Клубеньковые бактерии дикорастущих бобовых растений Южного Урала и молекулярное конструирование их искусственных ассоциаций с небобовыми растениями

Список литературы

1. Баймиев Ал.Х., Губайдуллин И. И., Баймиев Ан.Х., Чемерис A.B. Сайт-направленный мутагенез углеводсвязывающих участков лектинов бобовых растений с использованием инвертированной ПЦР // Мол. биология. 2007. -Т. 41,-С. 940−942.
2. Баулина О.И., Агафодорова М. Н., Корженевская Т. Г., Гусев М. В., Бутенко Р. Г. Цианобактерии в искусственно созданной ассоциации с каллусной тканью табака // Микробиология. 1984. — Т. 53, — № 6. — С. 9 971 002.
3. Белимов A.A., Сафронова В. И. АЦК деаминаза и растительно-микробные взаимодействия // Сельхоз. биология. 2011. — № 3. — С. 23−28.
4. Вишнякова М.А., Бурляева М. О., Алпатьева Н. В., Чесноков Ю.В. RAPD анализ видового полиморфизма рода чина Lathyrus L. семейства Fabaceae Lindl. // Вестник ВОГиС. 2008. — Т. 12, — № 4. — С. 595−607.
5. Глаголева О.Б., Ковальская Н. Ю., Киреев И. И., Лобакова Е. С., Умаров М. М. Паранодуляция рапса при инокуляции азотфиксирующими ризосферными бактериями // Микробиология. 1997. — № 66. — С. 545−552.
6. Горелова O.A., Лобакова Е. С., Корженевская Т. Г. Инфекционная активность изолированных из природных симбиозов цианобактерий вотношении нееимбиотрофных растений // Вестн. Московского ун-та. Сер. 16, Биология. 2004. — № 3. — С. 39−44.
7. Долгих Е. А., Леппянен И. В., Жуков В. А., Цыганов В. Е., Тихонович И. А. Экспрессия рекомбинантных белков-рецепторов SymlO и Sym37 Pisum sativum, вовлеченных в связывание липохитоолигосахаридов nod-факторов // Экол. генет. .-2010.-Т. 8, № i.c. 3−11.
8. Дрейпер Д., Скотт Р., Армитидж Ф., Уолден Р. / Генная инженерия растений (лабораторное руководство). М.: Мир, 1991. 173 с.
9. Жуков В.А., Рычагова Т. С., Штарк О. Ю., Борисов А. Ю., Тихонович И. А. Генетический контроль специфичности взаимодействия бобовых растений с клубеньковыми бактериями // Экол. генет. 2008. — Т. 7, — № 4. — С. 12−19
10. Карпунина Л.В. Значение углевод-белкового узнавания и роль лектинов при формировании различного рода азотфиксирующих систем // Успехи соврем, биологии. 2002. — Т. 122, — № 6. — С. 548−556.
11. Кауричева С.И. Практикум по почвоведению / М.: «Колос», 1973. 279 с.
12. Кацы Е.И. Молекулярная генетика ассоциативного взаимодействия бактерий и растений / М.: Наука, 2007.- 86 с.
13. Ковальская Н.Ю., Лобакова Е. С., Умаров М. М. Формирование искусственного азотфиксирующего симбиоза у растений рапса {Brassicanapus var. napus) в нестерильной почве // Микробиология. 2001. — Т. 50, — № 5.-С. 701−708.
14. Кретович В.А. Биохимия усвоения азота воздуха растениями / М.: Наука, 1994.- 168 с.
15. Лахтин В.М. Молекулярная организация лектинов // Мол. биология. -1994. Т. 28, — № 2. — С. 245−273.
16. Максимов И. В., Абизгильдина Р. Р., Пусенкова Л. И. Стимулирующие рост растений микроорганизмы как альтернатива химическим средствам защиты от патогенов (обзор) // Прикл биохим микробиол. 2011, — Т. 47, — № 4,-С. 373−385
17. Мишустин E.H., Шильникова В. К. Клубеньковые бактерии и инокуляционный процесс / М.: Наука, 1973.- 288 с.
18. Новикова Н.И., Сафронова В. И., Павлова Е. А. // Сельскохозяйств. биология. 1992. — Т.5. — С. 105−109.
19. Овцына А.О., Тихонович И. А. Структура, функции и возможность практического применения сигнальных молекул, инициирующих развитие бобово-ризобиального симбиоза // Экол. генет. 2004. — Т. 2, — № 3. — С. 1424.
20. Онищук О.П., Симаров Б. В. Генетическая изменчивость нодуляционной конкурентоспособности у клубеньковых бактерий и ее использование в селекции. // Генетика. 1995. — Т. 31, — № 3, — С. 293 — 303
21. Парийская А.Н., Клевенская И. Л. Распространение в природе и возможные пути эволюции азотфиксирующего симбиоза // Успехи микробиол. 1979. — Т. 14. — С. 124−147.
22. Пирузян Э.С., Андрианов В. М. Плазмиды агробактерий и генетическая инженерия растений / М.: Наука, 1985. 289 с.
23. Проворов H.A. Взаимосвязь между таксономией бобовых и специфичностью их взаимодействия с клубеньковыми бактериями // Ботан. журн. 1992. — Т. 77, — № 8. — С. 21−32.
24. Проворов H.A., Воробьев H.H. Эволюционная генетика клубеньковых бактерий: молекулярные и популяционные аспекты // Генетика. 2000. — Т. 36, -№ 12.-С. 1573−1587
25. Проворов H.A. Генетико-эволюционные основы учения о симбиозе // Журн. Общей биологии. 2001. — Т. 62,-№ 6.- С. 472−495.
26. Проворов H.A., Тихонович И. А. Экологогенетические принципы селекции растений на повышение эффективности взаимодействия с микроорганизмами // С.-х. биология. 2003. — № 3. — С. 11−25.
27. Проворов Н. А. Растительно-микробные симбиозы как эволюционный континуум // Журн. Общей биологии. 2009. — Т. 70, — № 1, — С. 10−34
28. Проворов H.A., Воробьев Н. И. Роль горизонтального переноса генов в эволюции клубеньковых бактерий, направляемой растением-хозяином // Успехи современной биологии. 2010. — Т. 130, — № 4. — С. 336−345
29. Радчук В.В., Блюм Я. Б. Успехи и проблемы генетической трансформации растений семейства крестоцветных // Цитология и генетика. -2005. -№ 3. С. 13−29.
30. Садовникова Ю.Н., Беспалова JI.A., Антонюк Л. П. Агглютинин зародышей пшеницы является фактором роста для бактерии Azospirillum brasilense II Докл. Акад. наук. 2003. — Т. 389, № 4. — С. 544−546.
31. Серебряков И.Г. Экологическая морфология растений. 1962. Жизненные формы покрытосеменных и хвойных. М.: Высш. шк., 387 с.
32. Сидорова К.К., Шумный В. К., Власова Е. Ю., Гляненко М. Н., Мищенко Т. М., Майстренко Г. Г. Симбиогенетика и селекция макросимбионта на повышение азотфиксации на примере гороха (Pisum sativum L.) // Вестник ВОГиС. 2010, — Т. 14, — № 2. — С. 357−374
33. Симаров Б.В., Аронштам A.A., Новикова Н. И. и др. Генетические основы селекции клубеньковых бактерий / Л.: Агропромиздат, 1990. 192 с.
34. Тильба В.А., Бегун С. А., Якименко М. В. Использование штаммов ризобий сои для стимулирования роста и оздоровления сельскохозяйственных культур (опыты с зернобобовыми культурами и томатами) // Вестн. РАСХН. 2004. — № 5. — С. 28−30.
35. Тихонович И.А., Проворов H.A. Пути использования адаптивного потенциала систем «растение-микроорганизм» для конструирования высокопродуктивных агрофитоценозов // С.-х. биология. 1993. — № 5. — С. 36−46.
36. Тихонович И.А., Проворов H.A. Генетика симбиотической азотфиксации с основами селекции / СПб.: Наука, 1998. 194 с.
37. Тихонович И.А., Проворов H.A. Принципы селекции растений на взаимодействие с симбиотическими микроорганизмами // Вестник ВОГиС. -2005. Т. 9, — № 3. — С. 295−305.
38. Тихонович И. А, Проворов H.A., 2009. Симбиозы растений и микроорганизмов / С.-Пб.: Изд-во С.-Петерб. ун-та, 210с.
39. Умаров М.М., Бурлуцкая Т. Р., Давидович О. Г., Матвеева Н. Г. Влияние инокуляции бактериями рода Pseudomonas на процессы азотного цикла в ризосфере небобовых растений // Микробиология. 1994. — Т. 63, — № 2. — С. 326−333.
40. Умаров М.М. Современное состояние и перспективы исследований микробной азотфиксации / Перспективы развития почвенной биологии. М.: МАКС Пресс, 2001. С. 47−56.
41. Шакирова Ф.М., Безрукова М. В. Современные представления о предпологаемых функциях лектинов растений // Журн. общ. биологии. -2007. Т. 68, — № 2. — С. 109−125.
42. Шестаков С.В. Как происходит и чем регулируется горизонтальный перенос у бактерий // Экологич. генетика. 2007. — Т. 5, — № 2. — С. 12−24.
43. Abd-Alla М.Н. Use of organic phosphorous by Rhizobium leguminosarum bv. viciae phosphatases. // Biol. Fertil. Soils. 1994. — V. 8. — P. 216−218.
44. Achouak W., Christen R., Barakat M., Martel M.H., Heulin T. Burkholderia caribensis sp. nov., an exopolysaccharide-producing bacterium isolated from vertisol microaggregates in Martinique // Int. J. Syst. Bacteriol. 1999. — V. 49. -P. 787−94.
45. Aguilar O.M., Grasso D.H., Riccillo P.M., Lopez M.V., Szafer E. Rapid identification of bean Rhizobium isolates by a niffl gene-pcr assay // Soil Biol Biochem. 1998.-V. 30. -P.1655−1661
46. Aguilar O.M., Riva O., Peltzer E. Analysis of Rhizobium etli and of its symbiosis with wild Phaseolus vulgaris supports coevolution in centers of host diversification // Proc. Natl. Acad. Sci. USA. 2004. — V.101. — P. 13 548−13 553
47. Akasaka Y., Mii M., Daimon H. Morphological alterations and root nodule formation in Agrobacterium rhizogenes-mediated transgenic hairy roots of peanut (Arachis hypogaea L.) // Ann. Bot. 1998. — V. 81. — P. 355−362.
48. Alexandre A., Laranjo M., Young J.P., Oliveira S. Dnaj is a useful phylogenetic marker for alphaproteobacteria // Int. J. Syst. Evol. Microbiol. 2008. -V. 58.-P. 2839−2849
49. Alikhani H.A., Saleh-Rastin N., Antoun H. Phosphate solubilization activity of rhizobia native to Iranian soils. // Plant Soil. 2006. — V. 287. — P. 35−41.
50. Algawadi A.R., Gaur A.C. Inoculation of Azospirillum brasilense and phosphate-solubilizing bacteria on yield of sorghum (Sorghum bicolor L. Moench) in dry land. // Trop. Agric. 1992. — V. 69. — P. 347−350.
51. Amara M.A.T., Dahdoh M.S.A. Effect of inoculation with plantgrowth promoting rhizobacteria (PGPR) on yield and uptake of nutrients by wheat grown on sandy soil. // Egyptian J. Soil Sci. 1997. — V. 37. — P. 467⁸⁴.
52. Amarger N., Macheret V., Laguerre G. Rhizobium gallicum sp. nov. and Rhizobium giardinii sp. nov., from Phaseolus vulgaris nodules // Int. J. Syst. Bacteriol. 1997. — V. 47. — P. 996−1006.
53. Aminov R. I. Horizontal gene exchange in environmental microbiota // Front Microbiol. 2011. — V. 2. — doi: 10.3389.
54. Andam C.P., Parker M.A. Novel alphaproteobacterial root nodule symbiont associated with Lupinus texensis // Appl. Environ. Microbiol. 2007a. — V. 73, -N. 17.-P. 5687−5691
55. Andam C. P., Mondo S. J., Parker M. A. Monophyly of nodA and nifH Genes across Texan and Costa Rican Populations of Cupriavidus Nodule Symbionts // Appl. Environ. Microbiol. 2007b. — V. 73, — N.14. — P. 4686−4690.
56. Andrade D.S., Murphy P.J., Giller K.J. The diversity of Phaseolus-nodulating rhizobial populations is altered by liming of acid soils planted with Phaseolus vulgaris L. in Brazil. // Appl. Environ. Microbiol. 2002. — V. 68. — P. 4025⁰³⁴
57. Antoine R., Locht C. Isolation and molecular characterization of a novel broad-host-range plasmid from Bordetella bronchiseptica with sequence similarities to plasmids from gram-positive organisms // Mol. Microbiol. 1992. -V. 6.-P. 1785−1799.
58. Antoun H., Beauchamp C.J., Goussard N., Chabot R., Lalande R. Potential of Rhizobium and Bradyrhizobium species as plant growth promoting rhizobacteria on non-legumes: Effect on radishes (Raphanus sativus L.). // Plant Soil.: 1998. -V. 204. P. 57−68.
59. Arora N.K., Kang S.C., Maheshwari D.K. Isolation of siderophoreproducing strains of Rhizobium meliloti and their biocontrol potential against Macrophomina phaseolina that causes charcoal rot of groundnut. // Curr. Sci. 2001. — V. 81. — P. 673−677.
60. Arshad M., Shaharoona B., Mahmood T. Inoculation with Pseudomonas spp. containing ACC deaminase partially eliminates the effects of drought stress on growth, yield, and ripening of pea (Pisum sativum L.). // Pedosphere. 2008. — V. 18.-P. 611−620.
61. Atzorn R., Crozier A., Wheeler C.T., Sandberg G. Production of gibberellins and indol-3-acetic acid by Rhizobium phaseoli in relation to nodulation of Phaseolus vulgaris roots. // Planta. 1988. — V. 175. — P. 532−538.
62. Ausubel F.M., Brent R., Kingston R.E., Moore D.D., Seidman J.G., Smith J.A., Struhl K. / Current protocols in molecular biology. 1987. John Wiley&Sons, NY
63. Baldani J.I., Weaver R.W., Hynes M.F., Eardly B.D. Utilization of carbon substrates, electrophoretic enzyme patterns, and symbiotic performance of plasmid-cured clover rhizobia // Appl. Environ. Microbiol. 1992. — V. 58. — N. 7. -P. 2308−2314
64. Baier R., Schiene K., Kohring B., Flaschen E., Niehaus K. Alfalfa and tobacco cells react differentially to chitin oligosaccharides and Sinorhizobium meliloti nodulation factors. // Planta. 1999. — V. 210. — P. 157−164.
65. Bailly X., Olivieri I., Brunei B., Cleyet-Marel J.C., Bena G. Horizontal gene transfer and homologous recombination drive the evolution of the nitrogen-fixing symbionts of Medicago species. // J. Bacteriol. 2007. — V. 189. — P. 5223^5236
66. Banerjee M., Yesmin L. Sulfur-oxidizing plant growth promoting rhizobacteria for enhanced canola performance / US Patent. 2002. N. 7 491 535.
67. Bardin S., Dan S., Osteras M., Finan T.M. A phosphate transport system is required for symbiotic nitrogen fixation by Rhizobium meliloti // J Bacteriol. -1996.-V. 178. -N. 15. P. 4540−4547.
68. Barnett M.J., Fisher R.F., Jones T., Komp C., Abola A.P. et al. Nucleotide sequence and predicted functions of the entire Sinorhizobium meliloti pSymA megaplasmid. // Proc. Natl. Acad. Sci. USA. 2001. — V. 98. — P. 9883−9888
69. Barnett M.J., Fisher R.F. Global gene expression in the rhizobial-legume symbiosis. // Symbiosis. 2006. — V. 42. — P. 1−24
70. Barrett C.F., Parker M.A. Prevalence of Burkholderia sp. nodule symbionts on four mimosoid legumes from Barro Colorado Island, Panama. // Syst Appl Microbiol. 2005. — V. 28. — P. 57−65
71. Bashan Y. Inoculants of plant growth-promoting bacteria for use in agriculture // Biotech. Adv. 1998. — V. 16, N 4. — P. 729−770.
72. Batut J., Andersson S.G., O’Callaghan D. The evolution of chronic infection strategies in the alpha-proteobacteria. // Nat Rev Microbiol. 2004. — V. 2. — P. 933−945
73. Becker A., Fraysse N., Sharypova L. Recent advances in studies on structure and symbiosisrelated function of rhizobial K-antigens and lipopolysaccharides. // Mol Plant Microbe Interact. 2005. — V. 18. — P. 899−905
74. Benata H., Mohammed O., Noureddine B., Abdelbasset B., Abdelmoumen H., Muresu R., Squartini A., El Idrissi M.M. Diversity of bacteria that nodulate Prosopis juliflora in the eastern area of Morocco. // Syst Appl Microbiol. 2008. -V. 31.-P. 378−386
75. Benhizia Y., Benhizia H., Benguedouar A., Muresu R., Giacomini A., Squartini A. Gamma proteobacteria can nodulate legumes of the genus Hedysarum. // Syst Appl Microbiol. 2004. — V. 27. — P. 462⁶⁸
76. Bentley S.D., Parkhill J. Comparative genomic structure of prokaryotes. // Annu Rev Genet. 2004. — V. 38. — P. 771−792
77. Belimov A.A., Kojemiakov P.A., Chuvarliyeva C.V. Interaction between barley andmixed cultures of nitrogen fixing and phosphate-solubilizing bacteria. // Plant Soil. // 1995. — V. 173. — P. 29−37.
78. Berg R.H., Liu L., Dawson J.O., Savka A.M., Farrand S.K. Induction of pseudoactinorhizae by the plant pathogen Agrobacterium rhizogenes // Plant Physiol. 1992. — V.98. — P. 777−779.
79. Birnboim H.C., Doly J. A rapid alkaline extraction procedure for screening recombinant plasmid DNA // Nucl. Acids Res. 1979. — V. 7. — PJ513−1523^
80. Biswas J.C., Ladha J.K., Dazzo F.B., Yanni Y.G., Rolfe B.G. Rhizobial inoculation influences seedling vigor and yield of rice //Agron. J. 2000. — V. 92. — P. 880−886.
81. Bhatia R., Dogra R.C., Sharma P.K. Construction of green fluorescent protein (GFP)-marked strains of Bradyrhizobium for ecological studies. // J. Appl. Microbiol. 2002. — V. 93. — P. 835−839.
82. Bohlool B.B., Schmidt E.L. Lectins: a possible basis for specificity in the Rhizobium-legume symbiosis // Science. 1974. — V. 185. — P. 269−275.
83. Boisson-Dernier A., Chabaud M., Garcia F., Becard G., Rosenberg C. and Barker D.G. Hairy roots of Medicago truncatula as tools for studying nitrogen-fixing and endomycorrhizal symbioses // Mol. Plant-Microbe Interact. 2001. — V. 14.-P. 693−700.
84. Bokman S. H., Ward W. W. Renaturation of Aequorea Green-Fluorescent Protein // Biochem. Biophys. Res. Commun. 1981. — V. 101. — P. 1372—1380.
85. Boussau B., Karlberg E.O., Frank A.C., Legault B.A., Andersson S.G. Computational inference of scenarios for alpha-proteobacterial genome evolution // Proc. Nat. Acad. Sci. USA. 2004. — V. 101. — P. 9722−9727.
86. Breil B.T., Ludden P.W., Triplett E. W. DNA sequence and mutational analysis of genes involved in the production and resistance of the antibiotic peptide trifolitoxin. // J. Bacteriol. 1993. — V. 175. — P. 3693−3702.
87. Brelles-Marino G., Costa G.A., Boiardi J.L. Enhancement of infection thread formation by Rhizobium etli incubated with bean seed lectin // Microbiol. Res. -1996.-V. 151.-P. 243−246.
88. Brewin N.J., Dejong T.M., Phillips D.A., B. Johnston A.W. Co-transfer of determinants for hydrogenase activity and nodulation ability in Rhizobium leguminosarum // Nature. 1980. — V. 288. — P. 77−79.
89. Brewin N.J. Tissue and cell invasion by Rhizobium'. the structure and development of infection threads and symbiosomes / The Rhizobiaceae. (Spaink H.P., Kondorosi A., Hooykaas P.J.J., Eds.). Kluwer Acad. Publ., Dordrecht, -1998. P. 417 -429.
90. Brewin N.J. Plant cell wall remodeling in the Rhizobium-legume symbiosis // Crit Rev Plant Sci. 2004. — V. 23. — P. 293−316.
91. Brockwell J., Bottomley P.J., Thies J.E. Manipulation of rhizobia microflora for improving legume productivity and soil fertility: a critical assessment // Plant Soil. 1995. — V. 174. — P. 143−180.
92. Broekaert W.F., van Parijs J., Leyns F., Joos H., Peumans W.J. A chitin-binding lectin from stinging nettle rhizomes with anti-fungal properties // Science. 1989. — V. 245. — P. 1100−1102.
93. Brom S., de los Santos A.G., de Lourdes Girard M., Davilla G., Palacios R., Romero D. Highfrequency rearrangements in Rhizobium leguminosarum bv. phaseoli plasmids // J. Bacteriol. 1991. — V. 173. — P. 1344−1346.
94. Bromfield E.S.P., Lewis D.M., Barran L.R. Cryptic plasmid and rifampin resistance in Rhizobium meliloti influencing nodulation competitiveness // J. Bacteriol. 1985.-V. 164.-P. 410−413
95. Broothaerts W., Mitchell H.J., Weir B., Kaines S., Smith L.M., Yang W., Mayer J.E., Roa-Rodnguez C., Jefferson R.A. Gene transfer to plants by diverse species of bacteria // Nature. 2005. — V. 433. — P. 629−633
96. Broughton W.J., Perret X. Genealogy of legume-Rhizobium symbioses // Curr Opin Plant Biol. 1999. — V. 2. — P. 305−311
97. Broughton W.J., Jabbouri S., Perret X. Keys to symbiotic harmony // J Bacteriol. 2000. — V. 182.-P. 5641−5652
98. Brown J. R. Ancient horizontal gene transfer // Nature Rev. Genet. 2003. — V. 4.-P. 121−132.
99. Buchanan R.E. What names should be used for the organisms producing nodules on the roots of leguminous plants? // Proc Iowa Acad Sci. 1926. — V. 33. -P. 81−90
100. Burd G.I., Dixon D.G., Glick B.R. Plant growth-promoting bacteria that decrease heavy metal toxicity in plants. // Can. J. Microbiol. 2000. — V. 46. — P. 237−245.
101. Campbell G.R.O., Reuhs B.L., Walker G.C. Chronic intracellular infection of alfalfa nodules by Sinorhizobium meliloti requires correct lipopolysaccharide core // Proc. Natl. Acad. Sci. USA. 2002. — V. 99. — P. 3938−3943
102. Capoen W., Goormachtig S., de Rycke R., Schroeyers K., Holsters M. SrSymRK, a plant receptor essential for symbiosome formation // Proc. Natl. Acad. Sci. U.S.A. 2005. — V. 102. — P.10 369−10 374.
103. Casida L.E. Ensifer adhaerens gen. nov., sp. nov.: a bacterial predator of bacteria in soil // Int. J. Syst. Bacteriol. 1982. — V. 32. — P. 339−345
104. Chabot R., Antoun H., Cescas M. P. Stimulation de la croissance du mais et de la laitue romaine par des microorganismes dissolvant le phosphore inorganique. // Can. J. Microbiol. 1993. — V. 39. — P. 941−947.
105. Chabot R. H., Antoun H., Kloepper J., Beauchamp C. Root colonization of maize and lettuce by bioluminescent Rhizobium leguminosarum biovar phaseolus II Appl. Environ. Microbiol. 1996. — V. 62. — P. 2767−2772.
106. Chahboune R., Carro L., Peix A., Barrijal S., Velazquez E., Bedmar E.J. Bradyrhizobium cytisi sp. nov., isolated from effective nodules of Cytisus villosus // Int. J. Syst. Evol. Microbiol. 2011. — V. 61, — N. 12. — P. 2922−2927
107. Chang Y.L., Wang J.Y., Wang E.T., Liu H.C., Sui X.H., Chen W.X. Bradyrhizobium lablabi sp. nov., isolated from effective nodules of Lablab purpureus and Arachis hypogaea // Int. J. Syst. Evol. Microbiol. 2011. — V. 61, -N. 10. -P. 2496−502.
108. Chalfie M., Tu Y., Euskirchen G., Ward W. W., Prasher D. C. Green fluorescent protein as a marker for gene expression // Science. 1994. — V. 263. -V. 802—805.
109. Chao W.L. Antagonistic activity of Rhizobium spp. against beneficial and plant pathogenic fungi // Lett. Appl. Microbiol. 1990. — V. 10, — N. 5. — P. 213 215.
110. Chen W.X., Yan G.H., Li J.L. Numerical taxonomy study of fast-growing soybean rhizobia and a proposal that Rhizobium fredii be assigned to Sinorhizobium gen. nov. // Int. J. Syst. Bacteriol. 1988. — V. 38. — P. 392−397
111. Chen W.X., Li G.S., Qi Y.L., Wang EI, Yuan H.L., Li J.L. Mizobium huakuii sp. nov., isolated from the root nodules of Astragalus sinicus // Int. J. Syst. Bacteriol. 1991. — V. 41. — P. 275−280
112. Chen W., Xie Y., Chen T. Studies on para-nodulation of wheat and nitrogen fixation //10 Int. Congr. on Nitrogen fixation: Abst. St.-Petersburg, 1995. P. 358.
113. Chen W.X., Tan Z.Y., Gao J.L., Li Y., Wang E.T. Rhizobium hainanense sp. nov., isolated from tropical legumes // Int. J. Syst. Bacteriol. 1997. — V. 47. — N. 3. P. 870−873.
114. Chen W.M., James E.K., Prescott A.R., Kierans M., Sprent J.I. Nodulation of Mimosa spp. by the beta-proteobacterium Ralstonia taiwanensis. // Mol. Plant Microbe Interact. 2003a. — V. 16. — P. 1051−1061
115. Chen W.M., Moulin L., Bontemps C., Vandamme P., Bena G., Boivin-Masson C. Legume symbiotic nitrogen fixation by beta-proteobacteria is widespread in nature // J Bacteriol. 2003b. — V. 185. — P. 7266−7272
116. Chen W.M., James E.K., Chou J.H., Sheu S.Y., Yang S.Z., Sprent J.I. Beta-rhizobia from Mimosa pigra, a newly discovered invasive plant in Taiwan // New Phytol. 2005. — V. 168. — P. 661−675
117. Chen W.M., Zhu W.F., Bontemps C., Young J.P.W., Wei G.H. Mesorhizobium alhagi sp. nov., isolated from wild Alhagi sparsifolia in northwestern China // Int. J. Syst. Evol. Microbiol. 2010. — V. 60. — P. 958−962
118. Chen W.M., Zhu W.F., Bontemps C., Young J.P., Wei G.H. Mesorhizobium camelthorni sp. nov., isolated from Alhagi sparsifolia // Int. J. Syst. Evol. Microbiol. -2011. -V. 61. P. 574−9.
119. Chrispeels M.J., Raikhel N.V. Lectins, lectin genes and their role in plant defense. // Plant Cell. 1991. — V. 3. — P. 1−9
120. Christey M. C. Transgenic crop plants using Agrobacterium rhizogenes-mediated transformation // Hairy roots: culture and applications / Harwood Acad. Pub., Amsterdam, 1997. P. 99−110.
121. Clewell D.B., Helinski D.R. Supercoiled circular DNA-protein complex in Escherichia coli: purification and induced conversion to an open circular DNA form // Proc. Natl. Acad. Sci. USA. 1969. — V. 62, N4, — P.1159−1166.
122. Cocking E.C., Davey M. R Nitrogen from the air for non-legume crops // Chem. Industry. 1991. — P. 831−835.
123. Cohen S., Chang A., Hsu L. Nonchromosomal Antibiotic Resistance in Bacteria Genetic Transformation of E. coli by R-factor DNA // Proc. Natl. Acad. Sci. USA. — 1972. — V. 69. — P. 2110−2114.
124. Collier R., Fuchs B., Walter N., Lutke W.K., Taylor C.G. Ex vitro composite plants: an inexpensive, rapid method for root biology // Plant J. 2005. — V. 43. -P. 449−457.
125. Conn H.J. Taxonomic relationships of certain non-sporeforming rods in soil // J. Bacteriol. 1938. — V. 36. — P. 320−321
126. Cren M., Kondorosi A., Kondorosi E. NolR controls expression of the Rhizobium meliloti nodulation genes involved in the core Nod factor synthesis // Mol. Microbiol. 1995. — V. 15. — P. 733−747
127. Cubitt A. B., Heim R., Adams S. R., Boyd A. E., Gross L. A., Tsien R. Y. Understanding, improving and using green fluorescent proteins // Trends Biochem. Sci. 1995. — V.20. — P. 448—455.
128. Dakora F.D. Defining new roles for plant and rhizobial molecules in sole and mixed plant cultures involving symbiotic legumes. // New Phytol. 2003. — V. 58. — P. 39−49.
129. Dalton D.A., Boniface C., Turner Z., Lindahl A., Kim H.J., Jelinek L., Govindarajulu M., Finger R.E., Taylor C.G. Physiological Roles of Glutathione S-Transferases in Soybean Root Nodules // Plant Physiology. 2009. — V. 150. — P. 521−530
130. Day B.R., McAlvin C.B., Loh J.T., Denny R.L., Wood T.C., Young N.D., Stacey G. Differential expression of two soybean apyrases, one of which is an early nodulin. Mol. Plant-Microbe Interact. 2000. — V. 13. — P. 1053−1070.
131. Dazzo F.B., Hubbell D.H. Cross-reactive antigens and lectins as determinants of symbiotic specificity in the Rhizobium-clover association // Appl. Environ. Microbiol. 1975. — V. 48. — P. 1140−1150.
132. Dazzo F.B., Truchet G. L, Sherwood J.E. Alteration of the trifolin A-binding capsule of Rhizobium trifolii -0403 by enzymes released from clover roots // Appl. Environ. Microbiol. 1982. — V. 44. — P. 478−490.
133. D’Haeze W., Holsters M. Nod factor structures, responses and perception during initiation of nodule development // Glycobiol. -2002. -V. 12. -P. 79−105 De Bary A. Die Erschaenung der symbiose / Strassburg: Verlag Von Karl J. Trubner. 1879. 30p.
134. Debelle F., Rosenberg C., Vasse J., Maillet F., Martinez E., Denarie J., Truchet G. Assignment of symbiotic developmental phenotypes to common and specific nodulation (nod) genetic loci of Rhizobium meliloti // J Bacteriol. 1986. -V. 168.-P. 1075−1086
135. De Hoff P. L., Brill L. M., Hirsch A. M. Plant lectins: the ties that bind in root symbiosis and plant defense // Mol Genet Genomics. 2009. — V. 282^- P.1−15
136. Denarie J., Cullimore J. Lipo-oligosaccharide nodulation factors: New class of signaling molecules mediating recognition and morphogenesis // Cell. 1993. — V. 74.-P. 951−954
137. Denarie J., Debbelle F., Prome J.C. Rhizobium lipo-chitin-oligosaccharide nodulation factors: signaling molecules mediating recognition and morphogenesis // Ann. Rev. Biochem. 1996. — V. 65. — P. 503−535.
138. Depret G., Laguerre G. Plant phenology and genetic variability in root and nodule development strongly influence genetic structuring of Rhizobium leguminosarum biovar viciae populations nodulating pea // New Phytol. 2008. -V. 179.-P. 224−235
139. Deshwal V.K., Dubey R.C., Maheshwari D. K. Isolation of plant growth promoting strains of Bradyrhizobium (Arachis) sp. with biocontrol potential against Macrophomina phaseolina causing charcol rot of peanut. // Curr. Sci. -2003.-V. 84.-P. 443—444.
140. Devine T.E., Kuykendall L.D. Host genetic control of symbiosis in soybean 0Glycine max L.) // Plant and Soil. 1996. — V. 186. — P. 173−187.
141. Diaz C.L., Melchers L.S., Hooykaas P.J.J., Lugtenberg B.J.J., Kijne J.W. Root lectin as a determinant of host-plant specificity in the Rhizobium-legume symbiosis //Nature. 1989. — V. 338.-P. 579−581.
142. Diaz C.L., Spaink H.P., Kijne J.W. Heterologous rhizobal lipochitin oligosaccharides and chitin oligomers induce cortical cell divisions in red clover root, transformed with the pea lectin gene // Mol. Plant Microbe Interact. 2000. -V. 13.-P. 268−276.
143. Dietrich C., Maiss E. Fluorescent labelling reveals spatial separation of potyvirus populations in mixed infected Nicotiana benthamiana plants // J. Gen. Virol. 2003. — V. 84. — P. 2871—2876.
144. Diouf D., Gherbi H., Prin Y., Franche C., Duhoux E., Bogusz D. Hairy root nodulation of Casuarina glauca: a system for the study of symbiotic gene expression in an actinorhizal tree // Mol. Plant Microbe Interact. 1995. — V. 8. -P. 532−537.
145. Diouf D., Diop T.A., Ndoye I. Actinorhizal, mycorhizal and rhizobial symbioses: how much do we know? // Afr. J. Biotechnol. 2003. — V. 2, N 1. — P. 1−7.
146. Dombrecht B., Tesfay M.Z., Verreth C., Heusdens C., Napoles M.C., Vanderleyden J., Michiels J. The Rhizobium etli gene iscN is highly expressed in bacteroids and required for nitrogen fixation. // Mol Gen Genomics. 2002. — V. 267.-P. 820−828
147. Doolittle W. F. Lateral genomics //Trends Cell Biol. 1999. — N 9. — P. M51. M9.
148. Downie J.A. Signalling strategies for nodulation of legumes by rhizobia // Trends Microbiol. 1994. — V. 2. — P. 318−324
149. Doyle J.J. Phylogenetic perspectives of nodulation: evolving views of plants and symbiotic bacteria // Trends Plant Sci. 1998. — V. 3. — P. 473−478
150. Duckworth D.H. Who discovered bacteriophage? // Bacteriol. Rev. 1976. -V. 40. — P. 793−802.
151. Duodu S., Brophy C., Connolly J., Svenning M.M. Competitiveness of native Rhizobium leguminosarum bv. trifolii strain for nodule occupancy is manifested during infection // Plant Soil. 2009. — V. 318. — P. 117−126.
152. Dyachok J.V., Tobin A.E., Price N.P.J., von Arnold S. Rhizobial Nod factors stimulate somatic embryo development in Picea abies // Plant Cell Rep. 2000. -V. 19.-P. 290−297
153. Eckhardt M.M., Baldwin I.R., Fred E.B. Studies on the root-nodule bacteria of Lupinus//J. Bacteriol. 1931. — V. 21. — P. 273−285.
154. Eckhardt T. A rapid method for the identification of plasmiddesoxyribonucleic acid in bacteria // Plasmid. 1978. — V.l. — P.584−588.
155. Edelman G.M., Cunningham B.A., Reede G.N., Becher J.W., Waxdal M.J., Wang J.L. The covalent and three-dimensional structure of concanavalin A. // Proc. Natl. Acad. Sci. USA. 1972. — V. 69. — P. 2580−2584
156. Egan E.S., Fogel M.A., Waldor M.K. Divided genomes: negotiating the cell cycle in prokaryotes with multiple chromosomes // Mol Microbiol. 2005. — V. 56. -P. 1129−1138.
157. Elliott G.N., Chen W.M., Bontemps C., Chou J.H., Young J.P., Sprent J. L, James E.K. Nodulation of Cyclopia spp. (Leguminosae, Papilionoideae) by Burkholderia tuberum // Ann. Bot. (Lond). 2007a. — V. 100. — P. .1403−1411,
158. Elliott G.N., Chen W.M., Chou J.H. et al. Burkholderia phymatum is a highly effective nitrogen-fixing symbiont of Mimosa spp. and fixes nitrogen ex planta // New Phytol. 2007b. — V. 173.-P. 168−180.
159. Elmerich C., Dezamaroczy M., Arsene F. et al. Regulation of nif geneexpression and nitrogen-metabolism in Azospirillum II Soil Biol. Biochem. 1997. -V. 29, N5−6.-P. 847−852.
160. Elzer P.H., Kovach M.E., Phillips R.W., Robertson G.T., Peterson K.M., Roop R.M. In vivo and in vitro stability of the broad-host-range cloning vector pBBRlMCS in six Brucella species // Plasmid. 1995. — V. 33. — P. 51−57.
161. Esashi Y. Ethylene and seed germination / In: The Plant Hormone Ethylene. (Matoo A.K., Suttle J.C., Eds.). CRC Press, Boca Raton, FL. USA. 1991. -P. 133−157.
162. Estrella M. J., Munoz S., Soto M. J. Ruiz O., Sanjuan J. Genetic diversity and host range of rhizobia nodulating Lotus tenuis in typical soils of the Salado River Basin (Argentina) // Appl. environ, microbial. 2009. — V.75, — N.4. — P. 1088−1098
163. Etzler M.E., Kalsi G., Ewing N.N., Roberts N.J., Day R.B., Murphy J.B. A nod factor binding lectin with apyrase activity from legume roots // Proc. Natl. Acad. Sci. U.S.A. 1999. — V.96.-P. 5856−5861.
164. Fedorova M, van de Mortel J., Matsumoto P.A., Cho J., Town C.D., VandenBosch K.A., Gantt J.S., Vance C.P. Genome-wide identification of nodule-specific transcripts in the model legume Medicago truncatula // Plant Physiol. -2002.-V. 130.-P. 519−537.
165. Feng J., Li Q., Hu H.L., Chen X.C., Hong G.F. Inactivation of the nod box distal half-site allows tetrameric NodD to activate nodA transcription in an inducer-independent manner // Nucleic Acids Res. 2003. — V. 31. — P. 31 433 156.
166. Fernandez L.A., Zalba P., Gomez M.A., Sagardoy M.A. Phosphate-solubilization activity of bacterial strains in soil and their effect on soybean growth under greenhouse conditions. // Biol. Fertil. Soils. 2007. — V. 43. — P. 805−809.
167. Finan T.M. Evolving insights: symbiosis islands and horizontal gene transfer // J. Bacteriol. V. 184. — P. 2855−2856.
168. Finan T.M., Kunkel B., De Vos G.F., Signer E.R. Second symbiotic megaplasmid in Rhizobium meliloti carrying exopolysaccharide and thiamine synthesis genes//J. Bacteriol. 1986.-V. 167.-N.l.-P. 66−72.
169. Finan T.M., Oresnik I., Bottacin A. Mutants of Rhizobium meliloti defective in succinate metabolism // J. Bacteriol. 1988. — V.170. — P. 3396−3403.
170. Fisher R. F, LongS.R. Rhizobium plant signal exchange // Nature. — 1992. -V. 357.-P. 655−660.
171. Fischer H.M. Genetic regulation of nitrogen fixation in rhizobia // Microbiol. Mol. Biol. Rev. -1994. -V. 58. -P. 352−386.
172. Flandung M., Gieffers W. Resistance reactions of leaves and tubers of rolC transgenic tetraploid potato to bacterial and fungal pathogens. Correlation with sugar, starch and clorophyll content // Physiol. Mol. PI. Pathol. 1993. — V. 42. -P. 123−132.
173. Fradkov A. F., Chen Y., Ding L., Barsova E. V., Matz M. V., Lukyanov S. A. Novel fluorescent protein from Discosoma coral and its mutants possesses a unique far-red fluorescence // FEBS Lett. 2000. — V. 479. — P. 127−130.
174. Frank B. Ueber die Pilzsymbiose der Leguminosen // Bet. Dtsch Bot. Ges. -1889.-V. 7.-P. 332−346.
175. Fraysse N., Couderc F., Poinsot V. Surface polysaccharide involvement in establishing the rhizobium-legume symbiosis // Eur. J. Biochem. 2003. — V. 270. -P. 1365−1380
176. Freiberg C., Fellay R., Bairoch A., Broughton W.J., Rosenthal A., Perret X. Molecular basis of symbiosis between Rhizobium and legumes // Nature. 1997. -V.387. — P. 394−401
177. Frost L.S., Leplae R., Summers A.O., Toussaint A. Mobile genetic elements: the agents of open source evolution // Nature Rev. Microbiol. 2005. — V. 3. — P. 722−732.
178. Frugier F., Kosuta S., Murray J.D., Crespi M., Szczyglowski K. Cytokinin: secret agent of symbiosis // Trends Plant Sci. 2008. — V. 13. — P. 115−120
179. Fujishige N.A., Lum M.R., de Hoff P.L., Whitelegge J.P., Faull K.F., Hirsch A.M. Rhizobium common nod genes are required for biofilm formation // Mol. Microbiol. 2008. — V. 67. — P. 504−515
180. Gage D.J. Infection and invasion of roots by symbiotic nitrogen-fixing rhizobia during nodulation of temperate legumes // Microbiol. Mol. Biol. Rev. -2004.-V. 68.-P. 280−300
181. Galal Y.G.M. Assessment of nitrogen availability to wheat (Triticum aestivum L.) from inorganic and organicNsources as affected by Azospirillum brasilense and Rhizobium leguminosarum inoculation. // Egyptian J.Microbiol. -2003.-V. 38.-P. 57−73.
182. Galibert F., Finan T.M., Long S.R., Puhler A., Abola P. et al. The composite genome of the legume symbiont Sinorhizobium meliloti // Science. 2001. — V. 293.-P. 668−672
183. Gamborg O.L., Miller R.A., Ojima K. Nutrient requirements of suspension cultures of soybean root cells // Exp. Cell Res. 1968. V.50. — P. 151−158.
184. Garcia-Fraile P., Rivas R., Willems A., Peix A., Martens M., Martinez-Molina E., Mateos P.F., Velazquez E. Rhizobium cellulosilyticum sp. nov., isolated from sawdust of Populus alba // Int. J. Syst. Evol. Microbiol. 2007. — V. 57. — P. 844 848
185. Garrity G.M., Bell J.A., Liburn T. Class I. Alphaproteobacteria class, nov. / In: Bergey’s manual of systematic bacteriology, part C. 2nd edn. (Brenner D.J., Krieg N.R., Staley J.T., Garrity G.M., Eds.). Springer, New York. 2005. — V. 2.
186. Gaunt M.W., Turner S.L., Rigottier-Gois L., Lloyd-Macgilp S.A., Young J.P.W. Phylogenies of atpD and recA support the small subunit rRNA-basedclassification of rhizobia // Int. J. Syst. Evol. Microbiol. 2001. — V. 51. — P. 2037−2048
187. Geurts R., Fedorova E., Bisseling T. Nod factor signaling genes and their function in the early stages of Rhizobium infection. // Curr Opin Plant Biol. 2005. -V. 8.-P. 346−352
188. Gevers D., Cohan F. M., Lawrence J. G. et al. Re-evaluating prokaryotic species // Nature Rev. Microbiol. 2005. — V. 3. — P. 733−739.
189. Gibson A.H., Child J.J., Pagan J.D., Scowcroft W.R. The induction of nitrogenase activity in Rhizobium by non-legume plant cells // Planta. 1976. — V. 128,-N.3.-P. 233−242.
190. Gibson D.M., Stack S., Krell K., House J. A comparison of soybean agglutinin in cultivars resistant and susceptible to Phytophthora megasperma var. sojae (race 1) // Plant Physiol. 1982. — V. 70. — P. 560−566
191. Gibson K.E., Kobayashi H., Walker G.C. Molecular determinants of a symbiotic chronic infection // Annu Rev Genet. 2008. — V. 42. — P. 413¹⁴¹
192. Giraud E., Moulin L., Vallenet D., Barbe V., Cytryn E. et al. Legumes symbioses: absence of nod genes in photosynthetic bradyrhizobia // Science. -2007.-V. 316.-P. 1307−1312
193. Giri A., Narasu M.L. Transgenic hairy roots. Recent trends and applications // Biotechnol. Adv. 2000. — V. 18. — P. 1−22.
194. Glagoleva O.B., Kovalskaya N.U., Umarov M.M. Endosymbiosis formation between nitrogen-fixing bacteria Pseudomonas caryophylli and rape root cells // Endosymbiosis Cell Res. 1996. — V. 11.-P. 147−158.
195. Glick B.R. The enhancement of plant growth by free-living bacteria // Can J Microbiol. 1995,-V. 41.-P. 109−117
196. Glick B.R., Penrose D.M., Li J. A model for the lowering of plant ethylene concentrations by plant growth promoting bacteria. // J. Theor. Biol. 1998. — V. 190.-P. 63−68.
197. Glick B.R., Patten C.L., Holguin G., Penrose D.M. Biochemical and Genetic Mechanisms Used by Plant Growth Promoting Bacteria / Imperial College Press, London. 1999. — 267p.
198. Gogarten J.P., Doolittle W.F., Lawrence J.G. Prokaryotic evolution in light of gene transfer. // Mol Biol Evol. 2002. — V. 19, — N. 12. — P. 2226−2238.
199. Gonzalez V., Bustos P., Ramirez-Romero M. A. et al. The mosaic structure of the symbiotic plasmid of Rhizobium etli CFN42 and its relation to other symbiotic genome compartments // Genome Biology. 2003. — V. 4, — N. 6. -R36
200. Gottfert M., Grob P., Hennecke H. Proposed regulatory pathway encoded by the nodV and nodW genes, determinants of host specificity in Bradyrhizobium japonicum. // Proc. Natl. Acad. Sci. USA. 1990. — V. 87. — P. 2680−2684
201. Graham D.E. The Isolation of high molecular weight DNA from whole organisms or large tissue masses // Anal. Biochem. 1978. — V. 85, N 2. — P. 609 613.
202. Graham P.H., Vance C.P. Legumes: importance and constraints to greater utilization. // Plant Physiol. 2003. — V. 131. — P. 872−877
203. Grichko V.P., Glick B.R. Amelioration of flooding stress by ACC deaminase containing plant growth promoting bacteria. // Plant Physiol. Biochem. 2001. -V. 39.-P. 11−17.
204. Gu C.T., Wang E.T., Tian C.F., Han T.X., Chen W.F., Sui X.H., Chen W.X. Rhizobium miluonense sp. nov., a symbiotic bacterium isolated from Lespedeza root nodules.// Int. J. Syst. Evol. Microbiol. 2008. — V. 58. — P. 1364−1368
205. Guan S.H., Chen W.F., Wang E.T., Lu Y.L., Yan X.R., Zhang X.X., Chen W.X. Mesorhizobium caraganae sp. nov., a novel rhizobial species nodulated with Caragana spp. in China // Int. J. Syst. Evol. Microbiol. 2008. — V. 58. — P. 26 462 653.
206. Gusev M.V., Korzhenevskaya T.G., Pyvovarova L.V., Baulina O.I., Butenko R.G. Introduction of a nitrogen-fixing cyanobacterium into tobacco shoot regenerates // Plant. 1986. — V. 167, N. 1. — P. 1−8.
207. Guo X., Flores M., Mavingui P., Fuentes S.I., Hernandez G., Davila G., Palacios R. Natural genomics design in Sinorhizobium meliloti: novel genomic architectures. // Genome Res. 2003. -V. 8. — P. 1810−1817
208. Gyaneshwar P., Hirsch A. M., Moulin L. et al. Legume-Nodulating Betaproteobacteria: Diversity, Host Range and Future Prospects // MPMI. 2011. — V. 24, -N. 11.-P. 1276−1288.
209. Hafeez F.Y., Safdar M.E., Chaudhry A.U., Malik K. A. Rhizobial inoculation improves seedling emergence, nutrient uptake and growth of cotton. // Aust. J. Exp. Agric. 2004. — V. 44. — P. 617−622.
210. Hakkila K., Matsimov M., Karp M., Virta M. Reporter genes lucFF, luxCDABE, gfp, and dsred have different characteristics in whole-cell bacterial sensors. // Anal. Biochem. 2002. — V. 301. — P. 235—242.
211. Hamblin J., Kent S.P. Possible role of phytohemagglutinin in Phaseolus vulgaris L. // Nature New Biol. 1973. — V. 245. — P. 28−29.
212. Hamelryck T.W., Loris R., Bouckaert J., Wyns L. Structural features of the legume lectins // Trends Glycosc. Glycotechnol. 1998. — V. 10. — P. 349−360.
213. Hamill J. D., Lidgett A. J. Hairy root cultures opportunities and key protocols for studies in metabolic engineering / Hairy roots: Culture and Applications. (Doran P., Ed.) Harwood Academic Publishers. Amsterdam, — 1997. -P. 1−30.
214. Han H.S. Lee K.D. Plant growth promoting rhizobacteria effect on antioxidant status, photosynthesis, mineral uptake and growth of lettuce under soil salinity. // Res. J. Agric. Biol. Sci. 2005. — V. 1. — P. 210−215.
215. Han T.X., Wang E.T., Wu L.J., Chen W.F., Gu J.G., Gu C.T., Tian C.F., Chen W.X. Rhizobium multihospitium sp. nov., isolated from multiple legume species native of Xinjiang, China. // Int. J. Syst. Evol. Microbiol. 2008. — V. 58. — P. 1693−1699
216. Handelsman J., Stabb E.V. Biocontrol of soilborne plant pathogens. // Plant Cell. 1996.-V. 8.-P. 1855−1869.
217. Hansen J., Jorgensen J.E., Stougaard J., Marcker A.K. Hairy roots a short cut to transgenic root nodules // Plant Cell Rep. — 1989. — V. 8. — P. 12−15.
218. Hara F., de Oliveira L.A. Physiological and ecological characteristics of rhizobio isolated deriving of acid and alic soils of Presidente Figueiredo. // Acta Amazonica. 2004. — V. 34. — P. 343−357.
219. Hara-Nishimura I., Inoue K., Nishimura M. A unique vauolar processing enzyme responsible for conversion several proprotein precursors into the mature forms // FEBS Letters. 1991. — V. 294. — P. 89−93.
220. Hardarson G. Methods for enhancing symbiotic nitrogen fixation // Plant and Soil. 1993,-V. 152.-P. 1−17.
221. Harrison M.J., Dewbre G.R. and Liu J. A Phosphate transporter from Medicago truncatula involved in the acquisition of phosphate released by arbuscular mycorrhizal fungi // Plant Cell. 2002. — V. 14. — P. 2413−2429.
222. Hawes M.C., Brigham L.A., Wen F., Woo H.H., Zhu Y. Function of root border cells in plant health: pioneers in the rhizosphere // Annu Rev Phytopathol. -V. 36.-P. 311−327.
223. Hawley T. S., Telford W. G., Hawley R. G. «Rainbow» reporters for multispectral marking and lineage analysis of hematopoietic stem cells. // Stem Cells. -2001a.-V.19.-P. 118—124.
224. Hawley T. S., Telford W. G., Ramezani A., Hawley R. G. Four-color flow cytometric detection of retrovirally expressed red, yellow, green, and cyan fluorescent proteins. // Biotechniques. 2001b. — V. 30. — P. 1028—1034.
225. Heidstra R., Bisseling T. Nod factor-induced hostresponsesi and mechanisms of Nod factor perception. // New Phytol. 1996. — V. 133. — P. 25¹³
226. Heim R., Prasher D. C., Tsien R. Y. Wavelength mutations and posttranslational autoxidation of green fluorescent protein. // Proc. Nat. Acad. Sci. USA. 1994,-V. 91.-P. 12 501—12 504.
227. Henzi M.X., Christey M.C., McNeil D.L. Factors that influence Agrobacterium r/zzzogewes-mediated transformation of broccoli (Brassica oleracea L. var. italica) // Plant Cell Rep. 2000. — V. 19. — P. 994−999.
228. Herridge D.F., Peoples M.B., Boddey R.M. Global inputs of biological nitrogen fixation in agricultural systems. // Plant Soil. 2008. — V. 311. — P. 1−18
229. Hirsch P. R, Van Montagu M., Johnston A.W.B., Brewin N.J., Schell, J. Physical identification of bacteriocinogenic, nodulation and other plasmids in strains of Rhizobium leguminosarum // Journal of General Microbiology. 1980. -V. 120.-P. 403−412
230. Hirsch A.M., Brill L.M., Lim P.O., Scambray J., Van Rhijn P. Steps toward defining the role of lectins in nodule development in legumes // Symbiosis. 1995. -V. 19.-P. 155−173.
231. Hirsch P.R. Population dynamics of indigenous and genetically modified rhizobia in the field // New Phytologist. 1996. — V. 133, — N. 1. — P. 159−171.
232. Hirsch A.M., Fang Y., Asad S., Kapulnik Y. The role of phytohormones in plant-microbe symbioses. // Plant Soil. 1997. — V. 194. — P. 171−184.
233. Hirsch A.M. Role of lectins (and rhizobial exopolysaccharides) in legume nodulation // Curr Opin Plant Biol. 1999. — V. 2. — P. 320−326
234. Hoang H.H., Gurich N., Gonzalez J.E. Regulation of motility by the ExpR/Sin quorumsensing system in Sinorhizobium meliloti. // J Bacteriol. 2008. — V. 190. -P. 861−871
235. Hoflich G., Wiehe W., Kohn G. Plant growth stimulation by inoculation with symbiotic and associative rhizosphere microorganisms. // Experienca. 1994. — V. 50.-P. 897−905.
236. Hong G.F., Burn J.E., Johnston A.W.B. Evidence that DNA involved in the expression of nodulation (nod) genes in Rhizobium binds to the product ofthe regulatory gene nodD. // Nucleic Acids Res. 1987. — V. 15. — P. 9677−9690
237. Horsh R.B., Fry J.E., Hoffmann N.L., Eichholtz D., Rogers S.C., Fraley R.T. A simple and general method for transferring genes into plants // Science. 1985. -V. 227.-P. 1229−1231.
238. Hotter G.S., Scott D.B. Exopolysaccharide mutants of Rhizobium loti are fully effective on a determinate nodulating host but are ineffective on an indeterminate nodulating host. // J Bacteriol. 1991. — V. 173. — P. 851−859
239. Hou B. C., Wang E. T., Li Y., et al. Rhizobial Resource Associated with Epidemic Legumes in Tibet // Microb Ecol. 2009a. — V. 57. — P.69−81
240. Hungria M., Stacey G. Molecular signals exchanged between host plants and rhizobia: basic aspects and potential application in agriculture. // Soil Biol Biochem. 1997. — V. 29. — P. 819−830
241. Hynes M.F., McGregor N.F. Two plasmids other than the nodulation plasmid are necessary for formation of nitrogen-fixing nodules by Rhizobium leguminosarum // Mol. Microbiol. 1990a. — V. 4, — N. 4. — P. 567−74.
242. Jackson M. B. Ethylene in root growth and development / In: The Plant Hormone Ethylene. (Matoo A.K., Suttle J. C., Eds.). CRC Press, Boca Raton, FL. USA. 1991.-P. 159−181.,
243. Jefferson R.A. Assaying Chimeric Genes in Plants: The GUS Gene Fusion System // Plant Mol. Biol. Rep. 1987. — V. 5. — P. 387⁰⁵.
244. Jensen J.S., Marcker K.A., Otten L., Schell J. Nodule-specific expression of chimaeric soybean leghaemoglobin gene in transgenicLotus corniculatus // Nature- 1986. V. 321.-P. 669−674.
245. Jones K.M., Kobayashi H., Davies B.W., Taga M.E., Walker G.C. How symbionts invade plants: the Sinorhizobium-Medicago model. // Nat Rev Microbiol. 2007. — V. 5. — P. 619−633
246. Jong J.P., Johnston A.W.B. The evolution of specificity in the legume-rhizobium symbiosis // Tree. 1989. — V. 4, — N. 11. — P. 341−349.
247. Jensen E.S., Sorensen L.H. Survival of Rhizobium leguminosarum is soil after addition as inoculant. // FEMS Microbiol Ecol. 1987. — V. 45. — P. 221−226
248. Jordan D.C., Allen O.N. Family I, Rhizobiaceae Conn, 1938 / In: Bergey’s manual of determinative bacteriology, 8th edn. (Buchanan R.E., Gibbons N.E., Eds.). The Williams & Wilkins Co, Baltimore. 1974. — P. 261−264
249. Jordan D.C. Transfer of Rhizobium japonicum Buchanan 1980 to Bradyrhizobium gen. nov., a genus of slow-growing, root nodule bacteria from leguminous plants. // Int. J. Syst. Bacteriol. 1982. — V. 32. — P. 136−139
250. Jordan D.C. Family III Rhizobiaceae / In: Bergeys manual of systematic bacteriology. (Krieg N.R., Holt J.G., Eds.). Williams and Wilkins Co., Baltimore.- 1984.-V. 1. P. 234−242
251. Jorgensen J.-E., Stougaard J., Marcker A., Marcker K.A. Root nodule specific gene regulation: Analysis of the soybean nodulin N23 gene promoter in heterologous symbiotic systems // Nucl. Acids Res. 1988. — V. 16. — P. 3940.
252. Juhas M., van der Meer J. R., Gaillard M., Harding R. M., Hood D. W., Crook D. W. Genomic islands: tools of bacterial horizontal gene transfer and evolution // FEMS Microbiol. Rev. 2009. — V. 33. — P. 376−393.
253. Jumas-Bilak E., Michaux-Charachon S., Bourg G., Ramuz M., Allardet-Servent A. Unconventional genomic organization in the alpha subgroup of the Proteobacteria. // J Bacteriol. 1998. — V. 180. — P. 2749−2755
254. Karsi A., Menanteau-Ledouble S., Lawrence M.L. Development of bioluminescent Edwardsiella ictaluri for noninvasive disease monitoring // FEMS Microbiol. Lett. 2006. — V. 260. — P. 216−223.
255. Kennedy I.R., Pereggerk L.L., Wood C. et al. Biological nitrogen fixation in non-leguminous field crops facilitating the evolution of an effective association between Azospirillum and wheat // Plant Soil. 1997. — Vol. 194, N. 1−2. — P. 6579.
256. Kannenberg E.L., Perzl M., Hartner T. The occurrence of hopanoid lipids in Bradyrhizobium bacteria. // FEMS Microbiol Lett. 1995. — V. 127. — P. 255−262
257. Kereszt A., Li D., Indrasumunar A., Nguyen C.D., Nontachaiyapoom S., Kinkema M., Gresshoff P.M. Agrobacterium rhizogenes-mediated transformation of soybean to study root biology // Nat. Protoc. 2007. — V. 2. — P. 948−952.
258. Kijne J.W., Diaz C.L., Pater S. Lectins in the symbiosis between Rhizobia and leguminous plants / In: Adv. Lectin Res. (Franz H., van Driessche E., Kasai K.J., Eds). Berlin: Ullstein Mosby. 1992. — P. 15−50.
259. Kijne J.W., Bauchrowitz M.A., Diaz C.L. Root lectin and Rhizobia II Plant Physiol. 1997. — V. 115. — P. 869−973.
260. Klee H.J., Hayford M.B., Kretzmer K.A., Barry G.F., Kishore G.M. Control of ethylene synthesis by expression of a bacterial enzyme in transgenic tomato plants.//Plant Cell. 1991,-V. 3.-P. 1187−1193.
261. Knosel D.H. Prufung von Bakterien auf Fahigkeit zur Sternbildung // Zentralbl Bakteriol Parasitenkd Infektionskr Hyg. 1962 — V.116. — P.79−100 (in German).
262. Knosel D.H. Genus IV. Phyllobacterium nom. Rev / In: Bergey’s manual of systematic bacteriology, vol 1 (Krieg N.R., Holt J.G., Eds). The Williams & Wilkins Co., Baltimore. 1984. — P. 254−256
263. Kobayashi H., Naciri-Graven Y., Broughton W.J., Perret X. Flavonoids induce temporal shifts in gene-expression of nod-box controlled loci in Rhizobium sp. NGR234. // Mol Microbiol. 2004. — V. 51. — P. 335−347
264. Konami Y., Yamamoto K., Osawa T., Irimura T. The primary structure of the Cytisus scoparus seed lectin and carbohydrareD binding peptide //J. Biochem. -1992. V. 112, — № 3. — P. 366−375.
265. Kondorosi E., Gyuris J., Schmidt J., John E., Hofmann D.B., Schell J., Kondorosi A. Positive and negative control of nod gene expression in Rhizobium meliloti is reqiured for optimal nodulation. // EMBO J. 1989. — V. 8. — P. 13 311 340
266. Kondorosi E., Pierre M., Cren M., Haumann U., Buire M., Hoffmann B., Schell J., Kondorosi A. Identification of NolR, a negative transacting factor controlling the nod regulon in Rhizobium meliloti. // J Mol Biol. 1991. — V. 222. -P. 885−896
267. Koonin E. V., Makarova K. S., Arvind L. Horizontal gene transfer in prokaryotes. Quantification and classification // Annu. Rev. Microbiol. 2001. — V. 55. — P. 709−742.
268. Kosugi S., Ohashf Y., Nakajima K., Arai Y. An Improved Assay for (3-Glucuronidase in Transformed Cells: Methanol Almost Completely Suppresses a Putative Endogenous -Glucuronidase Activity // Plant Sci. 1990. — V. 70. — P. 133−140.
269. Kovach M.E., Elzer P.H., Hill D.S., Robertson G.T., Farris M.A., Roop 2nd R.M., Peterson K.M. Four new derivatives of the broad-host-range cloning vector pBBRlMCS, carrying diVerent antibiotic-resistance cassettes // Gene. 1995. — V. 166.-P. 175−176
270. Krol M.J., Kobus J., Fuk B. Wiazanie azotu w parabrodawkach korzeni zboz przez Azospirillum lip. i Acin. like // Zezz. Nauk. Pol. AR Szczecinie. — 1997. -N. 68.-P. 153−161.
271. Krol J., Mazur A., Marczak M., Skorupska A. Syntenic arrangements of the surface polysaccharide biosynthesis genes in Rhizobium leguminosarum. // Genomics. 2007. — V. 89. — P. 237−247
272. Kundig C., Hennecke H., and Gottfert M. Correlated physical and genetic map of the Bradyrhizobium japonicum 110 genome // J. Bacteriol. 1993. — V. 75, -N. 3. — P. 613−622.
273. Kuykendall L.D., Saxena B., Devine T.E., Udell S.E. Genetic diversity in Bradyrhizobium japonicum Jordan 1982 and a proposal for Bradyrhizobium elkanii sp. nov. // Can J Microbiol. 1992. — V. 38. — P. 501−505
274. Y.L., Chen W.F., Han L.L., Wang E.T., Chen W.X. Rhizobium alkalisoli sp. nov., isolated from the legume Caragana intermedia growing in saline-alkaline soils. // Int. J. Syst. Evol. Microbiol. 2009a. — V. 59. — P. 3006−3011
275. Y.L., Chen W.F., Han L.L., Wang E.T., Zhang X.X., Chen W.X., Han S.Z. Mesorhizobium shangrilense sp. nov., isolated from root nodules of Caragana spp. // Int. J. Syst. Evol. Microbiol. -2009b. V. 59. — P. 3012−3018.
276. Maiden M.C. Multilocus sequence typing of bacteria. // Annu Rev Microbiol. 2006. — V. 60.-P. 561−88
277. Mandaci S., Dobres M. Sequence of a vegetative homolog of the pea seed lectin gene // Plant. Physiol. 1993. — V. 103, — N. 2. — P. 663−664.
278. Marchetti M., Capela D., Glew M. et al. Experimental evolution of a plant pathogen into a legume symbiont // PLoS Biology. 2010. — Vol.8, -N.l. -el000280.
279. Martens M., Delaere M., Coopman R., De Vos P., Gillis M., Willems A. Multilocus sequence analysis of Ensifer and related taxa. // Int. J. Syst. Evol. Microbiol. 2007. — V. 57. — P. 489−503
280. Martinez E., Pardo M.A., Palacios R., Cevallos M.A. Reiteration of nitrogen fixation gene sequences and specificity of Rhizobium in nodulation and nitrogen fixation in Phaseolus vulgaris. // J. Gen. Microbiol. 1985. — V. 131. — P. 1779— 1786
281. Martinez-Abarca F., Herrera-Cervera J.A., Bueno P., Sanjuan J., Bisseling T., Olivares J. Involvement of salicylic acid in the establishment of the Rhizobium meliloti-alfalfa symbiosis. // Mol. Plant Microbe Interact. 1998. — V. 11. — P. 153−155
282. Martinez-Romero E., Segovia L., Mercante F.M., Franco A.A., Graham P., Pardo M.A. Rhizobium tropici: a novel species nodulating Phaseolus vulgaris L. beans and Leucaena sp. trees. // Int. J. Syst. Bacteriol. 1991. — V. 41. — P. 417— 426
283. Martinez-Romero E. Coevolution in Rhizobium-legume symbiosis? // DNA Cell Biol. -2009. V. 28. — P. 361−370
284. Martyniuk S., Oron J., Martyniuk M. Diversity and numbers of root-nodule bacteria (rhizobia) in Polish soils. // Acta Soc Bot Polon. 2005. — V. 74. — P. 8386
285. Matz M. V., Fradkov A. F., Labas Y. A., Savitsky A. P., Zaraisky A. G., Markelov M. L., Lukyanov S. A. Fluorescent proteins from nonbioluminescent Anthozoa species. // Nat. Biotechnol. 1999. — V. 17. — P. 969—973.
286. Mavingui P., Flores M., Guo X., Davila G., Perret X., Broughton W.J., Palacios R. Dynamics of genome architecture in Rhizobium sp. strain NGR234. // J Bacteriol.-2002.-V. 184.-P. 171−176
287. McCormick D.B. Two interconnected B vitamins: Rhiboflavin and pyridoxine. // Physiol. Rev. 1989. — V. 69. — P. 1170−1198.
288. Mehboob I., Naveed M., Rhizobial Z.A.Z. Association with Non-Legumes: Mechanisms and Applications // Critical Reviews in Plant Science. 2009. — V. 28.-P. 432⁵⁶,
289. Menze A., Mollers C. Transformation of different Brassica napus cultivars with three different strains of Agrobacterium rhizogenes II Proc. 10th Int. Rapeseed Congress.- 1999. -P. 15−20.
290. Mercier A., Kay E., Simonet P. Horizontal Gene Transfer by Natural Transformation in Soil Environment // Soil Biology. 2006. — V. 8. — P. 355−373
291. Merzlyak E.M., Goedhart J., Shcherbo D. et al. Bright monomeric red fluorescent protein with an extended fluorescence lifetime // Nat Methods. 2007. -V. 4.-P. 555−557.
292. Michiels J., Dombrecht B., Vermeiren N., Xi C., Luyten E., Vanderleyden J. Phaseolus vulgaris is a non-selective host for nodulation. // FEMS Microbiol Ecol. 1998.-V. 26.-P. 193−205
293. Miller J. H Experiments in Molecular Genetics / Cold Spring Harbor: Cold Spring Harbor Lab. 1972. — 432 p.
294. Mimmack M.L., Hong G.F., Johnston A.W.B. Sequence and regulation of psrA, a gene on the Sym plasmid of Rhizobium leguminosarum biovar phaseoli which inhibits transcription of the psi genes. // Microbiology. 1994. — V. 140. -P. 455−461.
295. Minamisawa K., Ogawa K.I., Fukuhara H., Koga J. Indolepyruvate pathway for indol-3-acetic acid biosynthesis in Bradyrhizobium elkanii. // Plant Cell Physiol. 1996. — V. 37. — P. 449⁵³.
296. Mirelman D.E., Galun E., Sharon N., Lotan R. Inhibition of fungal growth by wheat germ agglutinin // Nature. 1975. — V. 256. — P. 414−416
297. Mishra R.P.N., Singh R.K., Jaiswal H.K., Kumar V., Maurya S. Rhizobium-mediated induction of phenolics and plant growth promotion in rice (Oryza sativa L.) // Curr. Microbiol. 2006. — V. 52. — P. 383−389.
298. Mitra R.M., Long S.R. Plant and bacterial symbiotic mutants define three transcriptionally distinct stages in the development of the Medicago truncatula/Sinorhizobium meliloti symbiosis. // Plant Physiol. 2004. — V.134. — P. 595−604
299. Moenne-Loccoz Y., Weaver R.W. Involvement of plasmids in saprophytic performance and sodium chloride tolerance of clover rhizobia W14−2 in vitro // Appl. Soil Ecol. 1996. — V. 3, — N. 2. — P. 137−148
300. Moulin L., Munive A., Dreyfus B., Boivin-Masson C. Nodulation of legumes by members of the beta-subclass of proteobacteria. // Nature. 2001. — V. 411. — P. 948−950
301. Moulin L., Bena G., Boivin-Masson C., Stepkowski T. Phylogenetic analyses of symbiotic nodulation genes support vertical and lateral gene co-transfer within the Bradyrhizobium genus. // Mol Phylogenet Evol. 2004. — V. 30. — P. 720−732
302. Muglia C. I., Grasso D. H., Mario Aguilar O. Rhizobium tropici response to acidity involvesactivation of glutathione synthesis // Microbiology. 2007. -V.153, — N4. — P.1286−1296
303. Munoz J.A., Coronado C., Perez-Hormaeche J., Kondorosi A., Ratet P., Palomares A.J. MsPG3, a Medicago sativa polygalacturonase gene expressed during the alfalfa-Rhizobium meliloti interaction // Proc. Natl. Acad. Sci. 1998. -V. 95.-P. 9687−9692.
304. Murashige T., Skoog F. A Revised Medium for Rapid Growth and Bioassays with Tobacco Tissue Cultures // Physiol. Plant. 1962. — V. 15. — P. 473⁹⁷.
305. Mutch L.A., Young J.P.W. Diversity and specifity of Rhizobium leguminosarum biovar viciae on wild and cultivated legumes. // Mol Ecol. 2004. — V. 13.-P. 2435−2444
306. Nautiyal S.S. Amethod for selection and characterization of rhizospherecompetent bacteria of chickpea. // Curr. Microbiol. 1997. — V. 34. — P. 12−17.
307. Nickoloff J.A. Methods in molecular biology / Humana Press. Totowa, NY. -1995.-V. 47.
308. Nie Y.E., Vesk M., Kennedy I.R., Srickandarajah S., Lane E., Tchan Y.T. Structure of 2,4-D induced 125 paranodules with Rhizobium on wheat // Phytochem. (Life Sci. Adv.). 1992. -N. 11. — P. 67−73.
309. Nie Y.F. Nitrogen fixation in 2,4-D forced associative wheat-diazotroph system // Intern. Workshop Assoc. Interactions Nitrogen-Fix. Bact. Plants (Saratov, June 5−8, 1995): Abstr. Saratov, 1995. P. 32−34.
310. Nilsson O., Olsson O. Getting to the root: The role of the Agrobacterium rhizogenes rol genes in the formation of hairy roots // Physiol. Plant. 1997. — V. 100.-P. 463-^73.
311. Normander B., Christensen B.B., Molin S., Kroer N. Effect of bacterial distribution and activity on conjugal gene transfer on the phylloplane of the bush bean (Phaseolus vulgaris) // Ibid. 1998. — V. 64, — N. 5. — P. 1902−1909.
312. Oldroyd G.E.D., Downie J.A. Calcium, kinases and nodulation signalling in legumes. // Nat Rev Mol Cell Biol. 2004. — V. 5. — P. 566−576
313. Oldroyd G.E.D., Downie J.A. Coordinating nodule morphogenesis with rhizobial infection in legumes // Annu Rev Plant Biol. 2008. — V. 59. — P. 519 546
314. Oresnik I.J., Twelker S., Hynes M.F. Cloning and characterization of a Rhizobium leguminosarum gene encoding a bacteriocin with similarities to RTX toxins. // Appl. Environ. Microbiol. 1999. — V. 65. — P. 2833−2840
315. Otten L., Heifer A. Biological activity of the rolB-like 5' end of the A4-orfS gene from the Agrobacterium rhizogenes TL-DNA // Mol. Plant-Microbe Interact. -2001.-V. 14.-P. 405−411.
316. Ozkoc I., Deliveli M.H. In vitro inhibition of the mycelial growth of some root rot fungi by Rhizobium leguminosarum biovar phaseoli isolates. // Turkish J. Biol. 2001. — V. 25. — P. 435−445.
317. Palmer K.M., Young J.P.W. Higher diversity of Rhizobium leguminosarum biovar viciae populations in arable soils than in grass soils. // Appl. Environ. Microbiol. 2000. — V. 66. — P. 2445−2450
318. Parniske M. Arbuscular mycorrhiza: the mother of plant root endosymbioses //Nat. Rev. Microbiol. -2008. V. 6, -N. 10. — P. 763−775.
319. Peck M.C., Fisher R.F., Long S.R. Diverse flavonoids stimulate NodDl binding to nod gene promoters in Sinorhizobium meliloti. // J Bacteriol. 2006. -V. 188.-P. 5417−5427
320. Peloquin J. J., Lauzon C. R., Potter S., Miller T. A. Transformed bacterial symbionts reintroduced to and detected in host gut. // Curr. Microbiol. 2002. -V.45.-P. 41—45.
321. Pena H.B., Reyes I. Nitrogen fixing bacteria and phosphate solubilizers isolated in lettuce (Lactuca sativa L.) and evaluated as plant growth promoters. // Intersciencia. 2007. — V. 32. — P. 560−565.
322. Peng G., Yuan Q., Li H., Zhang W., Tan Z. Rhizobium oryzae sp. nov., isolated from the wild rice Oryza alta. // Int. J. Syst. Evol. Microbiol. 2008. — V. 58.-P. 2158−2163
323. Perret X., Staehelin C., Broughton W.J. Molecular basis of symbiotic promiscuity. // Microbiol Mol Biol Rev. 2000. — V. 64. — P. 80−201
324. Perrine F.M., Prayito J., Frank J.J., Dazzo B., Rolfe B.G. Rhizobium plasmids are involved in the inhibition or stimulation of rice growth and development. // Aust. J. Plant Physiol. 2001. — V. 28. — P. 923−937.
325. Perrine-Walker F.M., Prayitno J., Rolfe B.G., Weinman J.J., Hocart C.H. Infection process and the interaction of rice roots with rhizobia // J. Exp. Bot. -2007. V. 58. — P. 3343−3350.
326. Petit A., Kuhle A., Marcker K.A., Tempe J. Transformation and regeneration of the legume Lotus corniculatus: a system for molecular studies of symbiotic nitrogen fixation // Mol. Gen Genet. 1987. — V. 207. — P. 245−250.
327. Peumans W.J., van Damme E.J.M. Lectins as plant defense proteins // Plant Physiol. 1995. — V. 109. — P. 347−353
328. Peumans W.J., Barre A., Hao Q., Rouge P., van Damme, Els J.M. Higher plants developed structurally different motifs to recognize foreign glycans // Trends Glycosci. Glycotechnol. 2000. — V. 12, N 64. — P. 83−101.
329. Pheler M., Petit M., Martin L., Duhoux E., Tempe J. Transformation and regeneration of a nitrogen-fixing tree, Allocasuarina verticillata II Lam. Biotechnol. 1991. — V. 9.-P. 461−466.
330. Phillips D.A., Joseph C.M., Yang G.-P., Martinez-Romero E., Sanborn J.R., Volpin H. Identification of lumichrome as a Sinorhizobium enhancer of alfalfa root respiration and shoot growth. // Proc. Nat. Acad. Sei. USA. 1999. — V. 96. — P. 12 275−12 280.
331. Porter J. R. Host range and implications of plant infection by Agrobacterium rhizogenes II Crit. Rev. Plant. Sei. 1991. — V. 10. — P. 387−421.
332. Prasher D. C., Eckenrode V. K., Ward W. W., Prendergast F. G., Cormier M. J. Primary structure of the Aequorea victoria green-fluorescent protein. // Gene. -1992.-V. 111.-P. 229—233.
333. Prell J., Poole P. Metabolic changes of rhizobia in legume nodules. // Trends Microbiol. 2006. — V. 14. — P. 161−168
334. Pueppke S.G., Broughton W.J. Rhizobium sp. strain NGR234 and R. fredii USDA257 share exceptionally broad, nested host ranges. // Mol Plant-Microbe Interact. 1999. — V. 12. — P. 293−318
335. Quan Z.X., Bae H.S., Baek J.H., Chen W.F., Im W.T., Lee S.T. Rhizobium daejeonense sp. nov. isolated from a cyanide treatment bioreactor. // Int. J. Syst. Evol. Microbiol. 2005. — V. 55. — P. 2543−2549
336. Quandt H.J., Puehler A., Broer I. Transgenic root nodules of Vicia hirsuta: A fast and efficient system for the study of gene expression in indeterminate-type nodules // Mol. Plant Microbe Interact. 1993. — V. 6, N 6. — P. 699−706.
337. Radeva G., Jurgens G., Niemi M., Nick G., Suominen L., Lindstrom K. Description of two biovars in the Rhizobium galegae species: biovar orientalis and biovar officinalis. // Syst Appl Microbiol. 2001. — V. 24. — P. 192−205
338. Radutoiu S., Madsen L. H., Madsen E. B. et al. Plant recognition of symbiotic bacteria requires two LysM receptor-like kinases // Nature. 2003. — V. 425, — N 6958. — P. 585−592.
339. Redecker D. Molecular identification and phylogeny of arbuscular mycorrhizal fungi // Plant and Soil. 2002. — V. 244. — P. 67−73.
340. Reid M. Ethylene in plant growth, development and senescence / In: Plant Hormones and Their Role in Plant Growth and Development. (Davies P.J., Ed.). Martinus Nijhoff, Den Hague. 1987. — P. 257−279.,
341. Relic B., Talmont F., Korsinska J., Golinowski W., Prome J.-C., Broughton W. J. Biological activity of Rhizobium sp. NGR234 Nod factors on macroptilium atropurpureum. // Mol. Plant-Microbe Interact. 1993. — V. 6. — P. 764−774.
342. Ren D.W., Chen W.F., Sui X.H., Wang E.T., Chen W.X. Rhizobium vignae sp. nov., a symbiotic bacterium isolated from multiple legume species // Int. J. Syst. Evol. Microbiol. 2011b. — V. 61. — P. 580−586.
343. Ribeiro R.A., Barcellos F.G., Thompson F.L., Hungria M. Multilocus sequence analysis of Brazilian Rhizobium microsymbionts of common bean (Phaseolus vulgaris L.) reveals unexpected taxonomic diversity. // Res Microbiol. -2009.-V. 160.-P. 297−306
344. Rivas R., Martens M., de Lajudie P., Willems A. Multilocus sequence analysis of the genus Bradyrhizobium. // Syst Appl Microbiol. 2009. — V. 32. — P. 101−110
345. Robertson B.K., Dreyfus B., Alexander M. Ecology of stem-nodulating Rhizobium and Azorhizobium in four vegetation zones of Senegal. // Microb Ecol. 1995.-V. 29.-P. 71−81
346. Robleto E.A., Kmiecik K., Oplinger E.S., Nienhuis J., Triplett E.W. Trifolitoxin production increases nodulation competitiveness of Rhizobium etli
347. CE3 under agricultural conditions. // Appl. Environ. Microbiol. 1998. — V. 64. -P. 2630−2633
348. Roche P., Maillet F., Plazanet C., Debelle F., Ferro M., Truchet G., Prome J.C., Denarie J. The common nodabc genes of Rhizobium meliloti are host-range determinants. // Proc. Natl. Acad. Sci. USA. 1996. — V. 93. — P. 15 305−15 310
349. Rodrigues F., van Hemert M., Steensma H. Y., Corte-Real M., Leao C. Red fluorescent protein (DsRed) as a reporter in Saccharomyces cerevisiae // J. Bacteriol. 2001. — V. 183.-P. 3791—3794.
350. Rodriguez H., Fraga R., Gonzalez T., Bashan Y. Genetics of phosphate solubilization and its potential applications for improving plant growthpromoting bacteria. // Plant Soil. 2006. — V. 287. — P. 15−21.
351. Rogel M.A., Hernandez-Lucas I., Kuykendall L.D., Balkwill D.L., Martinez-Romero E. Nitrogen-fixing nodules with Ensifer adhaerens harboring Rhizobium tropici symbiotic plasmids. // Appl. Environ. Microbiol. 2001. — V. 67. — P. 3264−3268.
352. Rossbach S., Kulpa D.A., Rossbach U., de Bruijn F.J. Molecular and genetic characterization of the rhizopine catabolism (mocABRC) genes of Rhizobium meliloti L5−30. // Mol Gen Genet. 1994. — V. 245. — P. 11−24
353. Rouge P., Pere D., Bourne Y. In vitro cleavage of the Lathyrus nissolia isolectin//Plant Sci. 1989.-V. 62.-P. 181−189.
354. Rouge P., Risler J. Evidence for the internal sequence homologies in leguminosae lectins: phylogenetical implications // Biochem. Systematics and Ecol. 1990.-V. 18.-P. 29−37.
355. Rudiger H. Purification and properties of blood group specific lectins from Vicia cracca // Eur. J. Biochem. 1977. — V. 72, — N. 2. — P. 317−322.
356. Rudiger H. Plant lectins more than just tools for glycoscientists: occurrence, structure, and possible functions of plant lectins // Acta Anat (Basel). — 1998. — V. 161.-P. 130−52.
357. Safronova V., Chizhevskaya E., Bullitta S., Andronov E., Belimov A., Charles T.C., Lindstrom K. Presence of a novel 16S-23S rRNA gene intergenicspacer insert in Bradyrhizobium canariense strains. // FEMS Microbiol Lett. -2007.-V. 269.-P. 207−212
358. Saha U., Sen M. Nitrogenase activity of diazotrophic strains of Candida tropicalis II Proc. Indian. Acad. Sci. (Plant Sci.). 1990. — V. 100, N 5. — P. 353 359
359. Sambrook J., Fritsch E., Maniatis T. Molecular Cloning: A Laboratory Manual, 2nd edn. / Cold Spring Harbor Laboratory Press, New York, Cold Spring Lab., 1989.- 1626 p.
360. Sanjuan J., Grob P., Gottfert M., Hennecke H., Stacey G. NodW is essential for full expression of the common nodulation genes in Bradyrhizobium japonicum. // Mol Plant-Microbe Interact. 1994. — V. 7. — P. 364−369
361. Sawada H., Kuykendall L. D., Young J. M. Changing concepts in the systematics of bacterial nitrogen-fixing legume symbionts //J. Gen. Appl. Microbiol. 2003. — V. 49. — P. 155−179.
362. Savka M.A., Liu L., Farrand S.K., Berg R.H., Dawson J.O. Induction of hairy roots or pseudoactinorhizae on Alnus glutinosa, A. acuminata and Elaeagnus angustifolia by Agrobacterium rhizogenes II Acta Ecol. 1992. — V. 13. — P. 423 431.
363. Schlaman H.R.M., Horvath B., Vijgenboom E., Okker R.J.H., Lugtenberg B.J.J. Suppression of nodulation gene expression in bacteroids of Rhizobium leguminosarum biovar viciae.// J Bacteriol. 1991. — V. 173. — P. 4277¹−287
364. Schmidt J., Rohrig H., John M., Wieneke U., Stacey G., Koncz C., Schell J. Alteration of plant growth and development by Rhizobium nodA and nodB genes involved in the synthesis of oligosaccharide signal molecules. // Plant J. 1993. -V. 4.-P. 651−658
365. Scholia M.H., Elkan G.H. Rhizobium fredii sp. nov., a fast-growing species that effectively nodulates soybeans. // Int. J. Syst. Bacteriol. 1984. — V. 34. — P. 484−486
366. Schwedock J., Long S.R. Nucleotide sequence and protein products of two new nodulation genes of Rhizobium meliloti, nodP and nodQ. // Mol. Plant-Microbe Interact. 1989. — V. 2. — P. 181−194
367. Scott M.P., Jung R., Muntz K., Nielsen N.C. A protease responsible for post-translational cleavage of a conserved Asn-Gly linkage in glycinin, the major seed storage protein of soybean // Proc. Natl. Acad. Sci. USA. 1992. — V. 89. — P. 685−662.
368. Sealey P.G., Southern E.M. Gel electrophoresis of DNA / In: Gel electrophoresis of nucleic acids. A practical approach. IRL Press, Oxford. 1982. -P. 3976.
369. Segovia L, Young JP, Martinez-Romero E. Reclassification of American Rhizobium leguminosarum biovar phaseoli type I strains as Rhizobium etli sp. nov. // Int. J. Syst. Bacteriol. 1993. — V. 43, — N. 2. — P. 374−377.
370. Sekar C., Prasad N.N., Sundaran M.D. Enhancement of polygalacturonase activity during auxing induced paranodulation and endorhizospphere colonization of Azospirillum in rice roots // Indian J. Exp. Biol. 2000. — V. 38, N 1. — P. 8083.
371. Sessitsch A., Hardarson G., de Vos W.M., Wilson K.J. Use of marker genes in competition studies of Rhizobium. // Plant and Soil. 1998. — V. 204. — P. 35−45.
372. Sharma V., Surolia A. Analyses of carbohydrate recognition by legume lectins: size of the combining site loops and their primary specificity // J. Mol. Biol. 1997. — V. 267. -N. 2. — P. 433¹⁴⁵.
373. Sharon N., Lis H. Lectins as cell recognition molecules. // Science. 1989. -V. 246. — P. 227−234
374. Sharon N., Lis H. Legume lectins a large family of homologous proteins // FASEB J. — 1990. — V. 4, — N. 14. — P. 3198−208.
375. Sheikh L.I., Dawar S., Zaki M.J., Ghaffar A. Efficacy of Bacillus thuringensis and Rhizobium meliloti wth nursery fertilizers in the control of root infecting fungi on mung bean and okra plants. // Pak. J. Bot. 2006. — V. 38. — P. 465⁷³.
376. Shimomura O., Johnson F. H., Saiga Y. Extraction, purification and properties of aequorin, a bioluminescent protein from the luminous hydromedusan, Aequorea. II J. Cell. Comp. Physiol. 1962. — V. 59. — P. 223—239.
377. Shoemaker N. B., Wang G. R., Salyers A. A. Multiple gene products and sequences required for excision of the mobilizable integrated Bacteroides element NBU1 // J. Bacteriol. 2000. — V. 182. — P. 928−936
378. Silva C., Kan F.L., Martinez-Romero E. Population genetic structure of Sinorhizobium meliloti and S. medicae isolated from nodules Medicago spp. in Mexico. // FEMS Microbiol Ecol. 2007. — V. 60. — P. 477¹⁸⁹
379. Singh C.D., Dadarwal K.R., Subba Rao N.S. Effectiveness of rhizobia from wild species of Arachis on the cultivated species A. hypogaea and their physiological characteristics // Zblt. Bakt. II. 1976. — V. 131, — N 1. — P. 72−78.
380. Skerman V.B.D., McGowan V., Sneath P.H.A. Approved lists of bacterial names. // Int. J. Syst. Bacteriol. 1980. — V. 30. — P. 225−420
381. Skorupska A., Janczarek M., Marczak M., Mazur A., Krol J. Rhizobial exopolysaccharides: genetic control and symbiotic functions. // Microb Cell Fact. -2006.-N. 5,-V. 7.-P. 1−19
382. Smith D.L., Prithiviraj B., Zhang F. Rhizobial signals and control of plant growth / In: Nitrogen Fixation: Global Perspectives. (Finan T.M., Brian M.R., Layzell D.B., Vessey K., Newton W.E., Eds.). CABI Publishing, Wallingford, UK. -2002.-P. 327−330.
383. Spaink H.P. Root nodulation and infection factors produced by rhizobial bacteria. // Annu Rev Microbiol. 2000. — V. 54. — P. 257−288
384. Spaink H.P. Regulation of plant morphogenesid by lipo-chitin oligosaccharides. // Crit. Rev. Plant Sci. 1996. — V. 15. — P. 559−582.
385. Stiller J., Martirani L., Tuppale S., Chian R.-J., Chiurazzi M., Gresshoff P.M. High frequency transformation and regeneration of transgenic plants in the model legume Lotus japonicus II J. Exp. Bot. 1997. — V. 48. — P. 1357−1365.
386. Streit W., Kosh K. Werner D. Nodulation competitiveness of Rhizobium leguminosarum bv phaseoli and Rhizobium tropici strains measured by glucuronidase (gus) gene fusion. // Biol. Fertil. Soil. 1992. — V. 14. — P. 140−144.
387. Stougaard J., Sandal N., Gren A., Kuhle A., Marcker K.A. 5' Analysis of the soybean leghemoglobin lbc3 gene: Regulatory elements required for promoter activity and organ specificity // EMBO J. 1987. — V. 6. — P. 3565−3369.
388. Stubbs M.E., Carver J.P., Dunn R.J. Production of pea lectin in Escherichia coli // J. Biol. Chem. 1986. — V. 261, — N. 14. — P. 6141−6142.
389. Sui X.H., Han L.L., Wang E.T. et al. Novel associations between rhizobial populations and legume species within the genera Lathyrus and Oxytropis grown in the temperate region of China. // Sei China Ser C-Life Sei. 2009. — V. 52, — N.2. -P. 182−192
390. Sullivan J. T, Patrick H. N, Lowther W. L, Scott D. B, Ronson C.W. Nodulating strains of Rhizobium loti arise through chromosomal symbiotic gene transfer in the environment. // Proc Natl Acad Sei U S A. 1995. — V. 92. — P. 8985−8989.
391. Sullivan J., Ronson C. Evolution of rhizobia by acquisition of a 500-kb symbiosis island that integrates into a phe-tRNA gene. // Proc. Natl. Acad. Sei. USA. 1998.-V. 95.-P. 5145−5149
392. Sujatha M.S., Balaji Petety V. Identification of common structural features of binding sites in galactose specific proteins // Proteins. — 2004. — V. 55, — N. 1. — P. 44−65.
393. Svenning M.M., Gudmundsson J., Fagerli I.L., Leinonen P. Competition for nodule occupancy between introduced strains of Rhizobium leguminosarum bv. trifolii and its influence on plant production. // Ann Bot. 2001. — V. 88. — P. 781— 787
394. Tan Z.Y., Kan F.L., Peng G.X., Wang E.T., Reinhold-Hurek B., Chen W.X. Rhizobium yanglingense sp. nov., isolated from arid and semi-arid regions in China // Int. J. Syst. Evol. Microbiol. 2001b. — V. 51. — P. 909−14.
395. Terskikh A., Fradkov A., Ermakova G., Zaraisky A., Tan P., Kajava A. V., Zhao X., Lukyanov S., Matz M., Kim S., Weissman I., Siebert P. «Fluorescent timer»: protein that changes color with time. // Science. 2000. — V. 290. — P. 1585—1588.
396. Timmers A.C., Soupene E., Auriac M.C., de Billy F., Vasse J., Boistard P., Truchet G. Saprophytic intracellular rhizobia in alfalfa nodules. // Mol Plant-Microbe Interact. 2000. — V. 13. — P. 1204−121
397. Thomas C.M., Nielsen K.M. Mechanisms of, and Barriers to, Horizontal Gene Transfer between Bacteria //Nature Rev. Microbiol. 2005. — V. 3. — P. 711−721.
398. Terskikh A., Fradkov A., Ermakova G., Zaraisky A., Tan P., Kajava A.V., Zhao X., Lukyanov S., Matz M., Kim S., Weissman I., Siebert P. «Fluorescent timer»: protein that changes color with time. // Science. 2000. — V. 290. — P. 1585—1588.
399. Teyssier C., Marchandin H., Jumas-Bilak E. The genome of alphaproteobacteria: complexity, reduction, diversity and fluidity. // Can. J. Microbiol. 2004. — V. 50. — P. 383−396
400. Treangen T. J., Rocha E. P. C. Horizontal Transjer, Not Duplication, Drives the Expansion of Protein Families in Prokaryotes // PLoS Genetics. 2011. -journal.pgen. 1 001 284.
401. Trujillo M.E., Willems A., Abril A., Planchuelo A.M., Rivas R., Ludena D., Mateos P.F., Martinez-Molina E., Velazquez E. Nodulation of Lupinus albus by strains of Ochrobactrum lupine sp. nov. //Appl. Environ. Microbiol. 2005. — V. 71.-P. 1318−1327
402. Tsien R. Y. The green fluorescent protein. // Annu. Rev. Biochem. 1998. -V. 67. — P. 509—544.
403. Toledo I., Lloret L., Martinez-Romero E. Sinorhizobium americanus sp. nov., a new Sinorhizobium species nodulating native Acacia spp. in Mexico // Syst. Appl. Microbiol. 2003. — V. 26. — P. 54−64.
404. Tombolini R., Unge A., Davey M.E., de Bruijn F.J., Jansson J.K. Flow cytometric and microscopic analysis of GFP-tagged Pseudomonas fluorescens bacteria // FEMS Microbiol. Ecol. 1997. — V. 22. — P. 17−28.
405. Validation List no. 107. List of new names and new combinations previously effectively, but not validly, published // Int. J. Syst. Evol. Microbiol. 2006. -V.56. -P. 1−6.
406. Van Damme E.J.M., Barre A., Rouge P., Peumans W.J. Cytoplasmic/nuclear plant lectins: a new story. // Trends Plant Sei. 2004. — V. 9. — P. 484⁸⁹
407. Van Damme E.J.M., Nausicaa L., Peumans W.J. Plant Lectins. / Eds Kader J.C., Delseny M. Advances in botanical research, 2008. — V. 48. Elsevier Ltd, San Diego, — P. 107−209
408. Vandamme P., Goris J., Chen W.M., de Vos P., Willems A. Burkholderia tuberum sp. nov. and Burkholderia phymatum sp. nov., nodulate the roots of tropical legumes. // Syst Appl Microbiol. 2002. — V. 25. — P. 507−512
409. Vandamme P., Coenye T. Taxonomy of the genus Cupriavidus: a tale of lost and found. // Int. J. Syst. Evol. Microbiol. 2004. — V. 54. — P. 2285−2289
410. Velazquez E., Cruz-Sanchez J.M., Mateos P.F., Martinez-Molina E. Analysis of stable lowmolecular weight RNA profiles of members of the family Rhizobiaceae. // Appl. Environ. Microbiol. 1998. — V. 64. — P. 1555−1559
411. Verkhusha V. V., Akovbian N. A., Efremenko E. N., Varfolomeyev S. D., Vrzhershch P. V. Kinetic analysis of maturation and denaturation of DsRed, a coral-derived red fluorescent protein. // Biochemistry. 2001a. — V. 66. — P. 1342—1351.
412. Verkhusha V. V., Otsuna H., Awasaki T., Oda H., Tsukita S., Ito K. An enhanced mutant of red fluorescent protein DsRed fore double labeling and developmental timer of neural fiber bundle formation // J. Biol. Chem. 2001b. -V. 276.-P. 29 621−29 624.
413. Vilaine F., Casse-Delbart F. Independent induction of transformed roots by the TL and TR regions of the Ri plasmid of agropine type Agrobacterium rhizogenes II Mol. Gen. Genet. 1987. — V. 206. — P. 17−23.
414. Vincent, J. M. A Manual for the Practical Study of Root Nodule Bacteria / Oxford: Blackwell Scientific. 1970. 164 p.
415. Viprey V., Rosenthal A., Broughton W.K., Perret X. Genetic snapshots of the Rhizobium species NGR234 genome // Genome Biol. 2000. — V. 1. — P. 1−17
416. Vlassak K.M., Vanderleyden J. Factors influencing nodule occupancy by inoculant rhizobia. // Crit Rev Plant Sci. 1997. — V. 16. — P. 163−229
417. Vulic M., Dionisio F., Tazddei F., Radman M. Molecular keys to speciation: DNA polymorphismand control of exchange to enterobacteria // Proc. Natl. Acad. Sci. USA. 1997. — V. 94. — P. 9763−9769.
418. Wang E.T., Rogel M.A., Garcia-de los Santos A., Martinez-Romero J., Cevallos M.A., Martinez-Romero E. Rhizobium etli bv. mimosae, a novel biovar isolated from Mimosa affmis.-// Int.-J. Syst, Bacteriol. 1−999^—V.-49,—P. -147−9- -1491
419. Wang F.Q., Wang E.T., Liu J., Chen Q., Sui X.H., Chen W.F., Chen W.X. Mesorhizobium albiziae sp. nov., a novel bacterium that nodulates Albizia kalkora in a subtropical region of China // Int. J. Syst. Evol. Microbiol. 2007. — V. 57. — P. 1192−1199.
420. Ward W.W., Prentice H.J., Poth A.F., Cody C.W., Reeves S.C. Spectral perturbations of the Aequorea green-fluorescent protein // Photochem. Photobiol. -1982a. V.35. — P.803—808.
421. Ward W.W., Bokman S.H. Reversible denaturation of Aequorea Green-fluorescent protein: physical separation and characterization of the renatured protein // Biochemistry. 1982b. — V.21. — P. 4535—4540.
422. White J., Prell J., James E.K., Poole P. Nutrient sharing between symbionts. // Plant Physiol. 2007. — V. 144. — P. 604−614
423. Webster G., Jain V., Davey M.R., Gouch C., Vasse J., Denarie J., Cocking E.C. The flavonoid naringenin stimulates the intracellular colonization of wheat roots by Azorhizobium caulinodans II Plant Cell Environ. 1998. — V. 21. — P. 373−383.
424. Wei G. H., Zhang Z. X., Chen C., et al. Phenotypic and genetic diversity of rhizobia isolated from nodules of the legume genera Astragalus, Lespedeza and Hedysarum in northwestern China // Microbiological research. 2008. — V.163, -N. 6,-P. 651−662.
425. Werdien D., Peiler G., Ryffel G. U. FLP and Cre recombinase function in Xenopus embryos. // Nucl. Acids Res. 2001. — V. 29. -E53.
426. Wielbo J., Mazur A., Krol J., Marczak M., Kutkowska J., Skorupska A. Complexity of phenotypes and symbiotic behaviour of Rhizobium leguminosarum biovar trifolii exopolysaccharide mutants. // Arch Microbiol. 2004a. — V. 182. -P. 331−336
427. Wielbo J., Mazur A., Krol J., Marczak M., Skorupska A. Environmental modulation of the pssTNOP gene expression in Rhizobium leguminosarum bv. trifolii. // Can J Microbiol. 2004b. — V. 50. — P. 201−211
428. Wielbo J., Marek-Kozaczuk M., Kubik-Komar A., Skorupska A. Increased metabolic potential of Rhizobium spp. is associated with bacterial competitiveness. // Can J Microbiol. 2007. — V. 53. — P. 957−967
429. Wielbo J., Golus J., Marek-Kozaczuk M., Skorupska A. Symbiosis stage-associated alterations in quorum sensing autoinducer molecules biosynthesis in Sinorhizobium meliloti. // Plant Soil. 2009. — V. 1−2. — P. 399−410
430. Wielbo-J., Marek-Kozaczuk M., Mazur A. T Kubik-Komar A. T Skorupska-A. Genetic and metabolic divergence within a Rhizobium leguminosarum bv. trifolii population recovered from clover nodules. // Appl. Environ. Microbiol. 2010. -V. 76,-N. 14.-P. 4593−4600
431. Willems A., Collins M.D. Phylogenetic analysis of rhizobia and agrobacteria based on 16S rRNA gene sequences. // Int. J. Syst. Bacteriol. 1993. — V. 43. — P. 305−313
432. Willems A., Coopman R., Gillis M. Comparison of sequence analysis of 16S-23 S rDNA spacer regions, AFLP analysis and DNA-DNA hibridization in Bradyrhizobium. // Int. J. Syst. Evol. Microbiol. -2001. V. 51. — P. 623- 632
433. Willems A. The taxonomy of rhizobia: an overview // Plant Soil. 2006. — V. 287.-P. 3−14.
434. Wijffelman C.A., Pees E., Brussel A.A.N. Hooykaas P.J.J. Repression of Small bacteriocin excretion in Rhizobium leguminosarum and Rhizobium trifolii by transmissible plasmids//Мої. Gen. Genet. 1983. -V. 192.-P. 171−176
435. Woese C.R., Stackebrandt E., Weisburg W.G., Paster B.J., Madigan M.T., Fowler V.J., Hahn C.M., Blanz P., Gupta R., Nealson K.H., Fox G.E. The phylogeny of purple bacteria: the alpha subdivision. // Syst Appl Microbiol. -1984.-V. 5.-P. 315−326
436. Wong P. Interactions between Rhizobia and Lentil, Pea, Broad, Bean, and Jackbean. // Plant Physiol. 1980. — V. 65. — P. 1049−1052.
437. WozniakR.A.,-Waldor-M.K. Integrative-and-conjugative elements: mosaic mobile genetic elements enabling dynamic lateral gene flow // Nat Rev Microbiol. 2010. — V. 8. — N. 8. — P. 552−63
438. Xia B., Kawar Z.S., Ju T., Alvarez R.A., Sachdev G.P., Cummings R.D. Versatile Xuorescent derivatization of glycans for glycomic analysis. // Nat Methods. 2005. — V. 2. — P. 845−850
439. Xu L.M., Ge C., Cui Z., Li J., Fan H. Bradyrhizobium liaoningense sp nov, isolated from the root nodules of soybeans // Int. J. Syst. Bact. 1995. — V. 45. — P. 706−707.
440. Xu L., Shi J.F., Zhao P., Chen W.M., Qin W., Tang M., Wei G. H. Rhizobium sphaerophysae sp. nov., a novel species isolated from root nodules of Sphaerophysa salsula in China // Antonie van Leeuwenhoek. 2011. — V. 99. — P. 845−854
441. Yagi K. Chemical determination of flavins // In: Methods of Biochemical Analysis. (Glick, D., Ed.) Interscience Publishers, London, UK.- 1962. -V. 10. -P. 319−356.
442. Yamamoto K., Konami Y., Kusui K. Purification and characterization of a carbohydrate-binding peptide from Bauhinia purpurea lectin // FEBS Letters. -1991.-V. 281.-P. 258−262.
443. Yamamoto K., Konami Y., Osawa T. Alteration of the carbohydrate-binding specificity of the Bauhinia purpurea lectin trough the preparation of a chimeric lectin // J. Biochem. 1992a. — V. 111. — P. 87−90.
444. Yamamoto K., Konami Y., Osawa T. Carbohydrate-binding peptides from several anti-H (O) lectins // J. Biochem. 1992b. — V. 111. — P. 436¹³⁹.
445. Yamamoto M., Yoshizaki K., Kishimoto T., Ito H. IL-6 is required for the development of-Th-1 cell-mediated murine colitis // J. Immunol. -=-2000. =¦ V—164. -P. 4878^1882.
446. Yan X.R., Chen W.F., Fu J.F., Lu Y.L., Xue C.Y., Sui X.H., Li Y., Wang E.T., Chen W.X. Mesorhizobium spp. are the main microsymbionts of Caragana spp. grown in Liaoning Province of China. // FEMS Microbiol Lett. 2007. — V. 271.-P. 265−273
447. Yanagi M., Yamasato K. Phylogenetic analysis of the family Rhizobiaceae and related bacteria by sequencing of 16S rRNA gene using PCR and DNA sequencer. // FEMS Microbiol Lett. 1993. — V. 107. — P. 115−120
448. Yang S.F., Hoffman N.E. Ethylene biosynthesis and its regulation in higher plants. // Annu. Rev. Plant Physiol. 1984. — V. 35. — P. 155−189.
449. Yanni Y.G., Rizk R.Y., Abd El-Fattah F.K., Squartini A., Corich V. et al. The beneficial plant growth-promoting association of Rhizobium leguminosarum bv. trifolii with rice roots. // Aust. J. Plant Physiol. 2001. — V. 28. — P. 845−870.
450. Yao Z.Y., Kan F.L., Wang E.T., Wei G.H., Chen W.X. Characterization of rhizobia that nodulate legume species of the genus Lespedeza and description of
451. Bradyrhizobium yuanmingense sp. nov. // Int. J. Syst. Evol. Microbiol. 2002. — V. 52. — P. 2219−30.
452. Yoon J.H., Kang S.J., Yi H.S., Oh T.K., Ryu C.M. Rhizobium soli sp. nov., isolated from soil // Int. J. System. Evol. Microbiol. 2010. — V. 60. — P. 13 871 393
453. Young N.M., Oomen R.P. Analysis of sequence variation among legume lectins: a ring of hypervariable residues forms the perimeter of the carbohydrate-binding site // J. Mol. Biol. 1992. — V. 228. — P. 924−934.
454. Young J.P., Crossman L.C., Johnston A.W., et al. The genome of Rhizobium leguminosarum has recognizable core and accessory components. // Genome Biol. 2006.-V. 7. -R34
455. Young JM. Sinorhizobium versus Ensifer: may a taxonomy subcommittee of the ICSP contradict the Judicial Commission? // Int. J. Syst. Evol. Microbiol. -2010. V. 60.-P. 1711−1713
456. Zacharias D.A., Baird G.S., Tsien R.Y. Recent advances in technology for measuring and manipulating cell signals. // Curr. Opin. Neurobiol. 2000. — V. 10. -P. 416—421.
457. Zahir Z.A., Arshad M., Frankenberger W.T. Jr. Plant growth promoting rhizobacteria: applications and perspectives in agriculture // Adv. Agron. 2004. -V.81.-P. 97−168.
458. Zahran H. H. Rhizobia from wild legumes: diversity, taxonomy, ecology, nitrogen fixation and biotechnology // Journ. Biotechnol. 2001. — V. 91. — P. 143 153 «-----. ... .
459. Zakhia F., de Lajudie P. Modern bacterial taxonomy: techniques review application to bacteria that nodulate leguminous plants (BNL) // Can. J. Microbiol. 2006. — V. 52.-P. 169−181
460. Zehr J.P., Jenkins B.D., Short S.M., Steward G.F. Nitrogenase gene diversity and microbial community structure: a cross-system comparison. // Environ Microbiol. 2003. — V. 5. — P. 539−554
461. Zeigler D.R. Gene sequences useful for predicting relatedness of whole genomes in bacteria. // Int. J. Syst. Evol. Microbiol. 2003. — V. 53. — P. 18 931 900
462. Zhang X., Sun L., Ma X., Sui X. H., Jiang R. Rhizobium pseudoryzae sp. nov., isolated from the rhizosphere of rice // Int. J. System. Evol. Microbiol. -201 la.-V. 61.-P. 2425−2429
463. Zhang R.J., Hou B.C., Wang E.T., Li Y., Jr, Zhang X.X., Chen W.X. Rhizobium tubonense sp. nov., isolated from root nodules of Oxytropis glabra //1.ternational Journal of Systematic and Evolutionary Microbiology. 2011b. — V. 61.-P. 512−7.
464. Zhang J.J., Liu T.Y., Chen W.F., Wang E.T., Sui X.H., Zhang X.X., Li Y., Li Y., Chen W.X. Mesorhizobium muleiense sp. nov., nodulating with Cicer arietinum L. in Xinjiang, China // Int. J. Syst-Evol. Microbiol, -2012. V. 6. Epub ahead of print.
465. Zhao C.T., Wang E.T., Zhang Y.M., Chen W.F., Sui X.H., Chen W.X., Liu H.C., Zhang X.X. Mesorhizobium silamurunense sp. nov., a novel species nodulated with Astragalus species in China // Int. J. Syst. Evol. Microbiol. 2011.- V. 4. Epub ahead of print.
466. Zhaxybayeva O., Lapierre P., Gogarten J. P. Genome mosaicism and organismallineages // Trends Genet. 2004. — V. 20, N 5. — P. 254−260.
467. Zhou PF, Chen WM, Wei GH. Mesorhizobium robiniae sp. nov., isolated from root nodules of Robinia pseudoacacia // Int. J. Syst. Evol. Microbiol. 2010.- V. 60.-P. 2552−2556.
468. Zurdo-Pineiro J.L., Rivas R., Trujillo M.E., Vizcaino N., Carrasco J.A., Chamber M., Palomares A., Mateos P.F., Martinez-Molina E., Velazquez E.
469. Ochrobactrum cytisi sp. nov., isolated from nodules of Cytisus scoparius in Spain. // Int. J. Syst. Evol. Microbiol. 2007. — V. 57. — P. 784−788
470. Zurkowski W., Lorkiewicz Z. Plasmid-mediated control of nodulation in Rhizobium trifolii. // Arch Microbiol. 1979. — V. 123. — P. 195−201