Применение эндофитных микроорганизмов для интенсификации ростовых процессов сельскохозяйственных культур
Аннотация и ключевые слова
Аннотация (русский):
Повышение продуктивности основных сельскохозяйственных культур (пшеницы, ячменя и овса) является актуальной проблемой. Урожайность данных культур во многом зависит от плодородия почвы. Недостаток биогенных веществ в почвах восполняют минеральными удобрениями, которые при неправильном применении неэкологичны и малоэффективны. Обеспечить растения необходимыми питательными элементами способны микроорганизмы. Цель данной работы – выделение эндофитных микроорганизмов, обладающих ростостимулирующими свойствами, а также оценка их влияния на рост пшеницы, ячменя и овса. Объектами исследования являлись яровая мягкая пшеница сорта «Сибирский Альянс», яровой овес сорта «Маручак», яровой ячмень сорта «Никита» и стандартные штаммы бактерий (Azospirillum brasilense В-11094 и Azotobacter chrococcum В-8739). Выделенные бактерии идентифицировали с помощью автоматического микробиологического анализатора Vitex 2 Compact. Способность изолятов микроорганизмов продуцировать индолил-3-уксусную и гиббереллиновую кислоты оценивали спектрофотометрическими методами. Способность к фиксации азота штаммами определяли с помощью Rapid N Cube. Способность изолятов солюбилизировать фосфаты тестировали на среде, содержащей кальций фосфорнокислый. Влияние наиболее перспективных штаммов на сельскохозяйственные культуры оценивали в лабораторных условиях. Выделено и идентифицировано 7 изолятов эндофитных микроорганизмов, таких как Pantoea allii Tri, Bacillus subtilis Tri 2, Bacillus subtilis Ave 1, Pantoea allii Ave 2, Bacillus subtilis Hor 1, Bacillus subtilis Hor 2, Bacillus subtilis Hor 3. Изучены ростостимулирующие свойства штаммов и отобраны наиболее перспективные. Штамм Bacillus subtilis Ave 1 продуцировал 7100 мкг/мл индолил-3-уксусной и 343 мкг/мл гиббереллиновой кислот, фиксировал 790 мкг/мл азота, солюбилизировал фосфаты (индекс 1,60). Bacillus subtilis Hor 1 демонстрировал способность к синтезу 4490 мкг/мл индолил-3-уксусной и 409 мкг/мл гиббереллиновой кислот, фиксировал азот в количестве 760 мкг/мл, а также солюбилизировал фосфаты (индекс 1,44). Лабораторная апробация штаммов показала, что наибольшей ростостимулирующей активностью обладает штамм Bacillus subtilis Ave 1. Выделенный в ходе работы штамм обладает способностью к синтезу фитогормонов, фиксирует атмосферный азот и солюбилизирует фосфаты. Лабораторная апробация показала, что штамм увеличивает длину побега и корня пшеницы и ячменя, а также повышает всхожесть, энергию прорастания и длину побега у овса. Это обуславливает высокие перспективы применения выделенного штамма в сельском хозяйстве.

Ключевые слова:
Овес, пшеница, ячмень, эндофитные микроорганизмы, Bacillus, Pantoea, Azotobacter, Azospirillum
Список литературы

1. Качутова А. А. Эффективное производство зерна – основа продовольственной безопасности страны // Вестник НГИЭИ. 2013. № 3. С. 76–88. https://elibrary.ru/PZFFSL

2. Albahri G, Alyamani AA, Badran A, Hijazi A, Nasser M, Maresca M, et al. Enhancing essential grains yield for sustainable food security and bio-safe agriculture through latest innovative approaches. Agronomy. 2023;13(7):1709. https:// doi.org/10.3390/agronomy13071709

3. Serazetdinova Y, Borodina E, Kolpakova D, Frolova A, Fotina N, Tikhonov S, et al. The biopotential of extremophilic microorganisms isolated from Kuzbass for protection and growth stimulation of oat (Avena sativa L.). BIO Web of Conferences. 2024;82:03009. https://doi.org/10.1051/bioconf/20248203009

4. Sullivan P, Arendt E, Gallagher E. The increasing use of barley and barley by-products in the production of healthier baked goods. Trends in Food Science and Technology. 2013;29(2):124–134. https://doi.org/10.1016/j.tifs.2012.10.005

5. Langridge P. Economic and academic importance of barley. In: Stein N, Muehlbauer GJ, editors. The Barley Genome. Cham: Springer International Publishing; 2018. pp. 1–10. https://doi.org/10.1007/978-3-319-92528-8_1

6. Kolmanič A, Sinkovič L, Nečemer M, Ogrinc N, Meglič V. The effect of cultivation practices on agronomic performance, elemental composition and isotopic signature of spring Oat (Avena sativa L.). Plants. 2022;11(2):169. https://doi.org/https://doi.org/10.3390/plants11020169

7. FAOSTAT [Internet]. [cited 2024 Jun 5]. Available from: http://www.fao.org/faostat/en/#data/QCL

8. Daniel AI, Fadaka AO, Gokul A, Bakare OO, Aina O, Fisher S, et al. Biofertilizer: The future of food security and food safety. Microorganisms. 2022;10(6):1220. https://doi.org/10.3390/microorganisms10061220

9. Просеков А. Ю. Современные аспекты производства продуктов питания. Кемерово: Кемеровский технологический институт пищевой промышленности, 2005. 381 с.. https://elibrary.ru/ZRZGCT

10. Abebe TG, Tamtam MR, Abebe AA, Abtemariam KA, Shigut TG, Dejen YA, et al. Growing use and impacts of chemical fertilizers and assessing alternative organic fertilizer sources in Ethiopia. Applied and Environmental Soil Science. 2022;2022(1):1–14. https://doi.org/10.1155/2022/4738416

11. Юрина Т. А., Ткаленко А. Е. Обзор инновационных препаратов для биологизации сельскохозяйственного производства // АгроФорум. 2020. № 1. С. 51–53. https://elibrary.ru/WLIKOC

12. Kumar R, Kumawat N, Sahu YK. Role of biofertilizers in agriculture. Popular Kheti. 2017;5(4):63–66.

13. Mahmud AA, Upadhyay SK, Srivastava AK, Bhojiya AA. Biofertilizers: A nexus between soil fertility and crop productivity under abiotic stress. Current Research in Environmental Sustainability. 2021;3:100063. https://doi.org/10.1016/ j.crsust.2021.100063

14. Chaudhary P, Agri U, Chaudhary A, Kumar A, Kumar G. Endophytes and their potential in biotic stress management and crop production. Frontiers in Microbiology. 2022;13:933017. https://doi.org/10.3389/fmicb.2022.933017

15. Liu H, Carvalhais LC, Crawford M, Singh E, Dennis PG, Pieterse CMJ, et al. Inner plant values: diversity, colonization and benefits from endophytic bacteria. Frontiers in Microbiology. 2017;8:2552. https://doi.org/10.3389/fmicb.2017.02552

16. Milentyeva IS, Fotina NV, Zharko MYu, Proskuryakova LA. Microbial treatment and oxidative stress in agricultural plants. Food Processing: Techniques and Technology. 2022;52(4):750–61. https://doi.org/10.21603/2074-9414-2022-4-2403

17. Asyakina LK, Vorob’eva EE, Proskuryakova LA, Zharko MYu. Evaluating extremophilic microorganisms in industrial regions. Foods and Raw Materials. 2023:11(1)162–71. https://doi.org/10.21603/2308-4057-2023-1-556

18. Backer R, Rokem JS, Ilangumaran G, Lamont J, Praslickova D, Ricci E, et al. Plant growth-promoting rhizobacteria: context, mechanisms of action, and roadmap to commercialization of biostimulants for sustainable agriculture. Frontiers in Plant Science. 2018;9:1473. https://doi.org/10.3389/fpls.2018.01473

19. Mahanty T, Bhattacharjee S, Goswami M, Bhattacharyya P, Das B, Ghosh A, et al. Biofertilizers: a potential approach for sustainable agriculture development. Environmental Science and Pollution Research. 2017;24:3315–3335. https:// doi.org/10.1007/s11356-016-8104-0

20. Steenhoudt O, Vanderleyden J. Azospirillum, a free-living nitrogen-fixing bacterium closely associated with grasses: genetic, biochemical and ecological aspects. FEMS Microbiology Reviews. 2000;24(4):487–506. https://doi.org/10.1111/ j.1574-6976.2000.tb00552.x

21. Iqbal R, Valipour M, Ali B, Zulfiqar U, Aziz U, Zaheer MS, et al. Maximizing wheat yield through soil quality enhancement: A combined approach with Azospirillum brasilense and bentonite. Plant Stress. 2024;11:100321. https://doi.org/https://doi.org/10.1016/j.stress.2023.100321

22. Fukami J, Cerezini P, Hungria M. Azospirillum: benefits that go far beyond biological nitrogen fixation. AMB Express. 2018;8:73. https://doi.org/10.1186/s13568-018-0608-1

23. Turan M, Gulluce M, Von Wirén N, Sahin F. Yield promotion and phosphorus solubilization by plant growth–promoting rhizobacteria in extensive wheat production in Turkey. Journal of Plant Nutrition and Soil Science. 2012;175(6):818–826. https://doi.org/10.1002/jpln.201200054

24. Aroca R. Plant responses to drought stress: from morphological to molecular features. Heidelberg: Springer; 2012. p. 466. https://doi.org/10.1007/978-3-642-32653-0

25. Kızılkaya R. Yield response and nitrogen concentrations of spring wheat (Triticum aestivum) inoculated with Azoto- bacter chroococcum strains. Ecological Engineering. 2008;33(2):150–156. https://doi.org/10.1016/j.ecoleng.2008.02.011

26. Dal Cortivo C, Ferrari M, Visioli G, Lauro M, Fornasier F, Barion G, et al. Effects of Seed-Applied Biofertilizers on Rhizosphere Biodiversity and Growth of Common Wheat (Triticum aestivum L.) in the Field. Frontiers in Plant Science. 2020; 11:72. https://doi.org/10.3389/fpls.2020.00072

27. Mishra P, Dash D. Rejuvenation of biofertilizer for sustainable agriculture and economic development. Consilience: The Journal of Sustainable Development. 2014;11(1):41–61.

28. Das HK. Azotobacters as biofertilizer. Advances in Applied Microbiology. 2019;108:1–43. https://doi.org/10.1016/ bs.aambs.2019.07.001

29. Harper SHT, Lynch JM. Effects of Azotobacter chroococcum on barley seed germination and seedling development. Journal of General Microbiology. 1979;112(1):45–51. https://doi.org/10.1099/00221287-112-1-45

30. Bageshwar UK, Srivastava M, Pardha-Saradhi P, Paul S, Gothandapani S, Jaat RS, et al. An environmentally friendly engineered Azotobacter Strain that replaces a substantial amount of urea fertilizer while sustaining the same wheat yield. Applied and Environmental Microbiology. 2017;83(15):e00590-17. https://doi.org/10.1128/AEM.00590-17

31. Kopylov IP, Spyrydonov VH, Patyka VP. Identification of Azospirillum genus bacteria isolated from the spring wheat root zone. Mikrobiolohichnyi Zhurnal. 2009;71:13–19.

32. Ayyaz K, Zaheer A, Rasul G, Mirza MS. Isolation and identification by 16S rRNA sequence analysis of plant growth-promoting azospirilla from the rhizosphere of wheat. Brazilian Journal of Microbiology. 2016;47(3):542–550. https:// doi.org/10.1016/j.bjm.2015.11.035

33. Camilios-Neto D, Bonato P, Wassem R, Tadra-Sfeir MZ, Brusamarello-Santos LC, Valdameri G, et al. Dual RNA- seq transcriptional analysis of wheat roots colonized by Azospirillum brasilense reveals up-regulation of nutrient acquisition and cell cycle genes. BMC Genomics. 2014;15:378. https://doi.org/10.1186/1471-2164-15-378

34. Kumar V, Narula N. Solubilization of inorganic phosphates and growth emergence of wheat as affected by Azotobacter chroococcum mutants. Biology and Fertility of Soils. 1999;28:301–305. https://doi.org/10.1007/s003740050497

35. Iqbal Z, Ahmad M, Raza MA, Hilger T, Rasche F. Phosphate-Solubilizing Bacillus sp. Modulate Soil Exoenzyme Activities and Improve Wheat Growth. Microbial Ecology. 2024;87:31. https://doi.org/10.1007/s00248-023-02340-5

36. Iqbal Z, Ahmad M, Jamil M, Akhtar MFUZ. Appraising the potential of integrated use of Bacillus strains for improving wheat growth. International Journal of Agriculture and Biology. 2020;24:1439‒1448.

37. Kaur T, Devi R, Kumar S, Sheikh I, Kour D, Yadav AN. Microbial consortium with nitrogen fixing and mineral solubilizing attributes for growth of barley (Hordeum vulgare L.). Heliyon. 2022;8(4):e09326. https://doi.org/10.1016/ j.heliyon.2022.e09326

38. Pang F, Tao A, Ayra-Pardo C, Wang T, Yu Z, Huang S. Plant organ- and growth stage-diversity of endophytic bacteria with potential as biofertilisers isolated from wheat (Triticum aestivum L.). BMC Plant Biology. 2022;22:276. https:// doi.org/10.1186/s12870-022-03615-8

39. Da Silva MF, De Souza Antônio C, De Oliveira PJ, Xavier GR, Rumjanek NG, De Barros Soares LH, et al. Survival of endophytic bacteria in polymer-based inoculants and efficiency of their application to sugarcane. Plant Soil. 2012;356:231–243. https://doi.org/10.1007/s11104-012-1242-3

40. Cavalcante VA, Dobereiner J. A new acid-tolerant nitrogen-fixing bacterium associated with sugarcane. Plant Soil. 1988;108:23–31. https://doi.org/10.1007/BF02370096

41. Tarrand JJ, Krieg NR, Döbereiner J. A taxonomic study of the Spirillum lipoferum group, with descriptions of a new genus, Azospirillum gen. nov. and two species, Azospirillum lipoferum (Beijerinck) comb. nov. and Azospirillum brasilense sp. nov. Canadian Journal of Microbiology. 1978;24:967–980. https://doi.org/10.1139/m78-160

42. Wisniewski-Dyé F, Borziak K, Khalsa-Moyers G, Alexandre G, Sukharnikov LO, Wuichet K, et al. Azospirillum Genomes Reveal Transition of Bacteria from Aquatic to Terrestrial Environments. PLoS Genetics. 2011;7(12):e1002430. https:// doi.org/10.1371/journal.pgen.1002430

43. Khammas KM, Ageron E, Grimont PAD, Kaiser P. Azospirillum irakense sp. nov., a nitrogen-fixing bacterium associated with rice roots and rhizosphere soil. Research in Microbiology. 1989;140(9):679–693. https://doi.org/10.1016/0923- 2508(89)90199-X

44. Baldani VLD, Alvarez MADB, Baldani JI, Döbereiner J. Establishment of inoculated Azospirillum spp. in the rhizosphere and in roots of field grown wheat and sorghum. Plant and Soil. 1986;90:35–46. https://doi.org/10.1007/BF02277385

45. Bhatia R, Ruppel S, Narula N. Diversity studies of Azotobacter spp. from cotton‐wheat cropping systems of India. Journal of Basic Microbiology. 2008;48(6):455–463. https://doi.org/10.1002/jobm.200800059

46. Kumawat KC, Razdan N, Saharan K. Rhizospheric microbiome: Bio-based emerging strategies for sustainable agriculture development and future perspectives. Microbiological Research. 2022;254:126901. https://doi.org/10.1016/j.micres. 2021.126901

47. Li H, Parmar S, Sharma VK, White JF. Seed endophytes and their potential applications. In: Verma SK, White, Jr JF, editors. Seed Endophytes. Cham: Springer International Publishing; 2019. pp. 35–54. https://doi.org/10.1007/978- 3-030-10504-43

48. Sa R, He S, Han D, Liu M, Yu Y, Shang R, et al. Isolation and identification of a new biocontrol bacteria against Salvia miltiorrhiza root rot and optimization of culture conditions for antifungal substance production using response surface methodology. BMC Microbiology. 2022;22:231. https://doi.org/10.1186/s12866-022-02628-5

49. Amna, Ud Din B, Sarfraz S, Xia Y, Kamran MA, Javed MT, et al. Mechanistic elucidation of germination potential and growth of wheat inoculated with exopolysaccharide and ACC- deaminase producing Bacillus strains under induced salinity stress. Ecotoxicology and Environmental Safety. 2019;183:109466. https://doi.org/10.1016/j.ecoenv.2019.109466

50. Masi C, Tebiso A, Selva Kumar KV. Isolation and characterization of potential multiple extracellular enzymeproducing bacteria from waste dumping area in Addis Ababa. Heliyon. 2023;9(2):e12645. https://doi.org/10.1016/j.heliyon. 2022.e12645

51. Wu SC, Gao J-K, Chang B-S. Isolation of lindane- and endosulfan-degrading bacteria and dominance analysis in the microbial communities by culture-dependent and independent methods. Microbiological Research. 2021;251:126817. https://doi.org/10.1016/j.micres.2021.126817

52. Borodina E, Asyakina L, Proskuryakova L, Osintseva M, Milentyeva I, Prosekov A. The potential of using plantgrowth-stimulating bacteria in phytoremediation of coal dumps. BIO Web of Conferences. 2024;82:06011. https://doi.org/10.1051/ bioconf/20248206011

53. Medfu Tarekegn M, Zewdu Salilih F, Ishetu AI. Microbes used as a tool for bioremediation of heavy metal from the environment. Cogent Food and Agriculture. 2020;6(1):1783174. https://doi.org/10.1080/23311932.2020.1783174

54. Atuchin VV, Asyakina LK, Serazetdinova YuR, Frolova AS, Velichkovich NS, Prosekov AYu. Microorganisms for bioremediation of soils contaminated with heavy metals. Microorganisms. 2023;11(4):864. https://doi.org/10.3390/ microorganisms11040864

55. Исследование потенциала естественной микробиоты яровой мягкой пшеницы в повышении урожайности / Л. К. Асякина [и др.] // Достижения науки и техники АПК. 2023. Т. 37. № 11. С. 12–17. https:// elibrary.ru/HXXGEC

56. Ризобактерии для снижения биотического стресса яровой пшеницы (Triticum aestivum L.), вызванного фитопатогенными грибами / Ю. Р. Серазетдинова [и др.] // Хранение и переработка сельхозсырья. 2023. № 4. С. 98–113. https://elibrary.ru/JTKRHL

57. Asyakina LK, Isachkova ОА, Kolpakova DE, Borodina ЕЕ, Boger VYu, Prosekov AYu. The effect of a microbial consortium on spring barley growth and development in the Kemerovo region, Kuzbass. Grain Economy of Russia. 2024; 16(1):104–112. (In Russ.). https://doi.org/10.31367/2079-8725-2024-90-1-104-112

58. Fotina NV, Serazetdinova YuR, Kolpakova DE, Asyakina LK, Atuchin VV, Alotaibi KM, et al. Enhancement of wheat growth by plant growth-stimulating bacteria during phytopathogenic inhibition. Biocatalysis and Agricultural Biotechnology. 2024;60:103294. https://doi.org/10.1016/j.bcab.2024.103294

59. Faskhutdinova ER, Fotina NV, Neverova OA, Golubtsova YuV, Mudgal G, Asyakina LK, et al. Extremophilic bacteria as biofertilizer for agricultural wheat. Foods and Raw Materials. 2024;12(2):348–360. https://doi.org/10.21603/2308- 4057-2024-2-613

60. Albassam M, Aslam M. Testing Internal Quality Control of Clinical Laboratory Data Using Paired t-Test under Uncertainty. BioMed Research International. 2021:5527845. https://doi.org/10.1155%2F2021%2F5527845

61. Singh RK, Singh P, Guo D-J, Sharma A, Li D-P, Li X, et al. Root-Derived Endophytic Diazotrophic Bacteria Pantoea cypripedii AF1 and Kosakonia arachidis EF1 Promote Nitrogen Assimilation and Growth in Sugarcane. Frontiers in Microbiology. 2021;12:774707. https://doi.org/10.3389/fmicb.2021.774707

62. Ma Q, He S, Wang X, Rengel Z, Chen L, Wang X, et al. Isolation and characterization of phosphate-solubilizing bacterium Pantoea rhizosphaerae sp. nov. from Acer truncatum rhizosphere soil and its effect on Acer truncatum growth. Frontiers in Plant Science. 2023;14:1218445. https://doi.org/10.3389/fpls.2023.1218445

63. Rfaki A, Zennouhi O, Aliyat FZ, Nassiri L, Ibijbijen J. Isolation, selection and characterization of root-associated rock phosphate solubilizing bacteria in moroccan wheat (Triticum aestivum L.). Geomicrobiology Journal. 2020;37(3):230–241. https://doi.org/10.1080/01490451.2019.1694106

64. Shao J, Xu Z, Zhang N, Shen Q, Zhang R. Contribution of indole-3-acetic acid in the plant growth promotion by the rhizospheric strain Bacillus amyloliquefaciens SQR9. Biology and Fertility of Soils. 2015;51:321–330. https://doi.org/https://doi.org/10.1007/s00374-014-0978-8

65. Özdal M, Gür Özdal Ö, Sezen A, Algur ÖF. Biosynthesis of indole-3-acetic acid by Bacillus cereus Immobilized Cells. Cumhuriyet Science Journal. 2016;37(3):212. https://doi.org/10.17776/csj.34085

66. Lee J-C, Whang K-S. Optimization of Indole-3-acetic Acid (IAA) Production by Bacillus megaterium BM5. Korean Journal of Soil Science and Fertilizer. 2016;49(5):461–468. https://doi.org/10.7745/KJSSF.2016.49.5.461

67. Rivera D, Mora V, Lopez G, Rosas S, Spaepen S, Vanderleyden J, et al. New insights into indole-3-acetic acid metabolism in Azospirillum brasilense. Journal of Applied Microbiology. 2018;125(6):1774–1785. https://doi.org/10.1111/ jam.14080

68. Shokri D, Emtiazi G. Indole-3-Acetic acid (IAA) production in symbiotic and non-symbiotic nitrogen-fixing bacteria and its optimization by taguchi design. Current Microbiology. 2010;61:217–25. https://doi.org/10.1007/s00284-010-9600-y

69. Lv L, Luo J, Ahmed T, Zaki HEM, Tian Y, Shahid MS, et al. Beneficial effect and Potential risk of Pantoea on rice production. Plants. 2022;11(19):2608. https://doi.org/10.3390/plants11192608

70. Lenin G, Jayanthi M. Indole Acetic Acid, Gibberellic Acid and Siderophore Production by PGPR Isolates from Rhizospheric Soils of Catharanthus roseus. International Journal of Pharmaceutical and Biological Archives. 2012;3(4):933–938

71. Dahiya A, Sharma R, Sindhu S, Sindhu SS. Resource partitioning in the rhizosphere by inoculated Bacillus spp. towards growth stimulation of wheat and suppression of wild oat (Avena fatua L.) weed. Physiology and Molecular Biology of Plants. 2019;25:1483–1495. https://doi.org/10.1007/s12298-019-00710-3

72. Platonov AV, Rassokhina II, Laptev GY, Bolshakov VN. Preparations Use Based on Bacteria of the Genus Bacillus to Increase the Yield of Oats (Avena sativa L.). AGRIVITA Journal of Agricultural Science. 2023;45(1):48–55. https:// doi.org/10.17503/agrivita.v45i1.3757

73. Mohan V, Devi KS, Anushya A, Revathy G, Viji Kuzhalvaimozhi G, Vijayalakshmi KS. Screening of Salt Tolerant and Growth Promotion Efficacy of Phosphate Solubilizing Bacteria. Journal of Academia and Industrial Research. 2017;5(12):168–172.

74. Kumari S, Kumar P, Kiran S, Kumari S, Singh A. Characterization of culture condition dependent, growth responses of phosphate solubilizing bacteria (Bacillus subtilis DR2) on plant growth promotion of Hordeum vulgare. Vegetos. 2023;37:266–276. https://doi.org/10.1007/s42535-023-00589-2


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