Growth-promoting potential of Herbaspirillum rhizosphaerae bacteria on wheat seedlings (Triticum aestivum L.)

Мұқаба

Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Рұқсат ақылы немесе тек жазылушылар үшін

Аннотация

The development of sustainable agriculture requires reducing the chemical load on agroecosystems. One of the ecological approaches is the use of biopreparations based on rhizobacteria that stimulate plant growth. Inoculation of early wheat (Triticum aestivum L.) sprouts with Herbaspirillum rhizosphaerae UMS-37T bacteria resulted in an increase in the length of roots and shoots, and also affected the content of proline, malondialdehyde, nitric oxide and catalase activity in sprouts, which indicates the induction of systemic plant resistance mechanisms. The strain H. rhizosphaerae UMS-37T demonstrated pronounced antifungal activity against field strains of mycelial fungi of the genus Fusarium. The results of this work can be used in the development of environmentally friendly and competitive biopreparations in adaptive agriculture that are capable of activating plant defense systems and controlling fusarium of the most important agricultural crops.

Авторлар туралы

N. Velichko

Institute of Biochemistry and Physiology of Plants and Microorganisms, FRC Saratov Scientific Centre of Russian Academy of Sciences

Email: velichko_n@ibppm.ru
Saratov, 410049, Russia

Y. Fedonenko

Institute of Biochemistry and Physiology of Plants and Microorganisms, FRC Saratov Scientific Centre of Russian Academy of Sciences

Хат алмасуға жауапты Автор.
Email: velichko_n@ibppm.ru
Saratov, 410049, Russia

Әдебиет тізімі

  1. Баймиев Ан.Х., Ямиданов Р. С., Матниязов Р. Т., Благова Д. К., Баймиев Ал.Х., Чемерис А. В. Получение флуоресцентно меченых штаммов клубеньковых бактерий дикорастущих бобовых для их детекции in vivo и in vitro // Мол. биология. 2011. Т. 45. С. 984–991.
  2. Baymiev A. K., Yamidanov R. S., Matniyazov R. T., Blagova D. K., Baymiev Al.Kh., Chemeris A. V. Preparation of fluorescent labeled nodule bacteria strains of wild legumes for their detection in vivo and in vitro // Mol. Biol. 2011. V. 45. P. 904‒910.
  3. Пестинская Т. В. О взаимоотношениях грибов, обитающих в почве // Ботан. журн. 1958. Т. 43. С. 1270–1277.
  4. Смолькина О. Н., Шишонкова (Величко) Н.С., Юрасов Н. А., Игнатов В. В. Капсульные и экстраклеточные полисахариды диазотрофных ризобактерий Herbaspirillum seropedicae Z78 // Микробиология. 2012. Т. 81. № 3. С. 345–352.
  5. Smol’kina O.N., Shishonkova (Velichko) N.S., Yurasov N. A., Ignatov V. V. Capsular and extracellular polysaccharides of the diazotrophic rhizobacterium Herbaspirillum seropedicae Z78 Microbiology (Moscow). 2012. V. 81. P. 317–323.
  6. Arnon D. I., Hoagland D. R. A comparison of water culture and soil as media for crop production // Science. 1939. V. 89. P. 512–514.
  7. Bates L. S., Waldren R. P., Teare I. D. Rapid determination of free proline for water-stress studies // Plant Soil. 1973. V. 39. P. 205–207.
  8. Batista B. D., Lacava P. T., Ferrari A., Teixeira-Silva N.S., Bonatelli M. L., Tsui S., Mondin M., Kitajima E. W., Pereira J. O., Azevedo J. L., Quecine M. C. Screening of tropically derived, multi-trait plant growth- promoting rhizobacteria and evaluation of corn and soybean colonization ability // Microbiol. Res. 2018. V. 206. P. 33–42.
  9. Batista M. B., Muller-Santos M., Pedrosa F. O., Souza E. M. Potentiality of Herbaspirillum seropedicae as a platform for bioplastic production // Microbial models: from environmental to industrial sustainability / Eds. Sowinski S. C. Singapore: Springer, 2016.
  10. Berendsen R. L., Pieterse C. M., Bakker P. A. The rhizosphere microbiome and plant health // Trends Plant Sci. 2012. V. 17. P. 478–486.
  11. Carril P., Cordeiro C., Silva M. S., Ngendahimana E., Tenreiro R., Cruz C. Exploring the plant-growth promoting bacterium Herbaspirillum seropedicae as catalyst of microbiome remodeling and metabolic changes in wheat plants // Planta. 2025. V. 261. Art. 36.
  12. Glick B. R. Plant growth-promoting bacteria: mechanisms and applications // Scientifica (Cairo). 2012. Art. 963401. https://doi.org/10.6064/2012/963401
  13. Hodges D. M., DeLong J.M., Forney C. F. Improving the thiobarbituric acid reactive substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds // Planta. 1999. V. 207. P. 604–611.
  14. Hu H., Young Y. Biocidal activity in plant pathogenic Acidovorax, Burkholderia, Herbaspirillum, Ralstonia and Xanthomonas spp. // J. Appl. Microbiol. 1998. V. 84. P. 263–271.
  15. Iqbal S., Begum F., Rabaan A. A., Aljeldah M., Al Shammari B. R., Alawfi A., Alshengeti A., Sulaiman T., Khan A. Classification and multifaceted potential of secondary metabolites produced by Bacillus subtilis group: a comprehensive review // Molecules. 2023. V. 28. Art. 927.
  16. Kaleh A. M., Singh P., Ooi Chua K., Harikrishna J. A. Modulation of plant transcription factors and priming of stress tolerance by plant growth-promoting bacteria: a systematic review // Ann. Bot. 2025. V. 135. P. 387–402.
  17. Matteoli F. P., Olivares F. L., Venancio T. M., da Rocha L. O., da Silva Irineu L.Ed.S., Canellas L. P. Herbaspirillum // Beneficial microbes in agro-ecology / Eds. Amaresan N., Senthil Kumar M., Annapurna K., Kumar K., Sankaranarayanan A. Academic Press, Chapter, 2020. P. 493–508.
  18. Meier U., Bleiholder H., Buhr L., Feller C., Hack H., Heß M., Lancashire P. D., Schnock U., Stauß R., van den Boom T., Weber E., Zwerger P. P. The BBCH system to coding the phenological growth stages of plants – history and publications // J. fur Kult. 2009. V. 61. P. 41–52.
  19. Murashige T., Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue cultures // Physiol. Plant. 1962. V. 15. P. 473–497.
  20. Negi R., Sharma B., Kumar S., Chaubey K. K., Kaur T., Devi R., Yadav A., Kour D., Yadav A. N. Plant endophytes: unveiling hidden applications toward agro-environment sustainability // Folia Microbiol. 2024. V. 25. P. 1–26.
  21. Pellegrini M., Pagnani G., Bernardi M., Mattedi A., Spera D. M., Del Gallo M. Cell-free supernatants of plant growth-promoting bacteria: a review of their use as biostimulant and microbial biocontrol agents in sustainable agriculture // Sustainability. 2020. V. 12. Art. 9917.
  22. Ramos A. C., Melo J.,·de Souza S. B., Bertolazi A. A., Silva R. A., Rodrigues W. P., Campostrini E., Olivares F. L., Eutrópio F. J., Cruz C., Dias T. Inoculation with the endophytic bacterium Herbaspirillum seropedicae promotes growth, nutrient uptake and photosynthetic efficiency in rice // Planta. 2020. V. 252. Art. 87.
  23. Sambrook J., Fritsch E., Maniatis T. Molecular cloning: a laboratory manual. N.Y.: Cold Spring Harbor Lab. Press, 1989. 1626 p.
  24. Tapia-García E.Y., Hernández-Trejo V., Guevara-Luna J., Rojas-Rojas F.U., Arroyo-Herrera I., Meza-Radilla G., Vásquez-Murrieta M.S., Estrada-de los Santos P. Plant growth-promoting bacteria isolated from wild legume nodules and nodules of Phaseolus vulgaris L. trap plants in central and southern Mexico // Microbiol. Res. 2020. V. 239. Art. 126522.
  25. Velichko N. S., Bagavova A. R., Burygin G. L., Pylaev T. E., Fedonenko Y. P. In situ localization and penetration route of an endophytic bacteria into roots of wheat and the common bean // Rhizosphere. 2022. V. 23. Art. 100567.
  26. Velichko N. S., Kondyurina N. K., Fedonenko Y. P. Antagonistic activity of some Herbaspirillum species against phytopathogenic micromycetes // Izvestiya of Saratov University Chemistry Biology Ecology. 2023. V. 23. P. 337–344.
  27. Velikova V., Yordanov I., Edreva A. Oxidative stress and some antioxidant systems in acid rain-treated bean plants // Plant Sci. 2000. V. 151. P. 59–66.
  28. Venkatachalam J., Mohan H., Seralathan K. K. Significance of Herbaspirillum sp. in biodegradation and biodetoxification of herbicides, pesticides, hydrocarbons and heavy metals – a review // Environ. Res. 2023. V. 239. Art. 117367.
  29. Wang F. Phytochrome A and B function antagonistically to regulate cold tolerance via abscisic acid-dependent jasmonate signaling // Plant Physiol. 2016. V. 170. P. 459–471.
  30. Wellburn A. R. The spectral determination of chlorophylls a and b, as well as total carotenoids, using various solvents with spectrophotometers of different resolution // J. Plant. Physiol. 1994. V. 144. P. 307–313.
  31. Zhou B., Guo Z., Xing J., Huang B. Nitric oxide is involved in abscisic acid-induced antioxidant activities in Stylosanthes guianensis // J. Exp. Bot. 2005. V. 56. P. 3223–3228.
  32. Zaninotto F., La Camera S., Polverari A. and Delledonne M. Cross talk between reactive nitrogen and oxygen species during the hypersensitive disease resistance response // Plant Physiol. 2006. V. 141. P. 379–383.

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML
Жүктеу

© Russian Academy of Sciences, 2025