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Biosynthesis of exopolysaccharides by soil bacteria Paenibacillus mucilaginosus on a nutrient molasses medium

https://doi.org/10.21285/2227-2925-2020-10-4-708-718

Abstract

Bacterial exopolysaccharides exhibiting water-retaining and cementing properties play an essential role in such processes as the formation and stabilization of soil aggregates, regulation of nutrients and water flow through plant roots, as well as reduction of salt stress in plants. When bacteria producing exopolysaccharides are introduced into a soil, plants become more resistant to water stress due to improved structure and significant accumulation of proline, sugars and free amino acids under the conditions of water deficiency. In this work, we set out to determine the efficiency of exopolysaccharide biosynthesis by the soil bacteria Paenibacillus mucilaginosus when cultivated on a nutrient molasses medium. The bacterial strains P. mucilaginosus 560 and 574 provided by the Departmental collection of non-pathogenic microorganisms for agricultural purposes (All-Russia Research Institute for Agricultural Microbiology, St. Petersburg) were used as exopolysaccharide producers. In order to determine the influence of cultivation conditions on the synthesis of exopolysaccharides by P. mucilaginosus, the one-factor-at-a-time (OFAT) method was used. On the basis of the obtained results, we determined the most effective producer of exopolysaccharides, the age and dose of the inoculum, the optimal values of the cultivation temperature and medium pH, the source of nitrogen and its concentration, as well as the aeration conditions affecting exopolysaccharide biosynthesis and the growth of the selected bacterial strain P. mucilaginosus. It was established that the P. mucilaginosus 574 strain is the most effective producer of exopolysaccharides. It was shown that the biosynthesis of exopolysaccharides is most effective and economical upon the cultivation of P. mucilaginosus 574 on a nutrient medium containing 2% molasses without addition of minerals and nitrogen. The maximum amount of exopolysaccharides can reach 9.55 g/L on a nutrient medium containing 2% molasses at a volume of 50 ml with the addition of 0.1% corn extract as an inducer of exopolysaccharide synthesis at a cultivation temperature of 30±1 °C, a medium pH of 6.0±0.2 with the introduction of 5% inoculum after 24 hours of inoculation. The obtained research results are recommended for use when creating new technologies for the production of microbiological fertilizers.

About the Authors

D. T. Ha
Kazan National Research Technological University, Russian Federation
Russian Federation

Dung T. Ha - Postgraduate Student, Department of Food Biotechnology.

8, Tolstov St., Kazan, 420015



A. V. Kanarsky
Kazan National Research Technological University, Russian Federation
Russian Federation

Albert V. Kanarsky - Dr. Sci. (Engineering), Professor, Department of Food Biotechnology.

8, Tolstov St., Kazan, 420015



Z. A. Kanarskaya
Kazan National Research Technological University, Russian Federation
Russian Federation

Zosia A. Kanarskaya - Cand. Sci. (Engineering), Associate Professor, Department of Food Biotechnology.

8, Tolstov St., Kazan, 420015


A. V. Shcherbakov
All-Russian Research Institute of Agricultural Microbiology
Russian Federation

Andrei V. Shcherbakov - Cand. Sci. (Biology), Researcher, laboratory of Microbial Technology.

3, Podbelsky Highway, St. Petersburg, 196608



E. N. Shcherbakova
All-Russian Research Institute of Agricultural Microbiology
Russian Federation

Elena N. Shcherbakova - Cand. Sci. (Agriculture), Researcher, laboratory of Microbial Technology.

 

3, Podbelsky Highway, St. Petersburg, 196608



References

1. Khan N, Bano A, Rahman MA, Rathinasabapa-thi B, Babar MA. UPLC-HRMS-based untargeted metabolic profiling reveals changes in chickpea (Cicer ari-etinum) metabolome following long-term drought stress. Plant, Cell & Environment. 2019;42(1):115-132. https://doi.org/10.1111/pce.13195

2. Vejan P, Abdullah R, Khadiran T, Ismail S, Boyce AN. Role of plant growth promoting rhizobac-teria in agricultural sustainability - a review. Molecules. 2016;21(5):573. https://doi.org/10.3390/mole-cules21050573

3. Sade N, Gebretsadik M, Seligmann R, Schwartz A, Wallach R, Moshelion M. The role of tobacco Aquaporin1 in improving water use efficiency, hydraulic conductivity, and yield production under salt stress. Plant Physiology. 2010;152(1):245-254. https://doi.org/10.1104/pp.109.145854

4. Kloeppe JW, Rodriguez-Kabana R, Zehnder AW, Murphy JF, Sikora E, Fernandez C. Plant root-bacterial interactions in biological control of soil-borne diseases and potential extension to systemic and foliar diseases. Australasian Plant Pathology. 1999;28(1):21-26. https://doi.org/10.1071/AP99003

5. Hilliou L, Freitas F, Oliveira R, Reis MAM, Lespineux D, Grandfils C, et al. Solution properties of an exopolysaccharide from a Pseudomonas strain obtained using glycerol as single carbon source. Carbohydrate Polymers. 2009;78(3):526-532. https://doi.org/10.1016/j.carbpol.2009.05.011

6. Rottava I, Batesini G, Silva FM, Lerin L, de Oliveira D, Padilha FF, et al. Xanthan gum production and rheological behavior using different strains of Xanthomonas sp. Carbohydrate Polymers. 2009;77(1):65-71. https://doi.org/10.1016Zj.carbpol. 2008.12.001

7. Freitas F, Alves VD, Pais J, Carvalheira M, Costa N, Oliveira R, et al. Production of a new exopolysaccharide (EPS) by Pseudomonas oleo-vorans NRRL B-14682 grown on glycerol. Process Biochemistry. 2010;45(3):297-305. https://doi.org/10.1016/j.procbio.2009.09.020

8. Liang T-W, Wang S-L. Recent advances in exopolysaccharides from Paenibacillus spp.: production, isolation, structure, and bioactivities. Marine Drugs. 2015;13(4):1847-1863. https://doi.org/10.3390/md13041847

9. Roberson EB, Firestone MK. Relationship between Desiccation and Exopolysaccharide Production in a Soil Pseudomonas sp. Applied and Environmental Microbiology. 1992;58(4):1284-1291. https://doi.org/10.1128/AEM.58.4.1284-1291.1992

10. Tisdall JM, Oades JM. Organic matter and water stable aggregates in soils. European Journal of Soil Science. 1982;33(2):141-163. https://doi.org/10.1111/j.1365-2389.1982.tb01755.x

11. Sabra W, Zeng AP, Lunsdorf H, Deckwer WD. Effect of oxygen on formation and structure of Azotobacter vinelandii alginate and its role in protecting nitrogenase. Applied and environmental microbiology. 2000;66(9):4037-4044. https://doi.Org/10.1128/aem.66.9.4037-4044.2000

12. Leigh JA, Coplin DL. Exopolysaccharides in plant-bacterial interactions. Annual Review of Microbiology. 1992;46:307-346. https://doi.org/10.1146/annurev.mi.46.100192.001515

13. Ashraf M. Photosynthetic capacity and ion accumulation in a medicinal plant henbane (Hyos-cyamus niger L.) under salt stress. Journal of Applied Botany and Food Quality. 2004;78(2):91-96.

14. Naseem H, Ahsan M, Shahid MA, Khan N. Exopolysaccharides producing rhizobacteria and their role in plant growth and drought tolerance. Journal of Basic Microbiology. 2018;58(12):1009-22. https://doi.org/10.1002/jobm.201800309

15. Bashan Y, Holguin G, de-Bashan LE. Azospirillum-plant relationships: physiological, molecular, agricultural, and environmental advances (1997-2003). Canadian Journal of Microbiology. 2004;50(8):521-577. https://doi.org/10.1139/W04-035

16. Li X, Yang SH, Yu XC, Jin ZX, Li WD, Li L, et al. Construction of transgenic Bacillus mucilagi-nosus strain with improved phytase secretion // Journal of Applied Microbiology. 2005. Vol. 99. Issue 4. P. 878-884. https://doi.org/10.1111/j.1365-2672.2005.02683.x

17. Czitrom V. One-factor-at-a-time versus designed experiments. The American Statistician. 1999;53(2):126-131. https://doi.org/10.1080/00031305.1999.10474445

18. Maier RM. Bacterial Growth. In: Maier RM, Pepper II, Gerba CP. Environmental Microbiology. San Diego, CA: Academic Press; 2000. Chapter 3. p. 43-60.

19. Barley MJ, Biely P, Poutanen K. Interlaboratory testing of methods for assay of xylanase activity. Journal of Biotechnology. 1992;23(3):257-270.

20. Morozova YuA, Skvortsov EV, Alimova FK, Kanarsky AV. The biosynthesis of xylanases and cellulases by Trichoderma fungi on the post-alcohol bard. Vestnik Kazanskogo tekhnologicheskogo uni-versiteta = Bulletin of the Technological University. 2012;15(19):120-122. (In Russian)

21. Ha DT, Kanarsky AV, Kanarskaya ZA, Shcherbakov AV, Shcherbakova EN. The efficiency of Paenibacillus mucilaginosus bacteria cultivation on nutrient medium based on sucrose. Nauchnyi zhurnal NIU ITMO. Seriya: Protsessy i apparaty pishchevykh proizvodstv = Scientific Journal NRU ITMO. Processes and Food Production Equipment. 2019;3:62-72. (In Russian) https://doi.org/10.17586/2310-1164-2019-12-3-62-72

22. Ha DT, Kanarskaya ZA, Kanarsky AV, Shcherbakov AV, Shcherbakova EN. The effect of carbon source on the biomass and exopolysaccharide synthesis by Paenibacillus mucilaginosus bacteria. Izvestiya Vuzov. Prikladnaya khimiya i bio-tekhnologiya = Proceedings of Universities. Applied Chemistry and Biotechnology. 2019;9(3):509-518. (In Russian) https://doi.org/10.21285/2227-2925-2019-9-3-509-518

23. Yarovenko VL, Marinchenko VA, Smirnov VA, Ustinnikov BA, Tsygankov PS, Shvets VN, et al. Technology of alcohol. Moscow: Kolos-Press; 2002. 464 p. (In Russian)

24. Emtiazia G, Ethemadifara Z, Habibib MH. Production of extra-cellular polymer in Azotobacter and biosorption of metal by exopolymer. African Journal of Biotechnology. 2004;3(6):330-333. https://doi.org/10.5897/AJB2004.000-2060

25. Razack SA, Velayutham V, Thangavelu V. Medium optimization for the production of exopolysaccharide by Bacillus subtilis using synthetic sources and agro wastes. Turkish Journal of Biology. 2013;3(37):280-288. https://doi.org/10.3906/biy-1206-50

26. Chaijamrus S, Udpuay N. Production and Characterisation of Polyhydroxybutyrate from Molasses and Corn Steep Liquor produced by Bacillus megaterium ATCC 6748. Agricultural Engineering International: the CIGR Ejournal. X p. 1-12, 2008.

27. Sharma N, Prasad GS, Choudhury AR. Utilization of corn steep liquor for biosynthesis of pullu-lan, an important exopolysaccharide. Carbohydrate Polymers. 2013;93(1):95—101. https://doi.org/10.1016/j.carbpol.2012.06.059

28. Elisashvili VI, Kachlishvili ET, Wasser SP. Carbon and nitrogen source effects on basidiomy-cetes exopolysaccharide production. Applied Biochemistry and Microbiology. 2009;45(5):531-535. https://doi.org/10.1134/S0003683809050135

29. Wang C-L, Huang T-H, Liang T-W, Fang C-Y, Wang S-L. Production and characterization of exopolysaccharides and antioxidant from Paeni-bacillus sp. TKU023. New Biotechnology. 2011;28(6):559-565. https://doi.org/10.1016/j.nbt.2011.03.003


Review

For citations:


Ha D.T., Kanarsky A.V., Kanarskaya Z.A., Shcherbakov A.V., Shcherbakova E.N. Biosynthesis of exopolysaccharides by soil bacteria Paenibacillus mucilaginosus on a nutrient molasses medium. Proceedings of Universities. Applied Chemistry and Biotechnology. 2020;10(4):708-718. (In Russ.) https://doi.org/10.21285/2227-2925-2020-10-4-708-718

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