Changes in the chemical, physical-chemical and biological properties of Ochrobactrum cytisi IPA7.2 lipopolysaccharide during О-deacylation
- Authors: Filip’echeva Y.A.1, Sigida E.N.1, Tkachenko O.V.2, Burygin G.L.1
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Affiliations:
- Institute of Biochemistry and Physiology of Plants and Microorganisms of the Russian Academy of Sciences - Subdivision of the Federal State Budgetary Research Institution Saratov Federal Scientific Centre of the Russian Academy of Sciences (IBPPM RAS)
- Saratov State University of Genetics, Biotechnology and Engineering named after N. I. Vavilov
- Issue: Vol 24, No 1 (2024)
- Pages: 44-50
- Section: Chemistry
- URL: https://journal-vniispk.ru/1816-9775/article/view/357152
- DOI: https://doi.org/10.18500/1816-9775-2024-24-1-44-50
- EDN: https://elibrary.ru/AJKDRB
- ID: 357152
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About the authors
Yulia A. Filip’echeva
Institute of Biochemistry and Physiology of Plants and Microorganisms of the Russian Academy of Sciences - Subdivision of the Federal State Budgetary Research Institution Saratov Federal Scientific Centre of the Russian Academy of Sciences (IBPPM RAS)410049, Russia, Saratov, Entuziastov Avenue, 13
Elena N. Sigida
Institute of Biochemistry and Physiology of Plants and Microorganisms of the Russian Academy of Sciences - Subdivision of the Federal State Budgetary Research Institution Saratov Federal Scientific Centre of the Russian Academy of Sciences (IBPPM RAS)410049, Russia, Saratov, Entuziastov Avenue, 13
Oksana V. Tkachenko
Saratov State University of Genetics, Biotechnology and Engineering named after N. I. Vavilov
ORCID iD: 0000-0001-8327-6763
Scopus Author ID: 36808551900
Saratov 410012, Russia
Gennady L. Burygin
Institute of Biochemistry and Physiology of Plants and Microorganisms of the Russian Academy of Sciences - Subdivision of the Federal State Budgetary Research Institution Saratov Federal Scientific Centre of the Russian Academy of Sciences (IBPPM RAS)410049, Russia, Saratov, Entuziastov Avenue, 13
References
- Raetz C. R., Whitfield C. Lipopolysaccharide endotoxins // Ann. Rev. Biochem. 2002. Vol. 71, iss. 1. P. 635–700. https://doi.org/10.1146/annurev.biochem.71.110601.135414
- Kagan J. C. Lipopolysaccharide detection across the kingdoms of life // Trends Immunol. 2017. Vol. 38, iss. 10. P. 696 –704. https://doi.org/10.1016/j.it.2017.05.001
- Valvano M. A. Genetics and biosynthesis of lipopolysaccharide // Molecular medical microbiology / eds. Y.-W. Tang, M. Sussman, D. Liu, I. Pexton, J. Schwartzman. 2nd ed. Academic Press, 2015. P. 55–89. https:// doi.org/10.1016/B978-0-12-397169-2.00004-4
- Vanacore A., Vitiello G., Wanke A., Cavasso D., Clifton L. A., Mahdi L., Campanero-Rhodes M. A., Solís D., Wuhrer M., Nicolardi S., Molinaro A. Lipopolysaccharide O-antigen molecular and supramolecular modifi cations of plant root microbiota are pivotal for host recognition // Carbohydr. Polym. 2022. Vol. 277. Article number 118839. P. 1–11. https://doi.org/10.1016/j. carbpol.2021.118839
- Ryan M. P., Pembroke J. T. The genus Ochrobactrum as major opportunistic pathogens // Microorganisms. 2020. Vol. 8 (11). Article number 1797. https://doi. org/10.3390/microorganisms8111797 6
- Burygin G. L., Kargapolova K. Yu., Kryuchkova Ye. V., Avdeeva E. S., Gogoleva N. E., Ponomaryova T. S., Tkachenko O. V. Ochrobactrum cytisi IPA7.2 promotes growth of potato microplants and is resistant to abiotic stress // World J. Microbiol. Biotechnol. 2019. Vol. 35, iss. 4. Article number 55. P. 1–12. https://doi.org/10.1007/s11274-019-2633-x
- Sigida E. N., Kargapolova K. Y., Shashkov A. S., Zdorovenko E. L., Ponomaryova T. S., Meshcheryakova A. A., Tkachenko O. V., Burygin G. L., Knirel Y. A. Structure, gene cluster of the O antigen and biological activity of the lipopolysaccharide from the rhizospheric bacterium Ochrobactrum cytisi IPA7.2 // Int. J. Biol. Macromol. 2020. Vol. 154. P. 1375–1381. https://doi.org/10.1016/j.ijbiomac.2019.11.017
- DuBois M., Gilles K. A., Hamilton J. K., Rebers P. T., Smith F. Colorimetric method for determination of sugars and related substances // Anal. Chem. 1956. Vol. 28, iss. 3. P. 350–356. https://doi.org/10.1021/ac60111a017
- Bailey G. S. Ouchterlony double immunodiffusion // The protein protocols handbook. 1996. P. 749–752. https:// doi.org/10.1007/978-1-60327-259-9_135
- Zdorovenko E. L., Kadykova A. A., Shashkov A. S., Varbanets L. D., Bulyhina T. V., Knirel Y. A. Lipopolysaccharide of Pantoea agglomerans 7969: Chemical identifi cation, function and biological activity // Carbohydr. Polym. 2017. Vol. 165. P. 351–358. https://doi. org/10.1016/j.carbpol.2017.02.053
- Tkachenko O. V., Burygin G. L., Evseeva N. V., Fedonenko Y. P., Matora L. Y., Lobachev Y. V., Shchyogolev S. Y. Morphogenesis of wheat calluses treated with Azospirillum lipopolysaccharides // Plant Cell Tissue Organ Cult. 2021. Vol. 147, iss. 1. P. 147–155. https:// doi.org/10.1007/s11240-021-02114-2
- Velasco J., Moll H., Knirel Y. A., Sinnwell V., Moriyón I., Zähringer U. Structural studies on the lipopolysaccharide from a rough strain of Ochrobactrum anthropi containing a 2,3-diamino-2,3-dideoxy-Dglucose disaccharide lipid A backbone // Carbohydr. Res. 1998. Vol. 306, iss. 1–2. P. 283–290. https://doi.org/10.1016/S0008-6215(97)10029-5
- Zamlynska K., Komaniecka I., Zebracki K., Mazur A., Sroka-Bartnicka A., Choma A. Studies on lipid A isolated from Phyllobacterium trifolii PETP02T lipopolysaccharide // Antonie Van Leeuwenhoek. 2017. Vol. 110. P. 1413–1433. https://doi.org/10.1007/s10482- 017-0872-0
- Wang J., Villeneuve S., Zhang J., Lei P.S., Miller C. E., Lafaye P., Nato F., Szu S. C., Karpas A., Bystricky S., Robbins J. B. On the antigenic determinants of the lipopolysaccharides of Vibrio cholerae O: 1, serotypes Ogawa and Inaba // J. Biol. Chem. 1998. Vol. 273, iss. 5. P. 2777–2783. https://doi.org/10.1074/jbc. 273.5.2777
- Haji-Ghassemi O., Blackler R. J., Martin Young N., Evans S. V. Antibody recognition of carbohydrate epitopes // Glycobiology. 2015. Vol. 25, iss. 9. P. 920–952. https://doi.org/10.1093/glycob/cwv037
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