α-Galactosidases and α-N-acetylgalactosaminidases of Planctomycetes: Origin and Genetic Diversity
- Authors: Naumoff D.G.1
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Affiliations:
- Winogradsky Institute of Microbiology, Research Center of Biotechnology, Russian Academy of Sciences
- Issue: Vol 94, No 5 (2025)
- Pages: 389-397
- Section: EXPERIMENTAL ARTICLES
- URL: https://journal-vniispk.ru/0026-3656/article/view/317081
- DOI: https://doi.org/10.7868/S3034546425050037
- ID: 317081
Cite item
Abstract
Keywords
About the authors
D. G. Naumoff
Winogradsky Institute of Microbiology, Research Center of Biotechnology, Russian Academy of Sciences
Email: daniil_naumoff@yahoo.com
Moscow, 119071, Russia
References
- Иванова А. А., Наумов Д. Г., Куличевская И. С., Мещерякова А. А., Дедыш С. Н. Paludisphaera mucosa sp. nov., новый планктомицет семейства Isosphaeraceae из бореального низинного болота // Микробиология. 2023. Т. 92. C. 347–357.
- Ivanova A. A., Naumoff D. G., Kulichevskaya I. S., Meshcheriakova A. A., Dedysh S. N. Paludisphaera mucosa sp. nov., a novel planctomycete of the family Isosphaeraceae from a boreal fen // Microbiology (Moscow). 2023. V. 92. P. 483–492.
- Наумов Д. Г. Идентификация генов α-галактозидазы и β-ксиланазы в геномной последовательности Humisphaera borealis // Сборник тезисов 10-й Всероссийской научно-практической конференции центров геномных исследований мирового уровня “Геномное секвенирование и редактирование”. 19.05.2022. Москва. С. 15. https://ngsconference.ru/wp-content/uploads/2022/12/Сборник-тезисов-NGS-2022.pdf
- Наумов Д. Г. Иерархическая классификация гликозил-гидролаз // Биохимия. 2011a. Т. 76. С. 764–780.
- Naumoff D. G. Hierarchical classification of glycoside hydrolases // Biochemistry (Moscow). 2011a. V. 76. P. 622–635.
- Наумов Д. Г. Иерархическая классификация гликозил-гидролаз // Матер. Пятого съезда общества биотехнологов России им. Ю.А. Овчинникова. 2–4 декабря 2008 г. Москва. С. 116–117. https://biorosinfo.ru/upload/file/vcongress/Naumov.pdf
- Наумов Д. Г. GHL1–GHL15: новые семейства гипотетических гликозилгидролаз // Мол. биология. 2011b. Т. 45. С. 1073–1083.
- Naumoff D. G. GHL1–GHL15: new families of the hypothetical glycoside hydrolases // Mol. Biol. (Moscow). 2011b. V. 45. P. 983–992.
- Наумов Д. Г., Степущенко О. О. Эндо-α-1,4-поли-галактозаминидазы и их гомологи: структура и эволюция // Мол. биология. 2011. Т. 45. С. 703–714.
- Naumoff D. G., Stepuschenko O. O. Endo-α-1,4-polygalactosaminidases and their homologs: structure and evolution // Mol. Biol. (Moscow). 2011. V. 45. P. 647–657.
- Наумов Д. Г., Куличевская И. С., Дедыш С. Н. Генетические детерминанты утилизации ксилана у планктомицета класса Phycisphaerae, Humisphaera borealis M1803T // Микробиология. 2022. Т. 91. C. 300–311.
- Naumoff D. G., Kulichevskaya I. S., Dedysh S. N. Genetic determinants of xylane utilization in Humisphaera borealis M1803T, a planctomycete of the class Phycisphaerae // Microbiology (Moscow). 2022. V. 91. P. 249–258.
- Altschul S. F., Madden T. L., Schaffer A. A., Zhang J., Zhang Z., Miller W., Lipman D. J. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs // Nucleic Acids Res. 1997. V. 25. P. 3389–3402.
- Brouns S. J.J., Smits N., Wu H., Snijders A. P.L., Wright P. C., de Vos W. M., van der Oost J. Identification of a novel α-galactosidase from the hyperthermophilic archaeon Sulfolobus solfataricus // J. Bacteriol. 2006. V. 188. P. 2392–2399.
- Calcutt M. J., Hsieh H.-Y., Chapman L. F., Smith D. S. Identification, molecular cloning and expression of an α-N-acetylgalactosaminidase gene from Clostridium perfringens // FEMS Microbiol. Lett. 2002. V. 214. P. 77–80.
- Davis M. O., Hata D. J., Johnson S. A., Jones D. E., Harmata M. A., Evans M. L., Walker J. C., Smith D. S. Cloning, sequence, and expression of a blood group B active recombinant α-D-galactosidase from pinto bean (Phaseolus vulgaris) // Biochem. Mol. Biol. Int. 1997. V. 42. P. 453–467. https://doi.org/10.1080/15216549700202861
- Drula E., Garron M.-L., Dogan S., Lombard V., Henrissat B., Terrapon N. The carbohydrate-active enzyme database: functions and literature // Nucleic Acids Res. 2022. V. 50 (Database issue). P. D571–D577.
- Fei Y., Jiao W., Wang Y., Liang J., Liu G., Li L. Cloning and expression of a novel α-galactosidase from Lactobacillus amylolyticus L6 with hydrolytic and transgalactosyl properties // PLoS One. 2020. V. 15. Art. e0235687.
- Felsenstein J. PHYLIP – Phylogeny Inference Package (Version 3.2) // Cladistics. 1989. V. 5. P. 164–166.
- Garron M.-L., Henrissat B. The continuing expansion of CAZymes and their families // Curr. Opin. Chem. Biol. 2019. V. 53. P. 82–87.
- Hall T. A. Bioedit: a user-friendly biological sequence alignment editor and analysis program for windows 95/98/nt // Nucleic Acids Symp. Ser. 1999. V. 41. P. 95–98.
- Henrissat B. A classification of glycosyl hydrolases based on amino acid sequence similarities // Biochem J. 1991. V. 280. Pt. 2. P. 309–316.
- Ivanova A. A., Naumoff D. G., Kulichevskaya I. S., Rakitin A. L., Mardanov A. V., Ravin N. V., Dedysh S. N. Planctomycetes of the genus Singulisphaera possess chitinolytic capabilities // Microorganisms. 2024. V. 12. Art. 1266.
- Ivanova A. A., Naumoff D. G., Miroshnikov K. K., Liesack W., Dedysh S. N. Comparative genomics of four Isosphaeraceae planctomycetes: a common pool of plasmids and glycoside hydrolase genes shared by Paludisphaera borealis PX4T, Isosphaera pallida IS1BT, Singulisphaera acidiphila DSM 18658T, and strain SH-PL62 // Front. Microbiol. 2017. V. 8. Art. 412.
- Katrolia P., Jia H., Yan Q., Song S., Jiang Z., Xu H. Characterization of a protease-resistant α-galactosidase from the thermophilic fungus Rhizomucor miehei and its application in removal of raffinose family oligosaccharides // Bioresour. Technol. 2012. V. 110. P. 578–586.
- Kulichevskaya I. S., Ivanova A. A., Naumoff D. G., Beletsky A. V., Rijpstra W. I.C., Sinninghe Damsté J. S., Mardanov A. V., Ravin N. V., Dedysh S. N. Frigoriglobus tundricola gen. nov., sp. nov., a psychrotolerant cellulolytic planctomycete of the family Gemmataceae from a littoral tundra wetland // Syst. Appl. Microbiol. 2020b. V. 43. Art. 126129.
- Kulichevskaya I. S., Ivanova A. A., Naumoff D. G., Zlatogorskaya A. A., Kachmazov G. S., Dedysh S. N. Schlesneria sphaerica sp. nov., a neutrophilic, xylan-degrading planctomycete from a mountain wetland, and emended description of the genus Schlesneria // FEMS Microbiol. Lett. 2025. V. 372. Art. fnaf006. https://doi.org/10.1093/femsle/fnaf006
- Kulichevskaya I. S., Naumoff D. G., Miroshnikov K. K., Ivanova A. A., Philippov D. A., Hakobyan A., Rijpstra W. I.C., Damsté J. S.S., Liesack W., Dedysh S. N. Limnoglobus roseus gen. nov., sp. nov., a novel freshwater planctomycete with a giant genome from the family Gemmataceae // Int. J. Syst. Evol. Microbiol. 2020a. V. 70. P. 1240–1249.
- Lombard V., Golaconda Ramulu H., Drula E., Coutinho P. M., Henrissat B. The carbohydrate-active enzymes database (CAZy) in 2013 // Nucleic Acids Res. 2014. V. 42 (Database issue). P. D490–D495.
- Lombard V., Henrissat B., Garron M. L. CAZac: an activity descriptor for carbohydrate-active enzymes // Nucleic Acids Res. 2025. V. 53 (Database issue). P. D625–D633.
- Marraccini P., Rogers W. J., Caillet V., Deshayes A., Granato D., Lausanne F., Lechat S., Pridmore D., Pétiard V. Biochemical and molecular characterization of α-D-galactosidase from coffee beans // Plant Physiol. Biochem. 2005. V. 4. P. 909–920.
- McDonald A.G., Boyce S., Tipton K. F. ExplorEnz: the primary source of the IUBMB enzyme list // Nucleic Acids Res. 2009. V. 37 (Database issue). P. D593–D597.
- Page R. D.M. TREEVIEW: An application to display phylogenetic trees on personal computers // Comput. Appl. Biosci. 1996. V. 12. P. 357–358.
- Rahfeld P., Sim L., Moon H., Constantinescu I., Morgan-Lang C., Hallam S. J., Kizhakkedathu J. N., Withers S. G. An enzymatic pathway in the human gut microbiome that converts A to universal O type blood // Nat. Microbiol. 2019. V. 4. P. 1475–1485.
- Rakitin A. L., Naumoff D. G., Beletsky A. V., Kulichevskaya I. S., Mardanov A. V., Ravin N. V., Dedysh S. N. Complete genome sequence of the cellulolytic planctomycete Telmatocola sphagniphila SP2T and characterization of the first cellulolytic enzyme from planctomycetes // Syst. Appl. Microbiol. 2021. V. 44. Art. 126276.
- Sasaki Y., Togo N., Kitahara K., Fujita K. Characterization of a GH36 β-L-arabinopyranosidase in Bifidobacterium adolescentis // J. Appl. Glycosci. 2018. V. 65. P. 23–30.
- Shibuya H., Kobayashi H., Sato T., Kim W. S., Yoshida S., Kaneko S., Kasamo K., Kusakabe I. Purification, characterization, and cDNA cloning of a novel α-galactosidase from Mortierella vinacea // Biosci. Biotechnol. Biochem. 1997. V. 61. P. 592–598.
- Terrapon N., Lombard V., Drula E., Coutinho P. M., Henrissat B. Chapter 6. The CAZy database/the Carbohydrate-Active Enzyme (CAZy) database: principles and usage guidelines // A practical guide to using glycomics databases / Ed. Aoki-Kinoshita K.F. Tokyo: Springer, 2017. P. 117–131.
- Tsuji S., Yamauchi T., Hiraiwa M., Isobe T., Okuyama T., Sakimura K., Takahashi Y., Nishizawa M., Uda Y., Miyatake T. Molecular cloning of a full-length cDNA for human α-N-acetylgalactosaminidase (α-galactosidase B) // Biochem. Biophys. Res. Commun. 1989. V. 163. P. 1498–1504.
- van Lieshout J. F.T., Verhees C. H., Ettema T. J.G. et al. Identification and molecular characterization of a novel type of α-galactosidase from Pyrococcus furiosus // Biocatal. Biotransform. 2003. V. 21. P. 243–252.
- Zheng J., Ge Q., Yan Y., Zhang X., Huang L., Yin Y. dbCAN3: automated carbohydrate-active enzyme and substrate annotation // Nucleic Acids Res. 2023. V. 51. Iss. W1. P. W115–W121.
- Zhou J., Liu Y., Lu Q., Zhang R., Wu Q., Li C., Li J., Tang X., Xu B., Ding J., Han N., Huang Z. Characterization of a glycoside hydrolase family 27 α-galactosidase from Pontibacter reveals its novel salt-protease tolerance and transglycosylation activity // J. Agric. Food Chem. 2016. V. 64. P. 2315–2324.
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