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Cellulose biosynthesis and function in bacteria
Open accessAbstract
The current model of cellulose biogenesis in plants, as well as bacteria, holds that the membranous cellulose synthase complex polymerizes glucose moieties from UDP-Glc into beta-1,4-glucan chains which give rise to rigid crystalline fibrils upon extrusion at the outer surface of the cell. The distinct arrangement and degree of association of the polymerizing enzyme units presumably govern extracellular chain assembly in addition to the pattern and width of cellulose fibril deposition. Most evident for Acetobacter xylinum, polymerization and assembly appear to be tightly coupled. To date, only bacteria have been effectively studied at the biochemical and genetic levels. In A. xylinum, the cellulose synthase, composed of at least two structurally similar but functionally distinct subunits, is subject to a multicomponent regulatory system. Regulation is based on the novel nucleotide cyclic diguanylic acid, a positive allosteric effector, and the regulatory enzymes maintaining its intracellular turnover: diguanylate cyclase and Ca2(+)-sensitive bis-(3',5')-cyclic diguanylic acid (c-di-GMP) phosphodiesterase. Four genes have been isolated from A. xylinum which constitute the operon for cellulose synthesis. The second gene encodes the catalytic subunit of cellulose synthase; the functions of the other three gene products are still unknown. Exclusively an extracellular product, bacterial cellulose appears to fulfill diverse biological roles within the natural habitat, conferring mechanical, chemical, and physiological protection in A. xylinum and Sarcina ventriculi or facilitating cell adhesion during symbiotic or infectious interactions in Rhizobium and Agrobacterium species. A. xylinum is proving to be most amenable for industrial purposes, allowing the unique features of bacterial cellulose to be exploited for novel product applications.
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“Bacterial cellulose (BC), produced by acetic acid bacteria Gluconobacter xylinum, is obtainable in a pure form which requires no intensive processing to remove undesirable impurities and contaminants such as lignin, pectin and hemicellulose.75,76”
From Sustainable hybrid photocatalysts: titania immobilized on carbon materials derived from renewable and biodegradable resources (2016) · cites this paper as [76]
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Gilles‐Gonzalez, M. (2003) · CRC Press eBooks · doi:10.1201/b14819-3 · Cited by 4
Bacterial cellulose : from culturing to the development of functional materials
Vadanan, S. V. (2020) · doi:10.32657/10356/143357 · Cited by 4
Hyodo, M., & Hayakawa, Y. (2008) · doi:10.1002/9783527623112.ch13 · Cited by 4
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Sathish, S. K., & Vitta, S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-803581-8.11489-4 · Cited by 4
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Pértile, R. A. N., Siqueira, J. M., Rambo, C. R., et al. (2008) · Exacta · doi:10.5585/exacta.v5i2.1184 · Cited by 3
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Mathivanan, Y., Shahir, S., Ibrahim, Z., et al. (2024) · Polymer Bulletin · doi:10.1007/s00289-024-05433-4 · Cited by 3
“Bacterial nanocellulose has an incredibly thin fibril texture with more crystalline regions consolidated by intra and intermolecular hydrogen bonds that contribute to the rigidity of the structure [46].”
Wolfe, A. J., & Visick, K. L. (2014) · ASM Press eBooks · doi:10.1128/9781555816667.ch13 · Cited by 3
Khanafari, A., Zangeneh, G. Y. N., & Sharifnia, F. (2013) · Jundishapur Journal of Microbiology · doi:10.5812/jjm.4807 · Cited by 3
“Medical application of microbial cellulose in the treatment of different types of wounds on a large scale was initiated in the early 1980s (17).”
BackgroundGhafoor, A. (2014) · Journal of Infection and Molecular Biology · doi:10.14737/jimb.2307-5465/2.4.61.73 · Cited by 3
“Comparative genome analysis of many other species has revealed the presence of genes homologous to- the G. xylinus BCS (Bacterial Cellulose Synthesis), indicating their capability to produce cellulose (Ross et al., 1991).”
Biomolecules in Space: The Way to Search for Life on Mars
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de Carvalho, K. A. T. (2016) · Elsevier eBooks · doi:10.1016/b978-0-444-63660-7.00014-0 · Cited by 2
Vidotto, F. L., Ribeiro, G. P., & Tischer, C. A. (2018) · Brazilian Archives of Biology and Technology · doi:10.1590/1678-4324-2016160696 · Cited by 2
Metadata
- Authors
- Ross, P., Mayer, R., & Benziman, M.
- Affiliations
- Hebrew University of Jerusalem (IL)
- Venue
- Microbiological Reviews
- Publisher
- American Society for Microbiology
- Published
- 1991-03
- Volume
- 55
- Issue
- 1
- Pages
- 35-58
- ISSN
- 0146-0749 (ISSN-L)
- PMC
- PMC372800
- OpenAlex
- W1911657064
- Cited by
- 1,231
- References
- 145
- Citations by year
- 2026: 18 · 2025: 43 · 2024: 45 · 2023: 64 · 2022: 67 · 2021: 74 · 2020: 56 · 2019: 59 · 2018: 60 · 2017: 56 · 2016: 48 · 2015: 70 · 2014: 67 · 2013: 53 · 2012: 47
- FWCI
- 8.86
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Locations
- Microbiological Reviews (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Materials Science › Biomaterials › Advanced Cellulose Research Studies
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Polysaccharides and Plant Cell Walls
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- bacterial cellulose, cellulose biosynthesis, cellulose synthase, Acetobacter xylinum, c-di-GMP, diguanylate cyclase, c-di-GMP phosphodiesterase, allosteric regulation, Sarcina ventriculi, Rhizobium, Agrobacterium, cell adhesion
- MeSH terms
- Bacteria, Cellulose
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