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Sporulation capability and amylosome conservation among diverse human colonic and rumen isolates of the keystone starch-degrader Ruminococcus bromii.

Mukhopadhya, I; Moraïs, S; Laverde-Gomez, J; Sheridan, PO; Walker, AW; Kelly, W; Klieve, AV; Ouwerkerk, D; Duncan, SH; Louis, P; et al. Mukhopadhya, I; Moraïs, S; Laverde-Gomez, J; Sheridan, PO; Walker, AW; Kelly, W; Klieve, AV; Ouwerkerk, D; Duncan, SH; Louis, P; Koropatkin, N; Cockburn, D; Kibler, R; Cooper, PJ; Sandoval, C; Crost, E; Juge, N; Bayer, EA; Flint, HJ (2018) Sporulation capability and amylosome conservation among diverse human colonic and rumen isolates of the keystone starch-degrader Ruminococcus bromii. Environ Microbiol, 20 (1). pp. 324-336. ISSN 1462-2920 https://doi.org/10.1111/1462-2920.14000
SGUL Authors: Cooper, Philip John

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Abstract

Ruminococcus bromii is a dominant member of the human colonic microbiota that plays a 'keystone' role in degrading dietary resistant starch. Recent evidence from one strain has uncovered a unique cell surface 'amylosome' complex that organizes starch-degrading enzymes. New genome analysis presented here reveals further features of this complex and shows remarkable conservation of amylosome components between human colonic strains from three different continents and a R. bromii strain from the rumen of Australian cattle. These R. bromii strains encode a narrow spectrum of carbohydrate active enzymes (CAZymes) that reflect extreme specialization in starch utilization. Starch hydrolysis products are taken up mainly as oligosaccharides, with only one strain able to grow on glucose. The human strains, but not the rumen strain, also possess transporters that allow growth on galactose and fructose. R. bromii strains possess a full complement of sporulation and spore germination genes and we demonstrate the ability to form spores that survive exposure to air. Spore formation is likely to be a critical factor in the ecology of this nutritionally highly specialized bacterium, which was previously regarded as 'non-sporing', helping to explain its widespread occurrence in the gut microbiota through the ability to transmit between hosts.

Item Type: Article
Additional Information: © 2017 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Keywords: Animals, Carbohydrate Metabolism, Cattle, Child, Colon, Humans, Male, Microbiota, Multiprotein Complexes, Rumen, Ruminococcus, Spores, Bacterial, Starch, Colon, Rumen, Animals, Cattle, Humans, Ruminococcus, Spores, Bacterial, Multiprotein Complexes, Starch, Child, Male, Carbohydrate Metabolism, Microbiota, 0603 Evolutionary Biology, 0605 Microbiology, Microbiology
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Environ Microbiol
ISSN: 1462-2920
Language: eng
Dates:
DateEvent
11 January 2018Published
7 December 2017Published Online
16 November 2017Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
UNSPECIFIEDWellcome Trusthttp://dx.doi.org/10.13039/100004440
BB/L008602/1Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
BB/L009951/1Biotechnology and Biological Sciences Research Councilhttp://dx.doi.org/10.13039/501100000268
UNSPECIFIEDScottish Government Food, Land and People programUNSPECIFIED
1349/13Israel Science Foundationhttp://dx.doi.org/10.13039/501100003977
1339/13Israel Science Foundationhttp://dx.doi.org/10.13039/501100003977
UNSPECIFIEDUnited States-Israel Binational Science Foundationhttp://dx.doi.org/10.13039/501100001742
PubMed ID: 29159997
Web of Science ID: WOS:000419784100025
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116501
Publisher's version: https://doi.org/10.1111/1462-2920.14000

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