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The Cytosolic Oligosaccharide-Degrading Proteome of Butyrivibrio Proteoclasticus
The growth and productivity of ruminants depends on a complex microbial community found in their fore-stomach (rumen), which is able to breakdown plant polysaccharides and ferment the released sugars. Butyrivibrio proteoclasticus B316(T) is a Gram-positive polysaccharide-degrading, butyrate-producin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217386/ https://www.ncbi.nlm.nih.gov/pubmed/28248275 http://dx.doi.org/10.3390/proteomes3040347 |
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author | Dunne, Jonathan C. Kelly, William J. Leahy, Sinead C. Li, Dong Bond, Judy J. Peng, Lifeng Attwood, Graeme T. Jordan, T. William |
author_facet | Dunne, Jonathan C. Kelly, William J. Leahy, Sinead C. Li, Dong Bond, Judy J. Peng, Lifeng Attwood, Graeme T. Jordan, T. William |
author_sort | Dunne, Jonathan C. |
collection | PubMed |
description | The growth and productivity of ruminants depends on a complex microbial community found in their fore-stomach (rumen), which is able to breakdown plant polysaccharides and ferment the released sugars. Butyrivibrio proteoclasticus B316(T) is a Gram-positive polysaccharide-degrading, butyrate-producing bacterium that is present at high numbers in the rumen of animals consuming pasture or grass silage based diets. B316(T) is one of a small number of rumen fibrolytic microbes capable of efficiently degrading and utilizing xylan, as well as being capable of utilizing arabinose, xylose, pectin and starch. We have therefore carried out a proteomic analysis of B316(T) to identify intracellular enzymes that are implicated in the metabolism of internalized xylan. Three hundred and ninety four proteins were identified including enzymes that have potential to metabolize assimilated products of extracellular xylan digestion. Identified enzymes included arabinosidases, esterases, an endoxylanase, and β-xylosidase. The presence of intracellular debranching enzymes indicated that some hemicellulosic side-chains may not be removed until oligosaccharides liberated by extracellular digestion have been assimilated by the cells. The results support a model of extracellular digestion of hemicellulose to oligosaccharides that are then transported to the cytoplasm for further digestion by intracellular enzymes. |
format | Online Article Text |
id | pubmed-5217386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-52173862017-02-27 The Cytosolic Oligosaccharide-Degrading Proteome of Butyrivibrio Proteoclasticus Dunne, Jonathan C. Kelly, William J. Leahy, Sinead C. Li, Dong Bond, Judy J. Peng, Lifeng Attwood, Graeme T. Jordan, T. William Proteomes Article The growth and productivity of ruminants depends on a complex microbial community found in their fore-stomach (rumen), which is able to breakdown plant polysaccharides and ferment the released sugars. Butyrivibrio proteoclasticus B316(T) is a Gram-positive polysaccharide-degrading, butyrate-producing bacterium that is present at high numbers in the rumen of animals consuming pasture or grass silage based diets. B316(T) is one of a small number of rumen fibrolytic microbes capable of efficiently degrading and utilizing xylan, as well as being capable of utilizing arabinose, xylose, pectin and starch. We have therefore carried out a proteomic analysis of B316(T) to identify intracellular enzymes that are implicated in the metabolism of internalized xylan. Three hundred and ninety four proteins were identified including enzymes that have potential to metabolize assimilated products of extracellular xylan digestion. Identified enzymes included arabinosidases, esterases, an endoxylanase, and β-xylosidase. The presence of intracellular debranching enzymes indicated that some hemicellulosic side-chains may not be removed until oligosaccharides liberated by extracellular digestion have been assimilated by the cells. The results support a model of extracellular digestion of hemicellulose to oligosaccharides that are then transported to the cytoplasm for further digestion by intracellular enzymes. MDPI 2015-10-27 /pmc/articles/PMC5217386/ /pubmed/28248275 http://dx.doi.org/10.3390/proteomes3040347 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dunne, Jonathan C. Kelly, William J. Leahy, Sinead C. Li, Dong Bond, Judy J. Peng, Lifeng Attwood, Graeme T. Jordan, T. William The Cytosolic Oligosaccharide-Degrading Proteome of Butyrivibrio Proteoclasticus |
title | The Cytosolic Oligosaccharide-Degrading Proteome of Butyrivibrio Proteoclasticus |
title_full | The Cytosolic Oligosaccharide-Degrading Proteome of Butyrivibrio Proteoclasticus |
title_fullStr | The Cytosolic Oligosaccharide-Degrading Proteome of Butyrivibrio Proteoclasticus |
title_full_unstemmed | The Cytosolic Oligosaccharide-Degrading Proteome of Butyrivibrio Proteoclasticus |
title_short | The Cytosolic Oligosaccharide-Degrading Proteome of Butyrivibrio Proteoclasticus |
title_sort | cytosolic oligosaccharide-degrading proteome of butyrivibrio proteoclasticus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217386/ https://www.ncbi.nlm.nih.gov/pubmed/28248275 http://dx.doi.org/10.3390/proteomes3040347 |
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