Unraveling essential cellulosomal components of the (

Biotechnology CBM Cellulases Cellulolytic bacteria Cohesin Dockerin Enzymatic hydrolysis Glycoside hydrolases Scaffoldin

Journal

Biotechnology for biofuels
ISSN: 1754-6834
Titre abrégé: Biotechnol Biofuels
Pays: England
ID NLM: 101316935

Informations de publication

Date de publication:
2019
Historique:
received: 18 02 2019
accepted: 20 04 2019
entrez: 16 5 2019
pubmed: 16 5 2019
medline: 16 5 2019
Statut: epublish

Résumé

( The current proteome-wide work reveals patterns of protein expression of the various cellulosomal components, and explores the signature of differential expression upon growth of the bacterium on two major carbon sources-cellobiose and microcrystalline cellulose. Mass spectrometry analysis of the bacterial secretome revealed the expression of 24 scaffoldin structural units and 166 dockerin-bearing components (mainly enzymes), in addition to free enzymatic subunits. The dockerin-bearing components comprise cell-free and cell-bound cellulosomes for more efficient carbohydrate degradation. Various glycoside hydrolase (GH) family members were represented among 102 carbohydrate-degrading enzymes, including the omnipresent, most abundant GH48 exoglucanase. Specific cellulosomal components were found in different molecular-weight fractions associated with cell growth on different carbon sources. Overall, microcrystalline cellulose-derived cellulosomes showed markedly higher expression levels of the structural and enzymatic components, and exhibited the highest degradation activity on five different cellulosic and/or hemicellulosic carbohydrates. The cellulosomal activity of The current research demonstrates the involvement of key cellulosomal factors that participate in the mechanism of carbohydrate degradation by

Sections du résumé

BACKGROUND BACKGROUND
(
RESULTS RESULTS
The current proteome-wide work reveals patterns of protein expression of the various cellulosomal components, and explores the signature of differential expression upon growth of the bacterium on two major carbon sources-cellobiose and microcrystalline cellulose. Mass spectrometry analysis of the bacterial secretome revealed the expression of 24 scaffoldin structural units and 166 dockerin-bearing components (mainly enzymes), in addition to free enzymatic subunits. The dockerin-bearing components comprise cell-free and cell-bound cellulosomes for more efficient carbohydrate degradation. Various glycoside hydrolase (GH) family members were represented among 102 carbohydrate-degrading enzymes, including the omnipresent, most abundant GH48 exoglucanase. Specific cellulosomal components were found in different molecular-weight fractions associated with cell growth on different carbon sources. Overall, microcrystalline cellulose-derived cellulosomes showed markedly higher expression levels of the structural and enzymatic components, and exhibited the highest degradation activity on five different cellulosic and/or hemicellulosic carbohydrates. The cellulosomal activity of
CONCLUSIONS CONCLUSIONS
The current research demonstrates the involvement of key cellulosomal factors that participate in the mechanism of carbohydrate degradation by

Identifiants

pubmed: 31086567
doi: 10.1186/s13068-019-1447-2
pii: 1447
pmc: PMC6507058
doi:

Types de publication

Journal Article

Langues

eng

Pagination

115

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

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Auteurs

Olga Zhivin-Nissan (O)

1Department of Biomolecular Sciences, The Weizmann Institute of Science, Rehovot, Israel.

Bareket Dassa (B)

2Bioinformatics Unit, Life Sciences Core Facilities, Weizmann Institute of Science, Rehovot, Israel.

Ely Morag (E)

1Department of Biomolecular Sciences, The Weizmann Institute of Science, Rehovot, Israel.

Meital Kupervaser (M)

3Proteomics Unit, Nancy and Stephen Grand Israel National Center for Personalized Medicine, Weizmann Institute of Science, Rehovot, Israel.

Yishai Levin (Y)

3Proteomics Unit, Nancy and Stephen Grand Israel National Center for Personalized Medicine, Weizmann Institute of Science, Rehovot, Israel.

Edward A Bayer (EA)

1Department of Biomolecular Sciences, The Weizmann Institute of Science, Rehovot, Israel.

Classifications MeSH