In vivo Functional Characterization of Hydrophilic X2 Modules in the Cellulosomal Scaffolding Protein
As part of free cellulases or scaffolding proteins in cellulosomes, the hydrophilic non-catalytic X2 module is widely distributed in cellulolytic or other bacteria. Previous biochemical studies suggest that X2 modules might increase the solubility and substrate binding affinity of X2-bearing protein...
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Published in | Frontiers in microbiology Vol. 13; p. 861549 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Research Foundation
07.04.2022
Frontiers Media S.A |
Subjects | |
Online Access | Get full text |
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Summary: | As part of free cellulases or scaffolding proteins in cellulosomes, the hydrophilic non-catalytic X2 module is widely distributed in cellulolytic
or other
bacteria. Previous biochemical studies suggest that X2 modules might increase the solubility and substrate binding affinity of X2-bearing proteins. However, their
biological functions remain elusive. Here we employed CRISPR-Cas9 editing to genetically modify X2 modules by deleting the conserved motif (NGNT) from the CipC scaffoldin. Both single and double X2 mutants (X2-N: near the N terminus of CipC; X2-C: near the C terminus of CipC) presented similar stoichiometric compositions in isolated cellulosomes as the wildtype strain (WT). These X2 mutants had an elongated adaptation stage during growth on cellulose compared to cellobiose. Compared to WT, the double mutant ΔX2-NC reduced cellulose degradation by 15% and the amount of released soluble sugars by 63%. Since single X2 mutants did not present such obvious physiological changes as ΔX2-NC, there seems to be a functional redundancy between X2 modules in CipC. The
adhesion assay revealed that ΔX2-NC decreased cell attachment to cellulose by 70% but a weaker effect was also overserved in single X2 mutants. These results highlight the
biological role of X2 in increasing cellulose degradation efficiency by enhancing the binding affinity between cells and cellulose, which provides new perspectives for microbial engineering. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 USDOE AC02-05CH11231 Edited by: Xinqing Zhao, Shanghai Jiao Tong University, China Reviewed by: Fu-Li Li, Qingdao Institute of Bioenergy and Bioprocess Technology (CAS), China; Roberto Mazzoli, University of Turin, Italy This article was submitted to Microbial Physiology and Metabolism, a section of the journal Frontiers in Microbiology These authors have contributed equally to this work and share first authorship |
ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2022.861549 |