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 inFrontiers in microbiology Vol. 13; p. 861549
Main Authors Tao, Xuanyu, Liu, Jiantao, Kempher, Megan L, Xu, Tao, Zhou, Jizhong
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Research Foundation 07.04.2022
Frontiers Media S.A
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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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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