Construction of Chitinase Complexes Using Self-Assembly Systems for Efficient Hydrolysis of Chitin

Chitin biomass is the second most abundant natural polysaccharide after cellulose on the earth, yet its recalcitrance to degrade and utilize severely limits its application. However, many microorganisms, such as <i>Serratia marcescen</i>, can secrete a range of free chitinases to degrade chitin, though their activity is typically insufficient to meet industrial demands. In this study, we employed self-assembly systems, named SpyTag/SpyCatcher and SnoopTag/SnoopCatcher, to modularize the molecular design of CHB, ChiB, ChiC, and CBP21 derived from <i>S. marcescens</i> ATCC14756, and we successfully constructed a variety of chitinase complexes. The assembled complexes showed higher chitinolytic activity and stability, compared to free chitinase mixture. Moreover, the distinct arrangements and combinations of chitinases within these complexes led to varied activities, suggesting that the spatial proximity and substrate channeling effects contribute to the synergy of chitinase complexes. The findings lay a solid technical foundation for the application of chitinosome in the industrial production of <i>N</i>-acetylglucosamine and chitooligosaccharides.

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Publication Details

Journal
ACS Synthetic Biology
Published
2024-11-20
DOI
https://doi.org/10.1021/acssynbio.4c00613
Citations
8
Primary Topic
Biochemical and Structural Characterization
Type
article
Field-Weighted Citation Impact
1.87

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article

Construction of Chitinase Complexes Using Self-Assembly Systems for Efficient Hydrolysis of Chitin

Yu‐Chen Pan, Yuansheng Liu, Houhui Song, Zhewei Shen et al.
8 citations
ACS Synthetic Biology
Biochemical and Structural Characterization
1.87
article

Construction of Chitinase Complexes Using Self-Assembly Systems for Efficient Hydrolysis of Chitin

Yu‐Chen Pan, Yuansheng Liu, Houhui Song, Zhewei Shen, Chenggang Xu
article en
8 citations

Abstract

Chitin biomass is the second most abundant natural polysaccharide after cellulose on the earth, yet its recalcitrance to degrade and utilize severely limits its application. However, many microorganisms, such as <i>Serratia marcescen</i>, can secrete a range of free chitinases to degrade chitin, though their activity is typically insufficient to meet industrial demands. In this study, we employed self-assembly systems, named SpyTag/SpyCatcher and SnoopTag/SnoopCatcher, to modularize the molecular design of CHB, ChiB, ChiC, and CBP21 derived from <i>S. marcescens</i> ATCC14756, and we successfully constructed a variety of chitinase complexes. The assembled complexes showed higher chitinolytic activity and stability, compared to free chitinase mixture. Moreover, the distinct arrangements and combinations of chitinases within these complexes led to varied activities, suggesting that the spatial proximity and substrate channeling effects contribute to the synergy of chitinase complexes. The findings lay a solid technical foundation for the application of chitinosome in the industrial production of <i>N</i>-acetylglucosamine and chitooligosaccharides.

ACS Synthetic BiologyVol. 13(12)
Zhejiang A & F University (CN), Shanxi University (CN)
National Natural Science Foundation of China, Scientific Research Foundation of Zhejiang A and F University, Natural Science Foundation of Zhejiang Province
Openalex Percentile: Top 14%
Biochemical and Structural Characterization
1.87
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