Crystal structure of ChbG from Klebsiella pneumoniae reveals the molecular basis of diacetylchitobiose deacetylation

被引:2
|
作者
Lee, So Yeon [1 ,2 ]
Pardhe, Bashu Dev [3 ]
Oh, Tae-Jin [3 ,4 ,5 ]
Park, Hyun Ho [1 ,2 ]
机构
[1] Chung Ang Univ, Coll Pharm, Seoul 06974, South Korea
[2] Chung Ang Univ, Grad Sch, Dept Global Innovat Drugs, Seoul 06974, South Korea
[3] Sunmoon Univ, Dept Life Sci & Biochem Engn, Chungnam 31460, South Korea
[4] Sunmoon Univ, Dept Pharmaceut Engn & Biotechnol, Chungnam 31460, South Korea
[5] Genome Based BioIT Convergence Inst, Chungnam 31460, South Korea
基金
新加坡国家研究基金会;
关键词
CHITIN DEACETYLASE; OLIGOSACCHARIDE DEACETYLASE; PROTEIN; PURIFICATION; MECHANISM; CHITOSAN; TOOLS; MODEL;
D O I
10.1038/s42003-022-03824-9
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The chitobiose (chb) operon is involved in the synthesis of chitooligosaccharide and is comprised of a BCARFG gene cluster. ChbG encodes a chitooligosaccharide deacetylase (CDA) which catalyzes the removal of one acetyl group from N,N'-diacetylchitobiose. It is considered a novel type of CDA due to its lack of sequence homology. Although there are various structural studies of CDAs linked to the kinetic properties of the enzyme, the structural information of ChbG is unavailable. In this study, the crystal structure of ChbG from Klebsiella pneumoniae is provided. The molecular basis of deacetylation of diacetylchitobiose by ChbG is determined based on structural analysis, mutagenesis, biophysical analysis, and in silico docking of the substrate, diacetylchitobiose. This study contributes towards a deeper understanding of chitin and chitosan biology, as well as provides a platform to engineer CDA biocatalysts. Structural and functional characterization of Klebsiella pneumonia ChbG (which lacks sequence homology) reveals the mechanism of chitooligosaccharide processing by ChbG.
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页数:11
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