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Food Chem ; 453: 139675, 2024 Sep 30.
Article in English | MEDLINE | ID: mdl-38781901

ABSTRACT

Bioproduction of diverse N-acetyl chitooligosaccharides from chitin is of great value. In the study, a novel GH family 18 bifunctional chitinase gene (PsChi82) from Paenibacillus shirakamiensis was identified, expressed and biochemically characterized. PsChi82 was most active at pH 5.0, and 55 °C, and displayed remarkable pH stability with the broad pH range of 3.0-12.0. It showed high chitosanase activity of 10.6 U mg-1 and diverse hydrolysis products of GlcNAc, (GlcNAc)2, GlcN-GlcNAc and (GlcN)2-GlcNAc, which may facilitate comprehensively understanding of structure-function relationships of N-acetyl COSs. Three engineered variants were then expressed and characterized. Among them, PsChi82-CBM26 possessed specific activity of 25.1 U mg-1 against colloidal chitin, which was 2.1 folds higher than that of PsChi82. The diverse N-acetyl COSs were subsequently produced by PsChi82-CBM26 with a sugar content of 23.2 g L-1. These excellent properties may make PsChi82-CBM26 potentially useful for N-acetyl COSs production in the food and chemical industries.


Subject(s)
Bacterial Proteins , Chitin , Chitinases , Chitosan , Oligosaccharides , Paenibacillus , Chitinases/chemistry , Chitinases/genetics , Chitinases/metabolism , Oligosaccharides/chemistry , Oligosaccharides/metabolism , Chitin/chemistry , Chitin/analogs & derivatives , Chitin/metabolism , Chitosan/chemistry , Chitosan/metabolism , Paenibacillus/enzymology , Paenibacillus/genetics , Paenibacillus/chemistry , Bacterial Proteins/genetics , Bacterial Proteins/chemistry , Bacterial Proteins/metabolism , Hydrogen-Ion Concentration , Enzyme Stability , Hydrolysis , Protein Engineering
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