期刊
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
卷 104, 期 5, 页码 2079-2096出版社
SPRINGER
DOI: 10.1007/s00253-020-10388-3
关键词
Carbohydrate-binding module family 3; Endo-; exotype enzyme; Glycoside hydrolase family 9; Multifunctional enzyme; Oligosaccharide; Paenibacillus curdlanolyticus
资金
- Office of the Higher Education Commission [214/2551]
- KMUTT 55th Anniversary Commemorative Fund
- Japan International Research Center for Agricultural Sciences
PcMulGH9, a novel glycoside hydrolase family 9 (GH9) from Paenibacillus curdlanolyticus B-6, was successfully expressed in Escherichia coli. It is composed of a catalytic domain of GH9, two domains of carbohydrate-binding module family 3 (CBM3) and two domains of fibronectin type 3 (Fn3). The PcMulGH9 enzyme showed broad activity towards the beta-1,4 glycosidic linkages of cellulose, mannan and xylan, including cellulose and xylan contained in lignocellulosic biomass, which is rarely found in GH9. The enzyme hydrolysed substrates with bifunctional endo-/exotypes cellulase, mannanase and xylanase activities, but predominantly exhibited exo-activities. This enzyme released cellobiose as a major product from cellohexaose, while mannotriose and xylotriose were major hydrolysis products from mannohexaose and xylohexaose, respectively. Moreover, PcMulGH9 could hydrolyse untreated corn hull and rice straw into xylo- and cello-oligosaccharides. Enzyme kinetics, site-directed mutagenesis and molecular docking revealed that Met394, located at the binding subsite + 2, was involved in broad substrate specificity of PcMulGH9 enzyme. This study offers new knowledge of the multifunctional cellulase/mannanase/xylanase in GH9. The PcMulGH9 enzyme showed a novel function of GH9, which increases its potential for saccharification of lignocellulosic biomass into value-added products, especially oligosaccharides.
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