TY - JOUR
T1 - Carbohydrate-binding modules facilitate the enzymatic hydrolysis of lignocellulosic biomass
T2 - Releasing reducing sugars and dissociative lignin available for producing biofuels and chemicals
AU - Shi, Qicheng
AU - Abdel-Hamid, Ahmed M.
AU - Sun, Zhanying
AU - Cheng, Yanfen
AU - Tu, Tao
AU - Cann, Isaac
AU - Yao, Bin
AU - Zhu, Weiyun
N1 - This work was supported by the National Key Research and Development Program [grant number 2021YFD1300302 ], the National Natural Science Foundation of China [grant numbers 32061143034 , 32161143028 ].
PY - 2023/7/1
Y1 - 2023/7/1
N2 - The microbial decomposition and utilization of lignocellulosic biomass present in the plant tissues are driven by a series of carbohydrate active enzymes (CAZymes) acting in concert. As the non-catalytic domains widely found in the modular CAZymes, carbohydrate-binding modules (CBMs) are intimately associated with catalytic domains (CDs) that effect the diverse hydrolytic reactions. The CBMs function as auxiliary components for the recognition, adhesion, and depolymerization of the complex substrate mediated by the associated CDs. Therefore, CBMs are deemed as significant biotools available for enzyme engineering, especially to facilitate the enzymatic hydrolysis of dense and insoluble plant tissues to acquire more fermentable sugars. This review aims at presenting the taxonomies and biological properties of the CBMs currently curated in the CAZy database. The molecular mechanisms that CBMs use in assisting the enzymatic hydrolysis of plant polysaccharides and the regulatory factors of CBM-substrate interactions are outlined in detail. In addition, guidelines for the rational designs of CBM-fused CAZymes are proposed. Furthermore, the potential to harness CBMs for industrial applications, especially in enzymatic pretreatment of the recalcitrant lignocellulose, is evaluated. It is envisaged that the ideas outlined herein will aid in the engineering and production of novel CBM-fused enzymes to facilitate efficient degradation of lignocellulosic biomass to easily fermentable sugars for production of value-added products, including biofuels.
AB - The microbial decomposition and utilization of lignocellulosic biomass present in the plant tissues are driven by a series of carbohydrate active enzymes (CAZymes) acting in concert. As the non-catalytic domains widely found in the modular CAZymes, carbohydrate-binding modules (CBMs) are intimately associated with catalytic domains (CDs) that effect the diverse hydrolytic reactions. The CBMs function as auxiliary components for the recognition, adhesion, and depolymerization of the complex substrate mediated by the associated CDs. Therefore, CBMs are deemed as significant biotools available for enzyme engineering, especially to facilitate the enzymatic hydrolysis of dense and insoluble plant tissues to acquire more fermentable sugars. This review aims at presenting the taxonomies and biological properties of the CBMs currently curated in the CAZy database. The molecular mechanisms that CBMs use in assisting the enzymatic hydrolysis of plant polysaccharides and the regulatory factors of CBM-substrate interactions are outlined in detail. In addition, guidelines for the rational designs of CBM-fused CAZymes are proposed. Furthermore, the potential to harness CBMs for industrial applications, especially in enzymatic pretreatment of the recalcitrant lignocellulose, is evaluated. It is envisaged that the ideas outlined herein will aid in the engineering and production of novel CBM-fused enzymes to facilitate efficient degradation of lignocellulosic biomass to easily fermentable sugars for production of value-added products, including biofuels.
KW - CBM-fused enzymes
KW - CBM-substrate interaction
KW - Carbohydrate-binding modules
KW - Enzymatic pretreatment
KW - Lignocellulosic biomass
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U2 - 10.1016/j.biotechadv.2023.108126
DO - 10.1016/j.biotechadv.2023.108126
M3 - Review article
C2 - 36921877
AN - SCOPUS:85150360828
SN - 0734-9750
VL - 65
JO - Biotechnology Advances
JF - Biotechnology Advances
M1 - 108126
ER -