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Reengineering CelA2 cellulase for hydrolysis in aqueous solutions of deep eutectic solvents and concentrated seawater

机译:重新设计CelA2纤维素酶以在深共熔溶剂和浓海水的水溶液中水解

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Cellulases are promising catalysts for the depolymerization of cellulose under mild conditions. Reengineered cellulases are required to match application demands in biorefineries and to avoid cost-intensive downstream processing. This manuscript provides a novel fluorescence-based high throughput screening method for directed evolution of cellulases, based on 4-methylumbelliferyl-β-D-cellobioside (4-MUC). The 4-MUC high throughput screening system was successfully employed to identify CelA2 variants with enhanced stability and activity in mixtures of water with deep eutectic solvents like choline chloride : glycerol (ChCl: Gly), and seawater. The cellulase variant 4D1 (L21P; L184Q; H288R; K299I; D330G; N442D) was isolated and showed, compared to wild type, an increase in specific activity in 30% (v/v) ChCl: Gly (7.5-fold; 0.4 to 3.0 U mg~(-1)) and in concentrated seawater (1.6-fold: 5.5 to 9.3 U mg~(-1)). In addition, the residual activity of 4D1 in the presence of 3-fold concentrated seawater is unaffected whereas CelA2 wild type loses >50% of its activity. Furthermore, the position H288 was identified as a key position for activity and resistance in 4D1.
机译:纤维素酶是在温和条件下纤维素解聚的有前途的催化剂。需要重新设计的纤维素酶来满足生物精炼厂的应用需求,并避免成本高昂的下游加工。该手稿提供了一种新颖的基于荧光的高通量筛选方法,用于基于4-甲基伞形基-β-D-纤维二糖苷(4-MUC)的纤维素酶定向进化。 4-MUC高通量筛选系统已成功用于鉴定在水与深共熔溶剂(如氯化胆碱:甘油(ChCl:Gly))和海水的混合物中具有增强的稳定性和活性的CelA2变体。分离了纤维素酶变体4D1(L21P; L184Q; H288R; K299I; D330G; N442D),与野生型相比,在30%(v / v)ChCl:Gly(7.5倍; 0.4至3.0 U mg〜(-1))和浓海水中(1.6倍:5.5至9.3 U mg〜(-1))。此外,在3倍浓缩海水存在下4D1的残留活性不受影响,而CelA2野生型则失去了其活性的50%以上。此外,位置H288被确定为4D1中活性和抗性的关键位置。

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