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半理性改造提升细菌漆酶Lac15的催化活性
引用本文:谢雅楠,王瑞,李治,李杰,方泽民,房伟,张学成,肖亚中.半理性改造提升细菌漆酶Lac15的催化活性[J].微生物学报,2022,62(4):1501-1512.
作者姓名:谢雅楠  王瑞  李治  李杰  方泽民  房伟  张学成  肖亚中
作者单位:安徽大学生命科学学院, 安徽 合肥 230601;安徽省微生物与生物催化工程技术研究中心, 安徽 合肥 230601;安徽省现代生物制造重点实验室, 安徽 合肥 230601
基金项目:国家自然科学基金(31370114);安徽省国际科技合作计划(1503062010);国家高技术研究发展计划(2011AA09070305);教育部博士点基金(20133401110006)
摘    要:目的]漆酶可氧化各种底物,在多个工业领域有很好的潜在应用价值.Lac15是一种微生物漆酶,已表现出可观的应用潜能,可望通过蛋白质工程改造提升和拓展其应用.方法]通过基于结构分析的半理性改造策略,选取推测与电子/质子转移或底物结合直接或间接相关的位点进行定点突变,并测定突变酶对各种底物的活性及酶学性质.结果]部分突...

关 键 词:细菌漆酶  Lac15  半理性改造  活性  特异性
收稿时间:2021/8/18 0:00:00
修稿时间:2021/12/12 0:00:00

Semi-rational engineering of microbial laccase Lac15 for enhanced activity
XIE Yanan,WANG Rui,LI Zhi,LI Jie,FANG Zemin,FANG Wei,ZHANG Xuecheng,XIAO Yazhong.Semi-rational engineering of microbial laccase Lac15 for enhanced activity[J].Acta Microbiologica Sinica,2022,62(4):1501-1512.
Authors:XIE Yanan  WANG Rui  LI Zhi  LI Jie  FANG Zemin  FANG Wei  ZHANG Xuecheng  XIAO Yazhong
Institution:School of Life Sciences, Anhui University, Hefei 230601, Anhui, China;Anhui Provincial Engineering Technology Research Center of Microorganisms and Biocatalysis, Hefei 230601, Anhui, China;Anhui Provincial Key Laboratory of Modern Biomanufacturing, Hefei 230601, Anhui, China
Abstract:Objective] Laccases can oxidize a wide range of compounds and have great application value in diverse industries.Lac15,a microbial laccase with considerable application potential,can be modified by protein engineering to expand the application range.Methods] By structure-based analysis,we chose some residues supposed to contribute directly or indirectly to electron/proton transfer or substrate interaction for site-directed mutagenesis,and measured the activities of the mutants for various substrates and the enzymatic properties.Results] Some of the mutants showed significantly enhanced activity towards particular substrates.To be specific,the catalysis efficiency of mutant D216N toward 2,2''-azino-bis (3-ethylbenzthiazoline-6-suphonic acid)(ABTS) was 1.0 fold higher,and that of mutants R178V and K433T toward dopamine was 1.2 and 11.1 folds,respectively,higher than that of Lac15.Moreover,the mutants maintained the advantages of Lac15 in application,such as the neutral optimum pH and salt activation.Conclusion] By structure-based semi-rational engineering,the specific activities of Lac15 toward some substrates can be improved.A conserved Asp in laccases,corresponding to D216 in Lac15,can be a common engineering target for enhancing the activity of the enzymes with ABTS as substrate or mediator.
Keywords:microbial laccase  Lac15  semi-rational engineering  activity  specificity
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