Wang Xinye, Nie Yao, Mu Xiaoqing, Xu Yan, Xiao Rong
School of Biotechnology and Key Laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan University, Wuxi 214122, China.
State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi 214122, China.
Sci Rep. 2016 Apr 19;6:24574. doi: 10.1038/srep24574.
Pullulanase is a well-known starch-debranching enzyme. However, the production level of pullulanase is yet low in both wide-type strains and heterologous expression systems. We predicted the disorder propensities of Bacillus naganoensis pullulanase (PUL) using the bioinformatics tool, Disorder Prediction Meta-Server. On the basis of disorder prediction, eight constructs, including PULΔN5, PULΔN22, PULΔN45, PULΔN64, PULΔN78 and PULΔN106 by deleting the first 5, 22, 45, 64, 78 and 106 residues from the N-terminus, and PULΔC9 and PULΔC36 by deleting the last 9 and 36 residues from the C-terminus, were cloned into the recombinant expression vector pET-28a-PelB and auto-induced in Escherichia coli BL21 (DE3) cells. All constructs were evaluated in production level, specific activities and kinetic parameters. Both PULΔN5 and PULΔN106 gave higher production levels of protein than the wide type and displayed increased specific activities. Kinetic studies showed that substrate affinities of the mutants were improved in various degrees and the catalytic efficiency of PULΔN5, PULΔN45, PULΔN78, PULΔN106 and PULΔC9 were enhanced. However, the truncated mutations did not change the advantageous properties of the enzyme involving optimum temperature and pH for further application. Therefore, Disorder prediction-based truncation would be helpful to efficiently improve the enzyme activity and catalytic efficiency.
普鲁兰酶是一种著名的淀粉脱支酶。然而,在野生型菌株和异源表达系统中,普鲁兰酶的生产水平都还很低。我们使用生物信息学工具“无序预测元服务器”预测了长野芽孢杆菌普鲁兰酶(PUL)的无序倾向。基于无序预测,通过从N端删除前5、22、45、64、78和106个残基构建了8种突变体,即PULΔN5、PULΔN22、PULΔN45、PULΔN64、PULΔN78和PULΔN106,以及通过从C端删除最后9和36个残基构建的PULΔC9和PULΔC36,将它们克隆到重组表达载体pET-28a-PelB中,并在大肠杆菌BL21(DE3)细胞中进行自诱导表达。对所有构建体的生产水平、比活性和动力学参数进行了评估。PULΔN5和PULΔN106的蛋白质生产水平均高于野生型,且比活性有所提高。动力学研究表明,突变体的底物亲和力有不同程度的提高,PULΔN5、PULΔN45、PULΔN78、PULΔN106和PULΔC9的催化效率增强。然而,截短突变并未改变该酶在最适温度和pH等方面有利于进一步应用的特性。因此,基于无序预测的截短有助于有效提高酶活性和催化效率。