基于易错PCR技术的短小芽孢杆菌YZ02脂肪酶基因BpL的定向进化  

Directed Evolution of Lipase of Bacillus pumilus YZ02 by Error-prone PCR

作　　者：黄瑛[1] 蔡勇[1] 杨江科[1] 闫云君[1] 

机构地区：[1]分子生物物理教育部重点实验室,华中科技大学生命科学与技术学院,武汉430074

出　　处：《生物工程学报》2008年第3期445-451,共7页Chinese Journal of Biotechnology

基　　金：国家十一五“863”计划(No.2006AA020203,No.2007AA05Z417);武汉市攻关计划(No.200720422138)~~

摘　　要：利用易错PCR技术对短小芽胞杆菌(Bacillus pumilus)YZ02脂肪酶基因BpL进行两轮定向进化研究,分别获得最佳突变株BpL1-7和BpL2-1369,其脂肪酶活力比出发酶分别提高了2倍和6倍。序列分析表明,突变体BpL2-1369有4个碱基发生了突变:T61C/C147T/A334G/T371A,其中有3个碱基突变导致了氨基酸的改变。通过SWISS-MODEL数据库模拟脂肪酶的结构显示,3个突变氨基酸分别位于第1个α螺旋的第3个氨基酸、第4和第5个β折叠之间的转角以及第5个β折叠的第1个氨基酸位置。将野生型脂肪酶基因BpL和进化后的基因BpL2-1369的高效表达产物经Ni-Agarose柱和Sephadex-G75纯化后,酶学性质测定表明:突变脂肪酶的比活力比野生型脂肪酶提高了1.31倍,Km值由8.24mmol/L降低至7.17mmol/L;在pH>8.0时的稳定性较野生型脂肪酶有所提高。Random mutagenesis on Bacillus pumilus lipase YZ02 gene was conducted by using error-prone PCR strategy. Through two cycles of directed evolution, two optimum mutants BpL1-7 and BpL2-1369 with lipase activity improved 2 folds and 6 folds respectively were screened. The sequence of BpL2-1369 lipase gene showed that four nucleotides substitution, T61C, C 147T, A334G and T371A have occurred, and three of them caused amino acid changes. Thus, amine acid Set21 was changed into Pro21, Arg 112 to Gly 112, and Leu 124 to His124. According to the 3D structure of Bacillus pumilus lipase mimicked by SWISS-MODEL Repository, three mutated amino acids were located at the third amino acid of the first α-helix, the turn between the fourth and fifth β fold, and the first amino acid of the fifth β fold, respectively. The BpL and BpL2-1369 genes were ligated into pET28a vector, and transferred into E. coli BL21 （DE3）. After induced by IPTG. the lipases were purified and characterized. The results showed that the specific activity of the evolved lipase was 1.31-fold than that of the wild lipase, and the Km decreased from 8.24 mmol/L to 7.17 mmol/L. The pH stability of the evolved lipase was better than wild lipase when pH〉8.0.

关 键 词：短小芽胞杆菌 脂肪酶 定向进化 易错PCR 

分 类 号：Q78[生物学—分子生物学]