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ε-聚赖氨酸生物合成及其产生菌遗传转化研究进展
引用本文:吴清平,刘盛荣,张菊梅. ε-聚赖氨酸生物合成及其产生菌遗传转化研究进展[J]. 微生物学报, 2011, 51(6): 718-724
作者姓名:吴清平  刘盛荣  张菊梅
作者单位:1. 广东省微生物研究所,广东省菌种保藏与应用重点实验室,广东省微生物应用新技术公共实验室,广州510070
2. 广东省微生物研究所,广东省菌种保藏与应用重点实验室,广东省微生物应用新技术公共实验室,广州510070;华南理工大学生物科学与工程学院,广州510006
基金项目:省部产学研项目(2009B090300300);粤港关键领域重点突破项目(2007A020902003)
摘    要:ε-聚赖氨酸(ε-poly-L-lysine,ε-PL)是由25-35个L-赖氨酸(L-lysine)通过α-ε酰胺键连接的具有很强抗菌活性的聚合物,是自然界中迄今为止仅发现的2种均聚氨基酸(ε-聚赖氨酸和γ-聚谷氨酸)之一。目前,研究发现ε-聚赖氨酸的合成酶是一种非核糖体肽合成酶,它催化前体物质L-lysine经多轮缩合反应合成链长不均一的ε-聚赖氨酸,与I型聚酮合成酶的合成过程相似。ε-聚赖氨酸的合成不受降解酶控制。同时,针对产生菌遗传转化的穿梭质粒载体pLAE001和pLAE003已构建成功,为进一步探索ε-聚赖氨酸生物合成提供了条件。本文主要就ε-聚赖氨酸生物合成及产生菌遗传转化体系进行综述。另外,扼要介绍了作者所在课题组的相关研究工作、取得的进展并提出了相应的见解,论文最后部分对组合生物合成在ε-PL产生菌菌种改造中的应用前景进行了探讨。

关 键 词:ε-聚赖氨酸  生物合成  遗传转化体系  组合生物合成
收稿时间:2010-10-17
修稿时间:2010-12-24

Progress in biosynthesis of epsilon-poly-L-lysine and genetic transformation for epsilon-poly-L-lysine producer--a review
Qingping Wu,Shengrong Liu and Jumei Zhang. Progress in biosynthesis of epsilon-poly-L-lysine and genetic transformation for epsilon-poly-L-lysine producer--a review[J]. Acta microbiologica Sinica, 2011, 51(6): 718-724
Authors:Qingping Wu  Shengrong Liu  Jumei Zhang
Affiliation:Guangdong Institute of Microbiology, Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Open Laboratory of Applied Microbiology, Guangzhou 510070, China;Guangdong Institute of Microbiology, Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Open Laboratory of Applied Microbiology, Guangzhou 510070, China;Guangdong Institute of Microbiology, Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Open Laboratory of Applied Microbiology, Guangzhou 510070, China
Abstract:Epsilon-Poly-L-lysine (epsilon-PL) is a polymer with strong antimicrobial activity and consists of 25-35 L-lysine monomers linked via epsilon-amino-alpha-carboxyl peptide bond. This polymer is one of only two homo-poly (amino acid) polymers known in nature. To date, the biosynthesis mechanism of epsilon-PL was remained unclear. Recently, epsilon-PL synthetase was identified as a nonribosomal peptide synthetase and it utilized L-lysine to synthesize epsilon-PLs of various chain length by iteratively condensing reaction, which was similar to type I polyketide synthase and was not determined by epsilon-PL-degrading enzyme. Meanwhile, the shutter vectors pLAE001 and pLAE003, special for epsilon-PL producer have been constructed, which is significant for studying epsilon-PL biosynthesis. In this review, the biosynthesis of epsilon-PL and the genetic transformation were introduced. Also, the study in our group was presented and the views related to e-PL study were raised. Finally, the prospect of application of combinational biosynthesis in epsilon-PL-producing strain improvement was also discussed considering epsilon-PL synthetase is a nonribosomal peptide synthetase containing several modules.
Keywords:ε-poly-L-lysine  biosynthesis  genetic transformation system  combinational biosynthesis
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