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编码6-甲基水杨酸合酶的细菌迭代型I聚酮合酶基因的克隆与表征

Cloning and characterization of a bacterial iterative type I polyketide synthase gene encoding the 6-methylsalicyclic acid synthase.

作者信息

Shao Lei, Qu Xu-Dong, Jia Xin-Ying, Zhao Qun-Fei, Tian Zhen-Hua, Wang Min, Tang Gong-Li, Liu Wen

机构信息

School of Life Science and Technology, Chinese Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, China.

出版信息

Biochem Biophys Res Commun. 2006 Jun 23;345(1):133-9. doi: 10.1016/j.bbrc.2006.04.069. Epub 2006 Apr 25.

Abstract

Unusual polyketide synthases (PKSs), that are structurally type I but act in an iterative manner for aromatic polyketide biosynthesis, are a new family found in bacteria. Here we report the cloning of the iterative type I PKS gene chlB1 from the chlorothricin (CHL) producer Streptomyces antibioticus DSM 40725 by a rapid PCR approach, and characterization of the function of the gene product as a 6-methylsalicyclic acid synthase (6-MSAS). Sequence analysis of various iterative type I PKSs suggests that the resulting aromatic or aliphatic structure of the products might be intrinsically determined by a catalytic feature of the paired KR-DH domains in the control of the double bond geometry. The finding of ChlB1 as a 6-MSAS not only enriches the current knowledge of aromatic polyketide biosynthesis in bacteria, but will also contribute to the generation of novel polyketide analogs via combinatorial biosynthesis with engineered PKSs.

摘要

不同寻常的聚酮合酶(PKSs)在结构上属于I型,但在芳香族聚酮生物合成中以迭代方式起作用,是在细菌中发现的一个新家族。在此,我们报告通过快速PCR方法从氯丝菌素(CHL)产生菌抗生链霉菌DSM 40725中克隆迭代型I型PKS基因chlB1,并将该基因产物的功能鉴定为6-甲基水杨酸合酶(6-MSAS)。对各种迭代型I型PKSs的序列分析表明,产物最终的芳香族或脂肪族结构可能本质上由控制双键几何结构的配对KR-DH结构域的催化特征决定。ChlB1作为6-MSAS的发现不仅丰富了目前关于细菌中芳香族聚酮生物合成的知识,还将通过与工程化PKSs的组合生物合成,为新型聚酮类似物的产生做出贡献。

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