Zhao Qunfei, He Qingli, Ding Wei, Tang Mancheng, Kang Qianjin, Yu Yi, Deng Wei, Zhang Qi, Fang Jie, Tang Gongli, Liu Wen
State Key Laboratory of Bioorganic and Natural Product Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, China.
Chem Biol. 2008 Jul 21;15(7):693-705. doi: 10.1016/j.chembiol.2008.05.021.
Azinomycin B is a complex natural product containing densely assembled functionalities with potent antitumor activity. Cloning and sequence analysis of the azi gene cluster revealed an iterative type I polyketide synthase (PKS) gene, five nonribosomal peptide synthetases (NRPSs) genes and numerous genes encoding the biosynthesis of unusual building blocks and tailoring steps for azinomycin B production. Characterization of AziB as a 5-methyl-naphthoic acid (NPA) synthase showed a distinct selective reduction pattern in aromatic polyketide biosynthesis governed by bacterial iterative type I PKSs. Heterologous expression established the PKS-post modification route from 5-methyl-NPA to reach the first building block 3-methoxy-5-methyl-NPA. This proposed azinomycin B biosynthetic pathway sets the stage to investigate the enzymatic mechanisms for building structurally unique and pharmaceutically important groups, including the unprecedented azabicyclic ring system and highly active epoxide moiety.
阿齐霉素B是一种复杂的天然产物,含有紧密组装的官能团,具有强大的抗肿瘤活性。azi基因簇的克隆和序列分析揭示了一个迭代型I聚酮合酶(PKS)基因、五个非核糖体肽合成酶(NRPSs)基因以及众多编码阿齐霉素B生产中不寻常构建模块生物合成和修饰步骤的基因。将AziB鉴定为5-甲基萘甲酸(NPA)合酶,显示出细菌迭代型I聚酮合酶在芳香族聚酮生物合成中具有独特的选择性还原模式。异源表达建立了从5-甲基-NPA到第一个构建模块3-甲氧基-5-甲基-NPA的PKS后修饰途径。这一提出的阿齐霉素B生物合成途径为研究构建结构独特且具有药学重要性的基团(包括前所未有的氮杂双环系统和高活性环氧基团)的酶促机制奠定了基础。