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首页> 外文期刊>Chemistry & biology >The biosynthetic gene cluster for the antitumor drug bleomycin from Streptomyces verticillus ATCC15003 supporting functional interactions between nonribosomal peptide synthetases and a polyketide synthase
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The biosynthetic gene cluster for the antitumor drug bleomycin from Streptomyces verticillus ATCC15003 supporting functional interactions between nonribosomal peptide synthetases and a polyketide synthase

机译:轮状链霉菌ATCC15003的抗肿瘤药物博来霉素的生物合成基因簇,支持非核糖体肽合成酶和聚酮化合物合酶之间的功能相互作用

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Background: The structural and catalytic similarities between modular nonribosomal peptide synthetases (NRPSs) and polyketide synthases (PKSs) inspired us to search for a hybrid NRPS-PKS system. The antitumor drug bleomycin (BLM) is a natural hybrid peptide-polyketide metabolite, the biosynthesis of which provides an excellent opportunity to investigate intermodular communication between NRPS and PKS modules. Here, we report the cloning, sequencing, and characterization of the BLM biosynthetic gene cluster from Streptomyces verticillus ATCC15003. Results: A set of 30 genes clustered with the previously characterized blmAB resistance genes were defined by sequencing a 85-kb contiguous region of DNA from S. verticillus ATCC15003. The sequenced gene cluster consists of 10 NRPS genes encoding nine NRPS modules, a PKS gene encoding one PKS module, five sugar biosynthesis genes, as well as genes encoding other biosynthesis, resistance, and regulatory proteins. The substrate specificities of individual NRPS and PKS modules were predicted based on sequence analysis, and the amino acid specificities of two NRPS modules were confirmed biochemically in vitro. The involvement of the cloned genes in BLM biosynthesis was demonstrated by bioconversion of the BLM aglycones into BLMs in Streptomyces lividans expressing a part of the gene cluster. Conclusion: The blm gene cluster is characterized by a hybrid NRPS-PKS system, supporting the wisdom of combining individual NRPS and PKS modules for combinatorial biosynthesis. The availability of the blm gene cluster has set the stage for engineering novel BLM analogs by genetic manipulation of genes governing BLM biosynthesis and for investigating the molecular basis for intermodular communication between NRPS and PKS in the biosynthesis of hybrid peptide-polyketide metabolites. [References: 99]
机译:背景:模块化非核糖体肽合成酶(NRPS)和聚酮化合物合酶(PKS)之间的结构和催化相似性激发了我们寻找混合NRPS-PKS系统的希望。抗肿瘤药博来霉素(BLM)是天然的杂合肽-聚酮化合物代谢产物,其生物合成为研究NRPS和PKS模块之间的互调通讯提供了极好的机会。在这里,我们报告了来自链霉菌ATCC15003的BLM生物合成基因簇的克隆,测序和表征。结果:通过测序来自网状葡萄球菌ATCC15003的85kb连续DNA区域,定义了与先前表征的blmAB抗性基因簇集的30个基因。测序的基因簇由编码9个NRPS模块的10个NRPS基因,编码1个PKS模块的PKS基因,5个糖类生物合成基因以及编码其他生物合成,抗性和调节蛋白的基因组成。根据序列分析预测了各个NRPS和PKS模块的底物特异性,并在体外通过生化方法确定了两个NRPS模块的氨基酸特异性。通过将表达部分基因簇的淡紫色链霉菌中的BLM糖苷配基生物转化为BLM,证明了克隆的基因参与BLM生物合成。结论:blm基因簇具有NRPS-PKS杂交系统的特点,支持将单个NRPS和PKS模块结合在一起进行组合生物合成的智慧。 blm基因簇的可用性为通过控制BLM生物合成基因的遗传操作工程化新型BLM类似物以及研究NRPS和PKS之间在杂肽-聚酮化合物代谢物生物合成中进行模块间通讯的分子基础奠定了基础。 [参考:99]

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