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首页> 外文期刊>Chemistry & biology >The neocarzinostatin biosynthetic gene cluster from Streptomyces carzinostaticus ATCC 15944 involving two iterative type I polyketide synthases
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The neocarzinostatin biosynthetic gene cluster from Streptomyces carzinostaticus ATCC 15944 involving two iterative type I polyketide synthases

机译:来自Carzinostaticus ATCC 15944的新carzinostatin生物合成基因簇,涉及两个迭代的I型聚酮化合物合酶

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The biosynthetic gene cluster for the enediyne antitumor antibiotic neocarzinostatin (NCS) was localized to 130 kb continuous DNA from Streptomyces carzinostaticus ATCC15944 and confirmed by gene inactivation. DNA sequence analysis of 92 kb of the cloned region revealed 68 open reading frames (ORFs), 47 of which were determined to constitute the NCS cluster. Sequence analysis of the genes within the NCS cluster suggested dNDP-D-mannose as a precursor for the deoxy aminosugar, revealed two distinct type I polyketide synthases (PKSs), and supported a convergent model for NCS chromophore biosynthesis from the deoxy aminosugar, naphthoic acid, and enediyne core building blocks. These findings shed light into deoxysugar biosynthesis, further support the iterative type I PKS paradigm for enediyne core biosynthesis, and unveil a mechanism for microbial polycyclic aromatic polyketide biosynthesis by an iterative type I PKS.
机译:烯二炔抗肿瘤抗生素新carzinostatin(NCS)的生物合成基因簇被定位到来自Carzinostaticus链霉菌ATCC15944的130 kb连续DNA,并通过基因失活得到证实。对92 kb克隆区域的DNA序列分析显示68个开放阅读框(ORF),其中47个被确定构成NCS簇。 NCS簇内基因的序列分析表明,dNDP-D-甘露糖是脱氧氨基糖的前体,揭示了两种截然不同的I型聚酮化合物(PKS),并支持了由脱氧氨基糖,萘甲酸合成NCS生色团的收敛模型。 ,以及恩尼迪恩核心组成部分。这些发现为脱氧糖的生物合成提供了启示,进一步支持了二烯二烯核心生物合成的迭代I型PKS范式,并揭示了由迭代I型PKS进行微生物多环芳族聚酮化合物生物合成的机理。

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