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首页> 外文期刊>DNA Sequence: The Journal of DNA Sequencing and Mapping >Analysis of a 108-kb region of the Saccharopolyspora spinosa genome covering the obscurin polyketide synthase locus
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Analysis of a 108-kb region of the Saccharopolyspora spinosa genome covering the obscurin polyketide synthase locus

机译:糖多孢菌多酮合酶基因座的糖多孢菌基因组的108 kb区域的分析。

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摘要

A 108-kb genomic DNA region of Saccharopolyspora spinosa NRRL 18395, producer of the agriculturally important insecticidal antibiotics spinosyns, has been cloned, sequenced and analyzed to reveal clustered genes encoding a type I polyketide synthase (PKS) complex. The genes for the PKS are flanked by genes encoding homologs of enzymes that are involved in the urea cycle, valine, leucine and isoleucine biosynthesis and energy metabolism. While the disruption of the PKS genes by insertional inactivation was not expected to abolish the production of spinosyns, no differences were found in the antibacterial, antifungal, or insecticidal activities either of the parental and the knockout mutant strains under the growth conditions tested. Deduction of the most likely structure of the polyketide core of the cryptic metabolite, termed obscurin, from the predicted modules and domains of the PKS suggests the formation of a highly unsaturated substituted C22 carboxylic acid that might undergo further processing after its release from the PKS.
机译:已克隆,测序和分析了农业上重要的杀虫抗生素多杀菌素的生产者-棘糖多孢菌NRRL 18395的108 kb基因组DNA区,进行了测序和分析,揭示了编码I型聚酮化合物合酶(PKS)复合物的簇状基因。 PKS的基因两侧是编码与尿素循环,缬氨酸,亮氨酸和异亮氨酸生物合成和能量代谢有关的酶的同源物的基因。虽然预期不会因插入失活而破坏PKS基因而消除多杀菌素的产生,但在测试的生长条件下,亲本和敲除突变菌株的抗菌,抗真菌或杀虫活性均未发现差异。从PKS的预测模块和结构域中推断隐性代谢物的聚酮化合物核的最可能结构(称为obscurin),这表明形成了高度不饱和的取代C22羧酸,该羧酸在从PKS释放后可能会进行进一步处理。

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