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解淀粉芽孢杆菌 JX-47 大片段细菌人工染色体文库的构建及其覆盖格尔德霉素生物合成基因簇的克隆的鉴定。

Streptomyces autolyticus JX-47 large-insert bacterial artificial chromosome library construction and identification of clones covering geldanamycin biosynthesis gene cluster.

机构信息

Key Laboratory of Marine Bio-Resources Sustainable Utilization, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, 510301, People's Republic of China.

出版信息

Curr Microbiol. 2011 Jul;63(1):68-74. doi: 10.1007/s00284-011-9940-2. Epub 2011 May 5.

Abstract

Geldanamycin belongs to benzoquinone ansamycin antibiotic and has potent antitumor activities. In this study, a bacterial artificial chromosome (BAC) library with an average insert size of up to 150 kb was constructed from genomic DNA of Streptomyces autolyticus JX-47. A genetic-screening strategy was established using BAC end-sequencing and three pairs of primers designed to target the remote regions, gdmA1, gdmA3 and gdmRI, of the geldanamycin gene cluster. Three clones covering geldanamycin biosynthesis gene cluster were obtained, which together spanned a 250-kb genomic region, and a 150227-bp insert in the clone p4E9 was sequenced. Comparison with the reported geldanamycin gene cluster sequences from S. hygroscopicus revealed that it had the same gene arrangement and high gene homology in the polyketide synthase (PKS) region and its downstream with 84-100% DNA identity and 81-100% amino acid (AA) identity. Its DNA homology with the whole gene cluster sequence from S. hygroscopicus strain 17997 reached 99% identity. However, upstream of the PKS region exhibited great diversity, where only ORF16 was conserved, and the other genes including gdmL and gdmX were displaced.

摘要

金霉素属于苯醌安莎霉素抗生素,具有很强的抗肿瘤活性。本研究从解淀粉芽孢杆菌 JX-47 的基因组 DNA 构建了一个平均插入片段长达 150kb 的细菌人工染色体(BAC)文库。采用 BAC 末端测序和三对引物设计针对金霉素基因簇的远程区域 gdmA1、gdmA3 和 gdmRI 建立了遗传筛选策略。获得了三个覆盖金霉素生物合成基因簇的克隆,它们共同跨越了 250kb 的基因组区域,并且克隆 p4E9 中的一个 150227-bp 插入片段被测序。与报道的吸水链霉菌中的金霉素基因簇序列进行比较,发现其在聚酮合酶(PKS)区域及其下游具有相同的基因排列和高度的基因同源性,DNA 同一性为 84-100%,氨基酸(AA)同一性为 81-100%。其与吸水链霉菌 17997 株全基因簇序列的 DNA 同源性达到 99%。然而,PKS 区域的上游表现出很大的多样性,只有 ORF16 被保守,而其他基因包括 gdmL 和 gdmX 则被取代。

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