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Cloning and expression of daunorubicin biosynthesis genes from Streptomyces peucetius and S. peucetius subsp. caesius.

机译:青霉链霉菌和青霉链霉菌亚种柔红霉素生物合成基因的克隆和表达。凯撒斯。

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摘要

Genes for the biosynthesis of daunorubicin (daunomycin) and doxorubicin (adriamycin), important antitumor drugs, were cloned from Streptomyces peucetius (the daunorubicin producer) and S. peucetius subsp. caesius (the doxorubicin producer) by use of the actI/tcmIa and actIII polyketide synthase gene probes. Restriction mapping and Southern analysis of the DNA cloned in a cosmid vector established that the DNA represented three nonoverlapping regions of the S. peucetius subsp. caesius genome. These three regions plus an additional one that hybridized to the same probes are present in the S. peucetius genome, as reported previously (K. J. Stutzman-Engwall and C. R. Hutchinson, Proc. Natl. Acad. Sci. USA 86:3135-3139, 1989). Functional analysis of representative clones from some of these regions in S. lividans, S. peucetius ATCC 29050, S. peucetius subsp. caesius ATCC 27952, and two of its blocked mutants (strains H6101 and H6125) showed that many of the antibiotic production genes reside in the region of DNA represented by the group IV clones. This conclusion is based on the production of epsilon-rhodomycinone, a key intermediate of the daunorubicin pathway, in certain S. lividans transformants and on the apparent complementation of mutations that block daunorubicin biosynthesis in strains H6101 and H6125. Some of the transformants of strains 29050, 27952, and H6125 exhibited substantial overproduction of epsilon-rhodomycinone and daunorubicin.
机译:从抗性链霉菌(Streptomyces peucetius)(柔红霉素生产商)和S. peucetius subsp。中克隆了重要的抗肿瘤药物柔红霉素(道柔霉素)和阿霉素(阿霉素)的生物合成基因。通过使用actI / tcmIa和actIII聚酮化合物合酶基因探针来确定caesius(阿霉素的产生者)。对在粘粒载体中克隆的DNA的限制性作图和Southern分析证实,该DNA代表了S. peucetius亚种的三个非重叠区域。 caesius基因组。如先前所报道的,这三个区域以及与相同探针杂交的另外一个区域存在于peucetius基因组中(KJ Stutzman-Engwall和CR Hutchinson,美国国家科学院院刊86:3135-3139,1989)。 )。来自S. lividans,S。peucetius ATCC 29050,S。peucetius亚种中某些区域的代表性克隆的功能分析。 caesius ATCC 27952及其两个受阻突变体(菌株H6101和H6125)显示,许多抗生素生产基因位于IV组克隆代表的DNA区域。该结论是基于ε-柔红霉素,柔红霉素途径的关键中间体,在某些S. lividans转化子中的产生,以及突变体H6101和H6125中阻断柔红霉素生物合成的突变的明显互补。菌株29050、27952和H6125的某些转化株显示出过量的ε-溶菌素和柔红霉素过量生产。

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