Otten S L, Stutzman-Engwall K J, Hutchinson C R
Department of Bacteriology, University of Wisconsin, Madison 53706.
J Bacteriol. 1990 Jun;172(6):3427-34. doi: 10.1128/jb.172.6.3427-3434.1990.
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.
通过使用actI/tcmIa和actIII聚酮合酶基因探针,从产柔红霉素的佩西链霉菌以及产阿霉素的佩西链霉菌亚种中克隆了重要抗肿瘤药物柔红霉素(柔毛霉素)和阿霉素(阿霉素)的生物合成基因。对克隆于黏粒载体中的DNA进行限制性图谱分析和Southern分析,确定该DNA代表了佩西链霉菌亚种基因组的三个不重叠区域。如先前报道(K. J. Stutzman-Engwall和C. R. Hutchinson,《美国国家科学院院刊》86:3135 - 3139,1989年),佩西链霉菌基因组中存在这三个区域以及另一个与相同探针杂交的区域。对来自这些区域中某些区域的代表性克隆在变铅青链霉菌、佩西链霉菌ATCC 29050、佩西链霉菌亚种ATCC 27952及其两个阻断突变体(菌株H6101和H6125)中的功能分析表明,许多抗生素生产基因位于IV组克隆所代表的DNA区域。这一结论基于某些变铅青链霉菌转化体中柔红霉素途径的关键中间体ε-红霉酮的产生,以及菌株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的一些转化体表现出ε-红霉酮和柔红霉素的大量过量生产。