Decker H, Haag S
Lehrbereich Mikrobiologie/Antibiotika, Universität Tübingen, Germany.
J Bacteriol. 1995 Nov;177(21):6126-36. doi: 10.1128/jb.177.21.6126-6136.1995.
A DNA fragment was cloned as cosmid purd8, which encodes a polyketide synthase involved in the production of the angucycline antibiotic urdamycin from Streptomyces fradiae Tü2717. Deletion of the polyketide synthase genes from the chromosome abolished urdamycin production. In addition, purd8 conferred urdamycin resistance on introduction into Streptomyces lividans TK24. Sequence analysis of 5.7 kb of purd8 revealed six open reading frames transcribed in the same direction. The deduced amino acid sequences of the six open reading frames strongly resemble proteins from known type II polyketide synthase gene clusters: a ketoacyl synthase, a chain length factor, an acyl carrier protein, a ketoreductase, a cyclase, and an oxygenase. Heterologous expression of the urdamycin genes encoding a ketoacyl synthase and a chain length factor in Streptomyces glaucescens tetracenomycin C-nonproducing mutants impaired in either the TcmK ketoacyl synthase or TcmL chain length factor resulted in the production of tetracenomycin C. Heterologous expression of a putative oxygenase gene from the urdamycin gene cluster in S. glaucescens GLA.O caused production of the hybrid antibiotic 6-hydroxy tetracenomycin C.
一个DNA片段被克隆为黏粒purd8,它编码一种聚酮合酶,参与来自弗氏链霉菌Tü2717的安古霉素类抗生素乌达霉素的产生。从染色体上缺失聚酮合酶基因消除了乌达霉素的产生。此外,将purd8导入变铅青链霉菌TK24时赋予其对乌达霉素的抗性。对purd8的5.7 kb进行序列分析,发现有六个开放阅读框按相同方向转录。这六个开放阅读框推导的氨基酸序列与已知的II型聚酮合酶基因簇中的蛋白质非常相似:一个酮酰基合酶、一个链长因子、一个酰基载体蛋白、一个酮还原酶、一个环化酶和一个加氧酶。在青灰链霉菌中,编码酮酰基合酶和链长因子的乌达霉素基因在tetracenomycin C不产生突变体中进行异源表达,这些突变体在TcmK酮酰基合酶或TcmL链长因子中受损,结果导致了tetracenomycin C的产生。在青灰链霉菌GLA.O中,来自乌达霉素基因簇的一个假定加氧酶基因的异源表达导致了杂合抗生素6-羟基tetracenomycin C的产生。