Dickens M L, Ye J, Strohl W R
Department of Microbiology, Ohio State University, Columbus, 43210, USA.
J Bacteriol. 1996 Jun;178(11):3384-8. doi: 10.1128/jb.178.11.3384-3388.1996.
DNA sequence analysis of a region of the Streptomyces sp. strain C5 daunomycin biosynthesis gene cluster, located just upstream of the daunomycin polyketide biosynthesis genes, revealed the presence of six complete genes. The two genes reading right to left include genes encoding the potentially translationally coupled gene products, an acyl carrier protein and a ketoreductase, and the four genes reading divergently, left to right, include two open reading frames of unknown function followed by a gene encoding an apparent glycosyltransferase and dauE, encoding aklaviketone reductase. Extracts of Streptomyces lividans TK24 containing recombinant DauE catalyzed the NADPH-specific conversion of aklaviketone, maggiemycin, and 7-oxodaunomycinone to aklavinone, epsilon-rhodomycinone, and daunomycinone, respectively. Neither the product of dauB nor that of the ketoreductase gene directly downstream of the acyl carrier protein gene demonstrated aklaviketone reductase activity.
对链霉菌属菌株C5柔红霉素生物合成基因簇中位于柔红霉素聚酮生物合成基因上游区域的一段DNA序列进行分析,发现存在六个完整基因。两个从右向左读码的基因包括编码可能翻译偶联的基因产物的基因,一个酰基载体蛋白和一个酮还原酶,而四个从左向右反向读码的基因包括两个功能未知的开放阅读框,接着是一个编码明显糖基转移酶的基因和dauE,dauE编码阿克拉酮还原酶。含有重组DauE的变铅青链霉菌TK24提取物催化阿克拉酮、马吉霉素和7-氧柔红霉素酮分别特异性地转化为阿克拉文酮、ε-红霉内酯酮和柔红霉素酮。酰基载体蛋白基因直接下游的dauB产物和酮还原酶基因产物均未表现出阿克拉酮还原酶活性。