Ml. Dickens et al., CLONING, SEQUENCING, AND ANALYSIS OF AKLAVIKETONE REDUCTASE FROM STREPTOMYCES SP STRAIN C5, Journal of bacteriology, 178(11), 1996, pp. 3384-3388
DNA sequence analysis of a region of the Streptomyces sp. strain C5 da
unomycin biosynthesis gene cluster, located just upstream of the dauno
mycin polyketide biosynthesis genes, revealed the presence of six comp
lete genes. The two genes reading right to left include genes encoding
the potentially translationally coupled gene products, an acyl carrie
r protein and a ketoreductase, and the four genes reading divergently,
left to right, include two open reading frames of unknown function fo
llowed by a gene encoding an apparent glycosyltransferase and dauE, en
coding aklaviketone reductase. Extracts of Streptomyces lividans TK24
containing recombinant DauE catalyzed the NADPH-specific conversion of
aklaviketone, maggiemycin, and 7-oxodaunomycinone to aklavinone, epsi
lon-rhodomycinone, and daunomycinone, respectively. Neither the produc
t of dauB nor that of the ketoreductase gene directly downstream of th
e acyl carrier protein gene demonstrated aklaviketone reductase activi
ty.