AbstractBackground: Elloramycin is an anthracycline-like antitumor drug related to tetracenomycin C which is produced by Streptomyces olivaceus Tü2353. Structurally is a tetracyclic aromatic polyketide derived from the condensation of 10 acetate units. Its chromophoric aglycon is glycosylated with a permethylated L-rhamnose moiety at the C-8 hydroxy group. Only limited information is available about the genes involved in the biosynthesis of elloramycin. From a library of chromosomal DNA from S. olivaceus, a cosmid (16F4) was isolated that contains part of the elloramycin gene cluster and when expressed in Streptomyces lividans resulted in the production of a non-glycosylated intermediate in elloramycin biosynthesis, 8-demethyl-tetracenomyci...
Sch47554 and Sch47555 are antifungal compounds from Streptomyces sp. SCC‐2136. The availability of t...
Elloramycin and oleandomycin are two polyketide compounds produced by Streptomyces olivaceus Tü2353 ...
SummaryAs glycosyltransferases found in nature often show distinct substrate specificity, glycosyltr...
AbstractBackground: Elloramycin is an anthracycline-like antitumor drug related to tetracenomycin C ...
SummarySugar biosynthesis cassette genes have been used to construct plasmids directing the biosynth...
AbstractBackground: The genetic engineering of antibiotic-producing Streptomyces strains is an appro...
AbstractA plasmid (pLN2) was generated in which genes involved in the biosynthesis of L-oleandrose i...
AbstractBackground: The biological activity of many microbial products requires the presence of one ...
Natural products occupy a central role as the majority of currently used antibiotic and anticancer a...
AbstractBackground: Mithramycin, chromomycin, and olivomycin belong to the aureolic acid family of c...
AbstractBackground: Urdamycin A, the principle product of Streptomyces fradiae Tü2717, is an angucyc...
SummaryDetailed studies on the biosynthesis of the hexasaccharide side chain of landomycin A, produc...
Natural products continue to be a major chemical lead matter for drug discovery due to their diverse...
AbstractThe biosynthetic gene cluster of the aureolic acid type antitumor drug chromomycin A3 from S...
AbstractA 3 kb DNA fragment from the Streptomyces globisporus 1912 landomycin E (LaE) biosynthetic g...
Sch47554 and Sch47555 are antifungal compounds from Streptomyces sp. SCC‐2136. The availability of t...
Elloramycin and oleandomycin are two polyketide compounds produced by Streptomyces olivaceus Tü2353 ...
SummaryAs glycosyltransferases found in nature often show distinct substrate specificity, glycosyltr...
AbstractBackground: Elloramycin is an anthracycline-like antitumor drug related to tetracenomycin C ...
SummarySugar biosynthesis cassette genes have been used to construct plasmids directing the biosynth...
AbstractBackground: The genetic engineering of antibiotic-producing Streptomyces strains is an appro...
AbstractA plasmid (pLN2) was generated in which genes involved in the biosynthesis of L-oleandrose i...
AbstractBackground: The biological activity of many microbial products requires the presence of one ...
Natural products occupy a central role as the majority of currently used antibiotic and anticancer a...
AbstractBackground: Mithramycin, chromomycin, and olivomycin belong to the aureolic acid family of c...
AbstractBackground: Urdamycin A, the principle product of Streptomyces fradiae Tü2717, is an angucyc...
SummaryDetailed studies on the biosynthesis of the hexasaccharide side chain of landomycin A, produc...
Natural products continue to be a major chemical lead matter for drug discovery due to their diverse...
AbstractThe biosynthetic gene cluster of the aureolic acid type antitumor drug chromomycin A3 from S...
AbstractA 3 kb DNA fragment from the Streptomyces globisporus 1912 landomycin E (LaE) biosynthetic g...
Sch47554 and Sch47555 are antifungal compounds from Streptomyces sp. SCC‐2136. The availability of t...
Elloramycin and oleandomycin are two polyketide compounds produced by Streptomyces olivaceus Tü2353 ...
SummaryAs glycosyltransferases found in nature often show distinct substrate specificity, glycosyltr...