Seno E T, Pieper R L, Huber F M
Antimicrob Agents Chemother. 1977 Mar;11(3):455-61. doi: 10.1128/AAC.11.3.455.
Tylosin, a macrolide antibiotic, was co-produced with four structurally similar antibiotics in fermentation cultures of Streptomyces fradiae. Macrocin, desmycosin, lactenocin, and relomycin were found to be components of a common pathway that functions in tylosin biosynthesis. Data obtained by the addition of the purified (14)C-labeled antibiotics to cultures of S. fradiae revealed that macrocin and desmycosin were direct precursors of tylosin, whereas lactenocin was an immediate precursor of both macrocin and desmycosin. Incubation of these cultures with [(14)C]tylosin resulted in an equivalent distribution of radioactive label between relomycin and an unidentified component. The kinetics of incorporation of label into the two species were similar, suggesting that both were derived directly from tylosin. A system that supported that methylation of macrocin to tylosin by cell-free extracts of S. fradiae was developed. A proposed scheme defining the terminal stages of tylosin biosynthesis is presented.
泰乐菌素是一种大环内酯类抗生素,在弗氏链霉菌的发酵培养物中与四种结构相似的抗生素共同产生。发现大霉素、去甲基泰乐菌素、乳链菌素和瑞洛霉素是泰乐菌素生物合成中共同途径的组成部分。通过向弗氏链霉菌培养物中添加纯化的(14)C标记抗生素获得的数据表明,大霉素和去甲基泰乐菌素是泰乐菌素的直接前体,而乳链菌素是大霉素和去甲基泰乐菌素的直接前体。用[(14)C]泰乐菌素培养这些培养物,导致放射性标记在瑞洛霉素和一种未鉴定成分之间等量分布。标记掺入这两种物质的动力学相似,表明两者都直接来源于泰乐菌素。开发了一种支持弗氏链霉菌无细胞提取物将大霉素甲基化为泰乐菌素的系统。提出了一个定义泰乐菌素生物合成终末阶段的方案。