Schlegel B, Stengel C, Schumann G, Prauser H, Eckardt K
Akademie der Wissenschaften der DDR.
J Basic Microbiol. 1987;27(2):107-11. doi: 10.1002/jobm.3620270212.
A number of blocked mutants was investigated which were obtained from taxonomically identified Streptomyces strains producing anthracyclines. Two of these mutants, NTG 061 derived from S. galilaeus F 198 and mutant 135 derived from S. peucetius var. caesius 601 F.I.1), accumulated an anthraquinone derivative which was identified as aklanonic acid. The results supplied further evidence that this compound was an intermediate of the biosynthetic pathway leading to different types of anthracyclines. It occurred before ring closure to the final tetracyclic anthracyclinone skeleton.
对从分类鉴定的产蒽环类抗生素的链霉菌菌株中获得的多个阻断突变体进行了研究。其中两个突变体,即源自加利利链霉菌F 198的NTG 061和源自佩鲁贾链霉菌变种天蓝链霉菌601 F.I.1的突变体135,积累了一种蒽醌衍生物,经鉴定为阿克拉农酸。这些结果进一步证明该化合物是导致不同类型蒽环类抗生素生物合成途径的中间体。它发生在环合形成最终的四环蒽环酮骨架之前。