Kameda Y, Horii S, Yamano T
J Antibiot (Tokyo). 1975 Apr;28(4):298-306. doi: 10.7164/antibiotics.28.298.
Alpha- or beta-Glucosidic linkage of validamycin was selectively cleaved by microbial hydrolysis and especially the conversion of validamycin C into validamycin A by the selective hydrolysis of alpha-glucoside linkage has important significance because validamycin C is considerably less active than validamycin A. Semisyntheses of validamycins including a new validamycin, beta-D-galactosyl-validoxylamine A were carried out by microbial transglycosidation using validoxylamine A as a glycosyl acceptor. D-[U-14C]glucose and [14C]validoxylamine A were highly incorporated into validamycin A by validamycin-producing Streptomyces hygroscopicus var. limoneus.
井冈霉素的α-或β-糖苷键可通过微生物水解选择性断裂,特别是通过α-糖苷键的选择性水解将井冈霉素C转化为井冈霉素A具有重要意义,因为井冈霉素C的活性远低于井冈霉素A。以井冈霉胺A作为糖基受体,通过微生物转糖苷作用进行了包括一种新的井冈霉素β-D-半乳糖基-井冈霉胺A在内的井冈霉素的半合成。D-[U-14C]葡萄糖和[14C]井冈霉胺A被产井冈霉素的吸水链霉菌柠檬变种高效掺入井冈霉素A中。