Yamasaki K, Kaneda M, Watanabe K, Ueki Y, Ishimaru K, Nakamura S, Nomi R, Yoshida N, Nakajima T
J Antibiot (Tokyo). 1983 May;36(5):552-8. doi: 10.7164/antibiotics.36.552.
The carbazomycin-producing microorganism, strain H 1051-MY 10, was determined to a strain of Streptoverticillium ehimense. Biosynthesis of carbazomycin B was studied using 14C-labeled and 13C-enriched precursors in combination with 13C NMR spectroscopy. The C-2 carbon of [2-13C]trytophan was shown to be involved at the C-3 carbon in carbazomycin B and both carbons of [1,2-13C]acetate at the C-1 and C-10 moiety of the antibiotic. [CH3-13C]Methionine was involved at the methoxyl group but not at the methyl group on the C-2 carbon of the antibiotic. Neither of the labeled carbons, [1-14C]tryptophan nor [2,3-13C]propionic acid, was detected in the antibiotic, and a progenitor of the C-2 and C-11 moiety of the antibiotic has not been determined.
产生咔唑霉素的微生物菌株H 1051-MY 10被鉴定为埃希氏链霉菌。使用14C标记和13C富集的前体结合13C核磁共振光谱研究了咔唑霉素B的生物合成。结果表明,[2-13C]色氨酸的C-2碳参与了咔唑霉素B的C-3碳的合成,[1,2-13C]乙酸盐的两个碳参与了抗生素的C-1和C-10部分的合成。[CH3-13C]甲硫氨酸参与了抗生素C-2碳上的甲氧基合成,但未参与甲基合成。在抗生素中未检测到标记的碳[1-14C]色氨酸和[2,3-13C]丙酸,并且抗生素C-2和C-11部分的前体尚未确定。