Reuter G, Köster H, Liebermann B
Z Allg Mikrobiol. 1977;17(7):543-7.
Distribution of radioactivity in paromomycin ascertained after application of 14C-D-glucose, 14C-D-glucosamine, 14C-2-deoxystreptamine, respectively, 14C-D-ribose is taken as basis for a biosynthesis scheme: While ribose bound in the antibiotic originates from glucose by oxidation and following decarboxylation, glucosamine is formed via fructose-6-phosphate. Paromose I arises from glucosamine, but not the cyclohexan derivative 2-deoxystreptamine, whose biosynthesis pathway is directly branching off glucose.
分别应用¹⁴C-D-葡萄糖、¹⁴C-D-葡糖胺、¹⁴C-2-脱氧链霉胺后确定的巴龙霉素中放射性分布,以¹⁴C-D-核糖为基础构建生物合成方案:抗生素中结合的核糖源于葡萄糖经氧化及随后的脱羧反应,葡糖胺则通过6-磷酸果糖形成。巴龙糖I由葡糖胺产生,但环己烷衍生物2-脱氧链霉胺并非如此,其生物合成途径直接从葡萄糖分支而来。