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通过两种小单孢菌属的阻断突变体共发酵进行抗生素生物合成。

Antibiotic biosynthesis by cofermentation of blocked mutants of two Micromonospora species.

作者信息

Lee B K, Nagabhushan T L, Condon R G, Cooper A B, Waitz J A

出版信息

Antimicrob Agents Chemother. 1978 Jul;14(1):73-7. doi: 10.1128/AAC.14.1.73.

Abstract

Two aminocyclitol-negative Micromonospora mutants representing two different species, M. purpurea and M. inyoensis, and blocked at different steps in the biosynthetic pathway were paired and cofermented for the synthesis of antibiotics. The two blocked mutants were incapable of producing antibiotics alone except when 2-deoxystreptamine was added. When combined they produced gentamicins A, X(2), C(1a), and C(2b), which all have an amino group at the 2' position, and gentamicin B, which has a hydroxyl group at this position instead.

摘要

两个代表不同物种(紫色小单孢菌和因约小单孢菌)的氨基环醇阴性小单孢菌突变体,它们在生物合成途径的不同步骤被阻断,将它们配对并共同发酵以合成抗生素。这两个阻断突变体单独无法产生抗生素,除非添加2-脱氧链霉胺。当它们组合时,产生了在2'位都有一个氨基的庆大霉素A、X(2)、C(1a)和C(2b),以及在该位置有一个羟基的庆大霉素B。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/352407/5fd2ddfaa92d/aac00289-0080-a.jpg

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