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通过基因改造的欧文氏菌生产 2-酮-L-古洛糖酸,这是 L-抗坏血酸合成的中间产物。

Production of 2-Keto-L-Gulonate, an Intermediate in L-Ascorbate Synthesis, by a Genetically Modified Erwinia herbicola.

出版信息

Science. 1985 Oct 11;230(4722):144-9. doi: 10.1126/science.230.4722.144.

Abstract

A new metabolic pathway has been created in the microorganism Erwinia herbicola that gives it the ability to produce 2-keto-L-gulonic acid, an important intermediate in the synthesis of L-ascorbic acid. Initially, a Corynebacterium enzyme that could stereoselectively reduce 2,5-diketo-D-gluconic acid to 2-keto-L-gulonic acid was identified and purified. DNA probes based on amino acid sequence information from 2,5-diketo-D-gluconic acid reductase were then used to isolate the gene for this enzyme from a Corynebacterium genomic library. The 2,5-diketo-D-gluconic acid reductase coding region was fused to the Escherichia coli trp promoter and a synthetic ribosome binding site and was then introduced into E. herbicola on a multicopy plasmid. Erwinia herbicola naturally produces 2,5-diketo-D-gluconic acid via glucose oxidation, and when recombinant cells expressing the plasmid-encoded reductase were grown in the presence of glucose, 2-keto-L-gulonic acid was made and released into the culture medium. The data demonstrate the feasibility of creating novel in vivo routes for the synthesis of important specialty chemicals by combining useful metabolic traits from diverse sources in a single organism.

摘要

一种新的代谢途径已经在微生物欧文氏菌中创建,该途径使它能够生产 2-酮-L-古洛糖酸,这是合成 L-抗坏血酸的重要中间体。最初,鉴定并纯化了一种能够立体选择性还原 2,5-二酮-D-葡萄糖酸为 2-酮-L-古洛糖酸的棒状杆菌酶。然后,使用基于 2,5-二酮-D-葡萄糖酸还原酶的氨基酸序列信息的 DNA 探针从棒状杆菌基因组文库中分离出该酶的基因。将 2,5-二酮-D-葡萄糖酸还原酶编码区与大肠杆菌 trp 启动子和合成核糖体结合位点融合,并将其引入埃希氏菌属的多拷贝质粒上。欧文氏菌属通过葡萄糖氧化自然产生 2,5-二酮-D-葡萄糖酸,当表达质粒编码的还原酶的重组细胞在葡萄糖存在下生长时,会产生 2-酮-L-古洛糖酸并释放到培养基中。这些数据证明了通过在单个生物体中结合来自不同来源的有用代谢特征,为合成重要特种化学品创造新的体内途径的可行性。

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