首页> 外文OA文献 >Cloning, characterization, and expression in Escherichia coli of the Streptomyces clavuligerus gene encoding deacetoxycephalosporin C synthetase.
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Cloning, characterization, and expression in Escherichia coli of the Streptomyces clavuligerus gene encoding deacetoxycephalosporin C synthetase.

机译:编码脱乙酰氧基头孢菌素C合成酶的克拉维链霉菌基因的克隆,鉴定和在大肠杆菌中的表达。

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摘要

Biosynthesis of cephalosporin antibiotics involves an expansion of the five-membered thiazolidine ring of penicillin N to the six-membered dihydrothiazine ring of deacetoxycephalosporin C by a deacetoxycephalosporin C synthetase (DAOCS) enzyme activity. Hydroxylation of deacetoxycephalosporin C to form deacetylcephalosporin C by a deacetylcephalosporin C synthetase (DACS) activity is the next step in biosynthesis of cephalosporins. In Cephalosporium acremonium, both of these catalytic activities are exhibited by a bifunctional enzyme, DAOCS-DACS, encoded by a single gene, cefEF. In Streptomyces clavuligerus, separable enzymes, DAOCS (expandase) and DACS (hydroxylase), catalyze these respective reactions. We have cloned, sequenced, and expressed in E. coli an S. clavuligerus gene, designated cefE, which encodes DAOCS but not DACS. The deduced amino acid sequence of DAOCS from S. clavuligerus (calculated Mr of 34,519) shows marked similarity (approximately 57%) to the deduced sequence of DAOCS-DACS from C. acremonium; however, the latter sequence is longer by 21 amino acid residues.
机译:头孢菌素抗生素的生物合成涉及通过去乙酰氧基头孢菌素C合成酶(DAOCS)酶将青霉素N的五元噻唑烷环扩展到去乙酰氧基头孢菌素C的六元二氢噻嗪环。通过脱乙酰头孢菌素C合成酶(DACS)活性将脱乙酰氧基头孢菌素C羟化以形成脱乙酰头孢菌素C是头孢菌素生物合成的下一步。在顶头孢霉中,这两种催化活性均由双功能酶DAOCS-DACS展现,该酶由单个基因cefEF编码。在棒状链霉菌中,可分离的酶DAOCS(扩展酶)和DACS(羟化酶)催化这些各自的反应。我们已经在大肠杆菌中克隆,测序并表达了一种名为cefE的链霉链球菌基因,该基因编码DAOCS,但不编码DACS。棒状链球菌DAOCS的推导氨基酸序列(计算为34519)显示出与顶头孢霉的DAOCS-DACS推导序列具有显着相似性(约57%)。但是,后者的序列长21个氨基酸残基。

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