首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Genes Specific for the Biosynthesis of Clavam Metabolites Antipodal to Clavulanic Acid Are Clustered with the Gene for Clavaminate Synthase 1 in Streptomyces clavuligerus
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Genes Specific for the Biosynthesis of Clavam Metabolites Antipodal to Clavulanic Acid Are Clustered with the Gene for Clavaminate Synthase 1 in Streptomyces clavuligerus

机译:克拉维酸对立的克拉瓦姆代谢产物生物合成的特异性基因与克拉维链霉菌中克拉维酸合酶1的基因簇集在一起

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摘要

Portions of the Streptomyces clavuligerus chromosome flanking cas1, which encodes the clavaminate synthase 1 isoenzyme (CAS1), have been cloned and sequenced. Mutants of S. clavuligerus disrupted in cvm1, the open reading frame located immediately upstream of cas1, were constructed by a gene replacement procedure. Similar techniques were used to generate S. clavuligerus mutants carrying a deletion that encompassed portions of the two open reading frames, cvm4 and cvm5, located directly downstream of cas1. Both classes of mutants still produced clavulanic acid and cephamycin C but lost the ability to synthesize the antipodal clavam metabolites clavam-2-carboxylate, 2-hydroxymethyl-clavam, and 2-alanylclavam. These results suggested that cas1 is clustered with genes essential and specific for clavam metabolite biosynthesis. When a cas1 mutant of S. clavuligerus was constructed by gene replacement, it produced lower levels of both clavulanic acid and most of the antipodal clavams except for 2-alanylclavam. However, a double mutant of S. clavuligerus disrupted in both cas1 and cas2 produced neither clavulanic acid nor any of the antipodal clavams, including 2-alanylclavam. This outcome was consistent with the contribution of both CAS1 and CAS2 to a common pool of clavaminic acid that is shunted toward clavulanic acid and clavam metabolite biosynthesis.
机译:已克隆并测序了链霉菌链霉菌cas1侧翼的染色体部分,该部分编码棒状合酶1同工酶(CAS1)。通过基因替换程序构建了在cvm1(紧邻cas1上游的开放阅读框)中破坏的克拉维链球菌突变体。类似的技术被用于产生携带缺失的链霉链球菌突变体,该缺失包含两个直接位于cas1下游的开放阅读框cvm4和cvm5的部分。这两类突变体仍然产生棒酸和头霉素C,但是丧失了合成对立的克拉瓦姆代谢产物克拉瓦姆-2-羧酸盐,2-羟甲基克拉瓦姆和2-丙氨酰克拉瓦姆的能力。这些结果表明,cas1聚集了克拉瓦姆代谢物生物合成必不可少的基因。当通过基因置换构建克拉维链霉菌的cas1突变体时,除了2-丙氨酰克拉维菌以外,它产生的克拉维酸和大多数对足的克拉瓦姆都较低。但是,在cas1和cas2中都被破坏的克拉维链霉菌的双突变体既不产生克拉维酸也不产生任何对立的克拉维姆,包括2-丙氨酰克拉维姆。这一结果与CAS1和CAS2对共同的克拉维酸库的贡献相一致,克拉维酸被转移至克拉维酸和克拉瓦姆代谢物的生物合成中。

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