首页> 美国卫生研究院文献>Journal of Bacteriology >Molecular cloning DNA sequence and gene expression of the oxalyl-coenzyme A decarboxylase gene oxc from the bacterium Oxalobacter formigenes.
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Molecular cloning DNA sequence and gene expression of the oxalyl-coenzyme A decarboxylase gene oxc from the bacterium Oxalobacter formigenes.

机译:富氧草酸细菌的草酰辅酶A脱羧酶基因oxc的分子克隆DNA序列和基因表达。

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摘要

Oxalic acid, a highly toxic by-product of metabolism, is catabolized by a limited number of bacterial species by an activation-decarboxylation reaction which yields formate and CO2. oxc, the gene encoding the oxalic acid-degrading enzyme oxalyl-coenzyme A decarboxylase, was cloned from the bacterium Oxalobacter formigenes. The DNA sequence revealed a single open reading frame of 1,704 bp capable of encoding a 568-amino-acid protein with a molecular weight of 60,691. The identification of a presumed promoter region and a rho-independent termination sequence indicates that this gene is not part of a polycistronic operon. A PCR fragment encoding the open reading frame, when overexpressed in Escherichia coli, produced a product which cross-reacted antigenically with native enzyme on Western blots (immunoblots), appeared to form homodimers spontaneously, and exhibited enzymatic activity similar to that of the purified native enzyme.
机译:草酸是一种新的剧毒副产物,它通过活化-脱羧反应被有限数量的细菌分解代谢,生成甲酸盐和二氧化碳。 oxc是草酸降解酶草酸辅酶A脱羧酶的编码基因。 DNA序列揭示了一个1,704 bp的开放阅读框,能够编码分子量为60,691的568个氨基酸的蛋白质。推测的启动子区域和不依赖rho的终止序列的鉴定表明该基因不是多顺反子操纵子的一部分。当在大肠杆菌中过量表达时,编码开放阅读框的PCR片段产生的产物与天然酶在免疫印迹上与天然酶发生抗原交叉反应(免疫印迹),似乎自发形成同型二聚体,并表现出与纯化的天然酶相似的酶活性。酶。

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