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在瘤胃厌氧菌普氏栖瘤胃菌D31d中鉴定出一种新型腺苷酸环化酶。

Identification of a novel adenylate cyclase in the ruminal anaerobe, Prevotella ruminicola D31d.

作者信息

Cotta M A, Whitehead T R, Wheeler M B

机构信息

Fermentation Biochemistry Research Unit, National Center for Agricultural Utilization Research, USDA, Peoria, IL 61604, USA.

出版信息

FEMS Microbiol Lett. 1998 Jul 15;164(2):257-60. doi: 10.1111/j.1574-6968.1998.tb13095.x.

Abstract

Our previous evaluation of ruminal and other anaerobic bacteria showed only Prevotella ruminicola D31d produced detectable concentrations of cyclic AMP. In order to investigate the synthesis of this important metabolic regulator, the gene for adenylate cyclase (cya), which produces cyclic AMP, was cloned and expressed in a cyaA mutant of Escherichia coli. The cloned P. ruminicola D31d gene was able to complement the cyaA mutation and permitted fermentation of lactose on MacConkey Lactose agar plates. Analysis of the DNA sequence of the 2.5-kilobase pair insert revealed an open reading frame encoding for a 67-kDa protein. This protein was novel in that no amino acid similarity was observed with other procaryotic or eucaryotic adenylate cyclases in the GenBank database. Production of cyclic AMP in the E. coli clone was confirmed with a radioimmunoassay technique. This is the first example of an adenylate cyclase gene identified from an anaerobic bacterium.

摘要

我们之前对瘤胃及其他厌氧菌的评估表明,只有瘤胃普雷沃氏菌D31d能产生可检测浓度的环磷酸腺苷(cAMP)。为了研究这种重要代谢调节物的合成,编码产生环磷酸腺苷的腺苷酸环化酶(cya)的基因被克隆,并在大肠杆菌的cyaA突变体中表达。克隆的瘤胃普雷沃氏菌D31d基因能够弥补cyaA突变,并允许在麦康凯乳糖琼脂平板上发酵乳糖。对2.5千碱基对插入片段的DNA序列分析揭示了一个编码67 kDa蛋白质的开放阅读框。该蛋白质是新颖的,因为在GenBank数据库中未观察到与其他原核或真核腺苷酸环化酶有氨基酸相似性。用放射免疫测定技术证实了大肠杆菌克隆中环磷酸腺苷的产生。这是从厌氧菌中鉴定出腺苷酸环化酶基因的首个实例。

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