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产气克雷伯菌多聚磷酸激酶编码基因(ppk)的克隆、测序及特性分析

Cloning, sequence and characterization of the polyphosphate kinase-encoding gene (ppk) of Klebsiella aerogenes.

作者信息

Kato J, Yamamoto T, Yamada K, Ohtake H

机构信息

Department of Fermentation Technology, Hiroshima University, Japan.

出版信息

Gene. 1993 Dec 31;137(2):237-42. doi: 10.1016/0378-1119(93)90013-s.

Abstract

Polyphosphate kinase (PPK) catalyzes the formation of polyphosphate (polyP). The PPK-encoding gene (ppk) has been cloned from Klebsiella aerogenes ATCC9621. The gene possessed an open reading frame of 2055 bp capable of encoding a putative polypeptide with a deduced M(r) of 80,157. This polypeptide showed 93% similarity to the Escherichia coli PPK. The nucleotide sequence of the promoter region of K. aerogenes ppk differed from that of the previously sequenced E. coli ppk. A putative pho box sequence was found in the promoter region of K. aerogenes ppk. The expression of lacZ from the ppk promoter was increased in E. coli MV1184 under conditions of phosphate (Pi) limitation, but not in E. coli ANCS3 (phoB-), indicating that the ppk promoter is regulated by the phoB product. Increased levels of specific PPK activity were shown by expressing the cloned ppk at high levels, resulting in increased accumulation of polyP in E. coli.

摘要

多聚磷酸激酶(PPK)催化多聚磷酸(polyP)的形成。已从产气克雷伯菌ATCC9621中克隆出编码PPK的基因(ppk)。该基因具有一个2055 bp的开放阅读框,能够编码一个推定的多肽,推导的分子量为80,157。该多肽与大肠杆菌PPK具有93%的相似性。产气克雷伯菌ppk启动子区域的核苷酸序列与先前测序的大肠杆菌ppk不同。在产气克雷伯菌ppk的启动子区域发现了一个推定的pho框序列。在磷酸盐(Pi)限制条件下,ppk启动子驱动的lacZ在大肠杆菌MV1184中的表达增加,但在大肠杆菌ANCS3(phoB-)中未增加,这表明ppk启动子受phoB产物调控。通过高水平表达克隆的ppk,显示出特定PPK活性水平增加,导致大肠杆菌中多聚磷酸的积累增加。

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