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大肠杆菌K-12中一种新型温度敏感型多核苷酸磷酸化酶突变体的分离与鉴定。

Isolation and characterization of a new temperature-sensitive polynucleotide phosphorylase mutation in Escherichia coli K-12.

作者信息

Yancey S D, Kushner S R

机构信息

Department of Genetics, University of Georgia, Athens 30602.

出版信息

Biochimie. 1990 Nov;72(11):835-43. doi: 10.1016/0300-9084(90)90193-k.

Abstract

Polynucleotide phosphorylase (PNPase) has been studied in detail since its discovery in 1955 [1]. In an attempt to determine what role, if any, it has in mRNA decay in Escherichia coli, we have isolated and characterized a temperature-sensitive mutation, pnp-200, in the pnp gene. In vitro phosphorolysis, polymerization and exchange activities of the partially purified Pnp-200 enzyme are all reduced to 30-40% of wild-type activity at 50 degrees C compared to 32 degrees C. The pnp-200 mutation alone does not affect cell growth or mRNA stability. A triple mutant strain containing pnp-200 in combination with other temperature-sensitive mutations in genes known to affect mRNA metabolism (rnb-500 and ams-1) is conditionally lethal and shows increased mRNA stability after shift to the non-permissive temperature.

摘要

自1955年发现多核苷酸磷酸化酶(PNPase)以来,人们对其进行了详细研究[1]。为了确定它在大肠杆菌mRNA降解中可能扮演的角色,我们分离并鉴定了pnp基因中的一个温度敏感突变体pnp - 200。与32℃相比,部分纯化的Pnp - 200酶在50℃时的体外磷酸解、聚合和交换活性均降至野生型活性的30 - 40%。单独的pnp - 200突变不影响细胞生长或mRNA稳定性。一个含有pnp - 200以及已知影响mRNA代谢的基因中的其他温度敏感突变(rnb - 500和ams - 1)的三重突变菌株是条件致死的,并且在转移到非允许温度后显示出mRNA稳定性增加。

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