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在缺失ptsH基因的大肠杆菌K12突变体中诱导酶合成的抑制作用。

Repression of inducible enzyme synthesis in a mutant of Escherichia coli K 12 deleted for the ptsH gene.

作者信息

Gershanovitch V N, Ilyina T S, Rusina O Y, Yourovitskaya N V, Bolshakova T N

出版信息

Mol Gen Genet. 1977 Jun 8;153(2):185-90. doi: 10.1007/BF00264734.

Abstract

The genome of lambda phage with thermosensitive repressor was inserted into the pts region of the Escherichia coli chromosome. This lysogenic culture possessed the PTS1 phenotype at 30 degrees C. A mutant strain with a deletion covering the ptsH gene was isolated after a prophage curing procedure. The deletion nature of the pts mutation was confirmed in genetical and biochemical experiments. The deletion covered a small fragment of the bacterial genome not extending in the ptsI and lig genes. The isolated deltaptsH mutant possessed all characteristics of known pts mutants: pleiotropical disturbances of transport and utilization of a number of carbohydrates, repression of the enzyme inducible synthesis, and resistance to glucose catabolite repression. From these and other data we can conclude that the phosphorylated form of the heat-stable protein HPr is involved (directly or indirectly) in activation of the DNA transcription process.

摘要

将带有热敏阻遏物的λ噬菌体基因组插入大肠杆菌染色体的pts区域。这种溶原培养物在30℃时具有PTS1表型。经过原噬菌体消除程序后,分离出了一个缺失覆盖ptsH基因的突变菌株。在遗传和生化实验中证实了pts突变的缺失性质。该缺失覆盖了细菌基因组的一小段片段,未延伸到ptsI和lig基因。分离出的ΔptsH突变体具有已知pts突变体的所有特征:多种碳水化合物运输和利用的多效性紊乱、酶诱导合成的抑制以及对葡萄糖分解代谢物阻遏的抗性。从这些和其他数据中我们可以得出结论,热稳定蛋白HPr的磷酸化形式(直接或间接)参与了DNA转录过程的激活。

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