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产气克雷伯菌中芳基硫酸酯酶合成的遗传控制。

Genetic control of arylsulfatase synthesis in Klebsiella aerogenes.

作者信息

Murooka Y, Adachi T, Okamura H, Harada T

出版信息

J Bacteriol. 1977 Apr;130(1):74-81. doi: 10.1128/jb.130.1.74-81.1977.

Abstract

It was shown that at least four genes are specifically responsible for arylsulfatase synthesis in Klebsiella aerogenes. Mutations at chromosome site atsA result in enzymatically inactive arylsulfatase. Mutants showing constitutive synthesis of arylsulfatase (atsR) were isolated by using inorganic sulfate or cysteine as the sulfur source. Another mutation in which repression of arylsulfatase by inorganic sulfate or cysteine could not be relieved by tyramine was determined by genetic analysis to be on the tyramine oxidase gene (tyn). This site was distinguished from the atsC mutation site, which is probably concerned with the action or synthesis of corepressors of arylsulfatase synthesis. Genetic analysis with transducing phage PW52 showed that the order of mutation sites was atsC-atsR-atsA-tynA-tynB. On the basis of these results and previous physiological findings, we propose a new model for regulation of arylsulfatase synthesis.

摘要

结果表明,至少有四个基因专门负责产气克雷伯菌中芳基硫酸酯酶的合成。染色体位点atsA发生突变会导致产生无酶活性的芳基硫酸酯酶。通过使用无机硫酸盐或半胱氨酸作为硫源,分离出了显示芳基硫酸酯酶组成型合成的突变体(atsR)。通过遗传分析确定,另一种突变体中无机硫酸盐或半胱氨酸对芳基硫酸酯酶的阻遏不能被酪胺解除,该突变位于酪胺氧化酶基因(tyn)上。该位点与atsC突变位点不同,atsC突变位点可能与芳基硫酸酯酶合成的辅阻遏物的作用或合成有关。用转导噬菌体PW52进行的遗传分析表明,突变位点的顺序为atsC - atsR - atsA - tynA - tynB。基于这些结果和先前的生理学发现,我们提出了一种新的芳基硫酸酯酶合成调控模型。

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