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酪胺氧化酶和芳基硫酸酯酶基因的遗传定位及其在肠道细菌属间杂种中的调控

Genetic mapping of tyramine oxidase and arylsulfatase genes and their regulation in intergeneric hybrids of enteric bacteria.

作者信息

Murooka Y, Higashiura T, Harada T

出版信息

J Bacteriol. 1978 Nov;136(2):714-22. doi: 10.1128/jb.136.2.714-722.1978.

Abstract

The genes for arylsulfatase (atsA) and tyramine oxidase (tynA) have been mapped in Klebsiella aerogenes by P1 transduction. They are linked to gdhD and trp in the order atsA-tynA-gdhD-trp-pyrF. Complementation analysis using F' episomes from Escherichia coli suggested an analogous location of these genes in E. coli, although arylsulfatase activity was not detected in E. coli. P1 phage and F' episomes were used to create intergeneric hybrid strains of enteric bacteria by transfer of the ats and tyn genes between K. aerogenes, E. coli, and Salmonella typhimurium. Intergeneric transduction of the tynK gene from K. aerogenes to an E. coli restrictionless strain was one to two orders less frequent than that of the leuK gene. The tyramine oxidase of E. coli and S. typhimurium in regulatory activity resemble very closely the enzyme of K. aerogenes. The atsE gene from E. coli was expressed, and latent arylsulfatase protein was formed in K. aerogenes and S typhimurium. The results of tyramine oxidase and arylsulfatase synthesis in intergeneric hybrids of enteric bacteria suggest that the system for regulation of enzyme synthesis is conserved more than the structure or function of enzyme protein during evolution.

摘要

通过P1转导已将产碱克雷伯菌中的芳基硫酸酯酶(atsA)和酪胺氧化酶(tynA)基因进行了定位。它们与gdhD和trp连锁,顺序为atsA - tynA - gdhD - trp - pyrF。使用来自大肠杆菌的F'附加体进行的互补分析表明这些基因在大肠杆菌中有类似的定位,尽管在大肠杆菌中未检测到芳基硫酸酯酶活性。通过在产碱克雷伯菌、大肠杆菌和鼠伤寒沙门氏菌之间转移ats和tyn基因,利用P1噬菌体和F'附加体构建了肠道细菌的属间杂交菌株。从产碱克雷伯菌到无限制酶的大肠杆菌菌株的tynK基因的属间转导比leuK基因的转导频率低一到两个数量级。大肠杆菌和鼠伤寒沙门氏菌的酪胺氧化酶在调节活性方面与产碱克雷伯菌的酶非常相似。大肠杆菌的atsE基因得到表达,并且在产碱克雷伯菌和鼠伤寒沙门氏菌中形成了潜在的芳基硫酸酯酶蛋白。肠道细菌属间杂交体中酪胺氧化酶和芳基硫酸酯酶合成的结果表明,在进化过程中,酶合成的调节系统比酶蛋白的结构或功能更保守。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a6/218598/7b35a96decfc/jbacter00288-0267-a.jpg

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