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大肠杆菌K-12中参与荚膜多糖合成的两个不同调节基因突变导致鸟苷二磷酸甘露糖焦磷酸化酶活性降低。

Depression of guanosine diphosphate-mannose pyrophosphorylase by mutations in two different regulator genes involved in capsular polysaccharide synthesis in Escherichia coli K-12.

作者信息

Lieberman M M, Markovitz A

出版信息

J Bacteriol. 1970 Mar;101(3):965-72. doi: 10.1128/jb.101.3.965-972.1970.

Abstract

Mutations in a regulator gene (capR) that causes increased synthesis of capsular polysaccharide and derepressed synthesis of several enzymes involved in polysaccharide synthesis also derepress synthesis of guanosine diphosphate (GDP)-mannose pyrophosphorylase. In addition, a second mucoid mutation (capS, which maps separately from capR) also results in the derepression of GDP-mannose pyrophosphorylase. New conditions for assaying GDP-mannose hydrolyase and GDP-l-fucose synthetase permitted us to show that these enzymes are also derepressed in the capS mucoid strain. Although phosphomannose isomerase and uridine diphosphate-galactose-4-epimerase are derepressed in capR mucoid strains, they are not derepressed in capS mucoid strains. A nonmucoid mutant of a strain containing the capR9 (mucoid) allele was deficient in GDP-mannose pyrophosphorylase.

摘要

调节基因(capR)发生突变会导致荚膜多糖合成增加,同时参与多糖合成的几种酶的合成去阻遏,这也会使二磷酸鸟苷(GDP)-甘露糖焦磷酸化酶的合成去阻遏。此外,第二个黏液样突变(capS,其定位与capR不同)也会导致GDP-甘露糖焦磷酸化酶的去阻遏。用于检测GDP-甘露糖水解酶和GDP-L-岩藻糖合成酶的新条件使我们能够证明,这些酶在capS黏液样菌株中也被去阻遏。虽然磷酸甘露糖异构酶和尿苷二磷酸-半乳糖-4-表异构酶在capR黏液样菌株中被去阻遏,但在capS黏液样菌株中并未被去阻遏。含有capR9(黏液样)等位基因的菌株的非黏液样突变体缺乏GDP-甘露糖焦磷酸化酶。

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