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capR(lon)、capS 和 capT 突变体中尿苷二磷酸葡萄糖焦磷酸化酶(galU)的去阻遏及 galU 阻遏物的研究

Derepression of uridine diphosphate-glucose pyrophosphorylase (galU) in capR(lon), capS, and capT mutants and studies on the galU repressor.

作者信息

Buchanan C E, Markovitz A

出版信息

J Bacteriol. 1973 Sep;115(3):1011-20. doi: 10.1128/jb.115.3.1011-1020.1973.

Abstract

Mutation of the capR(lon), capS, or capT genes in Escherichia coli K-12 causes overproduction of capsular polysaccharide leading to a mucoid phenotype. Several of the enzymes involved in capsular polysaccharide synthesis are derepressed in cap mutants. Previously it was shown that uridine diphosphate-glucose (UDPG) pyrophosphorylase, an enzyme involved in the synthesis of three of the nucleotide sugar precursors of the capsule, is derepressed in capR mutants. The control of galU, the gene which codes for UDPG pyrophosphorylase, is described in this study. In addition, it has been found that the enzyme is also derepressed in capS and capT mutants. The effect of galU gene dosage in cap mutants and the wild-type strain (all lysogenic for phi80) was studied by infecting them with the purified transducing phage phi80dgalU. The level of UDPG pyrophosphorylase increased in proportion to the number of galU copies added. The rate of enzyme synthesis in the mutants was about sixfold higher than in the wild type per galU gene added for multiplicities of infection from one to twenty. Thus, all the galU copies added to the wild-type lysogen were repressed. We obtain greater than 20 galU copies per cell by infecting the nonlysogenic strain which allows multiplication of phi80dgalU. With some number of galU copies greater than 20, the rate of UDPG pyrophosphorylase synthesis in the wild type approaches the mutant rate of synthesis. The results suggest that there may indeed be a galU repressor pool in the cell which can be completely titrated. This pool must be composed of more than 20 galU repressor molecules. Since the capR, capS, and capT gene products or combinations thereof are known to control other widely separated operons of the cell besides the galU gene, it is postulated that the galU repressor may be capable of binding other operators. This would account for the relatively large pool of galU repressors per cell.

摘要

大肠杆菌K-12中capR(lon)、capS或capT基因的突变会导致荚膜多糖过量产生,从而产生黏液样表型。参与荚膜多糖合成的几种酶在cap突变体中会去阻遏。此前已表明,尿苷二磷酸葡萄糖(UDPG)焦磷酸化酶是参与荚膜三种核苷酸糖前体合成的一种酶,在capR突变体中会去阻遏。本研究描述了编码UDPG焦磷酸化酶的galU基因的调控。此外,还发现该酶在capS和capT突变体中也会去阻遏。通过用纯化的转导噬菌体phi80dgalU感染cap突变体和野生型菌株(均为phi80溶原菌),研究了galU基因剂量对它们的影响。UDPG焦磷酸化酶的水平与添加的galU拷贝数成比例增加。对于感染复数从1到20,每个添加的galU基因,突变体中的酶合成速率比野生型高约6倍。因此,添加到野生型溶原菌中的所有galU拷贝都被阻遏。通过感染允许phi80dgalU增殖的非溶原菌株,我们获得了每个细胞大于20个galU拷贝。当galU拷贝数大于20时,野生型中UDPG焦磷酸化酶的合成速率接近突变体的合成速率。结果表明细胞中可能确实存在一个可以被完全滴定的galU阻遏物库。这个库必须由超过20个galU阻遏物分子组成。由于已知capR、capS和capT基因产物或其组合除了控制galU基因外,还控制细胞中其他广泛分离的操纵子,因此推测galU阻遏物可能能够结合其他操纵基因。这将解释每个细胞中相对大量的galU阻遏物库。

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