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大肠杆菌中一个增加6-磷酸葡萄糖酸脱氢酶基因转录的缺失突变的适应性效应

Fitness effects of a deletion mutation increasing transcription of the 6-phosphogluconate dehydrogenase gene in Escherichia coli.

作者信息

Miller R D, Dykhuizen D E, Hartl D L

机构信息

Department of Genetics, Washington University School of Medicine, St. Louis, Missouri 63110-1095.

出版信息

Mol Biol Evol. 1988 Nov;5(6):691-703. doi: 10.1093/oxfordjournals.molbev.a040522.

DOI:10.1093/oxfordjournals.molbev.a040522
PMID:2464736
Abstract

Directed evolution in microbial organisms provides an experimental approach to molecular evolution in which selective forces can be controlled and favorable mutations analyzed at the molecular level. Here we present an analysis of a mutation selected in Escherichia coli in response to growth in a chemostat in which the limiting nutrient was gluconate. The selectively favored mutation, designated gnd+ (862), occurred in the gene gnd coding for 6-phosphogluconate dehydrogenase, used in gluconate metabolism. Although the allele is strongly favored in chemostats in which the limiting nutrient is gluconate, the selective effects of gnd+ (862) are highly dependent on growth conditions. In chemostats in which growth is limited by a mixture of gluconate and either ribose, glucose, or succinate, the gnd+ (862) allele is favored, disfavored, or neutral according to the relative concentrations of the substrates. The gnd+ (862) allele results from a deletion of 385 nucleotide pairs in the region 5' to the promoter of gnd, and one endpoint of the deletion is contiguous with the terminus of an IS5 insertion sequence located near gnd in E. coli K12. The gnd+ (862) allele shows a marked increase in transcription that accounts for most or all of the increased enzyme activity.

摘要

微生物中的定向进化为分子进化提供了一种实验方法,在这种方法中,可以控制选择力,并在分子水平上分析有利突变。在这里,我们对大肠杆菌中因在恒化器中以葡萄糖酸盐作为限制营养物生长而选择的一个突变进行了分析。这个选择性有利的突变被命名为gnd+(862),它发生在编码6-磷酸葡萄糖酸脱氢酶的gnd基因中,该酶用于葡萄糖酸盐代谢。尽管在以葡萄糖酸盐作为限制营养物的恒化器中该等位基因受到强烈青睐,但gnd+(862)的选择效应高度依赖于生长条件。在以葡萄糖酸盐与核糖、葡萄糖或琥珀酸的混合物作为生长限制因素的恒化器中,根据底物的相对浓度,gnd+(862)等位基因可能受到青睐、不被青睐或呈中性。gnd+(862)等位基因是由于gnd基因启动子5'端区域缺失了385个核苷酸对而产生的,缺失的一个端点与大肠杆菌K12中位于gnd附近的一个IS5插入序列的末端相邻。gnd+(862)等位基因的转录显著增加,这解释了大部分或全部酶活性的增加。

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