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导致大肠杆菌O157:H7中β-葡萄糖醛酸酶活性缺失的gusA基因突变的遗传与进化分析。

Genetic and evolutionary analysis of mutations in the gusA gene that cause the absence of beta-glucuronidase activity in Escherichia coli O157:H7.

作者信息

Monday S R, Whittam T S, Feng P C

机构信息

Division of Microbiological Studies, Food and Drug Administration, Washington, DC 20204, USA.

出版信息

J Infect Dis. 2001 Oct 1;184(7):918-21. doi: 10.1086/323154. Epub 2001 Aug 15.

Abstract

Escherichia coli serotype O157:H7 do not exhibit beta-glucuronidase (GUD) activity but carry the gusA gene (uidA) that encodes for GUD. In trans-complementation, the gusA gene cloned from the GUD-positive variant strain 493-89 effectively restored GUD activity in O157:H7 strain 35150. Comparison of gusA sequences from the GUD-negative 35150 strain to that of 493-89 revealed several base mutations, including a guanosine (G) dinucleotide insertion that caused a frameshift in the 35150 gusA gene and introduced a predicted premature termination codon. This explains the absence of GUD activity in O157:H7. A 35150 gusA construct from which the G-G insertion was deleted restored activity in GUD-negative O157:H7 transformants. The G-G insertion was present in all GUD-negative O157:H7 strains but was absent in their GUD-positive variants. The G-G insertion that produced the characteristic GUD-negative phenotype to O157:H7 strains appeared later than the other gusA mutations in the evolutionary emergence of O157:H7.

摘要

大肠杆菌O157:H7血清型不表现出β-葡萄糖醛酸酶(GUD)活性,但携带编码GUD的gusA基因(uidA)。在反式互补中,从GUD阳性变异株493-89克隆的gusA基因有效地恢复了O157:H7菌株35150中的GUD活性。将GUD阴性的35150菌株的gusA序列与493-89的gusA序列进行比较,发现了几个碱基突变,包括一个鸟苷(G)二核苷酸插入,该插入导致35150 gusA基因发生移码,并引入了一个预测的提前终止密码子。这解释了O157:H7中缺乏GUD活性的原因。删除了G-G插入的35150 gusA构建体在GUD阴性的O157:H7转化体中恢复了活性。G-G插入存在于所有GUD阴性的O157:H7菌株中,但在它们的GUD阳性变异株中不存在。在O157:H7的进化出现过程中,产生O157:H7菌株特征性GUD阴性表型的G-G插入比其他gusA突变出现得晚。

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