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鼠疫耶尔森氏菌钙离子不敏感突变体的分离与鉴定

Isolation and characterization of Ca2+-blind mutants of Yersinia pestis.

作者信息

Yother J, Goguen J D

出版信息

J Bacteriol. 1985 Nov;164(2):704-11. doi: 10.1128/jb.164.2.704-711.1985.

Abstract

The plasmid pCD1 is required for expression of the low-calcium response (LCR), virulence, and production of V antigen in Yersinia pestis KIM. Five independent mutants constitutive for the LCR at 37 degrees C (Lcrc) were obtained through ethyl methanesulfonate mutagenesis followed by ampicillin enrichment. A sixth, spontaneous mutant was obtained directly through ampicillin enrichment. These mutants failed to grow at 37 degrees C regardless of calcium concentration and produced V antigen constitutively at this temperature. All six mutations were located on pCD1. One mutation was mapped to a 1-kilobase region of lcrA. Based on complementation mapping of this mutation, the lcrA locus was divided into two new loci, lcrD and lcrE. This mutation, lcrE1, did not alter the transcription of other genes in the LCR region and was cis-recessive to lcr mutations. Several lower-molecular-weight outer membrane proteins which were observed in the parent strain grown at 37 degrees C in the presence of 2.5 mM calcium were reduced in quantity or absent from the mutant strain.

摘要

质粒pCD1是鼠疫耶尔森氏菌KIM中低钙应答(LCR)表达、毒力以及V抗原产生所必需的。通过甲磺酸乙酯诱变继以氨苄青霉素富集,获得了5个在37℃时LCR组成型的独立突变体(Lcrc)。通过氨苄青霉素富集直接获得了第6个自发突变体。这些突变体无论钙浓度如何,在37℃时均无法生长,并在此温度下组成型产生V抗原。所有6个突变均位于pCD1上。一个突变被定位到lcrA的一个1千碱基区域。基于该突变的互补定位,lcrA基因座被分为两个新的基因座,lcrD和lcrE。这个突变,即lcrE1,并未改变LCR区域中其他基因的转录,并且对lcr突变是顺式隐性的。在亲本菌株于37℃、2.5 mM钙存在的条件下生长时观察到的几种低分子量外膜蛋白,在突变菌株中数量减少或缺失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/694b/214309/45fc53f0ae13/jbacter00216-0225-a.jpg

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