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一个低钙应答操纵子编码鼠疫耶尔森菌的V抗原。

A low-Ca2+ response operon encodes the V antigen of Yersinia pestis.

作者信息

Perry R D, Harmon P A, Bowmer W S, Straley S C

出版信息

Infect Immun. 1986 Nov;54(2):428-34. doi: 10.1128/iai.54.2.428-434.1986.

Abstract

Yersinia pestis has a virulence regulon called the low-Ca2+ response that is mediated by the plasmid pCD and manifested as regulation of growth and of expression of several virulence-associated properties by Ca2+ and temperature. We used Mu dI(Ap lac) to obtain a mutation in pCD1 of Y. pestis KIM that rendered the bacteria unable to express one of these properties, the V antigen. This mutant also had lost the Ca2+ requirement for growth at 37 degrees C and was avirulent in mice. Two-dimensional protein gel electrophoresis showed that the Mu dI(Ap lac) insertion had eliminated 13,000- and 18,000-molecular-weight proteins in addition to the V antigen. We mapped the Mu dI(Ap lac) insertion within pCD1, cloned the HindIII fragment spanning the insertion location, prepared two subclones of this fragment, and identified the proteins these clones expressed in Escherichia coli minicells. The data indicated that the V gene lies within an operon containing three genes; lcrG (encoding the 13,000-molecular-weight protein), lcrV (encoding the 38,000-molecular-weight V antigen), and lcrH (encoding the 18,000-molecular-weight protein). Therefore, the V operon contains the structural gene for V antigen, at least one virulence gene, and at least one Ca2+-dependence gene.

摘要

鼠疫耶尔森菌有一个称为低钙应答的毒力调节子,它由质粒pCD介导,表现为钙和温度对生长及几种毒力相关特性表达的调节作用。我们利用Mu dI(Ap lac)在鼠疫耶尔森菌KIM的pCD1中获得一个突变,使该细菌无法表达这些特性之一,即V抗原。这个突变体在37℃生长时也失去了对钙的需求,并且在小鼠中无致病性。二维蛋白质凝胶电泳显示,除了V抗原外,Mu dI(Ap lac)插入还消除了分子量为13000和18000的蛋白质。我们将Mu dI(Ap lac)插入定位在pCD1内,克隆了跨越插入位置的HindIII片段,制备了该片段的两个亚克隆,并鉴定了这些克隆在大肠杆菌微小细胞中表达的蛋白质。数据表明,V基因位于一个包含三个基因的操纵子内;lcrG(编码分子量为13000的蛋白质)、lcrV(编码分子量为38000的V抗原)和lcrH(编码分子量为18000的蛋白质)。因此,V操纵子包含V抗原的结构基因、至少一个毒力基因和至少一个钙依赖性基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bd4/260179/548759712881/iai00098-0167-a.jpg

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