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大肠杆菌中调控1型菌毛形成的基因产物的鉴定与特性分析

Identification and characterization of a gene product that regulates type 1 piliation in Escherichia coli.

作者信息

Orndorff P E, Falkow S

出版信息

J Bacteriol. 1984 Oct;160(1):61-6. doi: 10.1128/jb.160.1.61-66.1984.

DOI:10.1128/jb.160.1.61-66.1984
PMID:6148338
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC214681/
Abstract

The recombinant plasmid pSH2 confers type 1 piliation (Pil+) on a nonpiliated (Pil-) strain of Escherichia coli K-12. At least four plasmid-encoded gene products are involved in pilus biosynthesis and expression. We present evidence which indicates that one gene encodes an inhibitor of piliation. Hyperpiliated (Hyp) mutants were isolated after Tn5 insertion mutagenesis of pSH2 and introduction of the plasmid DNA into a Pil- strain of E. coli as unique small, compact colonies. Also, Hyp mutants clumped during growth in static broth and were piliated under several cultural conditions that normally suppressed piliation. Electron microscopic examination of Hyp mutants associated an observed 40-fold increase in pilin antigen with an increase in the number and length of pili per cell. All Hyp mutants examined failed to produce a 23-kilodalton protein that was encoded by a gene adjacent to the structural (pilin) gene for type 1 pili, and all Tn5 insertion mutations that produced the Hyp phenotype mapped in this region (hyp). Piliation in Hyp mutants could be reduced to near parental levels by introducing a second plasmid containing a parental hyp gene. Thus the 23-kilodalton (hyp) protein appears to act in trans to regulate the level of piliation.

摘要

重组质粒pSH2可赋予大肠杆菌K - 12的非菌毛(Pil -)菌株1型菌毛(Pil +)。至少有四种质粒编码的基因产物参与菌毛的生物合成和表达。我们提供的证据表明,一个基因编码菌毛形成的抑制剂。在对pSH2进行Tn5插入诱变并将质粒DNA导入大肠杆菌的Pil - 菌株后,作为独特的小而紧密的菌落分离出了高菌毛(Hyp)突变体。此外,Hyp突变体在静态肉汤中生长时会聚集,并且在几种通常抑制菌毛形成的培养条件下仍具有菌毛。对Hyp突变体的电子显微镜检查发现,菌毛抗原增加了40倍,同时每个细胞的菌毛数量和长度也增加了。所有检测的Hyp突变体均未能产生一种由与1型菌毛的结构(菌毛蛋白)基因相邻的基因编码的23千道尔顿蛋白,并且所有产生Hyp表型的Tn5插入突变都定位在该区域(hyp)。通过引入含有亲本hyp基因的第二个质粒,Hyp突变体中的菌毛形成可降低至接近亲本水平。因此,23千道尔顿(hyp)蛋白似乎以反式作用来调节菌毛形成的水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e25/214681/3627e376d6a3/jbacter00227-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e25/214681/4097c37a5228/jbacter00227-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e25/214681/0c4e61584ace/jbacter00227-0073-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e25/214681/dfeebd040c22/jbacter00227-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e25/214681/3627e376d6a3/jbacter00227-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e25/214681/4097c37a5228/jbacter00227-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e25/214681/0c4e61584ace/jbacter00227-0073-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e25/214681/dfeebd040c22/jbacter00227-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e25/214681/3627e376d6a3/jbacter00227-0075-a.jpg

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