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溶血巴斯德氏菌白细胞毒素的分泌与表达。

Secretion and expression of the Pasteurella haemolytica Leukotoxin.

作者信息

Highlander S K, Engler M J, Weinstock G M

机构信息

Department of Biochemistry and Molecular Biology, University of Texas Medical School, Houston 77030.

出版信息

J Bacteriol. 1990 May;172(5):2343-50. doi: 10.1128/jb.172.5.2343-2350.1990.

Abstract

The Pasteurella haemolytica leukotoxin gene cluster (lktCABD) is homologous to the Escherichia coli hemolysin locus (hlyCABD). Since the cloned leukotoxin (LktA) is not secreted from E. coli cells, a heteroplasmid complementation system was developed that permits secretion of the leukotoxin from cells expressing the hemolysin transport proteins HlyB and HlyD. We observed that the secreted leukotoxin protein had weak hemolytic activity when activated by either the HlyC or LktC proteins and that LktC expressed in E. coli could confer weak hemolytic activity upon hemolysin. Thus, it appears that the accessory proteins of the leukotoxin and hemolysin gene clusters are functionally similar, although their expression in E. coli is not equivalent. Northern (RNA) blot analysis of the P. haemolytica leukotoxin gene cluster revealed a major 3.5-kilobase transcript that includes the lktC and lktA genes. The start site for this transcript mapped to a cytosine residue 30 nucleotides upstream from the putative start of lktC; a similar initiation site was observed in E. coli, although adjacent cytosine and adenine residues were also utilized. The 3.5-kilobase transcript terminated near the rho-independent terminator structure between lktA and lktB, but transcription may continue, via antitermination or de novo transcription initiation, into the downstream lktB and lktD genes. We propose that the lack of LktB and LktD function in E. coli is a result, at least in part, of poor lktBD transcription and suggest that a P. haemolytica-specific regulator is required for optimal expression of the leukotoxin genes.

摘要

溶血巴斯德氏菌白细胞毒素基因簇(lktCABD)与大肠杆菌溶血素基因座(hlyCABD)同源。由于克隆的白细胞毒素(LktA)不能从大肠杆菌细胞中分泌出来,因此开发了一种异质质粒互补系统,该系统允许白细胞毒素从表达溶血素转运蛋白HlyB和HlyD的细胞中分泌。我们观察到,当被HlyC或LktC蛋白激活时,分泌的白细胞毒素蛋白具有较弱的溶血活性,并且在大肠杆菌中表达的LktC可以赋予溶血素较弱的溶血活性。因此,尽管白细胞毒素和溶血素基因簇的辅助蛋白在大肠杆菌中的表达不等同,但它们在功能上似乎相似。对溶血巴斯德氏菌白细胞毒素基因簇的Northern(RNA)印迹分析揭示了一个主要的3.5千碱基转录本,其中包括lktC和lktA基因。该转录本的起始位点定位于lktC推定起始位点上游30个核苷酸处的一个胞嘧啶残基;在大肠杆菌中观察到类似的起始位点,尽管也利用了相邻的胞嘧啶和腺嘌呤残基。3.5千碱基的转录本在lktA和lktB之间的不依赖rho的终止子结构附近终止,但转录可能通过抗终止或从头转录起始继续进入下游的lktB和lktD基因。我们提出,大肠杆菌中LktB和LktD功能的缺失至少部分是由于lktBD转录不佳的结果,并表明溶血巴斯德氏菌特异性调节因子是白细胞毒素基因最佳表达所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fac/208868/cb1470685560/jbacter00119-0159-a.jpg

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