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溶血巴斯德氏菌A1白细胞毒素基因的核苷酸序列

Nucleotide sequence of the leukotoxin genes of Pasteurella haemolytica A1.

作者信息

Lo R Y, Strathdee C A, Shewen P E

出版信息

Infect Immun. 1987 Sep;55(9):1987-96. doi: 10.1128/iai.55.9.1987-1996.1987.

Abstract

A 4.4-kilobase-pair DNA fragment coding for the leukotoxin of Pasteurella haemolytica A1 has been isolated, and its nucleotide sequence has been determined. Two open reading frames, designated lktC and lktA, coding for proteins of 19.8 and 101.9 kilodaltons, respectively, were identified. Expression of the two genes in minicell-labeling experiments resulted in the production of the predicted proteins LKTC and LKTA. By using an antiserum against the soluble antigens of P. haemolytica A1 in Western blot (immunoblot) analysis of total cellular proteins from the Escherichia coli clones, LKTA was identified as an additional antigenic protein. Results from subcloning of the DNA fragment suggested that expression from both lktC and lktA is required for leukotoxin activity, indicating that the leukotoxin of P. haemolytica A1 is encoded by two genes. A comparison of the organization and the DNA sequence of the leukotoxin genes with those of the E. coli alpha-hemolysin genes showed a significant degree of homology between the two loci. This analysis suggested that the leukotoxin genes of P. haemolytica A1 and the E. coli alpha-hemolysin genes may have evolved from a common ancestor and that the two toxins may share similar activities or functional domains or both.

摘要

编码溶血巴斯德菌A1白细胞毒素的一个4.4千碱基对的DNA片段已被分离出来,并测定了其核苷酸序列。鉴定出了两个开放阅读框,分别命名为lktC和lktA,它们分别编码19.8千道尔顿和101.9千道尔顿的蛋白质。在小细胞标记实验中这两个基因的表达导致了预测蛋白LKTC和LKTA的产生。通过在对来自大肠杆菌克隆的总细胞蛋白进行蛋白质印迹(免疫印迹)分析时使用针对溶血巴斯德菌A1可溶性抗原的抗血清,LKTA被鉴定为一种额外的抗原性蛋白。DNA片段亚克隆的结果表明,lktC和lktA的表达对于白细胞毒素活性都是必需的,这表明溶血巴斯德菌A1的白细胞毒素由两个基因编码。将白细胞毒素基因的结构和DNA序列与大肠杆菌α-溶血素基因的结构和序列进行比较,结果显示这两个基因座之间存在显著程度的同源性。该分析表明,溶血巴斯德菌A1的白细胞毒素基因和大肠杆菌α-溶血素基因可能起源于一个共同的祖先,并且这两种毒素可能具有相似的活性或功能结构域,或者两者兼具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc34/260644/343f7b6fdda7/iai00093-0050-a.jpg

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