Khan A A, Kim E, Cerniglia C E
Division of Microbiology, Food and Drug Administration, Jefferson, Arkansas 72079, USA.
Appl Environ Microbiol. 1998 Jul;64(7):2473-8. doi: 10.1128/AEM.64.7.2473-2478.1998.
Aeromonas trota AK2, which was derived from ATCC 49659 and produces the extracellular pore-forming hemolytic toxin aerolysin, was mutagenized with the transposon mini-Tn5Km1 to generate a hemolysin-deficient mutant, designated strain AK253. Southern blotting data indicated that an 8.7-kb NotI fragment of the genomic DNA of strain AK253 contained the kanamycin resistance gene of mini-Tn5Km1. The 8.7-kb NotI DNA fragment was cloned into the vector pGEM5Zf(-) by selecting for kanamycin resistance, and the resultant clone, pAK71, showed aerolysin activity in Escherichia coli JM109. The nucleotide sequence of the aerA gene, located on the 1.8-kb ApaI-EcoRI fragment, was determined to consist of 1,479 bp and to have an ATG initiation codon and a TAA termination codon. An in vitro coupled transcription-translation analysis of the 1.8-kb region suggested that the aerA gene codes for a 54-kDa protein, in agreement with nucleotide sequence data. The deduced amino acid sequence of the aerA gene product of A. trota exhibited 99% homology with the amino acid sequence of the aerA product of Aeromonas sobria AB3 and 57% homology with the amino acid sequences of the products of the aerA genes of Aeromonas salmonicida 17-2 and A. sobria 33.
源自ATCC 49659并产生细胞外成孔溶血毒素气溶素的嗜水气单胞菌AK2,用转座子mini-Tn5Km1进行诱变,以产生溶血素缺陷型突变体,命名为AK253菌株。Southern印迹数据表明,AK253菌株基因组DNA的一个8.7kb NotI片段含有mini-Tn5Km1的卡那霉素抗性基因。通过选择卡那霉素抗性,将8.7kb NotI DNA片段克隆到载体pGEM5Zf(-)中,所得克隆pAK71在大肠杆菌JM109中表现出气溶素活性。位于1.8kb ApaI-EcoRI片段上的aerA基因的核苷酸序列被确定为由1479bp组成,具有一个ATG起始密码子和一个TAA终止密码子。对1.8kb区域的体外偶联转录-翻译分析表明,aerA基因编码一种54kDa的蛋白质,这与核苷酸序列数据一致。嗜水气单胞菌aerA基因产物的推导氨基酸序列与温和气单胞菌AB3的aerA产物的氨基酸序列具有99%的同源性,与杀鲑气单胞菌17-2和气单胞菌33的aerA基因产物的氨基酸序列具有57%的同源性。