Goldberg S L, Murphy J R
J Bacteriol. 1984 Oct;160(1):239-44. doi: 10.1128/jb.160.1.239-244.1984.
Vibrio cholerae El Tor RV79 is phenotypically nonhemolytic; however, strongly hemolytic convertants are occasionally observed on blood agar plates. We have cloned DNA sequences corresponding to the hemolysin determinant from RV79 (Hly+) in the lambda L47.1 and pBR322 vectors. A 2.3-kilobase fragment of V. cholerae DNA was found to be necessary for hemolytic activity. This cloned DNA sequence was used as a probe in Southern blot hybridization analysis of chromosomal restriction digests of a variety of El Tor and classical biotype V. cholerae strains. In all cases, DNA fragments with the same electrophoretic mobilities hybridized to the Hly probe. The results presented demonstrate that the cloned hemolysin determinant is the hly locus. By using mutator vibriophage VcA-3 insertion to promote high-frequency transfer, the hly locus was mapped between arg and ilv on the V. cholerae RV79 chromosome.
霍乱弧菌埃尔托生物型RV79在表型上是非溶血的;然而,在血琼脂平板上偶尔会观察到强溶血转化体。我们已在λL47.1和pBR322载体中克隆了与RV79(Hly+)溶血素决定簇相对应的DNA序列。发现霍乱弧菌DNA的一个2.3千碱基片段对溶血活性是必需的。该克隆的DNA序列用作探针,对多种埃尔托生物型和古典生物型霍乱弧菌菌株的染色体限制性消化产物进行Southern印迹杂交分析。在所有情况下,具有相同电泳迁移率的DNA片段都与Hly探针杂交。给出的结果表明,克隆的溶血素决定簇是hly基因座。通过使用诱变噬菌体VcA-3插入来促进高频转移,hly基因座被定位在霍乱弧菌RV79染色体上的arg和ilv之间。