Datta A R, Wentz B A, Russell J
Division of Microbiology, Food and Drug Administration, Washington, D.C. 20204.
Appl Environ Microbiol. 1990 Dec;56(12):3874-7. doi: 10.1128/aem.56.12.3874-3877.1990.
A clone containing 3.1 kb of Listeria DNA was selected from a gene library of Listeria monocytogenes Scott A strain. The Escherichia coli clone produced hemolysin on sheep blood agar and in sonicated extracts but very little in the culture supernatant. This 3.1-kb DNA fragment and a 650-bp HindIII fragment located within the listeriolysin gene were used as probes in a colony hybridization assay. Both probes were specific for L. monocytogenes and did not hybridize with any other Listeria strains at high stringency. Two synthetic probes, one from the 650-bp HindIII fragment and one from the carboxy-terminal region of the protein, were also specific for L. monocytogenes.
从单核细胞增生李斯特菌斯科特A菌株的基因文库中筛选出一个含有3.1 kb李斯特菌DNA的克隆。该大肠杆菌克隆在绵羊血琼脂平板上以及超声提取物中产生溶血素,但在培养上清液中产生的量很少。这个3.1 kb的DNA片段和位于李斯特菌溶血素基因内的一个650 bp的HindIII片段被用作菌落杂交试验的探针。两种探针都对单核细胞增生李斯特菌具有特异性,在高严谨度下不与任何其他李斯特菌菌株杂交。两种合成探针,一种来自650 bp的HindIII片段,另一种来自该蛋白质的羧基末端区域,也对单核细胞增生李斯特菌具有特异性。