Duncan M J, Hillman J D
Department of Molecular Genetics, Forsyth Dental Center, Boston, Massachusetts 02115.
Infect Immun. 1991 Nov;59(11):3930-4. doi: 10.1128/iai.59.11.3930-3934.1991.
Previously, the fructose-1,6-diphosphate-dependent L-(+)-lactate dehydrogenase gene of Streptococcus mutans JH1000 was cloned into Escherichia coli (J. D. Hillman, M. J. Duncan, and K. P. Stashenko, Infect. Immun. 58:1290-1295, 1990). In the present study, the nucleotide sequence of 1.29 kb of S. mutans DNA which contained the promoter and protein-coding region of the gene was determined. In vitro disruption of the gene was achieved by deletion of the promoter and a major portion of the protein-coding sequence. Subsequently, a tetracycline resistance gene from S. mutans was inserted at the deletion site as a marker for selection. In addition, evidence from Southern hybridization showed that S. mutans JH1000 contained a single copy of the lactate dehydrogenase gene.
先前,变形链球菌JH1000的果糖-1,6-二磷酸依赖性L-(+)-乳酸脱氢酶基因已被克隆到大肠杆菌中(J. D. 希尔曼、M. J. 邓肯和K. P. 斯塔申科,《感染与免疫》58:1290 - 1295,1990)。在本研究中,测定了包含该基因启动子和蛋白质编码区的1.29 kb变形链球菌DNA的核苷酸序列。通过缺失启动子和大部分蛋白质编码序列实现了该基因的体外破坏。随后,将来自变形链球菌的四环素抗性基因插入缺失位点作为选择标记。此外,Southern杂交的证据表明变形链球菌JH1000含有乳酸脱氢酶基因的单拷贝。