Ross P, O'Gara F, Condon S
Department of Food Microbiology, University College, Cork, Ireland.
Appl Environ Microbiol. 1990 Jul;56(7):2164-9. doi: 10.1128/aem.56.7.2164-2169.1990.
The potential of the thymidylate synthase thyA gene cloned from Lactococcus lactis subsp. lactis as a possible alternative selectable marker gene to antibiotic resistance markers has been examined. The thyA mutation is a recessive lethal one; thyA mutants cannot survive in environments containing low amounts of thymidine or thymine (such as Luria-Bertani medium) unless complemented by the thyA gene. The cloned thyA gene was strongly expressed in L. lactis subsp. lactis, Escherichia coli, Rhizobium meliloti, and a fluorescent Pseudomonas strain. In addition, when fused to a promoterless enteric lac operon, the thyA gene drove expression of the lac genes in a number of gram-negative bacteria. In transformation experiments with thyA mutants of E. coli and conjugation experiments with thyA mutants of R. meliloti, the lactococcal thyA gene permitted selection of transformants and transconjugants with the same efficiency as did genes for resistance to ampicillin, chloramphenicol, or tetracycline. Starting from the broad-host-range plasmid pGD500, a plasmid, designated pPR602, was constructed which is completely free of antibiotic resistance genes and has the lactococcal thyA gene fused to a promoterless lac operon. This plasmid will permit growth of thyA mutant strains in the absence of thymidine or thymine and has a number of unique restriction sites which can be used for cloning.
已对从乳酸乳球菌乳酸亚种克隆的胸苷酸合成酶thyA基因作为抗生素抗性标记物的可能替代选择标记基因的潜力进行了研究。thyA突变是一种隐性致死突变;thyA突变体在含有少量胸苷或胸腺嘧啶的环境(如Luria-Bertani培养基)中无法存活,除非由thyA基因进行互补。克隆的thyA基因在乳酸乳球菌乳酸亚种、大肠杆菌、苜蓿根瘤菌和荧光假单胞菌菌株中强烈表达。此外,当与无启动子的肠道乳糖操纵子融合时,thyA基因驱动了许多革兰氏阴性细菌中乳糖基因的表达。在大肠杆菌thyA突变体的转化实验和苜蓿根瘤菌thyA突变体的接合实验中,乳球菌thyA基因允许以与氨苄青霉素、氯霉素或四环素抗性基因相同的效率选择转化体和转接合子。从广宿主范围质粒pGD500出发,构建了一个名为pPR602的质粒,该质粒完全不含抗生素抗性基因,并且乳球菌thyA基因与无启动子的乳糖操纵子融合。该质粒将允许thyA突变菌株在无胸苷或胸腺嘧啶的情况下生长,并且具有许多可用于克隆的独特限制性酶切位点。