Jeffrey W H, Paul J H
Department of Marine Science, University of South Florida, St. Petersburg 33701.
Appl Environ Microbiol. 1990 May;56(5):1367-72. doi: 10.1128/aem.56.5.1367-1372.1990.
One assumption made in bacterial production estimates from [3H]thymidine incorporation is that all heterotrophic bacteria can incorporate exogenous thymidine into DNA. Heterotrophic marine bacterium isolates from Tampa Bay, Fla., Chesapeake Bay, Md., and a coral surface microlayer were examined for thymidine uptake (transport), thymidine incorporation, the presence of thymidine kinase genes, and thymidine kinase enzyme activity. Of the 41 isolates tested, 37 were capable of thymidine incorporation into DNA. The four organisms that could not incorporate thymidine also transported thymidine poorly and lacked thymidine kinase activity. Attempts to detect thymidine kinase genes in the marine isolates by molecular probing with gene probes made from Escherichia coli and herpes simplex virus thymidine kinase genes proved unsuccessful. To determine if the inability to incorporate thymidine was due to the lack of thymidine kinase, one organism, Vibrio sp. strain D19, was transformed with a plasmid (pGQ3) that contained an E. coli thymidine kinase gene. Although enzyme assays indicated high levels of thymidine kinase activity in transformants, these cells still failed to incorporate exogenous thymidine into DNA or to transport thymidine into the cells. These results indicate that the inability of certain marine bacteria to incorporate thymidine may not be solely due to the lack of thymidine kinase activity but may also be due to the absence of thymidine transport systems.
通过[3H]胸苷掺入量来估算细菌产量时所做的一个假设是,所有异养细菌都能将外源胸苷掺入DNA中。对从佛罗里达州坦帕湾、马里兰州切萨皮克湾以及一个珊瑚表面微层分离出的异养海洋细菌进行了胸苷摄取(转运)、胸苷掺入、胸苷激酶基因的存在情况以及胸苷激酶酶活性的检测。在测试的41株分离菌中,有37株能够将胸苷掺入DNA。那4株不能掺入胸苷的菌株胸苷转运能力也很差,并且缺乏胸苷激酶活性。用由大肠杆菌和单纯疱疹病毒胸苷激酶基因制成的基因探针进行分子探测,试图在海洋分离菌中检测胸苷激酶基因,但未成功。为了确定不能掺入胸苷是否是由于缺乏胸苷激酶,用含有大肠杆菌胸苷激酶基因的质粒(pGQ3)转化了一株细菌,即弧菌属D19菌株。尽管酶分析表明转化体中胸苷激酶活性水平很高,但这些细胞仍然无法将外源胸苷掺入DNA或把胸苷转运到细胞内。这些结果表明,某些海洋细菌不能掺入胸苷可能不仅仅是由于缺乏胸苷激酶活性,还可能是由于缺乏胸苷转运系统。