Speed R R, Winkler H H
Department of Microbiology and Immunology, University of South Alabama College of Medicine, Mobile 36688.
J Bacteriol. 1991 Mar;173(5):1704-10. doi: 10.1128/jb.173.5.1704-1710.1991.
The pathway for the acquisition of thymidylate in the obligate bacterial parasite Rickettsia prowazekii was determined. R. prowazekii growing in host cells with or without thymidine kinase failed to incorporate into its DNA the [3H]thymidine added to the culture. In the thymidine kinase-negative host cells, the label available to the rickettsiae in the host cell cytoplasm would have been thymidine, and in the thymidine kinase-positive host cells, it would have been both thymidine and TMP. Further support for the inability to utilize thymidine was the lack of thymidine kinase activity in extracts of R. prowazekii. However, [3H]uridine incorporation into the DNA of R. prowazekii was demonstrable (973 +/- 57 dpm/3 x 10(8) rickettsiae). This labeling of rickettsial DNA suggests the transport of uracil, uridine, uridine phosphates (UXP), or 2'-deoxyuridine phosphates, the conversion of the labeled precursor to thymidylate, and subsequent incorporation into DNA. This is supported by the demonstration of thymidylate synthase activity in extracts of R. prowazekii. The enzyme was determined to have a specific activity of 310 +/- 40 pmol/min/mg of protein and was inhibited greater than or equal to 70% by 5-fluoro-dUMP. The inability of R. prowazekii to utilize uracil was suggested by undetectable uracil phosphoribosyltransferase activity and by its inability to grow (less than 10% of control) in a uridine-starved mutant cell line (Urd-A) supplemented with 50 microM to 1 mM uracil. In contrast, the rickettsiae were able to grow in Urd-A cells that were uridine starved and supplemented with 20 microM uridine (117% of control). However, no measurable uridine kinase activity could be measured in extracts of R. prowazekii. Normal rickettsial growth (92% of control) was observed when the host cell was blocked with thymidine so that the host cell's dUXP pool was depressed to a level inadequate for growth and DNA synthesis in the host cell. Taken together, these data strongly suggest that rickettsiae transport UXP from the host cell's cytoplasm and that they synthesize TTP from UXP.
确定了专性细菌寄生虫普氏立克次体获取胸苷酸的途径。在有或没有胸苷激酶的宿主细胞中生长的普氏立克次体,均未能将添加到培养物中的[³H]胸苷掺入其DNA中。在胸苷激酶阴性的宿主细胞中,立克次体在宿主细胞胞质中可利用的标记物应为胸苷;而在胸苷激酶阳性的宿主细胞中,应为胸苷和TMP。普氏立克次体提取物中缺乏胸苷激酶活性,这进一步支持了其无法利用胸苷的观点。然而,[³H]尿苷掺入普氏立克次体DNA的现象是可证实的(973±57 dpm/3×10⁸立克次体)。立克次体DNA的这种标记表明尿嘧啶、尿苷、尿苷磷酸(UXP)或2'-脱氧尿苷磷酸被转运,标记前体转化为胸苷酸,随后掺入DNA。普氏立克次体提取物中胸苷酸合酶活性的证实支持了这一点。该酶的比活性测定为310±40 pmol/分钟/毫克蛋白质,并且被5-氟-dUMP抑制≥70%。未检测到尿嘧啶磷酸核糖基转移酶活性以及普氏立克次体在补充有50 μM至1 mM尿嘧啶的尿苷饥饿突变细胞系(Urd-A)中无法生长(小于对照的10%),提示其无法利用尿嘧啶。相反,立克次体能够在尿苷饥饿且补充有20 μM尿苷的Urd-A细胞中生长(为对照的117%)。然而,在普氏立克次体提取物中未检测到可测量的尿苷激酶活性。当宿主细胞用胸苷阻断,使宿主细胞的dUXP池降低到不足以支持宿主细胞生长和DNA合成的水平时,观察到立克次体正常生长(为对照的92%)。综上所述,这些数据强烈表明立克次体从宿主细胞胞质中转运UXP,并从UXP合成TTP。