...
首页> 外文期刊>Journal of bacteriology >Acquisition of thymidylate by the obligate intracytoplasmic bacterium Rickettsia prowazekii.
【24h】

Acquisition of thymidylate by the obligate intracytoplasmic bacterium Rickettsia prowazekii.

机译:专性胞质内立氏立克次体细菌获得胸苷。

获取原文
           

摘要

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.
机译:确定了专性细菌寄生立克次体立克次体中获取胸苷的途径。在有或没有胸苷激酶的宿主细胞中生长的普氏疟原虫不能将添加到培养物中的[3 H]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细胞质中可用的标记是胸苷,而在胸苷激酶阳性的宿主细胞中,则是胸苷和TMP。对于不能利用胸苷的进一步支持是在普氏疟原虫的提取物中缺乏胸苷激酶活性。然而,证实了[3 H]尿苷掺入普氏罗伊氏菌的DNA中(973 +/- 57dpm / 3×10(8)立克次氏体)。立克次体DNA的这种标记表明尿嘧啶,尿苷,尿苷磷酸盐(UXP)或2'-脱氧尿苷磷酸盐的转运,标记的前体向胸苷的转化以及随后掺入DNA。这证明了普氏罗非鱼提取物中的胸苷酸合酶活性。确定该酶具有310 +/- 40 pmol / min / mg蛋白质的比活性,并被5-氟-dUMP抑制大于或等于70%。不可检测的尿嘧啶磷酸核糖基转移酶活性及其在补充了50 microM至1 mM的尿苷饥饿的突变细胞系(Urd-A)中无法生长(少于对照的10%)提示了R. prowazekii无法利用尿嘧啶。尿嘧啶。相反,立克次体能够在缺乏尿苷并补充了20 microM尿苷(对照的117%)的Urd-A细胞中生长。但是,在Prowazekii的提取物中无法测量到可测量的尿苷激酶活性。当宿主细胞被胸腺嘧啶核苷封闭时,观察到正常的立克次氏体生长(对照组的92%),从而使宿主细胞的dUXP库被抑制到不足以在宿主细胞中生长和合成DNA的水平。综上所述,这些数据强烈表明立克次体从宿主细胞的细胞质中转运了UXP,并且它们从UXP合成了TTP。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号