Aldritt S M, Tien P, Wang C C
J Exp Med. 1985 Mar 1;161(3):437-45. doi: 10.1084/jem.161.3.437.
We have found that the anaerobic protozoan parasite Giardia lamblia is incapable of de novo pyrimidine metabolism, as shown by its inability to incorporate orotate, bicarbonate, and aspartate into the pyrimidine nucleotide pool. Results from high performance liquid chromatography of pyrimidine and pyrimidine nucleoside pulse-labeled nucleotide pools and enzyme assays suggest that the parasite satisfies its pyrimidine nucleotide needs predominantly through salvage of uracil by a cytoplasmic uracil phosphoribosyltransferase. Exogenous uridine and cytidine are primarily converted to uracil by the action of uridine hydrolase and cytidine deaminase before incorporation into nucleotide pools. Direct salvage of cytosine occurs to a relatively limited extent via cytosine phosphoribosyltransferase. G. lamblia relies on salvage of exogenous thymidine for ribosylthymine monophosphate (TMP) synthesis, accomplished primarily through the action of a 100,000 g-pelletable thymidine phosphotransferase.
我们发现,厌氧原生动物寄生虫蓝氏贾第鞭毛虫无法进行从头嘧啶代谢,这表现为它无法将乳清酸、碳酸氢盐和天冬氨酸掺入嘧啶核苷酸库。嘧啶和嘧啶核苷脉冲标记核苷酸库的高效液相色谱分析结果以及酶分析表明,该寄生虫主要通过细胞质尿嘧啶磷酸核糖基转移酶对尿嘧啶的补救合成来满足其嘧啶核苷酸需求。外源尿苷和胞苷在掺入核苷酸库之前,主要通过尿苷水解酶和胞苷脱氨酶的作用转化为尿嘧啶。胞嘧啶通过胞嘧啶磷酸核糖基转移酶进行的直接补救合成程度相对有限。蓝氏贾第鞭毛虫依靠外源胸苷的补救合成来合成单磷酸核糖胸腺嘧啶(TMP),这主要通过一种可在100,000 g离心力下沉降的胸苷磷酸转移酶来完成。