Schwartzman J D, Pfefferkorn E R
J Parasitol. 1981 Apr;67(2):150-8.
Pyrimidine biosynthesis was studied in actively dividing, intracellular Toxoplasma gondii, in mutant Chinese hamster ovary cells blocked in pyrimidine biosynthesis to eliminate any contribution by the host cell. The parasite grew normally in these cells even though pyrimidines were not supplied in the medium. Uninfected, mutant cultures showed negligible pyrimidine synthesis. However, mutant cultures infected wit T. gondii efficiently incorporated 14C from glucose or aspartic acid into the pyrimidine bases of nucleic acids. Thus T. gondii is capable of de novo pyrimidine biosynthesis. The parasite may also be able to use pyrimidines of the host cell, because of pyrazofurin, an antimetabolite that blocks pyrimidine biosynthesis, markedly inhibited only a mutant parasite defective in the salvage of pyrimidines.
在活跃分裂的细胞内型弓形虫中研究嘧啶生物合成,所用的是在嘧啶生物合成中受阻的中国仓鼠卵巢突变细胞,以消除宿主细胞的任何贡献。即使培养基中不供应嘧啶,该寄生虫仍能在这些细胞中正常生长。未感染的突变培养物显示嘧啶合成可忽略不计。然而,感染了弓形虫的突变培养物能有效地将葡萄糖或天冬氨酸中的14C掺入核酸的嘧啶碱基中。因此,弓形虫能够从头合成嘧啶。由于吡唑呋林(一种阻断嘧啶生物合成的抗代谢物)仅显著抑制嘧啶补救途径有缺陷的突变寄生虫,所以该寄生虫可能也能够利用宿主细胞的嘧啶。