Lujan H D, Nash T E
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892.
J Eukaryot Microbiol. 1994 Mar-Apr;41(2):169-75. doi: 10.1111/j.1550-7408.1994.tb01491.x.
The cysteine, cystine, methionine and sulfate uptake and cysteine metabolism of Giardia lamblia was studied. Initial experiments indicated that bathocuproine sulphonate (20 microM) added to Keister's modified TYI-S-33 medium supported the growth of G. lamblia at low L-cysteine concentration. This allowed the use of high specific activity radiolabeled L-cysteine for further studies. The analyses of L-cysteine uptake by G. lamblia indicate the presence of at least two different transport systems. The total cysteine uptake was non saturable, with a capacity of 3.7 pmoles per 10(6) cells per min per microM of cysteine, and probably represent passive diffusion. However, cysteine transport was partially inhibited by L-methionine, D-cysteine and DL-homocysteine, indicating that another system specific for SH-containing amino acids is also present. Cysteine uptake was markedly decreased in medium without serum. In contrast to cysteine, the uptake of L-methionine and sulfate were carried out by saturable systems with apparent Km of 71 and 72 microM, respectively, but the Vmax of the uptake of sulfate was six orders of magnitude lower than the Vmax of methionine uptake. Cystine was not incorporated into trophozoites. [35S]-labeled L-cysteine and L-methionine, but not [35S]sulfate, were incorporated into Giardia proteins, indicating that the parasite lacks the capacity to synthesize cysteine or methionine from sulfate. Neither cystathionine gamma lyase nor cystathionine gamma synthase activities was detected in homogenates of Giardia lamblia, suggesting that the transsulfuration pathway is not active and there is no conversion of methionine to cysteine.(ABSTRACT TRUNCATED AT 250 WORDS)
对蓝氏贾第鞭毛虫的半胱氨酸、胱氨酸、蛋氨酸和硫酸盐摄取以及半胱氨酸代谢进行了研究。初步实验表明,添加到基斯特改良TYI-S-33培养基中的磺酸浴铜灵(20微摩尔)在低L-半胱氨酸浓度下支持蓝氏贾第鞭毛虫的生长。这使得能够使用高比活度放射性标记的L-半胱氨酸进行进一步研究。对蓝氏贾第鞭毛虫摄取L-半胱氨酸的分析表明存在至少两种不同的转运系统。总半胱氨酸摄取是非饱和的,每微摩尔半胱氨酸每分钟每10^6个细胞的摄取量为3.7皮摩尔,可能代表被动扩散。然而,L-蛋氨酸、D-半胱氨酸和DL-高半胱氨酸可部分抑制半胱氨酸转运,表明还存在另一种对含巯基氨基酸特异的系统。在无血清培养基中半胱氨酸摄取明显减少。与半胱氨酸不同,L-蛋氨酸和硫酸盐的摄取是通过可饱和系统进行的,其表观Km分别为71和72微摩尔,但硫酸盐摄取的Vmax比蛋氨酸摄取的Vmax低六个数量级。胱氨酸未掺入滋养体中。[35S]标记的L-半胱氨酸和L-蛋氨酸,但不是[35S]硫酸盐,被掺入蓝氏贾第鞭毛虫蛋白质中,表明该寄生虫缺乏从硫酸盐合成半胱氨酸或蛋氨酸的能力。在蓝氏贾第鞭毛虫匀浆中未检测到胱硫醚γ-裂解酶或胱硫醚γ-合酶活性,提示转硫途径不活跃,蛋氨酸不能转化为半胱氨酸。(摘要截短于250字)