Ogunkolade B W, Robinson H A, McDonald V, Webster K, Evans D A
Department of Clinical Sciences, London School of Hygiene and Tropical Medicine, UK.
Parasitol Res. 1993;79(5):385-8. doi: 10.1007/BF00931827.
Soluble extracts of the oocysts of Cryptosporidium parvum had demonstrable, but low, activities of malate dehydrogenase (MDH, EC. 1.1.1.37), carboxylesterase (ES, EC 3.1.1.1) and lactate dehydrogenase (LDH, EC. 1.1.1.27) following thin-layer starch-gel electrophoresis. Much higher activities of glucose phosphate isomerase (GPI, EC. 5.3.1.9) and phosphoglucomutase (PGM, EC. 2.7.5.1) were found, and zymograms of these two enzymes were used to characterise isolates of C. parvum from human, bovine, ovine and cervine sources, C. muris from the brown rat and C. baileyi from young turkeys. PGM and GPI zymograms clearly distinguished between C. parvum, C. muris and C. baileyi. The five isolates of C. parvum showed the same electrophoretic mobility for GPI, whereas the PGM mobility of the single human isolate of C. parvum examined was clearly different from that of the other isolates. This is the first report of the use of isoenzymes to distinguish between species and isolates of Cryptosporidium.
经薄层淀粉凝胶电泳后,微小隐孢子虫卵囊的可溶性提取物显示出苹果酸脱氢酶(MDH,EC. 1.1.1.37)、羧酸酯酶(ES,EC 3.1.1.1)和乳酸脱氢酶(LDH,EC. 1.1.1.27)的活性,但其活性较低。葡萄糖磷酸异构酶(GPI,EC. 5.3.1.9)和磷酸葡萄糖变位酶(PGM,EC. 2.7.5.1)的活性则高得多,这两种酶的酶谱被用于鉴定来自人、牛、羊和鹿源的微小隐孢子虫分离株、来自褐家鼠的鼠隐孢子虫以及来自幼火鸡的贝氏隐孢子虫。PGM和GPI酶谱能清楚地区分微小隐孢子虫、鼠隐孢子虫和贝氏隐孢子虫。微小隐孢子虫的五个分离株的GPI电泳迁移率相同,而所检测的单个人源微小隐孢子虫分离株的PGM迁移率与其他分离株明显不同。这是关于使用同工酶区分隐孢子虫物种和分离株的首次报道。