Cooper A, Hatton C, Sardharwalla I B
Willink Biochemical Genetics Unit, Royal Manchester Children's Hospital, Pendlebury, UK.
J Inherit Metab Dis. 1987;10(3):229-33. doi: 10.1007/BF01800067.
Optimum conditions for assay of human plasma beta-mannosidase activity were determined. Maximum activity was observed at pH 3.0-3.4, the apparent Km was 0.9 mmol L-1 and enzymatic hydrolysis was linear for at least 60 min. Assays were performed on plasma from two siblings with the recently described condition beta-mannosidosis and their parents and controls. Both beta-mannosidosis patients showed a marked deficiency of beta-mannosidase activity. Control samples showed no variation between sexes (p greater than 0.05) but enzyme activity varied significantly with age (p less than 0.05). Highest activity was observed in the 0-1 year age group, activity then decreasing to adulthood, Both mother and father of the affected individuals showed reduced activity (34% and 53%, respectively) compared to age-matched controls. This suggests that heterozygote detection in this condition is possible using plasma, provided the variation of activity with age is taken into consideration.
确定了检测人血浆β-甘露糖苷酶活性的最佳条件。在pH 3.0 - 3.4时观察到最大活性,表观Km为0.9 mmol/L,酶促水解至少60分钟呈线性。对两名患有最近描述的β-甘露糖苷贮积症的同胞及其父母和对照的血浆进行了检测。两名β-甘露糖苷贮积症患者均表现出β-甘露糖苷酶活性明显缺乏。对照样本在性别间无差异(p大于0.05),但酶活性随年龄有显著变化(p小于0.05)。在0 - 1岁年龄组观察到最高活性,随后活性降至成年期。与年龄匹配的对照相比,受影响个体的母亲和父亲活性均降低(分别为34%和53%)。这表明,在这种情况下,如果考虑到活性随年龄的变化,利用血浆检测杂合子是可能的。