Hoogenraad N J, Weston H J, Mackenzie N
J Inherit Metab Dis. 1986;9(4):367-73. doi: 10.1007/BF01800486.
A partial carbamylphosphate synthetase (CPS: EC 6.3.4.16) deficiency (McKusick 23730) was found in a male child who presented with generalized convulsions, rickets and apnoeic attacks at six months of age. By his second year he showed serious developmental delay and a gut biopsy revealed an absence of CPS activity with an elevated ornithine transcarbamylase activity. Analysis of the gut biopsy sample on SDS-polyacrylamide gels, followed by electrophoretic transfer to a nitrocellulose filter probed with monospecific antibodies to CPS showed that the child had normal levels of immunoreactive enzyme, but instead of one band corresponding to normal CPS with a subunit size of 165,000 u, the patient had three immunoreactive bands, one larger and two smaller than that found in normal controls. The genetic defect in this child therefore results in an unusual form of CPS being made which has markedly reduced enzyme activity.
在一名男童中发现了部分氨甲酰磷酸合成酶(CPS:EC 6.3.4.16)缺乏症(麦库西克23730),该男童在6个月大时出现全身性惊厥、佝偻病和呼吸暂停发作。到他两岁时,出现严重发育迟缓,肠道活检显示缺乏CPS活性,而鸟氨酸转氨甲酰酶活性升高。对肠道活检样本进行SDS-聚丙烯酰胺凝胶分析,然后电泳转移至用CPS单特异性抗体探测的硝酸纤维素滤膜上,结果显示该患儿免疫反应性酶水平正常,但与正常CPS对应的一条亚基大小为165,000 u的条带不同,该患者有三条免疫反应性条带,一条比正常对照中的大,两条比正常对照中的小。因此,该患儿的基因缺陷导致产生了一种酶活性明显降低的异常形式的CPS。