微粒体
唾液酸转移酶
生物化学
酶
转移酶
化学
增溶
糖基转移酶
作者
Hélène Bador,Renée Morelis,Pierre Louisot
出处
期刊:International Journal of Biochemistry
[Elsevier]
日期:1983-01-01
卷期号:15 (3): 343-347
被引量:4
标识
DOI:10.1016/0020-711x(83)90102-7
摘要
1. Mouse liver microsomal sialyltransferase is strongly inhibited by 1-palmitoyl-sn-glyccro-3-phosphoryleholine. 2. The inhibiting ability is approximately the same whatever the enzyme form may be, microsomal or solubilized. 3. The microsomal enzyme requires neither Mn2+ ions nor exogenous glycoproteinic acceptor for maximal catalytic activity. 4. The lysophospholipid acts as a non-competitive or a mixed-type inhibitor whether the enzyme is respectively microsomal or solubilized. 5. The lysophospholipid and the colchicine prove additive effects in inhibiting the microsomal sialyl-transferase.
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