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通过辐射诱导聚合固定耻垢分枝杆菌脂肪酸合成酶

Immobilization of fatty acid synthetase from Mycobacterium smegmatis by radiation-induced polymerization.

作者信息

Kikuchi S, Kolattukudy P E

机构信息

Department of Chemical Engineering, Muroran Institute of Technology, Hokkaido, Japan.

出版信息

Agric Biol Chem. 1990 Jun;54(6):1411-6.

PMID:1368562
Abstract

Fatty acid synthetase of Type I from Mycobacterium smegmatis was immobilized by radiation-induced polymerization of 2-hydroxyethyl methacrylate (HEMA) in the presence of trimethylolpropane trimethacrylate (TMPTMA). The stability of immobilized synthetase toward low ionic strength increased in comparison with the free form, but the stabilities of immobilized preparations assessed by pH and temperature were identical to those of the free form. The apparent Km of immobilized enzyme for acetyl-CoA and malonyl-CoA were both 6 microM, essentially the same as those of the free form; acetyl-CoA, 5 microM and malonyl-CoA, 6 microM.

摘要

耻垢分枝杆菌I型脂肪酸合成酶通过在三羟甲基丙烷三甲基丙烯酸酯(TMPTMA)存在下对甲基丙烯酸2-羟乙酯(HEMA)进行辐射诱导聚合来固定化。与游离形式相比,固定化合成酶对低离子强度的稳定性有所提高,但通过pH和温度评估的固定化制剂的稳定性与游离形式相同。固定化酶对乙酰辅酶A和丙二酰辅酶A的表观Km均为6微摩尔,与游离形式基本相同;乙酰辅酶A为5微摩尔,丙二酰辅酶A为6微摩尔。

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