Bertram A U, Gersteuer T, Ohnesorge F K, Delin S
Biochim Biophys Acta. 1975 Feb 19;377(2):297-302. doi: 10.1016/0005-2744(75)90311-3.
Acetylcholinesterase (acetylcholine hydrolase, EC 3.1.1.7) and cholinesterase (acylcholine acylhydrolase, EC 3.1.1.8), respectively, were covalently attached to a cross-linked copolymerisate of maleinic anhydride and butanediol-divinylether. Based on the coupling procedure reported by Brümmer et al. (Brummer, W., Hennrich, N., Klockow, M., Lang, H. and Orth, H.D. (1972) Eur. J. Biochem. 2k, 129--135), a simple method is described which requires only 24 h for completion and provides a sufficient yield. Although a polyanionic carrier was used the Km and k2 values as well as the substrate and pH optima of the bound acetylcholinesterase and bound cholinesterase did not differ considerably from the corresponding values of the free enzymes. Bound acetylcholinesterase and to some extent also bound cholinesterase did not lose any enzymatic activity after storage in saline at 4 degrees C for 140 days.
乙酰胆碱酯酶(乙酰胆碱水解酶,EC 3.1.1.7)和胆碱酯酶(酰基胆碱酰基水解酶,EC 3.1.1.8)分别与马来酸酐和丁二醇 - 二乙烯基醚的交联共聚物共价连接。基于Brümmer等人报道的偶联方法(Brümmer, W., Hennrich, N., Klockow, M., Lang, H. 和 Orth, H.D. (1972) Eur. J. Biochem. 2k, 129 - 135),描述了一种简单的方法,该方法仅需24小时即可完成,且产率足够。尽管使用了聚阴离子载体,但结合的乙酰胆碱酯酶和结合的胆碱酯酶的Km和k2值以及底物和pH最佳值与游离酶的相应值相比没有显著差异。结合的乙酰胆碱酯酶以及在一定程度上结合的胆碱酯酶在4℃盐溶液中储存140天后没有失去任何酶活性。