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微生物法生产丙烯酰胺的研究(II)——腈水合酶的酶催化动力学及失活动力学

[Study on production of acrylamide by microbial method (II)--enzyme catalytic kinetics and de-active dynamics of nitrile hydratase].

作者信息

Chen Zhi, Sun Xu-Dong, Shi Yue, Shen Zhong-Yao, Zhao Jian-Xun, Sun Xiao-Ying

机构信息

Department of Chemical Engineering, Institute of Biochemical Engineering, Tsinghua University, Beijing 100084, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2002 Jan;18(2):225-30.

Abstract

The hydration reaction by microbial method is the crisis of the procedure of acrylamide production from acrylonitrile. This research studied the enzyme catalytic kinetics and de-active kinetics of nitrile hydratase in the type of free cell. Firstly, the effects of the concentration of cells, the temperature, pH value, the concentration of acrylonitrile and the concentration of acrylamide on the activity of nitrile hydratase was investigated. The result is that the temperature and the concentration of acrylamide are the most important among these factors. The activity of the nitrile hydratase was 5659 u/mL (broth) at 28 degrees C; the counterpart was only 663 u/mL (broth) at 5 degrees C. And the activity of NHase in solution of 45% acrylamide was just about half of that in solution of 5% acrylamide. After study on the relation of temperature and the reaction speed, It was found that the activation energy of the hydration of NHase was 65.57 kJ.mol-1. This paper studied the effects of concentration of cells, temperature, pH value, concentrations of acrylonitrile and acrylamide on the deactivation of Nhase, as well as the related enzyme de-active kinetics. The result also showed that the temperature and the concentration of acrylamide are the most important among these factors. In solution of 35% acrylamide, the residual activity was about 0% of the original value after 55 h; but in solution of 10% acrylamide, after the same period of time, the residual activity was 50% of the original one. It was also found that the concentration of acrylonitrile had little effect on the stability of NHase. The coefficient of deactivation at 28 degrees C was 21.77 times of the one at 5 degrees C. Correlating the temperature and the coefficient of deactivation, the activation energy of the de-active reaction was found to be 92.28 kJ.mol-1.

摘要

微生物法水合反应是丙烯腈生产丙烯酰胺过程中的关键环节。本研究对游离细胞型腈水合酶的酶催化动力学和失活动力学进行了研究。首先,考察了细胞浓度、温度、pH值、丙烯腈浓度和丙烯酰胺浓度对腈水合酶活性的影响。结果表明,温度和丙烯酰胺浓度是这些因素中最重要的。在28℃时,腈水合酶的活性为5659 u/mL(发酵液);在5℃时,相应活性仅为663 u/mL(发酵液)。在45%丙烯酰胺溶液中,NHase的活性约为5%丙烯酰胺溶液中的一半。研究温度与反应速度的关系后发现,NHase水合反应的活化能为65.57 kJ·mol-1。本文研究了细胞浓度、温度、pH值、丙烯腈和丙烯酰胺浓度对Nhase失活的影响以及相关的酶失活动力学。结果还表明,温度和丙烯酰胺浓度是这些因素中最重要的。在35%丙烯酰胺溶液中,55 h后残余活性约为初始值的0%;但在10%丙烯酰胺溶液中,相同时间后,残余活性为初始值的50%。还发现丙烯腈浓度对NHase的稳定性影响较小。28℃时的失活系数是5℃时的21.77倍。将温度与失活系数相关联,发现失活反应的活化能为92.28 kJ·mol-1。

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