Bollmeier J P, Middleman S
Biotechnol Bioeng. 1979 Dec;21(12):2303-21. doi: 10.1002/bit.260211210.
Experiments and appropriate mathematical models are presented in an attempt to elucidate and separate the effects of mass transfer and immobilization on the apparent kinetics of hydrolysis of urea by urease immobilized within a crosslinked gelatin film. Diffusion of urea through the gelatin matrix appears to exert the major influence on the observed kinetics. Diffusion coefficients are measured, and a model for the "effectiveness factor" is presented, accounting for this aspect of mass transfer control. A secondary, but significant, influence on apparent kinetics arises because the reaction products lead to an increased pH level which, because of diffusion resistance, remains high within the gelatin matrix. For pH levels in the 6.7 to 9.0 range the activity of urease is a strongly decreasing function of pH. An approximate model accounting for ionic equilibrium allows this pH-diffusion effect to be introduced in such a way as to lead to predictions of the apparent kinetics that are compared with experimental observations. Examination of these results indicates that the immobilization procedure leads to some loss of activity due to an interaction of the gelatin crosslinking reaction with the enzyme itself.
本文通过实验和适当的数学模型,试图阐明并区分传质和固定化对交联明胶膜中固定化脲酶催化尿素水解表观动力学的影响。尿素在明胶基质中的扩散似乎对观测到的动力学起主要作用。测量了扩散系数,并提出了一个“有效因子”模型,以解释传质控制的这一方面。反应产物导致pH值升高,由于扩散阻力,明胶基质内的pH值仍然很高,这对表观动力学产生了次要但显著的影响。在pH值为6.7至9.0的范围内,脲酶的活性是pH值的强烈递减函数。一个考虑离子平衡的近似模型允许以一种方式引入这种pH扩散效应,从而得出与实验观测结果相比较的表观动力学预测。对这些结果的检验表明,由于明胶交联反应与酶本身的相互作用,固定化过程导致了一定的活性损失。