Masaki A, Fukamizo T, Otakara A, Torikata T, Hayashi K, Imoto T
J Biochem. 1981 Oct;90(4):1167-75. doi: 10.1093/oxfordjournals.jbchem.a133569.
The rate constants of the cleavage of glycoside linkage, hydration (hydrolysis) and transglycosylation in a lysozyme-catalyzed reaction of substrate chitooligosaccharides were evaluated by computer analysis of the experimentally obtained reaction time-courses. In the computer analysis, the rate equation was numerically solved by use of the known binding constants for each subsite. Because of the complexity of the lysozyme-catalyzed reaction, optimal values of rate constants were determined by checking the sensitivity of each rate constant to the computed time-courses. It was not possible to estimate uniquely the rate constants for transglycosylation and hydration, owing to the nature of the enzymatic reaction, but it was possible to estimate accurately their ratio. The estimated values were 0.94 s-1 for the rate constant for the cleavage of glycosidic linkage and 133 for the ratio of rate constants of transglycosylation and hydration.
通过对实验获得的反应时间进程进行计算机分析,评估了溶菌酶催化底物壳寡糖反应中糖苷键裂解、水合(水解)和转糖基化的速率常数。在计算机分析中,利用每个亚位点的已知结合常数对速率方程进行数值求解。由于溶菌酶催化反应的复杂性,通过检查每个速率常数对计算出的时间进程的敏感性来确定速率常数的最佳值。由于酶促反应的性质,无法唯一估计转糖基化和水合的速率常数,但可以准确估计它们的比值。糖苷键裂解的速率常数估计值为0.94 s-1,转糖基化与水合速率常数的比值为133。