Substituent effect on lysozyme-catalysed hydrolysis of some beta-aryl di-N-acetylchitobiosides.

Substituent effect on lysozyme-catalysed hydrolysis of some beta-aryl di-N-acetylchitobiosides.
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取代基对溶菌酶催化某些 β-芳基二-N-乙酰壳二糖苷水解的影响。

DOI:
10.1042/bj1140529
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发表时间:
1969
期刊:
The Biochemical journal
影响因子:
--
通讯作者:
S. C. Subbarao
S. C. Subbarao
中科院分区:
--
文献类型:
--
作者:
C. Tsai;J. Tang;S. C. Subbarao

文献摘要

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本文报道了溶菌酶催化水解几种β -芳基二n -乙酰壳聚糖的动力学测量,其中一些是首次合成的。45度时的催化速率常数k(cat.)产生了一个弯曲的Hammett图(上凹),delta - tah(双匕首)和delta - tas(双匕首)的图有一个明显的断裂。具有吸电子基团的底物表现出动力学氘同位素效应(k(H) (cat))。/ k (D)(猫)。),而那些有供电子基团的则没有这种同位素效应。结果表明,这两种类型的衬底具有不同的运行机制。
Measurements are reported on the kinetics of the lysozyme-catalysed hydrolysis of several beta-aryl di-N-acetylchitobiosides, some of which have been synthesized for the first time. The catalytic rate constants (k(cat.)) at 45 degrees yield a curved Hammett plot (concave up) and the plot of DeltaH(double dagger) versus DeltaS(double dagger) has a sharp break. Substrates with electron-withdrawing groups exhibit a kinetic deuterium isotope effect (k(H) (cat.)/k(D) (cat.)), whereas those with electron-donating groups show no such isotope effect. The results suggest the operation of different mechanisms for the two types of substrates.