Väljamäe P, Sild V, Pettersson G, Johansson G
Institute of Molecular and Cell Biology, University of Tartu, Estonia.
Eur J Biochem. 1998 Apr 15;253(2):469-75. doi: 10.1046/j.1432-1327.1998.2530469.x.
Introduction of a novel method for the quantification of the cellobiose released made it possible to follow the initial stage of hydrolysis of bacterial microcrystalline cellulose (BMCC) by cellobiohydrolases 1,4-beta-D-glucan-cellobiohydrolase I (CBH I) and 1,4-beta-D-glucan-cellobiohydrolase II (CBH II) from Trichoderma reesei. A drastic retardation of the rate of the hydrolysis was observed already at a very low degree of conversion. Earlier-suggested retardation factors, such as product inhibition by cellobiose or enzyme inactivation, could be discounted as primary causes for the pattern. A model including steric hindrance by non-productive binding and erosion of the cellulose surface during the processive action of exoenzymes was proposed to describe the rate retardation observed. Simultaneous action of CBH I and CBH II on cellulose was not a prerequisite for synergy between them.
一种用于定量释放的纤维二糖的新方法的引入,使得跟踪里氏木霉的纤维二糖水解酶1,4-β-D-葡聚糖-纤维二糖水解酶I(CBH I)和1,4-β-D-葡聚糖-纤维二糖水解酶II(CBH II)对细菌微晶纤维素(BMCC)水解的初始阶段成为可能。在非常低的转化率下就已经观察到水解速率的急剧减慢。早期提出的减慢因素,如纤维二糖的产物抑制或酶失活,可以被排除为这种模式的主要原因。提出了一个模型,该模型包括外切酶的连续作用过程中非生产性结合的空间位阻和纤维素表面的侵蚀,以描述观察到的速率减慢。CBH I和CBH II对纤维素的同时作用不是它们之间协同作用的先决条件。