Stauffer C E, Sullivan J F
Procter and Gamble Company, Miami Valley Laboratories, Cincinnati, Ohio 45239, USA.
Biochim Biophys Acta. 1971 Dec 28;251(3):407-12. doi: 10.1016/0005-2795(71)90129-2.
As shown by viscosity and optical rotation dispersion measurements, subtilisin Carlsberg is not denatured in the presence of 10 M urea or 6 M guanidinium chloride. This unusual structural stability made it possible to investigate the effects of these hydrophobic-bond breaking solutes on various aspects of the enzymic interaction with substrates and inhibitors. The binding of the competitive inhibitor N-benzoylarginine was decreased by urea or guanidinium chloride. The nature of this effect was such as to implicate hydrophobic interaction as making a major contribution to the binding. By contrast, Ks for the substrates N-acetyltyrosine ethyl ester, N-benzoylarginine ethyl ester and N-trans-cinnamoylimidazole was apparently unchanged by the presence of urea or guanidinium chloride. The influence of these solutes on kcat for the substrates was rather involved. Tentative hypotheses are put forward to account for the effects seen.
如粘度和旋光色散测量所示,在10 M尿素或6 M氯化胍存在的情况下,嗜热栖热菌蛋白酶不会变性。这种不同寻常的结构稳定性使得研究这些破坏疏水键的溶质对酶与底物及抑制剂相互作用的各个方面的影响成为可能。竞争性抑制剂N-苯甲酰精氨酸的结合会因尿素或氯化胍而减少。这种效应的性质表明疏水相互作用对结合起主要作用。相比之下,尿素或氯化胍的存在对底物N-乙酰酪氨酸乙酯、N-苯甲酰精氨酸乙酯和N-反式肉桂酰咪唑的Ks显然没有影响。这些溶质对底物的kcat的影响相当复杂。文中提出了一些初步假说来解释所观察到的效应。