Kiener P A, Knott-Hunziker V, Petursson S, Waley S G
Eur J Biochem. 1980 Aug;109(2):575-80. doi: 10.1111/j.1432-1033.1980.tb04830.x.
beta-Lactamase I (from Bacillus cereus 569/H) is inactivated by certain substrates (e.g. methicillin or cloxacillin) but not by others (e.g. benzylpenicillin). Emzyme that had been inactivated was found to be labelled stoichiometrically, as shown by the use of radioactive methicillin. Use of the penamaldate reaction showed the presence of a penicilloyl group in the enzyme inactivated by either methicillin or cloxacillin. In conditions under which enzymic activity was regained the penicilloyl group was shed. When the activity of beta-lactamase I was measured in 0.3-1.2 M guanidinium chloride the rates of hydrolysis of methicillin or cloxacillin (but not benzylpenicillin) were greatly reduced. The unliganded enzyme was stable. The results are explained by supposing that a normal intermediate, the acyl enzyme, is prone to unfold.
β-内酰胺酶I(来自蜡样芽孢杆菌569/H)可被某些底物(如甲氧西林或氯唑西林)灭活,但不能被其他底物(如苄青霉素)灭活。已发现被灭活的酶按化学计量进行标记,这通过使用放射性甲氧西林得以证明。青霉素醛酸反应表明,被甲氧西林或氯唑西林灭活的酶中存在青霉素酰基。在酶活性恢复的条件下,青霉素酰基脱落。当在0.3 - 1.2 M氯化胍中测量β-内酰胺酶I的活性时,甲氧西林或氯唑西林(但不是苄青霉素)的水解速率大大降低。未结合配体的酶是稳定的。这些结果通过假设一种正常中间体——酰基酶易于展开来解释。