Alvaro G, Fernandez-Lafuente R, Blanco R M, Guisán J M
Instituto de Catálisis, C.S.I.C. Serrano, Madrid, Spain.
Enzyme Microb Technol. 1991 Mar;13(3):210-4. doi: 10.1016/0141-0229(91)90130-3.
We have found that penicillin G sulfoxide (pen G SO) behaves as a general stabilizing agent of two bacterial penicillin G acylases (PGAs) from E. coli and from K. citrophila), and this role is related to a strong inhibitory effect on the enzymes. The stabilizing effect has been observed during two different inactivation processes: (i) thermal inactivation of soluble enzymes at alkaline pH, and (ii) inactivation of immobilized enzymes as a consequence of covalent multiinteraction with highly activated agarose aldehyde gels. At the same time, pen G SO behaves as a strong competitive inhibitor of these two enzymes. The inhibition constant is more than 10-fold lower than the one corresponding to another smaller competitive inhibitor, phenylacetic acid (PAA), the structure of which is exactly the acyl donor moiety corresponding to pen G SO. In turn, PAA hardly exerts any stabilizing effect on PGAs. The stabilizing effect of pen G SO allowed the preparation of derivatives of these PGAs preserving full catalytic activity in spite of being 1,400- and 650-fold more stable than the corresponding soluble or one-point attached immobilized enzymes.
我们发现青霉素G亚砜(pen G SO)可作为来自大肠杆菌和嗜柠檬酸克雷伯菌的两种细菌青霉素G酰基转移酶(PGA)的通用稳定剂,并且该作用与对这些酶的强烈抑制作用有关。在两种不同的失活过程中均观察到了这种稳定作用:(i)碱性pH条件下可溶性酶的热失活,以及(ii)由于与高活性琼脂糖醛凝胶的共价多相互作用导致的固定化酶失活。同时,pen G SO是这两种酶的强竞争性抑制剂。其抑制常数比另一种较小的竞争性抑制剂苯乙酸(PAA)的抑制常数低10倍以上,而PAA的结构恰好是与pen G SO对应的酰基供体部分。反过来,PAA对PGA几乎没有任何稳定作用。pen G SO的稳定作用使得这些PGA的衍生物得以制备,尽管其稳定性比相应的可溶性或单点固定化酶高1400倍和650倍,但仍保留了全部催化活性。