Arisawa M, Then R
Biochem J. 1983 Mar 1;209(3):609-15. doi: 10.1042/bj2090609.
6-Acetylmethylenepenicillanic acid is a new kinetically irreversible inhibitor of various beta-lactamases. Interaction between 6-acetylmethylenepenicillanate and purified TEM-1 beta-lactamase during the inactivation process was investigated. 6-Acetylmethylenepenicillanate inhibited the enzyme in a second-order fashion with a rate constant of 0.61 microM-1 . S-1. The apparent inactivation constant decreased in the presence of increasing concentrations of the substrate benzylpenicillin. Native enzyme (pI 5.4) was converted into two inactive forms with pI 5.25 and 5.15, the latter form being transient and readily converted into the more stable form with pI 5.15. Even a 50-fold excess of inhibitor over enzyme did not produce any other inactivated species of the enzyme. All the results obtained suggest that 6-acetylmethylenepenicillanate is a potent irreversible and active-site-directed inhibitor of TEM-1 beta-lactamase.
6-乙酰亚甲基青霉烷酸是多种β-内酰胺酶的新型动力学不可逆抑制剂。研究了6-乙酰亚甲基青霉烷酸酯与纯化的TEM-1β-内酰胺酶在失活过程中的相互作用。6-乙酰亚甲基青霉烷酸酯以二级反应方式抑制该酶,速率常数为0.61 μM⁻¹·s⁻¹。在底物苄青霉素浓度增加时,表观失活常数降低。天然酶(pI 5.4)转变为两种失活形式,pI分别为5.25和5.15,后一种形式是短暂的,很容易转变为更稳定的pI 5.15形式。即使抑制剂相对于酶过量50倍,也不会产生该酶的任何其他失活形式。所有获得的结果表明,6-乙酰亚甲基青霉烷酸酯是TEM-1β-内酰胺酶的一种有效的不可逆且作用于活性位点的抑制剂。