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Iodometric Assay Method for Beta-Lactamase with Various Beta-Lactam Antibiotics as Substrates

机译:以各种β-内酰胺类抗生素为底物的β-内酰胺酶的碘量法

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摘要

The rapid fixed-time assay for penicillinase was modified for measuring β-lactamase activity with twelve substrates, i.e., benzylpenicillin, ampicillin, cloxacillin, methicillin, carbenicillin, cefazolin, cephalothin, cephaloglycin, cephalexin, cephalosporin C, 7-aminocephalosporanic acid, and cefoxitin. The method depends upon the reduction of iodine by the hydrolyzed substrate. Determined experimentally, 1 mol of hydrolyzed penicillins consumed 3.4 to 4.0 mol of iodine (I2). Iodine consumption of hydrolyzed cephalosporins varied widely from 1.7 for cephalothin to 3.7 for cefazolin. The method is useful for routine assay of β-lactamase activity with various substrates.
机译:修改了用于青霉素酶的快速固定时间测定法,以测量具有十二种底物的β-内酰胺酶活性,即苄青霉素,氨苄青霉素,氯西林,甲氧西林,羧苄青霉素,头孢唑林,头孢菌素,头孢甘油,头孢氨苄,头孢菌素C,7-氨基头孢菌素酸。该方法取决于水解底物对碘的还原作用。通过实验确定,1摩尔的水解青霉素消耗了3.4到4.0摩尔的碘(I2)。水解头孢菌素的碘消耗量从头孢菌素的1.7到头孢唑林的3.7很大。该方法可用于各种底物的β-内酰胺酶活性的常规测定。

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