Rashtchian A, Nouravarsani R, Miller G R, Gerlach E H
Antimicrob Agents Chemother. 1979 Dec;16(6):772-5. doi: 10.1128/AAC.16.6.772.
A simple biological assay to detect beta-lactamase activity exhibited by selected cultures of Escherichia coli was used to test enzyme production in cells incubated aerobically and anerobically. Anaerobic incubation resulted in increased size of zones of drug inactivation by some beta-lactamase-producing strains. The beta-lactamase activity of cell lysates was determined iodometrically for aerobically and anaerobically grown cells. The specific beta-lactamase activity for anaerobically grown cells was three to five times greater than for aerobically grown cells. Beta-lactamase production was determined to be constitutive in all strains and to be plasmid mediated, as demonstrated by transfer to E. coli K-12 by conjugation.
一种用于检测大肠杆菌特定培养物所表现出的β-内酰胺酶活性的简单生物学测定法,被用于测试在需氧和厌氧条件下培养的细胞中的酶产生情况。厌氧培养导致一些产生β-内酰胺酶的菌株使药物失活的区域增大。通过碘量法测定需氧和厌氧生长细胞的细胞裂解物的β-内酰胺酶活性。厌氧生长细胞的比β-内酰胺酶活性比需氧生长细胞高3至5倍。已确定β-内酰胺酶的产生在所有菌株中都是组成型的,并且是由质粒介导的,如通过接合转移到大肠杆菌K-12所证明的那样。