Galante D, Esposito S, Barba D, Scioli C
Boll Soc Ital Biol Sper. 1983 Nov 30;59(11):1678-82.
54 beta-lactamase producing E. coli were tested to observe their eventual capacity to transfer beta-lactamase production by conjugation to a receiving E. coli K12 C600 Na-. About 16% (9/54) of these strains transferred beta-lactamase producing capacity. MICs of five beta-lactam antibiotics (Ampicillin, Cephaloridine, Cephalexine, Cefuroxime, Cefotaxime) were performed against E. coli donors and E. coli K12 C600 transconjugates. It was observed a remarkable increase only of Ampicillin MICs against all transconjugates++. Beta-lactamases produced by donors and transconjugants were isolated and purified by sonication and high speed centrifugation. Sensitivity of the six antibiotics to these purified beta-lactamases was assessed by a spectrophotometric method that utilizes the velocity of cytochrome c reduction. beta-lactamases produced by transconjugants have identical substrate profile that beta-lactamases produced by donors.
对54株产β-内酰胺酶的大肠杆菌进行测试,以观察它们最终通过接合将β-内酰胺酶产生能力转移至受体大肠杆菌K12 C600 Na-的能力。这些菌株中约16%(9/54)转移了β-内酰胺酶产生能力。针对大肠杆菌供体和大肠杆菌K12 C600转接合子测定了五种β-内酰胺抗生素(氨苄西林、头孢利定、头孢氨苄、头孢呋辛、头孢噻肟)的最低抑菌浓度(MIC)。仅观察到所有转接合子对氨苄西林的MIC显著增加++。通过超声处理和高速离心分离并纯化供体和转接合子产生的β-内酰胺酶。利用细胞色素c还原速度的分光光度法评估六种抗生素对这些纯化的β-内酰胺酶的敏感性。转接合子产生的β-内酰胺酶与供体产生的β-内酰胺酶具有相同的底物谱。