Coombe R G, George A M
Antimicrob Agents Chemother. 1981 Jul;20(1):75-80. doi: 10.1128/AAC.20.1.75.
The same aminoglycoside 2"-adenylyltransferase was isolated from four gram-negative species which were among a random group of gentamicin-resistant isolates from the same hospital. The enzyme was partially purified from a crude extract which also contained a second modifying enzyme identified as APH(3')-I. The substrate range of the new aminoglycoside 2"-adenylyltransferase included the newer aminoglycosides sisomicin and amikacin, but showed much-reduced activity against gentamicins C2 and Cla. The pH optimum was 7.8 to 8.0 for every substrate, and the molecular weight of the enzyme molecule was estimated at approximately 29,000. Genetic experiments clearly established that both enzymes were expressed by a conjugative plasmid.
从同一医院随机选取的一组庆大霉素耐药菌株中的四种革兰氏阴性菌中分离出了相同的氨基糖苷2”-腺苷酸转移酶。该酶从粗提物中部分纯化得到,粗提物中还含有另一种被鉴定为APH(3')-I的修饰酶。新的氨基糖苷2”-腺苷酸转移酶的底物范围包括较新的氨基糖苷类药物西索米星和阿米卡星,但对庆大霉素C2和Cla的活性大大降低。每种底物的最适pH值为7.8至8.0,酶分子的分子量估计约为29,000。遗传学实验明确证实这两种酶均由接合质粒表达。