Rouch D A, Byrne M E, Kong Y C, Skurray R A
Department of Microbiology, Monash University, Clayton, Victoria, Australia.
J Gen Microbiol. 1987 Nov;133(11):3039-52. doi: 10.1099/00221287-133-11-3039.
The aacA-aphD aminoglycoside resistance determinant of the Staphylococcus aureus transposon Tn4001, which specifies resistance to gentamicin, tobramycin and kanamycin, has been cloned and shown to express these resistances in Escherichia coli. The determinant encoded a single protein with an apparent size of 59 kDa which specified both aminoglycoside acetyltransferase [AAC(6')] and aminoglycoside phosphotransferase [APH(2")] activities. Nucleotide sequence analysis of the determinant showed it to be capable of encoding a 479-amino-acid protein of 56.9 kDa. analysis of Tn1725 insertion mutants of the determinant indicated that resistance to tobramycin and kanamycin is due to the AAC activity specified by, approximately, the first 170 amino acids of the predicted protein sequence and is consistent with the gentamicin resistance, specified by the APH activity, being encoded within the C-terminal region of the protein. Comparison of the C-terminal end of the predicted amino acid sequence with the reported sequences of 13 APHs and a viomycin phosphotransferase revealed a region which is highly conserved among these phosphotransferases.
金黄色葡萄球菌转座子Tn4001的aacA - aphD氨基糖苷类抗性决定簇可赋予对庆大霉素、妥布霉素和卡那霉素的抗性,该决定簇已被克隆,并证明可在大肠杆菌中表达这些抗性。该决定簇编码一种表观大小为59 kDa的单一蛋白质,它同时具有氨基糖苷乙酰转移酶[AAC(6')]和氨基糖苷磷酸转移酶[APH(2")]活性。对该决定簇的核苷酸序列分析表明,它能够编码一种56.9 kDa的479个氨基酸的蛋白质。对该决定簇的Tn1725插入突变体的分析表明,对妥布霉素和卡那霉素的抗性归因于预测蛋白质序列中大约前170个氨基酸所具有的AAC活性,这与由APH活性赋予的庆大霉素抗性由该蛋白质的C末端区域编码是一致的。将预测氨基酸序列的C末端与已报道的13种APH和一种紫霉素磷酸转移酶的序列进行比较,发现了一个在这些磷酸转移酶中高度保守的区域。