Vliegenthart J S, Ketelaar-van Gaalen P A, van de Klundert J A
Department of Medical Microbiology, University Hospital, Leiden, The Netherlands.
Antimicrob Agents Chemother. 1991 May;35(5):892-7. doi: 10.1128/AAC.35.5.892.
A chromosomal gentamicin resistance determinant from Pseudomonas aeruginosa was cloned on a 2.4-kb fragment in the broad-host-range vector pLAFR3. Substrate profiles for eight aminoglycosides at three concentrations showed that resistance was due to aminoglycoside-(3)-N-acetyltransferase III. This enzyme was produced in Pseudomonas strains but not in an Escherichia coli strain bearing the aacC3 gene. Nucleotide sequencing revealed two contiguous open reading frames (ORFs) preceded by a potential promoter and a ribosome-binding site. ORF-1 was 642 bp in length and encoded a protein of unknown function with a molecular mass of 23.9 kDa. ORF-2 was 813 bp in length and encoded a protein of 29.6 kDa. From deletion mutagenesis, in vitro transcription-translation data, and protein analysis of bacterial lysates, it was inferred that this 29.6-kDa protein represents the aminoglycoside-(3)-N-acetyltransferase III enzyme. A polymerase chain reaction with two specific intragenic 20-mer primers was developed to detect the aacC3 gene. A BstEII restriction site in the amplified DNA region was used to demonstrate the specificity of the reaction. Tests of 23 reference strains, which produced 12 different aminoglycoside-modifying enzymes, confirmed the specificities of the primers. The gene proved to be absent from a collection of 50 gentamicin-resistant P. aeruginosa strains selected at random in The Netherlands.
来自铜绿假单胞菌的一种染色体庆大霉素抗性决定簇被克隆到广宿主范围载体pLAFR3的一个2.4 kb片段上。三种浓度下对八种氨基糖苷类药物的底物谱表明,抗性是由氨基糖苷-(3)-N-乙酰基转移酶III引起的。这种酶在假单胞菌菌株中产生,但在携带aacC3基因的大肠杆菌菌株中不产生。核苷酸测序揭示了两个相邻的开放阅读框(ORF),前面有一个潜在的启动子和一个核糖体结合位点。ORF-1长度为642 bp,编码一种分子量为23.9 kDa的功能未知的蛋白质。ORF-2长度为813 bp,编码一种29.6 kDa的蛋白质。通过缺失诱变、体外转录-翻译数据以及细菌裂解物的蛋白质分析,推断这种29.6 kDa的蛋白质代表氨基糖苷-(3)-N-乙酰基转移酶III。开发了一种使用两个基因内特异性20聚体引物进行的聚合酶链反应来检测aacC3基因。扩增DNA区域中的一个BstEII限制性位点用于证明反应的特异性。对产生12种不同氨基糖苷类修饰酶的23株参考菌株进行的测试证实了引物的特异性。在荷兰随机选择的50株庆大霉素抗性铜绿假单胞菌菌株中未发现该基因。