Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, Alberta, Canada.
Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, Ontario, Canada.
Protein Sci. 2020 Mar;29(3):803-808. doi: 10.1002/pro.3811. Epub 2020 Jan 30.
Acyl-coenzyme A-dependent N-acetyltransferases (AACs) catalyze the modification of aminoglycosides rendering the bacteria carrying such enzymes resistant to this class of antibiotics. Here we present the crystal structure of AAC(3)-Ia enzyme from Serratia marcescens in complex with coenzyme A determined to 1.8 Å resolution. This enzyme served as an architype for the AAC enzymes targeting the amino group at Position 3 of aminoglycoside main aminocyclitol ring. The structure of this enzyme has been previously determined only in truncated form and was interpreted as distinct from subsequently characterized AACs. The reason for the unusual arrangement of secondary structure elements of AAC(3)-Ia was not further investigated. By determining the full-length structure of AAC(3)-Ia we establish that this enzyme adopts the canonical AAC fold conserved across this family and it does not undergo through significant rearrangement of secondary structure elements upon ligand binding as was proposed previously. In addition, our results suggest that the C-terminal tail in AAC(3)-Ia monomer forms intramolecular hydrogen bonds that contributes to formation of stable dimer, representing the predominant oligomeric state for this enzyme.
酰基辅酶 A 依赖性 N-乙酰转移酶 (AACs) 催化氨基糖苷类抗生素的修饰,使携带这些酶的细菌对这类抗生素产生耐药性。在这里,我们展示了来自粘质沙雷氏菌的 AAC(3)-Ia 酶与辅酶 A 复合物的晶体结构,分辨率为 1.8 Å。该酶是针对氨基糖苷类抗生素主氨基环醇环第 3 位氨基的 AAC 酶的原型。该酶的结构之前仅以截断形式确定,并被解释为与随后表征的 AACs 不同。AAC(3)-Ia 中二级结构元件的异常排列的原因尚未进一步研究。通过确定 AAC(3)-Ia 的全长结构,我们确定该酶采用了在整个家族中保守的典型 AAC 折叠,并且在配体结合时不会像先前提出的那样发生二级结构元件的显著重排。此外,我们的结果表明,AAC(3)-Ia 单体中的 C 末端尾部形成分子内氢键,有助于形成稳定的二聚体,这代表了该酶的主要寡聚状态。