Toth Marta, Antunes Nuno Tiago, Stewart Nichole K, Frase Hilary, Bhattacharya Monolekha, Smith Clyde A, Vakulenko Sergei B
Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana, USA.
Stanford Synchrotron Radiation Lightsource, Stanford University, Menlo Park, California, USA.
Nat Chem Biol. 2016 Jan;12(1):9-14. doi: 10.1038/nchembio.1950. Epub 2015 Nov 9.
Production of β-lactamases of one of four molecular classes (A, B, C and D) is the major mechanism of bacterial resistance to β-lactams, the largest class of antibiotics, which have saved countless lives since their inception 70 years ago. Although several hundred efficient class D enzymes have been identified in Gram-negative pathogens over the last four decades, none have been reported in Gram-positive bacteria. Here we demonstrate that efficient class D β-lactamases capable of hydrolyzing a wide array of β-lactam substrates are widely disseminated in various species of environmental Gram-positive organisms. Class D enzymes of Gram-positive bacteria have a distinct structural architecture and employ a unique substrate-binding mode that is quite different from that of all currently known class A, C and D β-lactamases. These enzymes thus constitute a previously unknown reservoir of novel antibiotic-resistance enzymes.
产生四种分子类别(A、B、C和D)之一的β-内酰胺酶是细菌对β-内酰胺类抗生素产生耐药性的主要机制,β-内酰胺类抗生素是最大的一类抗生素,自70年前问世以来已挽救了无数生命。尽管在过去的四十年里,在革兰氏阴性病原体中已鉴定出数百种高效的D类酶,但在革兰氏阳性细菌中尚未有相关报道。在此,我们证明能够水解多种β-内酰胺底物的高效D类β-内酰胺酶广泛分布于各种环境革兰氏阳性生物体中。革兰氏阳性细菌的D类酶具有独特的结构架构,并采用一种独特的底物结合模式,这与目前已知的所有A、C和D类β-内酰胺酶截然不同。因此,这些酶构成了一个前所未知的新型抗生素耐药酶库。