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- Title
Structural Study of Metal Binding and Coordination in Ancient Metallo-β-Lactamase PNGM-1 Variants.
- Authors
Park, Yoon Sik; Kim, Tae Yeong; Park, Hyunjae; Lee, Jung Hun; Nguyen, Diem Quynh; Hong, Myoung-Ki; Lee, Sang Hee; Kang, Lin-Woo
- Abstract
The increasing incidence of community- and hospital-acquired infections with multidrug-resistant (MDR) bacteria poses a critical threat to public health and the healthcare system. Although β-lactam antibiotics are effective against most bacterial infections, some bacteria are resistant to β-lactam antibiotics by producing β-lactamases. Among β-lactamases, metallo-β-lactamases (MBLs) are especially worrisome as only a few inhibitors have been developed against them. In MBLs, the metal ions play an important role as they coordinate a catalytic water molecule that hydrolyzes β-lactam rings. We determined the crystal structures of different variants of PNGM-1, an ancient MBL with additional tRNase Z activity. The variants were generated by site-directed mutagenesis targeting metal-coordinating residues. In PNGM-1, both zinc ions are coordinated by six coordination partners in an octahedral geometry, and the zinc-centered octahedrons share a common face. Structures of the PNGM-1 variants confirm that the substitution of a metal-coordinating residue causes the loss of metal binding and β-lactamase activity. Compared with PNGM-1, subclass B3 MBLs lack one metal-coordinating residue, leading to a shift in the metal-coordination geometry from an octahedral to tetrahedral geometry. Our results imply that a subtle change in the metal-binding site of MBLs can markedly change their metal-coordination geometry and catalytic activity.
- Subjects
BETA lactam antibiotics; NOSOCOMIAL infections; ZINC ions; METALS; SITE-specific mutagenesis; BACTERIAL diseases
- Publication
International Journal of Molecular Sciences, 2020, Vol 21, Issue 14, p4926
- ISSN
1661-6596
- Publication type
Article
- DOI
10.3390/ijms21144926