Deletion Mutations Conferring Substrate Spectrum Extension in the Class A β-Lactamase
Author(s) -
Junghyun Hwang,
Kwang-Hwi Cho,
Han Song,
Hyojeong Yi,
Sun Kim
Publication year - 2014
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.02648-14
Subject(s) - genetics , class (philosophy) , extension (predicate logic) , spectrum (functional analysis) , mutation , biology , computational biology , gene , computer science , physics , artificial intelligence , quantum mechanics , programming language
We describe four new deletion mutations in a class A β-lactamase PenA in Burkholderia thailandensis, each conferring an extended substrate spectrum. Single-amino-acid deletions T171del, I173del, and P174del and a two-amino-acid deletion, R165_T167delinsP, occurred in the omega loop, increasing the flexibility of the binding cavity. This rare collection of mutations has significance, allowing exploration of the diverse evolutionary trajectories of β-lactamases and as potential future mutations conferring high-level ceftazidime resistance on isolates from clinical settings, compared with amino acid substitution mutations.
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