Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Substrate Spectrum Extension of PenA in Burkholderia thailandensis with a Single Amino Acid Deletion, Glu168del

Authors
Yi, HyojeongKim, KaranCho, Kwang-HwiJung, OksungKim, Heenam Stanley
Issue Date
Jul-2012
Publisher
AMER SOC MICROBIOLOGY
Keywords
A BETA-LACTAMASES; ANTIMICROBIAL SUSCEPTIBILITY; PSEUDOMALLEI; CEFTAZIDIME; DIVERSITY
Citation
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, v.56, no.7, pp.4005 - 4008
Indexed
SCIE
SCOPUS
Journal Title
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Volume
56
Number
7
Start Page
4005
End Page
4008
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/108103
DOI
10.1128/AAC.00598-12
ISSN
0066-4804
Abstract
We describe a deletion mutation in a class A beta-lactamase, PenA, of Burkholderia thailandensis that extended the substrate spectrum of the enzyme to include ceftazidime. Glu168del was located in a functional domain called the omega loop causing expansion of the space in the loop, which in turn increased flexibility at the active site. This deletion mutation represents a rare but significant alternative mechanical path to substrate spectrum extension in PenA besides more common substitution mutations.
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Health Sciences > School of Biosystems and Biomedical Sciences > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE