Back to Search Start Over

Identification and characterization of novel catalytic bioscavengers of organophosphorus nerve agents.

Authors :
Otto TC
Scott JR
Kauffman MA
Hodgins SM
Ditargiani RC
Hughes JH
Sarricks EP
Saturday GA
Hamilton TA
Cerasoli DM
Source :
Chemico-biological interactions [Chem Biol Interact] 2013 Mar 25; Vol. 203 (1), pp. 186-90. Date of Electronic Publication: 2012 Oct 03.
Publication Year :
2013

Abstract

In an effort to discover novel catalytic bioscavengers of organophosphorus (OP) nerve agents, cell lysates from a diverse set of bacterial strains were screened for their capacity to hydrolyze the OP nerve agents VX, VR, and soman (GD). The library of bacterial strains was identified using both random and rational approaches. Specifically, two representative strains from eight categories of extremophiles were chosen at random. For the rational approach, the protein sequence of organophosphorus hydrolase (OPH) from Brevundimonas diminuta was searched against a non-redundant protein database using the Basic Local Alignment Search Tool to find regions of local similarity between sequences. Over 15 protein sequences with significant sequence similarity to OPH were identified from a variety of bacterial strains. Some of these matches were based on predicted protein structures derived from bacterial genome sequences rather than from bona fide proteins isolated from bacteria. Of the 25 strains selected for nerve agent testing, three bacterial strains had measurable levels of OP hydrolase activity. These strains are Ammoniphilus oxalaticus, Haloarcula sp., and Micromonospora aurantiaca. Lysates from A. oxalaticus had detectable hydrolysis of VR; Haloarcula sp. had appreciable hydrolysis of VX and VR, whereas lysates from M. aurantiaca had detectable hydrolysis of VR and GD.<br /> (Published by Elsevier Ireland Ltd.)

Details

Language :
English
ISSN :
1872-7786
Volume :
203
Issue :
1
Database :
MEDLINE
Journal :
Chemico-biological interactions
Publication Type :
Academic Journal
Accession number :
23041042
Full Text :
https://doi.org/10.1016/j.cbi.2012.09.009