» Articles » PMID: 32591552

Functional Analysis of BPSS2242 Reveals Its Detoxification Role in Burkholderia Pseudomallei Under Salt Stress

Overview
Journal Sci Rep
Specialty Science
Date 2020 Jun 28
PMID 32591552
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

A bpss2242 gene, encoding a putative short-chain dehydrogenase/oxidoreductase (SDR) in Burkholderia pseudomallei, was identified and its expression was up-regulated by ten-fold when B. pseudomallei was cultured under high salt concentration. Previous study suggested that BPSS2242 plays important roles in adaptation to salt stress and pathogenesis; however, its biological functions are still unknown. Herein, we report the biochemical properties and functional characterization of BPSS2242 from B. pseudomallei. BPSS2242 exhibited NADPH-dependent reductase activity toward diacetyl and methylglyoxal, toxic electrophilic dicarbonyls. The conserved catalytic triad was identified and found to play critical roles in catalysis and cofactor binding. Tyr162 and Lys166 are involved in NADPH binding and mutation of Lys166 causes a conformational change, altering protein structure. Overexpression of BPSS2242 in Escherichia coli increased bacterial survival upon exposure to diacetyl and methylglyoxal. Importantly, the viability of B. pseudomallei encountered dicarbonyl toxicity was enhanced when cultured under high salt concentration as a result of BPSS2242 overexpression. This is the first study demonstrating that BPSS2242 is responsible for detoxification of toxic metabolites, constituting a protective system against reactive carbonyl compounds in B. pseudomallei..

Citing Articles

Homologous relationship between FabG involved in fatty acid biosynthesis and SDR on chromosome II in the multi-chromosome pathogen Vibrio anguillarum.

Kim D, Park S, Rafiquzzaman S, Lee J Sci Rep. 2025; 15(1):8706.

PMID: 40082627 PMC: 11906770. DOI: 10.1038/s41598-025-92645-x.


Rv0687 a Putative Short-Chain Dehydrogenase Is Required for In Vitro and In Vivo Survival of .

Bhargavi G, Mallakuntla M, Kale D, Tiwari S Int J Mol Sci. 2024; 25(14).

PMID: 39063103 PMC: 11277061. DOI: 10.3390/ijms25147862.


Approaches for completing metabolic networks through metabolite damage and repair discovery.

Griffith C, Walvekar A, Linster C Curr Opin Syst Biol. 2021; 28:None.

PMID: 34957344 PMC: 8669784. DOI: 10.1016/j.coisb.2021.100379.


Exogenous Myo-Inositol Alleviates Salt Stress by Enhancing Antioxidants and Membrane Stability via the Upregulation of Stress Responsive Genes in L.

Al-Mushhin A, Qari S, Fakhr M, Alnusairi G, Alnusaire T, ALrashidi A Plants (Basel). 2021; 10(11).

PMID: 34834781 PMC: 8623490. DOI: 10.3390/plants10112416.


Arginine glycosylation enhances methylglyoxal detoxification.

El Qaidi S, Scott N, Hardwidge P Sci Rep. 2021; 11(1):3834.

PMID: 33589708 PMC: 7884692. DOI: 10.1038/s41598-021-83437-0.

References
1.
Limmathurotsakul D, Golding N, Dance D, Messina J, Pigott D, Moyes C . Predicted global distribution of Burkholderia pseudomallei and burden of melioidosis. Nat Microbiol. 2016; 1:15008. DOI: 10.1038/nmicrobiol.2015.8. View

2.
Chewapreecha C, Holden M, Vehkala M, Valimaki N, Yang Z, Harris S . Global and regional dissemination and evolution of Burkholderia pseudomallei. Nat Microbiol. 2017; 2:16263. PMC: 5300093. DOI: 10.1038/nmicrobiol.2016.263. View

3.
Cheng A, Currie B . Melioidosis: epidemiology, pathophysiology, and management. Clin Microbiol Rev. 2005; 18(2):383-416. PMC: 1082802. DOI: 10.1128/CMR.18.2.383-416.2005. View

4.
Inglis T, Sagripanti J . Environmental factors that affect the survival and persistence of Burkholderia pseudomallei. Appl Environ Microbiol. 2006; 72(11):6865-75. PMC: 1636198. DOI: 10.1128/AEM.01036-06. View

5.
Limmathurotsakul D, Wongratanacheewin S, Teerawattanasook N, Wongsuvan G, Chaisuksant S, Chetchotisakd P . Increasing incidence of human melioidosis in Northeast Thailand. Am J Trop Med Hyg. 2010; 82(6):1113-7. PMC: 2877420. DOI: 10.4269/ajtmh.2010.10-0038. View