Chemistry and Redox Biology of Mycothiol
- PMID: 28372502
- DOI: 10.1089/ars.2017.7074
Chemistry and Redox Biology of Mycothiol
Abstract
Significance: Mycothiol (MSH, AcCys-GlcN-Ins) is the main low-molecular weight (LMW) thiol of most Actinomycetes, including the human pathogen Mycobacterium tuberculosis that affects millions of people worldwide. Strains with decreased MSH content show increased susceptibilities to hydroperoxides and electrophilic compounds. In M. tuberculosis, MSH modulates the response to several antituberculosis drugs. Enzymatic routes involving MSH could provide clues for specific drug design. Recent Advances: Physicochemical data argue against a rapid, nonenzymatic reaction of MSH with oxidants, disulfides, or electrophiles. Moreover, exposure of the bacteria to high concentrations of two-electron oxidants resulted in protein mycothiolation. The recently described glutaredoxin-like protein mycoredoxin-1 (Mrx-1) provides a route for catalytic reduction of mycothiolated proteins, protecting critical cysteines from irreversible oxidation. The description of MSH/Mrx-1-dependent activities of peroxidases helped to explain the higher susceptibility to oxidants observed in Actinomycetes lacking MSH. Moreover, the first mycothiol-S-transferase, member of the DinB superfamily of proteins, was described. In Corynebacterium, both the MSH/Mrx-1 and the thioredoxin pathways reduce methionine sulfoxide reductase A. A novel tool for in vivo imaging of the MSH/mycothiol disulfide (MSSM) status allows following changes in the mycothiol redox state during macrophage infection and its relationship with antibiotic sensitivity.
Critical issues: Redundancy of MSH with other LMW thiols is starting to be unraveled and could help to rationalize the differences in the reported importance of MSH synthesis observed in vitro versus in animal infection models.
Future directions: Future work should be directed to establish the structural bases of the specificity of MSH-dependent enzymes, thus facilitating drug developments. Antioxid. Redox Signal. 28, 487-504.
Keywords: Actinomycetes; mycobacteria; mycoredoxin-1; mycothiol; tuberculosis.
Similar articles
-
Thiol Redox and pKa Properties of Mycothiol, the Predominant Low-Molecular-Weight Thiol Cofactor in the Actinomycetes.Chembiochem. 2016 Sep 15;17(18):1689-92. doi: 10.1002/cbic.201600228. Epub 2016 Jul 28. Chembiochem. 2016. PMID: 27332744
-
A mycothiol synthase mutant of Mycobacterium smegmatis produces novel thiols and has an altered thiol redox status.J Bacteriol. 2005 Nov;187(21):7309-16. doi: 10.1128/JB.187.21.7309-7316.2005. J Bacteriol. 2005. PMID: 16237013 Free PMC article.
-
Mycothiol/mycoredoxin 1-dependent reduction of the peroxiredoxin AhpE from Mycobacterium tuberculosis.J Biol Chem. 2014 Feb 21;289(8):5228-39. doi: 10.1074/jbc.M113.510248. Epub 2013 Dec 30. J Biol Chem. 2014. PMID: 24379404 Free PMC article.
-
Redox regulation by reversible protein S-thiolation in Gram-positive bacteria.Redox Biol. 2019 Jan;20:130-145. doi: 10.1016/j.redox.2018.08.017. Epub 2018 Aug 24. Redox Biol. 2019. PMID: 30308476 Free PMC article. Review.
-
Application of genetically encoded redox biosensors to measure dynamic changes in the glutathione, bacillithiol and mycothiol redox potentials in pathogenic bacteria.Free Radic Biol Med. 2018 Nov 20;128:84-96. doi: 10.1016/j.freeradbiomed.2018.02.018. Epub 2018 Feb 15. Free Radic Biol Med. 2018. PMID: 29454879 Review.
Cited by
-
Antimicrobial Activity of Neutrophils Against Mycobacteria.Front Immunol. 2021 Dec 23;12:782495. doi: 10.3389/fimmu.2021.782495. eCollection 2021. Front Immunol. 2021. PMID: 35003097 Free PMC article. Review.
-
Precise and versatile microplate reader-based analyses of biosensor signals from arrayed microbial colonies.Front Microbiol. 2023 Jun 14;14:1187228. doi: 10.3389/fmicb.2023.1187228. eCollection 2023. Front Microbiol. 2023. PMID: 37389345 Free PMC article.
-
Stable integration of the Mrx1-roGFP2 biosensor to monitor dynamic changes of the mycothiol redox potential in Corynebacterium glutamicum.Redox Biol. 2019 Jan;20:514-525. doi: 10.1016/j.redox.2018.11.012. Epub 2018 Nov 17. Redox Biol. 2019. PMID: 30481728 Free PMC article.
-
The role of thiols in antioxidant systems.Free Radic Biol Med. 2019 Aug 20;140:14-27. doi: 10.1016/j.freeradbiomed.2019.05.035. Epub 2019 Jun 13. Free Radic Biol Med. 2019. PMID: 31201851 Free PMC article. Review.
-
The flavohaemoprotein hmp maintains redox homeostasis in response to reactive oxygen and nitrogen species in Corynebacterium glutamicum.Microb Cell Fact. 2023 Aug 18;22(1):158. doi: 10.1186/s12934-023-02160-9. Microb Cell Fact. 2023. PMID: 37596674 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources