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Novel functions of an iron-sulfur flavoprotein from Trichomonas vaginalis hydrogenosomes
T. Smutná, K. Pilarová, J. Tarábek, J. Tachezy, I. Hrdý,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 1972 do Před 6 měsíci
Freely Accessible Science Journals
od 1995 do Před 6 měsíci
PubMed Central
od 1972 do Před 6 měsíci
Europe PubMed Central
od 1972 do Před 6 měsíci
Open Access Digital Library
od 1972-01-01
Open Access Digital Library
od 1972-01-01
PubMed
24663020
DOI
10.1128/aac.02320-13
Knihovny.cz E-zdroje
- MeSH
- antitrichomonádové látky farmakologie MeSH
- ferredoxiny metabolismus MeSH
- flavoproteiny metabolismus MeSH
- geny hub MeSH
- katalýza MeSH
- léková rezistence MeSH
- metronidazol chemie farmakologie MeSH
- molekulární sekvence - údaje MeSH
- NAD metabolismus MeSH
- proteiny obsahující železo a síru metabolismus MeSH
- sekvence aminokyselin MeSH
- subcelulární frakce účinky léků metabolismus MeSH
- Trichomonas vaginalis metabolismus MeSH
- vodík metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Iron-sulfur flavoproteins (Isf) are flavin mononucleotide (FMN)- and FeS cluster-containing proteins commonly encountered in anaerobic prokaryotes. However, with the exception of Isf from Methanosarcina thermophila, which participates in oxidative stress management by removing oxygen and hydrogen peroxide, none of these proteins has been characterized in terms of function. Trichomonas vaginalis, a sexually transmitted eukaryotic parasite of humans, was found to express several iron-sulfur flavoprotein (TvIsf) homologs in its hydrogenosomes. We show here that in addition to having oxygen-reducing activity, the recombinant TvIsf also functions as a detoxifying reductase of metronidazole and chloramphenicol, both of which are antibiotics effective against a variety of anaerobic microbes. TvIsf can utilize both NADH and reduced ferredoxin as electron donors. Given the prevalence of Isf in anaerobic prokaryotes, we propose that these proteins are central to a novel defense mechanism against xenobiotics.
Citace poskytuje Crossref.org
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