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A novel enzyme of type VI sulfide:quinone oxidoreductases in purple sulfur photosynthetic bacteria.
Duzs, Ágnes; Tóth, András; Németh, Brigitta; Balogh, Tímea; Kós, Péter B; Rákhely, Gábor.
Afiliação
  • Duzs Á; Department of Biotechnology, University of Szeged, Közép fasor 52, Szeged, 6726, Hungary.
  • Tóth A; Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Temesvári krt 62, Szeged, 6726, Hungary.
  • Németh B; Department of Biotechnology, University of Szeged, Közép fasor 52, Szeged, 6726, Hungary.
  • Balogh T; Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Temesvári krt 62, Szeged, 6726, Hungary.
  • Kós PB; Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Temesvári krt 62, Szeged, 6726, Hungary.
  • Rákhely G; Department of Biotechnology, University of Szeged, Közép fasor 52, Szeged, 6726, Hungary.
Appl Microbiol Biotechnol ; 102(12): 5133-5147, 2018 Jun.
Article em En | MEDLINE | ID: mdl-29680900
ABSTRACT
Sulfide detoxification can be catalyzed by ancient membrane-bound flavoproteins, sulfidequinone oxidoreductases (Sqr), which have important roles in sulfide homeostasis and sulfide-dependent energy conservation processes by transferring electrons from sulfide to respiratory or photosynthetic membrane electron flow. Sqr enzymes have been categorized into six groups. Several members of the groups I, II, III, and V are well-known, but type IV and VI Sqrs are, as yet, uncharacterized or hardly characterized at all. Here, we report detailed characterization of a type VI sulfidequinone oxidoreductase (TrSqrF) from a purple sulfur bacterium, Thiocapsa roseopersicina. Phylogenetic analysis classified this enzyme in a special group composed of SqrFs of endosymbionts, while a weaker relationship could be observed with SqrF of Chlorobaculum tepidum which is the only type VI enzyme characterized so far. Directed mutagenesis experiments showed that TrSqrF contributed substantially to the sulfidequinone oxidoreductase activity of the membranes. Expression of the sqrF gene could be induced by sulfide. Homologous recombinant TrSqrF protein was expressed and purified from the membranes of a SqrF-deleted T. roseopersicina strain. The purified protein contains redox-active covalently bound FAD cofactor. The recombinant TrSqrF enzyme catalyzes sulfur-dependent quinone reduction and prefers ubiquinone-type quinone compounds. Kinetic parameters of TrSqrF show that the affinity of the enzyme is similar to duroquinone and decylubiquinone, but the reaction has substantially lower activation energy with decylubiquinone, indicating that the quinone structure has an effect on the catalytic process. TrSqrF enzyme affinity for sulfide is low, therefore, in agreement with the gene expressional analyis, SqrF could play a role in energy-conserving sulfide oxidation at high sulfide concentrations. TrSqrF is a good model enzyme for the subgroup of type VI Sqrs of endosymbionts and its characterization might provide deeper insight into the molecular details of the ancient, anoxic, energy-gaining processes using sulfide as an electron donor.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinona Redutases / Bacteroides Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinona Redutases / Bacteroides Idioma: En Ano de publicação: 2018 Tipo de documento: Article