4.6 Article

SdhE Is a Conserved Protein Required for Flavinylation of Succinate Dehydrogenase in Bacteria

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 287, Issue 22, Pages 18418-18428

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ELSEVIER
DOI: 10.1074/jbc.M111.293803

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Funding

  1. Royal Society of New Zealand
  2. Biotechnology and Biological Sciences Research Council
  3. Tertiary Education Commission, New Zealand
  4. Gates Foundation

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Conserved uncharacterized genes account for similar to 30% of genes in both eukaryotic and bacterial genomes and are predicted to encode what are often termed conserved hypothetical proteins. Many of these proteins have a wide phylogenetic distribution and might play important roles in conserved cellular pathways. Using the bacterium Serratia as a model system, we have investigated two conserved uncharacterized proteins, YgfY (a DUF339 protein, renamed SdhE; (s) under bar uccinate (d) under bare (h) under bar ydrogenase protein (E) under bar) and YgfX (a DUF1434 protein). SdhE was required for growth on succinate as a sole carbon source and for the function, but not stability, of succinate dehydrogenase, an important component of the electron transport chain and the tricarboxylic acid cycle. SdhE interacted with the flavoprotein SdhA, directly bound the flavin adenine dinucleotide co-factor, and was required for the flavinylation of SdhA. This is the first demonstration of a protein required for FAD incorporation in bacteria. Furthermore, the loss of SdhE was highly pleiotropic, suggesting that SdhE might flavinylate other flavoproteins. Our findings are of wide importance to central metabolism because SdhE homologues are present in alpha-, beta-, and gamma-proteobacteria and multiple eukaryotes, including humans and yeast.

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