首页 | 本学科首页   官方微博 | 高级检索  
     


SdhE is a conserved protein required for flavinylation of succinate dehydrogenase in bacteria
Authors:McNeil Matthew B  Clulow James S  Wilf Nabil M  Salmond George P C  Fineran Peter C
Affiliation:Department of Microbiology and Immunology, University of Otago, Dunedin 9054, New Zealand.
Abstract:Conserved uncharacterized genes account for ~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; succinate dehydrogenase protein E) 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 α-, β-, and γ-proteobacteria and multiple eukaryotes, including humans and yeast.
Keywords:Bacterial Metabolism   Electron Transport   FAD   Flavoproteins   Tricarboxylic Acid (TCA) Cycle   Co-factor   Prodigiosin   Sdh5   SdhA   Succinate Dehydrogenase
本文献已被 PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号