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

被引:55
作者
Mcneil, Matthew B. [1 ]
Clulow, James S. [1 ]
Wilf, Nabil M. [2 ]
Salmond, George P. C. [2 ]
Fineran, Peter C. [1 ]
机构
[1] Univ Otago, Dept Microbiol & Immunol, Dunedin 9054, New Zealand
[2] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
基金
英国生物技术与生命科学研究理事会;
关键词
GGDEF/EAL DOMAIN PROTEIN; COVALENTLY BOUND FLAVIN; ANTIBIOTIC BIOSYNTHESIS; 2-COMPONENT SYSTEM; ESCHERICHIA-COLI; SERRATIA; FAD; PRODIGIOSIN; ATTACHMENT; FLAVOPROTEIN;
D O I
10.1074/jbc.M111.293803
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:18418 / 18428
页数:11
相关论文
共 47 条
[1]   The MicrobesOnline web site for comparative genomics [J].
Alm, EJ ;
Huang, KH ;
Price, MN ;
Koche, RP ;
Keller, K ;
Dubchak, IL ;
Arkin, AP .
GENOME RESEARCH, 2005, 15 (07) :1015-1022
[2]   The genome sequence of Rickettsia prowazekii and the origin of mitochondria [J].
Andersson, SGE ;
Zomorodipour, A ;
Andersson, JO ;
Sicheritz-Pontén, T ;
Alsmark, UCM ;
Podowski, RM ;
Näslund, AK ;
Eriksson, AS ;
Winkler, HH ;
Kurland, CG .
NATURE, 1998, 396 (6707) :133-140
[3]  
[Anonymous], QIAEXPRESSIONIST
[4]   BACTERIAL ELECTRON-TRANSPORT CHAINS [J].
ANRAKU, Y .
ANNUAL REVIEW OF BIOCHEMISTRY, 1988, 57 :101-132
[5]   Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants:: the Keio collection [J].
Baba, Tomoya ;
Ara, Takeshi ;
Hasegawa, Miki ;
Takai, Yuki ;
Okumura, Yoshiko ;
Baba, Miki ;
Datsenko, Kirill A. ;
Tomita, Masaru ;
Wanner, Barry L. ;
Mori, Hirotada .
MOLECULAR SYSTEMS BIOLOGY, 2006, 2 (1) :2006.0008
[6]   Riboflavin uptake and FAD synthesis in Saccharomyces cerevisiae mitochondria -: Involvement of the Flx1p carrier in FAD export [J].
Bafunno, V ;
Giancaspero, TA ;
Brizio, C ;
Bufano, D ;
Passarella, S ;
Boles, E ;
Barile, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (01) :95-102
[7]  
Bateman A, 2004, NUCLEIC ACIDS RES, V32, pD138, DOI [10.1093/nar/gkp985, 10.1093/nar/gkh121, 10.1093/nar/gkr1065]
[8]   COVALENT COFACTOR BINDING TO FLAVOENZYMES REQUIRES SPECIFIC EFFECTORS [J].
BRANDSCH, R ;
BICHLER, V .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 182 (01) :125-128
[9]   DROPLET ENRICHMENT FACTORS OF PIGMENTED AND NONPIGMENTED SERRATIA-MARCESCENS - POSSIBLE SELECTIVE FUNCTION FOR PRODIGIOSIN [J].
BURGER, SR ;
BENNETT, JW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1985, 50 (02) :487-490
[10]   Function and structure of complex II of the respiratory chain [J].
Cecchini, G .
ANNUAL REVIEW OF BIOCHEMISTRY, 2003, 72 :77-109