Microbial conversion of choline to trimethylamine requires a glycyl radical enzyme

被引:528
作者
Craciun, Smaranda [1 ]
Balskus, Emily P. [1 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
关键词
fragmentation; choline trimethylamine-lyase; gastrointestinal tract; metabolism; trimethylaminuria; PYRUVATE FORMATE-LYASE; ANAEROBIC DEGRADATION; GLYCINE BETAINE; METABOLISM; INVOLVEMENT; MECHANISM; BACTERIUM; CATALYSIS; SEQUENCE; CULTURE;
D O I
10.1073/pnas.1215689109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Choline and trimethylamine (TMA) are small molecules that play central roles in biological processes throughout all kingdoms of life. These ubiquitous metabolites are linked through a single biochemical transformation, the conversion of choline to TMA by anaerobic microorganisms. This metabolic activity, which contributes to methanogenesis and human disease, has been known for over a century but has eluded genetic and biochemical characterization. We have identified a gene cluster responsible for anaerobic choline degradation within the genome of a sulfate-reducing bacterium and verified its function using both a genetic knockout strategy and heterologous expression in Escherichia coli. Bioinformatics and electron paramagnetic resonance (EPR) spectroscopy revealed the involvement of a C-N bond cleaving glycyl radical enzyme in TMA production, which is unprecedented chemistry for this enzyme family. Our discovery provides the predictive capabilities needed to identify choline utilization clusters in numerous bacterial genomes, underscoring the importance and prevalence of this metabolic activity within the human microbiota and the environment.
引用
收藏
页码:21307 / 21312
页数:6
相关论文
共 41 条
[31]   The HHpred interactive server for protein homology detection and structure prediction [J].
Söding, J ;
Biegert, A ;
Lupas, AN .
NUCLEIC ACIDS RESEARCH, 2005, 33 :W244-W248
[32]   Culture-independent methods for studying environmental microorganisms: methods, application, and perspective [J].
Su, Can ;
Lei, Liping ;
Duan, Yanqing ;
Zhang, Ke-Qin ;
Yang, Jinkui .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2012, 93 (03) :993-1003
[33]   CLUSTAL-W - IMPROVING THE SENSITIVITY OF PROGRESSIVE MULTIPLE SEQUENCE ALIGNMENT THROUGH SEQUENCE WEIGHTING, POSITION-SPECIFIC GAP PENALTIES AND WEIGHT MATRIX CHOICE [J].
THOMPSON, JD ;
HIGGINS, DG ;
GIBSON, TJ .
NUCLEIC ACIDS RESEARCH, 1994, 22 (22) :4673-4680
[34]   Radical catalysis in coenzyme B12-dependent isomerization (eliminating) reactions [J].
Toraya, T .
CHEMICAL REVIEWS, 2003, 103 (06) :2095-2127
[35]   THE FREE-RADICAL OF PYRUVATE FORMATE-LYASE - CHARACTERIZATION BY EPR SPECTROSCOPY AND INVOLVEMENT IN CATALYSIS AS STUDIED WITH THE SUBSTRATE-ANALOG HYPOPHOSPHITE [J].
UNKRIG, V ;
NEUGEBAUER, FA ;
KNAPPE, J .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 184 (03) :723-728
[36]   Structural Insights into Radical Generation by the Radical SAM Superfamily [J].
Vey, Jessica L. ;
Drennan, Catherine L. .
CHEMICAL REVIEWS, 2011, 111 (04) :2487-2506
[37]   Transposon mutagenesis in Desulfovibrio desulfuricans: Development of a random mutagenesis tool from Tn7 [J].
Wall, JD ;
Murnan, T ;
Argyle, J ;
English, RS ;
RappGiles, BJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (10) :3762-3767
[38]   Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease [J].
Wang, Zeneng ;
Klipfell, Elizabeth ;
Bennett, Brian J. ;
Koeth, Robert ;
Levison, Bruce S. ;
Dugar, Brandon ;
Feldstein, Ariel E. ;
Britt, Earl B. ;
Fu, Xiaoming ;
Chung, Yoon-Mi ;
Wu, Yuping ;
Schauer, Phil ;
Smith, Jonathan D. ;
Allayee, Hooman ;
Tang, W. H. Wilson ;
DiDonato, Joseph A. ;
Lusis, Aldons J. ;
Hazen, Stanley L. .
NATURE, 2011, 472 (7341) :57-U82
[39]   EFFECT OF PHOSPHATE ON THE CORROSION OF CARBON-STEEL AND ON THE COMPOSITION OF CORROSION PRODUCTS IN 2-STAGE CONTINUOUS CULTURES OF DESULFOVIBRIO-DESULFURICANS [J].
WEIMER, PJ ;
VANKAVELAAR, MJ ;
MICHEL, CB ;
NG, TK .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1988, 54 (02) :386-396
[40]  
ZEISEL SH, 1983, J PHARMACOL EXP THER, V225, P320