Microbial NAD Metabolism: Lessons from Comparative Genomics

被引:174
作者
Gazzaniga, Francesca [2 ,3 ,4 ]
Stebbins, Rebecca [2 ,3 ,4 ]
Chang, Sheila Z. [2 ,3 ,4 ]
McPeek, Mark A. [4 ]
Brenner, Charles [1 ,2 ,3 ]
机构
[1] Univ Iowa, Carver Coll Med, Dept Biochem, Iowa City, IA 52242 USA
[2] Dartmouth Med Sch, Dept Biochem & Genet, Lebanon, NH 03756 USA
[3] Dartmouth Med Sch, Norris Cotton Canc Ctr, Lebanon, NH 03756 USA
[4] Dartmouth Coll, Dept Biol Sci, Hanover, NH 03755 USA
基金
美国国家科学基金会;
关键词
NICOTINAMIDE MONONUCLEOTIDE ADENYLYLTRANSFERASE; L-ASPARTATE OXIDASE; ESCHERICHIA-COLI; DIPHOSPHOPYRIDINE NUCLEOTIDE; HAEMOPHILUS-INFLUENZAE; MYCOBACTERIUM-TUBERCULOSIS; TRANSCRIPTIONAL REGULATION; NMN ADENYLYLTRANSFERASE; CRYSTAL-STRUCTURE; IDENTIFICATION;
D O I
10.1128/MMBR.00042-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
NAD is a coenzyme for redox reactions and a substrate of NAD-consuming enzymes, including ADP-ribose transferases, Sir2-related protein lysine deacetylases, and bacterial DNA ligases. Microorganisms that synthesize NAD from as few as one to as many as five of the six identified biosynthetic precursors have been identified. De novo NAD synthesis from aspartate or tryptophan is neither universal nor strictly aerobic. Salvage NAD synthesis from nicotinamide, nicotinic acid, nicotinamide riboside, and nicotinic acid riboside occurs via modules of different genes. Nicotinamide salvage genes nadV and pncA, found in distinct bacteria, appear to have spread throughout the tree of life via horizontal gene transfer. Biochemical, genetic, and genomic analyses have advanced to the point at which the precursors and pathways utilized by a microorganism can be predicted. Challenges remain in dissecting regulation of pathways.
引用
收藏
页码:529 / +
页数:14
相关论文
共 69 条
[1]   Manipulation of a nuclear NAD+ salvage pathway delays aging without altering steady-state NAD+ levels [J].
Anderson, RM ;
Bitterman, KJ ;
Wood, JG ;
Medvedik, O ;
Cohen, H ;
Lin, SS ;
Manchester, JK ;
Gordon, JI ;
Sinclair, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (21) :18881-18890
[2]   NAD+ metabolism in health and disease [J].
Belenky, Peter ;
Bogan, Katrina L. ;
Brenner, Charles .
TRENDS IN BIOCHEMICAL SCIENCES, 2007, 32 (01) :12-19
[3]   Nicotinamide riboside promotes Sir2 silencing and extends lifespan via Nrk and Urh1/Pnp1/Meu1 pathways to NAD+ [J].
Belenky, Peter ;
Racette, Frances G. ;
Bogan, Katrina L. ;
McClure, Julie M. ;
Smith, Jeffrey S. ;
Brenner, Charles .
CELL, 2007, 129 (03) :473-484
[4]   Nicotinamide Riboside and Nicotinic Acid Riboside Salvage in Fungi and Mammals QUANTITATIVE BASIS FOR Urh1 AND PURINE NUCLEOSIDE PHOSPHORYLASE FUNCTION IN NAD+ METABOLISM [J].
Belenky, Peter ;
Christensen, Kathryn C. ;
Gazzaniga, Francesca ;
Pletnev, Alexandre A. ;
Brenner, Charles .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (01) :158-164
[5]  
BENSON DA, 2005, NUCLEIC ACIDS RES, V38, P33
[6]   Subcellular compartmentation and differential catalytic properties of the three human nicotinamide mononucleotide adenylyltransferase isoforms [J].
Berger, F ;
Lau, C ;
Dahlmann, M ;
Ziegler, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (43) :36334-36341
[7]   The new life of a centenarian:: signalling functions of NAD(P) [J].
Berger, F ;
Ramírez-Hernández, MH ;
Ziegler, M .
TRENDS IN BIOCHEMICAL SCIENCES, 2004, 29 (03) :111-118
[8]   Discoveries of nicotinamide riboside as a nutrient and conserved NRK genes establish a Preiss-Handler independent route to NAD+ in fungi and humans [J].
Bieganowski, P ;
Brenner, C .
CELL, 2004, 117 (04) :495-502
[9]   Eukaryotic NAD+ synthetase Qns1 contains an essential, obligate intramolecular thiol glutamine amidotransferase domain related to nitrilase [J].
Bieganowski, P ;
Pace, HC ;
Brenner, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (35) :33049-33055
[10]   Inhibition of silencing and accelerated aging by nicotinamide, a putative negative regulator of yeast Sir2 and human SIRT1 [J].
Bitterman, KJ ;
Anderson, RM ;
Cohen, HY ;
Latorre-Esteves, M ;
Sinclair, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (47) :45099-45107