Why did Nature select phosphate for its dominant roles in biology?

被引:149
作者
Bowler, Matthew W. [2 ]
Cliff, Matthew J. [1 ]
Waltho, Jonathan P. [1 ]
Blackburn, G. Michael [1 ]
机构
[1] Univ Sheffield, Krebs Inst, Dept Mol Biol & Biotechnol, Sheffield S10 2TN, S Yorkshire, England
[2] European Synchrotron Radiat Facil, Struct Biol Grp, F-38043 Grenoble, France
基金
英国生物技术与生命科学研究理事会;
关键词
TRANSITION-STATE; PHOSPHORYL TRANSFER; ORGANIC PHOSPHATES; HYDROLYSIS; PROTEIN; PROFICIENCIES; NUCLEOTIDES; MECHANISM; SULFATION; GEOMETRY;
D O I
10.1039/b9nj00718k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Evolution has placed phosphate mono- and diesters at the heart of biology. The enormous diversity of their roles has called for the evolution of enzyme catalysts for phosphoryl transfer that are among the most proficient known. A combination of high-resolution X-ray structure analysis and F-19 NMR definition of metal fluoride complexes of such enzymes, that are mimics of the transition state for the reactions catalysed, has delivered atomic detail of the nature of such catalysis for a range of phosphoryl transfer processes. The catalytic simplicity thus revealed largely explains the paradox of the contrast between the extreme stability of structural phosphate esters and the lability of phosphates in regulation and signalling processes. A brief survey of the properties of oxyacids and their esters for other candidate elements for these vital roles fails to identify a suitable alternative to phosphorus, thereby underpinning Todd's Hypothesis "Where there's life there's phosphorus" as a statement of truly universal validity.
引用
收藏
页码:784 / 794
页数:11
相关论文
共 52 条
[1]  
Arnett D., 1996, Supernovae and Nucleosynthesis: An Investigation of the History of Matter from the Big Bang to the Present
[2]   SYNTHESIS OF ADENOSINE TRIPHOSPHATE [J].
BADDILEY, J ;
MICHELSON, AM ;
TODD, AR .
NATURE, 1948, 161 (4098) :761-762
[3]   Anionic charge is prioritized over geometry in aluminum and magnesium fluoride transition state analogs of phosphoryl transfer enzymes [J].
Baxter, Nicola J. ;
Blackburn, G. Michael ;
Marston, James P. ;
Hounslow, Andrea M. ;
Cliff, Matthew J. ;
Bermel, Wolfgang ;
Williams, Nicholas H. ;
Hollfelder, Florian ;
Wemmer, David E. ;
Waltho, Jonathan P. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (12) :3952-3958
[4]   MgF3- and α-Galactose 1-Phosphate in the Active Site of β-Phosphoglucomutase Form a Transition State Analogue of Phosphoryl Transfer [J].
Baxter, Nicola J. ;
Hounslow, Andrea M. ;
Bowler, Matthew W. ;
Williams, Nicholas H. ;
Blackburn, G. Michael ;
Waltho, Jonathan P. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (45) :16334-+
[5]  
BAXTER NJ, 2010, P NATL ACAD IN PRESS
[7]   MECHANISM OF HYDROLYSIS OF DIETHYL 2-CARBOXYPHENYLPHOSPHONATE [J].
BLACKBURN, GM ;
BROWN, MJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1969, 91 (02) :525-+
[8]   Temporal analysis of phosphotyrosine-dependent signaling networks by quantitative proteomics [J].
Blagoev, B ;
Ong, SE ;
Kratchmarova, I ;
Mann, M .
NATURE BIOTECHNOLOGY, 2004, 22 (09) :1139-1145
[9]  
Bowler M. E., UNPUB
[10]   THE REACTIONS OF ORGANIC PHOSPHATES .1. THE HYDROLYSIS OF METHYL DIHYDROGEN PHOSPHATE [J].
BUNTON, CA ;
LLEWELLYN, DR ;
OLDHAM, KG ;
VERNON, CA .
JOURNAL OF THE CHEMICAL SOCIETY, 1958, (OCT) :3574-3587