Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 6 March 1987:
Vol. 235. no. 4793, pp. 1173 - 1178
DOI: 10.1126/science.2434996

Articles

Science, Vol 235, Issue 4793, 1173-1178
Copyright © 1987 by American Association for the Advancement of Science


articles

Why nature chose phosphates

FH Westheimer

Phosphate esters and anhydrides dominate the living world but are seldom used as intermediates by organic chemists. Phosphoric acid is specially adapted for its role in nucleic acids because it can link two nucleotides and still ionize; the resulting negative charge serves both to stabilize the diesters against hydrolysis and to retain the molecules within a lipid membrane. A similar explanation for stability and retention also holds for phosphates that are intermediary metabolites and for phosphates that serve as energy sources. Phosphates with multiple negative charges can react by way of the monomeric metaphosphate ion PO3- as an intermediate. No other residue appears to fulfill the multiple roles of phosphate in biochemistry. Stable, negatively charged phosphates react under catalysis by enzymes; organic chemists, who can only rarely use enzymatic catalysis for their reactions, need more highly reactive intermediates than phosphates.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Diphosphoinositol Polyphosphates: Metabolic Messengers?.
S. B. Shears (2009)
Mol. Pharmacol. 76, 236-252
   Abstract »    Full Text »    PDF »
The Role of Biomacromolecular Crowding, Ionic Strength, and Physicochemical Gradients in the Complexities of Life's Emergence.
J. Spitzer and B. Poolman (2009)
Microbiol. Mol. Biol. Rev. 73, 371-388
   Abstract »    Full Text »    PDF »
A recurrent magnesium-binding motif provides a framework for the ribosomal peptidyl transferase center.
C. Hsiao and L. D. Williams (2009)
Nucleic Acids Res. 37, 3134-3142
   Abstract »    Full Text »    PDF »
The Global Phosphorus Cycle: Past, Present, and Future.
G. M. Filippelli (2008)
Elements 4, 89-95
   Abstract »    Full Text »    PDF »
Rethinking early Earth phosphorus geochemistry.
M. A. Pasek (2008)
PNAS 105, 853-858
   Abstract »    Full Text »    PDF »
Nucleoside Phosphorylation by Phosphate Minerals.
G. Costanzo, R. Saladino, C. Crestini, F. Ciciriello, and E. Di Mauro (2007)
J. Biol. Chem. 282, 16729-16735
   Abstract »    Full Text »    PDF »
Phosphorus in prebiotic chemistry.
A. W Schwartz (2006)
Phil Trans R Soc B 361, 1743-1749
   Abstract »    Full Text »    PDF »
Potent Mechanism-based Inhibitors for Matrix Metalloproteinases.
M. Ikejiri, M. M. Bernardo, R. D. Bonfil, M. Toth, M. Chang, R. Fridman, and S. Mobashery (2005)
J. Biol. Chem. 280, 33992-34002
   Abstract »    Full Text »    PDF »
Semipermeable lipid bilayers exhibit diastereoselectivity favoring ribose.
M. G. Sacerdote and J. W. Szostak (2005)
PNAS 102, 6004-6008
   Abstract »    Full Text »    PDF »
Ribozyme speed limits.
G. M. EMILSSON, S. NAKAMURA, A. ROTH, and R. R. BREAKER (2003)
RNA 9, 907-918
   Abstract »    Full Text »    PDF »
Metaphosphate in the Active Site of Fructose-1,6-bisphosphatase.
J.-Y. Choe, C. V. Iancu, H. J. Fromm, and R. B. Honzatko (2003)
J. Biol. Chem. 278, 16015-16020
   Abstract »    Full Text »    PDF »
Peptide nucleic acids rather than RNA may have been the first genetic molecule.
K. E. Nelson, M. Levy, and S. L. Miller (2000)
PNAS 97, 3868-3871
   Abstract »    Full Text »    PDF »
Chemical Etiology of Nucleic Acid Structure.
A. Eschenmoser (1999)
Science 284, 2118-2124
   Abstract »    Full Text »
RNA-dependent phosphorylation of a nuclear RNA binding protein.
P. A. Fung, R. Labrecque, and T. Pederson (1997)
PNAS 94, 1064-1068
   Abstract »    Full Text »    PDF »
The X-ray Crystal Structures of Yersinia Tyrosine Phosphatase with Bound Tungstate and Nitrate. MECHANISTIC IMPLICATIONS.
E. B. Fauman, C. Yuvaniyama, H. L. Schubert, J. A. Stuckey, and M. A. Saper (1996)
J. Biol. Chem. 271, 18780-18788
   Abstract »    Full Text »    PDF »
The Structural Basis of the Myosin ATPase Activity.
I. Rayment and I. Rayment (1996)
J. Biol. Chem. 271, 15850-15853
   Full Text »    PDF »
Metal Dependence of Transcriptional Switching in Escherichia coli Ada.
L. C. Myers, F.ço. Jackow, and G. L. Verdine (1995)
J. Biol. Chem. 270, 6664-6670
   Abstract »    Full Text »    PDF »
Stereochemistry of RNA cleavage by the Tetrahymena ribozyme and evidence that the chemical step is not rate-limiting.
J. McSwiggen and T. Cech (1989)
Science 244, 679-683
   Abstract »    PDF »
DNA and RNA sequence determination based on phosphorothioate chemistry.
G Gish and F Eckstein (1988)
Science 240, 1520-1522
   Abstract »    PDF »
Summary.
A.M. Weiner (1987)
Cold Spring Harb Symp Quant Biol 52, 933-941
   Abstract »    PDF »
Conformational Changes in Four Regions of the Escherichia coli ArsA ATPase Link ATP Hydrolysis to Ion Translocation.
T. Zhou, S. Radaev, B. P. Rosen, and D. L. Gatti (2001)
J. Biol. Chem. 276, 30414-30422
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)