Dihydroxyacetone phosphate. Its structure and reactivity with -glycerophosphate dehydrogenase, aldolase and triose phosphate isomerase and some possible metabolic implications
- PMID: 4330197
- PMCID: PMC1176777
- DOI: 10.1042/bj1220285
Dihydroxyacetone phosphate. Its structure and reactivity with -glycerophosphate dehydrogenase, aldolase and triose phosphate isomerase and some possible metabolic implications
Abstract
1. Dihydroxyacetone phosphate exists in neutral aqueous solution at 20 degrees C as a mixture of keto, gem-diol and enolic forms in the ratio 55:44:1. 2. The three forms are freely interconvertible and rate constants for these reactions have been determined. 3. Keto-dihydroxyacetone phosphate is the primary reactive species in the reactions catalysed by alpha-glycerophosphate dehydrogenase, aldolase and triose phosphate isomerase. 4. The proportion of keto form to gem-diol forms of dihydroxyacetone phosphate is temperature-dependent. At 37 degrees C, 83% is keto-dihydroxyacetone phosphate. 5. The enzymological and metabolic consequences of these results are discussed.
Similar articles
-
The active chemical state of D-glyceraldehyde 3-phosphate in its reactions with D-glyceraldehyde 3-phosphate dehydrogenase, aldolase and triose phosphate isomerase.Biochem J. 1969 Aug;114(1):19-24. doi: 10.1042/bj1140019. Biochem J. 1969. PMID: 4309306 Free PMC article.
-
Haloacetol phosphates. Potential active-site reagents for aldolase, triose phosphate isomerase, and glycerophosphate dehydrogenase. I. Preparation and properties.Biochemistry. 1970 Apr 14;9(8):1776-82. doi: 10.1021/bi00810a017. Biochemistry. 1970. PMID: 5439038 No abstract available.
-
Proton exchange of the pro-S hydrogen at C-1 in dihydroxyacetone phosphate, D-fructose 1,6-bisphosphate and D-fructose 1-phosphate catalysed by rabbit-muscle aldolase.Eur J Biochem. 1976 Jun 15;66(1):95-104. doi: 10.1111/j.1432-1033.1976.tb10429.x. Eur J Biochem. 1976. PMID: 954748 No abstract available.
-
Disequilibrium in the triose phosphate isomerase system in rat liver.Biochem J. 1969 Dec;115(4):837-42. doi: 10.1042/bj1150837. Biochem J. 1969. PMID: 5357024 Free PMC article.
-
FROM THE TRIOSES TO THE SYNTHESIS OF NATURAL PHOSPHOLIPIDS: A RESEARCH TRIAL OF FORTY YEARS.J Am Oil Chem Soc. 1965 Apr;42:257-66. doi: 10.1007/BF02540126. J Am Oil Chem Soc. 1965. PMID: 14279109 Review. No abstract available.
Cited by
-
Thiol-catalyzed formation of lactate and glycerate from glyceraldehyde.J Mol Evol. 1983;19(3-4):237-43. doi: 10.1007/BF02099971. J Mol Evol. 1983. PMID: 6887266
-
A substrate in pieces: allosteric activation of glycerol 3-phosphate dehydrogenase (NAD+) by phosphite dianion.Biochemistry. 2008 Apr 22;47(16):4575-82. doi: 10.1021/bi8001743. Epub 2008 Apr 1. Biochemistry. 2008. PMID: 18376850 Free PMC article.
-
Enzyme-substrate and enzyme-inhibitor complexes of triose phosphate isomerase studied by 31P nuclear magnetic resonance.Biochem J. 1979 Jun 1;179(3):607-21. doi: 10.1042/bj1790607. Biochem J. 1979. PMID: 38777 Free PMC article.
-
Oxygen Isotope Exchange between Metabolites and Water during Biochemical Reactions Leading to Cellulose Synthesis.Plant Physiol. 1986 Oct;82(2):423-7. doi: 10.1104/pp.82.2.423. Plant Physiol. 1986. PMID: 16665045 Free PMC article.
-
Synthetic Biomaterials from Metabolically Derived Synthons.Chem Rev. 2016 Feb 24;116(4):2664-704. doi: 10.1021/acs.chemrev.5b00465. Epub 2016 Jan 29. Chem Rev. 2016. PMID: 26821863 Free PMC article. Review.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials