3-phosphoglyceric acid
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D -3-phosphoglyceric acid (protonated form of D -3-phosphoglycerate) | |||||||||||||
General | |||||||||||||
Surname | 3-phosphoglyceric acid | ||||||||||||
other names |
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Molecular formula | C 3 H 7 O 7 P | ||||||||||||
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properties | |||||||||||||
Molar mass | 186.06 g mol −1 | ||||||||||||
safety instructions | |||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
D -3-phosphoglyceric acid (also D -3-phosphoglycerate ) is an intermediate of gluconeogenesis and glycolysis as well as the end point of one of their byways, the Rapoport-Luebering cycle . It is produced by the reversible reaction of D - 1,3-bisphosphoglyceric acid and adenosine diphosphate (ADP) to adenosine triphosphate (ATP) and D -3-phosphoglyceric acid. This reaction is catalyzed by phosphoglycerate kinase . The phosphoglycerate mutase converts it to D - 2-phosphoglyceric acid .
D -3-phosphoglyceric acid is also an intermediate product of the Calvin cycle : The fixation of carbon dioxide is done by carboxylation of D -Ribulose-1,5-bisphosphate to an unstable intermediate which rapidly to two molecules of D -3-phosphoglyceric acid hydrolyzed is. This reaction is catalyzed by ribulose-1,5-bisphosphate carboxylase ( Rubisco for short ). D -3-phosphoglyceric acid reacts further with consumption of one molecule of ATP per molecule of D -3-phosphoglyceric acid to form D -1,3-biphosphoglyceric acid . This reacts further to D - glyceraldehyde-3-phosphate , from which energy-rich compounds such as z. B. D - glucose can be formed.
In addition, D -3-phosphoglyceric acid is an important precursor to the biosynthesis of the amino acids L - serine , L - cysteine and glycine .
The enantiomer L -3-phosphoglyceric acid has no biological significance.
literature
- Jeremy M. Berg, Lubert Stryer et al .: Biochemistry. 5th edition. Spektrum Akademischer Verlag, 2003, ISBN 3-8274-1303-6 , online version, full-text search
Individual evidence
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.