Ribulose
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| Fischer projection , open-chain representation | ||||||||||||||||
| General | ||||||||||||||||
| Surname | Ribulose | |||||||||||||||
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| Molecular formula | C 5 H 10 O 5 | |||||||||||||||
| Brief description |
colorless to yellowish viscous liquid |
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| Molar mass | 150.13 g · mol -1 | |||||||||||||||
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| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . | ||||||||||||||||
Ribulose is a simple sugar (monosaccharide) from the group of carbohydrates . Since it has five carbon atoms, ribulose is a pentose , and because of its keto group it is also a ketosis .
Occurrence
D- ribulose occurs naturally in all plants as a metabolic product. It is also a common metabolic intermediate in bacteria (as ribulose-5-phosphate ).
Manufacturing
D- ribulose can be obtained from D - arabinose in pyridine by epimerization .
properties
All pentoses have the empirical formula C 5 H 10 O 5 . Most monosaccharides can be both open-chain and ring-shaped. Because of the chirality of the molecule, there are two different stereoisomers ( D - and L -ribulose). Ribose and arabinose as aldopentoses are in tautomeric equilibrium with the ketopentose ribulose .
| D -Ribulosis - spellings | ||
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α- D -ribulofuranose |
β- D -ribulofuranose |
Biological importance
Ribulose is an important compound in the Calvin cycle , through which CO 2 is assimilated to glucose . For this so-called dark reaction of photosynthesis , energy gained from the light reaction is used. In the Calvin cycle, as D - ribulose-1,5-bisphosphate, it is the initial molecule that combines with carbon dioxide .
Individual evidence
- ↑ Entry on d-ribulose. In: Römpp Online . Georg Thieme Verlag, accessed on May 1, 2016.
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.