l-Glucose is an organic compound with formula C6H12O6 or O=CH[CH(OH)]5H, specifically one of the aldohexose monosaccharides. As the l-isomer of glucose, it is the enantiomer of the more common d-glucose.
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 Haworth projection of α-l-glucopyranose
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 Fischer projection of l-glucose
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| Names | |
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| IUPAC name
l-Glucose
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| Identifiers | |
3D model (JSmol)
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| Abbreviations | L-Glc |
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| ChemSpider | |
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PubChem CID
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| Properties | |
| C6H12O6 | |
| Molar mass | 180.156 g·mol−1 |
| Density | 1.54 g/cm3 |
| 91 g/100 mL | |
| Hazards | |
| Safety data sheet (SDS) | ICSC 0865 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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l-Glucose does not occur naturally in living organisms, but can be synthesized in the laboratory. l-Glucose is indistinguishable in taste from d-glucose,[1] but cannot be used by living organisms as a source of energy because it cannot be phosphorylated by hexokinase, the first enzyme in the glycolysis pathway. One of the known exceptions is in Burkholderia caryophylli, a plant pathogenic bacterium, which contains the enzyme d-threo-aldose 1-dehydrogenase which is capable of oxidizing l-glucose.[2]
Like the d-isomer, l-glucose usually occurs as one of four cyclic structural isomers—α- and β-l-glucopyranose (the most common, with a six-atom ring), and α- and β-l-glucofuranose (with a five-atom ring). In water solution, these isomers interconvert in matters of hours, with the open-chain form as an intermediate stage.
Uses
editl-Glucose was once proposed as a low-calorie sweetener and it is suitable for patients with diabetes mellitus, but it was never marketed due to excessive manufacturing costs.[1]
The acetate derivative of l-glucose, l-glucose pentaacetate, was found to stimulate insulin release, and might therefore be of therapeutic value for type 2 diabetes.[3] l-Glucose was also found to be a laxative, and has been proposed as a colon-cleansing agent which would not produce the disruption of fluid and electrolyte levels associated with the significant liquid quantities of bad-tasting osmotic laxatives conventionally used in preparation for colonoscopy.[4]
References
edit- ^ a b A Natural Way to Stay Sweet, NASA, retrieved 2009-09-02.
- ^ Sasajima, K.; Sinskey, A. (1979). "Oxidation of l-glucose by a Pseudomonad". Biochimica et Biophysica Acta (BBA) - Enzymology. 571 (1): 120–126. doi:10.1016/0005-2744(79)90232-8. PMID 40609.120-126&rft.date=1979&rft_id=info:doi/10.1016/0005-2744(79)90232-8&rft_id=info:pmid/40609&rft.aulast=Sasajima&rft.aufirst=K.&rft.au=Sinskey, A.&rfr_id=info:sid/en.wikipedia.org:L-Glucose" class="Z3988">
- ^ Malaisse, W. J. (1998), "The riddle of L-glucose pentaacetate insulinotropic action", Int. J. Mol. Med., 2 (4): 383–88, doi:10.3892/ijmm.2.4.383, PMID 9857221, archived from the original on 2011-07-16383-88&rft.date=1998&rft_id=info:doi/10.3892/ijmm.2.4.383&rft_id=info:pmid/9857221&rft.aulast=Malaisse&rft.aufirst=W. J.&rft_id=http://www.biomedexperts.com/Abstract.bme/9857221/The_riddle_of_L-glucose_pentaacetate_insulinotropic_action_review&rfr_id=info:sid/en.wikipedia.org:L-Glucose" class="Z3988">.
- ^ Raymer, Geoffrey S.; Hartman, Donald E.; Rowe, William A.; Werkman, Robert F.; Koch, Kenneth L. (2003), "An open-label trial of L-glucose as a colon-cleansing agent before colonoscopy", Gastrointest. Endosc., 58 (1): 30–35, doi:10.1067/mge.2003.293, PMID 1283821730-35&rft.date=2003&rft_id=info:doi/10.1067/mge.2003.293&rft_id=info:pmid/12838217&rft.aulast=Raymer&rft.aufirst=Geoffrey S.&rft.au=Hartman, Donald E.&rft.au=Rowe, William A.&rft.au=Werkman, Robert F.&rft.au=Koch, Kenneth L.&rfr_id=info:sid/en.wikipedia.org:L-Glucose" class="Z3988">
External links
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Media related to L-Glucose at Wikimedia Commons
