L-Glucose is an organic compound with formula C6H12O6 or H––(CHOH)5–H, specifically one of the aldohexose monosaccharides. As the L-isomer of glucose, it is the enantiomer of the more common D-glucose. L-Glucose does not occur naturally in higher living organisms, but can be synthesized in the laboratory. L-Glucose is indistinguishable in taste from D-glucose, but cannot be used by living organisms as 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, the enzyme D-threo-aldolse dehydrogenase is capable of oxidising L-glucose Like the 'D-' isomer, L-glucose usually occurs as one of four cyclic structural isomers — α- and β-L-glucopyranose, and α- and β-L-glucofuranose. In solution, these isomers interconvert in matters of hours, with the open-chain form as an intermediate stage.
The numerical value of l-glucose in Chaldean Numerology is: 6
The numerical value of l-glucose in Pythagorean Numerology is: 4
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