Glyceraldehyde

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Glyceraldehyde is a triose monosaccharide, or simple sugar, that plays a key role in many biochemical processes. It is the simplest of all common aldoses. Glyceraldehyde is a chiral molecule that can exist in either of two stereoisomers, D-glyceraldehyde and L-glyceraldehyde.

Structure and Properties[edit | edit source]

Glyceraldehyde is a three-carbon aldehyde. It is a chiral molecule, meaning it has two possible optical isomers, or stereoisomers. These are designated D-glyceraldehyde and L-glyceraldehyde. The D-isomer is the common form in nature.

Biological Role[edit | edit source]

Glyceraldehyde plays a key role in glycolysis, the metabolic pathway that converts glucose into pyruvate. It is also involved in the Calvin cycle, which is the light-independent reactions of photosynthesis.

Synthesis[edit | edit source]

Glyceraldehyde can be synthesized in the laboratory by the oxidation of glycerol, the triol that is the backbone of many lipids.

Health Implications[edit | edit source]

In the human body, glyceraldehyde can be converted to glycerol, which can then be used to produce triglycerides, a type of fat. High levels of triglycerides in the blood can increase the risk of heart disease.

See Also[edit | edit source]

Glyceraldehyde Resources
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Contributors: Prab R. Tumpati, MD