Ketose

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A type of monosaccharide containing a ketone group



Ketose is a type of monosaccharide (simple sugar) that contains a ketone group. Ketoses are important in various biological processes and are found in many natural sources. Unlike aldoses, which contain an aldehyde group, ketoses have a carbonyl group (C=O) located at the second carbon atom of the sugar chain.

Structure[edit | edit source]

Ketoses are characterized by the presence of a ketone group, which is a carbon atom double-bonded to an oxygen atom (C=O). This group is typically located at the second carbon atom in the sugar chain, distinguishing ketoses from aldoses, where the carbonyl group is at the terminal carbon.

Common Ketoses[edit | edit source]

Some common ketoses include:

  • Dihydroxyacetone - The simplest ketose, with the chemical formula C_H_O_. It is a triose, meaning it contains three carbon atoms.
  • Fructose - A hexose sugar with the formula C_H__O_, commonly found in fruits and honey. It is one of the most important ketoses in human metabolism.
  • Ribulose - A pentose sugar with the formula C_H__O_, involved in the Calvin cycle of photosynthesis.

Biological Importance[edit | edit source]

Ketoses play crucial roles in various metabolic pathways. For example, fructose is a key player in the glycolysis pathway, where it is phosphorylated and converted into intermediates that enter the energy-producing cycles of the cell.

Metabolism[edit | edit source]

In the human body, ketoses are metabolized through pathways such as glycolysis and the pentose phosphate pathway. Fructose, for instance, is converted into fructose-1-phosphate by the enzyme fructokinase, and then further processed into intermediates that can be used for energy production or biosynthesis.

Sources[edit | edit source]

Ketoses are naturally found in various foods. Fructose, for example, is abundant in fruits, vegetables, and honey. It is also a component of sucrose, a disaccharide composed of glucose and fructose.

Chemical Properties[edit | edit source]

Ketoses can undergo isomerization to form aldoses through a process called tautomerization. This isomerization is facilitated by the presence of an enediol intermediate, allowing the conversion between the ketone and aldehyde forms.

Images[edit | edit source]

Structure of fructose, a common ketose.
Structure of dihydroxyacetone, the simplest ketose.

Related pages[edit | edit source]

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Contributors: Prab R. Tumpati, MD