- Pentose
A pentose is a
monosaccharide with fivecarbon atom s.They either have an
aldehyde functional group in position 1 (aldopentoses), or aketone functional group in position 2 (ketopentoses).The aldopentoses have three chiral centres ("asymmetric carbon atoms") and so 8 different
stereoisomer s are possible.The 4 D-aldopentoses are:
CH=O CH=O CH=O CH=O
| |
HC-OH HO-CH HC-OH HO-CH
| |
HC-OH HC-OH HO-CH HO-CH
| |
HC-OH HC-OH HC-OH HC-OH
| |
CH2OH CH2OH CH2OH CH2OH D-Ribose D-Arabinose D-Xylose D-Lyxose The ketopentoses have 2 chiral centres and therefore 4 possible stereoisomers —
ribulose (L- and D-form) andxylulose (L- and D-form).The D-isomers of both are known to occur naturally as is the L-isomer of
xylulose : CH2OH CH2OH
| C=O C=O
| HC-OH HO-CH
| HC-OH HC-OH
| CH2OH CH2OH D-Ribulose D-Xylulose The aldehyde and ketone functional groups in these carbohydrates react with neighbouring
hydroxyl functional groups to formintramolecular hemiacetal s orhemiketal s, respectively. The resulting ring structure is related tofuran , and is termed afuranose . The ring spontaneously opens and closes, allowing rotation to occur about the bond between the carbonyl group and the neighbouring carbon atom — yielding two distinct configurations (α and β). This process is termedmutarotation .Ribose is a constituent ofRNA , and the relateddeoxyribose ofDNA .A
polymer composed of pentose sugars is called a pentosan.See also
*
Triose
*Tetrose
*Hexose
*Heptose
*Pentose phosphate pathway
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