Deoxy sugar

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File:Ribofuranose-2D-skeletal.png

File:Deoxyribose.svg
Comparison of the chemical
structures of ribose (top)
and deoxyribose (bottom).
File:Fucose2.png
fucose

Deoxy sugars are sugars that have had a hydroxyl group replaced with a hydrogen atom.[1]

Examples include:

In Escherichia coli bacteria, deoxyribose sugars are synthesized via two different pathways - one pathway involves aldol condensation, whereas the other pathway is conversion of a ribose sugar into a deoxyribose sugar by means of changes on the nucleotide or nucleoside level. Deoxyribose is synthesized through the reduction of ribose. Deoxyribose is derived from the same precursor as ribose being that the reduction of the sugar with the extra hydroxyl group results in the deoxy-sugar, which has its hydroxyl group replaced with a hydrogen atom.[2]

Dideoxy sugars

Some biologically important dideoxy sugars, sugars that have had two hydroxyl groups replaced with hydrogen atoms, include colitose, abequose, tyvelose, and paratose. These may be found in bacterial lipopolysaccharides[3]

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Colitose
(3,6-Dideoxy-L-xylo-hexose)
Abequose
(3,6-Dideoxy-D-xylo-hexose)

See also

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content.Lichtenthaler, Frieder W. (2010). "Carbohydrates: Occurrence, Structures and Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a05_079.pub2. ISBN 978-3-527-30385-4.
  2. ^ Page Module:Citation/CS1/styles.css has no content.Sable, Henry Z.; Wright, Elmer M.; Bagatell, Fillmore K. (1959-06-01). "Biosynthesis of Ribose and Deoxyribose in Escherichia coli". Journal of Biological Chemistry. 234 (6): 1369–1374. doi:10.1016/S0021-9258(18)70013-6. ISSN 1083-351X. PMID 13654380.
  3. ^ Page Module:Citation/CS1/styles.css has no content.McGraw-Hill encyclopedia of science & technology. Vol. 2 (11th ed.). New York, NY: McGraw-Hill. 2012. p. 550. ISBN 978-0-07-179273-8.

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