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 Encyclopedia of Physical Science and Technology  EN006P-81  June 29, 2001  21:48




















                                                           Glycoconjugates and



                                                                          Carbohydrates






              Eugene A. Davidson

              Georgetown University School of Medicine



               I. Monosaccharides
              II. Oligosaccharides
              III. Polysaccharides
              IV. Glycoconjugates
              V. Analytical Methods







              GLOSSARY                                            a single asymmetric center. Thus, D-galactose is the
                                                                  4-epimer of D-glucose.
              Aglycone Group attached to the hydroxyl of a furanose  Furanose Five-membered ring (derived from furan) with
                or pyranose sugar to form a glycoside. Can vary from  a single oxygen formed by reaction of the carbonyl
                a simple methyl group to other sugars to complex  carbon of an aldose or ketose with the appropriate hy-
                alkaloids.                                        droxyl group. Sugars commonly found as furanoses
              Aldose Polyhydroxy aldehyde with three or more car-  include ribose and 2-deoxyribose (in RNA and DNA,
                bon atoms. When of sufficient length will form five-  respectively), and fructose in combined form (sucrose,
                or six-membered ring (furanose or pyranose) hemiac-  for example).
                etals. Designated D-or L- based on the configuration of  Glycolipid Structure containing one or more saccharide
                the asymmetric center furthest from the carbonyl group  units covalently attached to the primary hydroxyl group
                relative to glyceraldehyde.                       of N-acyl sphingosine (ceramide), a C-18 amino alco-
              Anomer Formation of the cyclic ring structure confers  hol. Those containing sialic acid are termed ganglio-
                asymmetry on the original carbonyl carbon atom. The  sides.
                two anomers produced are alpha- (the newly formed  Glycoprotein Protein with covalently attached saccha-
                hydroxyl group projects on the same side as the five- or  rides. Linkage may be N- (amide nitrogen of aspara-
                six-membered ring) or beta- (the new hydroxyl projects  gine residues), or O- (serine and threonine are most
                on the opposite side of the newly formed ring). This  common). The saccharide units may be heterogeneous
                is combined with D-, or L-; α-D-glucopyranose, β-L-  within the same protein, even at the identical substitu-
                fructofuranose, for example.                      tion site.
              Epimer Saccharide that differs from a reference sugar at  Glycosaminoglycan  Polysaccharide  chain  found  in



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