Page 20 - Academic Press Encyclopedia of Physical Science and Technology 3rd Polymer
P. 20

P1: FPP 2nd Revised Pages
 Encyclopedia of Physical Science and Technology  EN002C-64  May 19, 2001  20:39






               224                                                                                      Biopolymers


                  TABLE II Examples of Linear and Branched Homo- and Heteroglycans
                           Type               Common name                    Monosaccharide sequence
                  Homoglycans
                  Linear, one linkage type      Amylose            4)-α-D-Glc p-(1         4)-α-D -Glc p-(1
                                                Cellulose          4)-β-D-Glc p-(1         4)-β-D-Glc p-(1
                  Linear, more than one linkage type  Cereal β-glucan  3)-β-D-Glc p-(1         4)-β-D-Glc p-(1
                  Branched                     Amylopectin            4)-α-D-Glc p-(1         4)-α-D -Glc p-(1
                                                                            6

                                                                   4)-α-D-Glc p-1
                  Heteroglycans
                  Linear, one linkage type     Glucomannans        4)-β-D-Man p-(1         4)-β-D-Man p-(1         4)β-D -Glc p-(1
                  Linear, more than one linkage type  Hyaluronic acid  4)-β-D-Glc pA-(1         3)-β-D -Glc pNAC-(1
                  Branched                    Galactomannan        4)-β-D-Man p-(1         4)-β-D-Man p-(1
                                                                        6

                                                                 α-D-Gal p-1


               Typical examples (Table II) of the first group would be  of cellulose present on the earth at any one time. Some
               amylose or cellulose, containing only (1 → 4)-glycosidic  plant fibers, such as ramie, hemp, jute, and notably cotton
               bonds, and of the second group, cereal β-glucans with  seed hairs, contain from 60% to over 90% cellulose and
               both β-(1 → 3) and β-(1 → 4)-bonds. The most com-  can be used with minimum processing as textile fiber. In
               plex homoglycans are branched, as is the case for amy-  wood, however, cellulose exists in close association with
               lopectin, also a glucan. Heteroglycans contain at least  hemicelluloses and lignin (Section II.D) and harsh chem-
               two kinds of sugar unit, and the systematic name re-  ical treatments must be used to obtain cellulose, mainly
               flects the monomer composition. Again, the polysaccha-  for paper making.
               ride molecules may be linear, with one or more linkage  Cellulose molecules are unbranched chains of β-
               type, or branched. Examples of linear heteroglycans (Ta-  (1 → 4)-linked glucopyranose units up to 5000 residues
               ble  II)  are  glucomannans  where  glucose  and  mannose  long and are essentially rigid and extended. Individual
                                                                                              4
               residues are linked by β-(1 → 4)-bonds and hyaluronic  β-D-glucopyranose units adopt the C 1 chair conforma-
               acid (here a trivial name is commonly used) containing  tion. Within one molecule, the ribbon-like shape is sta-
               glucuronic acid and N-acetyl glucosamine joined by β-  bilized by hydrogen bonding between the ring oxygen of
               (1 → 3)-andβ-(1 → 4)-linkages.Branchedheteroglycans  one glucose unit and the OH on carbon three of the ad-
               can be much more complex, with one or more type of  jacent monomer residue, and also between the oxygen
               monosaccharide in the main chain and yet other sugars  on carbon six of the first glucose and the OH on car-
               in the branches, as is the case for plant pectins. With this  bon two of the adjacent residue. Cellulose molecules can
               degree of complexity, systematic nomenclature becomes  align themselves side by side, with adjacent chains run-
               difficult.                                         ning in the same direction; these sheets are stabilized by
                 The functions and uses of the most widely studied and  hydrogen bonds between the OH on carbon six of glu-
               commerciallyimportantpolysaccharidesaredescribedbe-  cose on one molecule and the oxygen on carbon three
               low, grouped according to source.                 of the closest glucose residue on an adjacent molecule.
                                                                 This structure is found in native, untreated cellulose and
                                                                 is called cellulose I. The forces between sheets are van der
                 3. Plant Polysaccharides
                                                                 Waals forces, but the sheets associate to form microfibrils.
               Cellulose and starch are undoubtedly the plant polysac-  These in turn aggregate to give fibers, which, in asso-
               charides of greatest importance, both in abundance and  ciation with other polysaccharides and proteins, are the
               economic impact. Both are homopolymers of D-glucose,  main structural components of plant cell walls. Cellulose
               i.e., glucans.                                    II is a form of cellulose obtained by chemical treatment
                 Cellulose is the most abundant biopolymer and is the  with, for example, alkali. Here chains run antiparallel to
               main structural material of the cell walls of higher plants.  one another and intermolecular hydrogen bonding differs
               It has been estimated that there are approximately 10 12  t  from that in cellulose I. Where structure is well-ordered,
   15   16   17   18   19   20   21   22   23   24   25