Cl. Delgobo et al., GUM HETEROPOLYSACCHARIDE AND FREE REDUCING MONOSACCHARIDES AND OLIGOSACCHARIDES OF ANADENANTHERA-COLUBRINA, Phytochemistry, 47(7), 1998, pp. 1207-1214
The gum from Anadenanthera colubrina consists mainly of a complex high
-arabinose heteropolysaccharide with a (1-->3)-linked beta-D-Galp main
-chain and many different side-chains. These contain beta-D-Galp-[(1--
>6)-beta-D-Galp](m)-(1-->6)-, substituted in turn at O-3 by alpha-L-Ar
af-[(1-->3)-alpha-L-Araf-](0.2). Also present are (1) main-chain units
substituted at O-4 and O-6 by alpha-L-Araf units, (2) side-chains of
hap-(1-->4)-beta-D-GlcpA-(1-->6)-beta-Galp-groups, (3) alpha-L-Arap no
n-reducing end-units linked (1-->6) to D-Galp, and (4) beta-Araf and b
eta-Arap structures. For the first time, a plant gum exudate was found
to contain in the natural state, reducing low M-r carbohydrates. Thes
e were rhamnose (0.6%), arabinose (4.7%), mannose (0.1%), galactose (0
.8%) and many oligosaccharides (0.6%; 11 with different R(F)s with the
majority containing arabinose). They were all mixtures with the excep
tion of alpha-Rhap-(1-->4)-beta-D-GlcpA-(1-->6)-alpha beta-Gal and an
incompletely identified hexasaccharide, probably having alpha-L-Araf-(
1-->4)-beta-D-Galp- and -alpha-L-Araf-(1-->3)-beta-D-Galp-structures.
The mono- and oligosaccharides do not appear to arise via in situ auto
hydrolysis of the gum. (C) 1998 Published by Elsevier Science Ltd. All
rights reserved.