Structures of three pectic arabinogalactans, one from
Vernonia kotschyana (Vk2a) and t
wo from
Cochlospermumtinctorium (Ct50A1 and Ct50A2), and their complement fixation and induction of B cell proliferation in vitro
were compared. The polysaccharide Vk2a expressed potent biological activity in both assays compared
withCt50A1 and Ct50A2. Vk2a possessed a very high molecular
weight (1150 ± 20 kDa) compared
with Ct50A1and Ct50A2
which both sho
wed a polydisperse nature
with the highest molecular
weight polymers in each fractionestimated at ~105 kDa (Ct1a) and 640 ± 100 kDa (Ct2a), respectively. The HMW polymers sho
wed complementfixation in the same range as the native fractions. The arabinogalactan II content
was lo
w in Vk2a (2%) compared
with that in Ct50A1 (23%) and Ct50A2 (12%). The high molecular
weight polymers
were subjected to digestion
with a
-
D-(1, 3)-galactanase-rich fraction from Driselase, oligomers
were isolated by HPAEC, and their finerstructures
were determined by MALDI- and ES-qoToF-MS, linkage, and monosaccharide composition analyses.Vk2a consists of both a galacturonan core and a rhamnogalacturonan core rich in neutral side chains. The backbonesof both Ct-polysaccharides consist mainly of RG-I regions
with numerous neutral side chains dominated bygalactosyl residues,
whereas the homogalacturonan regions seem to be small. Differences in the chain lengths ofthe 6-linked galacto-oligosaccharides attached to the 3-linked galactan core could not be related to the differencesin the potencies of the biological activities observed.