When grown in sorbitol-asparagine-salts medium, cells of Erwinia amylo
vora isolate T83 released a mixture of oligosaccharides and lipopolysa
ccharide in place of extracellular polysaccharide. The oligosaccharide
fraction was usually readily separable from lipopolysaccharide by gel
permeation chromatography, but some samples required disaggregation b
y preliminary treatment with EDTA. By H-1- and C-13-NMR spectroscopy,
methylation analysis and mass spectrometry, the oligosaccharide fracti
on was shown to consist of terminal, beta-1,2- and beta-1,2,6-linked D
-glucose residues in the ratio 2.2:2.6:1, indicating a branched oligos
accharide structure. The purified oligosaccharide fraction was partial
ly resolved by gel permeation chromatography into two components conta
ining approximately equal amounts of glucose. When grown on pear slice
s, isolate T83 produced normal extracellular polysaccharide.