CONSTITUTION OF A GLUCOMANNAN FROM TAMARACK (LARIX LARICINA)
- 1 April 1961
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 39 (4) , 889-896
- https://doi.org/10.1139/v61-109
Abstract
A hemicellulose fraction containing D-mannose, D-glucose, and D-galactose in a ratio of 70:25:3 has been isolated from tamarack wood. The product was homogeneous under conditions of free boundary electrophoresis and of sedimentation in the ultracentrifuge. Hydrolysis of the fully methylated hemicellulose yielded 2,3,4,6-tetra-O-methyl-D-glucose (1.2%); 2,3,4,6-tetra-O-methyl-D-galactose (2.2%); 2,3,6-tri-O-methyl-D-glucose (24.0%); 2,3,6-tri-O-methyl-D-mannose (68.8%); 2,3-di-O-methyl-D-mannose (1.6%); and 2,3-di-O-methyl-D-glucose (1.7%). This data and that from periodate oxidation indicated that the glucomannan had a linear backbone of approximately 35 (1 → 4) linked β-D-glucopyranose and β-D-mannopyranose units; approximately two thirds of the chains were terminated at the non-reducing ends by D-galactose and the remainder by D-glucose. Branching, if present, must occur through C6 of the hexoses in the main chain.This publication has 16 references indexed in Scilit:
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