Wheat flour lipids: III. structure of the mono- and digalactosylglycerol lipids*

Determination of the structures of the mono- and digalactosylglycerol lipids of wheat flour is reported. Methylation of these lipids, followed by alkaline saponification, yielded partially methylated derivatives. Periodate oxidation of these substances in each case gave 1 mole uptake with the format...

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Main Authors: H.E. Carter, R.A. Hendry, N.Z. Stanacev
Format: Article
Language:English
Published: Elsevier 1961-07-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520390088
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spelling doaj-e9061e1f73ec4902bfb53cf006f678562021-04-23T06:10:49ZengElsevierJournal of Lipid Research0022-22751961-07-0123223227Wheat flour lipids: III. structure of the mono- and digalactosylglycerol lipids*H.E. Carter0R.A. Hendry1N.Z. Stanacev2Division of Biochemistry, Noyes Laboratory of Chemistry, University of Illinois, Urbana, IllinoisDivision of Biochemistry, Noyes Laboratory of Chemistry, University of Illinois, Urbana, IllinoisDivision of Biochemistry, Noyes Laboratory of Chemistry, University of Illinois, Urbana, IllinoisDetermination of the structures of the mono- and digalactosylglycerol lipids of wheat flour is reported. Methylation of these lipids, followed by alkaline saponification, yielded partially methylated derivatives. Periodate oxidation of these substances in each case gave 1 mole uptake with the formation of formaldehyde. These data establish the presence of two vicinal hydroxyls in the glycerol residue: and strongly indicate that in the original lipid the two acyl groups are attached to these hydroxyl groups. This assignment was confirmed by acidic hydrolysis studies. The monogalactosylglycerol derivative gave 2,3,4,6-tetra-O-methy1-d-galactose plus glycerol; the digalactosylglycerol derivative yielded, in addition, 2,3,4-tri-O-methyl-d-galactose. In a control experiment, free digalactosylglycerol was methylated and hydrolyzed, giving only on papergrams 2,3,4tri-O-methyl- and 2,3,4,6-tetra-O-methyl-d-galactose. These results clearly define the structure of the galactosylglycerol lipids as a 2,3-diglyceride with a carbohydrate moiety attached in the 1-position. Infrared data suggest the d-configuration for the glycerol residue.http://www.sciencedirect.com/science/article/pii/S0022227520390088
collection DOAJ
language English
format Article
sources DOAJ
author H.E. Carter
R.A. Hendry
N.Z. Stanacev
spellingShingle H.E. Carter
R.A. Hendry
N.Z. Stanacev
Wheat flour lipids: III. structure of the mono- and digalactosylglycerol lipids*
Journal of Lipid Research
author_facet H.E. Carter
R.A. Hendry
N.Z. Stanacev
author_sort H.E. Carter
title Wheat flour lipids: III. structure of the mono- and digalactosylglycerol lipids*
title_short Wheat flour lipids: III. structure of the mono- and digalactosylglycerol lipids*
title_full Wheat flour lipids: III. structure of the mono- and digalactosylglycerol lipids*
title_fullStr Wheat flour lipids: III. structure of the mono- and digalactosylglycerol lipids*
title_full_unstemmed Wheat flour lipids: III. structure of the mono- and digalactosylglycerol lipids*
title_sort wheat flour lipids: iii. structure of the mono- and digalactosylglycerol lipids*
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1961-07-01
description Determination of the structures of the mono- and digalactosylglycerol lipids of wheat flour is reported. Methylation of these lipids, followed by alkaline saponification, yielded partially methylated derivatives. Periodate oxidation of these substances in each case gave 1 mole uptake with the formation of formaldehyde. These data establish the presence of two vicinal hydroxyls in the glycerol residue: and strongly indicate that in the original lipid the two acyl groups are attached to these hydroxyl groups. This assignment was confirmed by acidic hydrolysis studies. The monogalactosylglycerol derivative gave 2,3,4,6-tetra-O-methy1-d-galactose plus glycerol; the digalactosylglycerol derivative yielded, in addition, 2,3,4-tri-O-methyl-d-galactose. In a control experiment, free digalactosylglycerol was methylated and hydrolyzed, giving only on papergrams 2,3,4tri-O-methyl- and 2,3,4,6-tetra-O-methyl-d-galactose. These results clearly define the structure of the galactosylglycerol lipids as a 2,3-diglyceride with a carbohydrate moiety attached in the 1-position. Infrared data suggest the d-configuration for the glycerol residue.
url http://www.sciencedirect.com/science/article/pii/S0022227520390088
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AT rahendry wheatflourlipidsiiistructureofthemonoanddigalactosylglycerollipids
AT nzstanacev wheatflourlipidsiiistructureofthemonoanddigalactosylglycerollipids
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