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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1981-6-13
pubmed:abstractText
Pure 3-sn-monogalactosyldilinolenoylglycerol and 3-sn-digalactosyldilinolenoylglycerol have been isolated from bean leaves. Distearoyl derivatives have been prepared by catalytic hydrogenation of the unsaturated galactolipids. The unsaturated lipids form stable monomolecular films at the air/water interface which are similar to liquid-expanded phospholipid monolayers. The limiting areas were about 0.57 nm2 and 0.62 nm2 for the mono- and digalactosyldiacylglycerols, respectively. The saturated galactolipids formed condensed monolayers that were relatively unstable. The surface pressure-area isotherm of the digalactosyl derivative was more expanded than that of the monogalactosyldiacylglycerol especially at low surface pressures. Low-angle X-ray diffraction and freeze-fracture electron microscopy studies of the monogalactosyldiacylglycerols showed that an hexagonal-type structure was formed by the unsaturated lipid in aqueous systems, whilst the saturated lipid was arranged in a lamellar configuration. Both digalactosyldiacylglycerols form lamellar structures in water. A gel-to-liquid-crystalline phase transition of distearoyldigalactosylglycerol was observed at about 51 degrees C by fluorescence depolarization measurements, using 1,6-diphenylhexatriene, and by differential scanning calorimetry. The saturated monogalactosyldiacylglycerol did not form dispersions suitable for fluorescence probe studies of a phase transition. A complex pattern of endotherms was observed for this lipid by differential scanning calorimetry.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0006-3002
pubmed:author
pubmed:issnType
Print
pubmed:day
23
pubmed:volume
663
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
380-9
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed:year
1981
pubmed:articleTitle
The structure and thermotropic properties of pure 1,2-diacylgalactosylglycerols in aqueous systems.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't