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2005
DOI: 10.1111/j.1745-4522.2005.00016.x
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CHARACTERIZATION IN THE FATTY ACID DISTRIBUTIONS OF TRIACYLGLYCEROLS AND PHOSPHOLIPIDS IN KIDNEY BEANS (PHASEOLUS VULGARIS L.)

Abstract: The fatty acid distribution of triacylglycerols (TAGs) and major phospholipids (PLs) in kidney beans ( Phaseolus vulgaris L.) was investigated. The lipids extracted from five cultivars were separated by thin-layer chromatography (TLC) into seven fractions. The major lipid components were TAGs and PLs, while hydrocarbons (HCs), steryl esters (SEs), free fatty acids (FFAs) and diacylglycerols (DAGs) (sn-1,3 and sn-1,2) were also present in minor proportions. With a few exceptions, the dominant phospholipid compo… Show more

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Cited by 29 publications
(38 citation statements)
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“…The extracted lipids were weighed to determine the lipid content of the peas and then transferred to a 25-mL brown glass volumetric flask with chloroform/methanol (2 : 1, vol/vol) [9].…”
Section: Extraction Of Lipidsmentioning
confidence: 99%
“…The extracted lipids were weighed to determine the lipid content of the peas and then transferred to a 25-mL brown glass volumetric flask with chloroform/methanol (2 : 1, vol/vol) [9].…”
Section: Extraction Of Lipidsmentioning
confidence: 99%
“…3; Applied Science, State College, PA), using an electronic integrator (Shimadzu C-R6A). The other GC conditions were the same as described previously (12). The detection limit was 0.05% of total FA for each FAME in a FAME mixture, and results are expressed as the weight percentage (%) of total FAME.…”
Section: Methodsmentioning
confidence: 99%
“…The residue was dissolved in the mobile phase used for HPLC analysis (n-hexane/1,4-dioxane/ethanol, 490:10:1, by vol). The chromatographic system was the same as previously described (12) and operated at a flow rate of 2.0 mL/min. An aliquot (5-10 µL) of these solutions was injected with a fully loaded 20-µL loop onto the column.…”
Section: Methodsmentioning
confidence: 99%
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“…After phase separation, the chloroform layer was withdrawn, dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under vacuum with a rotary evaporator at 35 7C. The extracted lipids were weighed to determine the lipid content of the beans and then transferred to a 25-mL brown-glass volumetric flask with chloroform/methanol (2 : 1, vol/vol) [17].…”
Section: Extraction Of Lipidsmentioning
confidence: 99%