The lipids of an untreated white flour, which had been milled commercially from Canadian wheat, were extracted a t -23" with chloroform-methanol and freed from contaminating non-lipids (including lipophilic protein) by means of aqueous potassium citrate. They were then eluted on a preparative scale from columns of silicic acid, using continuous, concave gradients of methanol in chloroform and also pure methanol. The fractions obtained were examined by infra-red and chemical methods, and by chromatography on aminoethylated paper. Eleven known classes of polar lipids were identified, each class being estimated to account for between I yo and 15% of the flour lipids. Other classes were detected but remain unidentified.
IntroductionAlthough the lipids of wheat flour normally constitute less than 2% of the weight of the flour, they are a complex mixture, including glycerides, glycolipids, phospholipids, sterols and free fatty acids, and they have important functions in bakery products. [1][2][3][4][5] Understanding their functions must ultimately depend upon knowledge of their chemical structures, physical properties, and amounts. In large measure by means of chromatography on silicic acid, much has recently been learnt about the classes of lipids present in flour ; gas chromatography has also yielded much information on the fatty acid composition of whole extracts and some separate classes.Roughly half of the flour lipids are so-called ' polar ' lipids-that is, those more polar than free long-chain fatty acids-which are considered to be of more functional importance than the others because they have more potential in surface phenomena and in interactions with starch and gluten. The aims of the studies to be described were, firstly, fractionation of the polar lipids on a relatively large scale (for future physical and functional studies) and, secondly, their characterisation by chemical and other means.Extraction was carried out at low temperature and non-lipid contaminants, including lipophilic protein, were removed from the extracted lipid by a new washing technique. The lipid was fractionated on silicic acid columns by elution with a continuous, concave which gave better resolution than that achieved with continuous, convex gradientss-11 or discontinuous gradient^.^^ [12][13][14][15][16] Infra-red monitoring of the effluents1' minimised the work required to locate peaks in repeated experiments. Because an antioxidant was incorporated in the solvents usedl8 the effluents were stable, and the lipids could be safely stored in solution at low temperature. The lipids were characterised chiefly by infra-red spectrophotometry, chromatography on aminoethylated paper,19 and deacylation. 2o