The triglyceride composition of linseed oils obtained under different ecological conditions and having different fatty acid compositions was determined by a combination of several chromatographic techniques. The triglyceride mixture was first separated in 8 fractions of different polarity by reversed‐phase paper chromatography. Each glyceride fraction was then separated in a partition chromatographic system as the triglyceride coordination complexes with silver ions into individual compounds. The fatty acid compositions of the original oil, single glyceride fractions, and individual triglycerides were determined by gas‐liquid chromatography. The molar ratio between the two neighboring glyceride fractions was determined by relating the fatty acid composition of each fraction to the fatty acid composition of their sum. The triglyceride composition of the total oil was then calculated from these results.
The presence of 18舑19 triglycerides was ascertained in the samples studied, and the molar concentration of each glyceride was estimated. Linseed oil contains only triunsaturated and monosaturated‐diunsaturated triglycerides. Within each of these types the fatty acid distribution is close to random. At the same time, the content of some triglycerides departed regularly from a random pattern.
A method for calculation of linseed oil triglyceride composition from the fatty acid composition is given.
The same general pattern of glyceride formation in linseed is followed regardless of ecological conditions; therefore, the qualitative and quantitative triglyceride composition reflects the differences in fatty acid composition of linseed oil.
Composition and content of lipids were studied in 5-day-old radish seedlings (Raphanus sativus L. var. radicula DC.) grown in lowlight and darkness in an extremely low frequency (ELF) magnetic field characterized by 50 Hz frequency and ∼500 µT flux density. The control seedlings were grown under the same conditions, but without exposure to the magnetic field. The products of lipid metabolism were compared with lipid composition in seeds. In control seedlings, reserve neutral lipids, mostly triacylglycerides, were utilized for the formation of polar lipids (PL). As a result, the amount of the latter doubled, particularly due to glycolipids (GL) and phospholipids (PhL) compared to their content in seeds. At 20-22 °C in light, magnetic field exposure increased the production of PL by threefold specifically, GL content increased fourfold and PhL content rose 2.5 times, compared to seeds. In darkness, the effect of magnetic field on lipids was weaker. At the lower temperature of 13-16 °C in light, the effect of the magnetic field was weak, but in the darkness, no magnetic field action was recorded. It is concluded that ELF magnetic field stimulated lipid synthesis in chloroplast, mitochondrial, and other cell membranes in radish seedlings grown in light at 20-22 °C and 13-16 °C.
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