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Tocopherol content in edible plant oils

86%
Edible vegetable oils were analysed for tocopherols by reversed-phase HPLC. These included refined corn, soybean, sunflower, rapeseed, grapeseed, and peanut oils, and cold-pressed extra-virgin olive, linseed, rapeseed, and sunflower oils. Total measured tocopherol concentrations varied in the range from 121 to 829 mg/kg. The contents of individual α-, (β+γ)-, and δ-tocopherols show a great diversity depending on the kind of oil. Moreover, the effect of photooxidation on the tocopherol content was studied in cold-pressed sunflower and rapeseed oils. These studies revealed only a minor decomposition of tocopherols under visible light.
The experiment determined the effect of gibberellic acid applied prior to harvest on the contents of plant pigments in cut leaves of wild ginger (Asarum europaeum L.), cultivated in an unheated plastic tunnel and in the field. Foliar application of GA3 at a concentration of 100, 200, 400, 600 mg x dm-3 was repeated four times every two weeks. It has been proven that pre-harvest spraying of plants with gibberellic acid at a concentration of 100 mg x dm-3 has a positive effect on the content of photosynthetically active pigments in the leaves of A. europaeum cultivated in an unheated plastic tunnel. Application of GA3 at a concentration of 600 mg x dm-3 led to the accumulation of the greatest amount of anthocyanins in the leaves of Asarum europaeum cultivated both in the unheated plastic tunnel and in the field. The response of plants to GA3 application, expressed in the amount of flavonoids, depended on conditions related to the cultivation site. Pre-harvest treatment of A. europaeum plants with gibberellic acid at concentrations of 100-600 mg x dm-3 reduced the production of flavonoids in tunnel-grown wild ginger, but enhanced their accumulation in plants cultivated in the field. Pre-harvest application of gibberellic acid did not affect the fresh weight or dry mass content in plant material.
The paper presents the results of experiments to determine the influence of selected physico-chemical factors – oxygen, visible light and temperature – on the decomposition of (1) chlorophylls a, b and c, chlorophyll a derivatives and β-carotene in acetone solution, and (2) chlorophyll a and β-carotene in axenic cultures of the blue-green algae Anabaena variabilis. The results indicate that both in acetone extracts and in blue-green algae cultures these pigments were most sensitive to light and oxygen; temperatures of up to 25◦C had no marked influence on these compounds. Under anoxia in acetone solution, the stability towards light decreased in the order chlorophyll a, chlorophyll b, chlorophylls c. Chlorophyll a, moreover, was less stable than its derivatives – phaeophorbides, phaeophytins, pyrophaeophytins and steryl chlorins – but more stable than β-carotene, in the last case also in the blue-green algae cultures. Decomposition of all the pigments proceeded mainly via the breakdown of the porphyrin macrocycle, since the decomposition products were not detected in the VIS range. On the basis of these experiments one can state that while light and oxygen may have a decisive direct influence on the distribution of chlorophylls and β-carotene in sediments, in the natural environment, temperatures of up to 25◦ C may have very little immediate effect.
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86%
Electrolyte efflux, chlorophyll, malondialdehyde content and enzymatic activities (catalase, peroxidase) in cucumber cotyledons as well as stability of model lipid membranes in the presence of some new, acyclic and cyclic, aminophosphonates were studied. They also differed in the substituents at the phosphorus and nitrogen atoms. It was found that the effectiveness of the compounds to influence mentioned parameters depended on their lipophilicity and structural features. The most active compounds were these with isopropyl substituents at the P atom unless their hydrocarbon chains at the N atom were not too long. Butyl substituents at phosphorus significantly decreased aminophosphonates efficiency. Similar effect was observed when trans-type hydrocarbon chain was replaced with a short-branched one. It also seems that cyclic compounds with hexane rings were weaker modifiers of model and biological membranes than these with pentane rings. Results show that aminophosphonates interact with plasma membranes and presumably induce oxidative stress.
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