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The utilization and desaturation of oleate and linoleate during glycerolipid biosynthesis in olive (Olea europaea L.) callus cultures

机译:橄榄(Olea europaea L.)愈伤组织培养物中甘油脂生物合成过程中油酸酯和亚油酸酯的利用和去饱和

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摘要

Callus cultures from olive (Olea europaea L.) were used to study characteristics of desaturation in this oil-rich tissue. The incorporation of [1-14C]oleate and [1-14C]linoleate into complex lipids and their further desaturation was followed in incubations of up to 48 h. Both radiolabelled fatty acids were rapidly incorporated into lipids, especially phosphatidylcholine and triacylglycerol. Radiolabelling of these two lipids peaked after 1–4 h, after which it fell. In contrast, other phosphoglycerides and the galactosylglycerides were labelled in a more sustained manner. [1-14C]Linoleate was almost exclusively found in the galactolipids. With [1-14C]linoleate as a precursor, the only significant desaturation to linolenate was in the galactolipids. Monogalactosyldiacylglycerol was the first lipid in which [1-14C]linoleate and [1-14C]linolenate appeared after incubation of the calli with [1-14C]oleate and [1-14C]linoleate, respectively. The presence of radioactivity in the plastidial lipids shows that both [1-14C]oleate and [1-14C]linoleate can freely enter the chloroplast. Two important environmental effects were also examined. Raised incubation temperatures (30–35 °C) reduced oleate desaturation and this was also reflected in the endogenous fatty acid composition. Low light also caused less oleate desaturation. The data indicate that lysophosphatidylcholine acyltransferase is important for the entry of oleate and linoleate into olive callus lipid metabolism and phospholipid:diacylglycerol acyltransferase may be involved in triacylglycerol biosynthesis. In addition, it is shown that plastid desaturases are mainly responsible for the production of polyunsaturated fatty acids. Individual fatty acid desaturases were differently susceptible to environmental stresses with FAD2 being reduced by both high temperature and low light, whereas FAD7 was only affected by high temperature.
机译:来自橄榄(油橄榄(Olea europaea L.))的愈伤组织培养物用于研究该富含油的组织中的去饱和特性。将[1- 14 C]油酸酯和[1- 14 C]亚油酸酯掺入复合脂质中,并在长达48小时的孵育中进行进一步的去饱和。两种放射性标记的脂肪酸均迅速掺入脂质中,尤其是磷脂酰胆碱和三酰基甘油。这两种脂质的放射性标记在1-4小时后达到峰值,然后下降。相反,其他磷酸甘油酯和半乳糖基甘油酯则以更持久的方式标记。 [1- 14 C]亚油酸酯几乎完全存在于半乳糖脂中。以[1- 14 C]亚油酸酯为前体,亚油酸酯的唯一显着去饱和是在半乳糖脂中。愈伤组织与[1- 14”孵育后,单半乳糖基二酰基甘油是第一个出现[1- 14 C]亚油酸酯和[1- 14 C]亚油酸酯的脂质 C]油酸酯和[1- 14 C]亚油酸酯。质体脂质中放射性的存在表明[1- 14 C]油酸酯和[1- 14 C]亚油酸酯均可自由进入叶绿体。还研究了两个重要的环境影响。升高的孵育温度(30–35°C)降低了油酸盐的去饱和度,这也反映在内源性脂肪酸成分中。弱光也导致较少的油酸盐去饱和。数据表明溶血磷脂酰胆碱酰基转移酶对于油酸酯和亚油酸酯进入橄榄愈伤组织脂质代谢是重要的,并且磷脂:二酰基甘油酰基转移酶可能参与三酰基甘油的生物合成。另外,已经表明,质体去饱和酶主要负责多不饱和脂肪酸的产生。个别脂肪酸去饱和酶对环境胁迫的敏感性不同,FAD2受高温和弱光影响均降低,而FAD7仅受高温影响。

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