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Regulation of the biosynthesis of 22:5n-6 and 22:6n-3: a complex intracellular process.

机译:调节22:5n-6和22:6n-3的生物合成:复杂的细胞内过程。

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摘要

Both 22:4n-6 and 22:5n-3 are synthesized from n-6 and n-3 fatty acid precursors in the endoplasmic reticulum. The synthesis of both 22:5n-6 and 22:6n-3 requires that 22:4n-6 and 22:5n-3 are metabolized, respectively, to 24:5n-6 and 24:6n-3 in the endoplasmic reticulum. These two 24-carbon acids must then move to peroxisomes for partial degradation followed by the movement of 22:5n-6 and 22:6n-3 back to the endoplasmic reticulum for use as substrates in membrane lipid biosynthesis. Clearly an understanding of the control of intracellular fatty acid movement as well as of the reactions carried out by microsomes, peroxisomes, and mitochondria are all required in order to understand not only what regulates the biosynthesis of 22:5n-6 and 22:6n-3 but also why most tissue lipids selectively accumulate 22:6n-3.
机译:22:4n-6和22:5n-3均由内质网中的n-6和n-3脂肪酸前体合成。 22:5n-6和22:6n-3的合成都要求22:4n-6和22:5n-3在内质网中分别代谢为24:5n-6和24:6n-3。然后,这两种24-碳酸必须移至过氧化物酶体中进行部分降解,然后将22:5n-6和22:6n-3移回内质网,以用作膜脂质生物合成的底物。显然,需要了解细胞内脂肪酸运动的控制以及微粒体,过氧化物酶体和线粒体进行的反应,以便不仅了解调节22:5n-6和22:6n-生物合成的因素。 3,也是为什么大多数组织脂质选择性地累积22:6n-3的原因。

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