Sprecher H
Department of Medical Biochemistry, Ohio State University, Columbus, USA.
Nutrition. 1996 Jan;12(1 Suppl):S5-7. doi: 10.1016/0899-9007(96)90009-x.
When [1-14C]7,10,13,16,19-22:5 was incubated with microsomes, it was not desaturated to 4,7,10,13,16,19-22:6 by an acyl-CoA-dependent 4-desaturase. Subsequent studies with rat hepatocytes showed that 7,10,13,16, 19-22:5 was the precursor of 4,7,10,13,16,19-22:6, but the pathway proceeded through 24-carbon fatty acids. The implication of this finding is that 24-carbon acids, when produced in microsomes, must move to a site for partial beta-oxidation. Subsequent studies using a number of labeled acids showed that peroxisomes chain-shorten fatty acids, which then move back to the endoplasmic reticulum for esterification. The biosynthesis of both 22:5(n-6) and 22:6(n-3) thus requires the extensive movement of fatty acids between subcellular compartments.
当[1-¹⁴C]7,10,13,16,19-22:5与微粒体一起温育时,它不会被酰基辅酶A依赖性4-去饱和酶去饱和为4,7,10,13,16,19-22:6。随后对大鼠肝细胞的研究表明,7,10,13,16,19-22:5是4,7,10,13,16,19-22:6的前体,但该途径是通过24碳脂肪酸进行的。这一发现的含义是,微粒体中产生的24碳脂肪酸必须转移到一个进行部分β-氧化的位点。随后使用多种标记酸进行的研究表明,过氧化物酶体可使脂肪酸链缩短,并随后回到内质网进行酯化。因此,22:5(n-6)和22:6(n-3)的生物合成都需要脂肪酸在亚细胞区室之间进行广泛移动。