Paturneau-Jouas M, Baumann N, Bourre J M
Biochimie. 1976;58(3):341-9. doi: 10.1016/s0300-9084(76)80441-5.
Incorporation of malonyl-CoA or acetyl-CoA is studied in mouse brain mitochondrial fatty acids. Rupture of mitochondria is necessary ; Triton X-100 gives the best result. Other detergents or sonication are of lesser efficiency. Cofactor requirements have been studied : NADH and NADPH have been tested ; ATP increases biosynthesis and CoA causes an inhibition. Two systems of biosynthesis are involved : -- One is a de novo system using malonyl-CoA. Malonyl-CoA alone is incorporated and synthesizes mainly C16, indicating the existence of a malonly-CoA decarboxylase although elongation of short chain fatty acids cannot be excluded. Addition of acetyl-CoA increases the biosynthesis and palmityl-CoA when added causes an inhibition. -- The other system, using acetyl-CoA, elongates exogenous palmityl-CoA ; endogenous acyl-CoAs are not elongated by acetyl-CoA. All these results are confirmed by radiogas chromatographic studies of the reactions products.
在小鼠脑线粒体脂肪酸中研究丙二酰辅酶A或乙酰辅酶A的掺入情况。线粒体破裂是必要的;Triton X-100效果最佳。其他去污剂或超声处理效率较低。已经研究了辅因子需求:测试了NADH和NADPH;ATP可增加生物合成,而辅酶A会导致抑制作用。涉及两种生物合成系统:——一种是使用丙二酰辅酶A的从头合成系统。单独的丙二酰辅酶A可掺入并主要合成C16,这表明存在丙二酰辅酶A脱羧酶,尽管不能排除短链脂肪酸的延长。添加乙酰辅酶A可增加生物合成,而添加棕榈酰辅酶A则会导致抑制作用。——另一种系统使用乙酰辅酶A,可延长外源性棕榈酰辅酶A;内源性酰基辅酶A不会被乙酰辅酶A延长。所有这些结果都通过对反应产物的放射性气相色谱研究得到了证实。