Faergeman N J, Black P N, Zhao X D, Knudsen J, DiRusso C C
Center for Cardiovascular Sciences, Albany Medical College, Albany, New York 12208, USA.
J Biol Chem. 2001 Oct 5;276(40):37051-9. doi: 10.1074/jbc.M100884200. Epub 2001 Jul 27.
Exogenous long-chain fatty acids are activated to coenzyme A derivatives prior to metabolic utilization. In the yeast Saccharomyces cerevisiae, the activation of these compounds prior to metabolic utilization proceeds through the fatty acyl-CoA synthetases Faa1p and Faa4p. Faa1p or Faa4p are essential for long-chain fatty acid import, suggesting that one or both of these enzymes are components of the fatty acid transport system, which also includes Fat1p. By monitoring the intracellular accumulation of the fluorescent long-chain fatty acid analogue 4,4-difluoro-5-methyl-4-bora-3a,4a-diaza-s-indacene-3-dodecanoic acid, long-chain fatty acid transport was shown to be severely restricted in a faa1 Delta faa4 Delta strain. These data established for the first time a mechanistic linkage between the import and activation of exogenous fatty acids in yeast. To investigate this linkage further, oleoyl CoA levels were defined following incubation of wild type and mutant cells with limiting concentrations of exogenous oleate. These studies demonstrated oleoyl CoA levels were reduced to less than 10% wild-type levels in faa1 Delta and faa1 Delta faa4 Delta strains. Defects in metabolic utilization and intracellular trafficking were also found in the fatty acyl-CoA synthetase-deficient strains. The faa1 Delta faa4 Delta strain had a marked reduction in endogenous acyl-CoA pools, suggesting these enzymes play a role in maintenance of endogenous acyl-CoA pools, metabolism and trafficking. In addition, this strain had levels of in vivo beta-oxidation of exogenous oleate reduced 3-fold when compared with the isogenic parent. Northern analyses demonstrated an additional defect in fatty acid trafficking as FAA1 or FAA4 were required for the transcriptional regulation of the genes encoding the peroxisomal enzymes acyl-CoA oxidase (POX1) and medium-chain acyl-CoA synthetase (FAA2). These data support the hypothesis that fatty acyl-CoA synthetase (Faa1p or Faa4p) functions as a component of the fatty acid import system by linking import and activation of exogenous fatty acids to intracellular utilization and signaling.
外源性长链脂肪酸在代谢利用之前会被激活为辅酶A衍生物。在酿酒酵母中,这些化合物在代谢利用之前的激活过程是通过脂肪酰辅酶A合成酶Faa1p和Faa4p进行的。Faa1p或Faa4p对于长链脂肪酸的导入至关重要,这表明这两种酶中的一种或两种都是脂肪酸转运系统的组成部分,该系统还包括Fat1p。通过监测荧光长链脂肪酸类似物4,4-二氟-5-甲基-4-硼-3a,4a-二氮杂-s-茚并-3-十二烷酸的细胞内积累情况,发现长链脂肪酸转运在faa1Δfaa4Δ菌株中受到严重限制。这些数据首次在酵母中建立了外源性脂肪酸的导入与激活之间的机制联系。为了进一步研究这种联系,在用有限浓度的外源性油酸孵育野生型和突变细胞后,测定了油酰辅酶A水平。这些研究表明,在faa1Δ和faa1Δfaa4Δ菌株中,油酰辅酶A水平降低至野生型水平的不到10%。在脂肪酰辅酶A合成酶缺陷型菌株中还发现了代谢利用和细胞内运输方面的缺陷。faa1Δfaa4Δ菌株的内源性酰基辅酶A库明显减少,这表明这些酶在内源性酰基辅酶A库的维持、代谢和运输中发挥作用。此外,与同基因亲本相比,该菌株中外源性油酸的体内β-氧化水平降低了3倍。Northern分析表明,脂肪酸转运还存在另一个缺陷,因为FAA1或FAA4是过氧化物酶体酶酰基辅酶A氧化酶(POX1)和中链酰基辅酶A合成酶(FAA2)编码基因转录调控所必需的。这些数据支持了这样一种假设,即脂肪酰辅酶A合成酶(Faa1p或Faa4p)通过将外源性脂肪酸的导入和激活与细胞内利用及信号传导联系起来,作为脂肪酸导入系统的一个组成部分发挥作用。