Miura S, Mori M, Takiguchi M, Tatibana M, Furuta S, Miyazawa S, Hashimoto T
J Biol Chem. 1984 May 25;259(10):6397-402.
Three peroxisomal enzymes of beta-oxidation from rat liver were synthesized in a cell-free protein-synthesizing system derived from a lysate of rabbit reticulocytes. The in vitro products of acyl-CoA oxidase (EC 1.3.99.3) and a bifunctional protein containing enoyl-CoA hydratase (EC 4.2.1.17) and 3-hydroxyacyl-CoA dehydrogenase (EC 1.1.1.35) activities were apparently the same in size and charge as the subunit of the respective mature enzymes; that of 3-ketoacyl-CoA thiolase (EC 2.3.1.16) was about 3,000 Da larger and more basic than its mature subunit. The free polysome fraction of rat liver was 3.1-5.7 times more active than the membrane-bound polysome fraction in the synthesis of the three peroxisomal enzymes; these values were similar to those for cytosolic enzymes and differed from that for serum albumin. In isolated rat hepatocytes, radiolabeled acyl-CoA oxidase and bifunctional protein increased with time with no appreciable change in the subunit size. On the other hand, the labeled putative precursor of 3-ketoacyl-CoA thiolase, as well as the mature form of the enzyme, was detected in the hepatocytes. The radioactivity of the putative precursor reached a plateau in 30 min; that of the mature subunit appeared after a lag time of about 5 min and increased with time up to 90 min. In pulse-chase experiments, the putative precursor disappeared with an apparent half-life of several minutes. When the hepatocytes were fractionated into the cytosolic and the particulate fractions, one half of labeled acyl-CoA oxidase and 60% of the bifunctional protein were recovered in the cytosolic fraction after 10 min of labeling, whereas 70-80% of the labeled enzymes were recovered in the particulate fraction after 40-60 min of labeling. These results indicate that the three enzymes of peroxisomal beta-oxidation are synthesized on free polysomes, released into the cytosol, and then transported into peroxisomes. Our findings also indicate that 3-ketoacyl-CoA thiolase undergoes proteolytic processing during maturation. The temporal sequence of the proteolytic cleavage and intracellular transport of the thiolase remains to be determined.
从兔网织红细胞裂解物衍生的无细胞蛋白质合成系统中合成了大鼠肝脏的三种过氧化物酶体β-氧化酶。酰基辅酶A氧化酶(EC 1.3.99.3)以及含有烯酰辅酶A水合酶(EC 4.2.1.17)和3-羟酰基辅酶A脱氢酶(EC 1.1.1.35)活性的双功能蛋白的体外产物,在大小和电荷上显然与各自成熟酶的亚基相同;3-酮酰基辅酶A硫解酶(EC 2.3.1.16)的体外产物比其成熟亚基大约3000 Da,碱性更强。在三种过氧化物酶体酶的合成中,大鼠肝脏的游离多核糖体部分的活性比膜结合多核糖体部分高3.1 - 5.7倍;这些值与胞质酶的值相似,与血清白蛋白的值不同。在分离的大鼠肝细胞中,放射性标记的酰基辅酶A氧化酶和双功能蛋白随时间增加,亚基大小没有明显变化。另一方面,在肝细胞中检测到了3-酮酰基辅酶A硫解酶的标记假定前体以及该酶的成熟形式。假定前体的放射性在30分钟达到平台期;成熟亚基的放射性在约5分钟的延迟时间后出现,并随时间增加直至90分钟。在脉冲追踪实验中,假定前体以明显的几分钟半衰期消失。当肝细胞被分离为胞质部分和颗粒部分时,标记10分钟后,一半的标记酰基辅酶A氧化酶和60%的双功能蛋白在胞质部分中回收,而标记40 - 60分钟后,70 - 80%的标记酶在颗粒部分中回收。这些结果表明,过氧化物酶体β-氧化的三种酶在游离多核糖体上合成,释放到胞质溶胶中,然后转运到过氧化物酶体中。我们的发现还表明,3-酮酰基辅酶A硫解酶在成熟过程中经历蛋白水解加工。硫解酶蛋白水解切割和细胞内转运的时间顺序仍有待确定。