{"title":"Protein synthesis in mitochondria","authors":"A.M. Kroon","doi":"10.1016/0926-6550(64)90178-1","DOIUrl":null,"url":null,"abstract":"<div><p></p><ul><li><span>1.</span><span><p>1. A procedure for preparing rat-liver mitochondria including a pre-incubation with RNAase (EC 2.7.7.16) to inactivate the microsomal system for amino acid incorporation is described.</p></span></li><li><span>2.</span><span><p>2. The inhibition of the incorporation of amino acids into mitochondrial protein by adding substrate is correlated with a lowering of the NADP<sup>+</sup>/NADPH ratio.</p></span></li><li><span>3.</span><span><p>3. It is shown that ammonia can relieve the inhibition by α-oxoglutarate or isocitrate of the incorporation into liver mitochondria, that this effect is not due to the glutamate formed, and that this is correlated with oxidation of NADPH to NADP<sup>+</sup>.</p></span></li><li><span>4.</span><span><p>4. The role of endogenous substrate is discussed. It is concluded that in the case of rat-liver mitochondria α-oxoglutarate plus ammonia give the best conditions for providing energy for incorporation, since a high NADP<sup>+</sup>/NADPH ratio is also assured.</p></span></li><li><span>5.</span><span><p>5. Judged by the effects of oligomycin and 2,4-dinitrophenol on the amino acid incorporation into protein by mitochondria, the possibility is discussed whether and in how far the high-energy intermediates of oxidative phosphorylation can meet the energy requirements for the incorporation process.</p></span></li></ul></div>","PeriodicalId":100173,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Nucleic Acids and Related Subjects","volume":"91 1","pages":"Pages 145-154"},"PeriodicalIF":0.0000,"publicationDate":"1964-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6550(64)90178-1","citationCount":"36","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Nucleic Acids and Related Subjects","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0926655064901781","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 36

Abstract

  • 1.

    1. A procedure for preparing rat-liver mitochondria including a pre-incubation with RNAase (EC 2.7.7.16) to inactivate the microsomal system for amino acid incorporation is described.

  • 2.

    2. The inhibition of the incorporation of amino acids into mitochondrial protein by adding substrate is correlated with a lowering of the NADP+/NADPH ratio.

  • 3.

    3. It is shown that ammonia can relieve the inhibition by α-oxoglutarate or isocitrate of the incorporation into liver mitochondria, that this effect is not due to the glutamate formed, and that this is correlated with oxidation of NADPH to NADP+.

  • 4.

    4. The role of endogenous substrate is discussed. It is concluded that in the case of rat-liver mitochondria α-oxoglutarate plus ammonia give the best conditions for providing energy for incorporation, since a high NADP+/NADPH ratio is also assured.

  • 5.

    5. Judged by the effects of oligomycin and 2,4-dinitrophenol on the amino acid incorporation into protein by mitochondria, the possibility is discussed whether and in how far the high-energy intermediates of oxidative phosphorylation can meet the energy requirements for the incorporation process.

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线粒体中的蛋白质合成
1.1. 描述了制备大鼠肝脏线粒体的程序,包括用RNAase (EC 2.7.7.16)进行预孵育,以使微粒体系统失活以使氨基酸结合。通过添加底物抑制氨基酸并入线粒体蛋白与NADP+/NADPH比值的降低相关。结果表明,氨可以缓解α-氧葡萄糖酸盐或异柠檬酸盐对肝脏线粒体掺入的抑制作用,这种作用不是由于谷氨酸的形成,而是与NADPH氧化为NADP+.4.4有关。讨论了内源性底物的作用。综上所述,在大鼠肝脏线粒体α-氧戊二酸加氨的情况下,由于NADP+/NADPH比值较高,因此为合并提供能量的条件最好。根据寡霉素和2,4-二硝基苯酚对线粒体将氨基酸整合到蛋白质中的影响,探讨氧化磷酸化的高能中间体是否能满足和在多大程度上满足整合过程的能量需求的可能性。
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Author index Erratum Subject index Changes in sedimentation properties of ribosomal ribonucleic acids during the course of ribosome formation in Escherichia coli The inhibition of deoxyribonucleotidyl transferase, DNAase and RNAase by sodium poly ethenesulfonic acid. Effect of the molecular weight of the inhibitor
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