Proteinsynthese in grünen Blättern

Dr. Benno Parthier
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Abstract

1. Protein synthesis in subcellular fractions from young, mature and old ("starved") leaves of tobacco plants was compared with protein synthesis in the same fractions from detached senescent leaves, To this purpose, leaf-disks have been infiltrated with solutions of methionine-35S or leucine-U-14C and exposed in light or darkness, then the tissues have been homogenized, and the specific activities of the proteins of chloroplast, mitochondria, ribosomes and soluble fractions have been determined.

2. The mitochondria fraction showed the highest specific activity (c. p. m./mg protein) in all of the investigated fractions, both exposing the disks in light or darkness.

3. Light promoted the incorporation of methionine-35S into leaf proteins. This promotion could be referred to the increase of the incorporated radioactivity into the proteins of the chloro, plast fraction.

4. In detached leaves a steady decrease of the specific activity in all fractions ran parallel to the decay of the tissues. But the mitochondria fraction seemed to be more influenced during senescence than the other fractions.

5. The occurence of roots at the petioles prevented the decrease of the specific activity of the proteins. Moreover, after rooting a significant increase of the specific activity has been observed in all fractions, especially in the mitochondria.

6. A comparison of protein synthesis in young and old leaves from the same plant indicated that the synthesis was in old > mature > young in terms of the specific activity. However, the reverse was obtained in terms of absolutely incorporated radioactivity into the proteins.

7. During 14CO2-photosynthesis young leaves synthesized more 14C-protein than the old ones. In the following dark period, however, the increase of the radioactivity in the proteins, expressed as per cent of the acid-insoluble substances, was higher in the old tissues.

8. The differences of protein synthesis in detached, ageing leaves and in old leaves from the plants have been discussed in connection with the problem of senescence.

Mein Dank gilt Herm Prof. Dr. K. Mothes für die vielseitige Förderung der Arbeit. Fräulein M. Klein hat mir bei der Durchführung der Versuche wertvolle technische Hilfe geleistet.

1.将来自烟草植物年轻、成熟和衰老(“饥饿”)叶片的亚细胞组分中的蛋白质合成与来自分离的衰老叶片的相同组分的蛋白质合成进行比较。为此,用蛋氨酸-35S或亮氨酸-U-14C溶液渗透叶盘,并在光照或黑暗中暴露,然后将组织匀浆,并测定了叶绿体、线粒体、核糖体和可溶性部分蛋白质的特异性活性。在所有研究的组分中,线粒体组分显示出最高的比活性(c.p.m./mg蛋白质),无论是在光照还是黑暗中暴露圆盘。光照促进了蛋氨酸-35S在叶片蛋白质中的结合。这种促进作用可能是指氯代质体部分蛋白质中结合放射性的增加。在分离的叶片中,所有部分的比活性的稳步下降与组织的衰退平行。但线粒体组分在衰老过程中似乎比其他组分受到更大的影响。根在叶柄处的出现阻止了蛋白质比活性的降低。此外,生根后,在所有组分中都观察到比活性的显著增加,尤其是在线粒体中。来自同一植物的幼叶和老叶中蛋白质合成的比较表明,合成在老>;成熟>;年轻人的具体活动。然而,从蛋白质中绝对含有放射性的角度来看,情况正好相反。在14CO2光合作用过程中,幼叶合成的14C蛋白比老叶多。然而,在随后的黑暗时期,蛋白质中放射性的增加,以酸不溶性物质的百分比表示,在旧组织中更高。关于衰老问题,已经讨论了分离的、衰老的叶片和植物老叶片中蛋白质合成的差异。Mein Dank gilt Herm教授K.Mothes für博士是Arbeit的förderung博士。Fräulein M.Klein是Hilfe geleistet技术总监。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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