Schröder J, Betz B, Hahlbrock K
Biologisches Institut II der Universität, Schänzlestrasse 1, D-7800 Freiburg im Breisgau, Germany.
Plant Physiol. 1977 Sep;60(3):440-5. doi: 10.1104/pp.60.3.440.
A specific antiserum, raised against purified phenylalanine ammonialyase from irradiated cell suspension cultures of parsley (Petroselinum hortense Hoffm.), was used to compare the enzyme species induced either by dilution or by irradiation of the cell suspensions, to investigate the effect of dilution on the rate of synthesis of the enzyme protein in vivo, and to analyze the changes in specific activity of polyribosomal mRNA for the enzyme subunits in vitro. The mRNA activity in vitro was measured by translation of the polyribosomal RNA in a rabbit reticulocyte lysate.The results of immunodiffusion assays indicated that dilution and irradiation of the cell suspensions induced immunologically identical molecular species of phenylalanine ammonia-lyase. Dilution resulted in a large but short term increase in the rate of synthesis of the enzyme. Highest rates of synthesis were reached after 5 to 6 hours, and were followed by a rapid decline. The curves obtained for the changes in the rate of enzyme synthesis, both in vivo and in vitro, coincided with the curve for changes in the rate of appearance of catalytically active enzyme, as calculated from the observed changes in enzyme activity. These results suggested that the changes in enzyme activity were caused by corresponding changes in the amount of enzyme-specific polyribosomal mRNA.The dilution of cell cultures had no significant effect on the total rate of incorporation of radioactivity into protein in vivo or on the general template activity of the polyribosomal RNA in vitro throughout at least 25 hours.
一种针对从欧芹(Petroselinum hortense Hoffm.)经辐照的细胞悬浮培养物中纯化的苯丙氨酸解氨酶制备的特异性抗血清,被用于比较通过稀释或辐照细胞悬浮液诱导产生的酶种类,研究稀释对体内酶蛋白合成速率的影响,并分析体外多核糖体mRNA对酶亚基的比活性变化。体外mRNA活性通过在兔网织红细胞裂解物中翻译多核糖体RNA来测定。免疫扩散试验结果表明,细胞悬浮液的稀释和辐照诱导产生免疫上相同的苯丙氨酸解氨酶分子种类。稀释导致酶合成速率大幅但短期增加。在5至6小时后达到最高合成速率,随后迅速下降。体内和体外获得的酶合成速率变化曲线,与根据观察到的酶活性变化计算出的催化活性酶出现速率变化曲线相吻合。这些结果表明,酶活性的变化是由酶特异性多核糖体mRNA量的相应变化引起的。细胞培养物的稀释在至少25小时内对体内蛋白质放射性掺入的总速率或体外多核糖体RNA的总体模板活性没有显著影响。