Institut für Biologie I der Universität, Auf der Morgenstelle 1, D-7400, Tübingen, Federal Republic of Germany.
Planta. 1977 Jan;135(1):63-7. doi: 10.1007/BF00387977.
When callus cells of Daucus carota are grown on a medium containing gibberellic acid (GA3) in a physiological concentration of 3x10(-6) M the cells cease to accumulate anthocyanins. This anthocyanin-free cell line has a very low activity of phenylalanine ammonia-lyase. After density labelling with D2O an intensive de novo synthesis of the phenylalanine ammonia-lyase (E.C. 4.3.1.5; PAL) in the anthocyanin-containing cells does occur. 58% of the C-bound H-atoms are replaced by deuterium. The anthocyanin-free cells show only a very low enzyme synthesis which is difficult to detect with density labelling experiments. To ascertain that de novo synthesis occurs in the anthocyanin-free cells, the incorporation of (14)C-labelled amino acids into the partially purified enzyme protein was measured after separation of the protein a) in CsCl gradients and b) on polyacrylamide gels. In both cases the enzyme bears (14)C-label. These results suggest that in the anthocyanin-free cells de novo synthesis of PAL is still occuring but the synthesis is reduced in comparison to the anthocyanin-containing cells.
当胡萝卜愈伤组织细胞在含有生理浓度 3x10(-6) M 的赤霉素 (GA3) 的培养基上生长时,细胞停止积累花青素。这个不含花青素的细胞系苯丙氨酸解氨酶的活性非常低。用 D2O 进行密度标记后,花青素含量高的细胞中苯丙氨酸解氨酶(E.C. 4.3.1.5;PAL)会发生强烈的从头合成。58%的 C 结合氢原子被氘取代。不含花青素的细胞只显示出非常低的酶合成,用密度标记实验很难检测到。为了确定无花青素细胞中是否发生从头合成,在用 CsCl 梯度和 b)聚丙烯酰胺凝胶分离部分纯化的酶蛋白后,测量了(14)C 标记的氨基酸掺入到部分纯化的酶蛋白中的情况。在这两种情况下,酶都带有(14)C 标记。这些结果表明,在无花青素的细胞中,PAL 的从头合成仍在进行,但与含有花青素的细胞相比,合成量减少了。