Zucker M
Plant Physiol. 1969 Jun;44(6):912-22. doi: 10.1104/pp.44.6.912.
A cycloheximide-sensitive increase in the activity of phenylalanine ammonia-lyase (EC 4.3.1.5) occurs in Xanthium leaf disks exposed to light. Radioactive ammonia-lyase has been isolated by means of sucrose density gradient centrifugation and starch gel electrophoresis from disks fed l-isoleucine-U-(14)C or l-arginine-U-(14)C. The incorporation of radioactive amino acids into phenylalanine ammonia-lyase together with the inhibitory effects of cycloheximide indicate that the observed increase in enzyme activity involves the induction of lyase synthesis.The light-dependent synthesis of the ammonia-lyase is completely inhibited by 50 mum 3-(4-chlorophenyl)-1,1-dimethylurea (CMU) indicating that photosynthesis is involved. Only a trace quantity of some photosynthetic product must be needed because half light saturation occurs at very low intensity (ca. 30 ft-c). Exogenous carbohydrate is also required for continuing enzyme synthesis over a 72 hr period. But carbohydrate does not replace the photosynthetic requirement in darkness. Enzyme formed in light disappears rapidly from disks placed in the dark. The decay of ammonia-lyase activity follows first order kinetics. The half-life of the lyase ranged from 6 to 15 hr in leaf material used. Cyoloheximide inhibits the decay of lyase activity. Thus the maintenance of turnover in Xanthium leaf disks requires de novo synthesis of protein. That turnover, i.e., degradation as well as synthesis of lyase protein occurs is suggested by the apparent loss of radioactive ammonia-lyase from leaf disks placed in darkness. Light-induced synthesis coupled with rapid turnover can produce a diurnal fluctuation of ammonia-lyase activity in Xanthium leaf disks. Alternating periods of enzyme synthesis and degradation were observed in disks exposed to 24 hr cycles of light and dark. The average level of enzyme activity maintained in the tissue was directly related to the length of the light period. Induction of lyase synthesis was also observed in excised leaves and to a lesser extent in leaves of whole plants.
在光照下的苍耳属植物叶圆片中,苯丙氨酸解氨酶(EC 4.3.1.5)的活性会出现对放线菌酮敏感的增加。通过蔗糖密度梯度离心和淀粉凝胶电泳,从用L-异亮氨酸-U-(14)C或L-精氨酸-U-(14)C喂养的叶圆片中分离出了放射性解氨酶。放射性氨基酸掺入苯丙氨酸解氨酶以及放线菌酮的抑制作用表明,观察到的酶活性增加涉及解氨酶合成的诱导。氨解氨酶的光依赖性合成完全被50 μM 3-(4-氯苯基)-1,1-二甲基脲(CMU)抑制,这表明光合作用参与其中。由于在非常低的强度(约30英尺烛光)下就出现了半光饱和,所以只需要微量的某些光合产物。在72小时的时间段内持续进行酶合成也需要外源碳水化合物。但是碳水化合物并不能在黑暗中替代光合作用的需求。在光照下形成的酶会迅速从置于黑暗中的叶圆片中消失。氨解氨酶活性的衰减遵循一级动力学。在所使用的叶片材料中,解氨酶的半衰期在6到15小时之间。放线菌酮抑制解氨酶活性的衰减。因此,苍耳属植物叶圆片中周转率的维持需要蛋白质的从头合成。从置于黑暗中的叶圆片中放射性氨解氨酶的明显损失表明,解氨酶蛋白会发生周转,即降解以及合成。光诱导的合成与快速周转可导致苍耳属植物叶圆片中氨解氨酶活性出现昼夜波动。在暴露于24小时明暗循环的叶圆片中观察到了酶合成和降解的交替时期。组织中维持的酶活性平均水平与光照期的长度直接相关。在离体叶片中也观察到了解氨酶合成的诱导,在整株植物的叶片中诱导程度较小。