Hyodo H
J Biochem. 1976 Feb;79(2):277-82. doi: 10.1093/oxfordjournals.jbchem.a131068.
Phenylalanine ammonia-lyase [EC 4.3.1.5.] activity increased rapidly after a 3-hr lag period in potato tuber (Solanum tuberosum L. cv. May Queen) disks incubated in a suitable medium in the dark at 25 degrees. The activity reached a maxinum after incubation for about 40 hr. The effects of actinomycin D, 6-methylpurine, cycloheximide, chloramphenicol, and mitomycin C on the induction of phenylalanine ammonia-lyase were investigated during incubation of the disks. Actinomycin D, 6-methylpurine, and cycloheximide all inhibited the formation of phenylalanine ammonia-lyase, though cycloheximide was the most effective at low concentrations. Application of actinomycin D for the initial lag period (3 hr) caused strong inhibition; however, if it was supplied later it did not inhibit but actually increased phenylalanine ammonialyase formation. In contrast, cycloheximide was effective over most of the incubation period. Chloramphenicol and mitomycin C did not inhibit phenylalanine phenylalanine ammonialyase induction, but markedly stimulated it. Light was not an essential factor for phenylalanine ammonia-lyase induction in the wounded tissue.
在25摄氏度黑暗条件下,将马铃薯块茎(Solanum tuberosum L. cv. May Queen)圆盘置于合适培养基中培养,苯丙氨酸解氨酶[EC 4.3.1.5.]活性在3小时的延迟期后迅速增加。培养约40小时后活性达到最大值。在圆盘培养期间,研究了放线菌素D、6-甲基嘌呤、环己酰亚胺、氯霉素和丝裂霉素C对苯丙氨酸解氨酶诱导的影响。放线菌素D、6-甲基嘌呤和环己酰亚胺均抑制苯丙氨酸解氨酶的形成,尽管环己酰亚胺在低浓度时最有效。在初始延迟期(3小时)应用放线菌素D会导致强烈抑制;然而,如果稍后供应,它不会抑制反而实际上会增加苯丙氨酸解氨酶的形成。相比之下,环己酰亚胺在大部分培养期都有效。氯霉素和丝裂霉素C不抑制苯丙氨酸解氨酶的诱导,但会显著刺激其诱导。光照不是受伤组织中苯丙氨酸解氨酶诱导的必要因素。