Biology Department, California State University, 90032, Los Angeles, CA, USA.
Planta. 1979 Jan;144(5):413-8. doi: 10.1007/BF00380116.
Exogenous ethylene enhances the synthesis of wound-induced ribonuclease (RNase) (EC2.7.7.16) in tissue discs of white turnip (Brassica rapa L. var. rapa (L.) Tell.). The half-maximal concentration is <0.01 μl/l ehtylene. Maximal response was obtained with either continuous ethylene treatment, or a 90-min pulse of ethylene followed by flushing with 1500 cm(3) of air/min at standard pressure or 500 cm(3)/min at hypobaric pressure for the remainder of the experiments. Addition of ethylene at 60-75 min after cutting had no effect on RNase activity. Also the effect of ethylene in enhancing RNase decreased about linearly when addition of ethylene was delayed for tissue discs. Since actinomycin-D inhibition of RNase synthesis, observed earlier, is also limited to the initial 45-60 min after cutting, these results are consistent with the view that ethylene is acting at transcription.
外源乙烯增强了白芥菜组织圆盘中外源乙烯诱导的核糖核酸酶(RNase)(EC2.7.7.16)的合成(Brassica rapa L. var. rapa(L.)Tell.)。半最大浓度<0.01μl/l 乙烯。最大反应是通过连续乙烯处理或 90 分钟的乙烯脉冲,然后在标准压力下用 1500cm(3)/min 或在低气压下用 500cm(3)/min 冲洗 90 分钟获得的,其余实验。在切割后 60-75 分钟添加乙烯对 RNase 活性没有影响。当添加乙烯延迟到组织圆盘时,增强 RNase 的乙烯效应也呈线性下降。由于之前观察到的放线菌素-D 对 RNase 合成的抑制作用也仅限于切割后 45-60 分钟,这些结果与乙烯在转录中起作用的观点一致。