Montague M J, Armstrong T A, Jaworski E G
Monsanto Agricultural Products Company, 800 North Lindbergh Boulevard, St. Louis, Missouri 63166.
Plant Physiol. 1979 Feb;63(2):341-5. doi: 10.1104/pp.63.2.341.
Embryogenic cultured cells of Daucus carota have been shown to synthesize putrescine from exogenously supplied [(14)C]arginine at twice the rate of control nonembryogenic cells. In the present paper, the activity of arginine decarboxylase (arginine carboxy-lyase, EC 4.1.1.19), an important enzyme in the synthesis of putrescine, was assayed and also found to be elevated by as much as 2-fold in embryogenic cells. This difference between embryogenic and nonembryogenic cells was observed as early as 6 hours after the induction of embryogenesis and appeared not to result from the presence of a diffusible inhibitor or activator. It seemed to be dependent upon concomitant RNA and protein synthesis, as judged using 6-methyl-purine and cycloheximide. After cycloheximide addition to the culture medium, arginine decarboxylase activity declined with a half-time of about 30 minutes in both embryogenic and nonembryogenic cells. It is suggested that elevated arginine decarboxylase activity is involved in the mechanism leading to elevated putrescine levels in these cells and hence may play a role in the embryogenic process.
已证明胡萝卜的胚性培养细胞从外源供应的[(14)C]精氨酸合成腐胺的速度是对照非胚性细胞的两倍。在本文中,对精氨酸脱羧酶(精氨酸羧基裂解酶,EC 4.1.1.19)的活性进行了测定,该酶是腐胺合成中的一种重要酶,结果发现其在胚性细胞中的活性也提高了多达2倍。早在胚胎发生诱导后6小时就观察到了胚性细胞和非胚性细胞之间的这种差异,而且似乎不是由可扩散的抑制剂或激活剂的存在导致的。根据使用6-甲基嘌呤和环己酰亚胺的判断,这种差异似乎取决于RNA和蛋白质的同步合成。向培养基中添加环己酰亚胺后,胚性细胞和非胚性细胞中的精氨酸脱羧酶活性均以约30分钟的半衰期下降。有人提出,精氨酸脱羧酶活性的提高参与了导致这些细胞中腐胺水平升高的机制,因此可能在胚胎发生过程中起作用。