Central Research and Development Department, Experimental Station, E. I. du Pont de Nemours and Company, Wilmington, Delaware 19898.
Plant Physiol. 1975 Aug;56(2):273-8. doi: 10.1104/pp.56.2.273.
The effects of various treatments on the recently reported system in pea (Pisum sativum cv. Alaska), which results in (a) the incorporation of (14)C(2)H(4) into the tissue and (b) the conversion of (14)C(2)H(4) to (14)CO(2), was investigated using 2-day-old etiolated seedlings which exhibit a maximum response. Heat treatment (80 C, 1 min) completely inhibited both a and b, whereas homogenization completely inhibited b but only partially inhibited a. Detaching the cotyledons from the root-shoot axis immediately before exposing the detached cotyledons together with the root-shoot axis to (14)C(2)H(4) markedly reduced both a and b. Increasing the (14)C(2)H(4) concentration from 0.14 to over 100 mul/l progressively increased the rate of a and b with tissue incorporation being greater than (14)C(2)H(4) to (14)CO(2) conversion only below 0.3 mul/l (14)C(2)H(4). Reduction of the O(2) concentration reduced both a and b, with over 99% inhibition occurring under anaerobic conditions. The addition of CO(2) (5%) severely inhibited (14)C(2)H(4) to (14)CO(2) conversion without significantly affecting tissue incorporation. Exposure of etiolated seedlings to fluorescent light during (14)C(2)H(4) treatment was without effect. Similarly, indoleacetic acid, gibberellic acid, benzyladenine, abscisic acid, and dibutyryl cyclic adenosine monophosphate had no significant effect on either a or b.The possibilities that the incorporation of (14)C(2)H(4) into pea tissues and its conversion to (14)CO(2) is linked to ethylene action, or that it represents a means of reducing the endogenous ethylene level, are discussed.Several problems encountered with the use of polyethylene vials, rubber serum stoppers, Clorox, and microbial contamination are also described.
用 2 天龄的黄化幼苗研究了最近在豌豆(Pisum sativum cv. Alaska)中报道的系统的各种处理的效果,该系统导致(a)将(14)C(2)H(4)掺入组织中,(b)将(14)C(2)H(4)转化为(14)CO(2),幼苗表现出最大的反应。热处理(80°C,1 分钟)完全抑制了 a 和 b,而匀浆完全抑制了 b,但仅部分抑制了 a。在将子叶与根-茎轴一起暴露于(14)C(2)H(4)之前,立即将子叶从根-茎轴上分离出来,显著降低了 a 和 b。将(14)C(2)H(4)浓度从 0.14 增加到 100 微升/升以上,逐渐增加了 a 和 b 的速率,只有在 0.3 微升/升(14)C(2)H(4)以下,组织掺入才大于(14)C(2)H(4)向(14)CO(2)的转化。降低 O(2)浓度降低了 a 和 b,在厌氧条件下抑制率超过 99%。添加 CO(2)(5%)严重抑制(14)C(2)H(4)向(14)CO(2)的转化,而对组织掺入没有显著影响。在(14)C(2)H(4)处理期间将黄化幼苗暴露于荧光灯下没有效果。同样,吲哚乙酸、赤霉素、苄基腺嘌呤、脱落酸和二丁酰环腺苷单磷酸对 a 或 b 均无明显影响。将(14)C(2)H(4)掺入豌豆组织并将其转化为(14)CO(2)与乙烯作用有关,或者它代表了降低内源性乙烯水平的一种手段的可能性进行了讨论。还描述了使用聚乙烯小瓶、橡胶血清瓶塞、Clorox 和微生物污染时遇到的几个问题。