Department of Botany, Division of Biological Sciences, University of Michigan, Ann Arbor, Michigan 48109.
Plant Physiol. 1976 Nov;58(5):670-4. doi: 10.1104/pp.58.5.670.
The rate of acidification of media by Avena stem segments was studied with a titrimeter. GA(3) increased this rate by an average of 17% if supplied to the segments 90 min prior to measurement. GA(3) inhibited the rate by 15% if supplied 10 min prior to measurement. After 90 min incubation, stimulation of elongation had started; at 10 min, GA(3) had not yet started to stimulate elongation in the segments.The acidification rates of the nodes (including the sheath-pulvinus), leaf sheath bases, and the internode bases of the stem segments were determined for plus and minus GA(3)-treated segments. The internode fraction contributes most to modification of the acidification rate, the node-pulvinus fraction less so, and the nongrowing sheath not at all.Acidification rates were measured for segments in different stages of elongation (lag, log, and plateau phases of growth). Segments in these growth stages were obtained from intact plants and from segments preincubated in sucrose and sucrose + GA(3). Segments from all sources which are in the log phase of growth have the highest rates, those in the plateau phase the lowest. For lag and log growth phases, segments preincubated in sucrose + GA(3) show the highest rates, those preincubated in sucrose the lowest rates. The opposite occurs for segments in the plateau phase of growth.Segments stimulated to grow by GA(3) cause the pH of their incubation media to drop to pH 5.15 from an initial pH of 6.5. Nonstimulated segments cause a drop to pH 5.6. Long term growth of the segments is maximal in media buffered to pH 5 in the presence and absence of GA(3).Our results support the idea that GA(3) stimulates an active acidification process in Avena stem segments just after GA(3) starts to stimulate growth in the segments, and that such an acidification process could play an important role in wall-loosening during active growth of the internode.
用滴定法研究了燕麦茎段对介质酸化的速率。如果在测量前 90 分钟向节段提供 GA(3),则平均可使该速率提高 17%。如果在测量前 10 分钟供应 GA(3),则该速率会抑制 15%。孵育 90 分钟后,伸长开始刺激;10 分钟时,GA(3)尚未开始刺激节段伸长。测定了加和不加 GA(3)处理的节段的节点(包括鞘-叶枕)、叶鞘基部和茎节间基部的酸化速率。节间部分对酸化速率的修饰贡献最大,节点-叶枕部分次之,非生长鞘部则没有贡献。测定了处于不同伸长阶段(生长的滞后、对数和平台阶段)的节段的酸化速率。这些生长阶段的节段取自完整植物和在蔗糖和蔗糖+GA(3)中预培养的节段。处于对数生长阶段的所有来源的节段具有最高的速率,处于平台生长阶段的节段具有最低的速率。对于滞后和对数生长阶段,在蔗糖+GA(3)中预培养的节段显示出最高的速率,在蔗糖中预培养的节段显示出最低的速率。对于处于平台生长阶段的节段则相反。被 GA(3)刺激生长的节段会将其培养介质的 pH 从初始的 6.5 降低到 5.15。未受刺激的节段会导致 pH 降低到 5.6。在存在和不存在 GA(3)的情况下,将节段的培养基缓冲至 pH 5 时,节段的长期生长达到最大值。我们的结果支持这样一种观点,即 GA(3)在 GA(3)开始刺激节段生长后立即刺激燕麦茎段中的一个主动酸化过程,并且这种酸化过程可能在节间活跃生长期间的细胞壁松弛中发挥重要作用。