Gifford R M, Thorne J H
CSIRO, Division of Plant Industry, GPO Box 1600, Canberra, A.C.T. 2601, Australia.
Plant Physiol. 1986 Feb;80(2):464-9. doi: 10.1104/pp.80.2.464.
The time-course of sucrose efflux from attached seedcoats (having their embryos surgically removed) into aqueous traps placed in the ;empty ovules' had three phases. The first phase lasted 10 minutes and probably was a period of apoplastic flushing. The second lasted 2 to 3 hours and is thought to be a phase of equilibration of seed coat symplast with the frequently refreshed liquid. The third phase of relatively steady efflux was postulated to reflect the continued import of sucrose from the plant, and hence to reflect the rate of sieve tube unloading. The average steady state efflux was equal under most conditions to the estimated rate of sucrose import. Efflux and import were unaffected by 150 millimolar osmoticum (mannitol or polyethylene glycol [molecular weight about 400]), by 0.5 millimolar CaCl(2), or by pretreatments up to 20 minutes with p-chloromercuribenzenesulfonic acid (PCMBS); they were enhanced by 40 micromolar abscisic acid, 40 micromolar indoleacetic acid, 20 micromolar fusicoccin, and 1 millimolar dithiothreitol (DTT) and were inhibited by 100 micromolar KCN, by 0.03% H(2)O(2), by 20 micromolar and 5 micromolar trifluoromethoxy (carbonyl cyamide) phenylhydrazone, by repeated 5 minutes per hour treatments with 5 millimolar PCMBS, and by 5 millimolar DTT. The ;steady state' sucrose efflux was able to account for about half the rate of dry weight growth of the embryo, but stabilization of the system with <1 millimolar DTT taken together with other considerations is likely to give good correspondence between experimental unloading rates and in vivo growth rates.
将附着的种皮(其胚已通过外科手术移除)中的蔗糖流出到置于“空胚珠”中的水相收集器中的时间进程有三个阶段。第一阶段持续10分钟,可能是质外体冲洗期。第二阶段持续2至3小时,被认为是种皮共质体与频繁更新的液体平衡的阶段。相对稳定流出的第三阶段被假定反映了蔗糖从植物中的持续输入,因此反映了筛管卸载的速率。在大多数条件下,平均稳态流出量等于估计的蔗糖输入速率。流出和输入不受150毫摩尔渗透压剂(甘露醇或聚乙二醇[分子量约400])、0.5毫摩尔氯化钙或用对氯汞苯磺酸(PCMBS)预处理长达20分钟的影响;它们被40微摩尔脱落酸、40微摩尔吲哚乙酸、20微摩尔壳梭孢菌素和1毫摩尔二硫苏糖醇(DTT)增强,被100微摩尔氰化钾、0.03%过氧化氢、20微摩尔和5微摩尔三氟甲氧基(羰基氰胺)苯腙、每小时重复5分钟用5毫摩尔PCMBS处理以及5毫摩尔DTT抑制。“稳态”蔗糖流出能够解释胚干重生长速率的约一半,但用<1毫摩尔DTT使系统稳定并结合其他因素可能会使实验卸载速率与体内生长速率之间有良好的对应关系。