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本文引用的文献

1
Sucrose Concentration at the Apoplastic Interface between Seed Coat and Cotyledons of Developing Soybean Seeds.发育中大豆种子种皮与子叶的质外体界面处的蔗糖浓度。
Plant Physiol. 1985 Apr;77(4):863-8. doi: 10.1104/pp.77.4.863.
2
Economy of water, carbon, and nitrogen in the developing cowpea fruit.豇豆果实发育过程中的水分、碳和氮经济性
Plant Physiol. 1985 Jan;77(1):142-7. doi: 10.1104/pp.77.1.142.
3
Abscisic Acid and its relationship to seed filling in soybeans.脱落酸及其与大豆种子充实的关系。
Plant Physiol. 1984 Oct;76(2):301-6. doi: 10.1104/pp.76.2.301.
4
Spontaneous Phloem bleeding from cryopunctured fruits of a ureide-producing legume.来自产生脲类的豆科植物冷冻穿刺果实的自发韧皮部出血。
Plant Physiol. 1984 Mar;74(3):499-505. doi: 10.1104/pp.74.3.499.
5
Role of amides, amino acids, and ureides in the nutrition of developing soybean seeds.酰胺、氨基酸和尿素在发育中大豆种子营养中的作用。
Plant Physiol. 1984 Feb;74(2):329-34. doi: 10.1104/pp.74.2.329.
6
An in vivo technique for the study of Phloem unloading in seed coats of developing soybean seeds.一种用于研究发育中大豆种子种皮韧皮部卸载的体内技术。
Plant Physiol. 1983 May;72(1):268-71. doi: 10.1104/pp.72.1.268.
7
Modeling C and N transport to developing soybean fruits.建立大豆果实发育过程中 C、N 转运模型。
Plant Physiol. 1982 Nov;70(5):1290-8. doi: 10.1104/pp.70.5.1290.
8
Morphology and ultrastructure of maternal seed tissues of soybean in relation to the import of photosynthate.与光合作用产物导入有关的大豆母体种子组织的形态和超微结构。
Plant Physiol. 1981 May;67(5):1016-25. doi: 10.1104/pp.67.5.1016.
9
Mechanism of cyanide inhibition of Phloem translocation.氰化物抑制韧皮部运输的机制。
Plant Physiol. 1977 Feb;59(2):178-80. doi: 10.1104/pp.59.2.178.

大豆种皮中的韧皮部卸载:向附着的“空胚珠”中流出的动态变化及稳定性

Phloem unloading in soybean seed coats: dynamics and stability of efflux into attached ;empty ovules'.

作者信息

Gifford R M, Thorne J H

机构信息

CSIRO, Division of Plant Industry, GPO Box 1600, Canberra, A.C.T. 2601, Australia.

出版信息

Plant Physiol. 1986 Feb;80(2):464-9. doi: 10.1104/pp.80.2.464.

DOI:10.1104/pp.80.2.464
PMID:16664644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1075136/
Abstract

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.

摘要

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。