Gepstein S, Thimann K V
Department of Biology, University of California, Santa Cruz, California 95064.
Plant Physiol. 1981 Aug;68(2):349-54. doi: 10.1104/pp.68.2.349.
The evolution of ethylene, both from the endogenous source and from added 1-aminocyclopropane-1-carboxylic acid (ACC), has been followed in close relationship with the senescent loss of chlorophyll from seedling oat leaves. In white light, where chlorophyll loss is slow, the ethylene evolution increases slowly at first, but when the loss of chlorophyll becomes more rapid, ethylene evolution accelerates. CoCl(2) inhibits this increase and correspondingly maintains the chlorophyll content, with an optimum concentration of 10 micromolar. The rapid rate of chlorophyll loss in the dark is slightly decreased by 3-aminoethoxyvinyl glycine (AVG), by cobalt, and slightly stimulated by ACC. The slower chlorophyll loss in white light, however, is almost completely inhibited by silver ions, greatly decreased by cobalt and by AVG, and strongly increased by ACC. Since the chlorophyll loss is accompanied by proteolysis, it represents true senescence. Chlorophyll loss in light is also strongly antagonized by CO(2), 1% CO(2) giving almost 50% chlorophyll maintenance in controls, while in the presence of added ACC or ethylene gas, the chlorophyll loss is 50% reversed by about 3% CO(2). The ethylene system in leaves is thus more sensitive to CO(2) than that in fruits. Indoleacetic acid also clearly decreases the effect of ACC. It is shown that kinetin, CO(2), Ag(+), and indoleacetic acid, all of which oppose the effect of ethylene, nevertheless increase the evolution of ethylene by the leaves, and it is suggested that ethylene evolution may, in many instances, mean that its hormonal metabolism is being prevented.Abscisic acid somewhat increases ethylene evolution also, but its action in promoting senescence in light is antagonized only partially by Ag(+), Co(2+), or AVG. For this and a number of other reasons it is concluded that ethylene and abscisic acid both independently control leaf senescence in the light.
已对燕麦幼苗叶片中叶绿素衰老损失的同时,内源乙烯以及添加的1-氨基环丙烷-1-羧酸(ACC)所产生的乙烯的释放情况进行了跟踪研究。在白光下,叶绿素损失缓慢,乙烯释放起初也缓慢增加,但当叶绿素损失加快时,乙烯释放加速。氯化钴抑制这种增加,并相应地维持叶绿素含量,最适浓度为10微摩尔。在黑暗中叶绿素快速损失的速率,因3-氨基乙氧基乙烯基甘氨酸(AVG)、钴而略有降低,并因ACC而略有增加。然而,白光下较慢的叶绿素损失几乎完全被银离子抑制,因钴和AVG而大幅降低,并因ACC而大幅增加。由于叶绿素损失伴随着蛋白质水解,它代表真正的衰老。光照下的叶绿素损失也受到二氧化碳的强烈拮抗,1%的二氧化碳使对照中的叶绿素维持率接近50%,而在添加ACC或乙烯气体的情况下,约3%的二氧化碳可使叶绿素损失逆转50%。因此,叶片中的乙烯系统比果实中的乙烯系统对二氧化碳更敏感。吲哚乙酸也明显降低了ACC的作用。结果表明,激动素、二氧化碳、银离子和吲哚乙酸,所有这些都与乙烯的作用相反,但却增加了叶片中乙烯的释放,并且有人提出,在许多情况下,乙烯的释放可能意味着其激素代谢受到了抑制。脱落酸也在一定程度上增加乙烯的释放,但其在光照下促进衰老的作用仅部分地被银离子、钴离子或AVG拮抗。基于这一点以及其他一些原因,可以得出结论,乙烯和脱落酸在光照下均独立控制叶片衰老。