Department of Botany, University of Toronto, Erindale College, Mississauga, Ontario, Canada L5L 1C6.
Plant Physiol. 1981 Feb;67(2):233-6. doi: 10.1104/pp.67.2.233.
Abscisic acid (AbA) treatments of concentrations of up to 135 micromolar did not inhibit photosynthesis in enzymatically isolated leaf mesophyll cells of Phaseolus vulgaris, Nicotiana tabacum, and Lycopersicum esculentum over periods of up to 5 hours. Thin slices of leaves preincubated in hypertonic solutions identical to those used to isolate cells were shown to synthesize AbA rapidly, although accumulation of AbA in the cells was low due to extensive release of the newly synthesized AbA into the medium. The levels of endogenously made AbA in leaf cells of Phaseolus vulgaris rose from a low of 0.27 micromolar to a high of 6.74 micromolar during 2 hours preincubation. Exogenously applied AbA can be taken up by the cells as was demonstrated using (14)[C]AbA. Thus, AbA applied at concentrations 19 times higher than endogenous levels does not change the rate of photosynthesis.
脱落酸(AbA)处理浓度高达 135 微摩尔,在长达 5 小时的时间内,不会抑制酶分离的菜豆、烟草和番茄叶片叶肉细胞的光合作用。在与分离细胞相同的高渗溶液中预孵育的叶片薄片被证明能够快速合成 AbA,尽管由于新合成的 AbA大量释放到培养基中,细胞内 AbA 的积累量很低。在 2 小时的预孵育过程中,菜豆叶片细胞内内源产生的 AbA 水平从 0.27 微摩尔的低值上升到 6.74 微摩尔的高值。如使用(14)[C]AbA 所证明的,细胞可以摄取外源施加的 AbA。因此,施加的 AbA 浓度比内源性水平高 19 倍不会改变光合作用的速率。