Laisk A, Kiirats O, Oja V
Institute of Astrophysics and Atmospheric Physics, Estonian Academy of Sciences, 202444 Tôravere, Tartu, Estonia, U.S.S.R.
Plant Physiol. 1984 Nov;76(3):723-9. doi: 10.1104/pp.76.3.723.
Assimilatory power was measured in ten C(3) species by means of a rapid-response gas exchange device as the total amount of CO(2) fixed in N(2)-CO(2) atmosphere after switching the light off. Different steady-state levels of the assimilatory power were obtained by varying light intensity and O(2) and CO(2) concentrations during the preexposition periods in the leaf chamber.Within the limits of the linear part of the CO(2) curve of photosynthesis in N(2), the assimilatory power is constant, being sufficient for the assimilation of about 20 nanomoles CO(2) per square centimeter leaf. The pool starts to decrease with the onset of the CO(2) saturation of photosynthesis. Increase in O(2) concentration from 0 to 100% at 350 microliters CO(2) per liter produces a considerable decrease in the assimilatory power.THE MESOPHYLL CONDUCTANCE (M) WAS FOUND TO BE PROPORTIONAL TO THE ASSIMILATORY POWER (A): M = mA. The most frequently occurring values of the proportionality constant (m) (called the specific efficiency of carboxylation) were concentrated between 0.03 and 0.04 centimeter per second per nanomole A per square centimeter but the measured extreme values were 0.01 and 0.06 centimeter per second per nanomole A per square centimeter. The specific rate of carboxylation (the rate per unit A) showed a hyperbolic dependence on CO(2) conentration with the most frequent values of K(m) (CO(2)) ranging from 25 to 35 micromolar in the liquid phase of mesophyll cells (extremes 23 and 100 micromolar).It is concluded that the CO(2(-) ) and light-saturated rate of photosynthesis is limited by the reactions of the formation of the assimilatory power and not by ribulose-1,5-bisphosphate carboxylase. O(2) is a competitive consumer of the assimilatory power, and the inhibitory effect of O(2) on photosynthesis is caused mainly by a decrease in the pool of the assimilatory power at high O(2) concentrations. In intact leaves, the kinetic properties of ribulose-1,5-bisphosphate carboxylase seem to be variable.
利用快速响应气体交换装置,在10种C(3)植物中测定了同化力,即关闭光照后在N(2)-CO(2)气氛中固定的CO(2)总量。在叶室预暴露期间,通过改变光照强度、O(2)和CO(2)浓度,获得了不同稳态水平的同化力。在N(2)中光合作用的CO(2)曲线线性部分的范围内,同化力是恒定的,足以同化每平方厘米叶片约20纳摩尔的CO(2)。随着光合作用的CO(2)饱和开始,该库开始减少。在每升350微升CO(2)的条件下,O(2)浓度从0增加到100%会使同化力显著降低。发现叶肉导度(M)与同化力(A)成正比:M = mA。比例常数(m)(称为羧化的比效率)最常出现的值集中在每秒0.03至0.04厘米每平方厘米每纳摩尔A之间,但测量的极值为每秒0.01至0.06厘米每平方厘米每纳摩尔A。羧化的比速率(每单位A的速率)对CO(2)浓度呈双曲线依赖性,叶肉细胞液相中K(m)(CO(2))最常出现的值范围为25至35微摩尔(极值为23和100微摩尔)。得出的结论是,光合作用的CO(2)和光饱和速率受同化力形成反应的限制,而不是受核酮糖-1,5-二磷酸羧化酶的限制。O(2)是同化力的竞争性消耗者,O(2)对光合作用的抑制作用主要是由于高O(2)浓度下同化力库的减少。在完整叶片中,核酮糖-1,5-二磷酸羧化酶的动力学特性似乎是可变的。