Ludwig L J, Canvin D T
Department of Biology, Queen's University, Kingston, Ontario, Canada.
Plant Physiol. 1971 Dec;48(6):712-9. doi: 10.1104/pp.48.6.712.
Single attached leaves of sunflower (Helianthus annus L. "Mennonite") were supplied (14)CO(2) of constant specific radioactivity in gas mixtures containing various CO(2) and O(2) concentrations. The (14)CO(2) and CO(2) fluxes were measured concurrently in an open system using an ionization chamber and infrared gas analyzer.The rate of photorespiration (5.7 +/- 0.3 mg CO(2).dm(-2).(-1)) during photosynthesis in 21% O(2) at 25 C and 3,500 footcandles was over three times the rate of dark respiration and was independent of CO(2) concentrations from 0 to 300 mul/l. The steady rate of CO(2) evolution into CO(2)-free air was about 30% lower. Low oxygen (1%) inhibited both (14)CO(2) and CO(2) evolution, both during photosynthesis and in CO(2)-free air in the light.At 300 mul/l CO(2) apparent photosynthesis was inhibited 41% by 21% O(2). Two-thirds of the inhibition was due to the inhibition of true photosynthesis by oxygen and one-third due to the stimulation of photorespiration. At 50 mul/l CO(2), where the percentage inhibition of apparent photosynthesis by 21% oxygen was 92%, photorespiration accounted for two-thirds of the total inhibition.The rate of (14)CO(2) uptake by the leaf decreased about 30 seconds after the introduction of (14)CO(2), indicating that (14)CO(2) was rapidly evolved from the leaf. The rate of (14)CO(2) evolution increased rapidly with time, the kinetics depending on the CO(2) concentration. The high specific radioactivity of the (14)CO(2) evolved during photosynthesis or in the early period of flushing in CO(2)-free air showed that the substrate for light respiration was an early product of photosynthesis. From the measurement of (14)CO(2) and CO(2) evolution into CO(2)-free air over a longer time period it was apparent that at least three compounds, each of decreased (14)C content, could supply the substrate for light respiration.Based on a consideration of the specific radioactivity of (14)CO(2) evolved under a variety of conditions, it is suggested that total CO(2) evolution in the light or photorespiration is composed of two processes, dark respiration and light respiration. Light respiration is a process that only occurs in the light, persists for some time on darkening, and metabolizes substrates that are quite different from those of dark respiration.
为向日葵(向日葵属“门诺派”)的单叶提供了具有恒定比放射性的(14)CO(2),这些(14)CO(2)存在于含有不同CO(2)和O(2)浓度的气体混合物中。使用电离室和红外气体分析仪在开放系统中同时测量(14)CO(2)和CO(2)通量。在25℃和3500英尺烛光下,21% O(2)条件下光合作用期间的光呼吸速率(5.7±0.3毫克CO(2)·分米(-2)·小时(-1))是暗呼吸速率的三倍多,且与0至300微升/升的CO(2)浓度无关。向无CO(2)空气中稳定释放CO(2)的速率约低30%。低氧(1%)在光合作用期间以及光照下的无CO(2)空气中均抑制(14)CO(2)和CO(2)的释放。在300微升/升CO(2)时,21% O(2)使表观光合作用受到41%的抑制。其中三分之二的抑制是由于氧气对真正光合作用的抑制,三分之一是由于光呼吸的刺激。在50微升/升CO(2)时,21%氧气对表观光合作用的抑制百分比为92%,光呼吸占总抑制的三分之二。引入(14)CO(2)约30秒后,叶片对(14)CO(2)的吸收速率下降,这表明(14)CO(2)从叶片中迅速释放。(14)CO(2)的释放速率随时间迅速增加,其动力学取决于CO(2)浓度。光合作用期间或在无CO(2)空气中冲洗早期释放的(14)CO(2)的高比放射性表明,光呼吸的底物是光合作用的早期产物。通过在更长时间段内测量进入无CO(2)空气中的(14)CO(2)和CO(2)释放量,很明显至少有三种(14)C含量降低的化合物可以为光呼吸提供底物。基于对在各种条件下释放的(14)CO(2)比放射性的考虑,表明光照下的总CO(2)释放或光呼吸由两个过程组成,即暗呼吸和光呼吸。光呼吸是一个仅在光照下发生、在黑暗中持续一段时间且代谢与暗呼吸底物截然不同的底物的过程。