John Pirt S
Department of Microbiology, Kings College, University of London, Kensington Campus, Campden Hill Road, London W8 7AH.
New Phytol. 1986 Jan;102(1):3-37. doi: 10.1111/j.1469-8137.1986.tb00794.x.
The commonly quoted values of maximum photosynthetic efficiency have been those obtained by determining the oxygen yield from suspensions of resting algal cells in which growth was disregarded. The unpredictability of the metabolism of resting cells severely vitiates the reliability of measurements made on their energy metabolism. Also the validity of the measurements with resting cells is made doubtful by anomalous values for the photosynthetic quotient (-δCO /δO ). The measurements on resting cells fall into two categories: one in which the cells were suspended in acid media (pH 5) with a CO partial pressure (p ) 5% atmospheric, and one in which the cells were suspended in alkaline media (about pH 9) with a p of 0.25% atmospheric. In acid media with 5% CO , the most probable value of the minimum quantum demand is 5 to 6 hv/O . With pH 9 media, equilibrated with 0.25% CO , the minimum quantum demand found is about 10 hv/O . This low efficiency seems to be caused by a sub-optimal CO partial presure, since it has been observed that the value at alkaline pH agrees with that at acid pH provided the p is maintained at 2 % atmospheric. This p effect has been neglected by many workers. To avoid the controversial methods using resting cells, it is essential to determine the photosynthetic efficiency of cells in a steady state of growth. The environmental conditions during growth of the cells have a strong influence on the efficiency of photosynthesis; for instance, the efficiency appears to be strongly dependent on the temperature during growth. Under light-limited conditions when the photosynthetic efficiency of growth is optimized the minimum quantum demand of algal cells is found to be 5 to 6 hv/O . The minimum quantum demand of CO fixation varies from 1.1 to 1.4 times the value for O depending on the nature of the nitrogen source for growth. Significant doubt must be attached to measurements of the maximum photosynthetic efficiency with isolated chloroplasts, on the grounds that in vitro conditions may impair their efficiency and that the efficiency may be affected by the growth conditions of the parent plant. Thus, a unified view of the experimental data indicates that the most probable value of the minimum quantum demand is 5 to 6 hv/O . The preference for the apparently sub-optimal value of about 10 hv/O found with alkaline media and a p of 0.25 %, which is the prevailing view, is necessitated by the requirement of the Z-scheme paradigm of the mechanism of the electron transfer. Thus it appears that hypothesis rather than a unified view of the experimental data on the efficiency is dictating the view of the mechanism involved. A cell of Chlorella (strain 211/8k) fully charged with reducing equivalents and energy can continue to assimilate CO and grow at the maximum rate (doubling time 3 h) for 9 s. It is calculated that exposure to 20 W m (daylight PAR) for 0.5 s is sufficient fully to charge such a cell with energy and reducing equivalents. This calculation predicts that, in the steady state of growth, cycles of exposure of each cell to 20 W m for 0.5 s followed by 9 s in the dark will support growth at the maximum rate. The theoretical expressions used to express the maximum thermodynamic efficiency of conversion of radiation to chemical work (η ) are shown to be inconsistent. The correct value is taken to be given by Spanner's equation η = 1 -(T/T ), where T is the ambient temperature and T is the radiation temperature. Hence, the maximum value of η for conversion of the PAR in sunlight to chemical work varies from 0.93 for unscattered sunlight to 0.70 if it is isotropically scattered. It is deduced that under the usual ambient conditions the value of η for photosynthesis will decrease by 0.043 for each log decrease in the irradiance. Contents Summary 3 I. Introduction 4 II. The stoichiometry of photosynthesis 6 III. Thermodynamic limits to photosynthetic efficiency 7 IV. The theoretical quantum demands for production of NADPH and ATP 8 V. The dynamics and energetics of photosynthetic growth 10 VI. The physiology of cells at or near zero growth rate 12 VII. Manometric measurements of quantum demands of resting cells 13 VIII. Non-manometric measurements of quantum demands of resting cells 16 IX. Quantum demands of vascular plants and isolated chloroplasts 18 X. The quantum demands of growing cells 19 XI. The influence of wavelength of radiation on photosynthetic efficiency 22 XII. Conclusion 23 XIII. Appendices 24 References 34.
通常引用的最大光合效率值是通过测定静止藻类细胞悬浮液中的氧气产量获得的,其中生长情况被忽略。静止细胞代谢的不可预测性严重损害了对其能量代谢进行测量的可靠性。此外,静止细胞测量值的有效性也因光合商(-δCO₂/δO₂)的异常值而受到质疑。对静止细胞的测量分为两类:一类是将细胞悬浮在酸性介质(pH 5)中,CO₂分压(pCO₂)为大气的5%;另一类是将细胞悬浮在碱性介质(约pH 9)中,pCO₂为大气的0.25%。在含5% CO₂的酸性介质中,最小量子需求的最可能值为5至6 hv/O₂。在与0.25% CO₂平衡的pH 9介质中,发现的最小量子需求约为10 hv/O₂。这种低效率似乎是由次优的CO₂分压引起的,因为据观察,只要pCO₂保持在大气的2%,碱性pH下的值与酸性pH下的值一致。许多研究人员忽略了这种pCO₂效应。为了避免使用静止细胞的有争议方法,确定处于稳定生长状态的细胞的光合效率至关重要。细胞生长期间的环境条件对光合作用效率有很大影响;例如,效率似乎强烈依赖于生长期间的温度。在光限制条件下,当生长的光合效率达到最佳时,藻类细胞的最小量子需求为5至6 hv/O₂。CO₂固定的最小量子需求根据生长的氮源性质在O₂固定值的1.1至1.4倍之间变化。对于用分离的叶绿体测量最大光合效率,必须有很大疑问,因为体外条件可能会损害其效率,并且效率可能会受到亲本植物生长条件的影响。因此,对实验数据的统一看法表明,最小量子需求的最可能值为5至6 hv/O₂。由于电子传递机制的Z方案范式的要求,对于在碱性介质和0.25%的pCO₂下发现的约10 hv/O₂这种明显次优值的偏好是主流观点。因此看来,关于效率的实验数据的观点似乎是由假设而不是统一看法决定的。充满还原当量和能量的小球藻(211/8k菌株)细胞可以继续同化CO₂并以最大速率(倍增时间3小时)生长9秒。据计算,暴露于20 W m⁻²(日光光合有效辐射)0.5秒足以使这样一个细胞充满能量和还原当量。该计算预测,在稳定生长状态下,每个细胞以0.5秒暴露于20 W m⁻²随后在黑暗中9秒的循环将支持最大速率的生长。用于表示辐射转化为化学功的最大热力学效率(η)的理论表达式被证明是不一致的。正确的值由斯潘纳方程η = 1 - (Tₐ/Tₑ)给出,其中Tₐ是环境温度,Tₑ是辐射温度。因此,如果日光光合有效辐射在阳光中无散射,则转化为化学功的η最大值为0.93;如果它是各向同性散射的,则为0.70。据推断,在通常的环境条件下,光合效率的η值将随着辐照度每降低一个对数单位而降低0.043。内容摘要3 一、引言4 二、光合作用的化学计量6 三、光合效率的热力学极限7 四、产生NADPH和ATP的理论量子需求8 五、光合生长的动力学和能量学10 六、零生长速率或接近零生长速率时细胞的生理学12 七、静止细胞量子需求的测压测量13 八、静止细胞量子需求的非测压测量16 九、维管植物和分离叶绿体的量子需求18 十、生长细胞的量子需求19 十一、辐射波长对光合效率的影响22 十二、结论23 十三、附录24 参考文献34