Delayed fluorescence induction in chloroplasts. Irradiance dependence

We have studied the delayed fluorescence in spinach chloroplasts produced 0.5 ms after each of a pair of (sub)-microsecond flashes. We observe an increase in the delayed fluorescence from the second flash relative to that produced by the first. This increase is proportional to the product of the first and second flash irradiances, appearing as an I² dependence if both flashes are increased together. The enhancement is observable at very weak flash levels (roughly 1 photon absorbed/100 PS II centers). If the irradiance of the first flash is increased, but the irradiance of the second held constant, the delayed fluorescence from the second flash is observed to increase, but then to saturate well below the first flash irradiance at which the delayed fluorescence from the first flash itself saturates. For most experiments, the dark time between flashes was 30 ms. If the dark time is varied, the enhancement changes, reaching a half-maximal value for a dark time of approx. 300 μs. The enhancement is stopped by hydroxylamine, but not by gramicidin, valinomycin, DCMU, or mild heating. These experiments are consistent with the notion that there are two different types of Photosystem II centers if we assume that only one type is responsible for the induction we see and has an optical cross-section about 4-times the size of the other type of center.     

Chloroplast development and the synthesis of chlorophyll and protochlorophyllide in Zostera transferred to darkness

Intact plants and isolated leaves of Zostera capricornii Martens ex Aschers were transferred from daylight to darkness. Substantial amounts of chloropyll a and b continued to accumulate in immature and mature tissue in the same ratio as in the light and were incorporated into chlorophyll-protein complexes in the thylakoids. A small amount of protochlorophyllide also accumulated in immature tissue in the dark. Proplastids and immature chloroplasts continued to develop into mature chloroplasts in the dark in the normal manner but prolamellar bodies, which are a conspicuous feature of immature chloroplasts, took longer to disperse than in the light. Protochlorophyllide accumulation and prolamellar-body formation were not correlated. The results indicate that Zostera has a genetic capacity for dark chlorophyll synthesis which is expressed in immature and mature leaf tissue and enables this plant to continue synthesising chlorophyll and assembling chloroplasts at night.Abbreviations Chl chlorophyll - T _o time of transfer to darkness     

Possible mechanisms for the inhibition of photosynthesis by ozone

Tropospheric ozone produced by industrial civilization is widespread. Although the levels are not clearly life threatening, they do have the potential to inhibit normal plant productivity, thought to be by an inhibition of photosynthesis. While the mechanism for this inhibition is not yet clear, there are several hypotheses for its cause. It is unlikely that ozone can penetrate the cell membrane unreacted; therefore, reactions at the plasma membrane either causing general ionic and metabolic disturbance within the cell or causing the production of unidentified toxic products must ultimately produce the alterations within the chloroplasts. While model systems, such as individual biochemicals, isolated chloroplasts, and algae, can give some understanding of possible reactions, they cannot provide the full story. One continuing controversy revolves about the role of stomata in the inhibition process-they play an important role, but the full interaction between stomatal closure and inhibition of photosynthesis has not yet emerged. In order to reach a political compromise on air quality standards, we need to have a good understanding of the fundamental mechanisms by which ozone causes any decline in plant productivity.     

Characterization of the reversible state of photoinhibition occurring in vitro under anaerobic conditions

Thylakoid membranes were subjected to photoinhibitory illumination. The use of oxygen-consuming enzymes to obtain strictly anaerobic conditions showed that while the absence of oxygen is a prerequisite for the formation of a reversibly photoinhibited state, the presence of oxygen is required for the recovery in the dark. The formation of the reversibly photoinhibited state did not protect the thylakoid membranes against irreversible damage. The effects of both bicarbonate and formate were found to be qualitatively different for photoinhibition under strictly anaerobic conditions compared to the effects observed under normal aerobic photoinhibition. It is suggested that there are two different mechanisms of photoinhibition, occurring to different extent under aerobic and anaerobic conditions, respectively, involving Q_A in both cases, but the Q_B-site in the former only.Abbreviations chl chlorophyll - PpBQ phenyl-p-benzoquinone - PS 2 Photosystem 2 - Q_A and Q_B primary and secondary quinone acceptors of Photosystem 2     

The phase behavior of lipids in photosynthetic membranes

The phase behavior of the main classes of polar lipids found in the photosynthetic membranes of higher plants and algae is reviewed and compared to that of binary lipid mixtures and total lipid extracts of such membranes. Particular interest is paid to the way in which factors such as temperature and acyl chain saturation influence the phase behavior of these lipids and the implications this has in terms of the ability of photosynthetic membranes to resist environmental stress.