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The changes in photosynthetic activity and composition of pigments induced by changes in temperature were examined in the third leaf of three chilling-tolerant and three chilling-sensitive genotypes of maize (Zea mays L.). The plants were grown under a controlled environment at a photon flux density of 550 µmol m−2 s−1, a 12 h photoperiod and at a suboptimal temperature of 14/12°C (day/night) until the full expansion of the third leaf. After this treatment, the chilling-tolerant genotypes, when compared with the sensitive ones, displayed a higher photosynthetic activity, a higher content of chlorophyll (Chl) a + b, a higher Chl a/b ratio, a larger total carotenoid pool size as well as a different carotenoid composition. When temperature was subsequently increased to 24/22°C for 3 d the composition of the pigments changed, but the chilling-sensitive genotypes, while adjusting their lower Chl a/b ratio and their different carotenoid composition, were unable to adjust their lower content of chlorophyll, their smaller total carotenoid pool size or their lower photosynthetic performance. Moreover, while the chilling-tolerant genotypes converted the most part of zeaxanthin to violaxanthin in the xanthophyll cycle, the chilling-sensitive genotypes retained high amounts of zeaxanthin. The changes in pigment composition that occurred over the 3 d at 24/22°C were largely conserved when the plants were returned to 14/12°C, but photosynthetic activity decreased and zeaxanthin accumulated again. The results suggest that the capability of the chilling-tolerant genotypes, when compared with the sensitive ones, to retain high amounts of pigments and to form a competent photosynthetic apparatus at low temperature is the basis for their more vigorous growth in cool climates

Chlorophyll a fluorescence rise kinetics (from 50 μs to 1 s) were used to investigate the non-photochemical reduction of the plastoquinone (PQ) pool in osmotically broken spinach chloroplasts (Spinacia oleracea L.). Incubation of the chloroplasts in the presence of exogenous NADPH or NADH resulted in significant changes in the shape of the fluorescence transient reflecting an NAD(P)H-dependent accumulation of reduced PQ in the dark, with an extent depending on the concentration of NAD(P)H and the availability of oxygen; the dark reduction of the PQ pool was saturated at lower NAD(P)H concentrations and reached a higher level when the incubation took place under anaerobic conditions than when it occurred under aerobic conditions. Under both conditions NADPH was more effective than NADH in reducing PQ, however only at sub-saturating concentrations. Neither antimycin A nor rotenone were found to alter the effect of NAD(P)H. The addition of mercury chloride to the chloroplast suspension decreased the NAD(P)H-dependent dark reduction of the PQ pool, with the full inhibition requiring higher mercury concentrations under anaerobic than under aerobic conditions. This is the first time that this inhibitory role of mercury is reported for higher plants. The results demonstrate that in the dark the redox state of the PQ pool is regulated by the reduction of PQ via a mercury-sensitive NAD(P)H-PQ oxidoreductase and the reoxidation of reduced PQ by an O2-dependent pathway, thus providing additional evidence for the existence of a chlororespiratory electron transport chain in higher plant chloroplasts

We analysed the changes of the chlorophyll (Chl) a fluorescence rise kinetic (from 50 μs to 1 s) that occur when leaves or chloroplasts of pea ( Pisum sativum L.) are incubated under anaerobic conditions in the dark. In control leaves, Chl a fluorescence followed a typical O-J-I-P polyphasic rise [Strasser et al. (1995) Photochem Photobiol 61: 32-42]. Anaerobiosis modified the shape of the transient with the main effect being a time-dependent increase in the fluorescence yield at the J-step (2 ms). Upon prolongation of the anaerobic treatment (> 60 min), the O-J-I-P fluorescence rise was eventually transformed to an O-J (J = P) rise. A similar transformation was observed when pea leaves were treated with DCMU or sodium dithionite. Anaerobiosis resulted in a 10-20% reduction in the maximum quantum yield of the primary photochemistry of Photosystem II, as measured by the ratio of the maximal values of variable and total fluorescence (FV/FM). When the leaves were returned to the air in the dark, the shape of the fluorescence transient showed a time-dependent recovery from the anaerobiosis-induced change. The original O-J-I-P shape could also be restored by illuminating the anaerobically treated samples with far-red light but not with blue or white light. Osmotically broken chloroplasts displayed under anaerobic conditions fluorescence transients similar to those observed in anaerobically treated leaves, but only when they were incubated in a medium comprising reduced pyridine nucleotides (NADPH or NADH). As in intact leaves, illumination of the anaerobically treated chloroplasts by far-red light restored the original O-J-I-P transient, although only in the presence of methyl viologen. The results provide additional evidence for the existence of a chlororespiratory pathway in higher plant cells. Furthermore, they suggest that the J-level of the fluorescence transient is strongly determined by the redox state of the electron carriers at the PS II acceptor side

The changes in photosynthetic activity and composition of pigments induced by changes in temperature were examined in the third leaf of three chilling-tolerant and three chilling-sensitive genotypes of maize (Zea mays L.). The plants were grown under a controlled environment at a photon flux density of 550 µmol m−2 s−1, a 12 h photoperiod and at a suboptimal temperature of 14/12°C (day/night) until the full expansion of the third leaf. After this treatment, the chilling-tolerant genotypes, when compared with the sensitive ones, displayed a higher photosynthetic activity, a higher content of chlorophyll (Chl) a + b, a higher Chl a/b ratio, a larger total carotenoid pool size as well as a different carotenoid composition. When temperature was subsequently increased to 24/22°C for 3 d the composition of the pigments changed, but the chilling-sensitive genotypes, while adjusting their lower Chl a/b ratio and their different carotenoid composition, were unable to adjust their lower content of chlorophyll, their smaller total carotenoid pool size or their lower photosynthetic performance. Moreover, while the chilling-tolerant genotypes converted the most part of zeaxanthin to violaxanthin in the xanthophyll cycle, the chilling-sensitive genotypes retained high amounts of zeaxanthin. The changes in pigment composition that occurred over the 3 d at 24/22°C were largely conserved when the plants were returned to 14/12°C, but photosynthetic activity decreased and zeaxanthin accumulated again. The results suggest that the capability of the chilling-tolerant genotypes, when compared with the sensitive ones, to retain high amounts of pigments and to form a competent photosynthetic apparatus at low temperature is the basis for their more vigorous growth in cool climates