Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-25T07:05:32.842Z Has data issue: false hasContentIssue false

The action of 2, 21 and 100% of oxygen on primary photochemistry of photosystem II (PS II), biosynthesis of pigments and carbon dioxide fixation by etiolated bean leaves during greening

Published online by Cambridge University Press:  05 December 2011

B. Wróblewska
Affiliation:
Department of Plant Physiology II, University of Warsaw, Krakowskie Przedmieście 26/28, 00–927 Warszawa, Poland
M. Siedlecka
Affiliation:
Department of Plant Physiology II, University of Warsaw, Krakowskie Przedmieście 26/28, 00–927 Warszawa, Poland
J. W. Poskuta
Affiliation:
Department of Plant Physiology II, University of Warsaw, Krakowskie Przedmieście 26/28, 00–927 Warszawa, Poland
Get access

Synopsis

The responses of photosynthesis to oxygen concentration 2, 21 and 100% by etiolated bean leaves upon illumination were determined. After 0.3, 3, 6, 10, 12 and 24 h of greening the following processes were measured. (1) Functioning of PS II as reflected by changes in Fv/Fm ratios and t1/2 values. (2) Content and composition of pigments. (3) Capacity for carbon dioxide assimilation. The results showed that O2 exerts a complex inhibitory action on examined processes. The magnitudes of inhibition increased with increasing of O2 concentration and time of its action. Under applied conditions the lag phase for development of examined processes (with the exception of carotenoids) was in the range 3-10 h. After 24 h of greening in 2, 21 and 100% of O2 the Fy/Fm ratios attained values 0.55, 0.45, 0.13 respectively as compared with typical 0.80 of normal green leaves of bean. After 24 h of greening the inhibition by 100% O2 as compared with zero inhibition by 2% O2 were, in percentages: Fw/Fm, 78; t1/2, 77; chlorophyll a, 59; chlorophyll b, 69; β-carotene, 78; neoxanthin, 60; zeaxanthin, 43; violaxanthin, 35; CO2 fixation, 95.

Type
Research Article
Copyright
Copyright © Royal Society of Edinburgh 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Arnon, D. J., Allen, M. B. & Whatley, F. R. 1954. Photosynthesis by isolated chloroplasts. Nature (London) 174, 394–6.CrossRefGoogle ScholarPubMed
Baker, N. R. 1991. A possible role of photosystem II in environmental perturbation of photosynthesis. Physiologia Plantarum 81, 563–70.CrossRefGoogle Scholar
Barber, J. & Anderson, B. 1992. Too much a good thing: light can be bad for photosynthesis. Trends in Biochemical Science 17, 61–6.CrossRefGoogle Scholar
Bjorkman, O. & Demmig, B. 1987. Photon yield of oxygen evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins, Planta 170, 489504.Google Scholar
Bradbury, M., Ireland, C. R. & Baker, N. R. 1985. Analysis of chlorophyll fluorescence transients from pea leaves generated by changes in atmospheric concentration of CO2 and O2. Biochimica et Biophysica Acta 806, 357–65.CrossRefGoogle Scholar
Demmig, B., Winter, K., Kruger, A. & Czygan, F. C. 1987. Photoinhibition and zeaxanthin formation in intact leaves. A possible role of xantophyll-cycle in the dissipation of excess light energy. Plant Physiology 84, 218–24.CrossRefGoogle Scholar
Elstner, E. F. 1982. Oxygen activation and oxygen toxicity. Annual Review of Plant Physiology 33, 7396.CrossRefGoogle Scholar
Gaffron, H. 1960. The energy storage: Photosynthesis. In Steward, F. C. (Ed.) Plant physiology. A treatise, pp. 3237. New York: Academic Press.Google Scholar
Genty, B., Briantais, J.-M. & Baker, N. R. 1989. The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochimica et Biophysica Acta 990, 8792.Google Scholar
Genty, B., Harbinson, J., Briantais, J.-M. & Baker, N. R. 1990. The relationship between nonphotochemical quenching of chlorophyll fluorescence and the rate of photosystem 2 photochemistry in leaves. Photosynthesis Research 25, 249–57.CrossRefGoogle ScholarPubMed
Grishina, G. S., Maleszewski, S., Frankiewicz, A. & Poskuta, J. W. 1974. Comparative study of the effects of red and blue light on 14CO2 uptake and carbon metabolism of maize leaves in air and oxygen. Zeitschrift für Pflanzenphysiologie 73, 189–97.CrossRefGoogle Scholar
Halliwell, B. 1981. The structure and function of chloroplasts in green leaf cells. In: Chloroplast metabolism, pp. 179205. Oxford: Oxford University Press.Google Scholar
Harris, G. C. & Heber, U. 1993. Effects of anaerobiosis on chlorophyll fluorescence yield in spinach (Spinacia oleracea) leaf discs. Plant Physiology 101, 1169–73.CrossRefGoogle ScholarPubMed
Krall, J. P. & Edwards, G. E. 1992. Relationship between photosystem II activity and CO2 fixation in leaves. Physiologia Plantarum 86, 180–7.CrossRefGoogle Scholar
Krause, G. H. & Laasch, H. 1987. Photoinhibition of photosynthesis. Studies on the mechanism of damage and protection in chloroplasts. In Biggins, J. (Ed.) Progress in photosynthesis research, Vol. 4, pp. 1926. Deordrecht: Martinius Nijhoff Publishers.Google Scholar
Krause, G. H. & Weis, E. 1984. Review: Chlorophyll fluorescence as a tool in plant physiology. II. Interpretation of fluorescence signals. Photosynthesis Research 5, 139–57.Google Scholar
Lichtenthaler, H. K. & Wellburn, A. B. 1983. Determination of total carotenoids and chlorophyll a and b of leaf extracts in different solvents. Biochemical Society Transactions 603, 591–2.CrossRefGoogle Scholar
Malkin, S. & Fork, D. C. 1981. Photosynthetic units of sun and shade plants. Plant Physiology 67, 580–3.CrossRefGoogle Scholar
Mikulska, M., Siedlecka, M., Poskuta, J. W. & Maleszewski, S., 1987. Effect of long term-action of high oxygen concentration on photosynthetic apparatus in French bean leaves. 1. Changes in net photosynthetic rate and in chlorophylls and carotenoids contents. Photosynthetica 21, 175–8.Google Scholar
Mikulska, M., Poskuta, J. W. & Maleszewski, S. 1988. Effect of long-term action of high concentration of oxygen on photosynthetic apparatus in French bean leaves. 2. Carbon dioxide exchange, enzyme activities and level of ribulose-1,5-biphosphate in leaves. Photosynthetica 22, 383–7.Google Scholar
Oberhuber, W. & Edwards, G. E. 1993. Temperature dependence of the linkage of quantum yield of PS II to carbon dioxide fixation in C-4 and C-3 plants. Plant Physiology 101, 507–12.Google Scholar
Oquist, S. & Wass, R. 1988. A portable, microprocessor operated instrument for measuring chlorophyll fluorescence kinetics in stress physiology. Physiologia Plantarum 73, 211–7.Google Scholar
Peterson, R. B. 1991. Analysis of changes in minimal and maximal fluorescence yields with irradiance and oxygen level in tobacco leaf tissue. Plant Physiology 96, 171–7.CrossRefGoogle Scholar
Poskuta, J. W. 1968. Photosynthesis, photorespiration and respiration of detached spruce twigs as influenced by oxygen concentration and light intensity. Physiologia Plantarum 21, 1129–36.Google Scholar
Poskuta, J. W., Nelson, C. D. & Krotkow, G. 1967. Effects of metabolic inhibitors on the rates of carbon dioxide evolution in light and in darkness by detached spruce twigs, wheat and soybean leaves. Plant Physiology 42, 1187–90.CrossRefGoogle Scholar
Poskuta, J. W., Mikulska, M., Faltynowicz, M., Bielak, B. & Wróblewska, B. 1974. The effect of oxygen concentration on the development of photosynthetic capacity by etiolated bean seedlings upon illumination. Zeitschrift für Pflanzenphysiologie 73, 387–93.CrossRefGoogle Scholar
Powles, S. B. 1984. Photoinhibition of photosynthesis induced by visible light. Annual Review of Plant Physiology 35, 1544.CrossRefGoogle Scholar
Sandmann, H., Kühn, M. & Boger, P. 1993. Carotenoids in photosynthesis: Protection of D1 degradation in the light. Photosynthesis Research 35, 185–90.CrossRefGoogle ScholarPubMed
Scandalios, J. G. 1993. Oxygen stress and superoxide dismutases. Plant Physiology 101, 712.CrossRefGoogle ScholarPubMed
Sironval, C. & Kandler, O. 1958. Photooxidation processes in normal green Chlorella cells. I. The bleaching process. Biochimica et Biophysica Acta 29, 359–69.CrossRefGoogle Scholar
Thayer, S. S. & Bjorkman, O. 1992. Carotenoids distribution and deepoxidation in thylakoid pigmentprotein complexes from cotton leaves and bundle-sheet cells of maize. Photosynthesis Research 33, 213–25.CrossRefGoogle ScholarPubMed
Walker, D. 1992. Tansley Review No 36. Excited leaves. New Phytologist 121, 325–45.CrossRefGoogle ScholarPubMed
Warburg, O. 1920. Uber die Geschwindigkeit der photochemischen Kohlensaurezersetzung in lebenden Zellen. II. Biochemische Zeitschrift 103, 188217.Google Scholar
Zelitch, I. 1966. Increased rate of net photosynthetic carbon dioxide uptake caused by the inhibition of glycolate oxidase. Plant Physiology 41, 1623–31.Google Scholar