Relationship between energy-dependent fluorescence quenching and xanthophyll-cycle-pigments in transgenic chlorophyll-deficient tobacco grown under different light intensities

Journal of Photochemistry and Photobiology B: Biology

Volumn 43, Issue 2, 1998, Pages 136-145

  Härtel, Heiko ^a,b,c   Reinhardt, Immo ^b   Grimm, Bernhard ^a  

^a LEIBNIZ INSTITUTE OF PLANT GENETICS AND CROP PLANT RESEARCH IPK   (Germany)

^b HUMBOLDT UNIVERSITY   (Germany)

^c 224 Biochemistry Building ^*  (United States)

Author keywords

Antisense RNA; Chlorophyll synthesis; High energy quenching; Light acclimation; Nicotiana tabacum; Xanthophyll cycle

Indexed keywords

AMINOTRANSFERASE; CHLOROPHYLL; COMPLEMENTARY RNA; VIOLAXANTHIN; XANTHOPHYLL;

ARTICLE; LIGHT; PLANT GROWTH; PRIORITY JOURNAL; TOBACCO; TRANSGENIC PLANT;

NICOTIANA TABACUM; TABACUM;

EID: 0032524681     PISSN: 10111344     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1011-1344(98)00096-7     Document Type: Article

References (44)

1. [1] G.H. Krause, E. Weis, Chlorophyll fluorescence and photosynthesis: the basics, Annu. Rev. Plant Physiol. Plant Mol. Biol. 42 (1991) 313-349.
2. [2] T.G. Owens, Processing of excitation energy by antenna pigments, in: N.R. Baker (Ed.) Photosynthesis and the Environment, Kluwer, Dordrecht, The Netherlands, 1996, pp. 1-23.
3. [3] P. Horton, A.V. Ruban, R.G. Walters, Regulation of light harvesting in green plants, Annu. Rev. Plant Physiol. Plant Mol. Biol. 47 (1996) 655-684.
4. [4] G.H. Krause, U. Behrend, ΔpH-dependent chlorophyll fluorescence quenching indicating a mechanism of protection against photoinhibition of chloroplasts, FEBS Lett. 200 (1986) 298-302.
5. [5] W. Bilger, O. Björkman, Role of the xanthophyll cycle in photoprotection elucidated by measurements of light-induced absorbance changes, fluorescence and photosynthesis in leaves of Hedera canariensis, Photosynth. Res. 25 (1990) 173-185.
6. [6] J.-M. Briantais, C. Vernotte, M. Picaud, G.H. Krause, A quantitative study of the slow decline of chlorophyll fluorescence in isolated chloroplasts, Biochim. Biophys. Acta 548 (1979) 128-138.
7. [7] B. Demmig-Adams, W.W. Adams III, Photoprotection and other responses of plants to high light stress, Annu. Rev. Plant Phys. Plant Mol. Biol. 43 (1992) 599-626.
8. [8] A.M. Gilmore, H. Y. Yamamoto, Linear models relating xanthophylls and lumen acidity to non-photochemical fluorescence quenching. Evidence that antheraxanthin explains zeaxanthin-independent quenching, Photosynth. Res. 35 (1993) 67-78.
9. [9] R.G. Walters, A.V. Ruban, P. Horton, Higher plant light-harvesting complexes LHCIIa and LHCIIc are bound by dicyclohexylcarbodiimide during inhibition of energy dissipation, Eur. J. Biochem. 226 (1994) 1063-1069.
10. [10] H. Lokstein, H. Härtel, P. Hoffmann, Photoprotective function of light-harvesting complex II: a chlorophyll fluorescence study in leaves of wild type and a chlorophyll b-less mutant of barley, Lithuanian J. Phys. 34 (1994) 306-312.
11. [11] H. Lokstein, H. Härtel, P. Hoffmann, P. Woitke, G. Renger, The role of light-harvesting complex II in excess excitation energy dissipation: an in vivo fluorescence study on the origin of high-energy quenching, J. Photochem. Photobiol., B: Biol. 26 (1994) 175-184.
12. [12] A.M. Gilmore, T.L. Hazlett, P.G. Debrunner, Govindjee, Photosystem II chlorophyll a fluorescence lifetimes and intensity are independent of the antenna size differences between barley wild-type and chlorina mutants: photochemical quenching and xanthophyll cycle-dependent nonphotochemical quenching of fluorescence, Photosynth. Res. 48 (1996) 171-187.
13. [13] H. Härtel, H. Lokstein, B. Grimm, B. Rank, Kinetic studies on the xanthophyll cycle in barley leaves. Influence of antenna size and relations to nonphotochemical chlorophyll fluorescence quenching, Plant Physiol. 110 (1996) 471-482.
14. [14] S.S. Thayer, O. Björkman, Leaf xanthophyll content and composition in sun and shade determined by HPLC, Photosynth. Res. 23 (1990) 331-343.
15. [15] G.N. Johnson, J.D. Scholes, P. Horton, AJ. Young, Relationships between carotenoid composition and growth habit in British plant species, Plant, Cell Environ. 16 (1993) 681-686.
16. [16] E. Brugnoli, A. Cona, M. Lauteri, Xanthophyll cycle components and capacity for non-radiative energy dissipation in sun and shade leaves of Ligustrum ovalifolium exposed to conditions limiting photosynthesis, Photosynth. Res. 41 (1994) 451-463.
17. [17] B. Demmig-Adams, W.W. Adams III, B.A. Logan, A.S. Verhoeven, Xanthophyll cycle-dependent energy dissipation and flexible photosystem II efficiency in plants acclimated to light stress, Austr. J. Plant Physiol. 22 (1995) 249-260.
18. [18] B. Demmig-Adams, A.M. Gilmore, W.W. Adams III, In vivo functions of carotenoids in plants, FASEB J. 10 (1996) 403-412.
19. [19] A.V. Ruban, A.Y. Young, P. Horton, Induction of nonphotochemical energy dissipation and absorbance changes in leaves, Plant Physiol. 102 (1993) 741-750.
20. [20] G.N. Johnson, A.J. Young, J.D. Scholes, P. Horton, The dissipation of excess excitation energy in British plant species, Plant, Cell Environ. 16 (1993) 673-679.
21. [21] N.K. Boardman, Comparative photosynthesis of sun and shade plants, Annu. Rev. Plant Physiol. 28 (1977) 355-377.
22. [22] J.M. Briantais, Light-harvesting chlorophyll a-b complex requirement for regulation of photosystem II photochemistry by non-photochemical quenching, Photosynth. Res. 40 (1994) 287-294.
23. [23] H. Härtel, H. Lokstein, Relationship between quenching of maximum and dark-level chlorophyll fluorescence in vivo: dependence on photosystem II antenna size, Biochim. Biophys. Acta 1228 (1995) 91-94.
24. [24] P. Jahns, S. Schweig, Energy-dependent fluorescence quenching in thylakoids from intermittent light grown pea plants: evidence for an interaction of zeaxanthin and the chlorophyll a/b binding protein CP26, Plant Physiol. Biochem. 33 (1995) 683-687.
25. [25] R. Höfgen, K.A. Axelsen, C.G. Kannangara, I. Schüttke, H.-D. Pohlenz, L. Willmitzer, B. Grimm, D. von Wettstein. A visible marker for antisense mRNA expression in plants: inhibition of chlorophyll synthesis with a glutamate 1-semialdehyde aminotransferase antisense gene, Proc. Nat. Acad. Sci. USA 91 (1994) 1726-1730.
26. [26] H. Härtel, E. Kruse, B. Grimm, Restriction of chlorophyll synthesis due to expression of glutamate-1 semialdehyde aminotransferase antisense RNA does not reduce the light harvesting antenna size in tobacco, Plant Physiol. 113 (1997) 1113-1124.
27. [27] H. Härtel, B. Grimm, Consequences of chlorophyll deficiency for leaf carotenoid composition in tobacco synthesizing glutamate 1-semi-aldehyde aminotransferase antisense RNA: dependency on developmental age and growth light, J. Exp. Bot. 49 (1998) 535-546.
28. [28] B. Genty, J.M. Briantais, N. R. Baker, The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence, Biochim. Biophys. Acta 990 (1989) 87-92.
29. [29] U. Schreiber, W. Bilger, C. Neubauer, Chlorophyll fluorescence as a nonintrusive indicator for rapid assessment of in vivo photosynthesis, in: E.-D. Schulze, M.M. Caldwell (Eds.), Ecophysiology of Photosynthesis, Springer, Berlin, 1993, pp. 49-70.
30. [30] O. van Kooten, J.F.H. Snel, The use of fluorescence nomenclature in plant stress physiology, Photosynth. Res. 25 (1990) 147-150.
31. [31] J.M. Anderson, Photoregulation of the composition, function, and structure of thylakoid membranes, Annu. Rev. Plant Physiol. 37 (1986) 93-136.
32. [32] W. Bilger, J. Fisahn, W. Brummet, J. Kossmann, L. Willmitzer, Violaxanthin cycle pigment contents in potato and tobacco plants with genetically reduced photosynthetic capacity, Plant Physiol. 108 (1995) 1479-1486.
33. [33] B.W. Dreyfuss, J.P. Thornber, Organization of the light-harvesting complex of photosystem I and its assembly during plastid development, Plant Physiol. 106 (1994) 841-848.
34. [34] W.W. Adams III, B. Demmig-Adams, The xanthophyll cycle and sustained energy dissipation activity in Vinca minor and Euonymus kiautschovicus in winter, Plant, Cell Environ. 18 (1995) 117-127.
35. [35] A.S. Verhoeven, B. Demmig-Adams, W.W. Adams III, Enhanced employment of the xanthophyll cycle and thermal energy dissipation in spinach exposed to high light and N stress, Plant Physiol. 113 (1997) 817-824.
36. [36] R.G. Walters, P. Horton, Resolution of components of non-photochemical chlorophyll fluorescence quenching in barley leaves, Photosynth. Res. 27 (1991) 121-133.
37. [37] A.R. Crofts, C.T. Yerkes, A molecular mechanism for qE-quenching, FEBS Lett. 352 (1994) 265-270.
38. [38] R. Bassi, B. Pineau, P. Dainese, J. Marquardt, Carotenoid-binding proteins of photosystem II, Eur. J. Biochem. 212 (1993) 297-303.
39. [39] A.V. Ruban, A.Y. Young, A.A. Pascal, P. Horton, The effects of illumination on the photosytem II light-harvesting complexes of spinach thylakoid mambranes, Plant Physiol. 104 (1994) 227-234.
40. [40] A.M. Gilmore, Mechanistic aspects of xanthophyll cycle-dependent photoprotection in higher plant chloroplasts and leaves, Physiol. Plant. 99 (1997) 197-209.
41. [41] S.S. Thayer, O. Björkman, Carotenoid distribution and deepoxidation in thylakoid pigment-protein complexes from cotton leaves and bundle-sheath cells of maize, Photosynth. Res. 33 (1992) 213-225.
42. [42] A.M. Gilmore, O. Björkman, Temperature-sensitive coupling and uncoupling of ATPase-mediated, nonradiative energy dissipation: similarities between chloroplasts and leaves, Planta 197 (1995) 646-654.
43. [43] C.B. Osmond, What is photoinhibition? Some insights from comparison of shade and sun plants, in: N.R. Baker, J.R. Bowyer (Eds.) Photoinhibition of Photosynthesis: From Molecular Mechanisms to the Field, Bios Scientific Publishers, Oxford, UK, 1994, pp. 1-24.
44. O in leaves is emission wavelength dependent: consequences for quenching analysis and its interpretation, Photosynth. Res. 26 (1990) 133-139.