Skip to main content
Log in

Cooperation of xanthophyll cycle with water-water cycle in the protection of photosystems 1 and 2 against inactivation during chilling stress under low irradiance

  • Published:
Photosynthetica

Abstract

The xanthophyll cycle and the water-water cycle had different functional significance in chilling-sensitive sweet pepper upon exposure to chilling temperature (4 °C) under low irradiance (100 µmol m−2 s−1) for 6 h. During chilling stress, effects of non-photochemical quenching (NPQ) on photosystem 2 (PS2) in dithiothreitol (DTT) fed leaves remained distinguishable from that of the water-water cycle in diethyldithiocarbamate (DDTC) fed leaves. In DTT-fed leaves, NPQ decreased greatly accompanied by visible inhibition of the de-epoxidized ratio of the xanthophyll cycle, and maximum photochemical efficiency of PS2 (Fv/Fm) decreased markedly. Thus the xanthophyll cycle-dependent NPQ could protect PS2 through energy dissipation under chilling stress. However, NPQ had a slighter effect on photosystem 1 (PS1) in DTT-fed leaves than in DDTC-fed leaves, whereas effects of the water-water cycle on PS1 remained distinguishable from that of NPQ. Inhibiting superoxide dismutase (SOD) activity increased the accumulation of \(\operatorname{O} \overline {^-- } _2\), the oxidation level of P700 (P700+) decreased markedly relative to the control and DTT-fed leaves. Both Fv/Fm and NPQ changed little in DDTC-fed leaves accompanied by little change of (A+Z)/(V+A+Z). This is the active oxygen species inducing PS1 photoinhibition in sweet pepper. The water-water cycle can be interrupted easily at chilling temperature. We propose that during chilling stress under low irradiance, the xanthophyll cycle-dependent NPQ has the main function to protect PS2, whereas the water-water cycle is not only the pathway to dissipate energy but also the dominant factor causing PS1 chilling-sensitivity in sweet pepper.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

A:

antheraxanthin

DDTC:

diethyldithiocarbamate

DTT:

dithiothreitol

Fm :

maximum yield of fluorescence after dark adaptation

Fm‘:

maximum yield of fluorescence in light-acclimated leaves

F0 :

initial fluorescence

Fv/Fm :

maximum photochemical efficiency of PS2 with all reaction centres open

FM:

fresh mass

NPQ:

non-photochemical quenching

P700:

reaction centre chlorophyll of PS1

PFD:

photon flux density

PS1:

photosystem 1

PS2:

photosystem 2

SOD:

superoxide dismutase (EC 1.15.1.1)

V:

violaxanthin

Z:

zeaxanthin

References

  • Asada, K.: The water-water cycle in chloroplasts: Scavenging of active oxygen and dissipation of excess photons. — Annu. Rev. Plant Physiol. Plant mol. Biol. 50: 601–639, 1999.

    Google Scholar 

  • Demmig-Adams, B., Adams, W.W., III: The role of xanthophyll cycle carotenoids in the protection of photosynthesis. — Trends Plant Sci. 1: 21–26, 1996.

    Article  Google Scholar 

  • Endo, T., Shikanai, T., Takabayashi, A., Asada, K., Sato, F.: The role of chloroplastic NAD(P)H dehydrogenase in photoprotection. — FEBS Lett. 457: 5–8, 1999.

    Article  PubMed  Google Scholar 

  • Giannopolitis, C.N., Ries, S.K.: Superoxide dismutases. I. Occurrence in higher plants. — Plant Physiol. 59: 309–314, 1977.

    Google Scholar 

  • Horton, P., Ruban, A., Walters, R.G.: Regulation of light harvesting in green plants. Indication by nonphotochemical quenching of chlorophyll fluorescence. — Physiol. Plant. 106: 415–420, 1994.

    Google Scholar 

  • Huner, N.P.A., Oquist, G., Sarhan, F.: Energy balance and acclimation to light and cold. — Trends Plant Sci. 3: 224–230, 1998.

    Article  Google Scholar 

  • Jakob, B., Heber, U.: Photoproduction and detoxification of hydroxyl radicals in chloroplasts and leaves and relation to photoinactivation of photosystem I and II. — Plant Cell Physiol. 37: 629–635, 1996.

    Google Scholar 

  • Krause, G.H.: Photoinhibition induced by low temperatures. — In: Baker, N.R., Bowyer, J.R. (ed.): Photoinhibition of Photosynthesis: From Molecular Mechanisms to the Field. Pp. 331–348. Bios Scientific Publ., Oxford 1994.

    Google Scholar 

  • Li, X.G., Duan, W., Meng, Q.W., Zou, Q., Zhao, S.J.: The function of chloroplastic NAD(P)H dehydrogenase in tobacco during chilling stress under low irradiance. — Plant Cell Physiol. 45: 103–108, 2004a.

    Article  PubMed  Google Scholar 

  • Li, X.-G., Meng, Q.-W., Jiang, G.-Q., Zou, Q.: The susceptibility of cucumber and sweet pepper to chilling under low irradiance is related to energy dissipation and water-water cycle. — Photosynthetica 41: 259–265, 2003.

    Article  Google Scholar 

  • Li, X.-G., Wang, X.-M., Meng, Q.-W., Zou, Q.: Factors limiting photosynthetic recovery in sweet pepper leaves after shortterm chilling stress under low irradiance. — Photosynthetica 42: 257–262, 2004b.

    Article  Google Scholar 

  • Liu, P., Meng, Q.W., Zou, Q., Zhao, S., Liu, Q.: Effects of coldhardening on chilling-induced photoinhibition of photosynthesis and on xanthophyll cycle pigments in sweet pepper. — Photosynthetica 39: 467–472, 2001.

    Article  Google Scholar 

  • Miszalski, Z.: Influence of DDTC on SO2 effect on tomato seedling (Lycopersicon esculentum Mill.) photosynthesis. — Environ. exp. Bot. 31: 125–130, 1991.

    Article  Google Scholar 

  • Muller, P., Li, X.P., Niyogi, K.K.: Non-photochemical quenching. A response to excess light energy. — Plant Physiol. 125: 1558–1566, 2001.

    Article  PubMed  Google Scholar 

  • Powles, S.B.: Photoinhibition of photosynthesis induced by visible light. — Annu. Rev. Plant Physiol. 35: 15–44, 1984.

    Article  Google Scholar 

  • Osmond, C.B., Grace, S.C.: Perspectives on photoinhibition and photorespiration in the field: Quintessential inefficiencies of the light and dark reactions of photosynthesis? — J. exp. Bot. 46: 1351–1362, 1995.

    Google Scholar 

  • Schreiber, U., Bilger, W., Neubauer, C.: Chlorophyll fluorescence as a nonintrusive indicator for rapid assessment of in vivo photosynthesis. — In: Schulze, E.-D., Caldwell, M.M. (ed.): Ecophysiology of Photosynthesis. Pp. 49–70. Springer-Verlag, Berlin 1994.

    Google Scholar 

  • Sonoike, K.: Photoinhibition of photosystem I: its physiological significance in the chilling sensitivity of plants. — Plant Cell Physiol. 37: 239–247, 1996.

    Google Scholar 

  • Sonoike, K., Kamo, M., Hihara, Y., Hiyama, T., Enami, I.: The mechanism of the degradation of psaB gene product, one of the photosynthetic reaction center subunits of photosystem I upon photoinhibition. — Photosynth. Res. 53: 55–63, 1997.

    Article  Google Scholar 

  • Thayer, S.S., Bjorkman, O.: Carotenoid distribution and deepoxidation in thylakoid pigment protein complexes from cotton leaves and bundle sheath cells of maize. — Photosynth. Res. 33: 213–225, 1992.

    Article  Google Scholar 

  • Tjus, S.E., Moller, B.L., Scheller, H.V.: Photosystem I is an early target of photoinhibition in barley illuminated at chilling temperatures. — Plant Physiol. 116: 755–764, 1998.

    Article  PubMed  Google Scholar 

  • van Kooten, O., Snel, J.F.H.: The use of chlorophyll fluorescence nomenclature in plant stress physiology. — Photosynth. Res. 25: 147–150, 1990.

    Article  Google Scholar 

  • Wang, A.G., Luo, G.H.: Quantitative relation between the reaction of hydroxylamine and superoxide anion radicals in plants. — Plant Physiol. Commun. 6: 55–57, 1990.

    Google Scholar 

  • Xu, C.C., Jeon, Y.A., Lee, C.H.: Relative contributions of photochemical and non-photochemical routes to excitation energy dissipation in rice and barley illuminated at a chilling temperature. — Physiol. Plant. 107: 447–453, 1999.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Q.-W. Meng.

Additional information

This research was supported by the State Key Basic Research and Development Plan of China (G1998010100), the Natural Science Foundation of China (30370854), and the open project from Key Lab of Crop Biology of Shandong Province.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Li, XG., Bi, YP., Zhao, SJ. et al. Cooperation of xanthophyll cycle with water-water cycle in the protection of photosystems 1 and 2 against inactivation during chilling stress under low irradiance. Photosynthetica 43, 261–266 (2005). https://doi.org/10.1007/s11099-005-0042-x

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11099-005-0042-x

Additional key words

Navigation