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Received: 2023-10-17

Revision Accepted: 2024-05-08

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Citations:  Bibtex RefMan EndNote GB/T7714

 ORCID:

Tao Lu

http://orcid.org/0000-0003-0098-4356

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Journal of Zhejiang University SCIENCE B 2017 Vol.18 No.7 P.635-648

http://doi.org/10.1631/jzus.B1600286


Response of linear and cyclic electron flux to moderate high temperature and high light stress in tomato


Author(s):  Tao Lu, Jie-wei Shi, Zhou-ping Sun, Ming-fang Qi, Yu-feng Liu, Tian-lai Li

Affiliation(s):  College of Horticulture, Shenyang Agricultural University, Shenyang 110866, China; more

Corresponding email(s):   lyf-3939@163.com, tianlaili@126.com

Key Words:  Photoinhibition, Photoprotection, Thylakoid membrane, Tomato


Tao Lu, Jie-wei Shi, Zhou-ping Sun, Ming-fang Qi, Yu-feng Liu, Tian-lai Li. Response of linear and cyclic electron flux to moderate high temperature and high light stress in tomato[J]. Journal of Zhejiang University Science B, 2017, 18(7): 635-648.

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author="Tao Lu, Jie-wei Shi, Zhou-ping Sun, Ming-fang Qi, Yu-feng Liu, Tian-lai Li",
journal="Journal of Zhejiang University Science B",
volume="18",
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publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B1600286"
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%T Response of linear and cyclic electron flux to moderate high temperature and high light stress in tomato
%A Tao Lu
%A Jie-wei Shi
%A Zhou-ping Sun
%A Ming-fang Qi
%A Yu-feng Liu
%A Tian-lai Li
%J Journal of Zhejiang University SCIENCE B
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%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1600286

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T1 - Response of linear and cyclic electron flux to moderate high temperature and high light stress in tomato
A1 - Tao Lu
A1 - Jie-wei Shi
A1 - Zhou-ping Sun
A1 - Ming-fang Qi
A1 - Yu-feng Liu
A1 - Tian-lai Li
J0 - Journal of Zhejiang University Science B
VL - 18
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%@ 1673-1581
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PB - Zhejiang University Press & Springer
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DOI - 10.1631/jzus.B1600286


Abstract: 
Objective: To evaluate the possible photoprotection mechanisms of cyclic and linear electron flux (CEF and LEF) under specific high temperature and high light (HH) stress. Methods: Six-leaf-stage tomato seedlings (“Liaoyuanduoli”, n=160) were divided into four parts: Part 1, served as control under 25 °C, 500 µmol/(m2·s); Part 2, spayed with distilled water (H2O) under 35 °C, 1000 µmol/(m2·s) (HH); Part 3, spayed with 100 µmol/L diuron (DCMU, CEF inhibitor) under HH; Part 4, spayed with 60 µmol/L methyl viologen (MV, LEF inhibitor) under HH. Energy conversion, photosystem I (PSI), and PSII activity, and trans-thylakoid membrane proton motive force were monitored during the treatment of 5 d and of the recovering 10 d. Results: HH decreased photochemical reaction dissipation (P) and the maximal photochemical efficiency of PSII (Fv/Fm), and increased the excitation energy distribution coefficient of PSII (β); DCMU and MV aggravated the partition imbalance of the excitation energy (γ) and the photoinhibition degree. With prolonged DCMU treatment time, electron transport rate and quantum efficiency of PSI (ETRI and YI) significantly decreased whereas acceptor and donor side limitation of PSI (YNA and YND) increased. MV led to a significant decline and accession of yield of regulated and non-regulated energy YNPQ and YNO, respectively. Membrane integrity and ATPase activity were reduced by HH stress, and DCMU and MV enhanced inhibitory actions. Conclusions: The protective effects of CEF and LEF were mediated to a certain degree by meliorations in energy absorption and distribution as well as by maintenance of thylakoid membrane integrity and ATPase activity.

线性电子传递和环式电子传递对缓解番茄亚高温强光胁迫的响应

目的:探讨特定高温和强光逆境下番茄叶片中的环式电子传递(CEF)和线性电子传递(LEF)的光保护机制。
创新点:通过引入电子抑制剂的方法系统分析了CEF和LEF对亚高温强光胁迫的响应。
方法:将品种为"辽园多丽"的番茄幼苗(n=160)平均分成四组(表1):组1,于常温常光照25 °C,500 µmol/(m2·s)条件下培养并作为对照;组2,叶片喷施蒸馏水并在亚高温强光35 °C,1000 µmol/(m2·s)(HH)条件下培养;组3,HH条件下叶片喷施100 µmol/L敌草隆(DCMU,CEF抑制剂);组4,HH条件下叶片喷施60 µmol/L甲基紫精(MV,LEF抑制剂)。在处理5 d及恢复10 d期间,分别测定番茄幼苗叶片的光能吸收、激发能分配、光系统活性、类囊体膜完整性和ATP酶活性等指标。
结论:CEF和LEF通过一定程度上改善叶片光能吸收及激发能分配,并且维持类囊体膜较高完整性和ATP酶活性,从而维持光系统活性并减少光抑制和光破坏程度。

关键词:光抑制;光保护;类囊体膜;番茄

Darkslateblue:Affiliate; Royal Blue:Author; Turquoise:Article

Reference

[1]Agrawal, D., Allakhverdiev, S.I., Jajoo, A., 2016. Cyclic electron flow plays an important role in protection of spinach leaves under high temperature stress. Russ. J. Plant Physiol., 63(2):210-215.

[2]Apostolova, E.L., Dobrikova, A.G., Ivanova, P.I., et al., 2006. Relationship between the organization of the PSII super complex and the functions of the photosynthetic apparatus. J. Photochem. Photobiol. B, 83(2):114-122.

[3]Bailey, S., Horton, P., Walters, R.G., 2004. Acclimation of Arabidopsis thaliana to the light environment: the relationship between photosynthetic function and chloroplast composition. Planta, 218(5):793-802.

[4]Bailey, S., Melis, A., Mackey, K.R., et al., 2008. Alternative photosynthetic electron flow to oxygen in marine Synechococcus. Biochim. Biophys. Acta, 1777(3):269-276.

[5]Bailleul, B., Cardol, P., Breyton, C., et al., 2010. Electrochromism: a useful probe to study algal photosynthesis. Photosynth. Res., 106(1-2):179-189.

[6]Bilger, W., Schreiber, U., 1990. Chlorophyll luminescence as an indicator of stress-induced damage to the photosynthetic apparatus. Effects of heat-stress in isolated chloroplasts. Photosynth. Res., 25(3):161-171.

[7]Bilger, W., Bjorkman, O., Thayer, S.S., 1989. Light-induced spectral absorbance changes in relation to photosynthesis and the epoxidation state of xanthophyll cycle components in cotton leaves. Plant Physiol., 91(2):542-551.

[8]Bose, S., Kuila, T., Nguyen, et al., 2011. Polymer membranes for high temperature proton exchange membrane fuel cell: recent advances and challenges. Prog. Polym. Sci., 36(6):813-843.

[9]Braun, G., Malkin, S., 1990. Regulation of the imbalance in light excitation between photosystem II and photosystem I by cations and by the energized state of the thylakoid membrane. Biochim. Biophys. Acta, 1017(1):79-90.

[10]Brestic, M., Zivcak, M., Kunderlikova, K., et al., 2016. High temperature specifically affects the photoprotective responses of chlorophyll b-deficient wheat mutant lines. Photosynth. Res., 62(3):281-283.

[11]Camejo, D., Rodriguez, P., Morales, M.A., et al., 2005. High temperature effects on photosynthetic activity of two tomato cultivars with different heat susceptibility. J. Plant Physiol., 162(3):281-289.

[12]Chen, L., Jia, H., Tian, Q., et al., 2012. Protecting effect of phosphorylation on oxidative damage of D1 protein by down-regulating the production of superoxide anion in photosystem II membranes under high light. Photosynth. Res., 112(2):141-148.

[13]Cruz, J.A., Sacksteder, C.A., Kanazawa, A., et al., 2001. Contribution of electric field (ψ) to steady-state transthylakoid proton motive force (PMF) in vitro and in vivo. control of parsing into ψ and pH by ionic strength. Biochemistry, 40(5):1226-1237.

[14]de Filippis, L.F., Ziegler, H., 1993. Effect of sublethal concentrations of zinc, cadmium and mercury on the photosynthetic carbon reduction cycle of Euglena. J. Plant Physiol., 142(2):167-172.

[15]de Filippis, L.F., Hampp, R., Ziegler, H., 1981. The effects of sublethal concentrations of zinc, cadmium and mercury on Euglena. Arch. Microbiol., 128(4):407-411.

[16]de la Rosa-Manzano, E., Andrade, J.L., Garcia-Mendoza, E., et al., 2015. Photoprotection related to xanthophyll cycle pigments in epiphytic orchids acclimated at different light microenvironments in two tropical dry forests of the Yucatan Peninsula, Mexico. Planta, 242(6):1425-1438.

[17]Deng, C., Zhang, D., Pan, X., et al., 2013. Toxic effects of mercury on PSI and PSII activities, membrane potential and transthylakoid proton gradient in Microsorium pteropus. J. Photochem. Photobiol. B, 127:1-7.

[18]Dzbek, J., Korzeniewski, B., 2008. Control over the contribution of the mitochondrial membrane potential (Δψ) and proton gradient (ΔpH) to the proton motive force (Δp). In silico studies. J. Biol. Chem., 283(48):33232-33239.

[19]Foyer, C.H., Neukermans, J., Queval, G., et al., 2012. Photosynthetic control of electron transport and the regulation of gene expression. J. Exp. Bot., 63(4):1637-1641.

[20]Gao, S., Niu, J., Chen, W., et al., 2013. The physiological links of the increased photosystem II activity in moderately desiccated Porphyra haitanensis (Bangiales, Rhodophyta) to the cyclic electron flow during desiccation and re-hydration. Photosynth. Res., 116(1):45-54.

[21]Guissé, B., Srivastava, A., Strasser, R.J., 1995. Effects of high temperature and water stress on the polyphasic chlorophyll a fluorescence transient of potato leaves. J. Gansu Agric. Univ., 324(3):3877-3880.

[22]Heber, U., Gerst, U., Krieger, A., et al., 1995. Coupled cyclic electron transport in intact chloroplasts and leaves of C3 plants: does it exist? If so, what is its function? Photosynth. Res., 46(1-2):269-275.

[23]Hendrickson, L., Furbank, R.T., Chow, W.S., 2004. A simple alternative approach to assessing the fate of absorbed light energy using chlorophyll fluorescence. Photosynth. Res., 82(1):73-81.

[24]Huang, W., Zhang, S.B., Cao, K.F., 2010a. The different effects of chilling stress under moderate light intensity on photosystem II compared with photosystem I and subsequent recovery in tropical tree species. Photosynth. Res., 103(3):175-182.

[25]Huang, W., Zhang, S.B., Cao, K.F., 2010b. Stimulation of cyclic electron flow during recovery after chilling-induced photoinhibition of PSII. Plant Cell Physiol., 51(11):1922-1928.

[26]Ioannidis, N.E., Kotzabasis, K., 2014. Polyamines in chemiosmosis in vivo: a cunning mechanism for the regulation of ATP synthesis during growth and stress. Front. Plant Sci., 5:71.

[27]Ioannidis, N.E., Cruz, J.A., Kotzabasis, K., et al., 2012. Evidence that putrescine modulates the higher plant photosynthetic proton circuit. PLoS ONE, 7(1):e29864.

[28]Ivanov, A.G., Morgan-Kiss, R.M., Krol, M., et al., 2015. Photoinhibition of photosystem I in a pea mutant with altered LHCII organization. J. Photochem. Photobiol. B, 152(3):335-346.

[29]Jiang, H., Qiu, B., 2010. Inhibition of photosynthesis by UV-B exposure and its repair in the bloom-forming cyanobacterium Microcystis aeruginosa. J. Appl. Phycol., 23(4):691-696.

[30]Jin, S.H., Li, X.Q., Hu, J.Y., et al., 2009. Cyclic electron flow around photosystem I is required for adaptation to high temperature in a subtropical forest tree, Ficus concinna. J. Zhejiang Univ.-Sci. B (Biomed. & Biotechnol.), 10(10):784-790.

[31]Johnson, G.N., 2005. Cyclic electron transport in C3 plants: fact or artefact? J. Exp. Bot., 56(411):407-416.

[32]Johnson, M.P., Ruban, A.V., 2014. Rethinking the existence of a steady-state Δψ component of the proton motive force across plant thylakoid membranes. Photosynth. Res., 119(1-2):233-242.

[33]Kanazawa, A., Kramer, D.M., 2002. In vivo modulation of nonphotochemical exciton quenching (NPQ) by regulation of the chloroplast ATP synthase. Proc. Natl. Acad. Sci. USA, 99(20):12789-12794.

[34]Klughammer, C., Schreiber, U., 2008. Complementary PS II quantum yields calculated from simple fluorescence parameters measured by PAM fluorometry and the Saturation Pulse method. PAM Appl. Notes, 1:27-35.

[35]Kramer, D.M., Avenson, T.J., Edwards, G.E., 2004. Dynamic flexibility in the light reactions of photosynthesis governed by both electron and proton transfer reactions. Trends Plant Sci., 9(7):349-357.

[36]Liu, D., Li, S., Islam, E., et al., 2015. Lead accumulation and tolerance of Moso bamboo (Phyllostachys pubescens) seedlings: applications of phytoremediation. J. Zhejiang Univ.-Sci. B (Biomed. & Biotechnol.), 16(2):123-130.

[37]Liu, D.F., Zhang, D., Liu, G.Q., et al., 2013. Influence of heat stress on leaf ultrastructure, photosynthetic performance, and ascorbate peroxidase gene expression of two pear cultivars (Pyrus pyrifolia). J. Zhejiang Univ.-Sci. B (Biomed. & Biotechnol.), 14(12):1070-1083.

[38]Miyake, C., Shinzaki, Y., Miyata, M., et al., 2004. Enhancement of cyclic electron flow around PSI at high light and its contribution to the induction of non-photochemical quenching of chl fluorescence in intact leaves of tobacco plants. Plant Cell Physiol., 45(10):1426-1433.

[39]Munekage, Y., Hojo, M., Meurer, J., et al., 2002. PGR5 is involved in cyclic electron flow around photosystem I and is essential for photoprotection in Arabidopsis. Cell, 110(3):361-371.

[40]Pagliano, C., Raviolo, M., Dalla Vecchia, F., et al., 2006. Evidence for PSII donor-side damage and photoinhibition induced by cadmium treatment on rice (Oryza sativa L.). J. Photochem. Photobiol. B, 84(1):70-78.

[41]Partelli, F.L., Batista-Santos, P., Scotti-Campos, P., et al., 2011. Characterization of the main lipid components of chloroplast membranes and cold induced changes in Coffea spp. Environ. Exp. Bot., 74(2)194-204.

[42]Pospisil, P., 2012. Molecular mechanisms of production and scavenging of reactive oxygen species by photosystem II. Biochim. Biophys. Acta, 1817(1):218-231.

[43]Schreiber, U., Klughammer, C., 2008. New accessory for the Dual-PAM-100: the P515/535 module and examples of its application. PAM Appl. Notes, 1:1-10.

[44]Setif, P., 2015. Electron-transfer kinetics in cyanobacterial cells: methyl viologen is a poor inhibitor of linear electron flow. Biochim. Biophys. Acta, 1847(2):212-222.

[45]Shikanai, T., 2007. Cyclic electron transport around photosystem I: genetic approaches. Annu. Rev. Plant Biol., 58:199-217.

[46]Shikanai, T., 2014. Central role of cyclic electron transport around photosystem I in the regulation of photosynthesis. Curr. Opin. Biotechnol., 26:25-30.

[47]Takahashi, S., Badger, M.R., 2011. Photoprotection in plants: a new light on photosystem II damage. Trends Plant Sci., 16(1):53-60.

[48]Tu, W., Li, Y., Liu, W., et al., 2015. Spring ephemerals adapt to extremely high light conditions via an unusual stabilization of photosystem II. Front. Plant Sci., 6:1189.

[49]Wang, P., Ye, J., Shen, Y., et al., 2006. The role of chloroplast NAD(P)H dehydrogenase in protection of tobacco plant against heat stress. Sci. China C Life Sci., 49(4):311-321.

[50]Yamori, W., Sakata, N., Suzuki, Y., et al., 2011. Cyclic electron flow around photosystem I via chloroplast NAD(P)H dehydrogenase (NDH) complex performs a significant physiological role during photosynthesis and plant growth at low temperature in rice. Plant J., 68(6):966-976.

[51]Yamori, W., Makino, A., Shikanai, T., 2016. A physiological role of cyclic electron transport around photosystem I in sustaining photosynthesis under fluctuating light in rice. Sci. Rep., 6:20147.

[52]Yi, X., McChargue, M., Laborde, S., et al., 2005. The manganese-stabilizing protein is required for photosystem II assembly/stability and photoautotrophy in higher plants. J. Biol. Chem., 280(16):16170-16174.

[53]Yin, H.L., Tian, C.Y., 2013. Effects of nitrogen regulation on photosystem II chlorophyll fluorescence characteristics of functional leaves in sugar beet (Beta vulgaris) under salt environment. Chin. J. Plant Ecol., 37(2):122-131.

[54]Zhang, G., Liu, Y., Ni, Y., et al., 2014. Exogenous calcium alleviates low night temperature stress on the photosynthetic apparatus of tomato leaves. PLoS ONE, 9(5):e97322.

[55]Zhou, Y.H., Huang, L.F., Yu, J.Q., 2004. Effects of sustained chilling and low light on gas exchange, chlorophyll fluorescence quenching and absorbed light allocation in cucumber leaves. J. Plant Physiol. Mol. Biol., 30(2):153-160 (in Chinese).

[56]Zhou, Y.H., Lam, H.M., Zhang, J.H., 2007. Inhibition of photosynthesis and energy dissipation induced by water and high light stresses in rice. J. Exp. Bot., 58(5):1207-1217.

[57]Zhou, Y.H., Zhang, Y.L., Wang, X.M., et al., 2011. Effects of nitrogen form on growth, CO2 assimilation, chlorophyll fluorescence, and photosynthetic electron allocation in cucumber and rice plants. J. Zhejiang Univ.-Sci. B (Biomed. & Biotechnol.), 12(2):126-134.

[58]Zivcak, M., Brestic, M., Kalaji, H.M., et al., 2014. Photosynthetic responses of sun- and shade-grown barley leaves to high light: is the lower PSII connectivity in shade leaves associated with protection against excess of light? Photosynth. Res., 119(3):339-354.

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