Upregulation of the mitochondrial alternative oxidase pathway improves PSII function and photosynthetic electron transport in tomato seedlings under chilling stress
Status PubMed-not-MEDLINE Jazyk angličtina Země Česko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
39650763
PubMed Central
PMC11558502
DOI
10.32615/ps.2022.019
PII: PS60271
Knihovny.cz E-zdroje
- Klíčová slova
- JIP-test, OJIP curve, Solanum lycopersicum, chlorophyll fluorescence, salicylhydroxamic acid,
- Publikační typ
- časopisecké články MeSH
The aim of this study was to explore how the mitochondrial alternative oxidase (AOX) pathway alleviates photoinhibition in chilled tomato (Solanum lycopersicum) seedlings. Chilling induced photoinhibition in tomato seedlings despite the increases in thermal energy dissipation and cyclic electron flow around PSI (CEF-PSI). Chilling inhibited the function of PSII and blocked electron transport at the PSII acceptor side, however, it did not affect the oxygen-evolving complex on the donor side of PSII. Upregulation of the AOX pathway protects against photoinhibition by improving PSII function and photosynthetic electron transport in tomato seedlings under chilling stress. The AOX pathway maintained the open state of PSII and the stability of the entire photosynthetic electron transport chain. Moreover, the protective role of the AOX pathway on PSII was more important than that on PSI. However, inhibition of the AOX pathway could be compensated by increasing CEF-PSI activity under chilling stress.
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Akhter M.S., Noreen S., Mahmood S. et al. : Influence of salinity stress on PSII in barley (
Alber N.A., Vanlerberghe G.C.: The flexibility of metabolic interactions between chloroplasts and mitochondria in PubMed DOI
Allakhverdiev S.I.: Recent progress in the studies of structure and function of photosystem II. – J. Photoch. Photobio. B 104: 1-8, 2011. https://www.sciencedirect.com/science/article/pii/S1011134411000868?via%3Dihub PubMed
Allen D.J., Ort D.R.: Impacts of chilling temperatures on photosynthesis in warm-climate plants. – Trends Plant Sci. 6: 36-42, 2001. https://www.sciencedirect.com/science/article/pii/S1360138500018082?via%3Dihub PubMed
Analin B., Mohanan A., Bakka K., Challabathula D.: Cytochrome oxidase and alternative oxidase pathways of mitochondrial electron transport chain are important for the photosynthetic performance of pea plants under salinity stress conditions. – Plant Physiol. Bioch. 154: 248-259, 2020. https://www.sciencedirect.com/science/article/pii/S0981942820302461?via%3Dihub PubMed
Bartoli C.G., Gomez F., Gergoff G. et al. : Up-regulation of the mitochondrial alternative oxidase pathway enhances photosynthetic electron transport under drought conditions. – J. Exp. Bot. 56: 1269-1276, 2005. https://academic.oup.com/jxb/article/56/415/1269/493725 PubMed
Bertamini M., Muthuchelian K., Rubinigg M. et al. : Photoinhibition of photosynthesis in leaves of grapevine (
Challabathula D., Analin B., Mohanan A., Bakka K.: Differential modulation of photosynthesis, ROS and antioxidant enzyme activities in stress-sensitive and -tolerant rice cultivars during salinity and drought upon restriction of COX and AOX pathway of mitochondrial oxidative electron transport. – J. Plant Physiol. 268: 153583, 2022. https://www.sciencedirect.com/science/article/pii/S0176161721002224?via%3Dihub PubMed
Chen S., Strasser R.J., Qiang S.: PubMed
Cheng D., Gao H., Zhang L.: Upregulation of mitochondrial alternative oxidase pathway protects photosynthetic apparatus against photodamage under chilling stress in
Cheng D.D., Zhang L.T.: Mitochondrial alternative oxidase pathway acts as an electron sink during photosynthetic induction in
Clifton R., Lister R., Parker K.L. et al. : Stress-induced co-expression of alternative respiratory chain components in PubMed DOI
Dąbrowski P., Baczewska-Dąbrowska A.H., Kalaji H.M. et al. : Exploration of chlorophyll PubMed PMC
Dahal K., Martyn G.D., Vanlerberghe G.C.: Improved photosynthetic performance during severe drought in PubMed DOI
Dahal K., Vanlerberghe G.C.: Improved chloroplast energy balance during water deficit enhances plant growth: more crop per drop. – J. Exp. Bot. 69: 1183-1197, 2018. https://academic.oup.com/jxb/article/69/5/1183/4769838?login=true PubMed PMC
Florez-Sarasa I., Flexas J., Rasmusson A.G. et al. : PubMed DOI
Gan P., Liu F., Li R.B. et al. : Chloroplasts – beyond energy capture and carbon fixation: tuning of photosynthesis in response to chilling stress. – Int. J. Mol. Sci. 20: 5046, 2019. https://www.mdpi.com/1422-0067/20/20/5046 PubMed PMC
Gandin A., Duffes C., Day D.A., Cousins A.B.: The absence of alternative oxidase AOX1a results in altered response of photosynthetic carbon assimilation to increasing CO PubMed
Garmash E.V.: Role of mitochondrial alternative oxidase in the regulation of cellular homeostasis during development of photosynthetic function in greening leaves. – Plant Biol. 23: 221-228, 2021. https://onlinelibrary.wiley.com/doi/10.1111/plb.13217 PubMed DOI
Giraud E., Ho L.H.M., Clifton R. et al. : The absence of ALTERNATIVE OXIDASE1a in PubMed PMC
Grabelnych O.I., Borovik O.A., Tauson E.L. et al. : Mitochondrial energy-dissipating systems (alternative oxidase, uncoupling proteins, and external NADH dehydrogenase) are involved in development of frost-resistance of winter wheat seedlings. – Biochemistry-Moscow 79: 506-519, 2014. https://link.springer.com/article/10.1134/S0006297914060030 PubMed DOI
Guo Y., Zhang Y., Liu Y. et al. : Effect of AtLFNR1 deficiency on chlorophyll
Hu W.H., Yan X.H., He Y., Ye X.L.: Role of alternative oxidase pathway in protection against drought-induced photoinhibition in pepper leaves. – Photosynthetica 56: 1297-1303, 2018. https://ps.ueb.cas.cz/artkey/phs-201804-0035_role-of-alternative-oxidase-pathway-in-protection-against-drought-induced-photoinhibition-in-pepper-leaves.php
Hu W.H., Yan X.H., Yu J.Q.: Importance of the mitochondrial alternative oxidase (AOX) pathway in alleviating photoinhibition in cucumber leaves under chilling injury and subsequent recovery when leaves are subjected to high light intensity. – J. Hortic. Sci. Biotech. 92: 31-38, 2017. https://www.tandfonline.com/doi/abs/10.1080/14620316.2016.1219239 DOI
Huang W., Zhang S.B., Cao K.F.: 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: 175-182, 2010. https://link.springer.com/article/10.1007/s11120-010-9539-7 PubMed DOI
Ikkonen E.N., Grabelnykh O.I., Sherudilo E.G., Shibaeva T.G.: Salicylhydroxamic acid-resistant and sensitive components of respiration in chilling-sensitive plants subjected to a daily short-term temperature drop. – Russ. J. Plant Physiol. 67: 60-67, 2020. https://link.springer.com/article/10.1134/S1021443719050066 DOI
Jiang Z.X., Watanabe C.K.A., Miyagi A. et al. : Mitochondrial AOX supports redox balance of photosynthetic electron transport, primary metabolite balance, and growth in PubMed PMC
Kiener C.M., Bramlage W.J.: Temperature effects on the activity of the alternative respiratory pathway in chill-sensitive PubMed PMC
Kramer D.M., Johnson G., Kiirats O., Edwards G.E.: New fluorescence parameters for the determination of Q PubMed
Lei Y., Zheng Y., Dai K. et al. : Different responses of photosystem I and photosystem II in three tropical oilseed crops exposed to chilling stress and subsequent recovery. – Trees 28: 923-933, 2014. https://link.springer.com/article/10.1007/s00468-014-1007-0 DOI
Li J.W., Zhang S.B.: Differences in the responses of photosystems I and II in PubMed DOI PMC
Lyons J.M.: Chilling injury in plants. – Ann. Rev. Plant Physio. 24: 445-466, 1973. https://www.annualreviews.org/doi/abs/10.1146/annurev.pp.24.060173.002305 DOI
Maxwell K., Johnson G.N.: Chlorophyll fluorescence – a practical guide. – J. Exp. Bot. 51: 659-668, 2000. https://academic.oup.com/jxb/article/51/345/659/652534 PubMed
Noguchi K., Yoshida K.: Interaction between photosynthesis and respiration in illuminated leaves. – Mitochondrion 8: 87-99, 2008. https://www.sciencedirect.com/science/article/pii/S1567724907002474?via%3Dihub PubMed
Nunes-Nesi A., Sulpice R., Gibon Y., Fernie A.R.: The enigmatic contribution of mitochondrial function in photosynthesis. – J. Exp. Bot. 59: 1675-1684, 2008. https://academic.oup.com/jxb/article/59/7/1675/641429 PubMed
Ort D.R., Baker N.R.: A photoprotective role for O PubMed
Raghavendra A.S., Padmasree K.: Beneficial interactions of mitochondrial metabolism with photosynthetic carbon assimilation. – Trends Plant Sci. 8: 546-553, 2003. https://www.sciencedirect.com/science/article/pii/S1360138503002474?via%3Dihub PubMed
Ramazan S., Bhat H.A., Zargar M.A. et al. : Combined gas exchange characteristic, chlorophyll fluorescence and response curves as selection traits for temperature tolerance in maize genotypes. – Photosynth. Res. 150: 213-225, 2021. https://link.springer.com/article/10.1007/s11120-021-00829-z PubMed DOI
Sonoike K.: Photoinhibition of photosystem I: its physiological significance in the chilling sensitivity of plants. – Plant Cell Physiol. 37: 239-247, 1996. https://academic.oup.com/pcp/article/37/3/239/1930802
Strasser R.J., Srivastava A., Govindjee.: Polyphasic chlorophyll DOI
Takagi D., Amako K., Hashiguchi M. et al. : Chloroplastic ATP synthase builds up a proton motive force preventing production of reactive oxygen species in photosystem I. – Plant J. 91: 306-324, 2017. https://onlinelibrary.wiley.com/doi/10.1111/tpj.13566 PubMed DOI
Umbach A.L., Fiorani F., Siedow J.N.: Characterization of transformed PubMed PMC
Vanlerberghe G.C., Cvetkovska M., Wang J.: Is the maintenance of homeostatic mitochondrial signaling during stress a physiological role for alternative oxidase? – Physiol. Plantarum 137: 392-406, 2009. https://onlinelibrary.wiley.com/doi/10.1111/j.1399-3054.2009.01254.x PubMed DOI
Vanlerberghe G.C., Dahal K., Alber N. et al. : Photosynthesis, respiration and growth: a carbon and energy balancing act for alternative oxidase. – Mitochondrion 52: 197-211, 2020. https://www.sciencedirect.com/science/article/pii/S1567724919303289?via%3Dihub PubMed
Vishwakarma A., Bashyam L., Senthilkumaran B. et al. : Physiological role of AOX1a in photosynthesis and maintenance of cellular redox homeostasis under high light in PubMed
Watanabe C.K.A., Yamori W., Takahashi S. et al. : Mitochondrial alternative pathway-associated photoprotection of photosystem II is related to the photorespiratory pathway. – Plant Cell Physiol. 57: 1426-1431, 2016. https://academic.oup.com/pcp/article/57/7/1426/2755845 PubMed
Yamori W., Sakata N., Suxuki Y. et al. : 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: 966-976, 2011. https://onlinelibrary.wiley.com/doi/10.1111/j.1365-313X.2011.04747.x PubMed DOI
Yoshida K., Terashima I., Noguchi K.: Up-regulation of mitochondrial alternative oxidase concomitant with chloroplast over-reduction by excess light. – Plant Cell Physiol. 48: 606-614, 2007. https://academic.oup.com/pcp/article/48/4/606/2756913 PubMed
Yoshida K., Watanabe C.K., Terashima I., Noguchi K.: Physiological impact of mitochondrial alternative oxidase on photosynthesis and growth in PubMed DOI
Yu J.Q., Matsui Y.: Effects of roots exudates and allelochemicals on ion uptake by cucumber seedlings. – J. Chem. Ecol. 23: 817-827, 1997. https://link.springer.com/article/10.1023/B:JOEC.0000006413.98507.55 DOI
Zhang L.T., Xu R., Liu J.G.: Efficacy of botanical pesticide for rotifer extermination during the cultivation of
Zhang L.T., Zhang Z.S., Gao H.Y. et al. : The mitochondrial alternative oxidase pathway protects the photosynthetic apparatus against photodamage in PubMed DOI PMC
Zheng J., Fang C., Ru L. et al. : Glutathione-ascorbate cycle and photosynthetic electronic transfer in alternative oxidase-manipulated waterlogging tolerance in watermelon seedlings. – Horticulturae 7: 130, 2021. https://www.mdpi.com/2311-7524/7/6/130