Estimating the redox state of the plastoquinone pool in algae and cyanobacteria via OJIP fluorescence: perspectives and limitations
Status In-Process Jazyk angličtina Země Nizozemsko Médium electronic
Typ dokumentu časopisecké články
PubMed
41553583
PubMed Central
PMC12816086
DOI
10.1007/s11120-025-01194-x
PII: 10.1007/s11120-025-01194-x
Knihovny.cz E-zdroje
- Klíčová slova
- Chlorella, Synechocystis, Chlorophyll a fluorescence, OJIP curves, PQ pool, Photosystem II, Quinone A, Redox state,
- Publikační typ
- časopisecké články MeSH
UNLABELLED: The redox state of the plastoquinone pool (PQ-redox) acts as a central element in a variety of intracellular signal pathways. Several methods for determining PQ-redox have been established. Although some of these methods are quantitative, such as those based on liquid chromatography, they are typically sensitive to sample preparation. Here, we critically evaluate the use of fast chlorophyll a fluorescence induction kinetics (the so-called OJIP transient) for semi-quantitative PQ-redox estimation in green algae (Chlorella vulgaris) and cyanobacteria (Synechocystis sp. PCC 6803). The method, based on the evaluation of relative fluorescence yield at the J-step of the OJIP transient (VJ, VJ’), has already been reported; however, thus far, it has been used mostly for studying dark-acclimated leaves, which limits its range of application. Here, we show that the OJIP transient can be used for semi-quantitative estimation of PQ-redox in algal and cyanobacterial cell cultures, in addition to plants. We further show that it can reflect PQ-redox in both dark-acclimated and light-acclimated samples. Our systematic comparison of Multi-Color PAM, AquaPen, and FL 6000 fluorometers demonstrates that accurate measurement of VJ and VJ’ parameters in suspension cultures requires low culture density and a high-intensity saturation pulse. We further show that with increasing light intensity to which the cells are exposed, the state of photosystem II (PSII) changes due to light-induced reduction of quinone A (QA−) and conformational changes, which in turn influence both the sensitivity and dynamic range of the VJ’ parameter towards PQ-redox estimation. A comparison of fluorescence transients in Chlorella and Synechocystis revealed relatively narrow range of PQ-redox states across diverse conditions in Synechocystis, maintained by terminal oxidases present at the thylakoid membrane. While we discuss certain limitations, our systematic assessment suggests that the OJIP method has great potential to become a routine tool for semi-quantitative PQ-redox estimation under a wide range of experimental conditions in green algae and cyanobacteria. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11120-025-01194-x.
Bio Inspired Energy Conversion Technical University Darmstadt Darmstadt Germany
Cluster of Excellence on Plant Sciences Heinrich Heine University Düsseldorf Düsseldorf Germany
Computational Life Science Department of Biology RWTH Aachen University Aachen Germany
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Akinyemi OO, Čepl J, Keski-Saari S et al (2023) Derivative-based time-adjusted analysis of diurnal and within-tree variation in the OJIP fluorescence transient of silver Birch. Photosynth Res 157:133–146 PubMed DOI PMC
Bates H, Zavafer A, Szabó M, Ralph PJ (2019) A guide to Open-JIP, a low-cost open-source chlorophyll fluorometer. Photosynth Res 142:361–368 PubMed DOI
Belyaeva NE, Bulychev AA, Riznichenko GY, Rubin AB (2016) Thylakoid membrane model of the Chl PubMed DOI
Berg SP, Krogmann DW (1975) Mechanism of KCN Inhibition of photosystem I. J Biol Chem 250:8957–8962 PubMed DOI
Bernát G, Rögner M (2011) Center of the cyanobacterial electron transport network: the cytochrome b6/f complex. In: Peschek GA, Obinger Ch, Renger G (ed) Bioenergetic processes of cyanobacteria. Springer Netherlands, Dordrecht, pp 573–606
Bernát G, Steinbach G, Kaňa R et al (2018) On the origin of the slow M-T chlorophyll PubMed DOI
Bernát G, Zavřel T, Kotabová E et al (2021) Photomorphogenesis in the picocyanobacterium includes increased phycobilisome abundance under blue light, phycobilisome decoupling under near far- red light, and wavelength- specific photoprotective strategies. Front Plant Sci 12:612302 PubMed DOI PMC
Berry S, Schneider D, Vermaas WFJ, Rögner M (2002) Electron transport routes in whole cells of PubMed DOI
Bhatti AF, Kirilovsky D, van Amerongen H, Wientjes E (2021) State transitions and photosystems spatially resolved in individual cells of the cyanobacterium PubMed DOI PMC
Blankenship RE (2002) Molecular mechanisms of photosynthesis. Wiley, Oxford, UK
Calzadilla PI, Kirilovsky D (2020) Revisiting cyanobacterial state transitions. Photochem Photobiol Sci 19:585–603 PubMed DOI
Campbell D, Oquist G (1996) Predicting light acclimation in cyanobacteria from nonphotochemical quenching of photosystem II fluorescence, which reflects state transitions in these organisms. Plant Physiol 111:1293–1298 PubMed DOI PMC
Campbell D, Hurry V, Clarke AK et al (1998) Chlorophyll fluorescence analysis of cyanobacterial photosynthesis and acclimation. Microbiol Mol Biol Rev 62:667–683 PubMed DOI PMC
Du W, Jongbloets JA, Pineda Hernández H et al (2016) Photonfluxostat: a method for light-limited batch cultivation of cyanobacteria at different, yet constant, growth rates. Algal Res 20:118–125 DOI
Espinoza-Corral R, Zavřel T, Sutter M et al (2025) The linker protein ApcI regulates light harvesting under red light in PubMed DOI
Fei C, Wilson AT, Mangan NM et al (2022) Modelling the pyrenoid-based CO PubMed DOI PMC
Fu A, Aluru M, Rodermel SR (2009) Conserved active site sequences in PubMed DOI PMC
Fuerst EP, Norman MA (1991) Interactions of herbicides with photosynthetic electron transport. Weed Sci 39:458–464 DOI
Fukunaga T, Ogawa T, Iwasaki W, Sonoike K (2024) Phylogenetic profiling analysis of the phycobilisome revealed a novel State-Transition regulator gene in PubMed DOI PMC
Gog L, Berenbaum MR, DeLucia EH (2019) Mediation of impacts of elevated CO PubMed DOI
Harbinson J, Hedley CL (1993) Changes in P-700 oxidation during the early stages of the induction of photosynthesis. Plant Physiol 103:649–660 PubMed DOI PMC
Havaux M (2020) Plastoquinone in and beyond photosynthesis. Trends Plant Sci 25:1252–1265 PubMed DOI
He S, Crans VL, Jonikas MC (2023) The pyrenoid: the eukaryotic CO PubMed DOI PMC
Heldt WH, Werdan K, Milovancev M, Geller G (1973) Alkalization of the chloroplast stroma caused by light-dependent proton flux into the thylakoid space. Biochim Biophys Acta 314:224–241 PubMed DOI
Hill R, Szabó M, ur Rehman A et al (2014) Inhibition of photosynthetic CO₂ fixation in the coral PubMed
Höper R, Komkova D, Zavřel T, Steuer R (2024) A quantitative description of light-limited cyanobacterial growth using flux balance analysis. PLoS Comput Biol 20:e1012280 PubMed DOI PMC
Howitt CA, Vermaas WF (1998) Quinol and cytochrome oxidases in the cyanobacterium PubMed DOI
Ivanov B, Mubarakshina M, Khorobrykh S (2007) Kinetics of the plastoquinone pool oxidation following illumination oxygen incorporation into photosynthetic electron transport chain. FEBS Lett 581:1342–1346 PubMed DOI
Jablonsky J, Lazar D (2008) Evidence for intermediate S-states as initial phase in the process of oxygen-evolving complex oxidation. Biophys J 94:2725–2736 PubMed DOI PMC
Jahn M, Vialas V, Karlsen J et al (2018) Growth of cyanobacteria is constrained by the abundance of light and carbon assimilation proteins. Cell Rep 25:478–486e8 PubMed DOI
Joët T, Genty B, Josse E-M et al (2002) Involvement of a plastid terminal oxidase in plastoquinone oxidation as evidenced by expression of the PubMed DOI
Joliot P, Johnson GN (2011) Regulation of cyclic and linear electron flow in higher plants. Proc Natl Acad Sci USA 108:13317–13322 PubMed DOI PMC
Kalaji HM, Schansker G, Ladle RJ et al (2014) Frequently asked questions about in vivo chlorophyll fluorescence: practical issues. Photosynth Res 122:121–158 PubMed DOI PMC
Kanervo E, Mäenpää P, Aro E-M (1993) D1 protein degradation and PsbA transcript levels in DOI
Khorobrykh S, Tyystjärvi E (2018) Plastoquinol generates and scavenges reactive oxygen species in organic solvent: potential relevance for thylakoids. Biochim Biophys Acta Bioenerg 1859:1119–1131 PubMed DOI
Khorobrykh S, Tsurumaki T, Tanaka K et al (2020) Measurement of the redox state of the plastoquinone pool in cyanobacteria. FEBS Lett 594:367–375 PubMed DOI
Kirilovsky D, Kerfeld CA (2013) The orange carotenoid protein: a blue-green light photoactive protein. Photochem Photobiol Sci 12:1135–1143 PubMed DOI
Kopecná J, Komenda J, Bucinská L, Sobotka R (2012) Long-term acclimation of the cyanobacterium PubMed DOI PMC
Kramer M, Rodriguez-Heredia M, Saccon F et al (2021) Regulation of photosynthetic electron flow on dark to light transition by ferredoxin:NADP(H) oxidoreductase interactions. Elife 10:e56088 PubMed DOI PMC
Kruk J, Karpinski S (2006) An HPLC-based method of estimation of the total redox state of plastoquinone in chloroplasts, the size of the photochemically active plastoquinone-pool and its redox state in thylakoids of PubMed DOI
Kumar Panigrahi S, Kumar Mishra A (2019) Inner filter effect in fluorescence spectroscopy: as a problem and as a solution. J Photochem Photobiol C: Photochem Rev 41:100318 DOI
Kusama S, Kojima S, Kimura K et al (2022) Order-of-magnitude enhancement in photocurrent generation of PubMed DOI PMC
Lazár D (2003) Chlorophyll PubMed DOI
Lea-Smith DJ, Ross N, Zori M et al (2013) Thylakoid terminal oxidases are essential for the cyanobacterium PubMed DOI PMC
Lepetit B, Sturm S, Rogato A et al (2013) High light acclimation in the secondary plastids containing diatom PubMed DOI PMC
Li H, Nakajima Y, Nango E et al (2024) Oxygen-evolving photosystem II structures during S 1-S 2-S 3 transitions. Nature 626:670–677 PubMed DOI PMC
Lichtenthaler HK, Buschmann C, Knapp M (2005) How to correctly determine the different chlorophyll fluorescence parameters and the chlorophyll fluorescence decrease ratio R DOI
Lindahl M, Svensson LA, Liljas A (1993) Metal poison Inhibition of carbonic anhydrase. Proteins 15:177–182 PubMed DOI
Mattila H, Khorobrykh S, Hakala-Yatkin M et al (2020) Action spectrum of the redox state of the plastoquinone pool defines its function in plant acclimation. Plant J 104:1088–1104 PubMed DOI
Michelet L, Zaffagnini M, Morisse S et al (2013) Redox regulation of the Calvin-Benson cycle: something old, something new. Front Plant Sci 4:470 PubMed DOI PMC
Miller NT, Vaughn MD, Burnap RL (2021) Electron flow through NDH-1 complexes is the major driver of cyclic electron flow-dependent proton pumping in cyanobacteria. Biochim Biophys Acta Bioenerg 1862:148354 PubMed DOI
Misumi M, Katoh H, Tomo T, Sonoike K (2016) Relationship between photochemical quenching and non- photochemical quenching in six species of cyanobacteria reveals species difference in redox state and species commonality in energy dissipation. Plant Cell Physiol 57:1510–1517 PubMed PMC
Miyake C (2010) Alternative electron flows (water-water cycle and cyclic electron flow around PSI) in photosynthesis: molecular mechanisms and physiological functions. Plant Cell Physiol 51:1951–1963 PubMed DOI
Mustila H, Muth-Pawlak D, Aro E-M, Allahverdiyeva Y (2021) Global proteomic response of unicellular cyanobacterium PubMed
Naydov I, Kozuleva M, Ivanov B et al (2024) Pathways of oxygen- dependent oxidation of the plastoquinone pool in the dark after illumination. Plants 13:1–17 PubMed DOI PMC
Nelson N, Yocum CF (2006) Structure and function of photosystems I and II. Annu Rev Plant Biol 57:521–565 PubMed DOI
Nikkanen L, Toivola J, Trotta A et al (2018) Regulation of cyclic electron flow by chloroplast NADPH-dependent thioredoxin system. Plant Direct 2:e00093 PubMed DOI PMC
Nikkanen L, Solymosi D, Jokel M, Allahverdiyeva Y (2021) Regulatory electron transport pathways of photosynthesis in cyanobacteria and microalgae: recent advances and biotechnological prospects. Physiol Plant 173:514–525 PubMed DOI
Noguchi K, Yoshida K (2008) Interaction between photosynthesis and respiration in illuminated leaves. Mitochondrion 8:87–99 PubMed DOI
Nosek M, Kornaś A, Kuźniak E, Miszalski Z (2015) Plastoquinone redox state modifies plant response to pathogen. Plant Physiol Biochem 96:163–170 PubMed DOI
Ogawa T, Sonoike K (2016) Effects of bleaching by nitrogen deficiency on the quantum yield of photosystem II in PubMed DOI
Pfennig T, Kullmann E, Zavřel T et al (2024) Shedding light on blue-green photosynthesis: a wavelength-dependent mathematical model of photosynthesis in PubMed DOI PMC
Pilarska M, Niewiadomska E, Kruk J (2023) Salinity-induced changes in plastoquinone pool redox state in halophytic PubMed DOI PMC
Pils D, Schmetterer G (2001) Characterization of three bioenergetically active respiratory terminal oxidases in the cyanobacterium PubMed DOI
Pralon T, Shanmugabalaji V, Longoni P et al (2019) Plastoquinone homoeostasis by PubMed DOI PMC
Pshybytko NL, Kruk J, Kabashnikova LF, Strzalka K (2008) Function of plastoquinone in heat stress reactions of plants. Biochim Biophys Acta 1777:1393–1399 PubMed DOI
Redinbo MR, Yeates TO, Merchant S (1994) Plastocyanin: structural and functional analysis. J Bioenerg Biomembr 26:49–66 PubMed DOI
Remelli W, Santabarbara S (2018) Excitation and emission wavelength dependence of fluorescence spectra in whole cells of the cyanobacterium PubMed DOI
Rippka R, Stanier RY, Deruelles J et al (1979) Generic assignments, strain histories and properties of pure cultures of cyanobacteria. Microbiology 111:1–61 DOI
Sanakis Y, Petrouleas V, Diner BA (1994) Cyanide binding at the non-heme Fe PubMed DOI
Santos-Merino M, Torrado A, Davis GA et al (2021) Improved photosynthetic capacity and photosystem I oxidation via heterologous metabolism engineering in cyanobacteria. Proc Natl Acad Sci USA 118:1–9 PubMed DOI PMC
Santos-Merino M, Nikkanen L, Kokarakis EJ et al (2025) Plastoquinone redox status influences carboxysome integrity via a RpaA- and reactive oxygen species-dependent regulatory network. Plant J 123:e70480 PubMed DOI PMC
Schansker G, Strasser RJ (2005) Quantification of non-QB-reducing centers in leaves using a far-red pre-illumination. Photosynth Res 84:145–151 PubMed DOI
Schansker G, Tóth SZ, Strasser RJ (2005) Methylviologen and dibromothymoquinone treatments of pea leaves reveal the role of photosystem I in the Chl PubMed DOI
Schansker G, Tóth SZ, Strasser RJ (2006) Dark recovery of the Chl PubMed DOI
Schansker G, Tóth SZ, Kovács L et al (2011) Evidence for a fluorescence yield change driven by a light-induced conformational change within photosystem II during the fast chlorophyll PubMed DOI
Schansker G, Tóth SZ, Holzwarth AR, Garab G (2014) Chlorophyll PubMed DOI
Schmidt-Mende P, Witt HT (1968) Zur plastochinonoxydation Bei der photosynthese. Z Naturforsch B J Chem Sci 23:228–235 PubMed DOI
Schreiber U (1986) Detection of rapid induction kinetics with a new type of high-frequency modulated chlorophyll fluorometer. Photosynth Res 9:261–272 PubMed DOI
Schreiber U, Schliwa U, Bilger W (1986) Continuous recording of photochemical and non-photochemical chlorophyll fluorescence quenching with a new type of modulation fluorometer. Photosynth Res 10:51–62 PubMed DOI
Schuurmans RM, Schuurmans JM, Bekker M et al (2014) The redox potential of the plastoquinone pool of the cyanobacterium PubMed DOI PMC
Schuurmans RM, van Alphen P, Schuurmans JM et al (2015) Comparison of the photosynthetic yield of cyanobacteria and green algae: different methods give different answers. PLoS ONE 10:e0139061 PubMed DOI PMC
Senger H (1977) Changes in the sensitivity to inhibitors of photosynthesis during the life cycle of unicellular algae. Plant Cell Physiol 17:229–238
Sétif P (2015) Electron-transfer kinetics in cyanobacterial cells: methyl viologen is a poor inhibitor of linear electron flow. Biochim Biophys Acta 1847:212–222 PubMed DOI
Short A, Fay TP, Crisanto T et al (2023) Kinetics of the xanthophyll cycle and its role in photoprotective memory and response. Nat Commun 14:6621 PubMed DOI PMC
Siegień I, Bogatek R (2006) Cyanide action in plants — from toxic to regulatory. Acta Physiol Plant 28:483–497 DOI
Sipka GB, Magyar M, Mezzetti A et al (2021) Light-adapted charge-separated state of photosystem II: structural and functional dynamics of the closed reaction center. Plant Cell 33:1286–1302 PubMed DOI PMC
Stirbet A, Govindjee (2012) Chlorophyll PubMed DOI
Stirbet A, Lazár D, Kromdijk J, Govindjee G (2018) Chlorophyll DOI
Stirbet A, Lazár D, Papageorgiou GC, Govindjee (2019) Chlorophyll
Stokes DM, Walker DA (1972) Photosynthesis by isolated chloroplasts. Inhibition by DL-glyceraldehyde of carbon dioxide assimilation. Biochem J 128:1147–1157 PubMed DOI PMC
Strasser RJ, Govindjee (1992) The Fo and the O-J-I-P fluorescence rise in higher plants and algae. In: Argyroudi-Akoyunoglou JH (ed) Regulation of Chloroplast biogenesis. Springer US, Boston, MA, pp 423–42
Strasser RJ, Srivastava A, Govindjee (1995) Polyphasic chlorophyll DOI
Tamary E, Kiss V, Nevo R et al (2012) Structural and functional alterations of cyanobacterial phycobilisomes induced by high-light stress. Biochim Biophys Acta 1817:319–327 PubMed DOI
Tian L, van Stokkum IHM, Koehorst RBM et al (2011) Site, rate, and mechanism of photoprotective quenching in cyanobacteria. J Am Chem Soc 133:18304–18311 PubMed DOI
Tjus SE, Møller BL, Scheller HV (1998) Photosystem I is an early target of photoinhibition in barley illuminated at chilling temperatures. Plant Physiol 116:755–764 PubMed DOI PMC
Tomek P, Lazár D, Ilík P, Naus J (2001) Research note: on the intermediate steps between the O and P steps in chlorophyll
Tóth SZ, Schansker G, Strasser RJ (2005) In intact leaves, the maximum fluorescence level (F(M)) is independent of the redox state of the plastoquinone pool: a DCMU-inhibition study. Biochim Biophys Acta 1708:275–282 PubMed DOI
Tóth SZ, Schansker G, Strasser RJ (2007) A non-invasive assay of the plastoquinone pool redox state based on the OJIP-transient. Photosynth Res 93:193–203 PubMed DOI
Trinh MDL, Masuda S (2022) Chloroplast pH homeostasis for the regulation of photosynthesis. Front Plant Sci 13:919896 PubMed DOI PMC
Tsimilli-Michael M (2020) Special issue in honour of Prof. Reto J. Strasser - Revisiting JIP-test: an educative review on concepts, assumptions, approximations, definitions and terminology. Photosynthetica 58:275–292 DOI
Tsimilli-Michael M, Stamatakis K, Papageorgiou GC (2009) Dark-to-light transition in PubMed DOI
van Alphen P, Abedini Najafabadi H, Branco Dos Santos F, Hellingwerf KJ (2018) Increasing the photoautotrophic growth rate of PubMed DOI
Vass I (2012) Molecular mechanisms of photodamage in the photosystem II complex. Biochim Biophys Acta 1817:209–217 PubMed DOI
Velthuys BR (1981) Electron-dependent competition between plastoquinone and inhibitors for binding to photosystem II. FEBS Lett 126:277–281 DOI
Vermaas WFJ (2001) Photosynthesis and respiration in cyanobacteria. Encyclopedia of Life Sciences
Vermaas WF, Shen G, Styring S (1994) Electrons generated by photosystem II are utilized by an oxidase in the absence of photosystem I in the cyanobacterium PubMed DOI
Virtanen O, Tyystjärvi E (2023) Plastoquinone pool redox state and control of state transitions in PubMed DOI PMC
Wilson A, Ajlani G, Verbavatz J-M et al (2006) A soluble carotenoid protein involved in phycobilisome-related energy dissipation in cyanobacteria. Plant Cell 18:992–1007 PubMed DOI PMC
Wishnick M, Lane MD (1969) Inhibition of ribulose diphosphate carboxylase by cyanide. Inactive ternary complex of enzyme, ribulose diphosphate, and cyanide. J Biol Chem 244:55–59 PubMed DOI
Xia Q, Tan J, Cheng S et al (2019) Sensing plant physiology and environmental stress by automatically tracking F j and F i features in PSII chlorophyll fluorescence induction. Photochem Photobiol 95:1495–1503 PubMed DOI
Yoshida K, Shibata M, Terashima I, Noguchi K (2010) Simultaneous determination of in vivo plastoquinone and ubiquinone redox States by HPLC-based analysis. Plant Cell Physiol 51:836–841 PubMed DOI
Yu L, Zhao J, Muhlenhoff U et al (1993) PsaE is required for in vivo cyclic electron flow around photosystem I in the cyanobacterium PubMed DOI PMC
Zavřel T, Očenášová P, Červený J (2017) Phenotypic characterization of PubMed DOI PMC
Zavřel T, Faizi M, Loureiro C et al (2019) Quantitative insights into the cyanobacterial cell economy. Elife 8:e42508 PubMed DOI PMC
Zavřel T, Schoffman H, Lukeš M et al (2021) Monitoring fitness and productivity in cyanobacteria batch cultures. Algal Res 56:102328 DOI
Zavřel T, Segečová A, Kovács L et al (2024) A comprehensive study of light quality acclimation in PubMed DOI PMC