Subject, C. B., Behrenfeld, M. J., Randerson, J. T. & Falkowski, P. Major manufacturing of the biosphere: integrating terrestrial and oceanic parts. Science 281, 237–240 (1998).
Mackey, Ok. R., Morris, J. J., Morel, F. M. & Kranz, S. A. Response of photosynthesis to ocean acidification. Oceanography 28, 74–91 (2015).
Mackinder, L. C. M. et al. A spatial interactome reveals the protein group of the algal CO2-concentrating mechanism. Cell 171, 133–147.e114 (2017).
Mackinder, L. C. M. The Chlamydomonas CO2-concentrating mechanism and its potential for engineering photosynthesis in vegetation. New Phytol. 217, 54–61 (2018).
Raven, J. A. Inorganic carbon acquisition by eukaryotic algae: 4 present questions. Photosynth. Res. 106, 123–134 (2010).
Raven, J. A., Beardall, J. & Giordano, M. Vitality prices of carbon dioxide concentrating mechanisms in aquatic organisms. Photosynth. Res. 121, 111–124 (2014).
Maberly, S. C. & Gontero, B. Ecological imperatives for aquatic CO2-concentrating mechanisms. J. Exp. Bot. 68, 3797–3814 (2017).
Savir, Y., Noor, E., Milo, R. & Tlusty, T. Cross-species evaluation traces adaptation of Rubisco towards optimality in a low-dimensional panorama. Proc. Natl Acad. Sci. USA 107, 3475–3480 (2010).
Reinfelder, J. R. Carbon concentrating mechanisms in eukaryotic marine phytoplankton. Annu. Rev. Mar. Sci. 3, 291–315 (2011).
Moroney, J. V. et al. The carbonic anhydrase isoforms of Chlamydomonas reinhardtii: intracellular location, expression, and physiological roles. Photosynth. Res. 109, 133–149 (2011).
Duanmu, D., Miller, A. R., Horken, Ok. M., Weeks, D. P. & Spalding, M. H. Knockdown of limiting-CO2-induced gene HLA3 decreases HCO3− transport and photosynthetic Ci affinity in Chlamydomonas reinhardtii. Proc. Natl Acad. Sci. USA 106, 5990–5995 (2009).
Wang, Y. & Spalding, M. H. Acclimation to very low CO2: contribution of limiting CO2 inducible proteins, LCIB and LCIA, to inorganic carbon uptake in Chlamydomonas reinhardtii. Plant Physiol. 166, 2040–2050 (2014).
Yamano, T., Sato, E., Iguchi, H., Fukuda, Y. & Fukuzawa, H. Characterization of cooperative bicarbonate uptake into chloroplast stroma within the inexperienced alga Chlamydomonas reinhardtii. Proc. Natl Acad. Sci. USA 112, 7315–7320 (2015).
Mukherjee, A. et al. Thylakoid localized bestrophin-like proteins are important for the CO2 concentrating mechanism of Chlamydomonas reinhardtii. Proc. Natl Acad. Sci. USA 116, 16915–16920 (2019).
Karlsson, J. et al. A novel α-type carbonic anhydrase related to the thylakoid membrane in Chlamydomonas reinhardtii is required for development at ambient CO2. EMBO J. 17, 1208–1216 (1998).
Raven, J. A. CO2-concentrating mechanisms: a direct position for thylakoid lumen acidification? Plant Cell Environ. 20, 147–154 (1997).
Badger, M. R., Kaplan, A. & Berry, J. A. Inner inorganic carbon pool of Chlamydomonas reinhardtii. Plant Physiol. 66, 407–413 (1980).
Allen, J. F. Photosynthesis of ATP—electrons, proton pumps, rotors, and poise. Cell 110, 273–276 (2002).
Allen, J. F. Cyclic, pseudocyclic and noncyclic photophosphorylation: new hyperlinks within the chain. Developments Plant Sci. 8, 15–19 (2003).
Munekage, Y. et al. PGR5 is concerned in cyclic electron stream round photosystem I and is crucial for photoprotection in Arabidopsis. Cell 110, 361–371 (2002).
Johnson, X. et al. Proton gradient regulation 5-mediated cyclic electron stream underneath ATP- or redox-limited situations: a research of ΔATPase pgr5 and ΔrbcL pgr5 mutants within the inexperienced alga Chlamydomonas reinhardtii. Plant Physiol. 165, 438–452 (2014).
DalCorso, G. et al. A fancy containing PGRL1 and PGR5 is concerned within the swap between linear and cyclic electron stream in Arabidopsis. Cell 132, 273–285 (2008).
Tolleter, D. et al. Management of hydrogen photoproduction by the proton gradient generated by cyclic electron stream in Chlamydomonas reinhardtii. Plant Cell 23, 2619–2630 (2011).
Curien, G. et al. The water to water cycles in microalgae. Plant Cell Physiol. 57, 1354–1363 (2016).
Helman, Y. et al. Genes encoding a-type flavoproteins are important for photoreduction of O2 in cyanobacteria. Curr. Biol. 13, 230–235 (2003).
Gerotto, C. et al. Flavodiiron proteins act as security valve for electrons in Physcomitrella patens. Proc. Natl Acad. Sci. USA 113, 12322–12327 (2016).
Shimakawa, G. et al. The Liverwort, Marchantia, drives various electron stream utilizing a flavodiiron protein to guard PSI. Plant Physiol. 173, 1636–1647 (2017).
Chaux, F. et al. Flavodiiron proteins promote quick and transient O2 photoreduction in Chlamydomonas. Plant Physiol. 174, 1825–1836 (2017).
Dang, Ok. V. et al. Mixed will increase in mitochondrial cooperation and oxygen photoreduction compensate for deficiency in cyclic electron stream in Chlamydomonas reinhardtii. Plant Cell 26, 3036–3050 (2014).
Bailleul, B. et al. Energetic coupling between plastids and mitochondria drives CO2 assimilation in diatoms. Nature 524, 366 (2015).
Wang, Y., Stessman, D. J. & Spalding, M. H. The CO2 concentrating mechanism and photosynthetic carbon assimilation in limiting CO2: how Chlamydomonas works in opposition to the gradient. Plant J. 82, 429–448 (2015).
Kono, A. & Spalding, M. H. LCI1, a Chlamydomonas reinhardtii plasma membrane protein, capabilities in lively CO2 uptake underneath low CO2. Plant J. 102, 1127–1141 (2020).
Bonente, G. et al. Evaluation of LhcSR3, a protein important for suggestions de-excitation within the inexperienced alga Chlamydomonas reinhardtii. PLoS Biol. 9, e1000577 (2011).
Tian, L. et al. pH dependence, kinetics and light-harvesting regulation of nonphotochemical quenching in Chlamydomonas. Proc. Natl Acad. Sci. USA 116, 8320–8325 (2019).
Sültemeyer, D. F., Klug, Ok. & Fock, H. P. Impact of dissolved inorganic carbon on oxygen evolution and uptake by Chlamydomonas reinhardtii suspensions tailored to ambient and CO2-enriched air. Photosynth. Res. 12, 25–33 (1987).
Sültemeyer, D., Biehler, Ok. & Fock, H. P. Proof for the contribution of pseudocyclic photophosphorylation to the power requirement of the mechanism for concentrating inorganic carbon in Chlamydomonas. Planta 189, 235–242 (1993).
Lucker, B. & Kramer, D. M. Regulation of cyclic electron stream in Chlamydomonas reinhardtii underneath fluctuating carbon availability. Photosynthesis Res. 117, 449–459 (2013).
Qu, Z. & Hartzell, H. C. Bestrophin Cl− channels are extremely permeable to HCO3−. Am. J. Physiol. Cell Physiol. 294, C1371–C1377 (2008).
Rost, B., Riebesell, U., Burkhardt, S. & Sültemeyer, D. Carbon acquisition of bloom-forming marine phytoplankton. Limnol. Oceanogr. 48, 55–67 (2003).
Basu, S. & Mackey, Ok. R. M. Phytoplankton as key mediators of the organic carbon pump: their responses to a altering local weather. Sustainability 10, 869 (2018).
Atkinson, N. et al. Introducing an algal carbon-concentrating mechanism into larger vegetation: location and incorporation of key parts. Plant Biotechnol. J. 14, 1302–1315 (2016).
Meyer, M. T., McCormick, A. J. & Griffiths, H. Will an algal CO2-concentrating mechanism work in larger vegetation? Curr. Opin. Plant Biol. 31, 181–188 (2016).
Nölke, G. et al. The combination of algal carbon focus mechanism parts into tobacco chloroplasts will increase photosynthetic effectivity and biomass. Biotechnol. J. 14, 1800170 (2019).
Hennacy, J. H. & Jonikas, M. C. Prospects for engineering biophysical CO2 concentrating mechanisms into land vegetation to boost yields. Annu. Rev. Plant Biol. 71, 461–485 (2020).
Yamamoto, H., Takahashi, S., Badger, M. R. & Shikanai, T. Synthetic remodelling of different electron stream by flavodiiron proteins in Arabidopsis. Nat. Crops 2, 16012 (2016).
Wada, S. et al. Flavodiiron protein substitutes for cyclic electron stream with out competing CO2 assimilation. Plant Physiol. 176, 1509–1518 (2017).
Gómez, R. et al. Quicker photosynthetic induction in tobacco by expressing cyanobacterial flavodiiron proteins in chloroplasts. Photosynth. Res. 136, 129–138 (2018).
Vicino, P. et al. Expression of flavodiiron proteins Flv2–Flv4 in chloroplasts of Arabidopsis and tobacco vegetation supplies a number of stress tolerance. Int. J. Mol. Sci. 22, 1178 (2021).
Burlacot, A., Burlacot, F., Li-Beisson, Y. & Peltier, G. Membrane inlet mass spectrometry: a strong instrument for algal analysis. Entrance. Plant. Sci. 11, 1302 (2020).
Burlacot, A. et al. Flavodiiron-mediated O2 photoreduction hyperlinks H2 manufacturing with CO2 fixation through the anaerobic induction of photosynthesis. Plant Physiol. 177, 1639–1649 (2018).
Burlacot, A., Richaud, P., Gosset, A., Li-Beisson, Y. & Peltier, G. Algal photosynthesis converts nitric oxide into nitrous oxide. Proc. Natl Acad. Sci. USA 117, 2704–2709 (2020).
Desplats, C. et al. Characterization of Nda2, a plastoquinone-reducing kind II NAD(P)H dehydrogenase in Chlamydomonas chloroplasts. J. Biol. Chem. 284, 4148–4157 (2009).
Yamano, T. et al. Gentle and low-CO2-dependent LCIB–LCIC advanced localization within the chloroplast helps the carbon-concentrating mechanism in Chlamydomonas reinhardtii. Plant Cell Physiol. 51, 1453–1468 (2010).
Moroney, J. V. et al. Isolation and characterization of a mutant of Chlamydomonas reinhardtii poor within the CO2 concentrating mechanism. Plant Physiol. 89, 897–903 (1989).
Gerster, R. An try and interpret the kinetics of isotope trade between C18O2 and the water of a leaf: experiments in the dead of night. Planta 97, 155–172 (1971).
Silverman, D. N. In Strategies in Enzymology Vol. 87 (ed. Purich, D. L.) 732–752 (Educational Press, 1982).
Cruz, J. A., Sacksteder, C. A., Kanazawa, A. & Kramer, D. M. Contribution of electrical area (Δψ) to steady-state transthylakoid proton driver (pmf) in vitro and in vivo. management of pmf parsing into Δψ and ΔpH by ionic power. Biochem. 40, 1226–1237 (2001).
Douchi, D. et al. Membrane-inlet mass spectrometry allows a quantitative understanding of inorganic carbon uptake flux and carbon concentrating mechanisms in metabolically engineered cyanobacteria. Entrance. Microbiol. 10, 1356–1356 (2019).
Kramer, D. M. & Evans, J. R. The significance of power steadiness in bettering photosynthetic productiveness. Plant Physiol. 155, 70–78 (2011).