Oxygenic photosynthesis: translation to solar fuel technologies
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Shafiee S, Topal E. When will fossil fuel reserves be diminished? Energy Policy. 2009;37(1):181–189. http://dx.doi.org/10.1016/j.enpol.2008.08.016
Stephens E, Ross IL, Mussgnug JH, Wagner LD, Borowitzka MA, Posten C, et al. Future prospects of microalgal biofuel production systems. Trends Plant Sci. 2010;15(10):554–564. http://dx.doi.org/10.1016/j.tplants.2010.06.003
Industries [Internet]. Shell global. 2014 [cited 2014 Sep 9]; Available from: http://www.shell.com/global/products-services/solutions-for-businesses/lubes/industries.html
Barber J, Tran PD. From natural to artificial photosynthesis. Interface Focus. 2013;10(81):20120984. http://dx.doi.org/10.1098/rsif.2012.0984
Kargul J, Barber J. Structure and function of photosynthetic reaction centres. In: Wydrzynski TJ, Hillier W, editors. Molecular solar fuels. Cambridge: Royal Society of Chemistry; 2011. p. 107–142. http://dx.doi.org/10.1039/9781849733038-00107
Larkum AWD. Evolution of the reaction centers and photosystems. In: Renger G, editor. Primary processes of photosynthesis: principles and apparatus. Cambridge: Royal Society of Chemistry; 2008. p. 489–521.
Barber J. Engine of life and big bang of evolution: a personal perspective. Photosynth Res. 2004;80(1–3):137–155. http://dx.doi.org/10.1023/B:PRES.0000030662.04618.27
Hohmann-Marriott MF, Blankenship RE. Evolution of photosynthesis. Annu Rev Plant Biol. 2011;62(1):515–548. http://dx.doi.org/10.1146/annurev-arplant-042110-103811
Hurles M. Gene duplication: the genomic trade in spare parts. PLoS Biol. 2004;2(7):e206. http://dx.doi.org/10.1371/journal.pbio.0020206
Pennisi E. Genome duplications: the stuff of evolution? Science. 2001;294(5551):2458–2460. http://dx.doi.org/10.1126/science.294.5551.2458
Raymond J, Blankenship RE. Horizontal gene transfer in eukaryotic algal evolution. Proc Natl Acad Sci USA. 2003;100(13):7419–7420. http://dx.doi.org/10.1073/pnas.1533212100
Igarashi N, Harada J, Nagashima S, Matsuura K, Shimada K, Nagashima KV. Horizontal transfer of the photosynthesis gene cluster and operon rearrangement in purple bacteria. J Mol Evol. 2001;52(4):333–341. http://dx.doi.org/10.1007/s002390010163
Sadekar S. Conservation of distantly related membrane proteins: photosynthetic reaction centers share a common structural core. Mol Biol Evol. 2006;23(11):2001–2007. http://dx.doi.org/10.1093/molbev/msl079
Murray JW, Duncan J, Barber J. CP43-like chlorophyll binding proteins: structural and evolutionary implications. Trends Plant Sci. 2006;11(3):152–158. http://dx.doi.org/10.1016/j.tplants.2006.01.007
Blankenship RE, Tiede DM, Barber J, Brudvig GW, Fleming G, Ghirardi M, et al. Comparing photosynthetic and photovoltaic efficiencies and recognizing the potential for improvement. Science. 2011;332(6031):805–809. http://dx.doi.org/10.1126/science.1200165
Berardi S, Drouet S, Francàs L, Gimbert-Suriñach C, Guttentag M, Richmond C, et al. Molecular artificial photosynthesis. Chem Soc Rev. 2014;43(22):7501–7519. http://dx.doi.org/10.1039/C3CS60405E
Field CB. Primary production of the biosphere: integrating terrestrial and oceanic components. Science. 1998;281(5374):237–240. http://dx.doi.org/10.1126/science.281.5374.237
Kargul J, Janna Olmos JD, Krupnik T. Structure and function of photosystem I and its application in biomimetic solar-to-fuel systems. J Plant Physiol. 2012;169(16):1639–1653. http://dx.doi.org/10.1016/j.jplph.2012.05.018
Munekage Y, Hashimoto M, Miyake C, Tomizawa KI, Endo T, Tasaka M, et al. Cyclic electron flow around photosystem I is essential for photosynthesis. Nature. 2004;429(6991):579–582. http://dx.doi.org/10.1038/nature02598
Johnson GN. Physiology of PSI cyclic electron transport in higher plants. Biochim Biophys Acta. 2011;1807(3):384–389. http://dx.doi.org/10.1016/j.bbabio.2010.11.009
Joliot P, Johnson GN. Regulation of cyclic and linear electron flow in higher plants. Proc Natl Acad Sci USA. 2011;108(32):13317–13322. http://dx.doi.org/10.1073/pnas.1110189108
Hertle AP, Blunder T, Wunder T, Pesaresi P, Pribil M, Armbruster U, et al. PGRL1 is the elusive ferredoxin-plastoquinone reductase in photosynthetic cyclic electron flow. Mol Cell. 2013;49(3):511–523. http://dx.doi.org/10.1016/j.molcel.2012.11.030
DalCorso G, Pesaresi P, Masiero S, Aseeva E, Schünemann D, Finazzi G, et al. A complex containing PGRL1 and PGR5 is involved in the switch between linear and cyclic electron flow in Arabidopsis. Cell. 2008;132(2):273–285. http://dx.doi.org/10.1016/j.cell.2007.12.028
Peng L, Fukao Y, Fujiwara M, Takami T, Shikanai T. Efficient operation of NAD(P)H dehydrogenase requires supercomplex formation with photosystem I via minor LHCI in Arabidopsis. Plant Cell. 2009;21(11):3623–3640. http://dx.doi.org/10.1105/tpc.109.068791
Yamori W, Sakata N, Suzuki Y, Shikanai T, Makino A. 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. 2011;68(6):966–976. http://dx.doi.org/10.1111/j.1365-313X.2011.04747.x
Kukuczka B, Magneschi L, Petroutsos D, Steinbeck J, Bald T, Powikrowska M, et al. Proton gradient regulation5-like1-mediated cyclic electron flow is crucial for acclimation to anoxia and complementary to nonphotochemical quenching in stress adaptation. Plant Physiol. 2014;165(4):1604–1617. http://dx.doi.org/10.1104/pp.114.240648
Nelson N, Yocum CF. Structure and function of photosystems I and II. Annu Rev Plant Biol. 2006;57(1):521–565. http://dx.doi.org/10.1146/annurev.arplant.57.032905.105350
Cardona T, Sedoud A, Cox N, Rutherford AW. Charge separation in photosystem II: a comparative and evolutionary overview. Biochim Biophys Acta. 2012;1817(1):26–43. http://dx.doi.org/10.1016/j.bbabio.2011.07.012
Umena Y, Kawakami K, Shen JR, Kamiya N. Crystal structure of oxygen-evolving photosystem II at a resolution of 1.9 Å. Nature. 2011;473(7345):55–60. http://dx.doi.org/10.1038/nature09913
Kanady JS, Tsui EY, Day MW, Agapie T. A synthetic model of the Mn3Ca subsite of the oxygen-evolving complex in photosystem II. Science. 2011;333(6043):733–736. http://dx.doi.org/10.1126/science.1206036
Ananyev G, Dismukes GC. How fast can photosystem II split water? Kinetic performance at high and low frequencies. Photosynth Res. 2005;84(1-3):355–365. http://dx.doi.org/10.1007/s11120-004-7081-1
Badura A, Kothe T, Schuhmann W, Rögner M. Wiring photosynthetic enzymes to electrodes. Energy Environ Sci. 2011;4(9):3263. http://dx.doi.org/10.1039/c1ee01285a
Jordan P, Fromme P, Witt HT, Klukas O, Saenger W, Krauss N. Three-dimensional structure of cyanobacterial photosystem I at 2.5 A resolution. Nature. 2001;411(6840):909–917. http://dx.doi.org/10.1038/35082000
Ben-Shem A, Frolow F, Nelson N. Crystal structure of plant photosystem I. Nature. 2003;426(6967):630–635. http://dx.doi.org/10.1038/nature02200
Amunts A, Drory O, Nelson N. The structure of a plant photosystem I supercomplex at 3.4 A resolution. Nature. 2007;447(7140):58–63. http://dx.doi.org/10.1038/nature05687
Nguyen K, Bruce BD. Growing green electricity: progress and strategies for use of photosystem I for sustainable photovoltaic energy conversion. Biochim Biophys Acta. 2014;1837(9):1553–1566. http://dx.doi.org/10.1016/j.bbabio.2013.12.013
Ocakoglu K, Krupnik T, van den Bosch B, Harputlu E, Gullo MP, Olmos JDJ, et al. Photosystem I-based biophotovoltaics on nanostructured hematite. Adv Funct Mater. 2014 (in press). http://dx.doi.org/10.1002/adfm.201401399
Pandey D, Agrawal M. Carbon footprint estimation in the agriculture sector. In: Muthu SS, editor. Assessment of carbon footprint in different industrial sectors. Singapore: Springer; 2014. p. 25–47. (vol 1). http://dx.doi.org/10.1007/978-981-4560-41-2_2
Jajesniak P, Ali H, Wong TS. Carbon dioxide capture and utilization using biological systems: opportunities and challenges. J Bioprocess Biotech. 2014;4(155). http://dx.doi.org/10.4172/2155-9821.1000155
Zhao B, Su Y. Process effect of microalgal-carbon dioxide fixation and biomass production: a review. Renew Sustain Energy Rev. 2014;31:121–132. http://dx.doi.org/10.1016/j.rser.2013.11.054
Oliver JWK, Machado IMP, Yoneda H, Atsumi S. Combinatorial optimization of cyanobacterial 2,3-butanediol production. Metab Eng. 2014;22:76–82. http://dx.doi.org/10.1016/j.ymben.2014.01.001
Machado IMP, Atsumi S. Cyanobacterial biofuel production. J Biotech. 2012;162(1):50–56. http://dx.doi.org/10.1016/j.jbiotec.2012.03.005
Rabinovitch-Deere CA, Oliver JWK, Rodriguez GM, Atsumi S. Synthetic biology and metabolic engineering approaches to produce biofuels. Chem Rev. 2013;113(7):4611–4632. http://dx.doi.org/10.1021/cr300361t
Smith KS, Ferry JG. Prokaryotic carbonic anhydrases. FEMS Microbiol Rev. 2000;24(4):335–366. http://dx.doi.org/10.1111/j.1574-6976.2000.tb00546.x
Rosgaard L, de Porcellinis AJ, Jacobsen JH, Frigaard NU, Sakuragi Y. Bioengineering of carbon fixation, biofuels, and biochemicals in cyanobacteria and plants. J Biotech. 2012;162(1):134–147. http://dx.doi.org/10.1016/j.jbiotec.2012.05.006
Quintana N, van der Kooy F, Van de Rhee MD, Voshol GP, Verpoorte R. Renewable energy from cyanobacteria: energy production optimization by metabolic pathway engineering. Appl Microbiol Biotechnol. 2011;91(3):471–490. http://dx.doi.org/10.1007/s00253-011-3394-0
Das D. Hydrogen production by biological processes: a survey of literature. Int J Hydrog. Energy. 2001;26(1):13–28. http://dx.doi.org/10.1016/S0360-3199(00)00058-6
Abed RMM, Dobretsov S, Sudesh K. Applications of cyanobacteria in biotechnology. J Appl Microbiol. 2009;106(1):1–12. http://dx.doi.org/10.1111/j.1365-2672.2008.03918.x
Dutta D, De D, Chaudhuri S, Bhattacharya SK. Hydrogen production by cyanobacteria. Microb Cell Fact. 2005;4(1):36. http://dx.doi.org/10.1186/1475-2859-4-36
Melis A, Zhang L, Forestier M, Ghirardi M, Seibert M. Sustained photobiological hydrogen gas production upon reversible inactivation of oxygen evolution in the green alga Chlamydomonas reinhardtii. Plant Physiol. 2000;122(1):127–136. http://dx.doi.org/10.1104/pp.122.1.127
Kruse O, Rupprecht J, Bader K-P, Thomas-Hall S, Schenk PM, Finazzi G, et al. Improved photobiological H2 production in engineered green algal cells. J Biol Chem. 2005;280(40):34170–34177. http://dx.doi.org/10.1074/jbc.M503840200
Kargul J, Barber J. Photosynthetic acclimation: structural reorganisation of light harvesting antenna - role of redox-dependent phosphorylation of major and minor chlorophyll a/b binding proteins. FEBS J. 2008;275(6):1056–1068. http://dx.doi.org/10.1111/j.1742-4658.2008.06262.x
Oey M, Ross IL, Stephens E, Steinbeck J, Wolf J, Radzun KA, et al. RNAi knock-down of LHCBM1, 2 and 3 increases photosynthetic H2 production efficiency of the green alga Chlamydomonas reinhardtii. PLoS ONE. 2013;8(4):e61375. http://dx.doi.org/10.1371/journal.pone.0061375
Angermayr SA, Hellingwerf KJ, Lindblad P, Teixeira de Mattos MJ. Energy biotechnology with cyanobacteria. Curr Opin Biotechnol. 2009;20(3):257–263. http://dx.doi.org/10.1016/j.copbio.2009.05.011
Savakis P, Hellingwerf KJ. Engineering cyanobacteria for direct biofuel production from CO2. Curr Opin Biotechnol. 2015;33:8–14. http://dx.doi.org/10.1016/j.copbio.2014.09.007
van der Woude AD, Angermayr SA, Puthan Veetil V, Osnato A, Hellingwerf KJ. Carbon sink removal: increased photosynthetic production of lactic acid by Synechocystis sp. PCC6803 in a glycogen storage mutant. J Biotech. 2014;184:100–102. http://dx.doi.org/10.1016/j.jbiotec.2014.04.029
Wijffels RH, Kruse O, Hellingwerf KJ. Potential of industrial biotechnology with cyanobacteria and eukaryotic microalgae. Curr Opin Biotechnol. 2013;24(3):405–413. http://dx.doi.org/10.1016/j.copbio.2013.04.004
Gao Z, Zhao H, Li Z, Tan X, Lu X. Photosynthetic production of ethanol from carbon dioxide in genetically engineered cyanobacteria. Energy Environ Sci. 2012;5(12):9857. http://dx.doi.org/10.1039/c2ee22675h
Qi F, Yao L, Tan X, Lu X. Construction, characterization and application of molecular tools for metabolic engineering of Synechocystis sp. Biotechnol Lett. 2013;35(10):1655–1661. http://dx.doi.org/10.1007/s10529-013-1252-0
Ho SH, Ye X, Hasunuma T, Chang JS, Kondo A. Perspectives on engineering strategies for improving biofuel production from microalgae – a critical review. Biotechnol Adv. 2014;32(8):1448–1459. http://dx.doi.org/10.1016/j.biotechadv.2014.09.002
PC Lai E. Biodiesel: environmental friendly alternative to petrodiesel. J Pet Env. Biotechnol. 2014;5(1). http://dx.doi.org/10.4172/2157-7463.1000e122
Ragauskas AME, Ragauskas AJ. Re-defining the future of FOG and biodiesel. J Pet Environ Biotechnol. 2013;4(1). http://dx.doi.org/10.4172/2157-7463.1000e118
Talebi AF, Mohtashami SK, Tabatabaei M, Tohidfar M, Bagheri A, Zeinalabedini M, et al. Fatty acids profiling: a selective criterion for screening microalgae strains for biodiesel production. Algal Res. 2013;2(3):258–267. http://dx.doi.org/10.1016/j.algal.2013.04.003
Trudewind CA, Schreiber A, Haumann D. Photocatalytic methanol and methane production using captured CO2 from coal power plants. Part II – well-to-wheel analysis on fuels for passenger transportation services. J Clean Prod. 2014;70:38–49. http://dx.doi.org/10.1016/j.jclepro.2014.02.024
Sialve B, Bernet N, Bernard O. Anaerobic digestion of microalgae as a necessary step to make microalgal biodiesel sustainable. Biotechnol Adv. 2009;27(4):409–416. http://dx.doi.org/10.1016/j.biotechadv.2009.03.001
Rittmann BE. Opportunities for renewable bioenergy using microorganisms. Biotechnol Bioeng. 2008;100(2):203–212. http://dx.doi.org/10.1002/bit.21875
Thapper A, Styring S, Saracco G, Rutherford AW, Robert B, Magnuson A, et al. Artificial photosynthesis for solar fuels – an evolving research field within AMPEA, a joint programme of the european energy research alliance. Green. 2013;3(1):43–57. http://dx.doi.org/10.1515/green-2013-0007
Ocakoglu K, Joya KS, Harputlu E, Tarnowska A, Gryko DT. A nanoscale bio-inspired light-harvesting system developed from self-assembled alkyl-functionalized metallochlorin nano-aggregates. Nanoscale. 2014;6(16):9625. http://dx.doi.org/10.1039/C4NR01661K
Llansola-Portoles MJ, Bergkamp JJ, Tomlin J, Moore TA, Kodis G, Moore AL, et al. Photoinduced electron transfer in perylene-TiO2 nanoassemblies. Photochem Photobiol. 2013;89(6):1375–1382. http://dx.doi.org/10.1111/php.12108
Ihssen J, Braun A, Faccio G, Gajda-Schrantz K, Thöny-Meyer L. Light harvesting proteins for solar fuel generation in bioengineered photoelectrochemical cells. Curr Protein Pept Sci. 2014;15(4):374–384. http://dx.doi.org/10.2174/1389203715666140327105530
Duan L, Bozoglian F, Mandal S, Stewart B, Privalov T, Llobet A, et al. A molecular ruthenium catalyst with water-oxidation activity comparable to that of photosystem II. Nat Chem. 2012;4(5):418–423. http://dx.doi.org/10.1038/nchem.1301
Kanan MW, Nocera DG. In situ formation of an oxygen-evolving catalyst in neutral water containing phosphate and CO2+. Science. 2008;321(5892):1072–1075. http://dx.doi.org/10.1126/science.1162018
Reece SY, Hamel JA, Sung K, Jarvi TD, Esswein AJ, Pijpers JJH, et al. Wireless solar water splitting using silicon-based semiconductors and earth-abundant catalysts. Science. 2011;334(6056):645–648. http://dx.doi.org/10.1126/science.1209816
Kanan MW, Yano J, Surendranath Y, Dincă M, Yachandra VK, Nocera DG. Structure and valency of a cobalt−phosphate water oxidation catalyst determined by in situ X-ray spectroscopy. J Am Chem Soc. 2010;132(39):13692–13701. http://dx.doi.org/10.1021/ja1023767
Tran PD, Wong LH, Barber J, Loo JSC. Recent advances in hybrid photocatalysts for solar fuel production. Energy Environ Sci. 2012;5(3):5902. http://dx.doi.org/10.1039/c2ee02849b
Bensaid S, Centi G, Garrone E, Perathoner S, Saracco G. Towards artificial leaves for solar hydrogen and fuels from carbon dioxide. ChemSusChem. 2012;5(3):500–521. http://dx.doi.org/10.1002/cssc.201100661
Kim JH, Nam DH, Park CB. Nanobiocatalytic assemblies for artificial photosynthesis. Curr Opin Biotechnol. 2014;28:1–9. http://dx.doi.org/10.1016/j.copbio.2013.10.008
Benson EE, Kubiak CP, Sathrum AJ, Smieja JM. Electrocatalytic and homogeneous approaches to conversion of CO2 to liquid fuels. Chem Soc Rev. 2009;38(1):89. http://dx.doi.org/10.1039/b804323j
Bora DK, Braun A, Constable EC. “In rust we trust”. Hematite – the prospective inorganic backbone for artificial photosynthesis. Energy Environ Sci. 2013;6(2):407–425. http://dx.doi.org/10.1039/C2EE23668K
Bora DK, Braun A, Erni R, Müller U, Döbeli M, Constable EC. Hematite–NiO/α-Ni(OH)2 heterostructure photoanodes with high electrocatalytic current density and charge storage capacity. Phys Chem Chem Phys. 2013;15(30):12648. http://dx.doi.org/10.1039/c3cp52179f
Gajda-Schrantz K, Tymen S, Boudoire F, Toth R, Bora DK, Calvet W, et al. Formation of an electron hole doped film in the α-Fe2O3 photoanode upon electrochemical oxidation. Phys Chem Chem Phys. 2013;15(5):1443. http://dx.doi.org/10.1039/c2cp42597a
Bora DK, Rozhkova EA, Schrantz K, Wyss PP, Braun A, Graule T, et al. Functionalization of nanostructured hematite thin-film electrodes with the light-harvesting membrane protein C-phycocyanin yields an enhanced photocurrent. Adv Funct Mater. 2012;22(3):490–502. http://dx.doi.org/10.1002/adfm.201101830
Kothe T, Plumeré N, Badura A, Nowaczyk MM, Guschin DA, Rögner M, et al. Combination of a photosystem 1-based photocathode and a photosystem 2-based photoanode to a Z-scheme mimic for biophotovoltaic applications. Angew Chem Int Ed Engl. 2013;52(52):14233–14236. http://dx.doi.org/10.1002/anie.201303671
Badura A, Guschin D, Esper B, Kothe T, Neugebauer S, Schuhmann W, et al. Photo-induced electron transfer between photosystem 2 via cross-linked redox hydrogels. Electroanalysis. 2008;20(10):1043–1047. http://dx.doi.org/10.1002/elan.200804191
Badura A, Guschin D, Kothe T, Kopczak MJ, Schuhmann W, Rögner M. Photocurrent generation by photosystem 1 integrated in crosslinked redox hydrogels. Energy Environ Sci. 2011;4(7):2435. http://dx.doi.org/10.1039/c1ee01126j
Mershin A, Matsumoto K, Kaiser L, Yu D, Vaughn M, Nazeeruddin MK, et al. Self-assembled photosystem-I biophotovoltaics on nanostructured TiO2 and ZnO. Sci Rep. 2012;2:1–7. http://dx.doi.org/10.1038/srep00234
Wenk SO, Qian DJ, Wakayama T, Nakamura C, Zorin N, Rögner M, et al. Biomolecular device for photoinduced hydrogen production. Int J Hydrog. Energy. 2002;27(11–12):1489–1493. http://dx.doi.org/10.1016/S0360-3199(02)00094-0
Yehezkeli O, Tel-Vered R, Michaeli D, Nechushtai R, Willner I. Photosystem I (PSI)/photosystem II (PSII)-based photo-bioelectrochemical cells revealing directional generation of photocurrents. Small. 2013;9(17):2970–2978. http://dx.doi.org/10.1002/smll.201300051
Wang W, Chen J, Li C, Tian W. Achieving solar overall water splitting with hybrid photosystems of photosystem II and artificial photocatalysts. Nat Commun. 2014;5:4647. http://dx.doi.org/10.1038/ncomms5647
Kato M, Cardona T, Rutherford AW, Reisner E. Photoelectrochemical water oxidation with photosystem II integrated in a mesoporous indium–tin oxide electrode. J Am Chem Soc. 2012;134(20):8332–8335. http://dx.doi.org/10.1021/ja301488d
Kato M, Cardona T, Rutherford AW, Reisner E. Covalent immobilization of oriented photosystem II on a nanostructured electrode for solar water oxidation. J Am Chem Soc. 2013;135(29):10610–10613. http://dx.doi.org/10.1021/ja404699h
Sun J, Zhang J, Zhang M, Antonietti M, Fu X, Wang X. Bioinspired hollow semiconductor nanospheres as photosynthetic nanoparticles. Nat Commun. 2012;3:1139. http://dx.doi.org/10.1038/ncomms2152
Engel GS, Calhoun TR, Read EL, Ahn TK, Mančal T, Cheng YC, et al. Evidence for wavelike energy transfer through quantum coherence in photosynthetic systems. Nature. 2007;446(7137):782–786. http://dx.doi.org/10.1038/nature05678
Zhou H, Guo J, Li P, Fan T, Zhang D, Ye J. Leaf-architectured 3D hierarchical artificial photosynthetic system of perovskite titanates towards CO2 photoreduction into hydrocarbon fuels. Sci Rep. 2013;3:1667. http://dx.doi.org/10.1038/srep01667
Larkum AWD. Harvesting solar energy through natural or artificial photosynthesis: scientific, social, political and economic implications. In: Wydrzynski TJ, Hillier W, editors. Molecular solar fuels. Cambridge: Royal Society of Chemistry; 2011. p. 1–19. http://dx.doi.org/10.1039/9781849733038-00001
Kato M, Zhang JZ, Paul N, Reisner E. Protein film photoelectrochemistry of the water oxidation enzyme photosystem II. Chem Soc Rev. 2014;43(18):6485. http://dx.doi.org/10.1039/C4CS00031E
Redinbo MR, Cascio D, Choukair MK, Rice D, Merchant S, Yeates TO. The 1.5-.ANG. crystal structure of plastocyanin from the green alga Chlamydomonas reinhardtii. Biochemistry. 1993;32(40):10560–10567. http://dx.doi.org/10.1021/bi00091a005
Kameda H, Hirabayashi K, Wada K, Fukuyama K. Mapping of protein-protein interaction sites in the plant-type [2Fe-2S] ferredoxin. PloS One. 2011;6(7):e21947. http://dx.doi.org/10.1371/journal.pone.0021947
DOI: https://doi.org/10.5586/asbp.2014.037
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