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Photosystem II

May 02, 2024

"PSII" redirects here. For the video game console, see PlayStation 2. For the Indonesian political party, see Indonesian Islamic Union Party.

Photosystem II (or water-plastoquinone oxidoreductase) is the first protein complex in the light-dependent reactions of oxygenic photosynthesis. It is located in the thylakoid membrane of plants, algae, and cyanobacteria. Within the photosystem, enzymes capture photons of light to energize electrons that are then transferred through a variety of coenzymes and cofactors to reduce plastoquinone to plastoquinol. The energized electrons are replaced by oxidizing water to form hydrogen ions and molecular oxygen.

Cyanobacteria photosystem II, Dimer, PDB 2AXT

By replenishing lost electrons with electrons from the splitting of water, photosystem II provides the electrons for all of photosynthesis to occur. The hydrogen ions (protons) generated by the oxidation of water help to create a proton gradient that is used by ATP synthase to generate ATP. The energized electrons transferred to plastoquinone are ultimately used to reduce NADP+
 to NADPH or are used in non-cyclic electron flow.[1] DCMU is a chemical often used in laboratory settings to inhibit photosynthesis. When present, DCMU inhibits electron flow from photosystem II to plastoquinone.

Structure of complex edit

 
Cyanobacterial photosystem II, Monomer, PDB 2AXT.
 
Schematic of PSII, highlighting electron transfer.

The core of PSII consists of a pseudo-symmetric heterodimer of two homologous proteins D1 and D2.[2] Unlike the reaction centers of all other photosystems in which the positive charge sitting on the chlorophyll dimer that undergoes the initial photoinduced charge separation is equally shared by the two monomers, in intact PSII the charge is mostly localized on one chlorophyll center (70−80%).[3] Because of this, P680+ is highly oxidizing and can take part in the splitting of water.[2]

Photosystem II (of cyanobacteria and green plants) is composed of around 20 subunits (depending on the organism) as well as other accessory, light-harvesting proteins. Each photosystem II contains at least 99 cofactors: 35 chlorophyll a, 12 beta-carotene, two pheophytin, two plastoquinone, two heme, one bicarbonate, 20 lipids, the Mn
4CaO
5 cluster (including two chloride ions), one non heme Fe2+
 and two putative Ca2+
 ions per monomer.[4] There are several crystal structures of photosystem II.[5] The PDB accession codes for this protein are 3WU2, 3BZ1, 3BZ2 (3BZ1 and 3BZ2 are monomeric structures of the Photosystem II dimer),[4] 2AXT, 1S5L, 1W5C, 1ILX, 1FE1, 1IZL.

Protein Subunits (only with known function)
Subunit Family Function
D1 (PsbA) Photosynthetic reaction centre protein family Reaction center protein, binds Chlorophyll P680, pheophytin, beta-carotene, quinone and manganese center
D2 (PsbD) Reaction center protein
CP43 (PsbC) Photosystem II light-harvesting protein Binds manganese center
CP47 (PsbB)
O Manganese-stabilising protein (InterPro: IPR002628) Manganese Stabilizing Protein
By convention, gene names are formed by Psb + subunit letter. For example, subunit O is PsbO. The exceptions are D1 (PsbA) and D2 (PsbD).
Coenzymes/Cofactors
Cofactor Function
Chlorophyll Absorbs light energy and converts it to chemical energy
Beta-carotene Quench excess photoexcitation energy
Heme B559 Bound to Cytochrome b559 (PsbE–PsbF) as a secondary/protective electron carrier
Pheophytin Primary electron acceptor
Plastoquinone Mobile intra-thylakoid membrane electron carrier
Manganese center Also known as the oxygen evolving center, or OEC
Photosystem II
Identifiers
EC no.1.10.3.9
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Search
PMCarticles
PubMedarticles
NCBIproteins

Oxygen-evolving complex (OEC) edit

 
Proposed structure of Manganese Center
Main article: oxygen-evolving complex

The oxygen-evolving complex is the site of water oxidation. It is a metallo-oxo cluster comprising four manganese ions (in oxidation states ranging from +3 to +4)[6] and one divalent calcium ion. When it oxidizes water, producing oxygen gas and protons, it sequentially delivers the four electrons from water to a tyrosine (D1-Y161) sidechain and then to P680 itself. It is composed of three protein subunits, OEE1 (PsbO), OEE2 (PsbP) and OEE3 (PsbQ); a fourth PsbR peptide is associated nearby.

The first structural model of the oxygen-evolving complex was solved using X-ray crystallography from frozen protein crystals with a resolution of 3.8Å in 2001.[7] Over the next years the resolution of the model was gradually increased to 2.9Å.[8][9][10] While obtaining these structures was in itself a great feat, they did not show the oxygen-evolving complex in full detail. In 2011 the OEC of PSII was resolved to a level of 1.9Å revealing five oxygen atoms serving as oxo bridges linking the five metal atoms and four water molecules bound to the Mn
4CaO
5 cluster; more than 1,300 water molecules were found in each photosystem II monomer, some forming extensive hydrogen-bonding networks that may serve as channels for protons, water or oxygen molecules.[11] At this stage, it is suggested that the structures obtained by X-ray crystallography are biased, since there is evidence that the manganese atoms are reduced by the high-intensity X-rays used, altering the observed OEC structure. This incentivized researchers to take their crystals to a different X-ray facilities, called X-ray Free Electron Lasers, such as SLAC in the USA. In 2014 the structure observed in 2011 was confirmed.[12] Knowing the structure of Photosystem II did not suffice to reveal how it works exactly. So now the race has started to solve the structure of Photosystem II at different stages in the mechanistic cycle (discussed below). Currently structures of the S1 state and the S3 state's have been published almost simultaneously from two different groups, showing the addition of an oxygen molecule designated O6 between Mn1 and Mn4,[13][14] suggesting that this may be the site on the oxygen evolving complex, where oxygen is produced.

Water splitting edit

 
Water-splitting process: Electron transport and regulation. The first level (A) shows the original Kok model of the S-states cycling, the second level (B) shows the link between the electron transport (S-states advancement) and the relaxation process of the intermediate S-states ([YzSn], n=0,1,2,3) formation

Photosynthetic water splitting (or oxygen evolution) is one of the most important reactions on the planet, since it is the source of nearly all the atmosphere's oxygen. Moreover, artificial photosynthetic water-splitting may contribute to the effective use of sunlight as an alternative energy-source.

The mechanism of water oxidation is understood in substantial detail.[15][16][17] The oxidation of water to molecular oxygen requires extraction of four electrons and four protons from two molecules of water. The experimental evidence that oxygen is released through cyclic reaction of oxygen evolving complex (OEC) within one PSII was provided by Pierre Joliot et al.[18] They have shown that, if dark-adapted photosynthetic material (higher plants, algae, and cyanobacteria) is exposed to a series of single turnover flashes, oxygen evolution is detected with typical period-four damped oscillation with maxima on the third and the seventh flash and with minima on the first and the fifth flash (for review, see[19]). Based on this experiment, Bessel Kok and co-workers [20] introduced a cycle of five flash-induced transitions of the so-called S-states, describing the four redox states of OEC: When four oxidizing equivalents have been stored (at the S4-state), OEC returns to its basic S0-state. In the absence of light, the OEC will "relax" to the S1 state; the S1 state is often described as being "dark-stable". The S1 state is largely considered to consist of manganese ions with oxidation states of Mn3+, Mn3+, Mn4+, Mn4+.[21] Finally, the intermediate S-states[22] were proposed by Jablonsky and Lazar as a regulatory mechanism and link between S-states and tyrosine Z.

In 2012, Renger expressed the idea of internal changes of water molecules into typical oxides in different S-states during water splitting.[23]

Inhibitors edit

Inhibitors of PSII are used as herbicides. There are two main chemical families, the triazines derived from cyanuric chloride[24] of which atrazine and simazine are the most commonly used and the aryl ureas which include chlortoluron and diuron (DCMU).[25][26]

See also edit

References edit

  1. ^ Loll B, Kern J, Saenger W, Zouni A, Biesiadka J (December 2005). "Towards complete cofactor arrangement in the 3.0 A resolution structure of photosystem II". Nature. 438 (7070): 1040–4. Bibcode:2005Natur.438.1040L. doi:10.1038/nature04224. PMID 16355230. S2CID 4394735.
  2. ^ a b Rutherford AW, Faller P (January 2003). "Photosystem II: evolutionary perspectives". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 358 (1429): 245–53. doi:10.1098/rstb.2002.1186. PMC 1693113. PMID 12594932.
  3. ^ Okubo T, Tomo T, Sugiura M, Noguchi T (April 2007). "Perturbation of the structure of P680 and the charge distribution on its radical cation in isolated reaction center complexes of photosystem II as revealed by fourier transform infrared spectroscopy". Biochemistry. 46 (14): 4390–7. doi:10.1021/bi700157n. PMID 17371054.
  4. ^ a b Guskov A, Kern J, Gabdulkhakov A, Broser M, Zouni A, Saenger W (March 2009). "Cyanobacterial photosystem II at 2.9-A resolution and the role of quinones, lipids, channels and chloride". Nature Structural & Molecular Biology. 16 (3): 334–42. doi:10.1038/nsmb.1559. PMID 19219048. S2CID 23034289.
  5. ^ Junko Y, Kern J, Yachandra VK, Nilsson H, Koroidov S, Messinger J (2015). "Chapter 2, Section 3 X-Ray Diffraction and Spectroscopy of Photosystem II at Room Temperature Using Femtosecond X-Ray Pulses". In Kroneck PM, Sosa Torres ME (eds.). Sustaining Life on Planet Earth: Metalloenzymes Mastering Dioxygen and Other Chewy Gases. Metal Ions in Life Sciences. Vol. 15. Springer. pp. 13–43. doi:10.1007/978-3-319-12415-5_2. ISBN 978-3-319-12414-8. PMC 4688042. PMID 25707465.
  6. ^ Cox, Nicholas; Pantazis, Dimitrios A.; Lubitz, Wolfgang (2020). "Current Understanding of the Mechanism of Water Oxidation in Photosystem II and Its Relation to XFEL Data". Annual Review of Biochemistry. 89: 795–820. doi:10.1146/annurev-biochem-011520-104801. PMID 32208765. S2CID 214645936.
  7. ^ Zouni A, Witt HT, Kern J, Fromme P, Krauss N, Saenger W, Orth P (February 2001). "Crystal structure of photosystem II from Synechococcus elongatus at 3.8 A resolution". Nature. 409 (6821): 739–43. doi:10.1038/35055589. PMID 11217865. S2CID 4344756.
  8. ^ Kamiya N, Shen JR (January 2003). "Crystal structure of oxygen-evolving photosystem II from Thermosynechococcus vulcanus at 3.7-A resolution". Proceedings of the National Academy of Sciences of the United States of America. 100 (1): 98–103. Bibcode:2003PNAS..100...98K. doi:10.1073/pnas.0135651100. PMC 140893. PMID 12518057.
  9. ^ Ferreira KN, Iverson TM, Maghlaoui K, Barber J, Iwata S (March 2004). "Architecture of the photosynthetic oxygen-evolving center". Science. 303 (5665): 1831–8. Bibcode:2004Sci...303.1831F. doi:10.1126/science.1093087. PMID 14764885. S2CID 31521054.
  10. ^ Guskov A, Kern J, Gabdulkhakov A, Broser M, Zouni A, Saenger W (March 2009). "Cyanobacterial photosystem II at 2.9-A resolution and the role of quinones, lipids, channels and chloride". Nature Structural & Molecular Biology. 16 (3): 334–42. doi:10.1038/nsmb.1559. PMID 19219048. S2CID 23034289.
  11. ^ Umena Y, Kawakami K, Shen JR, Kamiya N (May 2011). "Crystal structure of oxygen-evolving photosystem II at a resolution of 1.9 Å" (PDF). Nature. 473 (7345): 55–60. Bibcode:2011Natur.473...55U. doi:10.1038/nature09913. PMID 21499260. S2CID 205224374.
  12. ^ Suga M, Akita F, Hirata K, Ueno G, Murakami H, Nakajima Y, Shimizu T, Yamashita K, Yamamoto M, Ago H, Shen JR (January 2015). "Native structure of photosystem II at 1.95 Å resolution viewed by femtosecond X-ray pulses". Nature. 517 (7532): 99–103. Bibcode:2015Natur.517...99S. doi:10.1038/nature13991. PMID 25470056. S2CID 205241611.
  13. ^ Young ID, Ibrahim M, Chatterjee R, Gul S, Fuller F, Koroidov S, et al. (December 2016). "Structure of photosystem II and substrate binding at room temperature". Nature. 540 (7633): 453–457. Bibcode:2016Natur.540..453Y. doi:10.1038/nature20161. PMC 5201176. PMID 27871088.
  14. ^ Suga M, Akita F, Sugahara M, Kubo M, Nakajima Y, Nakane T, et al. (March 2017). "Light-induced structural changes and the site of O=O bond formation in PSII caught by XFEL". Nature. 543 (7643): 131–135. Bibcode:2017Natur.543..131S. doi:10.1038/nature21400. PMID 28219079. S2CID 205254025.
  15. ^ Vinyard DJ, Brudvig GW (May 2017). "Progress Toward a Molecular Mechanism of Water Oxidation in Photosystem II". Annual Review of Physical Chemistry. 68 (1): 101–116. Bibcode:2017ARPC...68..101V. doi:10.1146/annurev-physchem-052516-044820. PMID 28226223.
  16. ^ Cox N, Pantazis DA, Lubitz W (June 2020). "Current Understanding of the Mechanism of Water Oxidation in Photosystem II and Its Relation to XFEL Data". Annual Review of Biochemistry. 89 (1): 795–820. doi:10.1146/annurev-biochem-011520-104801. PMID 32208765.
  17. ^ Ibrahim M, Fransson T, Chatterjee R, Cheah MH, Hussein R, Lassalle L, et al. (June 2020). "Untangling the sequence of events during the S2 → S3 transition in photosystem II and implications for the water oxidation mechanism". Proceedings of the National Academy of Sciences of the United States of America. 117 (23): 12624–12635. Bibcode:2020PNAS..11712624I. doi:10.1073/pnas.2000529117. PMC 7293653. PMID 32434915.
  18. ^ Joliot P.; Barbieri G.; Chabaud R. (1969). "Un nouveau modele des centres photochimiques du systeme II". Photochemistry and Photobiology. 10 (5): 309–329. doi:10.1111/j.1751-1097.1969.tb05696.x. S2CID 96744015.
  19. ^ Joliot P (2003). "Period-four oscillations of the flash-induced oxygen formation in photosynthesis". Photosynthesis Research. 76 (1–3): 65–72. doi:10.1023/A:1024946610564. PMID 16228566. S2CID 8742213.
  20. ^ Kok B, Forbush B, McGloin M (June 1970). "Cooperation of charges in photosynthetic O2 evolution-I. A linear four step mechanism". Photochemistry and Photobiology. 11 (6): 457–75. doi:10.1111/j.1751-1097.1970.tb06017.x. PMID 5456273. S2CID 31914925.
  21. ^ Kuntzleman T, Yocum CF (February 2005). "Reduction-induced inhibition and Mn(II) release from the photosystem II oxygen-evolving complex by hydroquinone or NH2OH are consistent with a Mn(III)/Mn(III)/Mn(IV)/Mn(IV) oxidation state for the dark-adapted enzyme". Biochemistry. 44 (6): 2129–42. doi:10.1021/bi048460i. PMID 15697239.
  22. ^ Jablonsky J, Lazar D (April 2008). "Evidence for intermediate S-states as initial phase in the process of oxygen-evolving complex oxidation". Biophysical Journal. 94 (7): 2725–36. Bibcode:2008BpJ....94.2725J. doi:10.1529/biophysj.107.122861. PMC 2267143. PMID 18178650.
  23. ^ Renger G (August 2012). "Mechanism of light induced water splitting in Photosystem II of oxygen evolving photosynthetic organisms". Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1817 (8): 1164–76. doi:10.1016/j.bbabio.2012.02.005. PMID 22353626.
  24. ^ "Chlorotraizine herbicides". alanwood.net. Retrieved 2021-03-26.
  25. ^ "Urea herbicides". alanwood.net. Retrieved 2021-03-26.
  26. ^ Oettmeier W (1992). "Herbicides of photosystem II". The Photosystems. pp. 349–408. doi:10.1016/B978-0-444-89440-3.50018-7. ISBN 9780444894403.

May 02, 2024
photosystem, psii, redirects, here, video, game, console, playstation, indonesian, political, party, indonesian, islamic, union, party, water, plastoquinone, oxidoreductase, first, protein, complex, light, dependent, reactions, oxygenic, photosynthesis, locate. PSII redirects here For the video game console see PlayStation 2 For the Indonesian political party see Indonesian Islamic Union Party Photosystem II or water plastoquinone oxidoreductase is the first protein complex in the light dependent reactions of oxygenic photosynthesis It is located in the thylakoid membrane of plants algae and cyanobacteria Within the photosystem enzymes capture photons of light to energize electrons that are then transferred through a variety of coenzymes and cofactors to reduce plastoquinone to plastoquinol The energized electrons are replaced by oxidizing water to form hydrogen ions and molecular oxygen Cyanobacteria photosystem II Dimer PDB 2AXT By replenishing lost electrons with electrons from the splitting of water photosystem II provides the electrons for all of photosynthesis to occur The hydrogen ions protons generated by the oxidation of water help to create a proton gradient that is used by ATP synthase to generate ATP The energized electrons transferred to plastoquinone are ultimately used to reduce NADP to NADPH or are used in non cyclic electron flow 1 DCMU is a chemical often used in laboratory settings to inhibit photosynthesis When present DCMU inhibits electron flow from photosystem II to plastoquinone Contents 1 Structure of complex 2 Oxygen evolving complex OEC 3 Water splitting 4 Inhibitors 5 See also 6 ReferencesStructure of complex edit nbsp Cyanobacterial photosystem II Monomer PDB 2AXT nbsp Schematic of PSII highlighting electron transfer The core of PSII consists of a pseudo symmetric heterodimer of two homologous proteins D1 and D2 2 Unlike the reaction centers of all other photosystems in which the positive charge sitting on the chlorophyll dimer that undergoes the initial photoinduced charge separation is equally shared by the two monomers in intact PSII the charge is mostly localized on one chlorophyll center 70 80 3 Because of this P680 is highly oxidizing and can take part in the splitting of water 2 Photosystem II of cyanobacteria and green plants is composed of around 20 subunits depending on the organism as well as other accessory light harvesting proteins Each photosystem II contains at least 99 cofactors 35 chlorophyll a 12 beta carotene two pheophytin two plastoquinone two heme one bicarbonate 20 lipids the Mn4 CaO5 cluster including two chloride ions one non heme Fe2 and two putative Ca2 ions per monomer 4 There are several crystal structures of photosystem II 5 The PDB accession codes for this protein are 3WU2 3BZ1 3BZ2 3BZ1 and 3BZ2 are monomeric structures of the Photosystem II dimer 4 2AXT 1S5L 1W5C 1ILX 1FE1 1IZL Protein Subunits only with known function Subunit Family Function D1 PsbA Photosynthetic reaction centre protein family Reaction center protein binds Chlorophyll P680 pheophytin beta carotene quinone and manganese center D2 PsbD Reaction center protein CP43 PsbC Photosystem II light harvesting protein Binds manganese center CP47 PsbB O Manganese stabilising protein InterPro IPR002628 Manganese Stabilizing Protein By convention gene names are formed by Psb subunit letter For example subunit O is PsbO The exceptions are D1 PsbA and D2 PsbD Coenzymes Cofactors Cofactor Function Chlorophyll Absorbs light energy and converts it to chemical energy Beta carotene Quench excess photoexcitation energy Heme B559 Bound to Cytochrome b559 PsbE PsbF as a secondary protective electron carrier Pheophytin Primary electron acceptor Plastoquinone Mobile intra thylakoid membrane electron carrier Manganese center Also known as the oxygen evolving center or OEC Photosystem IIIdentifiersEC no 1 10 3 9DatabasesIntEnzIntEnz viewBRENDABRENDA entryExPASyNiceZyme viewKEGGKEGG entryMetaCycmetabolic pathwayPRIAMprofilePDB structuresRCSB PDB PDBe PDBsumSearchPMCarticlesPubMedarticlesNCBIproteinsOxygen evolving complex OEC edit nbsp Proposed structure of Manganese Center Main article oxygen evolving complex The oxygen evolving complex is the site of water oxidation It is a metallo oxo cluster comprising four manganese ions in oxidation states ranging from 3 to 4 6 and one divalent calcium ion When it oxidizes water producing oxygen gas and protons it sequentially delivers the four electrons from water to a tyrosine D1 Y161 sidechain and then to P680 itself It is composed of three protein subunits OEE1 PsbO OEE2 PsbP and OEE3 PsbQ a fourth PsbR peptide is associated nearby The first structural model of the oxygen evolving complex was solved using X ray crystallography from frozen protein crystals with a resolution of 3 8A in 2001 7 Over the next years the resolution of the model was gradually increased to 2 9A 8 9 10 While obtaining these structures was in itself a great feat they did not show the oxygen evolving complex in full detail In 2011 the OEC of PSII was resolved to a level of 1 9A revealing five oxygen atoms serving as oxo bridges linking the five metal atoms and four water molecules bound to the Mn4 CaO5 cluster more than 1 300 water molecules were found in each photosystem II monomer some forming extensive hydrogen bonding networks that may serve as channels for protons water or oxygen molecules 11 At this stage it is suggested that the structures obtained by X ray crystallography are biased since there is evidence that the manganese atoms are reduced by the high intensity X rays used altering the observed OEC structure This incentivized researchers to take their crystals to a different X ray facilities called X ray Free Electron Lasers such as SLAC in the USA In 2014 the structure observed in 2011 was confirmed 12 Knowing the structure of Photosystem II did not suffice to reveal how it works exactly So now the race has started to solve the structure of Photosystem II at different stages in the mechanistic cycle discussed below Currently structures of the S1 state and the S3 state s have been published almost simultaneously from two different groups showing the addition of an oxygen molecule designated O6 between Mn1 and Mn4 13 14 suggesting that this may be the site on the oxygen evolving complex where oxygen is produced Water splitting edit nbsp Water splitting process Electron transport and regulation The first level A shows the original Kok model of the S states cycling the second level B shows the link between the electron transport S states advancement and the relaxation process of the intermediate S states YzSn n 0 1 2 3 formation Photosynthetic water splitting or oxygen evolution is one of the most important reactions on the planet since it is the source of nearly all the atmosphere s oxygen Moreover artificial photosynthetic water splitting may contribute to the effective use of sunlight as an alternative energy source The mechanism of water oxidation is understood in substantial detail 15 16 17 The oxidation of water to molecular oxygen requires extraction of four electrons and four protons from two molecules of water The experimental evidence that oxygen is released through cyclic reaction of oxygen evolving complex OEC within one PSII was provided by Pierre Joliot et al 18 They have shown that if dark adapted photosynthetic material higher plants algae and cyanobacteria is exposed to a series of single turnover flashes oxygen evolution is detected with typical period four damped oscillation with maxima on the third and the seventh flash and with minima on the first and the fifth flash for review see 19 Based on this experiment Bessel Kok and co workers 20 introduced a cycle of five flash induced transitions of the so called S states describing the four redox states of OEC When four oxidizing equivalents have been stored at the S4 state OEC returns to its basic S0 state In the absence of light the OEC will relax to the S1 state the S1 state is often described as being dark stable The S1 state is largely considered to consist of manganese ions with oxidation states of Mn3 Mn3 Mn4 Mn4 21 Finally the intermediate S states 22 were proposed by Jablonsky and Lazar as a regulatory mechanism and link between S states and tyrosine Z In 2012 Renger expressed the idea of internal changes of water molecules into typical oxides in different S states during water splitting 23 Inhibitors editInhibitors of PSII are used as herbicides There are two main chemical families the triazines derived from cyanuric chloride 24 of which atrazine and simazine are the most commonly used and the aryl ureas which include chlortoluron and diuron DCMU 25 26 See also editOxygen evolution P680 Photosynthesis Photosystem Photosystem I Photosystem II light harvesting protein Reaction Centre PhotoinhibitionReferences edit Loll B Kern J Saenger W Zouni A Biesiadka J December 2005 Towards complete cofactor arrangement in the 3 0 A resolution structure of photosystem II Nature 438 7070 1040 4 Bibcode 2005Natur 438 1040L doi 10 1038 nature04224 PMID 16355230 S2CID 4394735 a b Rutherford AW Faller P January 2003 Photosystem II evolutionary perspectives Philosophical Transactions of the Royal Society of London Series B Biological Sciences 358 1429 245 53 doi 10 1098 rstb 2002 1186 PMC 1693113 PMID 12594932 Okubo T Tomo T Sugiura M Noguchi T April 2007 Perturbation of the structure of P680 and the charge distribution on its radical cation in isolated reaction center complexes of photosystem II as revealed by fourier transform infrared spectroscopy Biochemistry 46 14 4390 7 doi 10 1021 bi700157n PMID 17371054 a b Guskov A Kern J Gabdulkhakov A Broser M Zouni A Saenger W March 2009 Cyanobacterial photosystem II at 2 9 A resolution and the role of quinones lipids channels and chloride Nature Structural amp Molecular Biology 16 3 334 42 doi 10 1038 nsmb 1559 PMID 19219048 S2CID 23034289 Junko Y Kern J Yachandra VK Nilsson H Koroidov S Messinger J 2015 Chapter 2 Section 3 X Ray Diffraction and Spectroscopy of Photosystem II at Room Temperature Using Femtosecond X Ray Pulses In Kroneck PM Sosa Torres ME eds Sustaining Life on Planet Earth Metalloenzymes Mastering Dioxygen and Other Chewy Gases Metal Ions in Life Sciences Vol 15 Springer pp 13 43 doi 10 1007 978 3 319 12415 5 2 ISBN 978 3 319 12414 8 PMC 4688042 PMID 25707465 Cox Nicholas Pantazis Dimitrios A Lubitz Wolfgang 2020 Current Understanding of the Mechanism of Water Oxidation in Photosystem II and Its Relation to XFEL Data Annual Review of Biochemistry 89 795 820 doi 10 1146 annurev biochem 011520 104801 PMID 32208765 S2CID 214645936 Zouni A Witt HT Kern J Fromme P Krauss N Saenger W Orth P February 2001 Crystal structure of photosystem II from Synechococcus elongatus at 3 8 A resolution Nature 409 6821 739 43 doi 10 1038 35055589 PMID 11217865 S2CID 4344756 Kamiya N Shen JR January 2003 Crystal structure of oxygen evolving photosystem II from Thermosynechococcus vulcanus at 3 7 A resolution Proceedings of the National Academy of Sciences of the United States of America 100 1 98 103 Bibcode 2003PNAS 100 98K doi 10 1073 pnas 0135651100 PMC 140893 PMID 12518057 Ferreira KN Iverson TM Maghlaoui K Barber J Iwata S March 2004 Architecture of the photosynthetic oxygen evolving center Science 303 5665 1831 8 Bibcode 2004Sci 303 1831F doi 10 1126 science 1093087 PMID 14764885 S2CID 31521054 Guskov A Kern J Gabdulkhakov A Broser M Zouni A Saenger W March 2009 Cyanobacterial photosystem II at 2 9 A resolution and the role of quinones lipids channels and chloride Nature Structural amp Molecular Biology 16 3 334 42 doi 10 1038 nsmb 1559 PMID 19219048 S2CID 23034289 Umena Y Kawakami K Shen JR Kamiya N May 2011 Crystal structure of oxygen evolving photosystem II at a resolution of 1 9 A PDF Nature 473 7345 55 60 Bibcode 2011Natur 473 55U doi 10 1038 nature09913 PMID 21499260 S2CID 205224374 Suga M Akita F Hirata K Ueno G Murakami H Nakajima Y Shimizu T Yamashita K Yamamoto M Ago H Shen JR January 2015 Native structure of photosystem II at 1 95 A resolution viewed by femtosecond X ray pulses Nature 517 7532 99 103 Bibcode 2015Natur 517 99S doi 10 1038 nature13991 PMID 25470056 S2CID 205241611 Young ID Ibrahim M Chatterjee R Gul S Fuller F Koroidov S et al December 2016 Structure of photosystem II and substrate binding at room temperature Nature 540 7633 453 457 Bibcode 2016Natur 540 453Y doi 10 1038 nature20161 PMC 5201176 PMID 27871088 Suga M Akita F Sugahara M Kubo M Nakajima Y Nakane T et al March 2017 Light induced structural changes and the site of O O bond formation in PSII caught by XFEL Nature 543 7643 131 135 Bibcode 2017Natur 543 131S doi 10 1038 nature21400 PMID 28219079 S2CID 205254025 Vinyard DJ Brudvig GW May 2017 Progress Toward a Molecular Mechanism of Water Oxidation in Photosystem II Annual Review of Physical Chemistry 68 1 101 116 Bibcode 2017ARPC 68 101V doi 10 1146 annurev physchem 052516 044820 PMID 28226223 Cox N Pantazis DA Lubitz W June 2020 Current Understanding of the Mechanism of Water Oxidation in Photosystem II and Its Relation to XFEL Data Annual Review of Biochemistry 89 1 795 820 doi 10 1146 annurev biochem 011520 104801 PMID 32208765 Ibrahim M Fransson T Chatterjee R Cheah MH Hussein R Lassalle L et al June 2020 Untangling the sequence of events during the S2 S3 transition in photosystem II and implications for the water oxidation mechanism Proceedings of the National Academy of Sciences of the United States of America 117 23 12624 12635 Bibcode 2020PNAS 11712624I doi 10 1073 pnas 2000529117 PMC 7293653 PMID 32434915 Joliot P Barbieri G Chabaud R 1969 Un nouveau modele des centres photochimiques du systeme II Photochemistry and Photobiology 10 5 309 329 doi 10 1111 j 1751 1097 1969 tb05696 x S2CID 96744015 Joliot P 2003 Period four oscillations of the flash induced oxygen formation in photosynthesis Photosynthesis Research 76 1 3 65 72 doi 10 1023 A 1024946610564 PMID 16228566 S2CID 8742213 Kok B Forbush B McGloin M June 1970 Cooperation of charges in photosynthetic O2 evolution I A linear four step mechanism Photochemistry and Photobiology 11 6 457 75 doi 10 1111 j 1751 1097 1970 tb06017 x PMID 5456273 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