ライフサイエンスコーパス: oxygenic

1 Oxygenic and anoxygenic photosynthesis were studied with

2 tabolic rhythm that controls the alternating oxygenic and microoxic processes of Cyanothece sp. ATCC

3 Both type I and type II (oxygenic and nonoxygenic, respectively) reaction centers

4 ers, genomic arguments for cyanobacteria, an oxygenic atmosphere and any comparably diverse suite of

5 Evolution of an oxygenic atmosphere required primordial life to accommod

6 litting process, which maintains the Earth's oxygenic atmosphere.

7 water would have competed with Earth's early oxygenic biosphere for essential nutrients.

8 III)-O-Fe(IV)]: there is no second inorganic oxygenic bridge, neither oxo nor hydroxo.

9 Given the absence of a second inorganic oxygenic bridge, the second bridging ligand must be prot

10 uivalent of O2 and produced water as a final oxygenic byproduct.

11 The possibility of oxygenic coordination for this molecular variant is disc

12 Glutathione metabolism is associated with oxygenic cyanobacteria and the oxygen-utilizing purple b

13 ring the Huronian glaciations, we argue that oxygenic cyanobacteria evolved and radiated shortly befo

14 esized only by photosynthetic eukaryotes and oxygenic cyanobacteria.

15 piration was likely linked to the origins of oxygenic Cyanobacteria.

16 a metabolically dormant spore to survive in oxygenic environments and be transmitted from host to ho

17 s essential for photosynthesis to proceed in oxygenic environments either by scavenging harmful react

18 , including very small molecules with single oxygenic groups, also strongly stimulated these posterio

19 imulations of light-harvesting proteins from oxygenic (LHCII) and anoxygenic organisms (LH2).

20 tative APX-II crystals indicate a protonated oxygenic ligand at 1.88 angstrom from the heme iron.

21 t interpreted in terms of one non-cysteinyl, oxygenic ligand for the [2Fe-2S] cluster.

22 Here, we have investigated the role of the oxygenic ligand in Av MoFeP, which natively contains a S

23 the D14C variant to three cysteines and one oxygenic ligand in each of the four serine variants.

24 ree variants were generated in which (1) the oxygenic ligand was eliminated (betaSer188Ala), (2) the

25 one or two Fe centers in the absence of the oxygenic ligand, while still retaining wild-type-like di

26 raised the possibility of one noncysteinyl, oxygenic ligand.

27 rmance to reexamine the protonation state of oxygenic ligands of the inorganic core of X by directly

28 eP (betaPhe99Tyr/betaSer188Ala), and (3) two oxygenic ligands were simultaneously included (betaPhe99

29 ariants with three cysteinate and one or two oxygenic ligands.

30 tion of both anoxygenic light-dependent- and oxygenic light-independent CO2 fixation as well as anoxy

31 products indicates a consistent grouping of oxygenic lineages that are distinct and descendent from

32 us, more potent HSCs associated with the low-oxygenic niche can be isolated by selecting for the low

33 solate primitive HSCs located within the low-oxygenic niche due to difficulties of direct physical ac

34 A low-oxygenic niche in bone marrow limits reactive oxygen spe

35 ay be consistent with the presence of either oxygenic or nitrogenic ligation.

36 Diatoms differ from the green lineage of oxygenic organisms by their photosynthetic pigments and

37 tosynthetic electron-transport system of all oxygenic organisms.

38 Many attributes of primitive HSCs in the low-oxygenic osteoblastic niche, such as quiescence, and cal

39 e of biofuels derived from aquatic microbial oxygenic photoautotrophs (AMOPs), more commonly known as

40 nthetic competence and their relationship to oxygenic photoautotrophs on global scales are unknown.

41 This gene is conserved in oxygenic photoautotrophs ranging from cyanobacteria to f

42 Oxygenic photoautotrophs require mechanisms for rapidly

43 d anoxygenic phototrophs largely outnumbered oxygenic photoautotrophs.

44 growth, and up to a 340% enhancement of the oxygenic photocurrent compared to the first generation Q

45 Oxygenic photogranules (OPGs), spherical aggregates comp

46 us cyanobacteria are an essential element of oxygenic photogranules for granule-based wastewater trea

47 A bioprocess using oxygenic photogranules is an attractive candidate for en

48 We describe the production of these oxygenic photogranules under static batch conditions, as

49 nm) than the wavelengths typically used for oxygenic photosynthesis (400-700 nm).

50 a and certain bacterial metabolisms, such as oxygenic photosynthesis and aerobic methanotrophy.

51 ified component to the regulatory network of oxygenic photosynthesis and conclude the more than 50-y-

52 Understanding the origins of oxygenic photosynthesis and Cyanobacteria is key when pi

53 n in Synechocystis 6803 is not essential for oxygenic photosynthesis and does not provide an importan

54 The evolution of oxygenic photosynthesis and ensuing oxygenation of Earth

55 annot be invoked to support the emergence of oxygenic photosynthesis and eukaryotes by approximately

56 as key evidence supporting the early rise of oxygenic photosynthesis and eukaryotes, but the syngenei

57 tem I and photosystem II reaction centers of oxygenic photosynthesis and generates a transmembrane el

58 Cyanothece 51142 performs oxygenic photosynthesis and nitrogen fixation, separatin

59 Before cyanobacteria invented oxygenic photosynthesis and O(2) and H(2)O began to cycl

60 Beyond its central position in oxygenic photosynthesis and primary metabolism - key tar

61 three billion years, the basic machinery of oxygenic photosynthesis and respiration has been perfect

62 sents a model membrane that can conduct both oxygenic photosynthesis and respiration simultaneously.

63 ell types, the vegetative cells that perform oxygenic photosynthesis and the dinitrogen-fixing hetero

64 a, the only known bacterial clade capable of oxygenic photosynthesis and the only group of organisms

65 Even after evidence for oxygenic photosynthesis appeared, the atmosphere remaine

66 yanobacteria and plants, the main engines of oxygenic photosynthesis are the pigment-protein complexe

67 tical to those used to date the evolution of oxygenic photosynthesis before the Great Oxidation Event

68 rd respiring microbial communities fueled by oxygenic photosynthesis before the oxygenation of the at

69 n achieve simultaneous nitrogen fixation and oxygenic photosynthesis by cooperation between two cell

70 The invention of oxygenic photosynthesis by cyanobacteria 2.4 billion yea

71 aging, we demonstrate substantial NIR-driven oxygenic photosynthesis by endolithic, Chl f-containing

72 patches Fe(III) alleviated the inhibition of oxygenic photosynthesis by sulfide.

73 Photosystem II (PSII) of oxygenic photosynthesis captures sunlight to drive the c

74 The cytochrome b6f complex of oxygenic photosynthesis carries out "dark reactions" of

75 xic world with high-Fe oceans indicates that oxygenic photosynthesis could have destroyed a methane g

76 The emergence of oxygenic photosynthesis created a new niche with dramati

77 Oxygenic photosynthesis crucially depends on proteins th

78 ection (ATCC) 51142 is capable of performing oxygenic photosynthesis during the day and microoxic nit

79 al clades are thought to have evolved before oxygenic photosynthesis emerged, including the Chlorofle

80 otopic evidence have been used to claim that oxygenic photosynthesis evolved by 2.8 giga-annum before

81 d provided the evolutionary stock from which oxygenic photosynthesis evolved ca. 2.3 billion years ag

82 Oxygenic photosynthesis evolved with cyanobacteria, the

83 s an artefact of lateral gene transfer after oxygenic photosynthesis evolved, an alternative is a geo

84 synthesis evolved at or around the time that oxygenic photosynthesis evolved.

85 ever, does not resolve the time of origin of oxygenic photosynthesis from its anoxygenic photosynthet

86 oligomeric dimeric cytochrome b6f complex of oxygenic photosynthesis from the thermophilic cyanobacte

87 Here we show that the origin of oxygenic photosynthesis gave rise to two simultaneously

88 Ca(1)Cl(y)) of the water oxidizing enzyme of oxygenic photosynthesis generates O(2) evolution capacit

89 Cytochrome f of oxygenic photosynthesis has an unprecedented structure,

90 Oxygenic photosynthesis has existed for more than three

91 ormation by the manganese-calcium cluster of oxygenic photosynthesis has shaped the biosphere, atmosp

92 The emergence of oxygenic photosynthesis in ancient cyanobacteria represe

93 During oxygenic photosynthesis in cyanobacteria and chloroplast

94 The origin of oxygenic photosynthesis in Cyanobacteria led to the rise

95 The evolution of oxygenic photosynthesis in cyanobacteria nearly three bi

96 a widely used model organism for studies of oxygenic photosynthesis in eukaryotes.

97 Light-driven water oxidation occurs in oxygenic photosynthesis in photosystem II and provides r

98 Oxygenic photosynthesis in plants involves highly reacti

99 is indicates an important role of NIR-driven oxygenic photosynthesis in primary production of endolit

100 The origin of oxygenic photosynthesis in the Archaeplastida common anc

101 history and was enabled by the evolution of oxygenic photosynthesis in the cyanobacteria.

102 e we report the presence of genes central to oxygenic photosynthesis in the genomes of three phages f

103 me in Earth's history, complete dominance of oxygenic photosynthesis in the oceans.

104 In situ microsensor data showed both oxygenic photosynthesis in the red surface layer and lig

105 Here we demonstrate that oxygenic photosynthesis in the secondary chlorophyll max

106 sible Glc-dependent repression/activation of oxygenic photosynthesis in the unicellular green alga Ch

107 We calculate that oxygenic photosynthesis in these millimeter-thick ecosys

108 Some cyanobacteria couple oxygenic photosynthesis in vegetative cells with O2-sens

109 D1 of the photosystem II reaction center of oxygenic photosynthesis is expressed in precursor form (

110 sed for transmembrane free energy storage in oxygenic photosynthesis is generated by the cytochrome b

111 that conducts the light-driven reactions of oxygenic photosynthesis is hosted within specialized pai

112 The initial event in oxygenic photosynthesis is light absorption by chlorophy

113 Light regulation of enzyme activities in oxygenic photosynthesis is mediated by ferredoxin:thiore

114 Our results indicate that the existence of oxygenic photosynthesis is not a sufficient condition fo

115 In many filamentous cyanobacteria, oxygenic photosynthesis is restricted to vegetative cell

116 icrobial innovations in Earth's history, and oxygenic photosynthesis is the largest source of O2 in t

117 Oxygenic photosynthesis is the principal converter of su

118 Oxygenic photosynthesis is the principal converter of su

119 Oxygenic photosynthesis is the process by which plants,

120 This transition took place long after oxygenic photosynthesis is thought to have evolved, but

121 The cytochrome b(6)f complex of oxygenic photosynthesis mediates electron transfer betwe

122 The oxygenic photosynthesis of green plants, green algae, an

123 The advent of oxygenic photosynthesis on Earth may have increased glob

124 on, suggesting a significant effect of local oxygenic photosynthesis on Pacific AMZ biogeochemical cy

125 ty to reconstruct events in the evolution of oxygenic photosynthesis on the scale of entire genomes.

126 During the oxygenic photosynthesis phase, nitrate deficiency limite

127 Oxygenic photosynthesis relies on accessory factors to p

128 The development of oxygenic photosynthesis spectacularly increased oxygen l

129 Oxygenic photosynthesis supplies organic carbon to the m

130 Oxygenic photosynthesis supports virtually all life form

131 Photochemical conversion in oxygenic photosynthesis takes place in two large protein

132 ear to have evolved during the transition to oxygenic photosynthesis to play various roles in chlorop

133 espite this, Anthocerotibacter is capable of oxygenic photosynthesis under a wide range of light inte

134 d the electrostatics of P680(+) reduction in oxygenic photosynthesis using histidine-tagged and histi

135 iological/organic nanoconstruct over in vivo oxygenic photosynthesis validates the concept of tetheri

136 easurements on retrieved samples showed that oxygenic photosynthesis was fully but reversibly inhibit

137 Oxygenic photosynthesis was limited to 4 h per day, due

138 subunits of the cytochrome b(6)f complex of oxygenic photosynthesis was measured by stopped-flow mix

139 Microbial mats fuelled by oxygenic photosynthesis were probably present in terrest

140 The development of anoxygenic and then oxygenic photosynthesis would have allowed life to escap

141 bacteria (the only microorganisms capable of oxygenic photosynthesis), their co-occurrence with anoxy

142 In oxygenic photosynthesis, a highly oxidising chlorophyll

143 dation of the global ocean by cyanobacterial oxygenic photosynthesis, about 2,100 Myr ago, is presume

144 se ancient evolutionary innovations, such as oxygenic photosynthesis, can be corroborated with fossil

145 lastoquinone photooxidoreductase involved in oxygenic photosynthesis, is modified.

146 In oxygenic photosynthesis, light energy is stored in the f

147 In oxygenic photosynthesis, light harvesting is regulated t

148 f (cytb(6) f ) complex has a central role in oxygenic photosynthesis, linking electron transfer betwe

149 During oxygenic photosynthesis, metabolic reactions of CO2 fixa

150 ous phototrophs, they are used as models for oxygenic photosynthesis, nitrogen fixation, circadian rh

151 late that in the early evolutionary phase of oxygenic photosynthesis, nitrogenase served as an electr

152 eria are unique among bacteria in performing oxygenic photosynthesis, often together with nitrogen fi

153 s a large membrane protein complex vital for oxygenic photosynthesis, one of the most important biolo

154 In oxygenic photosynthesis, photosystem I (PSI) conducts li

155 In oxygenic photosynthesis, photosystem I catalyzes the lig

156 In oxygenic photosynthesis, photosystem II (PSII) carries o

157 In oxygenic photosynthesis, photosystem II (PSII) is the mu

158 One of the major players in oxygenic photosynthesis, photosystem II (PSII), exhibits

159 ario, we demonstrated that a nuclear gene of oxygenic photosynthesis, psbO, is expressed in the sea s

160 In oxygenic photosynthesis, PSII carries out the oxidation

161 associated with the global carbon cycle and oxygenic photosynthesis, respectively.

162 e unicellular prokaryotic algae that perform oxygenic photosynthesis, similar to plants.

163 ia are the only known prokaryotes capable of oxygenic photosynthesis, the evolution of which transfor

164 In oxygenic photosynthesis, the initial charge separation o

165 anobacteria, algae, and plants is pivotal in oxygenic photosynthesis, the process that powers life on

166 During oxygenic photosynthesis, the reducing power generated by

167 of Earth's atmosphere since the evolution of oxygenic photosynthesis, thereby exerting key influence

168 tead, major innovations - from the origin of oxygenic photosynthesis, to the evolution of reefs or of

169 ria are the only prokaryotes to have evolved oxygenic photosynthesis, transforming the biology and ch

170 In oxygenic photosynthesis, two photosystems work in series

171 In oxygenic photosynthesis, two photosystems work in tandem

172 are necessary for the optimal functioning of oxygenic photosynthesis, we screened a large collection

173 e evolutionary transition from anoxygenic to oxygenic photosynthesis, which resulted in a substantial

174 omprise a phylum defined by the capacity for oxygenic photosynthesis.

175 he light-driven water-splitting reactions of oxygenic photosynthesis.

176 I (PSI) is a reaction center associated with oxygenic photosynthesis.

177 may enhance the rate of charge separation in oxygenic photosynthesis.

178 h levels of O2 on Earth-like worlds indicate oxygenic photosynthesis.

179 ses light-induced charge separation to power oxygenic photosynthesis.

180 ecific protein group that evolved to protect oxygenic photosynthesis.

181 rpinning a tight link between CEF and NPQ in oxygenic photosynthesis.

182 photosystems that drive electron transfer in oxygenic photosynthesis.

183 brane protease found in organisms performing oxygenic photosynthesis.

184 s a highly toxic and inevitable byproduct of oxygenic photosynthesis.

185 sed as a prerequisite for the development of oxygenic photosynthesis.

186 mbrane electrochemical potential gradient in oxygenic photosynthesis.

187 y in a diverse set of organisms that perform oxygenic photosynthesis.

188 abacteria prior or due to the acquisition of oxygenic photosynthesis.

189 cteria are the only prokaryotes that perform oxygenic photosynthesis.

190 w attain the electron transfer throughput of oxygenic photosynthesis.

191 the use of 2-methylhopanes as biomarkers for oxygenic photosynthesis.

192 cyanobacteria and their functional link with oxygenic photosynthesis.

193 ting an important role for these proteins in oxygenic photosynthesis.

194 been unlikely to influence the evolution of oxygenic photosynthesis.

195 saC inaccessible to dioxygen at the onset of oxygenic photosynthesis.

196 plays a central role in light regulation of oxygenic photosynthesis.

197 may constrain the timing of the evolution of oxygenic photosynthesis.

198 r-infrared radiation (NIR) at 700-780 nm for oxygenic photosynthesis.

199 n concerning the role of protein dynamics in oxygenic photosynthesis.

200 SII) catalyzes the oxidation of water during oxygenic photosynthesis.

201 n of water and reduction of plastoquinone in oxygenic photosynthesis.

202 t least 300 million years after the onset of oxygenic photosynthesis.

203 resent a transition step in the evolution of oxygenic photosynthesis.

204 paved the way for the eventual appearance of oxygenic photosynthesis.

205 ave evolved during or after the evolution of oxygenic photosynthesis.

206 d reductant before water in the evolution of oxygenic photosynthesis.

207 e photoperiod and occurs simultaneously with oxygenic photosynthesis.

208 of GSH production is related to evolution of oxygenic photosynthesis.

209 nsfer and proton-translocating enzyme in all oxygenic photosynthesis.

210 usion model" for the origin and evolution of oxygenic photosynthesis.

211 n of water and reduction of plastoquinone in oxygenic photosynthesis.

212 uctural analysis of a PetC Rieske protein of oxygenic photosynthesis.

213 Photosystems I and II drive oxygenic photosynthesis.

214 component of the photosynthetic apparatus of oxygenic photosynthesis.

215 solar-driven oxidation of water used to fuel oxygenic photosynthesis.

216 the planetary surface after the evolution of oxygenic photosynthesis.

217 hesis that aerobic respiration evolved after oxygenic photosynthesis.

218 ears ago), and thus cannot be progenitors of oxygenic photosynthesis.

219 ue to a rise of the pH in the zone of active oxygenic photosynthesis.

220 hem to use near-infrared-radiation (NIR) for oxygenic photosynthesis.

221 e supercomplex involved in the first step of oxygenic photosynthesis.

222 distribution between the two photosystems of oxygenic photosynthesis.

223 h are supported by solar energy harnessed by oxygenic photosynthesis.

224 g and photoprotective functions essential to oxygenic photosynthesis.

225 Carotenoids are essential in oxygenic photosynthesis: they stabilize the pigment-prot

226 The emergence of oxygen-producing (oxygenic) photosynthesis fundamentally transformed our p

227 core complex I subunits, as well as several oxygenic-photosynthesis-specific (OPS) subunits that are

228 Fe biomineralization may have protected oxygenic photosynthesizers against Fe(2+) toxicity durin

229 P pathway, in line with the observation that oxygenic photosynthesizers are nutrient-limited, rather

230 -microfossil Fe minerals are consistent with oxygenic photosynthesizers but not with other Fe-mineral

231 ecologically important prokaryotic group of oxygenic photosynthesizers that contain cyanobacteriochr

232 sites can expand the absorption spectrum of oxygenic photosynthetic and potentially modulate light h

233 a low concentration suggests that the first oxygenic photosynthetic bacteria in solitary form could

234 n and of the photosynthetic apparatus of non-oxygenic photosynthetic bacteria.

235 brane and intracellular proteins in isolated oxygenic photosynthetic cells are not subjected to exces

236 balance and reductant partitioning in these oxygenic photosynthetic cells under stress.

237 the photosynthetic membranes of functioning oxygenic photosynthetic cells was estimated using classi

238 the function and biological role of PntAB in oxygenic photosynthetic cyanobacteria capable of both au

239 ction center of photosystem II (PSII) of the oxygenic photosynthetic electron transport chain contain

240 e closest to the last common ancestor of all oxygenic photosynthetic lineages and that green sulfur b

241 ction is to protect the protein complexes in oxygenic photosynthetic membranes against toxic effects

242 al of photobiological hydrogen production by oxygenic photosynthetic microbes has attracted significa

243 Cyanobacteria are oxygenic photosynthetic microorganisms and are considere

244 However, only a few models are available for oxygenic photosynthetic microorganisms, particularly in

245 or bicarbonate in the evolution of the first oxygenic photosynthetic organism.

246 energy input, but the pigment composition of oxygenic photosynthetic organisms also reflects the spec

247 egulatory and catalytic functions of ChlH of oxygenic photosynthetic organisms and for a chaperoning

248 ical protein for disulfide bond formation in oxygenic photosynthetic organisms and required for their

249 s been conserved throughout the evolution of oxygenic photosynthetic organisms and suggest a role for

250 protein phosphorylation during evolution of oxygenic photosynthetic organisms and their colonization

251 Oxygenic photosynthetic organisms evolved mechanisms for

252 Oxygenic photosynthetic organisms possess a plastid-loca

253 Analysis of GUN4 found in oxygenic photosynthetic organisms reveals the evolution

254 mpared to other nonphotosynthetic organisms, oxygenic photosynthetic organisms such as cyanobacteria,

255 Cyanobacteria are the only oxygenic photosynthetic organisms that can fix nitrogen.

256 In these oxygenic photosynthetic organisms the assembly of the la

257 Photorespiration is an essential process in oxygenic photosynthetic organisms triggered by the oxyge

258 ) is a key component of this pathway in most oxygenic photosynthetic organisms(3,4) and is the last l

259 In oxygenic photosynthetic organisms, CtpA catalyzes C-term

260 Moreover, in oxygenic photosynthetic organisms, Mn is of special impo

261 In oxygenic photosynthetic organisms, photosystem II (PSII)

262 Cyanobacteria, like other oxygenic photosynthetic organisms, respond to increases

263 s required for sustainable photosynthesis in oxygenic photosynthetic organisms.

264 water oxidation reaction that takes place in oxygenic photosynthetic organisms.

265 light-harvesting and light-sensing roles in oxygenic photosynthetic organisms.

266 d type of flavin enzyme that is exclusive to oxygenic photosynthetic prokaryotes and that is based on

267 The cyanobacterial phylum encompasses oxygenic photosynthetic prokaryotes of a great breadth o

268 t the roles of glutathione in cyanobacteria, oxygenic photosynthetic prokaryotes that are the evoluti

269 Cyanobacteria are oxygenic photosynthetic prokaryotes that are the progeni

270 ) has long been known as a micronutrient for oxygenic photosynthetic resulting from its role an essen

271 pread use of bilins as retrograde signals in oxygenic photosynthetic species.

272 thrin, a novel rubrerythrin variant from the oxygenic phototroph Cyanophora paradoxa, at 1.20-1.40 A

273 anobacterium Prochlorococcus is the dominant oxygenic phototroph in the tropical and subtropical regi

274 57,990 base pairs, 1,716 genes) of any known oxygenic phototroph, whereas the genome of its low-light

275 Nanowires produced by the oxygenic phototrophic cyanobacterium Synechocystis PCC68

276 ts, algae and cyanobacteria that make up the oxygenic phototrophs and a diversity of bacteriochloroph

277 s rubredoxin and its orthologs are unique to oxygenic phototrophs and distinct from rubredoxins in Ar

278 t and nutrients in the surface ocean between oxygenic phototrophs and Fe(II)-oxidizing, anoxygenic ph

279 pha-Tocopherol is synthesized exclusively in oxygenic phototrophs and is known to function as a lipid

280 On the basis of the breadth of oxygenic phototrophs examined in this study, we conclude

281 Oxygenic phototrophs have played a fundamental role in E

282 ns in full solar exposure, light filtered by oxygenic phototrophs, and light filtered under seawater,

283 indicate that Ycf54 is a cyclase subunit in oxygenic phototrophs, and that different classes of the

284 subunit protein complex universally found in oxygenic phototrophs, as a reliable reporter protein to

285 In oxygenic phototrophs, chlorophylls, hemes, and bilins ar

286 emained elusive and paradoxical, in that, as oxygenic phototrophs, cyanobacteria tend to alkalinize t

287 charge separation and water oxidation in all oxygenic phototrophs.

288 ates, and in the photorespiratory pathway of oxygenic phototrophs.

289 (WOC) of photosystem II (PSII) in all known oxygenic phototrophs.

290 substrate than water for O(2) production by oxygenic phototrophs.

291 ne sensor technology, and complementation of oxygenic phototrophy.

292 ry, thereby precluding the possibility of an oxygenic prebiotic atmosphere caused by photodissociatio

293 ent increases in P bioavailability can raise oxygenic primary production and organic carbon burial, y

294 The prochlorophytes are oxygenic prokaryotes differing from other cyanobacteria

295 OX) state, whereby a backbone amidate and an oxygenic residue (Ser or Tyr) ligate to two of the clust

296 Oxygenic respiration and photosynthesis based on quinone

297 The analysis suggests that oxygenic respiration is quite an old process and, in fac

298 this is a unique molecular species mimicking oxygenic RuO2 surfaces.

299 ogen as an energy source in water-splitting, oxygenic systems.

300 on capture and conversion processes to drive oxygenic water-splitting and carbon fixation.