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

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

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

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

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

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

13 esized only by photosynthetic eukaryotes and oxygenic cyanobacteria.

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

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

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

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

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

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

20 raised the possibility of one noncysteinyl, oxygenic ligand.

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

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

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

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

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

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

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

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

29 tosynthetic electron-transport system of all oxygenic organisms.

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

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

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

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

34 Oxygenic photoautotrophs require mechanisms for rapidly

35 d anoxygenic phototrophs largely outnumbered oxygenic photoautotrophs.

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

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

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

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

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

41 The evolution of oxygenic photosynthesis and ensuing oxygenation of Earth

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

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

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

45 Cyanothece 51142 performs oxygenic photosynthesis and nitrogen fixation, separatin

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

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

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

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

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

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

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

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

54 The invention of oxygenic photosynthesis by cyanobacteria 2.4 billion yea

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

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

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

58 Oxygenic photosynthesis crucially depends on proteins th

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

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

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

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

63 Oxygenic photosynthesis evolved with cyanobacteria, the

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

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

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

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

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

69 Cytochrome f of oxygenic photosynthesis has an unprecedented structure,

70 Oxygenic photosynthesis has existed for more than three

71 The emergence of oxygenic photosynthesis in ancient cyanobacteria represe

72 During oxygenic photosynthesis in cyanobacteria and chloroplast

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

74 The evolution of oxygenic photosynthesis in cyanobacteria nearly three bi

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

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

77 Oxygenic photosynthesis in plants involves highly reacti

78 The origin of oxygenic photosynthesis in the Archaeplastida common anc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 Oxygenic photosynthesis is the principal converter of su

95 Oxygenic photosynthesis is the principal converter of su

96 Oxygenic photosynthesis is the process by which plants,

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

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

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

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

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

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

103 During the oxygenic photosynthesis phase, nitrate deficiency limite

104 The development of oxygenic photosynthesis spectacularly increased oxygen l

105 Oxygenic photosynthesis supports virtually all life form

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

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

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

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

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

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

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

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

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

115 In oxygenic photosynthesis, a highly oxidising chlorophyll

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

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

118 In oxygenic photosynthesis, light harvesting is regulated t

119 During oxygenic photosynthesis, metabolic reactions of CO2 fixa

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

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

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

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

124 In oxygenic photosynthesis, photosystem I catalyzes the lig

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

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

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

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

129 In oxygenic photosynthesis, PSII carries out the oxidation

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

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

132 In oxygenic photosynthesis, the initial charge separation o

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

134 During oxygenic photosynthesis, the reducing power generated by

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

136 In oxygenic photosynthesis, two photosystems work in series

137 In oxygenic photosynthesis, two photosystems work in tandem

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

139 hesis that aerobic respiration evolved after oxygenic photosynthesis.

140 cteria are the only prokaryotes that perform oxygenic photosynthesis.

141 w attain the electron transfer throughput of oxygenic photosynthesis.

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

143 cyanobacteria and their functional link with oxygenic photosynthesis.

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

145 been unlikely to influence the evolution of oxygenic photosynthesis.

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

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

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

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

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

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

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

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

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

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

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

157 e photoperiod and occurs simultaneously with oxygenic photosynthesis.

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

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

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

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

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

163 Photosystems I and II drive oxygenic photosynthesis.

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

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

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

167 distribution between the two photosystems of oxygenic photosynthesis.

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

169 g and photoprotective functions essential to oxygenic photosynthesis.

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

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

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

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

174 ecific protein group that evolved to protect oxygenic photosynthesis.

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

176 photosystems that drive electron transfer in oxygenic photosynthesis.

177 brane protease found in organisms performing oxygenic photosynthesis.

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

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

180 mbrane electrochemical potential gradient in oxygenic photosynthesis.

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

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

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

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

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

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

187 ecologically important prokaryotic group of oxygenic photosynthesizers that contain cyanobacteriochr

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

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

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

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

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

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

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

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

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

197 Cyanobacteria are oxygenic photosynthetic microorganisms and are considere

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

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

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

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

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

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

204 Oxygenic photosynthetic organisms evolved mechanisms for

205 Oxygenic photosynthetic organisms possess a plastid-loca

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

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

208 In these oxygenic photosynthetic organisms the assembly of the la

209 In oxygenic photosynthetic organisms, CtpA catalyzes C-term

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

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

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

213 s required for sustainable photosynthesis in oxygenic photosynthetic organisms.

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

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

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

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

218 Cyanobacteria are oxygenic photosynthetic prokaryotes that are the progeni

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

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

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

222 57,990 base pairs, 1,716 genes) of any known oxygenic phototroph, whereas the genome of its low-light

223 Nanowires produced by the oxygenic phototrophic cyanobacterium Synechocystis PCC68

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

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

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

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

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

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

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

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

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

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

234 charge separation and water oxidation in all oxygenic phototrophs.

235 ne sensor technology, and complementation of oxygenic phototrophy.

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

237 The prochlorophytes are oxygenic prokaryotes differing from other cyanobacteria

238 Oxygenic respiration and photosynthesis based on quinone

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

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

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

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