ライフサイエンスコーパス: green alga

1 n preventing transposon mobilization in this green alga.

2 sembly of the PSII holocomplex in this model green alga.

3 sing our knowledgebase by 10% for this model green alga.

4 r physiological processes in this eukaryotic green alga.

5 een acquired by secondary endosymbiosis of a green alga.

6 by secondary endosymbiosis, probably from a green alga.

7 , 10 invertebrates, 12 vascular plants and a green alga.

8 as food, as now demonstrated in an ancestral green alga.

9 vegetative wildtype cells of the uninucleate green alga Acetabularia acetabulum can differentiate a r

10 t of RNA polymerase II from two red algae, a green alga and a relatively derived amoeboid protist.

11 used affinity reagents for lipid A to probe green alga and tissues of the garden pea for a light mic

12 phosphate formation in several eubacteria, a green alga, and plant chloroplasts has been demonstrated

13 ated derivatives (C31-C37), generated by the green alga Botryococcus braunii race B have received sig

14 to Chlamydomonas, a biflagellate fresh water green alga, but intense autofluorescence from photosynth

15 Under nitrogen deprivation, the green alga C. reinhardtii showed substantial triacylglyc

16 of 5 nm with a polyacrylate coating) by the green alga C. reinhardtii was investigated in order to a

17 ates for the absence of an active Rca in the green alga C. reinhardtii.

18 ce of this signaling complex in a charophyte green alga, Chara braunii, proposed to be the closest li

19 in gamete membrane fusion in the unicellular green alga Chlamydomonas and the malaria pathogen Plasmo

20 Recent work with the green alga Chlamydomonas and the nematode C. elegans dem

21 -type minus (mt-) gametes of the unicellular green alga Chlamydomonas are mixed together, binding int

22 ium caudatum (P-trHb) and the other from the green alga Chlamydomonas eugametos (C-trHb).

23 parison to the truncated hemoglobin from the green alga Chlamydomonas eugametos also suggested how th

24 Among the eight organisms, the green alga Chlamydomonas has the most unusual pattern of

25 FUS1 gene in the unicellular, biflagellated green alga Chlamydomonas is one of the few sex-specific

26 In a culture of a B(12) -dependent green alga Chlamydomonas nivalis, we found a contaminati

27 In the green alga Chlamydomonas reinhardtii (Cr), three genes e

28 /beta-barrel active site of Rubisco from the green alga Chlamydomonas reinhardtii (methyl-Cys-256, Ly

29 t it may not be closely related to the model green alga Chlamydomonas reinhardtii A detailed survey o

30 The unicellular green alga Chlamydomonas reinhardtii acclimates to a low

31 At low-CO2 (air) conditions, the unicellular green alga Chlamydomonas reinhardtii acquires the abilit

32 The unicellular green alga Chlamydomonas reinhardtii adapts to anaerobic

33 cytochrome b(6)f from the chloroplast of the green alga Chlamydomonas reinhardtii and cytochrome bc(1

34 oredoxins from Escherichia coli and from the green alga Chlamydomonas reinhardtii and for a number of

35 sure studies on the well-characterized model green alga Chlamydomonas reinhardtii and identified temp

36 e control of the photoperiod response in the green alga Chlamydomonas reinhardtii and its influence o

37 The unicellular green alga Chlamydomonas reinhardtii and the vascular pl

38 was isolated from the unicellular eukaryotic green alga Chlamydomonas reinhardtii as a light-induced

39 The success of the green alga Chlamydomonas reinhardtii as a model organism

40 type and in the cell wall free mutant of the green alga Chlamydomonas reinhardtii at pH 7.5.

41 system II core dimers were isolated from the green alga Chlamydomonas reinhardtii by Ni(2+)-affinity

42 The [FeFe] hydrogenase from the green alga Chlamydomonas reinhardtii can catalyze the re

43 The green alga Chlamydomonas reinhardtii can grow photoautot

44 The unicellular biflagellate green alga Chlamydomonas reinhardtii can perceive light

45 e [FeFe] hydrogenases HydA1 and HydA2 in the green alga Chlamydomonas reinhardtii catalyze the final

46 Mutations at the APM1 and APM2 loci in the green alga Chlamydomonas reinhardtii confer resistance t

47 Rubisco from the green alga Chlamydomonas reinhardtii differs from higher

48 his study shows that the cpSRP system in the green alga Chlamydomonas reinhardtii differs significant

49 The unicellular green alga Chlamydomonas reinhardtii divides by multiple

50 by the screening and sorting of cells of the green alga Chlamydomonas reinhardtii encapsulated in dro

51 Chlorophycean VDE (CVDE) gene from the model green alga Chlamydomonas reinhardtii encodes an atypical

52 en plus and minus gametes of the unicellular green alga Chlamydomonas reinhardtii entails adhesion be

53 In anaerobiosis, the green alga Chlamydomonas reinhardtii evolves molecular h

54 mple, we detect the release of H2O2 from the green alga Chlamydomonas reinhardtii exposed to either 1

55 In the green alga Chlamydomonas reinhardtii flagellar adhesion

56 The green alga Chlamydomonas reinhardtii has a network of fe

57 The unicellular green alga Chlamydomonas reinhardtii has become an inval

58 directly light-gated cation channel from the green alga Chlamydomonas reinhardtii has been shown to b

59 The chloroplast of the green alga Chlamydomonas reinhardtii has been shown to c

60 The animal-like cryptochrome (aCRY) of the green alga Chlamydomonas reinhardtii has extended our vi

61 The genome of the green alga Chlamydomonas reinhardtii has multiple genes

62 The green alga Chlamydomonas reinhardtii has numerous genes

63 lar phosphatases produced by the terrestrial green alga Chlamydomonas reinhardtii in response to phos

64 The eyespot of the biflagellate unicellular green alga Chlamydomonas reinhardtii is a complex organe

65 The green alga Chlamydomonas reinhardtii is a leading unicel

66 The eyespot of the unicellular green alga Chlamydomonas reinhardtii is a photoreceptive

67 The green alga Chlamydomonas reinhardtii is a useful model o

68 The unicellular green alga Chlamydomonas reinhardtii is a widely used mo

69 The green alga Chlamydomonas reinhardtii is an invaluable re

70 The unicellular green alga Chlamydomonas reinhardtii is capable of accli

71 usly established that the Rh1 protein of the green alga Chlamydomonas reinhardtii is highly expressed

72 One such gene in the green alga Chlamydomonas reinhardtii is MCD1, whose prod

73 The unicellular green alga Chlamydomonas reinhardtii is the premier expe

74 generated a pgrl1 npq4 double mutant in the green alga Chlamydomonas reinhardtii lacking both PGRL1

75 otosynthetic apparatus using a mutant of the green alga Chlamydomonas reinhardtii lacking carotenoids

76 the low pH is the PsbS protein, while in the green alga Chlamydomonas reinhardtii LhcSR proteins appe

77 The green alga Chlamydomonas reinhardtii mutant 76-5EN lacks

78 CCS4 was genetically identified in the green alga Chlamydomonas reinhardtii on the basis of the

79 e redox regulation of autophagy in the model green alga Chlamydomonas reinhardtii Our results indicat

80 the preexisting centriole proteome from the green alga Chlamydomonas reinhardtii revealed additional

81 dissection of xanthophyll metabolism in the green alga Chlamydomonas reinhardtii revealed functions

82 State transitions in the green alga Chlamydomonas reinhardtii serve to balance ex

83 agenesis of cytochrome f from the eukaryotic green alga Chlamydomonas reinhardtii showed that a Phe4

84 anobacterium Mastigocladus laminosus and the green alga Chlamydomonas reinhardtii showed the presence

85 When the green alga Chlamydomonas reinhardtii swims, it uses the

86 splay for isolating genes of the unicellular green alga Chlamydomonas reinhardtii that exhibit elevat

87 Here, we have created a minimal cell of the green alga Chlamydomonas reinhardtii that is able to und

88 identified a gene (MUT68) in the unicellular green alga Chlamydomonas reinhardtii that is required fo

89 ve cloned a gene (Mut6) from the unicellular green alga Chlamydomonas reinhardtii that is required fo

90 Here, we report in the green alga Chlamydomonas reinhardtii that UVR8 induces a

91 of the animal-like cryptochrome aCRY in the green alga Chlamydomonas reinhardtii This finding was ex

92 loned and characterized from the unicellular green alga Chlamydomonas reinhardtii to begin to underst

93 enesis and chloroplast transformation of the green alga Chlamydomonas reinhardtii to create D473A and

94 Here we use the model green alga Chlamydomonas reinhardtii to discover that a

95 sponsive fluorescent dyes in the unicellular green alga Chlamydomonas reinhardtii to examine the spec

96 ble draft genome sequence of the unicellular green alga Chlamydomonas reinhardtii to guide clustering

97 critical for acclimation of the unicellular green alga Chlamydomonas reinhardtii to phosphorus starv

98 is of the evolutionarily distant unicellular green alga Chlamydomonas reinhardtii to quantify the eff

99 Gametes of the unicellular green alga Chlamydomonas reinhardtii undergo sexual adhe

100 The green alga Chlamydomonas reinhardtii undergoes gametogen

101 ays of PS I in whole cells of the deuterated green alga Chlamydomonas reinhardtii using high-time-res

102 The 2pac mutant of the unicellular green alga Chlamydomonas reinhardtii was isolated and fo

103 translational acetylation in the unicellular green alga Chlamydomonas reinhardtii was studied by trit

104 thetase (GS) in nitrogen assimilation in the green alga Chlamydomonas reinhardtii we used maize GS1 (

105 is study, the two small-subunit genes of the green alga Chlamydomonas reinhardtii were eliminated dur

106 cellular organization, using mutants of the green alga Chlamydomonas reinhardtii with known alterati

107 We have investigated a cryptochrome from the green alga Chlamydomonas reinhardtii with sequence homol

108 In the model green alga Chlamydomonas reinhardtii, a carbon-concentra

109 In the green alga Chlamydomonas reinhardtii, a Leu(290)-to-Phe

110 In the green alga Chlamydomonas reinhardtii, a luminal carbonic

111 In the green alga Chlamydomonas reinhardtii, a mutant, pmp1, wa

112 In the green alga Chlamydomonas reinhardtii, a photosynthetic m

113 ences from flowering plants with that of the green alga Chlamydomonas reinhardtii, a small number of

114 e 80S cytosolic ribosome from the eukaryotic green alga Chlamydomonas reinhardtii, and accompany this

115 similar to that recently demonstrated in the green alga Chlamydomonas reinhardtii, and for the first

116 lant Arabidopsis (Arabidopsis thaliana), the green alga Chlamydomonas reinhardtii, and the cyanobacte

117 oglycerate kinase (PGK1) from the eukaryotic green alga Chlamydomonas reinhardtii, and we show that C

118 ring plant, Commelina communis, cells of the green alga Chlamydomonas reinhardtii, and zygotes of the

119 optical spectroscopy in living cells of the green alga Chlamydomonas reinhardtii, between 277 and 31

120 In transformants of the unicellular green alga Chlamydomonas reinhardtii, expression of a eu

121 In the unicellular green alga Chlamydomonas reinhardtii, GTR and GSAT were

122 In the green alga Chlamydomonas reinhardtii, Mut11p, related to

123 In the green alga Chlamydomonas reinhardtii, non-photochemical

124 hat a qE-deficient mutant of the unicellular green alga Chlamydomonas reinhardtii, npq4, lacks two of

125 e found on unicellular organisms such as the green alga Chlamydomonas reinhardtii, on sperm cells, an

126 ) showed a dramatic daily oscillation in the green alga Chlamydomonas reinhardtii, peaking once each

127 We report that in the green alga Chlamydomonas reinhardtii, PPO and FeC are ea

128 onal, photosynthesis-deficient mutant of the green alga Chlamydomonas reinhardtii, previously recover

129 gly, a SU(VAR)3-9 homolog in the unicellular green alga Chlamydomonas reinhardtii, SET3p, functions i

130 In the unicellular green alga Chlamydomonas reinhardtii, single-copy transg

131 In the unicellular green alga Chlamydomonas reinhardtii, sRNAs derived from

132 In the unicellular green alga Chlamydomonas reinhardtii, the epigenetic sil

133 In the chloroplast of the green alga Chlamydomonas reinhardtii, two discontinuous

134 of native chloroplast ClpP complex from the green alga Chlamydomonas reinhardtii, using a strain tha

135 Using the unicellular green alga Chlamydomonas reinhardtii, we developed a gen

136 Using the green alga Chlamydomonas reinhardtii, we developed an ef

137 a heterologous psbA expression system in the green alga Chlamydomonas reinhardtii, we have measured g

138 chanisms exist in the evolutionarily distant green alga Chlamydomonas reinhardtii, we identified Chla

139 vivo, by manipulating the chloroplast of the green alga Chlamydomonas reinhardtii, where the translat

140 on two [FeFe]-hydrogenases, CrHydA1 from the green alga Chlamydomonas reinhardtii, which contains onl

141 remains poorly understood in the unicellular green alga Chlamydomonas reinhardtii, which contains thr

142 f these additional residues, a mutant of the green alga Chlamydomonas reinhardtii, which lacks both s

143 The AMT4 locus of the green alga Chlamydomonas reinhardtii, which we mapped to

144 anobacterium Mastigocladus laminosus and the green alga Chlamydomonas reinhardtii, whose appearance i

145 new spontaneous mutations in the unicellular green alga Chlamydomonas reinhardtii.

146 system I (PSI) biogenesis in the unicellular green alga Chlamydomonas reinhardtii.

147 e formation in a plant cryptochrome from the green alga Chlamydomonas reinhardtii.

148 dy of an unusual heteroplasmic strain of the green alga Chlamydomonas reinhardtii.

149 sociated with flagellar length change in the green alga Chlamydomonas reinhardtii.

150 es, including 6 eudicots, 5 monocots and the green alga Chlamydomonas reinhardtii.

151 1 and sac3 sulfur acclimation mutants of the green alga Chlamydomonas reinhardtii.

152 oved by conversion of each Tyr to Phe in the green alga Chlamydomonas reinhardtii.

153 aining protein cytochrome c6 (cyt c6) in the green alga Chlamydomonas reinhardtii.

154 volved in the microbodies of the unicellular green alga Chlamydomonas reinhardtii.

155 ntly identified in the hydEF-1 mutant of the green alga Chlamydomonas reinhardtii.

156 basal bodies (centrioles) isolated from the green alga Chlamydomonas reinhardtii.

157 ntify proteins in purified flagella from the green alga Chlamydomonas reinhardtii.

158 ype and mutant forms of photosystem I in the green alga Chlamydomonas reinhardtii.

159 ned and characterized the psbW gene from the green alga Chlamydomonas reinhardtii.

160 A from the chloroplast to the nucleus in the green alga Chlamydomonas reinhardtii.

161 subunit of the chloroplast ribosome from the green alga Chlamydomonas reinhardtii.

162 edominant components of the cell wall of the green alga Chlamydomonas reinhardtii.

163 properties similar to acidocalcisomes in the green alga Chlamydomonas reinhardtii.

164 ia the reversible hydrogenase pathway in the green alga Chlamydomonas reinhardtii.

165 ent, Tcr3, was identified in the unicellular green alga Chlamydomonas reinhardtii.

166 ) from non-Solanaceae species, including the green alga Chlamydomonas reinhardtii.

167 ated from the chloroplast of the unicellular green alga Chlamydomonas reinhardtii.

168 use observed in the chloroplast genes of the green alga Chlamydomonas reinhardtii.

169 ges during synchronized cell division in the green alga Chlamydomonas reinhardtii.

170 f nuclear gene expression in the unicellular green alga Chlamydomonas reinhardtii.

171 nsertion sites in the eukaryotic unicellular green alga Chlamydomonas reinhardtii.

172 utophagy activation in the model unicellular green alga Chlamydomonas reinhardtii.

173 hat are native to D1:1 were expressed in the green alga Chlamydomonas reinhardtii.

174 ative selectable marker for use in the model green alga Chlamydomonas reinhardtii.

175 t is found in the eyespot of the unicellular green alga Chlamydomonas reinhardtii.

176 The unicellular green alga Chlamydomonas swims with two flagella that ca

177 We screened the unicellular green alga Chlamydomonas using insertional mutagenesis t

178 ere, by use of gene discovery methods in the green alga Chlamydomonas, gene disruption in the rodent

179 In the unicellular, biflagellated green alga Chlamydomonas, the early steps in zygote deve

180 During fertilization in the green alga Chlamydomonas, the plus gamete-specific membr

181 biflagellated phytoplanktons resembling the green alga Chlamydomonas.

182 ontrol zygote development of the unicellular green alga Chlamydomonas.

183 counterparts of cilia) of the biflagellated green alga Chlamydomonas.

184 e to environmental cues in the biflagellated green alga Chlamydomonas.

185 s (Physcomitrella patens), and a unicellular green alga (Chlamydomonas reinhardtii), encode proteins

186 esulted in identification of KCBP in another green alga, Chlamydomonas reinhardtii, and several flowe

187 The model unicellular green alga, Chlamydomonas reinhardtii, employs diverse s

188 Here we use the green alga, Chlamydomonas reinhardtii, which regulates b

189 nd modifying the chloroplast genome from the green alga, Chlamydomonas reinhardtii.

190 animals are also present in the unicellular green alga, Chlamydomonas reinhardtii.

191 obacterium, Mastigocladus laminosus, and the green alga, Chlamydomonas reinhardtii.

192 ibody in the chloroplast of the unicellular, green alga, Chlamydomonas reinhardtii.

193 ized a second [Fe]-hydrogenase gene from the green alga, Chlamydomonas reinhardtii.

194 us, (ii) spinach chloroplasts, and (iii) the green alga, Chlamydomonas reinhardtii.

195 were changed in six mutants generated in the green alga, Chlamydomonas reinhardtii.

196 Sexual reproduction in the green alga, Chlamydomonas, is regulated by environmental

197 in many aspects of flagella function in the green alga, Chlamydomonas.

198 stically related in higher plants and in the green alga Chlorella protothecoides.

199 e-forming virus that infects the unicellular green alga Chlorella sp. strain NC64A.

200 hlorophyte plastid genomes, only that of the green alga Chlorella vulgaris appears to share this feat

201 diuron on the photosynthetic activity of the green alga Chlorella vulgaris in presence of different m

202 Experiments with the green alga Chlorella vulgaris presented here compared po

203 TCV-1, whose only known host is a eukaryotic green alga (Chlorella heliozoae) that is an endosymbiont

204 ntosa and two acetylated diterpenes from the green alga Chlorodesmis fastigiata as potent allelochemi

205 There is interest in the unicellular green alga Chromochloris zofingiensis, because it produc

206 The nuisance, macrophytic, green alga Cladophora (Chlorophyta; mostly Cladophora gl

207 diolabeled EE2 ((14)C-EE2) by the freshwater green alga Desmodesmus subspicatus were investigated.

208 DNA (mtDNA) of Chlamydomonas reinhardtii, a green alga, does not encode subunit 6 of F(0)F(1)-ATP sy

209 The halotolerant green alga Dunaliella bardawil is unique in that it accu

210 diatom, Pseudonitzshia delicatissima and the green alga, Dunaliella tertiolecta .

211 (APS) reductase from the marine macrophytic green alga Enteromorpha intestinalis uses reduced glutat

212 inant phytochromes from a higher plant and a green alga exhibit serine/threonine kinase activity simi

213 en plant lineage, including charophytes (the green alga group closest to the land plants), bryophytes

214 Chlamydomonas reinhardtii, a unicellular green alga, grows photoautotrophically at very low conce

215 In the model organism Dunaliella salina (a green alga), growth under low light (100 mol of photons

216 el alkaloids recently isolated from the blue-green alga Hapalosiphon welwitschii.

217 The green alga Hematococcus pluvialis accumulates large amou

218 elicits a lytic infection of its unicellular green alga host.

219 in Chlamydomonas reinhardtii, a unicellular green alga in the land plant lineage.

220 B(12) -dependent Lobomonas rostrata, another green alga, in return for fixed carbon.

221 nas sp. UWO 241 (UWO 241) is a psychrophilic green alga isolated from Antarctica.

222 osynthetic cell, because in this unicellular green alga LD dynamics can be readily manipulated by nit

223 The unicellular green alga Lobomonas rostrata requires an external suppl

224 of phytochrome isolated from the unicellular green alga Mesotaenium caldariorum is blue-shifted.

225 ornithine decarboxylase in the single-celled green alga Micromonas.

226 is, we show that gametogenesis in the marine green alga, Monostroma angicava, exhibits equal size cel

227 DNA possesses 4 derived features relative to green alga mtDNAs--increased genome size, RNA editing, i

228 sis obtusa (starry stonewort) is a dioecious green alga native to Europe and Asia that has emerged as

229 Chlamydomonas reinhardtii, a unicellular green alga, often experiences hypoxic/anoxic soil condit

230 Dendroamide A (1) was isolated from a blue-green alga on the basis of its ability to reverse drug r

231 During embryonic development, cells of the green alga Oophila amblystomatis enter cells of the sala

232 g was associated with POT1 proteins from the green alga Ostreococcus lucimarinus and two flowering pl

233 phytoplankton virus, which infects the small green alga Ostreococcus tauri, a host-derived ammonium t

234 nced the 13.5 Mbp genome of the halotolerant green alga Picochlorum SENEW3 (SE3) that was isolated fr

235 hthoquinone aulosirazole, isolated from blue-green alga, possesses selective antitumor cytotoxicity,

236 Green alga POT1 exhibited a strong preference for the ca

237 As NoDGAT2A, 2C, and 2D originated from the green alga, red alga, and eukaryotic host ancestral part

238 Arthrospira (Spirulina) platensis is a blue-green alga, rich with bioactive components and nutrients

239 -PS) on the growth and photosynthesis of the green alga Scenedesmus obliquus and the growth, mortalit

240 iforme and Anabaena spp., in addition to the green alga Scenedesmus obliquus.

241 cation to homogeneity of the enzyme from the green alga, Scenedesmus obliquus.

242 ene functions as a hormone in the charophyte green alga Spirogyra pratensis Since land plants evolved

243 d KCBP from a gymnosperm, Picea abies, and a green alga, Stichococcus bacillaris.

244 he glaucocystophyte Cyanophora, and the blue-green alga Synechocystis as an outgroup.

245 tegies of Chlamydomonas reinhardtii, a model green alga that can grow using various carbon sources an

246 Chlamydomonas reinhardtii is a unicellular green alga that has attracted interest due to its potent

247 s a unicellular, soil-dwelling (and aquatic) green alga that has significant metabolic flexibility fo

248 Chlamydomonas reinhardtii is a unicellular green alga that is a key model organism in the study of

249 hardtii is a motile single-celled freshwater green alga that is guided by photosensory, mechanosensor

250 Chlamydomonas reinhardtii is a single-celled green alga that phototaxes toward light by means of a li

251 ed into a putative genome-scale model of the green alga to in silico test hypotheses of underlying ca

252 he robust and flexible biology utilized by a green alga to successfully inhabit a desert coastline.

253 ar plant (fern, Dryopteris crassirhizoma), a green alga (Ulva pertusa), and cyanobacteria (Anabaena v

254 The multicellular green alga Volvox carteri and its morphologically divers

255 The green alga Volvox carteri possesses several thousand cel

256 (MT) of the sexually dimorphic multicellular green alga Volvox carteri specifies the production of eg

257 TIs is the origin of multicellularity in the green alga Volvox, a model system for the evolution of m

258 ly linked to the regA gene of the eukaryotic green alga Volvox.

259 poson called kangaroo from the multicellular green alga, Volvox carteri.

260 Chlamydomonas reinhardtii is a unicellular green alga whose lineage diverged from land plants over

261 Volvox carteri is a spherical green alga with a predominantly asexual mode of reproduc

262 n identified in Chlamydomonas reinhardtii, a green alga with a well-studied CCM.

263 Udotea flabellum is a marine, macroscopic green alga with C4-like photosynthetic characteristics,