ライフサイエンスコーパス: green algae

1 e with massive growth of cyanobacteria (blue-green algae).

2 elopment-specific expression were present in green algae.

3 ore ancestral third form (SLP3) was found in green algae.

4 rotein complex-based signaling mechanisms in green algae.

5 ay not explain the coexistence of freshwater green algae.

6 elrhodopsins are light-gated ion channels of green algae.

7 rent pesticides on Chlamydomonas reinhardtii green algae.

8 s described in higher plants is conserved in green algae.

9 onophyletic clade of homologs descended from green algae.

10 d be widely applicable to research involving green algae.

11 for regulation of "steering" motility in the green algae.

12 allmark of terrestrial plants and charophyte green algae.

13 s previously described in yeast, humans, and green algae.

14 n-evolving PSII complex in higher plants and green algae.

15 ic endosymbiont related to prasinophyte-like green algae.

16 er virus that infects unicellular eukaryotic green algae.

17 r specific high-throughput gene silencing in green algae.

18 nt role for phosphotyrosine signaling in the green algae.

19 hat infect certain eukaryotic chlorella-like green algae.

20 table nucleus-encoded proteins deriving from green algae.

21 o-cytochrome present in land plants and some green algae.

22 germ-soma differentiation in the volvocalean green algae.

23 major land plant taxa and in closely related green algae.

24 of all species rather than being confined to green algae.

25 randed DNA virus that infects chlorella-like green algae.

26 rtain unicellular, eukaryotic chlorella-like green algae.

27 land plants, preceding the emergence of the green algae.

28 to that found for Cab proteins in plants and green algae.

29 a feature shared only with some chlorophyte green algae.

30 rtain unicellular, eukaryotic chlorella-like green algae.

31 s conserved in dicots, monocots, mosses, and green algae.

32 yanobacteria, soon joined by eukaryotic blue-green algae.

33 light regulate GS transcript accumulation in green algae.

34 ascular plants from the avascular plants and green algae.

35 known proteins modulated by short-term -N in green algae.

36 from glaucophytes, red algae and chlorophyte green algae.

37 utative orthologous relationships with other green algae.

38 organisms, from angiosperms and monocots to green algae.

39 tid genomes yet observed from photosynthetic green algae.

40 h are not closely related to land plants and green algae.

41 evolution of isogamy and anisogamy in marine green algae.

42 mages of several elements in frozen-hydrated green algae.

43 in land plants, with none recognizable from green algae.

44 ips among land plants and (other) charophyte green algae.

45 strictly freshwater lineage, the charophyte green algae.

46 e a monophyletic lineage embedded within the green algae.

47 lated to land plants than to other groups of green algae.

48 tion in prasinophytes will differ from other green algae.

49 re unlikely crown-group animals or volvocine green algae.

50 ly known channelrhodopsins from chlorophyte (green) algae.

51 ago from a lineage of freshwater charophyte green algae(1).

52 s as a photoreceptor linked to phototaxis in green algae [2, 3] and has been implicated by chemical m

53 In chlorophytes (green algae), a protein termed major lipid-droplet prote

54 sing a data set of 14 taxa: 6 land plants, 2 green algae, a diatom, 2 red algae and a cryptophyte, th

55 isting of isolated nuclei of the unicellular green algae Acetabularia acetabulum.

56 ar protists, mesomycetozoean-like holozoans, green algae akin to Volvox, and blastula embryos of earl

57 ion as sensory photoreceptors in flagellated green algae, allowing these algae to identify optimal li

58 occurs also in homologous proteins in other green algae, amoebae, and pathogenic fungi.

59 tous green algae (Cladophora genus) and blue-green algae (Anabaena genus).

60 mon lichen-forming genus of aero-terrestrial green algae and all its species are desiccation tolerant

61 ts, but are entirely absent from liverworts, green algae and all other eukaryotes.

62 Bioinformatics of 1,000 oleosins of green algae and all plants emphasizing biological implic

63 rameterized model of a planktonic ecosystem, green algae and cyanobacteria coexist over a wide range

64 omponent of photosystem II in higher plants, green algae and cyanobacteria.

65 harvesting complex stress-related (LHCSR) in green algae and diatoms.

66 inhibition in the diatoms, prymnesiophytes, green algae and dinoflagellates of >2-3 mum cell sizes a

67 us 1 (PBCV-1) infects certain chlorella-like green algae and encodes a 120-kDa protein with a similar

68 lypeptides was identified that is present in green algae and flowering and nonflowering plants but is

69 s in photosynthetic bacteria, cyanobacteria, green algae and gymnosperms, dark-operative protochlorop

70 The oleosin gene first appeared in green algae and has evolved in enhancing promoter streng

71 A viruses known to infect certain eukaryotic green algae and have not been previously shown to infect

72 binding antenna of photosystem I (LHCI) from green algae and higher plants binds specific low energy

73 In green algae and higher plants, less efficient energy cou

74 nt and mobility, may also occur in wild-type green algae and higher plants.

75 for lipid A in free-living and endosymbiotic green algae and in the chloroplasts of vascular plants,

76 sponsible for light absorption in plants and green algae and is involved in photoprotective mechanism

77 ute polypeptides after the divergence of the green algae and land plant lineages.

78 two domains are mainly present in charophyte green algae and land plants but absent from glaucophytes

79 f myosins diverged prior to the radiation of green algae and land plants from a common ancestor and t

80 Green algae and land plants trace their evolutionary his

81 , an early divergent streptophyta (including green algae and land plants) in which both proteins are

82 CLMP1-like sequences are unique to green algae and land plants, and the CLMP1 sequence sugg

83 In contrast to green algae and land plants, inverted repeat regions in

84 teins in 20 model organisms, with a focus on green algae and land plants.

85 s indicates that KCBP is highly conserved in green algae and land plants.

86 e of phytochrome in the common progenitor of green algae and land plants.

87 Our protein sequence analyses indicate that green algae and major lineages of fungi were present 100

88 ein, which is responsible for dissipation in green algae and moss.

89 nary gap that exists between the chlorophyte green algae and most basal land plants, the bryophytes,

90 (31)P NMR detection, and low cytotoxicity on green algae and murine fibroblasts cell cultures.

91 representative land plant species but not in green algae and nonplant species, suggesting it is speci

92 n of entire mitochondrial genomes from three green algae and one moss.

93 nverted into zeaxanthin, is ubiquitous among green algae and plants and is necessary for the regulati

94 reenCut" gene set, a group of genes found in green algae and plants but not in non-photosynthetic org

95 cation of this information to sequences from green algae and plants suggested that a subset of the IT

96 imilar to that of metazoans but is absent in green algae and plants, facilitates rapid recovery from

97 e that was present in the common ancestor of green algae and plants, providing evidence of unexpected

98 ochrome c6A is a unique dithio-cytochrome of green algae and plants.

99 enes, named GreenCut2, that are conserved in green algae and plants.

100 (AtCGL160) protein (AtCGL160), conserved in green algae and plants.

101 All these gene families emerged in green algae and show concurrent expansions via serial du

102 nt transposons in the CHG context extends to green algae and that exclusion of histone H2A.Z from met

103 egulated enzyme in ascorbate biosynthesis in green algae and that, together with the ascorbate recycl

104 e Streptophyta, which consists of freshwater green algae and the land plants.

105 photosynthetic bacteria and eventually blue-green algae (and protoplastids) is described.

106 ght-harvesting complexes of prochlorophytes, green algae, and both nonvascular and vascular plants.

107 ause orthologs of ARC6 occur in land plants, green algae, and cyanobacteria but PDV2 occurs only in l

108 The oxygenic photosynthesis of green plants, green algae, and cyanobacteria is the major provider of

109 of photosystem II (PS II) in higher plants, green algae, and cyanobacteria, is encoded by the psbC g

110 es photosynthetic water oxidation in plants, green algae, and cyanobacteria.

111 omponent of photosystem II in higher plants, green algae, and cyanobacteria.

112 liverwort, and hornwort), from streptophyte green algae, and from a monocot (duckweed).

113 nctly different from those used by bacteria, green algae, and fungi to synthesize astaxanthin.

114 tida, consisting of glaucophytes, red algae, green algae, and land plants, share a common ancestor th

115 Thr-244 are conserved only in cyanobacteria, green algae, and land plants, whereas the other key amin

116 In prokaryotes, green algae, and most plants, this enzyme is a heteromer

117 In eubacteria, green algae, and plant chloroplasts, isopentenyl diphosp

118 nclude centrioles in humans, basal bodies in green algae, and spindle pole bodies in yeast.

119 east three independent times--in alveolates, green algae, and the ancestor of fungi and metazoans-acc

120 ble reactions of O(2) and H(2) production in green algae, and the second involves the use of classica

121 orophyta, which includes a wide diversity of green algae, and the Streptophyta, which consists of fre

122 The volvocine green algae are a tractable system for understanding the

123 he oral delivery of therapeutic proteins, as green algae are edible and do not contain endotoxins or

124 ecular studies have revealed that charophyte green algae are the closest relatives of the land plants

125 Cyanobacteria, formerly called blue-green algae, are abundant bacteria that carry out green

126 oducts, such as spirulina, derived from blue green algae, are believed to help reverse this effect du

127 , along with MSC1, a MscS family member from green algae, are implicated in the control of organelle

128 Cyanobacteria, blue-green algae, are the most abundant autotrophs in aquatic

129 Cyanobacteria, blue-green algae, are the most abundant autotrophs in aquatic

130 Green algae as a whole are among the oldest eukaryotic l

131 s of lichen species that exclusively include green algae as photobiont.

132 hyceae/phaeophyceae) and frequent loss among green algae, as well as in the red algae and their secon

133 from a streptomycete strain found in a blue-green algae associated with the ascidian Ecteinascidia t

134 vans are cell wall matrix polysaccharides in green algae belonging to the genus Ulva.

135 enomena were previously observed in other DT green algae, bryophytes and resurrection plants, other t

136 MET1 is conserved in C3 and C4 plants and green algae but is not found in prokaryotes.

137 eus-encoded proteins conserved in plants and green algae but not in non-photosynthetic organisms.

138 odel system for studying lipid metabolism in green algae, but current methods for isolating mutants o

139 s have been well characterized in plants and green algae, but little is known about transporters or t

140 The work shows that cpftsy deletion in green algae, but not in higher plants, can be employed t

141 B contains 21 or more residues in plants and green algae, but only 10 residues in prokaryotes and non

142 stress is conserved between land plants and green algae, but the distinct spatial and temporal dynam

143 (Girella nigricans) fed primarily on red and green algae, but there was significant variation in the

144 h core features similar to those of PSI from green algae, but with significant differences in shape a

145 isiae (Tpa1p), Schizosaccharomyces pombe and green algae catalyze an unprecedented dihydroxylation mo

146 psins (CCRs), structurally distinct from the green algae CCRs used extensively for neural activation

147 The charophyte green algae (CGA, Streptophyta, Viridiplantae) occupy a

148 ns, vertebrate rat rhodopsin 4 (RO4) and the green algae channelrhodospin 2 (ChR2), could be used to

149 ed effluent, the short-term toxicity for the green algae Chlamydomonas reinhardtii increased and reac

150 -sensitive [FeFe]-hydrogenase HydA1 from the green algae Chlamydomonas reinhardtii was exposed to def

151 tion-selective ion channel isolated from the green algae Chlamydomonas reinhardtii.

152 hort-term uptake of silver by two species of green algae, Chlamydomonas reinhardtii and Pseudokirchne

153 itrate transport system from the unicellular green algae, Chlamydomonas reinhardtii required two gene

154 hat the observed phenomenon extends to other green algae (Chlorella kesslerii and Scenedesmus obliquu

155 rticles (NPs) interacting with single-celled green algae, Chlorella sp., have been found to be bilate

156 Upper shore epiphytes were dominated by green algae (Chlorophyta) and single-celled diatoms (pri

157 ants as well as the two distinct lineages of green algae, chlorophytes and charophytes.

158 Thus light-activated vertebrate RO4 and green algae ChR2 allow the antagonistic control of neuro

159 The calculated profiles of 96-h green algae chronic toxicity show that the overall toxic

160 imes (archamoebae, calonymphids, chlorophyte green algae, ciliates, foraminifera).

161 algal blooms, which consisted of filamentous green algae (Cladophora genus) and blue-green algae (Ana

162 ting in proliferation of filamentous benthic green algae (Cladophora glomerata).

163 ella spp. are free-living, nonphotosynthetic green algae closely related to the model organism Chlamy

164 hotspots coinciding with abundant freshwater green algae (Closterium spp.).

165 Both red and green algae colonized marine environments early in their

166 tions to three food treatments consisting of green algae combined with cyanobacteria able/unable of p

167 AT values are increased in nonphotosynthetic green algae compared to their closest photosynthetic rel

168 Chloroplast genomes in plants and green algae contain numerous group II introns, large rib

169 loroplast-localized holoenzyme of plants and green algae contains eight nuclear-encoded small subunit

170 Freshwater with higher blue-green algae content produced higher number fractions of

171 ost cases, the blooms are predominantly blue-green algae (Cyanobacteria), which are favored by low ra

172 es form obligate symbiotic associations with green algae, cyanobacteria or with both photobionts.

173 The carbon material derived from blue-green algae demonstrated promising electrochemical perfo

174 lineages: animals, land plants, chlorophyte green algae, demosponges, slime molds and brown algae.

175 plexa, ciliates, land plants, and charophyte green algae--directly conflicts with the phylogeny of th

176 nce is eliminated or greatly restricted, and green algae dominate over a wide range of supply conditi

177 the natural organic ligands excreted by the green algae Dunaliella tertiolecta on the Fe(II) oxidati

178 ists representing Choanozoa, Archamoeba, and green algae efficiently suppressed all the phenotypes of

179 s 1 (PBCV-1), a large DNA virus that infects green algae, encodes a histone H3 lysine 27-specific met

180 rised nuclei of formerly independent red and green algae enslaved by separate eukaryote hosts over 50

181 ment analyses), particularly the diatoms and green algae, experienced only transient suppression then

182 Whereas green algae express many different OPR proteins, only a

183 hat infect certain eukaryotic chlorella-like green algae from the genus Chlorovirus.

184 , including Charophyceae algae, the group of green algae giving rise to land plants.

185 sulfate deficiency of plants and freshwater green algae has been extensively analysed by system biol

186 protein homologs in the sequenced genomes of green algae has led to the hypothesis that, in plants, t

187 ished role in the field of basic research in green algae has paved the way for understanding algal me

188 Only land plants and green algae have a kinesin with the MyTH4 and talin-like

189 Indeed, several charophyte green algae have historically been used as model systems

190 rce the cell walls of some red and siphonous green algae have not been well studied, yet they could p

191 t the bright promise studying the charophyte green algae holds for better understanding plant evoluti

192 major divisions of land plants as well as in green algae; homologs outside of the plant kingdom were

193 s are typically caused by the so-called blue-green algae in eutrophic waters.

194 ery different from those found in plants and green algae, including 3' poly(U) tail addition, and ext

195 chloroplast chaperonin system of plants and green algae is a curiosity as both the chaperonin cage a

196 f both mammalian sperm cells and unicellular green algae is primarily governed by direct ciliary cont

197 al diversity seen in the cyanobacteria (blue-green algae) is especially pronounced in the ubiquitous

198 gae Pseudokirchneriella subcapitata and blue-green algae Microcystis aeruginosa were separately incub

199 reveal five oleosin lineages: primitive (in green algae, mosses, and ferns), universal (U; all land

200 of foreign mitochondrial DNA, acquired from green algae, mosses, and other angiosperms.

201 AE gene families in the sequenced genomes of green algae, mosses, and trees; the size of the respecti

202 11-kDa protein from the cyanobacterium (blue-green algae) Nostoc ellipsosporum with potent virucidal

203 by photosynthesizing cyanobacteria and blue-green algae of nearly three billion years appeared to ha

204 , but recent studies of mating-type genes in green algae open a promising new way to explore molecula

205 genetic and genomic properties of charophyte green algae opens up new opportunities to study key prop

206 Plants and green algae optimize photosynthesis in changing light co

207 d colonial organisms such as the volvocalean green algae, organized beating by the somatic cells' fla

208 at support the expected monophyly of red and green algae/plants (i.e. the Plantae hypothesis) and 19

209 Several charophytes (advanced green algae) possessed low levels of transcripts encodin

210 l hormone during the evolution of charophyte green algae, prior to land colonization.

211 ever, it is not known if avascular plants or green algae produce this enzyme.

212 l algal blooms (HABs) of Cyanobacteria (blue-green algae) produce toxins that impact human health.

213 The freshwater green algae Pseudokirchneriella subcapitata and blue-gre

214 ent chloroplast genomes from land plants and green algae recovers the phylogeny congruent with prior

215 ation in chloroplasts of vascular plants and green algae, respectively.

216 e virus PBCV-1 that infects a chlorella-like green algae revealed an open reading frame, A98R, with s

217 Comparison with other sequenced green algae revealed unique protein families involved in

218 roup of spore-forming parasites that share a green algae symbiont and a predilection for causing chro

219 s obliquus) and at least one species of blue-green algae (Synechococcus leopoliensis).

220 yococcus braunii race B is a colony-forming, green algae that accumulates triterpene oils in excess o

221 Evidence is accumulating that in the green algae the evolution of female and male gametes dif

222 In plants and green algae the fastest response to high light is non-ph

223 is a spherical shell, such as the volvocine green algae, the current (molecules per second) of neede

224 Although state transitions are also found in green algae, the detailed architecture of the extant see

225 P. margaritaceum, a member of the charophyte green algae, the immediate ancestors of land plants, was

226 compounds have been identified in primitive green algae, the presence of true lignins in nonvascular

227 The accepted view is that in plants and green algae, the three extrinsic proteins are PsbO, PsbP

228 re the plastid genomes of two "transitional" green algae: the photosynthetic, mixotrophic Auxenochlor

229 tilization in taxa ranging from protozoa and green algae to flowering plants and invertebrate animals

230 is highly conserved from cyanobacteria, and green algae to land plants but not existing in the other

231 e the phenomic and genomic traits that allow green algae to survive in deserts, we characterized a ub

232 or understanding the transition from aquatic green algae to terrestrial plants.

233 plastids, photosynthesis spread from red and green algae to unrelated eukaryotes by secondary and ter

234 ted the organellar genomes of photosynthetic green algae, we generated the complete plastid genome (p

235 entified as a biotransformation product when green algae were exposed to environmentally relevant con

236 in situ hybridization images suggested that green algae were predominant in both the anode-based bio

237 se mediated by the two sensory rhodopsins in green algae were recorded.

238 ider aspects of the biology of the volvocine green algae, which contain both unicellular and multicel

239 deviant chloroplast genome of Cladophorales green algae, which is entirely fragmented into hairpin c

240 tes, recent efforts to purify molecules from green algae with structural features unique to lipid A h