ライフサイエンスコーパス: C. reinhardtii

1 C. reinhardtii BBS4 may be required for the export of si

2 C. reinhardtii cells deprived of iron have more saturate

3 C. reinhardtii cells exposed to oxidative stress show in

4 C. reinhardtii has contributed to our understanding of c

5 C. reinhardtii insertional mutants defective in BBS1, -4

6 C. reinhardtii is serving as an important model organism

7 C. reinhardtii knockdown mutants for GPD2 and GPD3 showe

8 C. reinhardtii mutants null for cia5 do not express seve

9 ibodies raised to PsbW we have examined: (1) C. reinhardtii mutants lacking either photosystem and (2

10 A C. reinhardtii insertional mutant null for IFT46 has sho

11 Gene g5047 encodes a C. reinhardtii homolog of the chloroplast-localized SRP4

12 scribe the cloning and characterization of a C. reinhardtii version of a TRP channel sharing key feat

13 for Rca was cloned and expressed in pSL18, a C. reinhardtii expression vector conferring paromomycin

14 An antibody raised against C. reinhardtii hydin was specific for an approximately 5

15 Under nitrogen deprivation, the green alga C. reinhardtii showed substantial triacylglycerol (TAG)

16 th a polyacrylate coating) by the green alga C. reinhardtii was investigated in order to assess the c

17 ng the atypically fast IFT in the green alga C. reinhardtii, on average, 10 kinesin-2 motors "line up

18 e absence of an active Rca in the green alga C. reinhardtii.

19 he most thoroughly studied unicellular alga, C. reinhardtii, is the current standard for algal resear

20 Although C. reinhardtii has a single gene encoding pyruvate carbo

21 ithii +, plus the new eastern North American C. reinhardtii isolates, comprise one morphological spec

22 ommon unicellular ancestor of V. carteri and C. reinhardtii and that this gene was lost in the latter

23 region with several predicted V. carteri and C. reinhardtii proteins and that this region, the VARL d

24 mplex obtained from spinach chloroplasts and C. reinhardtii.

25 nce between cytochrome f of P. laminosum and C. reinhardtii (E(m7) = 297 and 370 mV, respectively).

26 l cyt bc(1) complex and the M. laminosus and C. reinhardtii cyt b(6)f complexes.

27 lesser degree between the higher plants and C. reinhardtii.

28 determined for both E. coli thioredoxin and C. reinhardtii thioredoxin h.

29 pendent signaling cascades operate in anoxic C. reinhardtii cells.

30 of the wide array of experimental approaches C. reinhardtii offers, Lechtreck and Witman determined t

31 ned elusive in eukaryotic microalgae such as C. reinhardtii.

32 tion pathway in the dark, especially because C. reinhardtii PFR1 was also able to allow H(2) evolutio

33 response is physiologically relevant because C. reinhardtii experiences these growth conditions routi

34 nach and pea thioredoxin f, -300 mV for both C. reinhardtii and spinach thioredoxin m, -320 mV for sp

35 nd/or ASQD in photosynthesis as conducted by C. reinhardtii, particularly under phosphate-limited con

36 nic forms of Se, are readily internalized by C. reinhardtii, but selenite is accumulated around ten t

37 at Sc hydroxo-complexes were internalized by C. reinhardtii.

38 dentify the molecular basis of the classical C. reinhardtii mutation ac17.

39 ST) evidence and annotation of the completed C. reinhardtii genome identified genes for each of the f

40 In conclusion, C. reinhardtii hydin is a CP protein required for flagel

41 Co-culturing C. reinhardtii with M. loti also results in reduction of

42 The deduced C. reinhardtii mature GTR amino acid sequence has more t

43 thway for Hyd1 expression in oxygen-depleted C. reinhardtii demonstrates the existence of multiple ox

44 ived sequences among nuclear genome data for C. reinhardtii, which also contrasts with the situation

45 nd frequency of the oscillatory dynamics for C. reinhardtii.

46 toxicity and adaptive response pathways for C. reinhardtii exposed to silver.

47 ws for the generation of stable, marker-free C. reinhardtii transformants without the supplementation

48 ast FLA8/10 and slow KLP11/20 kinesin-2 from C. reinhardtii and C. elegans through a DNA tether to un

49 comparison of genomic Hind10 fragments from C. reinhardtii rs-3 and its wild-type progenitor CC-407

50 oxidant function, the nuclear VTE2 gene from C. reinhardtii was overexpressed in the npq1 lor1 double

51 dentical to the known HydA1 hydrogenase from C. reinhardtii.

52 ecificity and affinity as RB47 isolated from C. reinhardtii chloroplasts.

53 As isolated from C. reinhardtii flagella, IFT complex B can be further re

54 ty in the spectra for WT PS I particles from C. reinhardtii and Synechocystis sp. 6803 indicates that

55 For PS I particles from C. reinhardtii, substitution of HisA676 with serine has

56 00(+) formation, in both PS I particles from C. reinhardtii, the higher-frequency carbonyl band upshi

57 Evidently, docking of these proteins from C. reinhardtii is due to hydrophobic interaction, slight

58 and by nuclear transformation with VTE2 from C. reinhardtii, which resulted in 1.6-fold, 5-fold to 10

59 he previously identified SUMO conjugase gene C. reinhardtii ubiquitin-conjugating enzyme9 (CrUBC9) is

60 However, C. reinhardtii also possesses the pyruvate:ferredoxin ox

61 In C. reinhardtii cells synchronized by light to dark cycle

62 In C. reinhardtii, low levels of a transcript encoding an o

63 In C. reinhardtii, the STA7 isoamylase gene is important fo

64 signal for acclimation to limiting CO(2) in C. reinhardtii is unidentified, and it is not known how

65 arteri but that a similar array is absent in C. reinhardtii.

66 a crucial part of high-light acclimation in C. reinhardtii.

67 cular and nonvascular plant databases and in C. reinhardtii but absent from cyanobacterial genomes.

68 ot detection of CSRA and CSRB apoproteins in C. reinhardtii cells enabling assessment of the cellular

69 ER stress also triggered autophagy in C. reinhardtii based on the protein abundance, lipidatio

70 ne-folate cycle are also repressed by B12 in C. reinhardtii.

71 retinal-dependent photomotility behavior in C. reinhardtii.

72 rk provides insight into TAG biosynthesis in C. reinhardtii, and paves the way for engineering microa

73 cts with an antibody to lumen-directed CA in C. reinhardtii, and because it can be removed with 1 M C

74 tinct from the two mitochondrial beta-CAs in C. reinhardtii.

75 pyrenoid is required for a functional CCM in C. reinhardtii.

76 mponents of a high molecular mass complex in C. reinhardtii cells.

77 abundance or transient regulatory complex in C. reinhardtii that may be similar to DREAM-like complex

78 of at least one additional SUMO conjugase in C. reinhardtii, a conjugase tentatively identified as Cr

79 istinct and functional SUMO E2 conjugases in C. reinhardtii, with a clear division of labor between t

80 We predicted a large number of CREs in C. reinhardtii that are consistent with experimentally v

81 the first large-scale collection of CREs in C. reinhardtii to facilitate further experimental study

82 regulatory function is wired differently in C. reinhardtii to control qE capacity via cis-regulatory

83 ured airway epithelial cells, as was DRC2 in C. reinhardtii following deflagellation.

84 rafish embryos or mutation of TTC26/DYF13 in C. reinhardtii, produced short cilia with abnormal motil

85 h as much as approximately 10% efficiency in C. reinhardtii We demonstrate its use in transgene- and

86 cyanobacterial b(6)f, as well as eicosane in C. reinhardtii, are unique to the b(6)f complex.

87 ral dynamics of osmotic Ca(2+) elevations in C. reinhardtii suggest important mechanistic differences

88 y omega-3 fatty acid desaturase expressed in C. reinhardtii, and we discuss possible mechanisms of ho

89 When expressed in C. reinhardtii, we observed a differential metal-depende

90 known chloroplast ferredoxins (FDX1-FDX6) in C. reinhardtii, FDX1 and FDX2 were the most efficient el

91 ly regulated by the levels of PPO and FeC in C. reinhardtii.

92 t Asc has distinct roles in NPQ formation in C. reinhardtii as compared to vascular plants.

93 ults suggest a mechanism for LD formation in C. reinhardtii involving chloroplast envelope membranes

94 to both Class-1 and Class-2 enzyme-forms in C. reinhardtii.

95 rophycean violaxanthin de-epoxidase found in C. reinhardtii does not require Asc as a reductant.

96 he molecular cloning of the two Ppc genes in C. reinhardtii (CrPpc1, CrPpc2), each of which is transc

97 LciB and three related genes in C. reinhardtii compose a unique gene family that encode

98 ed expression of the LHCSR and PSBS genes in C. reinhardtii The spa1 and cul4 mutants accumulate incr

99 nt high-level expression of foreign genes in C. reinhardtii, which has not previously been reliably a

100 l transcripts derived from the same genes in C. reinhardtii.

101 rom specific photosynthesis-related genes in C. reinhardtii.

102 We monitored the accumulation of GFP in C. reinhardtii chloroplasts transformed with the codon-o

103 s expression with the accumulation of GFP in C. reinhardtii transformed with a non-optimized GFP cass

104 Overexpression of GPD2 and GPD3 in C. reinhardtii gave distinct phenotypes.

105 photoreceptor for light induction of gsa in C. reinhardtii is not a carotenoid.

106 The FeC content is higher in C. reinhardtii cells growing in continuous light than in

107 -regulatory element (CRE) identification, in C. reinhardtii.

108 s responsible for the atypically fast IFT in C. reinhardtii.

109 Calcium binding site IV in C. reinhardtii centrin was found to bind Ca2+ approximat

110 l to enforcing wild-type flagellar length in C. reinhardtii.

111 identification at the whole genome level in C. reinhardtii using a comparative genomics-based method

112 protein phosphorylation under high light in C. reinhardtii, known to fully induce the expression of

113 oarray and identified more than 50 lipids in C. reinhardtii without an extraction process.

114 omycin define three unlinked nuclear loci in C. reinhardtii.

115 sed a chloroplast luciferase gene, luxCt, in C. reinhardtii chloroplasts under the control of the ATP

116 gene family, which consists of 12 members in C. reinhardtii and 14 in V. carteri, has experienced a c

117 duced expression of Pcdp1 complex members in C. reinhardtii results in failure of the C1d central pai

118 of the transcriptome and mRNA metabolism in C. reinhardtii.

119 tal validation of several novel microRNAs in C. reinhardtii that were predicted by miRvial but missed

120 harge on the RS surface impaired motility in C. reinhardtii.

121 vement of DNA from chloroplast to nucleus in C. reinhardtii, which may reflect the ultrastructure of

122 the transgene silencing that often occurs in C. reinhardtii, the FPs were expressed from the nuclear

123 ectronic structure of P700 and/or P700(+) in C. reinhardtii and Synechocystis sp. 6803.

124 complex antenna phosphorylation patterns in C. reinhardtii compared to Arabidopsis are discussed in

125 Artificial microRNA silencing of PDAT in C. reinhardtii alters the membrane lipid composition, re

126 edoxin, is thus likely the partner of PFO in C. reinhardtii.

127 panying software tool and the predictions in C. reinhardtii are also made available through a Web-acc

128 yldiacylglycerol (ASQD), which is present in C. reinhardtii.

129 inglet oxygen-induced acclimation process in C. reinhardtii.

130 on of ATG8 and thus autophagy progression in C. reinhardtii.

131 Expression of the PsbS protein in C. reinhardtii has not been reported yet.

132 show that PsbS is a light-induced protein in C. reinhardtii, whose accumulation under high light is f

133 activation of non-photochemical quenching in C. reinhardtii, possibly by promoting conformational cha

134 together for coordinated gene regulation in C. reinhardtii.

135 vents in the global N starvation response in C. reinhardtii, starting within minutes with the upregul

136 uli, including a novel [Ca2+]cyt response in C. reinhardtii.

137 s associated with S deprivation responses in C. reinhardtii.

138 on factor-evolved from its ancestral role in C. reinhardtii as a mating-type specifier, to become a d

139 starch metabolism play an important role in C. reinhardtii H(2) photoproduction.

140 als that the miRNA-mediated RNA silencing in C. reinhardtii differs from that of higher plants and in

141 nsduction pathway controls organelle size in C. reinhardtii.

142 porally to synthesize diverse TAG species in C. reinhardtii.

143 d membranes occurs during iron starvation in C. reinhardtii.

144 rol of autophagy in response to ER stress in C. reinhardtii In close agreement, we also found that au

145 te that the rate of chlorophyll synthesis in C. reinhardtii is not directly controlled by the express

146 -mediated repression of protein synthesis in C. reinhardtii may involve alterations to the function/s

147 Functionality of the 5' UTRs was tested in C. reinhardtii chloroplasts using beta-glucuronidase rep

148 These data suggest that, in C. reinhardtii, (i) PHOT is involved in blue-light-media

149 Our results suggest that, in C. reinhardtii, miRNAs might be subject to relatively fa

150 hat mastigonemes enhance flagellar thrust in C. reinhardtii, and so, their function still remains eni

151 ardtii Here we analyzed state transitions in C. reinhardtii mutants of two phosphatases, PROTEIN PHOS

152 tioned for mRNA stability and translation in C. reinhardtii chloroplasts while the more divergent C.

153 used to regulate chloroplast translation in C. reinhardtii.

154 andidates for distributive iron transport in C. reinhardtii.

155 SUMO-conjugating enzyme (SCE) (E2, Ubc9) in C. reinhardtii was shown to be functional in an Escheric

156 unteracting phosphatase(s) remain unknown in C. reinhardtii Here we analyzed state transitions in C.

157 These tools are now being utilized in C. reinhardtii and in other algal species for the develo

158 9 kDa in extracts from anaerobically induced C. reinhardtii cells, strongly suggesting that HydA2 enc

159 arge-scale preparations and transformed into C. reinhardtii cells.

160 ed may vary in photosynthetic organisms like C. reinhardtii from anoxia to high light to limitations

161 phage library was demonstrated by using live C. reinhardtii cells to pan for VH H clones with specifi

162 ing its codon usage to reflect that of major C. reinhardtii chloroplast-encoded proteins.

163 utionary distance between algae and mammals, C. reinhardtii ATPase 6 functioned in human cells, becau

164 investigated in carotenoid-deficient mutant C. reinhardtii cells.

165 The native C. reinhardtii-PSII WOC cycles less efficiently at all l

166 environment (G x E) variation in 18 natural C. reinhardtii accessions in 30 environments.

167 hing 38% (5884) of the 15,501 nonoverlapping C. reinhardtii genes.

168 X proteins can participate in acclimation of C. reinhardtii cells to excess absorbed light energy.

169 ii Our results indicate that the activity of C. reinhardtii ATG4 is regulated by the formation of a s

170 eme inhibition was restored upon addition of C. reinhardtii soluble proteins.

171 Southern blot analysis of C. reinhardtii genomic DNA indicates that C. reinhardtii

172 lasticity of the photosynthetic apparatus of C. reinhardtii This alga is able to use various photoacc

173 w, using ODAs extracted from the axonemes of C. reinhardtii, that the C-terminal beta-propeller but n

174 tudying the biochemistry and cell biology of C. reinhardtii chloroplasts.

175 on-dense vacuoles or polyphosphate bodies of C. reinhardtii showed large amounts of phosphorus, magne

176 A possible role for Cah6 in the CCM of C. reinhardtii is proposed.

177 ; also named NAR1.2) and LCIB, in the CCM of C. reinhardtii.

178 nt results for deuterated wild-type cells of C. reinhardtii demonstrating that both radical pairs P70

179 ation of high light to dark-adapted cells of C. reinhardtii led to an increase in the amplitudes of 6

180 Therefore, in mixotrophically grown cells of C. reinhardtii, interpretations of the effects of enviro

181 ette and transformed into the chloroplast of C. reinhardtii and into E. coli.

182 ation in Escherichia coli by coexpression of C. reinhardtii HydEF and HydG and the HydA1 [FeFe] hydro

183 mentally measured steady-state Cd content of C. reinhardtii in the presence of low or high [Zn(2+)].

184 usly shown that when mixotrophic cultures of C. reinhardtii (which use both photosynthesis and mitoch

185 n the regulation of the sexual life cycle of C. reinhardtii, which is controlled by blue and red ligh

186 n important role in the sexual life cycle of C. reinhardtii: It controls the germination of the alga,

187 d on this we suggest that the development of C. reinhardtii as an industrial biotechnology platform c

188 n opportunity to expedite the development of C. reinhardtii as an industrial biotechnology platform,

189 e 251-residue extrinsic functional domain of C. reinhardtii cytochrome f was expressed in Escherichia

190 Further exploitation of C. reinhardtii as a model system to elucidate various mo

191 ent, indicated by 1) a consistent failure of C. reinhardtii vtc1 mutant strains, which are deficient

192 ed 309,278 raw EST sequencing trace files of C. reinhardtii and found that only 57% had cDNA termini

193 lustrate the marked metabolic flexibility of C. reinhardtii and contribute to the development of an i

194 The haploid genome of C. reinhardtii facilitates genetic analyses and offers m

195 CO2-concentrating mechanism or for growth of C. reinhardtii at limiting CO2 concentrations.

196 PSI-LHCI-LHCII of C. reinhardtii is the largest PSI supercomplex isolated

197 he current status of genetic manipulation of C. reinhardtii for metabolic engineering.

198 ple changes in the nutrition and motility of C. reinhardtii.

199 he wild type (WT) and the HS(A676) mutant of C. reinhardtii indicates that the mutation primarily exe

200 isolation of a plasmid disruption mutant of C. reinhardtii, designated Deltasqd1, which lacks ASQD a

201 S I particles from a site-directed mutant of C. reinhardtii, in which the axial histidine ligand (His

202 Eight independently isolated mutants of C. reinhardtii that require high CO(2) for photoautotrop

203 A set of nuclear mutants of C. reinhardtii were identified that specifically lack tr

204 e compared with two site-directed mutants of C. reinhardtii, in which the spin-polarized signal on ei

205 ropriate for the soil environmental niche of C. reinhardtii.

206 hemical properties of the homodimeric PFO of C. reinhardtii expressed in Escherichia coli.

207 gene that is critical for the protection of C. reinhardtii from photo-oxidative damage under high li

208 Several of the large subunit proteins of C. reinhardtii have short extension or insertion sequenc

209 s, and thus should represent a wide range of C. reinhardtii antigens.

210 lly validated genome-scale reconstruction of C. reinhardtii metabolism that should serve as a useful

211 e utility of the GFPct gene as a reporter of C. reinhardtii chloroplast gene expression.

212 oid membrane proteins and in the response of C. reinhardtii to light and macronutrient stress.

213 show how FtsH is involved in the response of C. reinhardtii to macronutrient stress.

214 es of the different acclimation responses of C. reinhardtii and B. braunii Knowledge of the specific

215 5, a protein that regulates the responses of C. reinhardtii to low-CO2 conditions.

216 Overall, the chloroplast ribosome of C. reinhardtii is similar to those of spinach chloroplas

217 nt a historical retrospective of the rise of C. reinhardtii to illuminate its past and present.

218 gA gene, we analyzed the genome sequences of C. reinhardtii and V. carteri to identify additional gen

219 ng microscopy how the motility statistics of C. reinhardtii are modulated by diurnal cycles.

220 . eugametos) and five independent strains of C. reinhardtii.

221 ned the high-resolution crystal structure of C. reinhardtii ODA16 (CrODA16) and mapped the binding to

222 tii and determined the crystal structures of C. reinhardtii IFT70/52 and Tetrahymena IFT52/46 subcomp

223 tools currently being applied to studies of C. reinhardtii.

224 Through the study of C. reinhardtii mutants deficient in flavodiiron proteins

225 ble thylakoid membrane appression to that of C. reinhardtii at its optimal growth condition, UWO241 g

226 le markers for the genetic transformation of C. reinhardtii.

227 e orientational and gravitactic transport of C. reinhardtii.

228 Moreover, we found that treatment of C. reinhardtii cells with norflurazon, an inhibitor of c

229 Treatment of C. reinhardtii cells with the ER stressors tunicamycin o

230 indicate that the electron-dense vacuoles of C. reinhardtii are very similar to acidocalcisomes with

231 The natural variation of C. reinhardtii accessions supports the hypothesis that,

232 with picosecond-fluorescence spectroscopy on C. reinhardtii cells that, although LHCs indeed detach f

233 s encoding the mouse homologues of the other C. reinhardtii C1d complex members are primarily express

234 component characteristic of photoautotrophic C. reinhardtii cultures grown at high light was not limi

235 gh TRP channels seem to be absent in plants, C. reinhardtii possesses genomic sequences encoding TRP

236 ansition from state 1 to state 2 can protect C. reinhardtii in high-light conditions and how this dif

237 We have characterized recombinant C. reinhardtii VTC2 as an active GDP-L-galactose phospho

238 with two cell types, one of which resembles C. reinhardtii cytologically but is terminally different

239 R sequences from four Chlamydomonas species (C. reinhardtii, C. incerta, C. moewusii and C. eugametos

240 The standard C. reinhardtii strains, plus C. smithii +, plus the new

241 RNA-Seq analysis of iron-starved C. reinhardtii cells revealed notable changes in many tr

242 We demonstrate that C. reinhardtii chloroplasts transformed with the GFPct c

243 We hypothesized that C. reinhardtii ATPase 6 is nucleus encoded and identifie

244 Physiological analyses indicate that C. reinhardtii possesses multiple Ci transport systems r

245 These results indicate that C. reinhardtii VTC2, like its plant homologs, is a highl

246 , systems-level investigation indicated that C. reinhardtii cells sense and respond on a large scale

247 of C. reinhardtii genomic DNA indicates that C. reinhardtii has only one gtr gene.

248 Phylogenetic analysis indicates that C. reinhardtii PPO and FeC are most closely related to p

249 Chlamydomonas reinhardtii, and we show that C. reinhardtii PGK1 (CrPGK1) activity is inhibited by th

250 Our results suggest that C. reinhardtii employs a clostridial type H(2) productio

251 Immunoblotting results suggest that C. reinhardtii PPO and FeC are targeted exclusively to t

252 The C. reinhardtii cofactor proteins alone were all unable t

253 The C. reinhardtii LD fraction contained minimal proteins wi

254 he possible interaction between CHT7 and the C. reinhardtii retinoblastoma tumor suppressor (RB) prot

255 of spinach chloroplast and E. coli, but the C. reinhardtii ribosome has proteins associated with the

256 We also examined the C. reinhardtii nuclear methylation map with base-level r

257 Moreover, the data generated for the C. reinhardtii double mutant clearly showed a complement

258 oplast was due to the codon bias seen in the C. reinhardtii chloroplast genome.

259 els of recombinant protein expression in the C. reinhardtii chloroplast was due to the codon bias see

260 In this report we study the changes in the C. reinhardtii cyclophilin transcript and protein levels

261 abidopsis thaliana which is conserved in the C. reinhardtii enzyme, indicated localization in the pla

262 In the C. reinhardtii genome, the HydEF gene is adjacent to ano

263 with two Rub1 genes and one Ufm1 gene in the C. reinhardtii genome.

264 last PSRP-7 and EF-Ts sequences found in the C. reinhardtii genome.

265 on by tunicamycin was more pronounced in the C. reinhardtii sor1 mutant, which shows increased expres

266 currently used to modify and interrogate the C. reinhardtii nuclear genome and explore several techno

267 The flanking sequence matched the C. reinhardtii Rca cDNA sequence previously deposited in

268 lowed brilliant and specific staining of the C. reinhardtii cell wall and analysis of cell-wall genes

269 which may reflect the ultrastructure of the C. reinhardtii cell.

270 Lipid profiling of the C. reinhardtii cells revealed that they degraded FAs but

271 small subunit protein to the pyrenoid of the C. reinhardtii chloroplast in cells maintained under amb

272 lthough paradoxically, the GC content of the C. reinhardtii genome is very high.

273 sduction effector for light induction of the C. reinhardtii gsa gene is a flavoprotein.

274 Moreover, co-expression of the C. reinhardtii HydEF, HydG, and HydA1 genes in Escherich

275 epigenetic programs during key stages of the C. reinhardtii life cycle.

276 P cassette (GFPct), under the control of the C. reinhardtii rbcL 5'- and 3'-UTRs.

277 Sequencing of the C. reinhardtii Rca gene revealed that it contains 10 exo

278 roteins were identified as components of the C. reinhardtii ribosome.

279 of the ALS promoter with the promoter of the C. reinhardtii Rubisco small subunit gene (RbcS2) permit

280 The GP1 protein, an HRGP of the C. reinhardtii wall, is shown to adopt a polyproline II

281 e betaC-plastoglobuli proteome resembles the C. reinhardtii eyespot and Arabidopsis (Arabidopsis thal

282 We conclude that the C. reinhardtii Flv participates in a Mehler-like reducti

283 , although developed for and tailored to the C. reinhardtii dataset, can be exploited by any eukaryot

284 NRT3.1 and AtNRT3.2, that are similar to the C. reinhardtii NAR2 gene.

285 Treating the C. reinhardtii wild type with mercuric ions, which were

286 essful complementation was achieved with the C. reinhardtii TLA2-CpFTSY gene, whose occurrence and fu

287 H H clones (designated B11 and H10) bound to C. reinhardtii with EC50 values </= 0.5 nm.

288 solated from the library show specificity to C. reinhardtii and lack of reactivity to antigens from f

289 e role against copper uptake and toxicity to C. reinhardtii.

290 ion of the chimeric gene using either of two C. reinhardtii chloroplast promoters and 5' and 3' RNA e

291 robically induced concomitantly with the two C. reinhardtii [Fe] hydrogenase genes, HydA1 and HydA2.

292 cation is present in the genome of wild-type C. reinhardtii but at a substantially lower level in a C

293 ses that accompany anaerobiosis in wild-type C. reinhardtii cells and a null mutant strain for the HY

294 Transformation of wild-type C. reinhardtii with the mutant ALS gene produced no tran

295 When C. reinhardtii was grown photomixotrophically at moderat

296 When C. reinhardtii was transferred from the dark to very low

297 tion of cilia, and other processes for which C. reinhardtii is a leading model system.

298 While C. reinhardtii is unicellular, V. carteri is multicellul

299 In contrast with C. reinhardtii, but similar to other biofilm-forming alg

300 -light (HL) photoacclimation strategies with C. reinhardtii and other frequently studied green algae: