ライフサイエンスコーパス: cyanobacterium

1 >1 billion y ago via the endosymbiosis of a cyanobacterium.

2 C 7120 as a model of a siderophore-secreting cyanobacterium.

3 p. PCC 7120 is a nitrogen-fixing filamentous cyanobacterium.

4 f the autotrophic CO2 fixation to one unique cyanobacterium.

5 r measurement of intracellular pH in a model cyanobacterium.

6 onnection between the host cell and captured cyanobacterium.

7 coccus elongatus PCC7942, a model freshwater cyanobacterium.

8 required for plastoquinone synthesis in the cyanobacterium.

9 enigmatic binding site of PsbQ in PSII in a cyanobacterium.

10 t not a critical role in the function of the cyanobacterium.

11 osperin, from a lichen-associated Nostoc sp. cyanobacterium.

12 protein in the outer membrane of an ancient cyanobacterium.

13 s in an ecologically important bloom-forming cyanobacterium.

14 an organelle derived from endosymbiosis of a cyanobacterium.

15 porous material and a frozen-hydrated marine cyanobacterium.

16 ase polymeric organic matter produced by the cyanobacterium.

17 PCC 7120 is a nitrogen-fixing filamentous cyanobacterium.

18 lic lipopeptide, yuvalamide A, from a marine cyanobacterium.

19 yochloris marina, a chlorophyll d-containing cyanobacterium.

20 tively present as chlorophyll (Chl) d in the cyanobacterium Acaryochloris marina, or dynamically expr

21 ae), three Bacillariophyta (diatoms) and one cyanobacterium, all of which consistently formed Mn(III/

22 that heterologous expression of OsPIP1;3 in cyanobacterium altered bacterial growth under different

23 The filamentous cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120 pro

24 ression during heterocyst development in the cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120.

25 (ABDH), a known beta-diketone hydrolase from Cyanobacterium anabaena (PDB ID 2j5s).

26 rate calmodulin and oxidized flavodoxin from Cyanobacterium anabaena .

27 The filamentous cyanobacterium Anabaena fixes nitrogen in specialized ce

28 mechanisms of the sensory rhodopsin from the cyanobacterium Anabaena PCC 7120 (ASR) and of the bovine

29 The filamentous nitrogen-fixing cyanobacterium Anabaena sp. PCC 7120 differentiates spec

30 HgdD of the filamentous, heterocyst-forming cyanobacterium Anabaena sp. PCC 7120 is part of multiple

31 e N-terminal POTRA domains of Omp85 from the cyanobacterium Anabaena sp. PCC 7120 using pulsed electr

32 logue of the filamentous, heterocyst-forming cyanobacterium Anabaena sp. PCC 7120, termed heterocyst

33 The filamentous, heterocyst-forming cyanobacterium Anabaena sp. strain PCC 7120 contains, be

34 ronmental combined nitrogen, the filamentous cyanobacterium Anabaena sp. strain PCC 7120 differentiat

35 cells called heterocysts by the filamentous cyanobacterium Anabaena sp. strain PCC 7120 is dependent

36 rogen-limiting conditions, the multicellular cyanobacterium Anabaena sp. strain PCC 7120 terminally c

37 ed in a periodic pattern on filaments of the cyanobacterium Anabaena sp. strain PCC 7120 under condit

38 In the filamentous cyanobacterium Anabaena sp. strain PCC 7120, heterocysts

39 dipeptidase in the model heterocyst-forming cyanobacterium Anabaena sp. strain PCC 7120.

40 We have characterized Prx6 from the cyanobacterium Anabaena sp. strain PCC7120 (AnPrx6) and

41 The cyanobacterium Anabaena variabilis has two Mo-nitrogenas

42 DABA AT ORF in a siderophore pathway in the cyanobacterium Anabaena variabilis, which was shown to b

43 In the cyanobacterium Anabaena, pretreatment of cells with NaCl

44 to monitor the photosynthetic activity of a cyanobacterium (Anabaena flos-aquae) contained within an

45 The nitrogen-fixing cyanobacterium, Anabaena PCC7120 encodes for a membrane-

46 The closely related cyanobacterium, Anabaena sp. PCC 7120 has the nif1 syste

47 This unusual partnership between a cyanobacterium and a unicellular alga is a model for sym

48 onal physiology of this toxic, bloom-forming cyanobacterium and the role of N in controlling microcys

49 trophic mode-dependent protein expression in cyanobacterium, and reveal the functional significance o

50 rk highlights the utility of a multicellular cyanobacterium as a model for the study of developmental

51 The symbiotic unicellular cyanobacterium Candidatus Atelocyanobacterium thalassa (

52 stigate how the acquisition of the symbiotic cyanobacterium Candidatus Synechococcus feldmannii pertu

53 cin A, a metabolite isolated from the marine cyanobacterium cf. Oscillatoria sp. that exhibits select

54 matic amino acid pathways in the filamentous cyanobacterium Chlorogloeopsis fritschii PCC 6912.

55 a tetrameric form of PSI in the thermophilic cyanobacterium Chroococcidiopsis sp TS-821 (TS-821).

56 This cyanobacterium coexists with many cyanophages in the oce

57 ochlorococcus, a numerically dominant marine cyanobacterium, continuously release lipid vesicles cont

58 in situ metabolism of the keystone N2-fixing cyanobacterium Crocosphaera, as well as the broader ecos

59 The unicellular cyanobacterium Cyanothece sp. American Type Culture Coll

60 -CVNH, a recently identified lectin from the cyanobacterium Cyanothece(7424), and elucidated its glyc

61 ng a genome-scale model for the diazotrophic cyanobacterium, Cyanothece sp. ATCC 51142.

62 A library of analogues of the cyanobacterium-derived depsipeptide natural product gall

63 usive to photosynthetic eukaryotes, encode a cyanobacterium-derived domain fused to one of cyanobacte

64 udy of plastid evolution because it contains cyanobacterium-derived photosynthetic organelles termed

65 ioses between two eukaryotes are also known; cyanobacterium-derived plastids have spread horizontally

66 The cyanobacterium dominating the submerged mat type does no

67 y, we describe the fam gene cluster from the cyanobacterium Fischerella ambigua UTEX 1903 encoding ha

68 ed nitrogen-fixing cell of the multicellular cyanobacterium Fischerella thermalis, has evolved multip

69 nechocystis sp. PCC 6803, an important model cyanobacterium for sustainable biofuel production.

70 In the filamentous cyanobacterium Fremyella diplosiphon UTEX 481, two syste

71 gene infCa was not lethal in the filamentous cyanobacterium Fremyella diplosiphon, and its genome was

72 a putative lyase-encoding gene, cpeF, in the cyanobacterium Fremyella diplosiphon.

73 xygen concentration within the plesiomorphic cyanobacterium Gloeobactor violaceus is only 0.025 muM,

74 Here, the cyanobacterium Gloeomargarita lithophora, capable of for

75 ant symbioses, the symbiotic nitrogen-fixing cyanobacterium has low photosynthetic activity and is su

76 ocystis sp., a common unicellular freshwater cyanobacterium, has been used as a model organism to stu

77 ns (A and B) were reported from an epilithic cyanobacterium Hassallia sp. and found to be active agai

78 ed Microcystis aeruginosa as the predominant cyanobacterium in the sample.

79 dispensable for biofilm development in this cyanobacterium, in contrast to their biofilm-promoting f

80 which is endosymbiotically associated with a cyanobacterium, in order to investigate the role of N-fi

81 During the endosymbiotic transformation of a cyanobacterium into the eukaryotic plastid, most cyanoba

82 No known cyanobacterium is equipped with flagella, but a diverse

83 sbA4, one of the five psbA orthologs in this cyanobacterium, is exclusively expressed during nighttim

84 ural geological environment, we cultivated a cyanobacterium isolate on gypsum rock samples under cont

85 plied to the extract of a filamentous marine cyanobacterium known to be a prolific producer of cytoto

86 sis revealed that bacteria were dominated by cyanobacterium Leptolyngbia ( approximately 35%), while

87 ransformants of a chlB-lacking mutant of the cyanobacterium Leptolyngbya boryana that was complemente

88 JSC1_58120g3, a frCBCR from the thermophilic cyanobacterium Leptolyngbya sp. JSC-1 that is a represen

89 The cyanobacterium, Leptolyngbya sp. strain JSC-1, exhibits

90 s striatus, a specialist grazer of the toxic cyanobacterium Lyngbya majuscula.

91 e of eukaryotic origin and that the captured cyanobacterium made a relatively minor (albeit important

92 The filamentous Section V cyanobacterium Mastigocladus laminosus is one of the mos

93 table isotopes and NanoSIMS to show that the cyanobacterium Mastigocoleus testarum derives most of it

94 and regional climate predictions, the latter cyanobacterium may replace the former in much of the stu

95 ns L-R (2-8) have been isolated from a mixed cyanobacterium-microbial culture.

96 e proteins of green and red algae and in the cyanobacterium Microcoleus sp PCC 7113 with unknown func

97 The filamentous cyanobacterium Microcoleus vaginatusis found in arid lan

98 ed strains support this contention, with one cyanobacterium (Microcoleus vaginatus) being more psychr

99 ess the transcriptomic response of the toxic cyanobacterium Microcystis aeruginosa during growth with

100 he exudate secreted by a toxic strain of the cyanobacterium Microcystis aeruginosa with Fe(II) and Fe

101 gy and risk assessment, exposed to the toxic cyanobacterium Microcystis aeruginosa.

102 c microbial assemblies and the bloom forming cyanobacterium Microcystis aeruginosa.

103 Harmful blooms of the cyanobacterium Microcystis sp. have become increasingly

104 We studied the cyanobacterium Microcystis, a notorious genus that can d

105 numerous fossil casts formed by the planktic cyanobacterium, Microcystis, a coccoid genus that at the

106 es, and their brominated analogues, from the cyanobacterium Moorea producens ASI16Jul14-2.

107 lete genome of a filamentous tropical marine cyanobacterium, Moorea producens PAL, which reveals that

108 s part of their study on osmoadaptation in a cyanobacterium, Nanatani et al. describe employing an in

109 nsisted of the cold-adapted photoautotrophic cyanobacterium Nodularia sp. and potential cold adapted

110 bined nitrogen starvation, the multicellular cyanobacterium Nostoc PCC 7120 develops nitrogen-fixing

111 ze novel dual-cysteine photosensors from the cyanobacterium Nostoc punctiforme ATCC 29133, we establi

112 or mycosporine sunscreen biosynthesis by the cyanobacterium Nostoc punctiforme ATCC 29133.

113 The filamentous cyanobacterium Nostoc punctiforme differentiates from ve

114 oxides, we detected a novel candidate in the cyanobacterium Nostoc punctiforme PCC 73102.

115 cally competent, facultatively heterotrophic cyanobacterium Nostoc punctiforme were constructed beari

116 , Npun_F4153 (SigG)/Npun_F4154 (SapG) of the cyanobacterium Nostoc punctiforme were hypothesized to e

117 In the model filamentous cyanobacterium Nostoc punctiforme, the T4P systems are a

118 ully survey the red/green subfamily from the cyanobacterium Nostoc punctiforme.

119 by the genome of the N2-fixing, filamentous cyanobacterium Nostoc sp. PCC7120 in the nblA1/nblA2 mut

120 resolution structure of the complex from the cyanobacterium Nostoc sp. revealed the presence of 23 li

121 thalene (a model substrate) into CO2 and the cyanobacterium PCC 7942 was used to provide the necessar

122 viral-encoded nblA is derived from the host cyanobacterium, Phormidium MIS-PhA.

123 a symbiotic relationship with an alga and/or cyanobacterium (photobiont), the non-photoautotrophic ba

124 e and significance in biogeochemical cycles, cyanobacterium-phytoplankton symbioses remain understudi

125 tom Asterionella formosa and the filamentous cyanobacterium Planktothrix agardhii.

126 cal flocculants for treating wastewaters and cyanobacterium-polluted freshwater.

127 tress in high-light ecotypes of the abundant cyanobacterium Prochlorococcus across a meridional trans

128 rements of natural populations of the marine cyanobacterium Prochlorococcus indicate this numerically

129 ell abundance of the dominant photosynthetic cyanobacterium Prochlorococcus is assumed to reflect a s

130 acterization of carboxysomes from the marine cyanobacterium Prochlorococcus marinus MED4.

131 irus P-SSM2 Fd (pssm2-Fd), which infects the cyanobacterium Prochlorococcus marinus, revealed high le

132 components L(2) and (NB)(2) from the marine cyanobacterium Prochlorococcus marinus.

133 reen alga Chlamydomonas reinhardtii, and the cyanobacterium Prochlorococcus marinus.

134 Studies of the cyanobacterium Prochlorococcus MED4 and its associated c

135 ter of ~1 mum, and the marine photosynthetic cyanobacterium Prochlorococcus, with a diameter of ~600

136 populations of the globally abundant marine cyanobacterium Prochlorococcus.

137 dant phytoplankter in the oceans, the marine cyanobacterium Prochlorococcus.

138 transcriptomic and field data for the marine cyanobacterium Prochlorococcus.

139 nship between tunicates and the uncultivated cyanobacterium Prochloron didemni has long provided a mo

140 echococcus OS-B', a thermophilic unicellular cyanobacterium, recently isolated from the microbial mat

141 ipal pacemaker of the circadian clock of the cyanobacterium S. elongatus is a protein phosphorylation

142 cellular clocks, we studied the unicellular cyanobacterium S. elongatus.

143 l, fast-growing, and naturally transformable cyanobacterium, S. elongatus PCC 11802, that shares 97%

144 Escherichia coli demonstrated that no other cyanobacterium-specific components are required for prop

145 on between the ecologically important marine cyanobacterium Synechococcus and a lytic virus.

146 Here we show that in the cyanobacterium Synechococcus elongate, non-optimal codon

147 r Rubisco large subunits (LSU) from the beta-cyanobacterium Synechococcus elongatus (Se) to form aggr

148 We argue that the cyanobacterium Synechococcus elongatus has evolved two f

149 The cyanobacterium Synechococcus elongatus is a model organi

150 The circadian input kinase of the cyanobacterium Synechococcus elongatus PCC 7942 (CikA) i

151 stigated the in vivo function of RbcX in the cyanobacterium Synechococcus elongatus PCC 7942 (Syn7942

152 The cyanobacterium Synechococcus elongatus PCC 7942 exhibits

153 ere, it was shown that the Min system in the cyanobacterium Synechococcus elongatus PCC 7942 oscillat

154 We have identified a putative OGT in the cyanobacterium Synechococcus elongatus PCC 7942 that sho

155 fluorescence microscopy in live cells of the cyanobacterium Synechococcus elongatus PCC 7942 to inves

156 In the model cyanobacterium Synechococcus elongatus PCC 7942, a funct

157 In the cyanobacterium Synechococcus elongatus PCC 7942, the gen

158 dian rhythms of gene expression in the model cyanobacterium Synechococcus elongatus PCC 7942.

159 rs, and it is present as two isoforms in the cyanobacterium Synechococcus elongatus PCC 7942.

160 genome-scale metabolic reconstruction of the cyanobacterium Synechococcus elongatus PCC 7942.

161 bacco lines with functional Rubisco from the cyanobacterium Synechococcus elongatus PCC7942 (Se7942).

162 ity of single beta-carboxysomes in the model cyanobacterium Synechococcus elongatus PCC7942.

163 The cyanobacterium Synechococcus elongatus possesses a circa

164 The cyanobacterium Synechococcus elongatus relies upon photo

165 um acetobutylicum in the non-nitrogen-fixing cyanobacterium Synechococcus elongatus sp. 7942.

166 ck, we constructed a chimeric protein in the cyanobacterium Synechococcus elongatus that structurally

167 photosynthetic machinery of the fast-growing cyanobacterium Synechococcus elongatus UTEX 2973 to prod

168 , we visualize individual chromosomes in the cyanobacterium Synechococcus elongatus via time-lapse fl

169 in beta-type carboxysomes of the freshwater cyanobacterium Synechococcus elongatus, CcmM, occurs in

170 on and responses to fluctuating light in the cyanobacterium Synechococcus elongatus.

171 The marine cyanobacterium Synechococcus is the second most abundant

172 In the presence of the cyanobacterium Synechococcus PCC 7002, aqueous Fe(II) (F

173 carbon pathway compatibility using the model cyanobacterium Synechococcus sp. PCC 7002 (S7002) by co-

174 bal transcript abundance data from the model cyanobacterium Synechococcus sp. PCC 7002 grown under 42

175 s of the fast-growing physiologically robust cyanobacterium Synechococcus sp. PCC 7002 to changing en

176 The cyanobacterium Synechococcus sp. PCC 7002 uses a hemoglo

177 ldehyde dehydrogenase were identified in the cyanobacterium Synechococcus sp. PCC 7002.

178 For example, a NOS protein in the marine cyanobacterium Synechococcus sp. PCC 7335 (syNOS) has re

179 Diverse strains of the marine planktonic cyanobacterium Synechococcus sp. show consistent differe

180 Here, we show that the abundant marine cyanobacterium Synechococcus synthesizes only pseudocoba

181 Among the pico-fraction, it is the cyanobacterium Synechococcus that flourishes when iron a

182 g-term chemostat experiment where the marine cyanobacterium Synechococcus was challenged with a lytic

183 beling proteomics approach in a model marine cyanobacterium Synechococcus WH8102 infected by a lytic

184 e SAR11 clade of Alphaproteobacteria and the cyanobacterium Synechococcus.

185 riven by the dominance of the photosynthetic cyanobacterium Synechococcus.

186 The model cyanobacterium, Synechococcus elongatus PCC 7942, is a g

187 omplexes in thylakoid membranes from a model cyanobacterium, Synechococcus elongatus PCC 7942, using

188 lization of beta-carboxysomes within a model cyanobacterium, Synechococcus elongatus PCC7942, in resp

189 3-hydroxypropionate bi-cycle into the model cyanobacterium, Synechococcus elongatus sp. PCC 7942.

190 Here we show that an abundant marine cyanobacterium, Synechococcus elongatus, contributes a v

191 , S-TIM5, that infects the ubiquitous marine cyanobacterium, Synechococcus.

192 sphate, in an engineered strain of the model cyanobacterium Synechocystis (DeltaglgC/xylAB), in which

193 We provide data that the cyanobacterium Synechocystis (Synechocystis sp. PCC 6803

194 SII assembly intermediate complexes from the cyanobacterium Synechocystis 6803 with chemical cross-li

195 Two of these, Sll1214 and Sll1874 from the cyanobacterium Synechocystis 6803, were FLAG-tagged in v

196 Active KDPG aldolases from the cyanobacterium Synechocystis and the plant barley (Horde

197 The truncated Hb from the freshwater cyanobacterium Synechocystis exhibits hexacoordinate hem

198 lorophyll synthase (ChlG), was tagged in the cyanobacterium Synechocystis PCC 6803 (Synechocystis) an

199 stability of PSII subunits in strains of the cyanobacterium Synechocystis PCC 6803 blocked at specifi

200 ression of the isoprene synthase gene in the cyanobacterium Synechocystis PCC 6803 conferred upon the

201 beta-carotene binding protein complex in the cyanobacterium Synechocystis PCC 6803 important for form

202 partially inhibited activity of FeCh in the cyanobacterium Synechocystis PCC 6803 leads to overprodu

203 a complex and photosystems I and II from the cyanobacterium Synechocystis PCC 6803.

204 NDH-C assembly in the cyanobacterium Synechocystis sp PCC 6803 and the moss Ph

205 d that the four FtsH homologs encoded by the cyanobacterium Synechocystis sp PCC 6803 are functionall

206 The genome of the model cyanobacterium Synechocystis sp PCC 6803 encodes four Ft

207 Here, we show that RubA in the cyanobacterium Synechocystis sp PCC 6803 is required for

208 In the cyanobacterium Synechocystis sp PCC 6803, early steps in

209 The endogenous CURT1 protein in the cyanobacterium Synechocystis sp PCC6803 can be partially

210 embly factors, Psb28-1 and Psb28-2, from the cyanobacterium Synechocystis sp.

211 In the cyanobacterium Synechocystis sp. PCC 6803 (hereafter Syn

212 cleic acids and polysaccharides-in the model cyanobacterium Synechocystis sp. PCC 6803 (S.6803) under

213 stigated the redox-insensitive APSK from the cyanobacterium Synechocystis sp. PCC 6803 (SynAPSK).

214 We substituted the D1-Asn(87) residue in the cyanobacterium Synechocystis sp. PCC 6803 (wildtype) wit

215 he CyanoGate system in the established model cyanobacterium Synechocystis sp. PCC 6803 and the more r

216 Knockouts of the rubredoxin orthologs in the cyanobacterium Synechocystis sp. PCC 6803 and the plant

217 loss-of-function mutants of the unicellular cyanobacterium Synechocystis sp. PCC 6803 as a model sys

218 system encoded on plasmid pSYSA of the model cyanobacterium Synechocystis sp. PCC 6803 as involving a

219 lastic neutron scattering experiments on the cyanobacterium Synechocystis sp. PCC 6803 assessed the f

220 In this study, we engineered the model cyanobacterium Synechocystis sp. PCC 6803 for sustainabl

221 The cyanobacterium Synechocystis sp. PCC 6803 harvests light

222 Recent work on the model unicellular cyanobacterium Synechocystis sp. PCC 6803 has shown that

223 found to be important for the growth of the cyanobacterium Synechocystis sp. PCC 6803 in high-salt (

224 P-protein from the cyanobacterium Synechocystis sp. PCC 6803 is an alpha2 h

225 se core in the DeltarpoZ strain of the model cyanobacterium Synechocystis sp. PCC 6803 leads to a uni

226 The unicellular cyanobacterium Synechocystis sp. PCC 6803 moves with Typ

227 The photosynthetic machinery of the cyanobacterium Synechocystis sp. PCC 6803 resides in fla

228 We grew a dense culture of the model cyanobacterium Synechocystis sp. PCC 6803 under a sinuso

229 saturated, and light-inhibited growth of the cyanobacterium Synechocystis sp. PCC 6803 using a reprod

230 rotein to probe microalgal metabolism (i.e., cyanobacterium Synechocystis sp. PCC 6803) in a mixed cu

231 nel, SynCaK, in the genome of the freshwater cyanobacterium Synechocystis sp. PCC 6803, a model photo

232 A potassium channel (SynK) of the cyanobacterium Synechocystis sp. PCC 6803, a photohetero

233 convert 2-oxoglutarate into succinate in the cyanobacterium Synechocystis sp. PCC 6803, a series of m

234 In the unicellular photosynthetic cyanobacterium Synechocystis sp. PCC 6803, individual ce

235 In the cyanobacterium Synechocystis sp. PCC 6803, the slr1796 g

236 stages of nitrogen starvation for the model cyanobacterium Synechocystis sp. PCC 6803, we performed

237 tant strain of the model non-nitrogen-fixing cyanobacterium Synechocystis sp. PCC 6803, which lacks a

238 embly factors, Psb28-1 and Psb28-2, from the cyanobacterium Synechocystis sp. PCC 6803.

239 system II under low carbon conditions in the cyanobacterium Synechocystis sp. PCC 6803.

240 es of site-directed PSII RC mutants from the cyanobacterium Synechocystis sp. PCC 6803.

241 an extensive study of Hox hydrogenase in the cyanobacterium Synechocystis sp. PCC 6803.

242 ole in photosystem (PS) II biogenesis in the cyanobacterium Synechocystis sp. PCC 6803.

243 ional [NiFe]-hydrogenase (HoxEFUYH) from the cyanobacterium Synechocystis sp. PCC 6803.

244 SI-IsiA complex isolated from the mesophilic cyanobacterium Synechocystis sp. PCC 6803.

245 We show here that the cyanobacterium Synechocystis sp. PCC6803 accumulates bot

246 Data indicate that strains of the cyanobacterium Synechocystis sp. PCC6803 engineered for

247 We generated transformants of the cyanobacterium Synechocystis sp. PCC6803 expressing GFP-

248 e-light-using FAD) photoreceptor used by the cyanobacterium Synechocystis sp. PCC6803 to control phot

249 s in genetically engineered membranes of the cyanobacterium Synechocystis sp. PCC6803 to elucidate th

250 The unicellular, photosynthetic cyanobacterium Synechocystis sp. PCC6803 transduces a li

251 sive generations of genetic modifications of cyanobacterium Synechocystis sp. PCC6803 wild type (SD10

252 s the surface layer (S-layer) protein of the cyanobacterium Synechocystis sp. strain PCC 6803.

253 the chromosome and the pSYSX plasmid in the cyanobacterium Synechocystis sp. strain PCC 6803.

254 lipoamide dehydrogenase) from plants and the cyanobacterium Synechocystis species strain PCC6803 and

255 he cognate thioesterase characterized in the cyanobacterium Synechocystis.

256 Experiments with a model photoautotroph cyanobacterium, Synechocystis sp. PCC 6803, in batch exp

257 dimeric PSII complex isolated from the model cyanobacterium, Synechocystis sp. PCC 6803, to determine

258 Cyanobacteria lack Lon (including the model cyanobacterium, Synechocystis sp. PCC6803), so maintenan

259 Nostoc punctiforme is a versatile cyanobacterium that can live either independently or in

260 rain PCC 7822 is a unicellular, diazotrophic cyanobacterium that can produce large quantities of H2 w

261 Nostoc punctiforme is a cyanobacterium that differentiates specialized gliding f

262 stoc punctiforme ATCC 29133 is a filamentous cyanobacterium that expresses the uptake hydrogenase Hup

263 is an invasive, filamentous, nitrogen-fixing cyanobacterium that forms frequent blooms in freshwater

264 Prochlorococcus is an abundant marine cyanobacterium that grows rapidly in the environment and

265 us PCC 7942 is a genetically tractable model cyanobacterium that has been engineered to produce indus

266 entered into a symbiotic relationship with a cyanobacterium (the cyanobiont).

267 f three cornerstone partners--the plastid (a cyanobacterium), the mitochondrion (a proteobacterium),

268 ith natural photosynthesis of a fast-growing cyanobacterium, the artificial photosynthetic system has

269 though it was long considered an autotrophic cyanobacterium, the uptake of organic compounds has been

270 dimeric b(6)f complex from the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1 enable

271 e 0.42-MDa NDH complex from the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1, obtai

272 nds using the plant-like Te-Rubisco from the cyanobacterium Thermosynechococcus elongatus BP1 identif

273 atase H subunit, ChlH, from the thermophilic cyanobacterium Thermosynechococcus elongatus.

274 the orientation of PSII from a thermophilic cyanobacterium, Thermosynechococcus elongatus , on a nan

275 ep in the transformation of an endosymbiotic cyanobacterium to a plastid some 1.5 billion years ago w

276 id microevolutionary adaptation of a harmful cyanobacterium to changes in inorganic carbon (Ci) avail

277 c gene transfer (EGT) from the intracellular cyanobacterium to the nucleus is widely recognized as a

278 nt phyA of oat and recombinant CphA from the cyanobacterium Tolypothrix PCC7601) have been investigat

279 tive system in the chromatically acclimating cyanobacterium Tolypothrix sp. PCC 7601, which encodes b

280 this gap, we cultured the globally important cyanobacterium Trichodesmium at both low and high CO2 fo

281 hat growth and N2-fixation of the ubiquitous cyanobacterium Trichodesmium decreased under acidified c

282 g these factors, we grew the nitrogen-fixing cyanobacterium Trichodesmium for 1 year under Fe/P co-li

283 stributed, biogeochemically important marine cyanobacterium Trichodesmium increase under high carbon

284 s of the biogeochemically significant marine cyanobacterium Trichodesmium showing increased growth an

285 The oceanic N2-fixing cyanobacterium Trichodesmium spp. form extensive surface

286 y in the bloom-forming, N(2) -fixing, marine cyanobacterium Trichodesmium, which undergoes PCD under

287 transcription in the marine nitrogen-fixing cyanobacterium Trichodesmium.

288 The diazotrophic cyanobacterium, Trichodesmium, is an integral component

289 The unicellular cyanobacterium UCYN-A, one of the major contributors to

290 One of these partnerships involves the cyanobacterium UCYN-A, which has been found in partnersh

291 ymbiosis between an uncultivated unicellular cyanobacterium (UCYN-A) and a haptophyte picoplankton al

292 ibuted planktonic uncultured nitrogen-fixing cyanobacterium (UCYN-A) was found to have unprecedented

293 read and significant nitrogen (N(2) )-fixing cyanobacterium, UCYN-A and its prymnesiophyte host was p

294 We used a cyanobacterium unable to take up glucose to engineer str

295 about 1.6 billion years ago (BYA) in which a cyanobacterium was engulfed and retained by a eukaryotic

296 be traced back to a single event, in which a cyanobacterium was incorporated into a protistan host.

297 smium erythraeum, a filamentous diazotrophic cyanobacterium which has cells with two distinct metabol

298 tsonii is a unicellular nitrogen (N2)-fixing cyanobacterium with ecological importance in oligotrophi

299 sp. ATCC 51142, a unicellular, diazotrophic cyanobacterium with the capacity to generate high levels

300 nsis) is a filamentous blue-green microalga (cyanobacterium) with potent dietary phytoantioxidant and