ライフサイエンスコーパス: cyanobacterium

1 coccus elongatus PCC7942, a model freshwater cyanobacterium.

2 required for plastoquinone synthesis in the cyanobacterium.

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

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

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

6 protein in the outer membrane of an ancient cyanobacterium.

7 porous material and a frozen-hydrated marine cyanobacterium.

8 ase polymeric organic matter produced by the cyanobacterium.

9 that has not previously been described in a cyanobacterium.

10 tion as either a redox or a NO sensor in the cyanobacterium.

11 s in several species of plants, algae, and a cyanobacterium.

12 erotrophic protist enslaved a photosynthetic cyanobacterium.

13 PCB to Cys-82 of the PC beta subunit in this cyanobacterium.

14 PCC 7120 is a nitrogen-fixing filamentous cyanobacterium.

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

16 yochloris marina, a chlorophyll d-containing cyanobacterium.

17 >1 billion y ago via the endosymbiosis of a cyanobacterium.

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

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

20 f the autotrophic CO2 fixation to one unique cyanobacterium.

21 r measurement of intracellular pH in a model cyanobacterium.

22 onnection between the host cell and captured cyanobacterium.

23 However, this cyanobacterium also produces a monocyclic myxoxanthophyl

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

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

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

27 rate calmodulin and oxidized flavodoxin from Cyanobacterium anabaena .

28 The filamentous cyanobacterium Anabaena fixes nitrogen in specialized ce

29 ra of intact collapsed gas vesicles from the cyanobacterium Anabaena flos-aquae show duplication of c

30 Intact, collapsed gas vesicles from the cyanobacterium Anabaena flos-aquae were studied by solid

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

32 cells that fix nitrogen in filaments of the cyanobacterium Anabaena PCC 7120.

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

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

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

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

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

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

39 The filamentous cyanobacterium Anabaena sp. strain PCC 7120 forms a peri

40 The filamentous cyanobacterium Anabaena sp. strain PCC 7120 forms nitrog

41 The genome of the heterocyst-forming cyanobacterium Anabaena sp. strain PCC 7120 harbors 14 g

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

43 gen-fixing cells, called heterocysts, by the cyanobacterium Anabaena sp. strain PCC 7120 requires Het

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

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

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

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

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

49 The cyanobacterium Anabaena variabilis has two Mo-nitrogenas

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

51 In the cyanobacterium Anabaena, pretreatment of cells with NaCl

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

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

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

55 tion of a MAA biosynthetic gene cluster in a cyanobacterium and the discovery of analogous pathways i

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

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

58 New work shows that the cyanobacterium Aphanizomenon ovalisporum obtains inorgan

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

60 y rcaC and L Boxes in the genome of a marine cyanobacterium capable of CCA, suggesting widespread use

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

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

63 This cyanobacterium coexists with many cyanophages in the oce

64 hich was isolated from a marine Leptolyngbya cyanobacterium collected from the Coiba National Park, P

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

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

67 The unicellular cyanobacterium Cyanothece sp. American Type Culture Coll

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

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

70 of the thylakoid membranes in a unicellular cyanobacterium, Cyanothece sp. ATCC 51142.

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

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

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

74 The cyanobacterium dominating the submerged mat type does no

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

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

77 The freshwater cyanobacterium Fremyella diplosiphon (also known as Toly

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

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

80 ses to changes in ambient light color in the cyanobacterium Fremyella diplosiphon.

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

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

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

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

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

86 of Prochlorococcus, the numerically dominant cyanobacterium in the world's oligotrophic oceans.

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

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

89 The UCYN-A cyanobacterium is a paradox in evolution and adaptation

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

91 ranscriptional activity in a nitrogen-fixing cyanobacterium is necessary to understand the impact of

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

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

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

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

96 ve been isolated from extracts of the marine cyanobacterium Lyngbya confervoides.

97 act of a Panamanian collection of the marine cyanobacterium Lyngbya majuscula showed strong in vitro

98 nticancer properties generated by the marine cyanobacterium Lyngbya majuscula.

99 ancer lead compound isolated from the marine cyanobacterium Lyngbya majuscula.

100 or, were isolated from the Madagascar marine cyanobacterium Lyngbya majuscula.

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

102 chanism of how Synechocystis sp. PCC 6803, a cyanobacterium, maintains redox homeostasis and coordina

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

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

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

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

107 The filamentous cyanobacterium Microcoleus vaginatusis found in arid lan

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

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

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

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

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

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

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

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

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

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

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

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

120 sociated with scytonemin biosynthesis in the cyanobacterium Nostoc punctiforme ATCC 29133; we now rep

121 The filamentous cyanobacterium Nostoc punctiforme differentiates from ve

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

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

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

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

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

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

128 BxmR from the cyanobacterium Osciliatoria brevis is the first characte

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

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

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

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

133 r from those of Trichodesmium, the N2-fixing cyanobacterium previously considered to be the most impo

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

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

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

137 The marine cyanobacterium Prochlorococcus is the most abundant phot

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

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

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

141 Studies of the cyanobacterium Prochlorococcus MED4 and its associated c

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

143 rain of the single-celled, planktonic marine cyanobacterium Prochlorococcus-which conducts a sizable

144 populations of the globally abundant marine cyanobacterium Prochlorococcus.

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

146 transcriptomic and field data for the marine cyanobacterium Prochlorococcus.

147 mary production contributions similar to the cyanobacterium Prochlorococcus.

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

149 h precision to both membrane systems in this cyanobacterium, raising the question of how, and when, i

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

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

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

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

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

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

156 circadian phases of individual cells of the cyanobacterium Synechococcus elongatus and fit the data

157 The circadian rhythms exhibited in the cyanobacterium Synechococcus elongatus are generated by

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

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

160 The cyanobacterium Synechococcus elongatus PCC 7942 exhibits

161 The cyanobacterium Synechococcus elongatus PCC 7942 exhibits

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

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

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

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

166 In the cyanobacterium Synechococcus elongatus PCC 7942, the gen

167 an oscillator of the unicellular fresh water cyanobacterium Synechococcus elongatus PCC 7942, the mod

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

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

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

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

172 The cyanobacterium Synechococcus elongatus relies upon photo

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

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

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

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

177 In the cyanobacterium Synechococcus elongatus, the circadian cl

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

179 The marine cyanobacterium Synechococcus is the second most abundant

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

181 Cyanobacterium Synechococcus sp. PCC 7002 contains a sin

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

183 Genome analyses of the unicellular, marine cyanobacterium Synechococcus sp. PCC 7002 identified thr

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

185 The cyanobacterium Synechococcus sp. PCC 7002 uses a hemoglo

186 the autofermentative metabolism in the model cyanobacterium Synechococcus sp. PCC 7002, for which int

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

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

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

190 riven by the dominance of the photosynthetic cyanobacterium Synechococcus.

191 e SAR11 clade of Alphaproteobacteria and the cyanobacterium Synechococcus.

192 genes, were likely acquired from an ancient cyanobacterium (Synechococcus) progenitor, and separate

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

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

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

196 3-hydroxypropionate bi-cycle into the model cyanobacterium, Synechococcus elongatus sp. PCC 7942.

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

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

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

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

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

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

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

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

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

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

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

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

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

210 cA (Mn(2+)-cupin A), in the periplasm of the cyanobacterium Synechocystis PCC 6803.

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

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

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

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

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

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

217 nes that encode PGL-like polypeptides in the cyanobacterium Synechocystis sp. PCC 6803 (pgl1 and pgl2

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

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

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

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

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

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

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

225 The cyanobacterium Synechocystis sp. PCC 6803 harvests light

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

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

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

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

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

231 proteomic analysis of PSII purified from the cyanobacterium Synechocystis sp. PCC 6803 was performed.

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

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

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

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

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

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

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

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

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

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

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

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

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

245 oautotrophy but not photoheterotrophy in the cyanobacterium Synechocystis sp. PCC 6803.

246 1) FTIR difference spectrum of PSII from the cyanobacterium Synechocystis sp. PCC 6803.

247 own by the characterization of ChlM from the cyanobacterium Synechocystis sp. PCC 6803.

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

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

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

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

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

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

254 to a loss of optimal photoautotrophy in the cyanobacterium Synechocystis sp. strain PCC 6803 grown u

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

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

257 he cognate thioesterase characterized in the cyanobacterium Synechocystis.

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

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

260 oromethyl carbinol, and may be produced by a cyanobacterium that also makes phorbasides.

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

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

263 Nostoc punctiforme is a cyanobacterium that differentiates specialized gliding f

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

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

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

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

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

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

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

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

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 diffraction (XRD) structure of PSII from the cyanobacterium Thermosynechococcus elongatus.

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

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

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

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

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

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

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

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

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

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

285 The marine cyanobacterium Trichodesmium is ubiquitous in tropical a

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

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

288 transcription in the marine nitrogen-fixing cyanobacterium Trichodesmium.

289 The diazotrophic cyanobacterium, Trichodesmium, is an integral component

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

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

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

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

294 ed, periodically abundant N(2)-fixing marine cyanobacterium, UCYN-A, was recently found to lack the o

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

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

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

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