ライフサイエンスコーパス: Anabaena

1 and oxidized flavodoxin from Cyanobacterium anabaena .

2 Haloarcula marismortui and the non-halophile anabaena.

3 d the FNR-Fld system from the cyanobacterium Anabaena.

4 nitrogen fixation gene (nifH) expression in Anabaena.

5 nobacteria; Synechococcus, Synechocystis and Anabaena.

6 of three anabaenolysin-producing strains of Anabaena.

7 ial N(2)-fixers were dominated by Nostoc and Anabaena.

8 dependent signal between vegetative cells of Anabaena.

9 rier from heterocysts to vegetative cells in Anabaena.

10 Anabaena, a filamentous cyanobacterium, is of developmen

11 or more GAF (cGMP-binding phosphodiesterase, Anabaena adenylyl cyclase, and Escherichia coli FhlA) su

12 om the proteins mammalian cGMP-binding PDEs, Anabaena adenylyl cyclases, and Escherichia coli (FhlA))

13 wo mammalian cGMP-binding phosphodiesterase, Anabaena adenylyl cyclases, Escherichia coli FhlAs (GAFs

14 syl residue (Lys 419) near the C-terminus of Anabaena ADP-glucose pyrophosphorylase is involved in th

15 ly is shared even in the adenylyl cyclase of Anabaena, an organism separated from mouse by 2 billion

16 anobacteria (e.g. Microcystis, Planktothrix, Anabaena and Cylindrospermopsis) will increase in freshw

17 Heterocysts of both hepK Anabaena and devRA Anabaena lack an envelope polysacchar

18 ly with GlbN antibodies was detected in four Anabaena and Nostoc strains and in Trichodesmium thiebau

19 stous cyanobacteria, belonging to the genera Anabaena and Nostoc, isolated from Iranian terrestrial a

20 the development of functional heterocysts in Anabaena and Nostoc, respectively.

21 (closest to the mouth of the Maumee River), Anabaena and Planktothrix were the dominant cyanobacteri

22 mponents that are similar between plants and Anabaena and that may be evolutionarily related.

23 the conserved core of both a cyanobacterial (Anabaena) and a eukaryotic (Tetrahymena) group I intron.

24 ong cyanobacterial populations (Microcystis, Anabaena, and Planktothrix) toward a greater dominance b

25 l proposed from the crystal structure of the Anabaena apoflavodoxin.

26 The Tn5 derivative transposed in Anabaena at ca. 1-4 x 10(-5) per cell and permitted high

27 the two MBDs of the Zn/Cd/Pb effluxing pump Anabaena AztA are functionally nonequivalent, but only w

28 tter local structural match is obtained with Anabaena beta-diketone hydrolase (ABDH), a known beta-di

29 Anabaena beta-diketone hydrolase (ABDH), in common with

30 Nowadays, the increasing Dolichospermum (Anabaena) blooms pose a major threat to the aquatic envi

31 is demonstrated that 20 strains of the genus Anabaena carry hassallidin synthetase genes and produce

32 r color-sensitive physiological responses in Anabaena cells.

33 at this strain belongs to the Trichormus and Anabaena cluster.

34 Filamentous cyanobacteria of the genus Anabaena contain a unique open reading frame, rbcX, whic

35 k state of one such frCBCR Anacy_2551g3 from Anabaena cylindrica PCC 7122 which exhibits a reversible

36 uced calcein, a 623-Da fluorophore, into the Anabaena cytoplasm.

37 Moreover, Anabaena deficient in KatB was susceptible to oxidative

38 We show that HepK is an autokinase and that Anabaena DevRA is its cognate response regulator, togeth

39 nobacteria Synechocystis, Synechococcus, and Anabaena do not form a coherent group and are as far fro

40 and the functional activities of Nostoc- and Anabaena-dominated or Microcystis-dominated communities,

41 Site-directed mutagenesis of Lys382 of the Anabaena enzyme was performed to determine the role of t

42 zed in five other euglenoid species, Euglena anabaena, Euglena granulata, Euglena myxocylindracea, Eu

43 The filamentous cyanobacterium Anabaena fixes nitrogen in specialized cells called hete

44 resonance techniques of several variants of Anabaena flavodoxin, where the naturally occurring FMN c

45 Mutagenesis of two acidic Anabaena Fld residues (D144A and E145A) significantly de

46 Anabaena Fld residues Asp144 and Glu145 align closely wi

47 proteolyzed vesicles from the cyanobacterium Anabaena flos-aquae and the archaea Halobacterium salina

48 forms the gas vesicle in the cyanobacterium Anabaena flos-aquae has been imaged by atomic force micr

49 xclusively in the extended N-terminus of the Anabaena flos-aquae protein and in the extended C-termin

50 llapsed gas vesicles from the cyanobacterium Anabaena flos-aquae show duplication of certain gas vesi

51 llapsed gas vesicles from the cyanobacterium Anabaena flos-aquae were studied by solid-state NMR spec

52 photosynthetic activity of a cyanobacterium (Anabaena flos-aquae) contained within an EGOFET's electr

53 ects of the antibiotics to the cyanobacteria Anabaena flos-aquae.

54 itute the ribs of the buoyancy organelles of Anabaena flos-aquae.

55 sient catalytically competent interaction of Anabaena FNR with its coenzyme, NADP(+).

56 ns of the hydride transfer processes between Anabaena FNR(rd)/FNR(ox) and NADP(+)/H, accounting also

57 and ferredoxin:NADP(+) reductase (FNR) from Anabaena function in photosynthetic electron transfer (e

58 A BLAST search of the Anabaena genome identified 166 hepA-like sites that occu

59 ss bacterial luciferase genes, luxAB, to the Anabaena genome.

60 gae (Cladophora genus) and blue-green algae (Anabaena genus).

61 ha-linolenic acids (which occur naturally in Anabaena) giving the respective 9R-hydroperoxides, the m

62 nucleophile to the ribozyme derived from the Anabaena group I intron, and find that they are similar

63 In a species such as Anabaena, growth in nitrogen-depleted medium, in which a

64 ANABAENA has nine DNA MTases.

65 Cocrystal structures of Anabaena HU bound to DNA (1P71, 1P78, 1P51) reveal that

66 of a gene, which we call hanA, that encodes Anabaena HU protein.

67 storted substrates in the recently published Anabaena HU(AHU)-DNA cocrystal structures.

68 ese proteins in cyanobacteria in general and Anabaena in particular.

69 Many mutations in HetR render Anabaena incapable of nitrogen fixation.

70 Heterocysts of both hepK Anabaena and devRA Anabaena lack an envelope polysaccharide layer and are n

71 e detected retinal binding to the protein in Anabaena membranes by SDS-PAGE and autofluorography of 3

72 e, transcript, protein, metabolite) model of Anabaena - nitrogen interaction.

73 The cyanobacterium Anabaena (Nostoc) PCC 7120 responds to starvation for ni

74 rk adaptation and photochemical reactions of Anabaena (Nostoc) sp. PCC7120 sensory rhodopsin (ASR).

75 in, a green light-activated photoreceptor in Anabaena (Nostoc) sp. PCC7120, a freshwater cyanobacteri

76 ive cells in filaments of the cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120 differentiate into

77 The novel asr1734 gene of Anabaena (Nostoc) sp. strain PCC 7120 inhibited heterocy

78 The filamentous cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120 maintains a genome

79 The filamentous cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120 produces specializ

80 The filamentous cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120 responds to starva

81 heterocyst development in the cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120.

82 This study establishes that all four Anabaena NTD-like proteins can bind a carotenoid and the

83 Two of the other Anabaena paralogs (All3221 and Alr4783) were shown to be

84 Oxidized flavodoxin from Cyanobacterium anabaena PCC 7119 is used as a model system to investiga

85 he sensory rhodopsin from the cyanobacterium Anabaena PCC 7120 (ASR) and of the bovine rhodopsin (Rh)

86 (1)H-NMR of proteins from P. aeruginosa, Anabaena PCC 7120 and E. coli generated fingerprints dia

87 yaB2 adenylyl cyclases of the cyanobacterium Anabaena PCC 7120 are inhibited by Na(+).

88 ed (1)H-NMR, identified histidine ligands in Anabaena PCC 7120 BmtA, analogous to SmtA.

89 ual function protein from the cyanobacterium Anabaena PCC 7120 forms 9R-hydroperoxy-C18.3omega3 in a

90 Thirty Anabaena PCC 7120 genes contain this repeat motif.

91 ses (MTases) possessed by the cyanobacterium ANABAENA PCC 7120 has been deduced.

92 on from a heterologous promoter in wild-type Anabaena PCC 7120 induced multiple-contiguous heterocyst

93 rentiation in the filamentous cyanobacterium Anabaena PCC 7120 requires a functional hetR gene.

94 ing the copper-responsive petE promoter from Anabaena PCC 7120 to drive hetR expression, we show that

95 rylase (EC 2.7.7.27) from the cyanobacterium Anabaena PCC 7120 with phenylglyoxal in 50 mM Hepes, pH

96 ble genetic tools, developed primarily using Anabaena PCC 7120, but employed also with Nostoc spp., a

97 2Fe-2S] vegetative cell ferredoxin (Fd) from Anabaena PCC 7120, each of which has a cluster ligating

98 lated bacterial metallothioneins (BmtA) from Anabaena PCC 7120, Pseudomonas aeruginosa and Pseudomona

99 nitrogen in filaments of the cyanobacterium Anabaena PCC 7120.

100 ed and characterized from the cyanobacterium Anabaena PCC 7120.

101 se pyrophosphorylase from the cyanobacterium Anabaena PCC 7120.

102 al method we have analyzed nine promoters of Anabaena PCC 7120.

103 The nitrogen-fixing cyanobacterium, Anabaena PCC7120 encodes for a membrane-targeted 30 kDa

104 ing of the 249-residue group I intron of the Anabaena PCC7120 tRNAleu precursor.

105 beta-diketone hydrolase from Cyanobacterium anabaena (PDB ID 2j5s).

106 In the cyanobacterium Anabaena, pretreatment of cells with NaCl resulted in un

107 abinitol 1-phosphate with the product of the Anabaena rca gene.

108 In contrast, the Anabaena reductase shows over 90% sequence similarity to

109 We conclude that Anabaena rhodopsin functions as a photosensory receptor

110 Anabaena ribonucleotide reductase is a monomer with a mo

111 ' and delta(S)degrees' for pG binding to the Anabaena ribozyme--RNA substrate complex (E x S) are 3.4

112 cernible effect after incubating recombinant Anabaena Rubisco and carboxyarabinitol 1-phosphate with

113 ength and C-terminally truncated versions of Anabaena sensory rhodopsin (ASR) demonstrate that the ch

114 Anabaena sensory rhodopsin (ASR) is a novel microbial rh

115 microbial rhodopsins characterized thus far, Anabaena sensory rhodopsin (ASR) is a photochromic senso

116 a seven-helical transmembrane (TM) protein, Anabaena Sensory Rhodopsin (ASR) reconstituted in lipids

117 a seven-transmembrane helical photoreceptor, Anabaena sensory rhodopsin (ASR), prepared in the Escher

118 of an oligomeric integral membrane protein, Anabaena sensory rhodopsin (ASR), reconstituted in a lip

119 rized eubacterial retinylidene photoreceptor Anabaena sensory rhodopsin (ASR).

120 med by a seven-helical transmembrane protein Anabaena Sensory Rhodopsin (ASR).

121 Anabaena sensory rhodopsin exhibits light-induced interc

122 ions with membrane-embedded transducers, the Anabaena sensory rhodopsin may signal through a soluble

123 tes in a seven transmembrane helical protein Anabaena Sensory Rhodopsin reconstituted in lipids.

124 We present crystal structures of the Anabaena sensory rhodopsin transducer (ASRT), a soluble

125 On exposure to H2O2, the NaCl-treated Anabaena showed reduced formation of reactive oxygen spe

126 miting conditions, in filaments of the genus Anabaena, some cells differentiate into heterocysts, whi

127 r steps from extracts of vegetative cells of Anabaena sp.

128 20% in Escherichia coli and 40% in wild-type Anabaena sp.

129 bsiella pneumoniae (49%), the cyanobacterium Anabaena sp. (44%), and the protozoan Trichomonas vagina

130 Bioinformatic analysis of the Anabaena sp. 90 genome identified a 59-kb cryptic inacti

131 A (NucA) is a nonspecific endonuclease from Anabaena sp. capable of degrading single- and double-str

132 bp2) are encoded by neighboring genes in the Anabaena sp. chromosome.

133 Heterocysts of patA and patL Anabaena sp. form nearly exclusively terminally in long

134 We have verified that 10 Anabaena sp. genes, all1338, all1591, alr1728, all3278,

135 Nuclease A (NucA) from Anabaena sp. is a non-specific endonuclease able to degr

136 Anabaena sp. ISs were often more closely related to exog

137 gnments of putative cellulose synthases from Anabaena sp. Pasteur Culture Collection 7120 and N. punc

138 similar to putative cellulose synthases from Anabaena sp. Pasteur Culture Collection 7120 and Nostoc

139 we approached the systems of the filamentous Anabaena sp. PCC 7120 as a model of a siderophore-secret

140 A) mutants of Synechocystis sp. PCC 6803 and Anabaena sp. PCC 7120 become arrested, resulting in cell

141 variabilis in anaerobic vegetative cells of Anabaena sp. PCC 7120 depended on the presence of cnfR2.

142 e filamentous nitrogen-fixing cyanobacterium Anabaena sp. PCC 7120 differentiates specialized cells,

143 alr4455 from the well-studied cyanobacterium Anabaena sp. PCC 7120 encodes a crotonase orthologue tha

144 he curated model of the metabolic network of Anabaena sp. PCC 7120 enhances our ability to understand

145 The closely related cyanobacterium, Anabaena sp. PCC 7120 has the nif1 system but lacks nif2

146 Anabaena sp. PCC 7120 is a nitrogen-fixing filamentous c

147 Tic22 in Anabaena sp. PCC 7120 is essential.

148 Anabaena sp. PCC 7120 is one of the few prokaryotes harb

149 lamentous, heterocyst-forming cyanobacterium Anabaena sp. PCC 7120 is part of multiple three-componen

150 6803 and in the filamentous, nitrogen-fixing Anabaena sp. PCC 7120 is stimulated through nitrogen lim

151 Summary In the filamentous cyanobacterium Anabaena sp. PCC 7120 patS and hetN suppress the differe

152 During a search for mutants of Anabaena sp. PCC 7120 that can overcome heterocyst suppr

153 ratricopeptide repeat protein - All4981 - in Anabaena sp. PCC 7120 that polymerized into filaments in

154 TRA domains of Omp85 from the cyanobacterium Anabaena sp. PCC 7120 using pulsed electron-electron dou

155 more common pentacylindrical phycobilisome (Anabaena sp. PCC 7120).

156 trolled gene at the individual cell level in Anabaena sp. PCC 7120, a multicellular filamentous cyano

157 that the L-array of the model cyanobacterium Anabaena sp. PCC 7120, encoding 23 functional tRNAs, is

158 lamentous, heterocyst-forming cyanobacterium Anabaena sp. PCC 7120, termed heterocyst glycolipid depo

159 al characterization of recombinant PcyA from Anabaena sp. PCC 7120.

160 ation when present on a multicopy plasmid in Anabaena sp. PCC 7120.

161 localization, and function of these genes in Anabaena sp. PCC 7120.

162 ase from spinach leaf and the cyanobacterium Anabaena sp. PCC 7120.

163 e major players for antibiotic resistance in Anabaena sp. PCC 7120.

164 and describe parameters of detoxification by Anabaena sp. PCC 7120.

165 The C-terminal 114-residue portion of the Anabaena sp. PCC7120 biotin carboxyl carrier protein (BC

166 Such tagged alpha or beta subunits of Anabaena sp. PCC7120 C-phycocyanin formed stoichiometric

167 The cyaB1 gene of the cyanobacterium Anabaena sp. PCC7120 codes for a multidomain protein wit

168 l populations (n < 616 +/- 76) of vegetative Anabaena sp. PCC7120 cyanobacterial cells are analyzed b

169 Thus the Alr1105 of Anabaena sp. PCC7120 functions as an arsenate reductase

170 constructed to express in the cyanobacterium Anabaena sp. PCC7120 recombinant C-phycocyanin subunits

171 nstitutes the first report on the Alr1105 of Anabaena sp. PCC7120 which functions as arsenate reducta

172 discovered in the freshwater cyanobacterium Anabaena sp. PCC7120.

173 ogen-deprived filaments of wild-type or hetC Anabaena sp. produce respectively, at semiregular interv

174 Anabaena sp. produces schizokinen and uptake of Fe-schiz

175 , we conclude that lindane dechlorination by Anabaena sp. requires a functional nir operon that encod

176 The purified recombinant Anabaena sp. strain CA RubisCO, much like the RubisCO en

177 smid constructions containing the genes from Anabaena sp. strain CA were prepared, and expression stu

178 Anabaena sp. strain PCC 7120 adapts to deprivation of fi

179 Fox- mutants of Anabaena sp. strain PCC 7120 are unable to fix dinitroge

180 Anabaena sp. strain PCC 7120 cell extracts contained a p

181 lamentous, heterocyst-forming cyanobacterium Anabaena sp. strain PCC 7120 contains, besides the four

182 Thus, although Anabaena sp. strain PCC 7120 could take up fructose and

183 Anabaena sp. strain PCC 7120 did not show any of these c

184 ned nitrogen, the filamentous cyanobacterium Anabaena sp. strain PCC 7120 differentiates nitrogen-fix

185 Two operons have been cloned from Anabaena sp. strain PCC 7120 DNA, each of which encodes

186 lly using fructose, while the close relative Anabaena sp. strain PCC 7120 does not.

187 otropic, transposon-generated mutant AB22 of Anabaena sp. strain PCC 7120 exhibits slow growth, alter

188 The filamentous cyanobacterium Anabaena sp. strain PCC 7120 forms a developmental patte

189 The filamentous cyanobacterium Anabaena sp. strain PCC 7120 forms a periodic pattern of

190 The filamentous cyanobacterium Anabaena sp. strain PCC 7120 forms nitrogen-fixing heter

191 The cyanobacterium Anabaena sp. strain PCC 7120 forms single heterocysts ab

192 Three new Anabaena sp. strain PCC 7120 genes encoding group 2 alte

193 er putative terminal oxidases present in the Anabaena sp. strain PCC 7120 genome are able to compensa

194 ome of the heterocyst-forming cyanobacterium Anabaena sp. strain PCC 7120 harbors 14 genes containing

195 Unlike unicellular strains, Anabaena sp. strain PCC 7120 has three additional group

196 fferentiation and function of heterocysts in Anabaena sp. strain PCC 7120 have been identified by mut

197 d survival of the filamentous cyanobacterium Anabaena sp. strain PCC 7120 in the absence of combined

198 Anabaena sp. strain PCC 7120 is a filamentous cyanobacte

199 eterocysts by the filamentous cyanobacterium Anabaena sp. strain PCC 7120 is dependent on regulators

200 Transposon-generated mutant C3 of Anabaena sp. strain PCC 7120 is unable to form heterocys

201 deduced amino acid sequence of the predicted Anabaena sp. strain PCC 7120 MoeA polypeptide shows 37%

202 The Anabaena sp. strain PCC 7120 ntcA gene showed multiple t

203 at are activated rapidly upon deprivation of Anabaena sp. strain PCC 7120 of fixed nitrogen.

204 ABC transporter, herein named frtRABC, into Anabaena sp. strain PCC 7120 on a replicating plasmid al

205 xed nitrogen, the filamentous cyanobacterium Anabaena sp. strain PCC 7120 provides a microoxic intrac

206 s, called heterocysts, by the cyanobacterium Anabaena sp. strain PCC 7120 requires HetR, which is con

207 on of one of the two annotated trpE genes in Anabaena sp. strain PCC 7120 resulted in a spike in the

208 Interruption of the moeA gene in Anabaena sp. strain PCC 7120 resulted in a strain, AMC36

209 The devH gene was identified in a screen for Anabaena sp. strain PCC 7120 sequences whose transcripts

210 conditions, the multicellular cyanobacterium Anabaena sp. strain PCC 7120 terminally commits approxim

211 Mutants of Anabaena sp. strain PCC 7120 that form heterocysts when

212 In Anabaena sp. strain PCC 7120 the presence and/or phospho

213 c pattern on filaments of the cyanobacterium Anabaena sp. strain PCC 7120 under conditions of limitin

214 The gene for ribonucleotide reductase from Anabaena sp. strain PCC 7120 was identified and expresse

215 from Escherichia coli to the cyanobacterium Anabaena sp. strain PCC 7120 was quantitated as a functi

216 Salt-induced genes in the cyanobacterium Anabaena sp. strain PCC 7120 were identified by use of a

217 ) and alr2834 (hepC) mutants, heterocysts of Anabaena sp. strain PCC 7120, a filamentous cyanobacteri

218 57 (hglB) of the filamentous cyanobacterium, Anabaena sp. strain PCC 7120, and hglE of Nostoc punctif

219 in other cyanobacteria (Nostoc punctiforme, Anabaena sp. strain PCC 7120, and Thermosynechococcus el

220 In the filamentous cyanobacterium Anabaena sp. strain PCC 7120, heterocysts are formed in

221 other Nostoc and Anabaena strains, including Anabaena sp. strain PCC 7120, provided no hybridization

222 gically and physiologically distant strains, Anabaena sp. strain PCC 7120, Synechococcus sp. strain P

223 In the model organism Anabaena sp. strain PCC 7120, the septal protein SepJ is

224 progression of heterocyst differentiation in Anabaena sp. strain PCC 7120, we have identified protein

225 Anabaena sp. strain PCC 7120, when mutated in genes orth

226 ication when expressed in the cyanobacterium Anabaena sp. strain PCC 7120, whether the ability of the

227 Anabaena sp. strain PCC 7120, widely studied, has 145 an

228 rentiation in the filamentous cyanobacterium Anabaena sp. strain PCC 7120.

229 heterocyst development in the cyanobacterium Anabaena sp. strain PCC 7120.

230 an otherwise wild-type genetic background in Anabaena sp. strain PCC 7120.

231 eterocysts in the filamentous cyanobacterium Anabaena sp. strain PCC 7120.

232 pS are required for heterocyst maturation in Anabaena sp. strain PCC 7120.

233 cyst pattern formation in the cyanobacterium Anabaena sp. strain PCC 7120.

234 , regulates plasmid maintenance functions in Anabaena sp. strain PCC 7120.

235 ysaccharide is dependent on the gene hepA in Anabaena sp. strain PCC 7120.

236 patS, blocked heterocyst differentiation in Anabaena sp. strain PCC 7120.

237 etwork were identified in the cyanobacterium Anabaena sp. strain PCC 7120.

238 omosome during heterocyst differentiation in Anabaena sp. strain PCC 7120.

239 cF phycoerythrocyanin alpha-subunit lyase of Anabaena sp. strain PCC 7120.

240 the model heterocyst-forming cyanobacterium Anabaena sp. strain PCC 7120.

241 e characterized Prx6 from the cyanobacterium Anabaena sp. strain PCC7120 (AnPrx6) and found that in a

242 lindane dechlorination by the cyanobacteria Anabaena sp. strain PCC7120 and Nostoc ellipsosporum, as

243 be the hassallidin biosynthetic pathway from Anabaena sp. SYKE748A, as well as the large chemical var

244 fied LPS may prevent cyanophage infection of Anabaena sp. vegetative cells and the formation of a fun

245 A fragment of the DNA of Anabaena sp. was cloned by complementation of a spontane

246 cyanin beta--BCCP114 constructs expressed in Anabaena sp. were >30% biotinylated.

247 e-cycle phases, e.g., Methanosarcina sp., or Anabaena sp., which have more periodicities than prokary

248 and the following odor producing algae taxa: Anabaena spp., Aphanizemenon spp., Oscillatoria spp., Ch

249 cyanobacteria such as Nostoc punctiforme and Anabaena spp., in addition to the green alga Scenedesmus

250 In Anabaena spp., synthesis of the heterocyst envelope poly

251 Analysis of an Anabaena strain bearing an All3922-GFP (green fluorescen

252 An Anabaena strain overexpressing SepJ made wider septa bet

253 We speculated that overexpression of other Anabaena strain PCC 7120 RGSGR-encoding genes might show

254 Anabaena strains expressing a version of HetN lacking th

255 ess tolerance was analysed using recombinant Anabaena strains overexpressing either different molecul

256 Genomic DNAs from 11 other Nostoc and Anabaena strains, including Anabaena sp. strain PCC 7120

257 The observations in Anabaena suggest that the MP modifies plasmodesmata by f

258 In the cyanobacterium, Anabaena, the cyaB1 and cyaB2 genes encode adenylyl cycl

259 bloom, a shift of dominance from Nostoc and Anabaena to Microcystis and an increase of microcystin a

260 locheilus striatus, a sea hare that feeds on Anabaena torulosa, a cyanobacterium that produces toxic

261 ocytes were loaded with recombinant PAL from Anabaena variabilis (rAvPAL) and their ability to perfor

262 r filamentous nitrogen-fixing cyanobacteria, Anabaena variabilis and Nostoc punctiforme.

263 reen alga (Ulva pertusa), and cyanobacteria (Anabaena variabilis and Synechococcus) have been investi

264 nd novel MITEs in the two bacterial genomes, Anabaena variabilis ATCC 29413 and Haloquadratum walsbyi

265 time PALs from cyanobacteria, in particular, Anabaena variabilis ATCC 29413 and Nostoc punctiforme AT

266 Anabaena variabilis ATCC 29413 fixes nitrogen in special

267 Anabaena variabilis ATCC 29413 is a filamentous heterocy

268 Anabaena variabilis ATCC 29413 is unusual in that it has

269 The cyanobacterium Anabaena variabilis ATCC 29413 uses nitrate and atmosphe

270 irected mutant strains of the cyanobacterium Anabaena variabilis ATCC 29413.

271 ent substrate specificity from that known in Anabaena variabilis ATCC 29413.

272 trogenase in the heterocystous cyanobacteria Anabaena variabilis ATTC 29413 using the acetylene reduc

273 Furthermore, Anabaena variabilis cultures grown in Mo or V media achi

274 The filamentous cyanobacterium Anabaena variabilis fixes nitrogen in the presence of va

275 Anabaena variabilis fixes nitrogen under aerobic growth

276 Anabaena variabilis grows heterotrophically using fructo

277 The cyanobacterium Anabaena variabilis has two Mo-nitrogenases that functio

278 In Anabaena variabilis it was shown that a NifE-N fusion pr

279 characteristics, and efficacy of recombinant Anabaena variabilis phenylalanine ammonia lyase (produce

280 with the calcium-dependent protease PrcA of Anabaena variabilis, HreP forms a new subfamily of bacte

281 ht to comprise multiple operons; however, in Anabaena variabilis, the promoter for the first gene in

282 og of Hen1 from Clostridium thermocellum and Anabaena variabilis, which are enzymatically indistingui

283 Anabaena variabilis, which can fix nitrogen by using an

284 a siderophore pathway in the cyanobacterium Anabaena variabilis, which was shown to be a bona fide D

285 ase (PAL) from Rhodosporidium toruloides and Anabaena variabilis.

286 o acid level with the vnfD gene product from Anabaena variabilis.

287 ntial screen for cold-induced transcripts in Anabaena variabilis.

288 metallo-intramembrane cleaving proteases in Anabaena variabilis.

289 e identified through a genome-wide survey in Anabaena variabilis.

290 ansient kinetic data on wild-type and mutant Anabaena vegetative cell ferredoxins has been used to in

291 toskeletal proteins and is indispensable for Anabaena viability.

292 y permuted self-splicing group I intron from Anabaena was used to generate covalently closed circular

293 re in the small (249 nt) group I intron from Anabaena, we used two independent assays to detect backb

294 ging activities dominated also by Nostoc and Anabaena were associated with low P and the Microcystis

295 etative cells, which are narrow in wild-type Anabaena, were notably enlarged in the SepJ-overexpressi

296 Cd(II) and Pb(II); this might have provided Anabaena with an evolutionary advantage to adapt to heav