ライフサイエンスコーパス: Anabaena

1 and oxidized flavodoxin from Cyanobacterium anabaena .

2 nitrogen fixation gene (nifH) expression in Anabaena.

3 nobacteria; Synechococcus, Synechocystis and Anabaena.

4 Haloarcula marismortui and the non-halophile anabaena.

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

6 of three anabaenolysin-producing strains of Anabaena.

7 dependent signal between vegetative cells of Anabaena.

8 rier from heterocysts to vegetative cells in Anabaena.

9 Anabaena, a filamentous cyanobacterium, is of developmen

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 r color-sensitive physiological responses in Anabaena cells.

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

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

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

34 Moreover, Anabaena deficient in KatB was susceptible to oxidative

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

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

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

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

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

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

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

42 Anabaena Fld residues Asp144 and Glu145 align closely wi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

59 ANABAENA has nine DNA MTases.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 Thirty Anabaena PCC 7120 genes contain this repeat motif.

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

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

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

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

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

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

91 2Fe-2S] vegetative cell ferredoxin (Fd) from Anabaena PCC 7120, each of which has a cluster ligating

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

93 ed and characterized from the cyanobacterium Anabaena PCC 7120.

94 se pyrophosphorylase from the cyanobacterium Anabaena PCC 7120.

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

96 nitrogen in filaments of the cyanobacterium Anabaena PCC 7120.

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

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

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

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

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

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

103 We conclude that Anabaena rhodopsin functions as a photosensory receptor

104 Anabaena ribonucleotide reductase is a monomer with a mo

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

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

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

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

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

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

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

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

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

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

115 Anabaena sensory rhodopsin exhibits light-induced interc

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

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

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

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

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

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

122 20% in Escherichia coli and 40% in wild-type Anabaena sp.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 Tic22 in Anabaena sp. PCC 7120 is essential.

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

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

144 6803 and in the filamentous, nitrogen-fixing Anabaena sp. PCC 7120 is stimulated through nitrogen lim

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

162 discovered in the freshwater cyanobacterium Anabaena sp. PCC7120.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

188 Anabaena sp. strain PCC 7120 is a filamentous cyanobacte

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

208 57 (hglB) of the filamentous cyanobacterium, Anabaena sp. strain PCC 7120, and hglE of Nostoc punctif

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

242 An Anabaena strain overexpressing SepJ made wider septa bet

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

244 Anabaena strains expressing a version of HetN lacking th

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

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

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

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

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

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

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

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

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

254 Anabaena variabilis ATCC 29413 fixes nitrogen in special

255 Anabaena variabilis ATCC 29413 is a filamentous heterocy

256 Anabaena variabilis ATCC 29413 is unusual in that it has

257 The cyanobacterium Anabaena variabilis ATCC 29413 uses nitrate and atmosphe

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

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

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

261 Anabaena variabilis fixes nitrogen under aerobic growth

262 Anabaena variabilis grows heterotrophically using fructo

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

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

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

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

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

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

269 Anabaena variabilis, which can fix nitrogen by using an

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

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

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

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

274 metallo-intramembrane cleaving proteases in Anabaena variabilis.

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

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

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

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

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

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