ライフサイエンスコーパス: Nostoc

1 and there are no genomes available for polar Nostoc.

2 es with N(2)-fixing cyanobacteria, primarily Nostoc.

3 Genomic DNAs from 11 other Nostoc and Anabaena strains, including Anabaena sp. stra

4 s-dominated bloom, a shift of dominance from Nostoc and Anabaena to Microcystis and an increase of mi

5 t, P-scavenging activities dominated also by Nostoc and Anabaena were associated with low P and the M

6 cyanobacterial N(2)-fixers were dominated by Nostoc and Anabaena.

7 in gene and a ferredoxin reductase gene from Nostoc and that the enzyme oxygenates the NS1 terpene pr

8 y employ different soluble sugars to attract Nostoc and, once the cyanobacteria are internalized, to

9 hout the known global phylogeny of the genus Nostoc, and that each appears to be evolving clonally.

10 hanizomenon, Cylindrospermopsis raciborskii, Nostoc, and Tolypothrix.

11 er CyanoHAB and the functional activities of Nostoc- and Anabaena-dominated or Microcystis-dominated

12 bunits and four small peripheral subunits of Nostoc are 88 and 80% identical to those in the M. lamin

13 Dinitrogen fixation by Nostoc azollae residing in specialized leaf pockets supp

14 that occurred in the whole genome of single Nostoc cells.

15 lose, a non-reducing disaccharide present in Nostoc colonies.

16 Increasing Nostoc colonization resulted in an enrichment of S and c

17 undance of Glc and Fru in the gland prior to Nostoc colonization, genes encoding key enzymes for sucr

18 Genomic DNA of Nostoc commune (Cyanobacteria) became covalently modifie

19 Cyanobacterium Nostoc commune can tolerate the simultaneous stresses of

20 rd most abundant soluble protein in cells of Nostoc commune CHEN/1986 after prolonged (13 years) stor

21 lobin and decades slower than in the related Nostoc commune cyanoglobin.

22 ysaccharide (glycan) of desiccation-tolerant Nostoc commune DRH-1 was determined through chromatograp

23 arried out the first genomic analysis of the Nostoc commune morphotype with a recent sample from the

24 ein phosphatase IphP from the cyanobacterium Nostoc commune UTEX 584 also dephosphorylated these prot

25 The glbN gene of the cyanobacterium Nostoc commune UTEX 584 encodes a hemoprotein, named cya

26 The glbN gene of Nostoc commune UTEX 584 is juxtaposed to nifU and nifH,

27 of, a terminal cytochrome oxidase complex in Nostoc commune UTEX 584 under microaerobic conditions, w

28 The globin from the cyanobacterium Nostoc commune, abbreviated GlbN, which appears to serve

29 Two unique aspects of the Nostoc complex are: (i) a dominant conformation of heme

30 lternative vanadium-based nitrogenase in the Nostoc cyanobiont of these lichens and its substantial c

31 potentially nitrogen-fixing community, with Nostoc decreasing and noncyanobacterial diazotrophs incr

32 Successful colonization by Nostoc drastically reduced sugar accumulation in the sur

33 n from the cyanobacterium (blue-green algae) Nostoc ellipsosporum with potent virucidal activity, was

34 yanobacteria Anabaena sp. strain PCC7120 and Nostoc ellipsosporum, as it is for dechlorination of oth

35 kDa protein isolated from the cyanobacterium Nostoc ellipsosporum, potently inactivates diverse strai

36 he unusual amino acid 4-methylproline in the Nostoc genus of cyanobacteria was investigated on the ge

37 were found for in vitro establishment of the Nostoc-Gunnera symbiosis by inoculating mature glands wi

38 the region near beta-C122 in the homologous Nostoc H-NOX crystal structure indicates that this resid

39 Purified b(6)f complex from Nostoc has a stable dimeric structure, eight subunits wi

40 me NO and oxygen binding domain (H-NOX) from Nostoc homologous to that of sGC reveals that the trifur

41 r Microbiology suggests that the motility of Nostoc hormogonia has much more in common with Synechocy

42 f catalase-related proteins and functions in Nostoc in specific transformation of the 10S-hydroperoxy

43 However, the genomic diversity of Nostoc is little known and there are no genomes availabl

44 PC synthase homolog from the cyanobacterium Nostoc, is capable of explaining the strict requirement

45 cteria, belonging to the genera Anabaena and Nostoc, isolated from Iranian terrestrial and aquatic ec

46 and identified a putative gene cluster from Nostoc linckia NIES-25 that encodes a short-chain dehydr

47 The Nostoc linoleate 10S-dioxygenase, the sequence of which

48 n of Sphagnum angustifolium hyaline cells by Nostoc muscorum modifies S abundance and speciation at t

49 s nidulans, Microcoleus chthonoplastes S.G., Nostoc muscorum, Oscillatoria amphigranulata, Oscillator

50 Nostoc (Nostocales, Cyanobacteria) has a global distribu

51 starvation, the multicellular cyanobacterium Nostoc PCC 7120 develops nitrogen-fixing heterocysts wit

52 The cyanobacterium Anabaena (Nostoc) PCC 7120 responds to starvation for nitrogen com

53 19 and Prochlorothrix hollandica) as well as Nostoc plastocyanin mutants showed a linear dependence o

54 s of cycad trees, cyanobacteria of the genus Nostoc produce beta-methylamino-l-alanine (BMAA), a neur

55 mophila (L1 H-NOX and L2 H-NOX) and one from Nostoc punctiforme (Np H-NOX).

56 Previous studies of the Nostoc punctiforme (Np) AD produced in Escherichia coli

57 dition, the in vitro activity of the AD from Nostoc punctiforme (Np) was shown to require a reducing

58 omplex of the diiron(II/II) form of ADO from Nostoc punctiforme (Np) with an aldehyde substrate react

59 netically introduced into a highly efficient Nostoc punctiforme (Npu) DnaE intein.

60 We show that both the diferric form of Nostoc punctiforme ADO and its (putative) diferric-perox

61 aena sp. Pasteur Culture Collection 7120 and Nostoc punctiforme American Type Culture Collection 2913

62 ction for diazotrophic cyanobacteria such as Nostoc punctiforme and Anabaena spp., in addition to the

63 xing, symbiotically competent cyanobacterium Nostoc punctiforme and designated sigH.

64 m, Anabaena sp. strain PCC 7120, and hglE of Nostoc punctiforme are required for synthesis of heteroc

65 Nostoc punctiforme ATCC 29133 is a filamentous cyanobact

66 nemin-deficient mutant of the cyanobacterium Nostoc punctiforme ATCC 29133 was obtained by random tra

67 rticular, Anabaena variabilis ATCC 29413 and Nostoc punctiforme ATCC 29133, identified by screening t

68 system involved in heterocyst development in Nostoc punctiforme ATCC 29133, purified affinity-tagged

69 ysteine photosensors from the cyanobacterium Nostoc punctiforme ATCC 29133, we establish that this sp

70 k heterotrophic growth of the cyanobacterium Nostoc punctiforme ATCC 29133.

71 orphan halogenase-encoding gene cluster from Nostoc punctiforme ATCC 29133.

72 sunscreen biosynthesis by the cyanobacterium Nostoc punctiforme ATCC 29133.

73 cytonemin biosynthesis in the cyanobacterium Nostoc punctiforme ATCC 29133; we now report on the expr

74 tive cells of the filamentous cyanobacterium Nostoc punctiforme can differentiate into three mutually

75 The filamentous cyanobacterium Nostoc punctiforme differentiates from vegetative cells

76 t high frequencies in a zwf mutant strain of Nostoc punctiforme following dark incubation in the pres

77 Here we confirm that Nostoc punctiforme hormogonia are positively phototactic

78 t the cloning and heterologous expression of Nostoc punctiforme HupS as a fusion protein, f-HupS.

79 Nostoc punctiforme is a cyanobacterium that differentiat

80 Nostoc punctiforme is a versatile cyanobacterium that ca

81 Nostoc punctiforme is an example of a filamentous cyanob

82 stem of the model filamentous cyanobacterium Nostoc punctiforme is capable of sensing light indirectl

83 The N-terminal domain in an STHK from Nostoc punctiforme is of unknown function yet is homolog

84 tic gene cluster (BGC) in the cyanobacterium Nostoc punctiforme NIES-2108 and functions as a nonheme

85 We examined the frequently used Nostoc punctiforme Npu DnaE intein after the C-extein cy

86 the sequence space of residues flanking the Nostoc punctiforme Npu DnaE intein and found that this i

87 . strain PCC 7120 (terpene synthase NS1) and Nostoc punctiforme PCC 73102 (terpene synthases NP1 and

88 cted a novel candidate in the cyanobacterium Nostoc punctiforme PCC 73102.

89 tures of Vipp1 rings from the cyanobacterium Nostoc punctiforme presented over a range of symmetries.

90 FEGSEM images of Nostoc punctiforme revealed a highly convoluted, not par

91 se-6-phosphate dehydrogenase (G6PD), zwf, in Nostoc punctiforme strain ATCC 29133 is part of a four-g

92 sence of a unique membrane protein, PatN, in Nostoc punctiforme strain ATCC 29133 leads to a threefol

93 evelopment in the filamentous cyanobacterium Nostoc punctiforme strain ATCC 29133.

94 was coupled with aldehyde decarbonylase from Nostoc punctiforme to use free FAs as substrates for alk

95 e-related cyanobacteriochrome NpR6012g4 from Nostoc punctiforme was studied by transient absorption p

96 , facultatively heterotrophic cyanobacterium Nostoc punctiforme were constructed bearing a neomycin r

97 igG)/Npun_F4154 (SapG) of the cyanobacterium Nostoc punctiforme were hypothesized to encode an ECF si

98 ymbiosis with nitrogen-fixing cyanobacteria (Nostoc punctiforme) presumably representing the ancestra

99 oculating mature glands with hormogonia from Nostoc punctiforme, a cyanobacterium strain for which th

100 ive genomics studies on hps and pil genes in Nostoc punctiforme, a species in which motility is restr

101 of Slr2013 are found in other cyanobacteria (Nostoc punctiforme, Anabaena sp. strain PCC 7120, and Th

102 genome of the multicellular cyanobacterium, Nostoc punctiforme, and its relatives for small disperse

103 methyl-accepting chemotaxis-like protein in Nostoc punctiforme, designated HmpD.

104 me sequences of other cyanobacteria, such as Nostoc punctiforme, Synechococcus sp. strain WH8102, and

105 In the model filamentous cyanobacterium Nostoc punctiforme, the T4P systems are arrayed in stati

106 In Nostoc punctiforme, they are also induced by the exudate

107 filamentous forms, including species such as Nostoc punctiforme, which can generate specialised motil

108 ailed characterization of the hmp locus from Nostoc punctiforme, which encodes chemotaxis-like protei

109 rimeric C termini of the Dps4 dodecamer from Nostoc punctiforme.

110 a PS I reaction center core preparation from Nostoc punctiforme.

111 red/green subfamily from the cyanobacterium Nostoc punctiforme.

112 ixing cyanobacteria, Anabaena variabilis and Nostoc punctiforme.

113 nt of functional heterocysts in Anabaena and Nostoc, respectively.

114 Different sugars affected Nostoc's ability to differentiate motile hormogonia in a

115 Nostoc sp. (Ns) H-NOX is a heme protein found in symbiot

116 s are potent anticancer agents isolated from Nostoc sp. ATCC 53789 and Nostoc sp. GSV 224.

117 s produced by the terrestrial cyanobacterium Nostoc sp. ATCC53789 that possess a unique imino linkage

118 s in E. coli demonstrates that the P450 from Nostoc sp. can be functionally expressed in E. coli when

119 In this work we subjected Nostoc sp. CCCryo 231-06, a cyanobacterium capable of li

120 BphG1 and the adenylate cyclase domain from Nostoc sp. CyaB1.

121 lyketide, nosperin, from a lichen-associated Nostoc sp. cyanobacterium.

122 ents isolated from Nostoc sp. ATCC 53789 and Nostoc sp. GSV 224.

123 cluster from the terrestrial cyanobacterium Nostoc sp. GSV224 is described.

124 y, the structure of BAY 58-2667 bound to the Nostoc sp. H-NOX domain was published.

125 The genome of Nostoc sp. PCC 7120 has been sequenced and is closer phy

126 We solved two crystal structures of the Nostoc sp. PCC 7120 HCP1 protein, each binding a differe

127 Three CCD homologs identified in Nostoc sp. PCC 7120 were purified, and their cleavage ac

128 ed to as H-NOX domains, including those from Nostoc sp. PCC 7120, Shewanella oneidensis, Shewanella w

129 ieske (PetC) protein from the cyanobacterium Nostoc sp. PCC 7906.

130 et charge more positive than -2.0 (including Nostoc sp. PCC7119 and Prochlorothrix hollandica) as wel

131 cyanobacteria Synechocystis sp. PCC6803 and Nostoc sp. PCC7120 are examined.

132 as the cyanobacterial T-type lyase CpcT from Nostoc sp. PCC7120 but overall is more compact and small

133 of the N2-fixing, filamentous cyanobacterium Nostoc sp. PCC7120 in the nblA1/nblA2 mutant of Synechoc

134 doxin oxidoreductase from the cyanobacterium Nostoc sp. PCC7120 through site-specific chemical modifi

135 03 is combined in the homodimeric protein of Nostoc sp. PCC7120.

136 cture of the complex from the cyanobacterium Nostoc sp. revealed the presence of 23 lipid-binding sit

137 in UCD 311 is a transposon-induced mutant of Nostoc sp. strain ATC C 29133 that is unable to fix nitr

138 iation of akinetes, its presence in trans in Nostoc sp. strain ATCC 29133 stimulated their formation

139 The nifU-nifH intergenic region of Nostoc sp. strain MUN 8820 was sequenced (1,229 bp) and

140 three sesquiterpene synthases identified in Nostoc sp. strain PCC 7120 (terpene synthase NS1) and No

141 The thermodynamic stability of Nostoc sp. strain PCC 8009 PsaE toward urea denaturation

142 on structure of PsaE from the cyanobacterium Nostoc sp. strain PCC 8009 was determined by NMR methods

143 of Escherichia coli is 55% identical to the Nostoc sp. strain PCC7120 gene encoding DNA methyltransf

144 e alkaloid, isolated from the cyanobacterium Nostoc sp. UIC 10771, demonstrated cytotoxic activity ag

145 N-fixing symbiosis between a cyanobacterium (Nostoc sp.) and the ubiquitous feather moss, Pleurozium

146 ion and photochemical reactions of Anabaena (Nostoc) sp. PCC7120 sensory rhodopsin (ASR).

147 n light-activated photoreceptor in Anabaena (Nostoc) sp. PCC7120, a freshwater cyanobacterium.

148 in filaments of the cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120 differentiate into nitrogen-

149 The novel asr1734 gene of Anabaena (Nostoc) sp. strain PCC 7120 inhibited heterocyst develop

150 The filamentous cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120 maintains a genome that is d

151 The filamentous cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120 produces specialized cells f

152 The filamentous cyanobacterium Anabaena (Nostoc) sp. strain PCC 7120 responds to starvation for f

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

154 In cyanobacterial Nostoc species, substratum-dependent gliding motility is

155 -Cas systems in the Arctic and two temperate Nostoc species.

156 Here, we present the complete genome of Nostoc sphaeroides, a paddy-field diazotroph used for fo

157 Functional expression of a selection Nostoc spp.

158 st-forming clades, some strains, such as the Nostoc spp. and Fisherella spp., are motile only as spec

159 ng Anabaena PCC 7120, but employed also with Nostoc spp., are reviewed.

160 antibodies was detected in four Anabaena and Nostoc strains and in Trichodesmium thiebautii.

161 here are pronounced genetic variations among Nostoc strains and species.

162 All Nostoc strains had a subtype I-D system, but the polar s

163 glbN was present in five Nostoc strains in a single copy.

164 ion and other stress genes were found in all Nostoc strains, but the two Arctic strains had markedly