ライフサイエンスコーパス: Nostoc

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

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

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

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

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

6 hanizomenon, Cylindrospermopsis raciborskii, Nostoc, and Tolypothrix.

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

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

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

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

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

12 Cyanobacterium Nostoc commune can tolerate the simultaneous stresses of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

39 19 and Prochlorothrix hollandica) as well as Nostoc plastocyanin mutants showed a linear dependence o

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

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

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

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

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

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

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

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

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

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

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

51 Nostoc punctiforme ATCC 29133 is a filamentous cyanobact

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

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

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

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

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

57 sunscreen biosynthesis by the cyanobacterium Nostoc punctiforme ATCC 29133.

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

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

60 The filamentous cyanobacterium Nostoc punctiforme differentiates from vegetative cells

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

62 Here we confirm that Nostoc punctiforme hormogonia are positively phototactic

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

64 Nostoc punctiforme is a cyanobacterium that differentiat

65 Nostoc punctiforme is a versatile cyanobacterium that ca

66 Nostoc punctiforme is an example of a filamentous cyanob

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

91 red/green subfamily from the cyanobacterium Nostoc punctiforme.

92 ixing cyanobacteria, Anabaena variabilis and Nostoc punctiforme.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

114 03 is combined in the homodimeric protein of Nostoc sp. PCC7120.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

132 Functional expression of a selection Nostoc spp.

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

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

135 documentation is available online at http://nostoc.stanford.edu/Docs/index.html

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

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