ライフサイエンスコーパス: Chlorella

1 ed on lipids extracted from three species of Chlorella and resulted in close agreement with triacylgl

2 f renewable diesel in the United States from Chlorella biomass by hydrothermal liquefaction (HTL).

3 ruction of the virus in the presence of host chlorella cell walls established that the spike at the u

4 of 7 ns in Bold's basal medium, and 8 ns in Chlorella cells.

5 n, M. conductrix is deeply nested within the Chlorella clade, suggesting that taxonomic revision is n

6 moeba, Cafeteria, Cercomonas, Chlamydomonas, Chlorella, Cyanophora, Dictyostelium, Dunaliella, Ectoca

7 Autonomous Chlorella densities increased monotonically with light i

8 nochloropsis oculata, Isochrysis galbana and Chlorella fusca, were supplemented to the diet of laying

9 Only supplementation of Chlorella gave rise to mainly alpha-linolenic acid enric

10 In Chlorella grown in sediments spiked with BaP, in 12 h th

11 ern cottonwood, peanut, salt marsh grass and Chlorella have been transformed with these genes.

12 only known host is a eukaryotic green alga (Chlorella heliozoae) that is an endosymbiont of the heli

13 uences from three green algal endosymbionts (Chlorella heliozoae, Chlorella variabilis and Micractini

14 we conclude that Prototheca is an apoplastic Chlorella (i.e., an alga) and that Dictyostelium as well

15 lipid species of two microalgae strains, Kyo-Chlorella in tablet form and Nannochloropsis in paste fo

16 aliella strains plus strains of Arthrospira, Chlorella, Isochrysis, Tetraselmis and a range of cultur

17 ved phenomenon extends to other green algae (Chlorella kesslerii and Scenedesmus obliquus) and at lea

18 a chlorella virus 1 (PBCV-1) infects certain chlorella-like green algae and encodes a 120-kDa protein

19 rming viruses that infect certain eukaryotic chlorella-like green algae from the genus Chlorovirus.

20 se genome of the virus PBCV-1 that infects a chlorella-like green algae revealed an open reading fram

21 large double-stranded DNA virus that infects chlorella-like green algae.

22 replicate in certain unicellular, eukaryotic chlorella-like green algae.

23 replicate in certain unicellular, eukaryotic chlorella-like green algae.

24 rming viruses that infect certain eukaryotic chlorella-like green algae.

25 ne loss also characterized the Chlamydomonas/Chlorella lineage, a phenomenon that might be independen

26 sis genes were found in the Nannochloropsis, Chlorella, or Chlamydomonas genomes.

27 Q)-based quantitative proteomics to identify Chlorella proteins with modulated expression under short

28 esh water microalgae (Chlorella vulgaris and Chlorella protothecoides) important for nutritional appl

29 lated in higher plants and in the green alga Chlorella protothecoides.

30 r to RDIs in almost all algal samples except Chlorella pyrenoidosa (C) and Palmaria palmata (D), wher

31 rations between various NPs and algal cells (Chlorella pyrenoidosa) and analyzed influencing factors

32 ynechococcus lividus], and eucaryotic algae (Chlorella pyrenoidsa, Chlorella vulgaris, Euglena gracil

33 tivity during the life cycle of synchronized Chlorella sorokiniana cells grown with a 7:5 light-dark

34 Chlorella sorokiniana has seven ammonium-inducible, chlo

35 bunits and a truncated mutant subunit of the Chlorella sorokiniana NADP-GDH isozymes were constructed

36 d that most of the kinetic properties of the Chlorella sorokiniana NADP-GDH isozymes were retained af

37 pumilus ES4 on growth of the green microalga Chlorella sorokiniana UTEX 2714 were studied.

38 d experiment in flat-panel photobioreactors, Chlorella sorokiniana was able to remove 100% of the pho

39 suggests that BaP does not aggregate inside Chlorella sp. (average brightness = 5.330), while it agg

40 t Paramecium bursaria and the algal symbiont Chlorella sp. [10].

41 that BaP accumulates in the lipid bodies of Chlorella sp. and that there is Forster resonance energy

42 ents were conducted with Scenedesmus sp. and Chlorella sp. in the presence and absence of carbonate a

43 irus that infects the unicellular green alga Chlorella sp. strain NC64A.

44 d the localization and aggregation of BaP in Chlorella sp., a microalga that is one of the primary pr

45 samples from three strains: Scenedesmus sp., Chlorella sp., and Nannochloropsis sp.

46 interacting with single-celled green algae, Chlorella sp., have been found to be bilateral.

47 rgy transfer between BaP and photosystems of Chlorella sp., indicating the close proximity of the two

48 such as milk, egg, fish, rice, soybean, pea, chlorella, spirulina, oyster and mussel.

49 ae which may serve to improve performance of Chlorella spp. for biotechnological applications.

50 Annotation of the virus host Chlorella strain NC64A genome revealed 482 putative tran

51 tent is highly variable among the members of Chlorella, suggesting very high rates of gain and/or los

52 nd beta-subunit antigens during induction in Chlorella, the larger mRNA is proposed to encode the lar

53 en algal endosymbionts (Chlorella heliozoae, Chlorella variabilis and Micractinium conductrix).

54 ell as 7- and 8-heptadecene were detected in Chlorella variabilis NC64A (Trebouxiophyceae) and severa

55 ed data were compared to PBCV-1 and its host Chlorella variabilis NC64A predicted proteomes.

56 eactivity to antigens from four other algae: Chlorella variabilis, Coccomyxa subellipsoidea, Nannochl

57 Paramecium bursaria chlorella virus (PBCV-1) is a large double-stranded DNA

58 Paramecium bursaria chlorella virus (PBCV-1) is the prototype of a family of

59 Paramecium bursaria chlorella virus (PBCV-1) is the prototype of a family of

60 capsid protein (Vp54) of Paramecium bursaria chlorella virus (PBCV-1) were recently described and fou

61 gue for T4-pdg has been found in a strain of Chlorella virus (strain Paramecium bursaria Chlorella vi

62 us to the chlorovirus Acanthocystis turfacea chlorella virus 1 (ATCV-1) in a metagenomic analysis of

63 he prototype chlorovirus Paramecium bursaria chlorella virus 1 (PBCV-1) contains four Asn-linked glyc

64 Paramecium bursaria chlorella virus 1 (PBCV-1) elicits a lytic infection of

65 The 331-kbp chlorovirus Paramecium bursaria chlorella virus 1 (PBCV-1) genome was resequenced and an

66 Paramecium bursaria chlorella virus 1 (PBCV-1) infects certain chlorella-lik

67 Paramecium bursaria chlorella virus 1 (PBCV-1) is the prototype of a family

68 Paramecium bursaria chlorella virus 1 (PBCV-1), a large DNA virus that infec

69 Paramecium bursaria chlorella virus 1 (PBCV-1), a member of the family Phyco

70 rototype of the genus is Paramecium bursaria chlorella virus 1 (PBCV-1).

71 1 and eukaryotic viruses Paramecium bursaria Chlorella virus 1 and adenovirus, suggesting a viral lin

72 ltransferase (vSET) from Paramecium bursaria chlorella virus 1 bound to cofactor S-adenosyl-L-homocys

73 ucture of the homologous Paramecium bursaria chlorella virus 1 Vp54 MCP.

74 e chlorovirus ATCV-1 (Acanthocystis turfacea chlorella virus 1, family Phycodnaviridae) and that thes

75 94-aa protein encoded by Paramecium bursaria chlorella virus 1, is the smallest known protein to form

76 lyltransferase and the crystal structures of Chlorella virus and Candida albicans guanylyltransferase

77 al. show that a DNA glycosylase derived from Chlorella virus and engineered to enhance tissue penetra

78 the RNA triphosphatases of fungi, protozoa, Chlorella virus and poxviruses.

79 eins are absent, causing Paramecium bursaria chlorella virus and the cellular contents to merge, poss

80 olog of this family, the Paramecium bursaria Chlorella virus arginine decarboxylase (cvADC), shares a

81 al results with the crystal structure of the Chlorella virus capping enzyme.

82 yotic topoisomerase II, type II enzymes from chlorella virus completely lack the C-terminal domain.

83 ast cells containing only the 298-amino acid Chlorella virus DNA ligase (a 'minimal' eukaryotic ATP-d

84 Chlorella virus DNA ligase (ChVLig) has pluripotent biol

85 Chlorella virus DNA ligase (ChVLig) is a minimized eukar

86 Chlorella virus DNA ligase (ChVLig) is an instructive mo

87 to study the conformational dynamics of the Chlorella virus DNA ligase (ChVLig), a minimized eukarya

88 ly efficient ligation of RNA-splinted DNA by Chlorella virus DNA ligase (PBCV-1 DNA ligase).

89 roRNA (miRNA) detection method that utilizes Chlorella virus DNA ligase (SplintR((R)) Ligase).

90 enesis the roles of conserved amino acids of Chlorella virus DNA ligase during the third step of the

91 Our findings indicate that Chlorella virus DNA ligase has the potential to affect g

92 Deletion analysis of the 298 amino acid Chlorella virus DNA ligase indicates that motif VI plays

93 Chlorella virus DNA ligase is the smallest eukaryotic AT

94 Chlorella virus DNA ligase is the smallest eukaryotic AT

95 KDAEAT(196)) in the nick joining reaction of Chlorella virus DNA ligase, an exemplary ATP-dependent e

96 eting Lig1 to the mitochondria or expressing Chlorella virus DNA ligase, the minimal eukaryal nick-se

97 In contrast, fungi and Chlorella virus encode monofunctional guanylyltransferas

98 f the family members resemble the fungal and Chlorella virus enzymes, which have a complex active sit

99 oding R.CviJI was cloned from the eukaryotic Chlorella virus IL-3A and expressed in Escherichia coli.

100 M x CviJI [RGmC(T/C/G)] produced by another chlorella virus IL-3A.

101 The Chlorella virus ligase binds to a nicked ligand containi

102 The domain structure of Chlorella virus ligase inferred from the solution experi

103 We find that the minimal Chlorella virus ligase is capable of catalyzing non-homo

104 phate moiety is essential for the binding of Chlorella virus ligase to nicked DNA.

105 The Chlorella virus ligase-adenylate intermediate has an int

106 ide effect is observed for bacterial LigA or Chlorella virus ligase.

107 cium bursaria chlorella virus-1 (PBCV-1) and chlorella virus Marburg-1 (CVM-1) displays an extraordin

108 cium bursaria chlorella virus-1 (PBCV-1) and chlorella virus Marburg-1 (CVM-1) topoisomerase II to re

109 Therefore, topoisomerase II from Chlorella virus Marburg-1 (CVM-1), a distant family memb

110 III) typical of C5 MTases, but, like another chlorella virus MTase M.CviJI, lacks conserved motifs IX

111 gnizing the dinucleotide GpC was cloned from Chlorella virus NYs-1 and expressed in both Escherichia

112 A nicking and modification system encoded by chlorella virus NYs-1 is described.

113 log of T4 endonuclease V was identified from chlorella virus Paramecium bursaria chlorella virus-1 (P

114 Such a pdg was identified in the Chlorella virus PBCV-1 and termed Cv-pdg.

115 Chlorella virus PBCV-1 DNA ligase seals nicked DNA subst

116 Chlorella virus PBCV-1 DNA ligase seals nicked duplex DN

117 We report that Chlorella virus PBCV-1 encodes a 298-amino-acid ATP-depe

118 We report that the A103R protein of Chlorella virus PBCV-1 is an mRNA capping enzyme that ca

119 e 298-amino acid ATP-dependent DNA ligase of Chlorella virus PBCV-1 is the smallest eukaryotic DNA li

120 Chlorella virus PBCV-1 topoisomerase II is the only func

121 xyuridine triphosphatase (dUTPase) gene from chlorella virus PBCV-1 was cloned, and the recombinant p

122 Like the prototype chlorella virus PBCV-1, the SC-1A genome contains invert

123 nsic DNA cleavage activity was isolated from Chlorella virus PBCV-1.

124 one of the major capsid glycoproteins of the Chlorella virus PBCV-1.

125 e known for T4-pdg, homology modeling of the Chlorella virus pyrimidine dimer glycosylase (cv-pdg) pr

126 ytic mechanism has been investigated for the Chlorella virus pyrimidine dimer glycosylase (cv-pdg).

127 sent the biochemical characterization of the chlorella virus pyrimidine dimer glycosylase, cv-PDG.

128 Chlorella virus RNA triphosphatase (cvRtp1) is the small

129 ate the proposal that protozoan, fungal, and Chlorella virus RNA triphosphatases belong to a single f

130 it a yeast-based genetic system to show that Chlorella virus RTP can function as a cap-forming enzyme

131 Chlorella virus RTP is more similar in structure to the

132 The 193-amino-acid Chlorella virus RTP is the smallest member of a family o

133 Chlorella virus SC-1A encodes at least six DNA methyltra

134 ggest that the high DNA cleavage activity of chlorella virus topoisomerase II on unmodified nucleic a

135 intrinsic to the viral enzyme and imply that chlorella virus topoisomerase II plays a physiological r

136 e whether methylation impacts the ability of chlorella virus topoisomerase II to cleave DNA, the effe

137 s critical to the physiological functions of chlorella virus topoisomerase II, then this remarkable c

138 Paramecium bursaria Chlorella virus type 1 (PBCV-1) is a very large, icosahe

139 al, internally enveloped Paramecium bursaria chlorella virus was used to interpret structures of the

140 resolved by ectopic expression of a foreign (Chlorella virus) but not endogenous topo II.

141 ctures of the eukaryotic Paramecium bursaria Chlorella virus, and the bacteriophage PRD1, and shows a

142 Topoisomerase II from Paramecium bursaria chlorella virus-1 (PBCV-1) and chlorella virus Marburg-1

143 pothesis, the ability of Paramecium bursaria chlorella virus-1 (PBCV-1) and chlorella virus Marburg-1

144 e prototypic chlorovirus Paramecium bursaria chlorella virus-1 (PBCV-1) that functioned as binding pa

145 ase II was discovered in Paramecium bursaria chlorella virus-1 (PBCV-1) that has an exceptionally hig

146 ied from chlorella virus Paramecium bursaria chlorella virus-1 (PBCV-1).

147 Paramecium bursaria Chlorella virus-1 is an icosahedrally shaped, 1,900-A-di

148 he C-terminal residue of Paramecium bursaria chlorella virus-1 topoisomerase II as determined by BLAS

149 at have either p6 (as in Paramecium bursaria Chlorella virus-1) or p3 symmetry (as in Mimivirus).

150 Chlorella virus (strain Paramecium bursaria Chlorella virus-1), which contains a gene that predicts

151 (d) Many chlorella virus-encoded proteins are either the smallest

152 tosine-5-DNA methyltransferase cloned from a Chlorella virus.

153 somerase II gene is widely distributed among Chlorella viruses and that the protein is expressed 60-9

154 To this point, the genomes of many chlorella viruses contain high levels of N6-methyladenin

155 Notably, paramecium bursaria chlorella viruses encode a conserved SET domain methyltr

156 Large dsDNA-containing chlorella viruses encode a pyrimidine dimer-specific gly

157 (e) Accumulating evidence indicates that the chlorella viruses have a very long evolutionary history.

158 In addition to their large genome size, the chlorella viruses have other features that distinguish t

159 The chlorella viruses have other features that distinguish t

160 nes were cloned and expressed from two other chlorella viruses IL-3A and SH-6A.

161 he pdg gene was cloned and sequenced from 42 chlorella viruses isolated over a 12-year period from di

162 Unlike the chlorella viruses, large double-stranded-DNA-containing

163 ke proteins were isolated from 40 additional chlorella viruses.

164 omers, M x CviRI and M x CviBIII, from other chlorella viruses.

165 elmis chuii) and two fresh water microalgae (Chlorella vulgaris and Chlorella protothecoides) importa

166 in a simple food web consisting of the algae Chlorella vulgaris and daphnid Daphnia magna.

167 Two commonly used algal strains, fresh-water Chlorella vulgaris and seawater Tetraselmis chuii, were

168 plastid genomes, only that of the green alga Chlorella vulgaris appears to share this feature.

169 Vitamin B12 was extracted from Chlorella vulgaris biomass under aqueous conditions, par

170 oceanica CCAP 849/10 and a marine isolate of Chlorella vulgaris CCAP 211/21A as the best lipid produc

171 In conclusion, the data proved that Chlorella vulgaris cell can be used as a new stable carr

172 onclusively the presence of selenocyanate in Chlorella vulgaris culture medium by electrospray mass s

173 this system by directly observing changes in Chlorella vulgaris genotype frequencies as the abundance

174 The green microalga Chlorella vulgaris has been widely recognized as a promi

175 he photosynthetic activity of the green alga Chlorella vulgaris in presence of different multiwalled

176 quantification method for cellular lipids in Chlorella vulgaris is demonstrated in this study.

177 Chlorella vulgaris NR mRNA levels are very responsive to

178 Experiments with the green alga Chlorella vulgaris presented here compared polyphosphate

179 n and Se removal from the water column was a Chlorella vulgaris strain (designated Cv).

180 rostatic interaction with negatively charged Chlorella vulgaris upon CO2-treatment.

181 Total protein measured in Chlorella vulgaris using this method compared closely wi

182 n (BOF) in a genome-scale metabolic model of Chlorella vulgaris UTEX 395 over time.

183 this, the accuracy of a model developed for Chlorella vulgaris was assessed against data collected f

184 ntents and water on the Raman spectrogram of Chlorella vulgaris were also addressed.

185 Here we show that novel microalgal strains (Chlorella vulgaris YSL01 and YSL16) upregulate the expre

186 ccessfully encapsulated in algae (Alg) cell (Chlorella vulgaris) as confirmed by fluorescence microsc

187 hermore, detection of individual algal cell (Chlorella vulgaris) was performed at the SERS substrate

188 s in different microalgae samples, including Chlorella vulgaris, Dunaliella salina, and Phaeodactylum

189 and eucaryotic algae (Chlorella pyrenoidsa, Chlorella vulgaris, Euglena gracilis, Scenedesmus obliqu

190 ated thermal tolerance in the phytoplankton, Chlorella vulgaris.