ライフサイエンスコーパス: microalgae

1 environmental stress responses by eukaryotic microalgae.

2 iological functions in astaxanthin-producing microalgae.

3 the metabolic processes of this and related microalgae.

4 rategies to mediate high lipid production in microalgae.

5 and enhance standard molecular taxonomy for microalgae.

6 cessfully demonstrated for complex lipids in microalgae.

7 hat represent natural aquatic conditions for microalgae.

8 neering of high-biomass/high-triacylglycerol microalgae.

9 nted pathways of anoxic dark fermentation in microalgae.

10 observed effect on the varphiPSII of marine microalgae.

11 including dicots, monocots, lycophytes, and microalgae.

12 m(3) with an associated cost of $0.282/kg of microalgae.

13 l improvement of hydrogen photoproduction in microalgae.

14 arbon footprint of 0.74-1.67 kg of CO2/kg of microalgae.

15 mental performance of biofuels produced from microalgae.

16 portion of total protein in eight species of microalgae.

17 carbon acquisition and utilization in marine microalgae.

18 rs for the mass production of biodiesel from microalgae.

19 eocystis that are cosmopolitan bloom-forming microalgae.

20 ormation and turnover of these organelles in microalgae.

21 ll death in naturally co-occurring competing microalgae.

22 esponsible for nonphotochemical quenching in microalgae.

23 smaller than the overall CO(2) uptake by the microalgae.

24 understand the mechanisms of LD dynamics in microalgae.

25 on temperatures of constituent lipids within microalgae.

26 advanced molecular tools for most eukaryotic microalgae.

27 and one of the most promising capitalizes on microalgae.

28 tion of the mechanism of oil accumulation in microalgae.

29 of unicellular organisms collectively called microalgae.

30 fatty acid synthesis is poorly understood in microalgae.

31 nd new evidence for programmed cell death in microalgae.

32 tabolism encourage the prospects of designer microalgae.

33 nsidered to be a promising method to harvest microalgae.

34 uctivity and quality of oils from industrial microalgae.

35 t physical attachment of the bacteria to the microalgae.

36 ally important dinoflagellate and haptophyte microalgae.

37 abundance, biomass and diversity of benthic microalgae.

38 as pseudocobalamin, a form not bioactive in microalgae.

39 imizing culture methods and screening mutant microalgae.

40 alization and detoxification of Cu in marine microalgae.

41 sed as a reversible coagulant for harvesting microalgae.

42 the carbon assimilation strategy of aquatic microalgae.

43 In microalgae, (1)O(2)-induced transcriptomic changes resul

44 dge on the protective antioxidant network of microalgae, a series of experiments to explore the role

45 Following N deprivation, microalgae accumulate triacylglycerols (TAGs).

46 Many microalgae acquire vitamin B12 from marine prokaryotes.

47 ray-based biosensor system employing diverse microalgae, aiming on the identification of five individ

48 However, microalgae anaerobic biodegradability is limited by thei

49 f 75-95 degrees C was effective at enhancing microalgae anaerobic biodegradability; increasing the me

50 Consumption of microalgae and absorption efficiency were significantly

51 at potential in high-throughput screening of microalgae and also provides valuable information for mo

52 lular polymeric substances (EPS) produced by microalgae and bacteria inhabiting the ice.

53 in antioxidants has arisen in recent years; microalgae and cyanobacteria are potential sources there

54 Microalgae and cyanobacteria are promising organisms for

55 Screening experiments with green microalgae and cyanobacteria showed that all tested gree

56 w innovations in feedstock development (e.g. microalgae and food wastes).

57 human consumer and examines the potential of microalgae and genetically modified crops as future sour

58 e most potent trigger of oil accumulation in microalgae and has been thoroughly investigated.

59 e only clear genetic link to Ci transport in microalgae and is one of only a very few mutants directl

60 volved in C4 acid metabolism in green plants/microalgae and prokaryotes.

61 Eukaryotic microalgae and prokaryotic cyanobacteria are the major c

62 the forces that shaped the genomes of marine microalgae and then discuss some of the metabolic conseq

63 mmary on advances in genetic manipulation of microalgae and thoughts on the future directions of mari

64 c chemical communication between conspecific microalgae and to identify the common traits and ecologi

65 quent air sparging, can also enmesh adjacent microalgae and/or microalgae-modified CNC aggregates, th

66 ing relevant bioenergy genes and pathways in microalgae, and powerful genetic techniques have been de

67 hesion and growth of marine bacteria, fungi, microalgae, and spores of macroalgae.

68 synergy for a systems-level understanding of microalgae, and thereby accelerate the improvement of in

69 Microalgae are a good source of carotenoids that can be

70 lternatives to traditional fossil fuels, and microalgae are a particularly promising source, but impr

71 Microalgae are attracting renewed interest from both the

72 Microalgae are considered a promising platform for the p

73 Microalgae are diverse microorganisms that are of intere

74 al synthesis of value-added natural products microalgae are emerging as a source of sustainable chemi

75 Photosynthetic microalgae are exposed to changing environmental conditi

76 Microalgae are good candidates for toxic metal remediati

77 Microalgae are good crops to produce natural pigments be

78 Most microalgae are obligate photoautotrophs and their growth

79 Within the gel, microalgae are observed to grow in large clusters rather

80 ical mechanisms underlying Se methylation in microalgae are poorly understood.

81 Microalgae are prolific photosynthetic organisms that ha

82 Microalgae are proposed as feedstock organisms useful fo

83 Marine microalgae are the primary producers of EPA/DHA and prom

84 Microalgae are versatile organisms capable of converting

85 While the concept of using microalgae as an alternative and renewable source of lip

86 cial metabolic networks will further promote microalgae as an attractive platform for the production

87 essential to evaluate the true potential of microalgae as an industrial feedstock.

88 ur isotope ((34)S) from its incorporation by microalgae as inorganic sulfate to its biosynthesis and

89 o, inorganic carbon was shown to be fixed in microalgae as the C3 compound phosphoglyceric acid.

90 polymerase from phycodnavirus (which infects microalgae) as the basis of this analysis, as it represe

91 these compounds have the potential to affect microalgae at the base of the pelagic food chain.

92 rainage water was metabolized differently in microalgae, bacteria, and diatoms where it was accumulat

93 technoeconomic, and resource assessments of microalgae-based biofuel production systems have relied

94 historical perspective and path forward for microalgae-based biofuel research and commercialization.

95 Results highlight the promising potential of microalgae-based biofuels compared with traditional terr

96 e investigation of chemical communication in microalgae, because of the relevance of these organisms

97 et both economic and environmental goals for microalgae biodiesel production.

98 the manner in which nitrogen is supplied to microalgae biorefineries will be an important driver of

99 DHA, or both derived from nonanimal sources (microalgae, biotech yeast, and, in the future, biotech p

100 The latter are not genetically modified microalgae, but a product of modified Luria-Delbruck flu

101 eins are found in cyanobacteria, mosses, and microalgae, but have been lost in angiosperms.

102 demonstrates that cpsrp43 deletion in green microalgae can be employed to generate tla mutants with

103 s cerevisiae, E. coli, Bacillus subtilis and microalgae can be used as protein sources, producing up

104 This study demonstrates that microalgae can effectively recover all P and N from anae

105 Microalgae can grow significantly faster than terrestria

106 However, some microalgae can remodel pseudocobalamin to the active cob

107 ng protein assay to measure total protein in microalgae cells that involves little or no extraction o

108 c images showed how the pretreatment damaged microalgae cells, enhancing subsequent anaerobic digesti

109 The marine microalgae, Ceratoneis closterium, Phaeodactylum tricorn

110 mical and immunological terms from two green microalgae, Chlamydomonas reinhardtii and Selenastrum mi

111 Like many microalgae, Chlamydomonas reinhardtii forms lipid drople

112 m and Tetraselmis chuii) and two fresh water microalgae (Chlorella vulgaris and Chlorella protothecoi

113 Microalgae constitute a diverse group of eukaryotic unic

114 As microalgae contain considerable amounts of carotenoids,

115 urred in living cells early in evolution and microalgae contain these important polymers in their cel

116 ving way to a new regime in which eukaryotic microalgae contributed nearly half of all export product

117 ns for biorefineries, for which high-protein microalgae could be used as a feedstock with a possibili

118 Therefore, biological Se methylation by microalgae could significantly contribute to environment

119 While the climate benefits of microalgae cultivation that result from the capture of a

120 le information for monitoring the quality of microalgae culture and determining parameters for the ma

121 enhancing knowledge of the diversity within microalgae culture collections.

122 Nevertheless, further developments in microalgae culture offer a promising alternative lipid s

123 well as pigment and protein concentration in microalgae cultures; and (2) 3D high-resolution imaging

124 Here we use diatom microalgae-derived nanoporous biosilica to deliver chemo

125 are able to accumulate biotoxins produced by microalgae directly from seawater, thus providing useful

126 density and nutrient availability on benthic microalgae (diversity, abundance and biomass) and ecosys

127 evaluate heterogeneous populations of motile microalgae due to the labelling requirements and limited

128 The halotolerant microalgae Dunaliella bardawil accumulates under nitroge

129 enetic affinity with other viruses infecting microalgae (e.g., phycodnaviruses), including those infe

130 conditions such as nitrogen (N) deprivation, microalgae enter cellular quiescence, a reversible cell

131 tion, the prophylactic effect of a Ca-SP and microalgae extract containing cream was superior to that

132 ed copper-sparing mechanism that operates in microalgae faced with copper deficiency is the replaceme

133 At low micromolar concentration, microalgae fixed all silver initially present in solutio

134 using triacylglycerides (TAGs) produced from microalgae for biodiesel feedstocks.

135 ent and sustainable approaches to harvesting microalgae for biofuel production and water treatment.

136 A key advantage of using microalgae for biofuel production is the ability of some

137 prospects for the engineering of oleaginous microalgae for biotechnological applications.

138 Thus, genetic modifications of microalgae for enhancing photosynthetic productivity, an

139 Starving microalgae for nitrogen sources is commonly used as a bi

140 inhardtii, and paves the way for engineering microalgae for production of biofuels and high-value bio

141 igated iron uptake mechanisms in five marine microalgae from different ecologically important phyla:

142 ed ion channels that enable photomobility of microalgae from the genus Chlamydomonas.

143 e coagulation treatment process for removing microalgae from water.

144 C16:4, an FA typical of green microalgae galactolipids, also was a major component of

145 dentify CREs and characterize their roles in microalgae gene regulation.

146 to facilitate further experimental study of microalgae gene regulation.

147 key factors that control the growth rate of microalgae growing photoautotrophically.

148 ge-scale, validated, outdoor photobioreactor microalgae growth model based on 21 reactor- and species

149 ly reduced to 0.90 kWh/m(3) and $0.058/kg of microalgae harvested.

150 quirement and associated carbon footprint of microalgae harvesting reported here do not forfeit the n

151 filtration was demonstrated to be a feasible microalgae harvesting technology allowing for more than

152 scale production of biofuels from cultivated microalgae has gained considerable interest in the last

153 gene, whose occurrence and function in green microalgae has not hitherto been investigated.

154 icle, whose occurrence and function in green microalgae has not hitherto been investigated.

155 Microalgae have great prospects as a sustainable resourc

156 Microalgae have potential to help meet energy and food d

157 Microalgae have reemerged as organisms of prime biotechn

158 This work thus demonstrates that microalgae have the ability to convert C16 and C18 fatty

159 Many microalgae have the ability to produce substantial amoun

160 Microalgae have the potential to revolutionize biotechno

161 Diatoms, a major group of photosynthetic microalgae, have a high biotechnological potential that

162 Eukaryotic microalgae hold great promise for the bioproduction of f

163 e screening and sorting of cyanobacteria and microalgae in a microdroplet platform.

164 f ocean acidification and warming on benthic microalgae in a seagrass community mesocosm experiment.

165 given rise to the introduction of macro and microalgae in food industry.

166 ficulties in growing cyanobacteria and other microalgae in large, open ponds for the production of bi

167 ity and PSI-CEF in the ecological success of microalgae in low-oxygen environments.

168 rated fatty acids producing photoautotrophic microalgae in one study.

169 Flagellated eukaryotic microalgae in particular, like the model organism Chlamy

170 Cell counts revealed a predominance of microalgae in the sediments.

171 After seeding microalgae in the TAPP medium in a solution phase at 15

172 Microalgae include cells derived from a primary endosymb

173 al growth and survival of many bloom-forming microalgae, including climatically important dinoflagell

174 Many microalgae induce an extracellular carbonic anhydrase (e

175 In marine environments, photosymbiosis with microalgae is best known for sustaining benthic coral re

176 Understanding metabolism in live microalgae is crucial for efficient biomaterial engineer

177 ntaminations with natural toxins produced by microalgae is discussed.

178 he physiology and biochemistry of oleaginous microalgae is lacking, especially under nitrogen depriva

179 Using captured CO(2) to grow microalgae is limited by the high cost of CO(2) capture

180 ss the nitrogen from the non-TAG portions of microalgae is recycled.

181 A mechanistic model of microalgae is used to explore the implications of modify

182 lls by diatoms (a large group of unicellular microalgae) is a well established model system for the s

183 nduce the accumulation of triacylglycerol in microalgae, leads to a state of cellular quiescence defi

184 Global maps of the current near-term microalgae lipid and biomass productivity were generated

185 The microalgae lipid productivity results of this study were

186 Compared to microalgae, macroalgae are larger in size, thereby impos

187 Microalgae may be responsible for a large portion of the

188 We review evidence that toxin production by microalgae may yield 'privatised' benefits for individua

189 techniques are being investigated to improve microalgae methane yield.

190 ng of biomass that could harvest the typical microalgae, Microcystis aeruginosa, using a bioflocculan

191 nas reinhardtii is one of the most important microalgae model organisms and has been widely studied t

192 , can also enmesh adjacent microalgae and/or microalgae-modified CNC aggregates, thereby further enha

193 Many eukaryotic microalgae modify their metabolism in response to nutrie

194 h production costs, commercial products from microalgae must command high prices.

195 osystem II efficiency (varphiPSII) in marine microalgae of the Dutch estuarine and coastal waters.

196 udy shows that besides Nannochloropsis other microalgae offer an alternative to current sources for e

197 Microalgae offer great potential for exploitation, inclu

198 Biofilms dominated by microalgae often show remarkable, yet unexplained fine-s

199 Consumption of microalgae oil ensures intake of sterols and carotenoids

200 ach is demonstrated to be suitable for crude microalgae oil from Phaeodactylum tricornutum geneticall

201 er definitely significant and could give the microalgae oils a nutritional added value compared to fi

202 In the microalgae oils an important part of the omega-3 long ch

203 It was shown that microalgae oils from Isochrysis, Nannochloropsis, Phaeod

204 A new route to convert crude microalgae oils using ZrO(2)-promoted Ni catalysts into

205 evelopment is underway to produce fuels from microalgae, one of several options being explored for in

206 Upon nutrient deprivation, microalgae partition photosynthate into starch and lipid

207 Four different omega-3 rich autotrophic microalgae, Phaeodactylum tricornutum, Nannochloropsis o

208 Microalgae play a major role as primary producers in aqu

209 Photosynthetic microalgae play a vital role in primary productivity and

210 ces in molecular and biochemical analyses of microalgae point toward interesting differences in lipid

211 Thus, studying lipid metabolism in microalgae points to new possible avenues of genetic eng

212 The use of this approach for harvesting microalgae presents an advantage to other current method

213 estimated to be 0.23 kWh or $0.029/batch of microalgae processed.

214 Many species of microalgae produce hydrocarbons, polysaccharides, and ot

215 Many unicellular microalgae produce large amounts ( approximately 20 to 5

216 eir transportation fuel requirements through microalgae production, without land resource restriction

217 show the potential for a 10 fold increase in microalgae productivity in genetically modified versus u

218 Occurrence of secondary metabolites in microalgae (protoctista) is discussed with respect to th

219 o investigate PtNP toxicity toward the green microalgae Pseudokirchneriella subcapitata and Chlamydom

220 E. oleoabundans within the trebouxiophycean microalgae, rather than with the Chlorophyceae class, in

221 delineate the role of CaCO3(S) nucleation on microalgae removal.

222 Microalgae represent a promising source of renewable bio

223 Microalgae represent an exceptionally diverse but highly

224 Microalgae represent one of the most promising groups of

225 able than cobalamin to several B12-dependent microalgae representing diverse lineages.

226 ducible CO2-concentrating mechanism (CCM) of microalgae represents an effective strategy to capture C

227 Supplementing these microalgae resulted in increased but different n-3 LC-PU

228 ch for the analysis of pigments in different microalgae samples, including Chlorella vulgaris, Dunali

229 The harvesting of the microalgae Scenedesmus species using a 200 L pilot-scale

230 crowave irradiation, thermal pretreatment of microalgae seems to be scalable.

231 ditions, Chlamydomonas reinhardtii and other microalgae show adaptive changes, such as induction of a

232 high silver amounts remained confined inside microalgae, showing their potential for the bioremediati

233 ity of endolithic stages among bloom-forming microalgae spanning different phyla, some of public heal

234 dy, aroma compounds produced by three marine microalgae species (Crypthecodinium cohnii, Schizochytri

235 into hydrogen is naturally realized by some microalgae species due to a coupling between the photosy

236 been proposed as one of the most attractive microalgae species for biodiesel and biomass production,

237 Recently, large-scale genomic data in microalgae species have become available, which enable t

238 d cyanobacteria showed that all tested green microalgae species successfully grew on anaerobically tr

239 r phenotypes allowed us to differentiate the microalgae species.

240 e and defendable taxonomic identification of microalgae strains is vital for culture collections, ind

241 yed to characterize the lipid species of two microalgae strains, Kyo-Chlorella in tablet form and Nan

242 As the biomass productivity of microalgae strongly depends on the cultivation temperatu

243 nsporters has remained elusive in eukaryotic microalgae such as C. reinhardtii.

244 Marine microalgae support world fisheries production and influe

245 R and the genetic identity of the symbiotic microalgae (Symbiodinium spp.) remained unchanged (type

246 Integrating microalgae systems (MAS) at municipal wastewater treatme

247 For example, microalgae tend to accumulate valuable compounds, such a

248 Marine diatoms are silica-precipitating microalgae that account for over half of organic carbon

249 potent neurotoxin produced by certain marine microalgae that can accumulate in the foodweb, posing a

250 Discovery of heat-tolerant marine microalgae that can synthesize EPA/DHA will solve these

251 ide biogenic habitats colonised by epiphytic microalgae that contribute significantly to community pr

252 llarophyceae) are photosynthetic unicellular microalgae that have risen to ecological prominence in o

253 Diatoms are microalgae that possess so-called "complex plastids," wh

254 Diatoms are eukaryotic microalgae that produce species-specifically structured

255 diatoms, a group of single-celled eukaryotic microalgae that produce their SiO2 (silica)-based cell w

256 As, in microalgae, the molecular mechanisms of this specific P

257 Compared with microalgae, the pace of knowledge acquisition in seaweed

258 on to the different metabolic routes used by microalgae to accumulate oil reserves depending on culti

259 oughout the viridiplantae ranging from green microalgae to bryophyta and pteridophyta, i.e. mosses an

260 lls exploit the ability of cyanobacteria and microalgae to convert light energy into electrical curre

261 chrysis, due to transfer of carotenoids from microalgae to eggs.

262 d demonstrate transcriptional engineering in microalgae to modulate starch biosynthesis.

263 and tightly regulated, the CCM enables these microalgae to respond rapidly to varying environmental C

264 strategy for carbon acquisition that enables microalgae to survive and proliferate when the CO2 conce

265 to understand the adaptations and limits of microalgae to survive changing salinities.

266 udy site, substantiating the hypothesis that microalgae undertake fermentation.

267 ve, in vivo lipid profiling of oil-producing microalgae using single-cell laser-trapping Raman spectr

268 at mediate ion transport across membranes in microalgae (vectorial catalysis).

269 Representative microalgae were grown in batch and continuous cultures u

270 In the absence of grazers, benthic microalgae were negatively and indirectly affected by se

271 Microalgae were reported to contain low amounts of pheno

272 The microalgae were supplemented in two doses: 125 mg and 25

273 a new paradigm on how PGPB promote growth of microalgae which may serve to improve performance of Chl

274 atter in permeable sediments is dominated by microalgae, which as eukaryotes have different anaerobic

275 Diatoms are unicellular microalgae whose cell walls are composed of, amorphous n

276 epresent 6-45% of the energy embedded in the microalgae with a carbon footprint of 0.74-1.67 kg of CO

277 ence species for basic research on oleogenic microalgae with biotechnological relevance.

278 However, targeted mutagenesis in microalgae with CRISPR-Cas9 is limited.

279 the identification of polar lipids in green microalgae with no sample preparation.

280 first time the storage locations of DMSP in microalgae, with high enrichments present in vacuoles, c

281 developed to efficiently culture and harvest microalgae without affecting the productivity as compare

282 to increase lipid accumulation in eukaryotic microalgae without compromising growth.

283 ect growth and metabolic parameters in green microalgae without physical attachment of the bacteria t