ライフサイエンスコーパス: microalgae

1 rge-capacity and rapid-turnover N reserve of microalgae.

2 nted pathways of anoxic dark fermentation in microalgae.

3 suggested to originate from zooplankton and microalgae.

4 nsidered to be a promising method to harvest microalgae.

5 uctivity and quality of oils from industrial microalgae.

6 t physical attachment of the bacteria to the microalgae.

7 ally important dinoflagellate and haptophyte microalgae.

8 abundance, biomass and diversity of benthic microalgae.

9 as pseudocobalamin, a form not bioactive in microalgae.

10 imizing culture methods and screening mutant microalgae.

11 alization and detoxification of Cu in marine microalgae.

12 sed as a reversible coagulant for harvesting microalgae.

13 the carbon assimilation strategy of aquatic microalgae.

14 iological functions in astaxanthin-producing microalgae.

15 the metabolic processes of this and related microalgae.

16 rategies to mediate high lipid production in microalgae.

17 and enhance standard molecular taxonomy for microalgae.

18 cessfully demonstrated for complex lipids in microalgae.

19 hat represent natural aquatic conditions for microalgae.

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

21 observed effect on the varphiPSII of marine microalgae.

22 including dicots, monocots, lycophytes, and microalgae.

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

24 l improvement of hydrogen photoproduction in microalgae.

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

26 mental performance of biofuels produced from microalgae.

27 portion of total protein in eight species of microalgae.

28 carbon acquisition and utilization in marine microalgae.

29 rs for the mass production of biodiesel from microalgae.

30 tically distant microorganisms such as green microalgae.

31 etic biology of these industrially important microalgae.

32 of bioelectricity generated from whole-cell microalgae.

33 timized production of high-value products in microalgae.

34 ellular metabolisms for oil storage in green microalgae.

35 he Haptophyta and Gymnodiniaceae families of microalgae.

36 rom that of higher plants, animals and other microalgae.

37 wish to expand their studies to the realm of microalgae.

38 environmental stress responses by eukaryotic microalgae.

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

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

41 Microalgae accumulate lipids during stress such as that

42 Many microalgae acquire vitamin B12 from marine prokaryotes.

43 n electrochemical immunosensor for the toxic microalgae Alexandrium minutum (A. minutum AL9T) detecti

44 presence of carotenoid esters in prokaryote microalgae, an event that has not been shown so far.

45 However, microalgae anaerobic biodegradability is limited by thei

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

47 Consumption of microalgae and absorption efficiency were significantly

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

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

50 Co-incubations between DMSP-producing microalgae and bacteria revealed an increase in cleavage

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

52 Microalgae and cyanobacteria are promising organisms for

53 Microalgae and cyanobacteria contribute roughly half of

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

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

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

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

58 Eukaryotic microalgae and prokaryotic cyanobacteria are the major c

59 However, these efforts primarily target microalgae and terrestrial plants.

60 r complex physiological interactions between microalgae and their associated bacteria.

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

62 oping planar hydrogel slabs with immobilized microalgae and with bulk optical properties similar to t

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

64 phytoplankton (Cyanobacteria and eukaryotic microalgae) and prokaryotes (bacteria and archaea), 2 mi

65 astic community diversity revealed bacteria, microalgae, and invertebrate groups adhered to debris.

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

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

68 Microalgae are a good source of carotenoids that can be

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

70 Microalgae are a precious source of polyunsaturated fatt

71 Microalgae are a sustainable alternative source of n-3 L

72 Microalgae are considered a promising platform for the p

73 Microalgae are currently considered one of the most prom

74 Microalgae are diverse microorganisms that are of intere

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

76 Photosynthetic microalgae are exposed to changing environmental conditi

77 Microalgae are good candidates for toxic metal remediati

78 Microalgae are good crops to produce natural pigments be

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 However, extensive studies showed that microalgae are rich in lutein content and potentially ex

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

85 Microalgae are versatile organisms capable of converting

86 s species, unicellular industrial oleaginous microalgae, are model organisms for microalgal systems a

87 Our results are promising for using microalgae as a novel, sustainable alternative as a nutr

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

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

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

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

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

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

94 fish oil with evidence of a cost-competitive microalgae-based tilapia feed that improves growth metri

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

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

97 Sixteen different microalgae biomasses were evaluated by both strategies.

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

99 actuation element, a detector element, and a microalgae bioreporter.

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

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

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

103 and to facilitate the cost-effective use of microalgae by the feed industry, in general.

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 e from yellow passion fruit albedo flour and microalgae carotenoid extract presented an average parti

108 Nanoparticles containing microalgae carotenoid extract showed average particle di

109 rial in the production of nanoparticles from microalgae carotenoids can be a polymeric alternative ca

110 extraction is difficult due to the peculiar microalgae cell structure.

111 The disruption of microalgae cell walls by a four-enzyme mixture (Mix) in

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

113 The marine microalgae, Ceratoneis closterium, Phaeodactylum tricorn

114 idated by measuring the lipid composition of microalgae, Chlamydomonas reinhardtii (ChRe) and Euglena

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

116 Microalgae constitute a diverse group of eukaryotic unic

117 As microalgae contain considerable amounts of carotenoids,

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

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

120 er containing a mixed assemblage of cultured microalgae (control), with the addition of ~50 microplas

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

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

123 enhancing knowledge of the diversity within microalgae culture collections.

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

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

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

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

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

129 The halotolerant microalgae Dunaliella bardawil accumulates under nitroge

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

131 highly pigmented biological specimens (e.g., microalgae) enabling interrogation by Raman microspectro

132 Microalgae enriched breads made with chemically acidifie

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

134 and associated trade-offs in a population of microalgae exposed to sublethal concentrations of organi

135 The aim of this study was to use microalgae expressing antiviral dsRNA as a sustainable f

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

137 We report the characterization of microalgae extracts via traveling wave ion mobility-mass

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

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

140 latform enables to measure the variations of microalgae fluorescence as well as oxygen production.

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

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

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

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

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

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

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

148 buted across taxonomically distant groups of microalgae from diverse habitats, from freshwater and ma

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

150 e coagulation treatment process for removing microalgae from water.

151 e-coagulation treatment process for removing microalgae from water.

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

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

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

155 Significant enhancements in microalgae growth were observed with all the tested IONP

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

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

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

159 The motility of microalgae has been studied extensively, particularly in

160 vices, biological-friendly materials such as microalgae have been explored for detecting toxic chemic

161 Microalgae have evolved B(12) dependence on multiple occ

162 Microalgae have great potential as an energy and feed re

163 Microalgae have great prospects as a sustainable resourc

164 Microalgae have potential to help meet energy and food d

165 Microalgae have reemerged as organisms of prime biotechn

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

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

168 Eukaryotic microalgae hold great promise for the bioproduction of f

169 ates the generation of renewable energy from microalgae; however, inadequate electron generation from

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

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

172 ange winners' evolve, we grew populations of microalgae in ameliorated environments for several hundr

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

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

175 rated fatty acids producing photoautotrophic microalgae in one study.

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

177 our understanding of this important class of microalgae in the context of evolution, cell biology, an

178 ely related aquatic and desert-derived green microalgae in the family Scenedesmaceae and capitalized

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

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

181 Microalgae incorporation increased the protein and ash c

182 Many microalgae induce an extracellular carbonic anhydrase (e

183 trogen (N) is an essential macronutrient for microalgae, influencing their productivity, composition,

184 however, inadequate electron generation from microalgae is a significant impediment for functional em

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

186 ntaminations with natural toxins produced by microalgae is discussed.

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

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

189 f how the physiology of high-latitude marine microalgae is regulated over a polar seasonal cycle, wit

190 ate the cellular processes of photosynthetic microalgae leading to transient changes in the productio

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

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

193 The microalgae lipid productivity results of this study were

194 Herein we report the novel concept of a microalgae living biosensor by enhancing photocurrent th

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

196 Microalgae may be responsible for a large portion of the

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

198 linseed oil (LSO) at 4-g/kg each; diet 5 had microalgae meal at 50-g/kg and equal amounts of LSO and

199 techniques are being investigated to improve microalgae methane yield.

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

201 Pathways that involve chemicals, fuels and microalgae might reduce emissions of carbon dioxide but

202 ChRe and EuGr microalgae mixed together in the same solution were diff

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

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

205 Many eukaryotic microalgae modify their metabolism in response to nutrie

206 The marine microalgae Nannochloropsis oceanica (CCMP1779) is a prol

207 Photosynthetic microalgae not only perform fixation of carbon dioxide b

208 Microalgae nutritional and healthy dietary pattern might

209 nd marine free-living forms to endosymbiotic microalgae of reef-building corals (Acropora millepora,

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

211 articular, the mandatory photosymbiosis with microalgae of the family Symbiodiniaceae and its consequ

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

213 Consumption of microalgae oil ensures intake of sterols and carotenoids

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

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

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

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

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

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

220 Microalgae play a major role as primary producers in aqu

221 Photosynthetic microalgae play a vital role in primary productivity and

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

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

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

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

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

227 ay an important role in the digestibility of microalgae proteins.

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

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

230 Jeunesse introduces the group of unicellular microalgae referred to as 'zooxanthellae'.

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

232 lineate the role of CaCO(3(S)) nucleation on microalgae removal.

233 Microalgae represent a promising source of renewable bio

234 Microalgae represent one of the most promising groups of

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

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

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

238 in cleavage pathway expression close to the microalgae's surface.

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

240 ized to achieve maximum lutein recovery from microalgae Scenedesmus sp. biomass.

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

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

243 Finally, the microalgae sensor was exploited to detect various light

244 Marine microalgae sequester as much CO(2) into carbohydrates as

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

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

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

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

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

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

251 r phenotypes allowed us to differentiate the microalgae species.

252 e and used for the selective capture of such microalgae strain.

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

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

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

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

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

258 Microalgae that acquire tolerance allocate resources to

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

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

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

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

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

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

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

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

267 Among the nutritional properties of microalgae, this study is focused in the presence of car

268 arvation, many free-living and endosymbiotic microalgae thrive in N-poor and N-fluctuating environmen

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

270 The capacity of microalgae to advance the limit of technology of nutrien

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

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

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

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

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

276 bility of development of multifunctionalized microalgae to simultaneously produce industrially useful

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

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

279 We combined two commercially available microalgae, to produce a high-performing fish-free feed

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

281 Representative microalgae were grown in batch and continuous cultures u

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

283 Microalgae were reported to contain low amounts of pheno

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

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

286 Diatoms (Bacillariophyta) are ubiquitous microalgae which produce a siliceous exoskeleton and whi

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

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

289 onal responses may provide insights into how microalgae will respond to long-term environmental chang

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

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

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

293 Microalgae with high growth rates have been considered a

294 3D printed bionic corals capable of growing microalgae with high spatial cell densities of up to 10(

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

296 Marine microalgae within seawater and sea ice fuel high-latitud

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

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

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

300 t can be used for early detection of harmful microalgae without the necessity of pre-concentration or