ライフサイエンスコーパス: heterotrophic

1 Pyrinomonas methylaliphatogenes, an aerobic heterotrophic acidobacterium isolated from New Zealand v

2 e results confirmed the potential of using a heterotrophic acidophile to facilitate the rapid commiss

3 microbial communities enriched for versatile heterotrophic Alpha- and Gammaproteobacteria.

4 omes inferring that these Archaea are organo-heterotrophic and autotrophic acetogens.

5 Multifarious heterotrophic and autotrophic microbes and plants have b

6 rous studies to measure the contributions of heterotrophic and autotrophic N2-producing metabolisms (

7 etween habitats but also as a bridge between heterotrophic and chemoautotrophic symbiosis for the gia

8 d sand content and the presence of microbial heterotrophic and nitrifying communities partially expla

9 phy metabolism classifies these strains into heterotrophic and obligately or facultatively autotrophi

10 s Rhodobacter sphaeroides can switch between heterotrophic and photosynthetic growth.

11 or a range of biosynthetic processes in both heterotrophic and photosynthetic tissues.

12 own metabolic behaviour of tomato leaf under heterotrophic and phototrophic conditions.

13 However, flowers, which are heterotrophic and relatively short-lived, may not be con

14 erences in the metabolic state of the North (heterotrophic) and South (autotrophic) Atlantic oligotro

15 predicts phenotypes under photoautotrophic, heterotrophic, and mixotrophic conditions.

16 ively, corresponding research has focused on heterotrophic, anodic EABs.

17 Heterotrophic Bacillus amyloliquefaciens associated with

18 data showed also a significant reduction of heterotrophic bacteria (36 degrees C) in 6/11 (55%) site

19 f monochloramine disinfection on Legionella, heterotrophic bacteria (36 degrees C), Pseudomonas aerug

20 9), but here we demonstrate that many marine heterotrophic bacteria also produce DMSP, probably using

21 However, diel cycles in naturally occurring heterotrophic bacteria and archaea have rarely been obse

22 ivities and interactions between anammox and heterotrophic bacteria and offer the first transcription

23 We investigated the relative role of heterotrophic bacteria and phytoplankton in P cycling by

24 persistent or increased cellular activity of heterotrophic bacteria and protists in the BW, which was

25 uptake rates of individual microbial groups (heterotrophic bacteria and the phytoplankton groups Syne

26 o examine the gene expression of anammox and heterotrophic bacteria and to identify their potential i

27 Some heterotrophic bacteria are able to oxidize sulfide (H2 S

28 Heterotrophic bacteria associated with microphytoplankto

29 Finally, our data indicate that heterotrophic bacteria can feed on the exoproteome of Sy

30 lipid production was significantly higher in heterotrophic bacteria compared with cyanobacterial phyt

31 Many heterotrophic bacteria contain sulfide:quinone oxidoredu

32 in the mode of polysaccharide utilization by heterotrophic bacteria during the course of a diatom-dom

33 Heterotrophic bacteria exploit diverse microhabitats in

34 s to recover 17 draft genomes of anammox and heterotrophic bacteria from a laboratory-scale anammox b

35 ditions, lactic acid bacteria and endogenous heterotrophic bacteria grew better.

36 rocesses can occur through biodegradation by heterotrophic bacteria growing on other organic wastewat

37 Comparatively, heterotrophic bacteria had a dual role in the anoxic pha

38 These findings indicate that heterotrophic bacteria have a uniquely P-oriented physio

39 expression of sulfonate catabolism genes in heterotrophic bacteria highlights active cycling of sulf

40 the more studied set-up, the anode contains heterotrophic bacteria in anaerobic conditions, capable

41 Heterotrophic bacteria in pelagic marine environments ar

42 Heterotrophic bacteria inactivation mirrored the trend i

43 and/or lower (BZ) degradation pathways, and heterotrophic bacteria involved indirectly in processing

44 Heterotrophic bacteria likely experience C-limitation wh

45 , we describe the growth of eight strains of heterotrophic bacteria on a variety of soluble and insol

46 of photosynthetic algae or cyanobacteria and heterotrophic bacteria or fungi are pervasive throughout

47 ce ocean is a result of de novo synthesis by heterotrophic bacteria or via modification of closely re

48 Biovolume normalized heterotrophic bacteria P uptake rate per cell (amol P mu

49 r, little is known about the functional role heterotrophic bacteria play in anammox granules.

50 showed that marine Thaumarchaeota and select heterotrophic bacteria produce cobalamin.

51 The adsorption of Fe colloids onto heterotrophic bacteria Pseudomonas aureofaciens produced

52 ustering of carotenoid biosynthetic genes in heterotrophic bacteria show that a non-clustered genome

53 emolithoautotrophic life support a 'belt' of heterotrophic bacteria significantly different from the

54 es, is cycled into the environment by marine heterotrophic bacteria using largely uncharacterized mec

55 greater than phytoplankton uptake rates, and heterotrophic bacteria were responsible for generally gr

56 We found that heterotrophic bacteria were the dominant consumers of P

57 Thus, the approaches applied to engineering heterotrophic bacteria will need to be revised for the c

58 The data demonstrated that heterotrophic bacteria with SQR and PDO can rapidly oxid

59 sulfite, providing the foundation for using heterotrophic bacteria with SQR and PDO for sulfide bior

60 ed SAR11, the ocean's most abundant clade of heterotrophic bacteria(16,17).

61 involved phytoplankton, particle-associated heterotrophic bacteria, and NADH-oxidizing enzymes.

62 Other groups, such as heterotrophic bacteria, may be relatively resilient to c

63 is the remineralization of algae biomass by heterotrophic bacteria, most notably during massive mari

64 promoting function in type IV pili-producing heterotrophic bacteria.

65 idetes but modified in other phyla of marine heterotrophic bacteria.

66 eria and well-studied type IV pili-producing heterotrophic bacteria.

67 om marine macroalgae and nutrient source for heterotrophic bacteria.

68 e response in cyanobacteria as starvation in heterotrophic bacteria.

69 titute an important energy source for marine heterotrophic bacteria.

70 compounds that fuel secondary production by heterotrophic bacteria.

71 e incomplete carbon oxidation metabolisms in heterotrophic bacteria.

72 uctured differently in cyanobacteria than in heterotrophic bacteria.

73 R11 clade, the most abundant group of marine heterotrophic bacteria.

74 N2 fixation and heterotrophic bacterial activity increased up-to tenfold

75 Furthermore, heterotrophic bacterial clades common to both ecosystems

76 to assess the effect of pCO(2) enrichment on heterotrophic bacterial community composition and metabo

77 the bloom-stage dependent composition of the heterotrophic bacterial community.

78 es of eukaryotic phytoplankton producers and heterotrophic bacterial consumers in the North Pacific S

79 obiont, especially between Trichodesmium and heterotrophic bacterial epibionts.

80 lication cycles in both photoautotrophic and heterotrophic bacterial hosts.

81 phosphorus lipids is well documented in some heterotrophic bacterial lineages, phosphorus-free lipid

82 ata from approximately 100 13C-MFA papers on heterotrophic bacterial metabolisms.

83 s may affect the function and composition of heterotrophic bacterial populations.

84 gion surrounding marine phytoplankton cells, heterotrophic bacterioplankton transform a major fractio

85 of marine primary production transformed by heterotrophic bacterioplankton within hours to weeks of

86 hat is, cyanobacteria and prasinophytes, and heterotrophic bacterioplankton, such as SAR11 and SAR116

87 cently described acidophilic, iron-oxidizing heterotrophic bacterium Acidithrix ferrooxidans grown in

88 d adriaticol, produced by the aerobic marine heterotrophic bacterium Eudoraea adriatica Phylogenetic

89 odel system and found that the presence of a heterotrophic bacterium induced a potential recognition

90 Prochlorococcus and the dominant cooccurring heterotrophic bacterium SAR11 form a coevolved mutualism

91 saccharides of red macroalgae, in the marine heterotrophic bacterium Zobellia galactanivorans.

92 eveal that Ruegeria pomeroyi, a model marine heterotrophic bacterium, can oxidize DMS to DMSO using t

93 Aerobic heterotrophic biofilms in MBBRs demonstrated limited ret

94 ivity of two extracellular enzymes of intact heterotrophic biofilms, beta-glucosidase (carbon-cycling

95 a 44%, 18% and 92% reduction in terrestrial heterotrophic biomass, metabolism, and fertility respect

96 The oligotrophic ocean is neither auto- nor heterotrophic, but functionally diverse.

97 thways while ketocarotenoid biosynthesis and heterotrophic carbon metabolism are upregulated.

98 uantified the lymphatic flow index following heterotrophic cardiac transplantation in a murine model

99 but plays a fundamental role in roots and in heterotrophic cells of the AP.

100 ipid renovation is a common strategy used by heterotrophic cells to reduce their requirement for phos

101 dehydrogenase (GAPCp) in photosynthetic and heterotrophic cells.

102 rient limited, the secondary productivity by heterotrophic communities is inherently carbon limited.

103 Microbial carbon oxidation by heterotrophic communities is likely to play an important

104 Our results suggest that the assembly of heterotrophic communities that degrade complex organic m

105 cycles driven by interacting autotrophic and heterotrophic communities.

106 Therefore, phytoplankton and heterotrophic community dynamics are important in modell

107 dynamics, it can more directly constrain the heterotrophic component of Rs, but global-scale models t

108 nine different autotrophic, mixotrophic, and heterotrophic conditions during nutrient-replete growth

109 of algae under autotrophic, mixotrophic, and heterotrophic conditions using metabolic flux analysis a

110 Under heterotrophic conditions, carbohydrate oxidation inside

111 e and succinate dehydrogenase is small under heterotrophic conditions, indicating that the newly disc

112 phase organic carbon oxidation indicate that heterotrophic consumption of oxidants could maintain the

113 dies that did not control for the effects of heterotrophic consumption.

114 ethod is a repetitive procedure for one-week heterotrophic cultivation, staining intracellular lipids

115 Heterotrophic cultures accumulated TAG and starch during

116 respiration, associated with production, and heterotrophic decomposition.

117 climate change if permafrost thaw increases heterotrophic decomposition.

118 rticular, notable differences emerged in the heterotrophic degrader communities in our microcosms; on

119 Heterotrophic denitrification and dissimilatory nitrate

120 Heterotrophic denitrification consists of the four-step

121 d nitrification-coupled denitrification) and heterotrophic denitrification in six soils (alkaline vs.

122 The experiments showed that heterotrophic denitrification was a negligible source of

123 In acid soils, however, heterotrophic denitrification was the main source for N2

124 cycling processes, including autotrophic and heterotrophic denitrification, anammox, ammonia oxidatio

125 o give rise to variable ratios of anammox to heterotrophic denitrification, providing a mechanism for

126 for nitrogen was in the range determined for heterotrophic denitrification, with only the absence of

127 se (Nar), which is generally prevalent among heterotrophic denitrifiers and is considered as the domi

128 pathways) and the N2O production pathway by heterotrophic denitrifiers to describe and provide insig

129 Transcripts associated with autotrophic and heterotrophic denitrifiers were mostly confined to the s

130 brated with data from batch experiments with heterotrophic denitrifying communities, where reduction

131 octiluca) is a cosmopolitan red tide forming heterotrophic dinoflagellate.

132 100% of dispersed oil in surface waters when heterotrophic dinoflagellates are abundant or bloom.

133 on of faecal pellets containing crude oil by heterotrophic dinoflagellates could contribute to the si

134 study indicates that crude oil ingestion by heterotrophic dinoflagellates is a noteworthy route by w

135 found after an oil spill (1 muL L(-1)), the heterotrophic dinoflagellates Noctiluca scintillans and

136 crude oil droplets (1-86 mum in diameter) by heterotrophic dinoflagellates, major components of marin

137 to chemical cues from copepods, ciliates and heterotrophic dinoflagellates, respectively, under nutri

138 more sensitive to toxic shocks than anodic, heterotrophic EABs.

139 x and wane, and often production cannot meet heterotrophic energy needs.

140 up by Trichodesmium or primarily consumed by heterotrophic epibiont bacteria that ultimately transfer

141 crose-secreting Synechococcus elongatus with heterotrophic Escherichia coli K-12, Escherichia coli W,

142 ce for this trade-off across a wide range of heterotrophic eukaryotes from unicellular nanoflagellate

143 on is sedimentation because it impedes coral heterotrophic feeding and their ability to photosynthesi

144 n or whether ingesting microplastics affects heterotrophic feeding in corals is unknown.

145 doubling the number of available samples of heterotrophic flagellate mitochondrial genomes.

146 by mycorrhizal partners during the initially heterotrophic gametophyte and early sporophyte stages of

147 n, and sulfur-cycling metabolisms, including heterotrophic genera Halolactibacillus, Vibrio, Marinoba

148 trophic (flag leaf), mixotrophic (ears), and heterotrophic (grains and roots) organs.

149 trophic planktonic growth to light-activated heterotrophic growth and biofilm initiation, knockout of

150 f the DeltandbC mutant under light-activated heterotrophic growth conditions but not under mixotrophy

151 calculated for autotrophic, mixotrophic and heterotrophic growth conditions, as well as knockout con

152 echanism in this bacterium under aerobic and heterotrophic growth conditions.

153 me SUP05 also have the genetic potential for heterotrophic growth, raising questions about the roles

154 yanobacteria capable of both autotrophic and heterotrophic growth, with support from structural three

155 the medium for photoautotrophic and 13% for heterotrophic growth.

156 ersion demonstrate strain PS1's capacity for heterotrophic growth.

157 from autotrophic respiration in wet years to heterotrophic in dry years.

158 icrobial metabolic pathways or dilution with heterotrophic isotope signals.

159 y of transition from a photoautotrophic to a heterotrophic life history.

160 Metabolic modelling predicted an aerobic heterotrophic lifestyle for the chlamydia, which were fo

161 Metabolic reconstruction indicates a heterotrophic lifestyle with conspicuous nutritional def

162 d in uptake of sugar and peptide perhaps for heterotrophic lifestyle.

163 e range and controls on the stoichiometry of heterotrophic marine bacteria will help improve understa

164 nderlying biochemical allocation patterns of heterotrophic marine bacteria.

165 tegy and elemental composition among taxa of heterotrophic marine bacteria.

166 ollow the 1:1 relationship characteristic of heterotrophic, marine denitrification.

167 Leaves are derived from heterotrophic meristem tissue that, at some point, must

168 psulate critical segments of autotrophic and heterotrophic metabolic pathways; they are functionally

169 When cells that were adapted to heterotrophic metabolism are shifted back to light condi

170 plastoquinone reduction confirm an impaired heterotrophic metabolism in the cph2 knockout.

171 totrophs are also fixing respired CO(2) from heterotrophic metabolism of the underlying microbial mat

172 and is degraded at night by BAM3 to support heterotrophic metabolism.

173 ntribution of the phosphoketolase pathway to heterotrophic metabolism.

174 organelles involved in both autotrophic and heterotrophic metabolism.

175 These methanogens are heterotrophic methyl-reducers that use C1-methylated com

176 This proves that lipid (2)H/(1)H ratios of heterotrophic microbes are quantitatively related to cen

177 connecting Prochlorococcus with the 'helper' heterotrophic microbes in its environment.

178 he euphotic zone, it has been suggested that heterotrophic microbes rely largely on solubilized parti

179 roduced was further assimilated by different heterotrophic microbes, demonstrating that the methane-o

180 osm experiments, dispersants did not enhance heterotrophic microbial activity or hydrocarbon oxidatio

181 In contrast, it has been demonstrated that heterotrophic microbial communities in soil are primaril

182 erous surveys of gene and species content in heterotrophic microbial communities, such as those found

183 The phylogenetic composition of the heterotrophic microbial community is depth stratified in

184 d phenomenon and is most often attributed to heterotrophic microbial metabolism for the purposes of n

185 and transcriptionally active autotrophic and heterotrophic microbial populations within low-biomass c

186 inciples that could be exploited to engineer heterotrophic microbiomes.

187 Heterotrophic microorganisms are commonly thought to be

188 n (DOC) is the main energy source for marine heterotrophic microorganisms, but a small fraction of DO

189 to organic matter that fuels the activity of heterotrophic microorganisms, creating intricate metabol

190 Compared to heterotrophic microorganisms, however, the cellular econ

191 focusing on distribution and capabilities of heterotrophic microorganisms.

192 sting of an assemblage of photosynthetic and heterotrophic microorganisms.

193 restrial environments and with single-celled heterotrophic, mixotrophic, and autotrophic protists in

194 as transparent exopolymer particles, enhance heterotrophic N2 fixation, by forming microenvironments

195 abundance of phototrophic, mixotrophic, and heterotrophic nanoflagellates, to ask whether there are

196 -mixed microbial community comprised of four heterotrophic natural isolates, experimentally quantifyi

197 d direct inhibition by nitrite produced from heterotrophic nitrate reduction were the most important

198 d by photosynthetic Cyanobacteria exhibiting heterotrophic nutrition (Calothrix and Chroococcidiopsis

199 xotrophy, the combination of autotrophic and heterotrophic nutrition, is a common trophic strategy am

200 fluxes) as well as experimental treatments (heterotrophic only, etc.).

201 Secondary (i.e., heterotrophic or animal) production is a main pathway of

202 e number of cytochrome c oxidase operons and heterotrophic or diazotrophic capabilities.

203 s predicted distinct proteome demands during heterotrophic or photoautotrophic growth.

204 ohydrates (i.e., glycans) provide carbon for heterotrophic organisms and constitute a carbon sink in

205 cal assimilation from the growth of ordinary heterotrophic organisms.

206 lag leaves, whereas it strongly increased in heterotrophic organs such as grains and roots.

207 In heterotrophic organs, delta(2)H was associated with post

208 direct interspecies electron transfer from a heterotrophic partner bacterium, Geobacter sulfurreducen

209 efit from enrichment at the expense of their heterotrophic partners.

210 ned with expression of a complete TCA cycle, heterotrophic pathways for carbon assimilation, and meth

211 This analysis suggested that competition by heterotrophic perchlorate reducers and direct inhibition

212 tic (Rubisco small subunit RBCS2B [RBCS]) or heterotrophic (phosphate transporter PHT1.2 [PHT]) cell-

213 different trophic modes, i.e., autotrophic, heterotrophic, photoheterotrophic, and mixotrophic modes

214 ods when the gross transport capacity of the heterotrophic plankton community exceeds the supply, dep

215 sotopic steady state have been used to study heterotrophic plant tissues, while nonstationary isotope

216 t of 660 photoautotrophic plants and all the heterotrophic plants are missing plastid-encoded cp-ndh

217 Whether this heterotrophic plasticity affects microplastics ingestion

218 f temperature, oxygen and pH changes through heterotrophic plasticity.

219 ng to the modified protein turnover rates in heterotrophic plastids.

220 EGA and heterotrophic plate counting (HPC) were used to evaluate

221 Leptospira exoproteins primarily function in heterotrophic processes (the processes by which organism

222 extent that the interacting autotrophic and heterotrophic processes are controlled by organisms that

223 Expression of genes involved in unexpected heterotrophic processes includes those with a role in th

224 Extensive heterotrophic processing of plant and soil-derived DOM r

225 on a community of both chemolithotrophic and heterotrophic prokaryotes in an unusual ecosystem isolat

226 lankton production is ultimately consumed by heterotrophic prokaryotes(2).

227 on of solute transporters indicates that the heterotrophic prokaryotic community is geared toward the

228 Heterotrophic Proteobacteria and Actinobacteria were iso

229 ed that both heterocystous cyanobacteria and heterotrophic proteobacteria had the genetic potential f

230 s been inferred in three main groups: select heterotrophic Proteobacteria, chemoautotrophic Thaumarch

231 expressing nifH was primarily represented by heterotrophic Proteobacteria.

232 eukaryotic plankton biodiversity belonged to heterotrophic protistan groups, particularly those known

233 onditions on the distribution of two related heterotrophic protistan lineages in marine plankton, kin

234 many organisms in the environment, including heterotrophic protists (protozoa).

235 factors that structure microbial eukaryotes (heterotrophic protists and fungi) are poorly characteriz

236 anion channelrhodopsins (ACRs), one from the heterotrophic protists labyrinthulea and the other from

237 n among early-branching unicellular Rhizaria-heterotrophic protists that play an important role in tr

238 , distributed across categories expected for heterotrophic protists.

239 r lineages of eukaryotes, mostly free-living heterotrophic protists.

240 The additional CO(2) originated from heterotrophic rather than autotrophic sources, and equat

241 cating that it plays a role predominantly in heterotrophic rather than autotrophic tissues, at least

242 itional barium and sulfate ions derived from heterotrophic remineralization of organic matter.

243 mal adaptation can lead to considerably less heterotrophic respiration (11.6 +/- 7.5%), and hence les

244 ies are the primary factors controlling soil heterotrophic respiration (R(h) ) in warming experiments

245 on ecosystem net primary productivity (NPP), heterotrophic respiration (Rh) and net ecosystem product

246 otal soil respiration, trenched chambers for heterotrophic respiration (Rh), and warmed trenched cham

247 range of microsites, which leads to a PDF of heterotrophic respiration and O(2) consumption among mic

248 on DeltaC(s,tau), which makes use of current heterotrophic respiration and the spatial variability of

249 wed that these high ratios resulted from low heterotrophic respiration and very low daylight autotrop

250 -2005), but at a lower rate due to increased heterotrophic respiration as well as lower productivity

251 fset the erosional carbon loss by increasing heterotrophic respiration implicitly.

252 g different seasons affected autotrophic and heterotrophic respiration in a bryophyte-dominated peatl

253 roduction (NPP), autotrophic respiration and heterotrophic respiration is measured separately, to dev

254 e.g., 2040-2060) as committed emissions from heterotrophic respiration of beetle-killed biomass are b

255 est predicts the measured mass-specific soil heterotrophic respiration rates in soils distributed glo

256 nd compared the simulated mass-specific soil heterotrophic respiration rates with multiple published

257 s about the timing and magnitude of seasonal heterotrophic respiration rates, again reflecting struct

258 imulate soil organic carbon (SOC) losses via heterotrophic respiration remains uncertain, in part bec

259 But as soil erosion and heterotrophic respiration respond differently to a warmi

260 em respiration and larger contributions from heterotrophic respiration than the Healy tundra, both sy

261 cessity to simulate the seasonal patterns of heterotrophic respiration to accurately simulate the net

262 rbon is slowly emitted to the atmosphere via heterotrophic respiration which subsequently feeds back

263 th increasing precipitation, suggesting that heterotrophic respiration will be more sensitive than au

264 ater mixing in the hyporheic zone stimulates heterotrophic respiration, alters organic carbon composi

265 lexity and competing mechanisms driving soil heterotrophic respiration-MAT relationships (e.g., carbo

266 nic matrices and how this ultimately affects heterotrophic respiration.

267 tion, and increased ratios of autotrophic to heterotrophic respiration.

268 soil respiration (RS) and its components of heterotrophic (RH) and rhizospheric (RR) respiration dur

269 ts components, that is, autotrophic (Ra) and heterotrophic (Rh) respiration.

270 s two components [i.e., autotrophic (Ra) and heterotrophic (Rh) respiration] to single global change

271 The persistent but less abundant heterotrophic Rhizobiales bacteria possibly contributed

272 Rubrimentiphilum act as efficient heterotrophic scavengers.

273 ong-term warming were observed regarding the heterotrophic soil CO2 efflux (R10 warmed: 2.31 +/- 0.15

274 As heterotrophic soil microbes are primarily carbon limited

275 Heterotrophic soil microbial respiration-one of the main

276 plore why a similar core model structure for heterotrophic soil respiration remains elusive and how a

277 which sustain the growth of autotrophic and heterotrophic species whose activities may have conseque

278 carbon, which is translocated to the largely heterotrophic SS.

279 o (Solanum lycopersicum) fruits representing heterotrophic storage organs important for agriculture a

280 sistent with the definition of an endogenous heterotrophic succession.

281 d by complete oxidation to carbon dioxide by heterotrophic sulfate-reducing bacteria, which closes th

282 pathways of organic matter oxidation by the heterotrophic SUP05.

283 We show that heterotrophic sycamore (Acer pseudoplatanus L.) cells in

284 biosis arose by displacement of an ancestral heterotrophic symbiosis and a report of pure culture of

285 1) subunit of 2-OGDH in both autotrophic and heterotrophic tissues and suggest that the two E(1) isof

286 equired for sulfide assimilation in specific heterotrophic tissues and that a lack of PPSB activity p

287 may increase sink strength in proliferating heterotrophic tissues by indicating low sugar availabili

288 lopmentally regulated starch turnover within heterotrophic tissues other than dedicated storage organ

289 nthetic processes in leaves, its function in heterotrophic tissues remains unclear.

290 rns in various tissues as well as individual heterotrophic tissues.

291 omocenter formation during the switch from a heterotrophic to a photosynthetically competent state du

292 microbiomes as well as seasonal shifts from heterotrophic to autotrophic microorganisms associated w

293 rming instead causes a persistent shift from heterotrophic to more autotrophic control of the growing

294 Of particular interest is the switch from heterotrophic to photoautotrophic seedling growth, for w

295 ating carbon metabolism and redox balance in heterotrophic tomato fruits, affecting fruit development

296 represents one of the largest and most rapid heterotrophic transformations of organic matter in the e

297 ediments host a large population of diverse, heterotrophic, uncultured microorganisms with unknown ph

298 hotopigment exclusion, we sorted flagellated heterotrophic unicellular eukaryotes from Pacific Ocean

299 as used to build an in silico model to study heterotrophic utilisation of autotroph biomass using ele

300 trated increased total carbon recovery above heterotrophic values associated to mixotrophic assimilat