ライフサイエンスコーパス: autotrophic

1 (14) C and delta(13) C into four sources-two autotrophic (above - and belowground plant structures) a

2 t these Archaea are organo-heterotrophic and autotrophic acetogens.

3 c evidence for the Ljungdahl-Wood pathway of autotrophic acetyl-CoA biosynthesis in the methanogenic

4 enzyme activities could be detected in other autotrophic alpha-proteobacteria or in gram-positive met

5 Autotrophic ammonia oxidizing bacteria (AOB) have been r

6 first time highly effective and sustainable autotrophic ammonia removal in a gas biofilter and there

7 Autotrophic ammonium oxidation in membrane-aerated biofi

8 ive tricarboxylic acid cycle, which in these autotrophic anaerobes is the stage for biosynthesis of a

9 In many autotrophic anaerobes, PFOR links the Wood-Ljungdahl pat

10 the last common ancestor of life, a complex autotrophic, anaerobic green bacterium.

11 Citrate synthase activity decreased in autotrophic and acetate-containing cultures compared to

12 pyruvate carboxylase activities increased in autotrophic and acetate-containing cultures.

13 eps of phylloquinone synthesis do not become autotrophic and are seedling lethals, even when grown on

14 hytes of the fern Ceratopteris richardii are autotrophic and develop independently of the diploid spo

15 biogeochemical cycles driven by interacting autotrophic and heterotrophic communities.

16 ange on Reco depends on the responses of its autotrophic and heterotrophic components.

17 CM) from Chlorella vulgaris cultivated under autotrophic and heterotrophic conditions.

18 robial nitrogen cycling processes, including autotrophic and heterotrophic denitrification, anammox,

19 Transcripts associated with autotrophic and heterotrophic denitrifiers were mostly c

20 he microbial fossils, which include putative autotrophic and heterotrophic eukaryotes, are similar to

21 photosynthetic cyanobacteria capable of both autotrophic and heterotrophic growth, with support from

22 nelles that encapsulate critical segments of autotrophic and heterotrophic metabolic pathways; they a

23 re proteinaceous organelles involved in both autotrophic and heterotrophic metabolism.

24 tributed viable and transcriptionally active autotrophic and heterotrophic microbial populations with

25 Mixotrophy, the combination of autotrophic and heterotrophic nutrition, is a common tro

26 To the extent that the interacting autotrophic and heterotrophic processes are controlled b

27 of warming during different seasons affected autotrophic and heterotrophic respiration in a bryophyte

28 How autotrophic and heterotrophic respiration sources respon

29 We quantified the response of autotrophic and heterotrophic respiration to permafrost

30 energy sources, which sustain the growth of autotrophic and heterotrophic species whose activities m

31 rtance of the E(1) subunit of 2-OGDH in both autotrophic and heterotrophic tissues and suggest that t

32 thylakoids, and it is present in plastids of autotrophic and heterotrophic tissues.

33 s and the vital role of microorganisms, both autotrophic and heterotrophic, in the coupled organic-ma

34 aracterization of the DeltapntA mutant under autotrophic and mixotrophic conditions.

35 In this report, we probed carbon flux during autotrophic and mixotrophic growth of the GSB Chlorobacu

36 thetic machinery in Ochromonas danica during autotrophic and mixotrophic growth.

37 llowing: (a) the RTCA cycle is active during autotrophic and mixotrophic growth; (b) the flux from py

38 Overall, growing season fluxes of autotrophic and old soil heterotrophic respiration incre

39 to increased proportional contributions from autotrophic and young soil respiration and decreased pro

40 thanococcus jannaschii, a hyperthermophilic, autotrophic, and strictly hydrogenotrophic inhabitant of

41 e- and quinone-based S(0)-reducing system in autotrophic archaea and bacteria.

42 Autotrophic archaeal and bacterial ammonia-oxidisers (AO

43 ete 1.66-megabase pair genome sequence of an autotrophic archaeon, Methanococcus jannaschii, and its

44 Arsenotrophy, growth coupled to autotrophic arsenite oxidation or arsenate respiratory r

45 tate of the North (heterotrophic) and South (autotrophic) Atlantic oligotrophic gyres, resulting from

46 Autotrophic bacteria convert carbon dioxide (CO(2)) into

47 mes in the carbon-concentrating mechanism of autotrophic bacteria predict the carboxysomal carbonic a

48 Autotrophic bacteria rely on various mechanisms to incre

49 ototypes of the BMCs are the carboxysomes of autotrophic bacteria.

50 in all plants and algae, as well as in some autotrophic bacteria.

51 e host, achieved by expressing genes from an autotrophic bacterium in an Escherichia coli strain engi

52 protein isolated from the ammonia-oxidizing autotrophic bacterium Nitrosomonas europaea, is shown to

53 Dominating the active community are four autotrophic beta-proteobacterial genera that are capable

54 However, autotrophic biological treatment is most environmentally

55 Directly observing autotrophic biomass at ecologically relevant frequencies

56 h whole-community chlorophyll a, a proxy for autotrophic biomass, suggest that ecological selection v

57 ize that altered mycorrhizal communities and autotrophic C inputs have led to positive 'priming' of s

58 approach to this question by quantifying the autotrophic carbon budget in 16 forest plots along a 330

59 ariaco Basin nitrogen cycle is influenced by autotrophic carbon cycling in addition to organic matter

60 Autotrophic carbon dioxide (CO(2) ) fixation by microbes

61 l microbes contain the genetic potential for autotrophic carbon fixation spreading over broad taxonom

62 er, no information exists on what pathway of autotrophic carbon fixation these bacteria might use.

63 All sediments contain abundant genes for autotrophic carbon fixation used in the Calvin-Benson-Ba

64 At 150 m and below, the potential for autotrophic carbon fixation via rubisco is dominated by

65 and use the reductive acetyl-CoA pathway for autotrophic carbon fixation.

66 that the most common form for deep-branching autotrophic carbon-fixation combines two disconnected su

67 he Proterozoic, possibly because of changing autotrophic carbon-isotope fractionation driven by biolo

68 abundance of culturable hydrogenotrophic and autotrophic cells of the three springs.

69 Autotrophic cells, including phototrophs and chemolithot

70 r parallels with the biochemistry of ancient autotrophic cells, notably the acetyl CoA pathway in arc

71 ultrathin sections that enzymes involved in autotrophic CO(2) assimilation are located in the interm

72 nerates low potential electrons required for autotrophic CO(2) assimilation.

73 f the reductive tricarboxylic acid cycle for autotrophic CO(2) fixation in epsilon-proteobacteria.

74 We further show that autotrophic CO(2) fixation in T. acidiphilum is accompli

75 r activities of the key enzymes of the known autotrophic CO(2) fixation pathways.

76 pyruvate links the Wood-Ljungdahl pathway of autotrophic CO(2) fixation to the reductive tricarboxyli

77 es, or oilfields, these results suggest that autotrophic CO(2) fixation via the reductive tricarboxyl

78 oxysomes (a polyhedral organelle involved in autotrophic CO(2) fixation), suggesting that the S. ente

79 oxidation to aerobic energy conservation and autotrophic CO(2) fixation.

80 entral role in the Wood-Ljungdahl pathway of autotrophic CO(2) fixation.

81 ential importance of mixotrophic rather than autotrophic CO2 fixation pathways in these organisms and

82 d functional analysis attributed most of the autotrophic CO2 fixation to one unique cyanobacterium.

83 xcept for Striga after divergence from their autotrophic common ancestor, suggesting that, in contras

84 f variation in flow regime modifications and autotrophic communities in rivers, it has been challengi

85 This mutant was seedling lethal under autotrophic conditions but could be partially rescued un

86 hic conditions (light and glucose) and under autotrophic conditions in a day/night cycle, which is pr

87 es in the presence of glucose, whereas under autotrophic conditions the mutant did not differ from th

88 1, was able to grow via photosynthesis under autotrophic conditions using H2 as an electron donor and

89 l predictions for cyclic electron flow under autotrophic conditions, and fluxes through the phosphoke

90 l of this transcript increased in high light autotrophic conditions, suggesting that it is involved i

91 genome results in synthetic lethality under autotrophic conditions.

92 of metabolic robustness in self-oscillating autotrophic continuous cultures of the gas-fermenting ac

93 arming with increased respiration, increased autotrophic contributions to ecosystem respiration, and

94 persistent shift from heterotrophic to more autotrophic control of the growing season carbon cycle i

95 appropriate biological process for achieving autotrophic conversion of methane (CH(4)) to methanol (C

96 four subgenera of Cuscuta and ten species of autotrophic Convolvulaceae.

97 representing a 45-60% reduction relative to autotrophic Convolvulaceae.

98 higher than ATP citrate synthase activity in autotrophic cultures.

99 Although it was long considered an autotrophic cyanobacterium, the uptake of organic compou

100 efficiency of anabolism exemplified by this autotrophic cycle perfectly suits the lifestyle of ammon

101 tions probably promoted complete S-oxidizing autotrophic denitrification at the sulfide interface.

102 n situ dark carbon fixation by sulfur-driven autotrophic denitrification in addition to anammox.

103 The use of autotrophic denitrification in microbial fuel cells (MFC

104 ciently reactive reductants that can promote autotrophic denitrification.

105 Additionally autotrophic denitrifiers could have used reduced iron or

106 release and nitrogen removal suggested that autotrophic denitrifiers oxidized Fe(II) sulfides using

107 The solid components are autotrophic denitrifying bacteria, autotrophic perchlora

108 that the FCA-mediated thermal adaptation of autotrophic development allows developing seedlings to c

109 Chlorophyll biosynthesis enables autotrophic development of developing seedlings.

110 shifting the chlorophyll-ROS balance toward autotrophic development.

111 nge, resulting in 289% and 281% increases in autotrophic dissolved inorganic N and P use efficiency (

112 cted using DNA extracted from soil and river autotrophic enrichments, a photosynthetic biofilm and a

113 , ndh genes are truncated or deleted in some autotrophic Epidendroideae orchid cp genomes.

114 ependent micro-organisms that began with the autotrophic eukaryotes.

115 eron was involved in the negative control of autotrophic events, whereas the plasmid operon was invol

116 nt fashion, the trophic activity may be a DA autotrophic factor.

117 ctors supported multiple taxa presumed to be autotrophic Fe(II) oxidizers based on their phylogeny.

118 that the long-term co-existence of multiple autotrophic Fe(II)-oxidizing populations in the reactors

119 The reaction is involved both in the autotrophic fixation of carbon and in the process of met

120 tained from reduced inorganic sulfur to fuel autotrophic fixation of carbon using RuBisCo.

121 70 m and 915 m), carbon derived from in situ autotrophic fixation supported a significant fraction of

122 t influenced the performance of delta(2)H in autotrophic (flag leaf), mixotrophic (ears), and heterot

123 nitrogen, temperature and photosynthesis on autotrophic flux from soils at the ecosystem level.

124 Recent advances in the partitioning of autotrophic from heterotrophic respiration processes in

125 off in allocating biomass to phagotrophy vs. autotrophic functions.

126 e CP43-357K mutation lost their capacity for autotrophic growth and exhibited a drastic reduction in

127 The mutants were not capable of autotrophic growth and produced extremely chlorotic coty

128 ions led us to propose a metabolic model for autotrophic growth by Ca. P. anaerolimi whereby DPO driv

129 cluster, is essential for CO(2) fixation and autotrophic growth by the WLP.

130 veral metabolic pathways in Synechocystis in autotrophic growth conditions without prominent effects

131 germination rate and is unable to establish autotrophic growth due to severe inhibition of cotyledon

132 Our study demonstrates microbial autotrophic growth fully supported by this highly ATP-ef

133 ng tobacco SSU and the Se LSU, allowing slow autotrophic growth in high CO(2) CcmM35 was able to form

134 ere expressed in each case and all permitted autotrophic growth in strains expressing cyt. c-550.

135 When both pathways are disrupted, autotrophic growth is abolished at ambient CO(2) We pres

136 gy and carbon for the growing seedling until autotrophic growth is possible.

137 dicating that RPL15 is an essential gene for autotrophic growth of Arabidopsis thaliana.

138 To learn more about autotrophic growth of methanococci, we isolated nine con

139 Finally, the potential for autotrophic growth of other Pseudonocardia spp. was expl

140 Here, we report autotrophic growth of Shewanella oneidensis MR-1 with ph

141 w and high CO(2) concentrations, and testing autotrophic growth phenotypes of gene deletion strains a

142 which is reflected in the dependence of the autotrophic growth rate on the ammonia concentration.

143 The autotrophic growth rates and maximum concentrations of c

144 Rescue of the DeltarbcL mutation and autotrophic growth stabilizes transgenic plastids in het

145 m, performing comparative transcriptomics of autotrophic growth under low and high CO(2) concentratio

146 In the absence of organic carbon sources, autotrophic growth via the Wood-Ljungdahl (WL) pathway a

147 timum for growth at pH 11 and are capable of autotrophic growth with hydrogen, calcium carbonate and

148 nt undergo photomorphogenesis, which enables autotrophic growth with optimized morphology and physiol

149 ere photosynthetically competent, supporting autotrophic growth, and their respective forms of Rubisc

150 During autotrophic growth, carbon dioxide is incorporated into

151 Whereas plastocyanin is essential for photo-autotrophic growth, copper/zinc superoxide dismutase is

152 delays the transition from heterotrophic to autotrophic growth, possibly due to MG toxicity.

153 d reductive directions for heterotrophic and autotrophic growth, respectively, but the control of car

154 Compared with autotrophic growth, the total pigmentation of O. danica

155 hus making these compounds indispensable for autotrophic growth.

156 naerobic CO(2) fixation for heterotrophic or autotrophic growth.

157 ole in this transition from heterotrophic to autotrophic growth.

158 gative mutant enzyme incapable of supporting autotrophic growth.

159 ion of cellular components but do not permit autotrophic growth.

160 mental conditions during their transition to autotrophic growth.

161 tively, could support photoheterotrophic and autotrophic growth.

162 egative mutant of Rhodobacter sphaeroides to autotrophic growth.

163 obably sugar-fermenting organisms capable of autotrophic growth.

164 reases CO affinity thirty-fold and abolishes autotrophic growth; however, a F229W substitution enhanc

165 the core populations into heterotrophic and autotrophic guilds.

166 e report on pyritized replicas of the iconic autotrophic Gunflintia-Huroniospora microfossil assembla

167 An autotrophic H(2)-oxidizing bacterium fixes CO(2) in dark

168 rocesses themselves form and maintain stable autotrophic habitats on the surface of the Greenland ice

169 ich upon germination develop as free-living, autotrophic haploid gametophyte consisting of a small (<

170 tified, indicating significant plasticity in autotrophic, heterotrophic, and diazotrophic strategies

171 e across four different trophic modes, i.e., autotrophic, heterotrophic, photoheterotrophic, and mixo

172 For example, parasitic plants and autotrophic hosts are similar in delta15N (with no parti

173 e community reveals a carbon cycle driven by autotrophic hydrogen oxidizers belonging to novel genera

174 organic carbon via a modified version of the autotrophic hydroxypropionate/hydroxybutyrate cycle of C

175 on of the total marine archaeal community is autotrophic in situ.

176 idans becoming increasingly displaced by the autotrophic iron-oxidizing acidophiles Ferrovum myxofaci

177 umping well oxic and anoxic zones, including autotrophic iron-oxidizing bacteria.

178 Here we assess whether synthetic autotrophic Komagataella phaffii (Pichia pastoris) can b

179 uality genomes of orobanchaceous plants, the autotrophic Lindenbergia luchunensis and the holoparasit

180 Autotrophic members of the Sulfolobales (crenarchaeota)

181 photosynthetic robustness drives the optimal autotrophic metabolism at the expense of metabolic versa

182 ral inclusion bodies that play a key role in autotrophic metabolism in many bacteria.

183 The autotrophic metabolism of this isolate, and its close ph

184 'Candidatus Altiarchaeum hamiconexum' has an autotrophic metabolism that uses a not-yet-reported Fact

185 athways was found to be critical for optimal autotrophic metabolism.

186 the synthesis of other proteins required for autotrophic metabolism.

187 al trends in carbon-heterotrophic and carbon-autotrophic metabolism.

188 lic demands, allowing the plant to switch to autotrophic metabolism.

189 eterotrophic and obligately or facultatively autotrophic methylotrophs.

190 Four different omega-3 rich autotrophic microalgae, Phaeodactylum tricornutum, Nanno

191 Multifarious heterotrophic and autotrophic microbes and plants have been studied for th

192 Autotrophic microbes can acquire electrons from solid do

193 al indicative of their origin from primarily autotrophic microbes.

194 ical barrier to SCN(-) biodegradation for an autotrophic microbial consortium enriched from mine tail

195 Microbial fuel cells operating with autotrophic microorganisms are known as biophotovoltaic

196 ell as seasonal shifts from heterotrophic to autotrophic microorganisms associated with increases in

197 fluxes in P. tricornutum were calculated for autotrophic, mixotrophic and heterotrophic growth condit

198 s (pico, nano and micro), nutritional modes (autotrophic, mixotrophic and heterotrophic) and taxonomi

199 as reinhardtii cultured under nine different autotrophic, mixotrophic, and heterotrophic conditions d

200 study carbohydrate metabolism of algae under autotrophic, mixotrophic, and heterotrophic conditions u

201 erential assimilation of fungal protein, and autotrophic, mycorrhizal plants are lower in 15N than th

202 asure the contributions of heterotrophic and autotrophic N2-producing metabolisms (denitrification an

203 Oxygen-limited autotrophic nitrification/denitrification (OLAND), appli

204 Hydroxylamine oxidoreductase (HAO) from the autotrophic nitrifying bacterium Nitrosomonas europaea c

205 Hydroxylamine oxidoreductase (HAO) from the autotrophic nitrifying bacterium Nitrosomonas europaea c

206 To understand how autotrophic nitrifying organisms respond to inorganic ca

207 ic basis for energy and biomass synthesis in autotrophic nitrifying organisms, which in turn are cruc

208 Autotrophic nitrogen removal from municipal wastewater e

209 Autotrophic nitrogen removal is regarded as a resource e

210 OM use by Trichodesmium as an alternative to autotrophic nutrition in oligotrophic open ocean waters.

211 rkers of an MCG community that may either be autotrophic or feeding on (13) C-depleted organic substr

212 metalloenzyme that is vitally important for autotrophic organism as it catalyzes the first and rate-

213 engineered Cupriavidus necator H16, a model autotrophic organism to express differing aromatic modif

214 Autotrophic organisms obtain phosphorus from the environ

215 Fluorescence in phytoplankton and other autotrophic organisms originates within the cell chlorop

216 Higher plants, as autotrophic organisms, are effective sources of molecule

217 s often the limiting factor in the growth of autotrophic organisms, intrinsically linking the nitroge

218 irst step of carbon dioxide fixation in most autotrophic organisms.

219 ced by photosynthesis within an ecosystem by autotrophic organisms.

220 gene expression in plants, which are biotin autotrophic organisms.

221 variation in A is known to exist in various autotrophic organs that represent an unexploited target

222 bably as a consequence of NADPH formation in autotrophic organs.

223 gests a role for this enzyme in the proposed autotrophic origin of life.

224 more energy efficient than any other aerobic autotrophic pathway.

225 th (14) C-labelling to investigate all known autotrophic pathways and CO(2) assimilation mechanisms i

226 Marker genes of six autotrophic pathways are detected in all soil samples, w

227 hic growth, genes encoding enzymes for known autotrophic pathways in other phototrophic organisms, in

228 However, the multiple autotrophic pathways of microbial carbon assimilation an

229 nents are autotrophic denitrifying bacteria, autotrophic perchlorate-reducing bacteria, heterotrophic

230 ut only those with a strategy that is mostly autotrophic persisted with high nutrient supply, and the

231 that the MSP-D159N mutant suppresses the non-autotrophic phenotype of MSP-R163L (or vice versa) in th

232 Autotrophic photosynthesis by PSI-deficient mutants was

233 lysogeny occurs in natural populations of an autotrophic picoplankton (Synechococcus) and that there

234 Autotrophic picoplankton dominate primary production ove

235 e to viral infection seen in common forms of autotrophic picoplankton.

236 fferent from that in either heterotrophic or autotrophic plant tissues or in most other organisms: (i

237 rowth rate ever reported for a multicellular autotrophic plant.

238 tid genome (plastome) is highly conserved in autotrophic plants but is often reduced in parasites, an

239 ground levels in protocorms, confirming that autotrophic plants supply carbon to juveniles via common

240 es of the 15N/14N (expressed as delta15N) of autotrophic plants, mycoheterotrophic plants, parasitic

241 In contrast to most autotrophic plants, which produce carbohydrates from car

242 e specialized towards mycorrhizal fungi than autotrophic plants.

243 itrification or the more recently discovered autotrophic process, anaerobic ammonia oxidation (anammo

244 Heterotrophic and autotrophic production data together with small subunit

245 However, warming can also stimulate autotrophic production leading to increased ecosystem ca

246 e ecosystem known to be supported by in situ autotrophic production, and it contains the only terrest

247 Thus, the autotrophic productive capacity of large aquatic ecosyst

248 The RTCA pathway occurs in several groups of autotrophic prokaryotes, including the green sulfur bact

249 ingle-celled heterotrophic, mixotrophic, and autotrophic protists in aquatic environments.

250 fixed carbon was visualised in intact entire autotrophic/protocorm systems using digital autoradiogra

251 espiration (Rs) and its components, that is, autotrophic (Ra) and heterotrophic (Rh) respiration.

252 esponses of Rs and its two components [i.e., autotrophic (Ra) and heterotrophic (Rh) respiration] to

253 ominant microbial communities, especially in autotrophic reactors performing nitrification or nitrita

254 cing equivalents, such as H2, which then fed autotrophic reduction of CO2 to methane.

255 mycoheterotrophic Ericaceae and their close autotrophic relatives.

256 arge portion of each bioreactor community is autotrophic, relying not on molasses in reactor feed but

257 ood vs foliage production (NPPfoliage ), and autotrophic respiration (Ra ) vs all biomass production

258 Autotrophic respiration (Ra) was calculated by subtracti

259 roductivity (GPP) and continuously increased autotrophic respiration (Ra).

260 fer the impacts of environmental stresses on autotrophic respiration and carbon-use-efficiency, with

261 h component of net primary production (NPP), autotrophic respiration and heterotrophic respiration is

262 Tight coupling between below-ground autotrophic respiration and the availability of recently

263 phic respiration will be more sensitive than autotrophic respiration if precipitation increases in th

264 sence of drought, with extended decreases in autotrophic respiration in the three driest plots.

265 ut dominant contribution to ER switched from autotrophic respiration in wet years to heterotrophic in

266 Autotrophic respiration is a major driver of the global

267 If increased autotrophic respiration is balanced by increased primary

268 the proportion of photosynthate allocated to autotrophic respiration is not sensitive to temperature.

269 Autotrophic respiration ranged from 40 to 70% of Reco an

270 he Rs decrease was mainly due to a decreased autotrophic respiration rate (Ra).

271 t increase in RH was offset by a decrease in autotrophic respiration such that the total ecosystem re

272 al NPP, trees prioritized growth by reducing autotrophic respiration that was unrelated to growth.

273 Despite the physiological acclimation of autotrophic respiration to warming, increases in tempera

274 First, the models predicted declines in autotrophic respiration under prolonged drought in contr

275 rbon to partition ecosystem respiration into autotrophic respiration, associated with production, and

276 However, towards the end of the drought, autotrophic respiration, especially in roots and stems,

277 ned WUE and CUE is driven by modeled NPP and autotrophic respiration, nitrogen cycle, carbon allocati

278 dences of gross primary production (GPP) and autotrophic respiration, the fraction of GPP respired by

279 erotrophic respiration and very low daylight autotrophic respiration.

280 tosynthesis and release by decomposition and autotrophic respiration.

281 ons to growth; feedbacks to nutrient uptake; autotrophic respiration; and the impact of low soil mois

282 development of a germinating embryo into an autotrophic seedling is arrested under conditions of wat

283 2) originated from heterotrophic rather than autotrophic sources, and equated to a loss of 8.2 +/- 4.

284 atory evolution to generate several distinct autotrophic strains.

285 zone, and large lakes may exhibit shifts in autotrophic structure analogous to the regime shifts see

286 n of algal production), or simply a shift in autotrophic structure with no net decline in PP?

287 to cell densities of > 10(7) cells mL(-1) in autotrophic sulfur comproportionation medium.

288 y of in situ SCN(-) bioremediation involving autotrophic sulfur-oxidizing bacteria.

289 Thermodynamic calculations showed that the autotrophic synthesis of all 20 protein-forming amino ac

290 diverse cyanobacterial symbioses exist with autotrophic taxa in phytoplankton, including dinoflagell

291 Seq data, which documented the prevalence of autotrophic taxa, such as Thiobacillus and Gallionellace

292 is inconsistent with known heterotrophic and autotrophic thaumarchaeal lifestyles.

293 that is a net producer of fixed carbon (net autotrophic) throughout the year, with episodic events n

294 e predominantly in heterotrophic rather than autotrophic tissues, at least under standard growth cond

295 This shift from an autotrophic to a heterotrophic profile occurred concurre

296 osystem respiration, and increased ratios of autotrophic to heterotrophic respiration.

297 L. cf. luymesi can be sufficient to fuel net autotrophic total dissolved inorganic carbon uptake.

298 the debate are that it is either hetero- or autotrophic, which suggests either substantial unaccount

299 However, products from autotrophic whole-cell biocatalysts are limited.

300 )MPT-dependent activities were also found in autotrophic Xanthobacter strains.