ライフサイエンスコーパス: anaerobic

1 +195 +/- 25 mV), anoxic (-15 +/- 50 mV), and anaerobic (-195 +/- 15 mV) conditions, and flow cytometr

2 transport-coupled phosphorylation indicated anaerobic acetogenesis was central to their catabolism.

3 nts and (iii) investigating the evolution of anaerobic alkane metabolisms and their impact on biogeoc

4 ethanogenesis in a laboratory batch reactor, anaerobic ammonia oxidation in a wastewater reactor and

5 2) production, whether by denitrification or anaerobic ammonia oxidation, yields proportions of (15)N

6 rucial role in the metabolism of aerobic and anaerobic ammonia oxidizers by converting hydroxylamine

7 Anaerobic ammonium oxidation (anammox) bacteria contribu

8 Anaerobic ammonium oxidation (anammox) is a microbial pr

9 The mainstream anaerobic ammonium oxidation (anammox) process provides

10 By coupling anaerobic ammonium oxidation (anammox) with nitrite/nitr

11 reference sites showed a dominant signal for anaerobic ammonium oxidation (anammox).

12 Anammox (anaerobic ammonium oxidation) bacteria are important for

13 ANAMMOX (anaerobic ammonium oxidation) represents an energy-effic

14 n restricted basins would prompt shoaling of anaerobic ammonium oxidation, leading to low observed 2-

15 re, we report evidence for in situ growth of anaerobic ammonium-oxidizing (anammox) bacteria in ~80,0

16 changes in proteome allocation, during both anaerobic and aerobic growth on glucose.

17 Clostridium difficile is an anaerobic and spore-forming bacterium responsible for 15

18 long-term stability of U(IV) solid phases in anaerobic aquifers depends upon their reactivity in the

19 Finally, we demonstrate that anaerobic arsenite oxidase and respiratory arsenate redu

20 on occurs in the cytosol of certain obligate anaerobic bacteria and archaea possessing the hgcAB gene

21 ly occurs in other bifurcating Etfs found in anaerobic bacteria and archaea.

22 les mechanistic investigation of the role of anaerobic bacteria in the tumor microenvironment.

23 Anaerobic bacteria seem to play a role in the occurrence

24 tain microbial populations, such as obligate anaerobic bacteria, is particularly critical if the purp

25 rticipate in the citric acid cycle, while in anaerobic bacteria, they are important in energy-conserv

26 ondary metabolites described from obligately anaerobic bacteria.

27 based family of antibiotics to fight against anaerobic bacteria.

28 es can be used in gene expression studies of anaerobic bacteria.

29 ful for heterologous expression of BGCs from anaerobic bacteria.

30 gulase-negative Staphylococci) and a lack of anaerobic bacteria.

31 el that can harbor and promote the growth of anaerobic bacteria.

32 synthesis is a common characteristic of many anaerobic bacteria; however, the uroS gene, encoding a u

33 rio cholerae is a Gram-negative, facultative anaerobic bacterial species that causes serious disease

34 ctron transfer flavoprotein (EtfAB) from the anaerobic bacterium Acidaminococcus fermentans bifurcate

35 The Gram-negative anaerobic bacterium Dichelobacter nodosus (Dn) causes fo

36 this study, we used the bza operon from the anaerobic bacterium Moorella thermoacetica (comprising b

37 to the development of periodontitis and the anaerobic bacterium Porphyromonas gingivalis plays a key

38 difficile is a Gram-positive, spore-forming, anaerobic bacterium that infects the human gastrointesti

39 Filifactor alocis, a Gram-positive anaerobic bacterium, is now a proposed diagnostic indica

40 ive transconjugants persisted much longer in anaerobic biofilms (~1.0 log reduction, after 72 h).

41 Anaerobic biological secondary treatment has the potenti

42 a stand-alone unit when integrated with the anaerobic bioprocess and demonstrated that we can select

43 ifferent MCCAs (MCCA oil) by integrating the anaerobic bioprocess with membrane-based liquid-liquid e

44 of sulfide from the process solution in the anaerobic bioreactor.

45 The anaerobic biosynthesis of 5,6-dimethylbenzimidazole (DMB

46 We implemented automatic anaerobic blood culture alongside aerobic blood cultures

47 pediatric patients, routine inclusion of an anaerobic blood culture alongside the aerobic remains co

48 Although inclusion of anaerobic blood cultures only recovered 2 (0.69%) obliga

49 cultures recovered 7.6% (349/4,615), whereas anaerobic blood cultures recovered 6.6% (286/4,363).

50 ms were only recovered from an aerobic or an anaerobic bottle in the paired cultures were 126 (30.0%)

51 n 27/5,594 (0.5%) bacterial culture-positive anaerobic bottles that contained cultures collected from

52 before a dose and utilizing resin-containing anaerobic bottles will maximize the likelihood of recove

53 c bottles and 810 bacterial culture-negative anaerobic bottles.

54 in-free BacT/Alert SN and BD Bactec standard anaerobic bottles.

55 l determination in cell-free samples from an anaerobic butanol fermentation.

56 Like most anaerobic ciliates, all studied species of the APM clade

57 w class-level lineages of free-living marine anaerobic ciliates, Muranotrichea, cl. nov. and Parablep

58 The putative anaerobic citrate fermentation genes in V. cholerae, con

59 ntermediate in the Wood-Ljungdahl pathway of anaerobic CO and CO(2) fixation.

60 n that the attachment of the lower ligand in anaerobic cobamide biosynthesis is regiospecific.

61 vation of the benzimidazolyl lower ligand in anaerobic cobamide biosynthesis.

62 Pg in vitro using the Human oxygen-Bacteria anaerobic coculture technique.

63 The human intestinal anaerobic commensal and opportunistic pathogen Bacteroid

64 Trend 1 OTUs comprised a mix of primarily anaerobic commensals and potential periodontopathogens.

65 reactive Fe and reduced Fe(II), a proxy for anaerobic conditions (reactive Fe: R(2) = .54-.79; Fe(II

66 H(2) evolution occurs under anaerobic conditions and is difficult to sustain due to

67 Here, we prepared samples under anaerobic conditions and then applied native MS to inves

68 Escherichia coli can utilize citrate under anaerobic conditions but not aerobic conditions.

69 tic resonance spectroscopy demonstrated that anaerobic conditions decreased protein-derived C but inc

70 ded litter under either aerobic (control) or anaerobic conditions for 1 year.

71 thesized with and without Hg(2+) and aged in anaerobic conditions for multiple time frames spanning f

72 Indeed, a pathway that produces UQ under anaerobic conditions in an UbiU-, UbiV-, and UbiT-depend

73 enhance the robustness of germination under anaerobic conditions in inbred and hybrid rice varieties

74 ription of l-lactate utilization genes under anaerobic conditions in vitro The ArcAB-mediated repress

75 n normoxia, they use ubiquinone (UQ), but in anaerobic conditions inside the host, they require rhodo

76 The adaptation of eukaryotic cells to anaerobic conditions is reflected by substantial changes

77 ery of microbial defluorination under common anaerobic conditions may provide valuable insights into

78 Anaerobic conditions mobilize phosphorus (P) in soils an

79 Germination under aerobic and anaerobic conditions showed very low correlation, indica

80 formed flow-through column experiments under anaerobic conditions to investigate the mechanisms and d

81 tive anaerobe, was grown both in aerobic and anaerobic conditions with an arabinose-inducible express

82 The assay occurred under anaerobic conditions with different time and temperature

83 ding setup, in which birch bark is heated in anaerobic conditions, a setup whose inherent complexity

84 te pathway, had a doubling time of 4 h under anaerobic conditions, in contrast to the 45 min doubling

85 Under anaerobic conditions, production of nitrite by nitrate-r

86 Under anaerobic conditions, pyruvate formate-lyase enabled 2-k

87 ulating isotopic compositions in aerobic and anaerobic conditions, respectively.

88 Conducting this analysis under fully anaerobic conditions, we solved the DHAD crystal structu

89 /thermodynamic C protection mechanisms under anaerobic conditions, whereby decreased decomposition of

90 the phenotypic variation for survival under anaerobic conditions.

91 can be cultivated on specialized media under anaerobic conditions.

92 transfer frequencies were also higher under anaerobic conditions.

93 coli, the most common early colonizer, under anaerobic conditions.

94 enes by global regulators ArcA and Fnr under anaerobic conditions.

95 btained in the case of B. longum cultured in anaerobic conditions.

96 ion of the ABTS radical cation by glucose in anaerobic conditions.

97 e formed on titanium specimens for 5 days in anaerobic conditions.

98 citrate fermentation genes in E. coli under anaerobic conditions.

99 findings were obtained from both aerobic and anaerobic cultivations.

100 cytotoxicity assay, isolated C. difficile by anaerobic culture, and performed PCR ribotyping.

101 The study reports on the effect of anaerobic digestate derived composts on the metabolite c

102 Using the anaerobic digestate of a pilot wastewater treatment plan

103 different fertiliser treatments (composts of anaerobic digested cattle (C) or pig slurry (P) at 30t/h

104 es initiated with non-augmented heat-treated anaerobic digester sludge (AS) and mono-culture of C. kl

105 he impact of bioaugmentation of heat-treated anaerobic digester sludge with Clostridium kluyveri (AS

106 he gap between the laboratory and real-world anaerobic digesters effectively.

107 ste induces community shifts in conventional anaerobic digesters treating sewage sludge at wastewater

108 sed to infer possible process instability of anaerobic digesters.

109 midpoint results of LCA show that CEPT with anaerobic digestion (AD) for sludge treatment achieves e

110 waste including landfilling, composting, dry anaerobic digestion (AD) for the production of renewable

111 Biomethanation through anaerobic digestion (AD) is the most reliable energy har

112 Dry anaerobic digestion (AD) of organic municipal solid wast

113 oach for enhancing mesophilic (37 degrees C) anaerobic digestion (AD) of organic waste using a low-te

114 Anaerobic digestion (AD) with hydrothermal (HT) pretreat

115 We investigated the viability of solid-state anaerobic digestion (SS-AD) as an alternative that reduc

116 e-pili in diverse biogeochemical processes, anaerobic digestion and electromicrobiological applicati

117 ng of volatile fatty acids (VFAs) during the anaerobic digestion of high strength wastewater, with a

118 ste MRF was used, and the higher values when anaerobic digestion was used.

119 VFAs are identified as a key intermediary in anaerobic digestion, hence their accumulation could be u

120 ne when producing biogas from food waste via anaerobic digestion, thus could help biogas project deve

121 ating no general preference for any specific anaerobic electron acceptor.

122 ia and whether the addition of Mars relevant anaerobic electron acceptors might enhance growth.

123 rformed to quantify the effects of the added anaerobic electron acceptors.

124 ed on five TSA-based media supplemented with anaerobic electron acceptors.

125 egrative real-time monitoring of aerobic and anaerobic energy metabolism in bovine embryos, with pote

126 Electron bifurcation plays a key role in anaerobic energy metabolism, but it is a relatively new

127 anaerobiosis drives expansion of facultative anaerobic Enterobacteriaceae, regardless of their pathog

128 Our discovery confirms that adaptation to an anaerobic environment is not unique to single-celled euk

129 biochar as the sole electron acceptor in an anaerobic environment, CH(4) was biologically oxidized,

130 termediate during ethanol fermentation in an anaerobic environment.

131 robes that inhabit organic- and Fe(III)-rich anaerobic environments may similarly reduce Fe(III) to F

132 ble to express nitrite reductase and grow in anaerobic environments, such as the urogenital and anore

133 h from COQ-2a to COQ-2e as they transit into anaerobic environments.

134 tiveness against aceticlastic methanogens in anaerobic environments.

135 rt, we describe the crystal structure of the anaerobic ergothioneine biosynthetic enzyme EanB from gr

136 Anaerobic ethylene production by this pathway apparently

137 vulnerability of mineral-associated C under anaerobic events characteristic of a warmer and wetter f

138 In this way, the anaerobic excellence and oxygen sensitivity of B. thetai

139 aining BacT/Alert FN Plus and BD Bactec Plus anaerobic/F bottles as well as resin-free BacT/Alert SN

140 munities and viral assemblages to stimulated anaerobic Fe(III)-bioreduction following electron donor

141 in particular methane, due to the microbial anaerobic fermentation of feed in the rumen.

142 The influence of dicarbonyl compounds on the anaerobic fermentation processes was confirmed by the re

143 gut microbial metabolic pathways, including anaerobic fermentation to generate short-chain fatty aci

144 d not only aerobic fitness but also parts of anaerobic fitness in young males.

145 ss was evaluated by 3000-meter run test, and anaerobic fitness was evaluated by 2-minute sit-ups and

146 by the time for a 3-kilometer run test, and anaerobic fitness was evaluated by the numbers of sit-up

147 A mainstream anaerobic fluidized-bed bioreactor and a partial nitrita

148 nsive patients were dominated by facultative anaerobic genera (Escherichia, Enterococcus, and Strepto

149 ate in the nucleus under hypoxia to activate anaerobic genes but are destabilized in normoxic conditi

150 Anaerobic germination is one of the most important trait

151 Four significant markers with an effect on anaerobic germination were identified through BSA.

152 identification of QTLs and causal genes for anaerobic germination will facilitate breeding for impro

153 derstand the effect of phenotyping method on anaerobic germination, which will lead to better phenoty

154 tant animals and mammalian cells to initiate anaerobic glycolysis and survive hypoxia.

155 yocardial glucose consumption mainly through anaerobic glycolysis while reducing utilization of free

156 In contrast, anaerobic glycolytic capacity is surprisingly high, and

157 ens (1-alk-1'-enyl, 2-acyl phospholipids) in anaerobic Gram-positive bacteria led to studies on the p

158 lized with equal affinity during aerobic and anaerobic growth conditions, suggesting that the dual-pu

159 The difference in anaerobic growth rate was traced to three amino acid cha

160 hylthio)acetaldehyde during both aerobic and anaerobic growth.

161 Mechanistic studies of anaerobic gut bacteria have been hindered by the lack of

162 The anaerobic gut fungi (AGF, Neocallimastigomycota) reside

163 The anaerobic gut microbial pathway that converts choline in

164 Using one defined anaerobic gut microbiota to track whether microbiota int

165 The anaerobic gut pathogen, Clostridioides difficile, forms

166 elium with stable communities of aerobic and anaerobic human gut microbiota, using a microfluidic int

167 terized the microbial populations capable of anaerobic hydrocarbon degradation coupled with sulfate r

168 se communities potentially sustained through anaerobic hydrocarbon, acetate and hydrogen metabolism.

169 rprisingly, we identified peroxisomes in the anaerobic, hydrogenosome-bearing protist Mastigamoeba ba

170 a protein levels under aerobic (normoxia) or anaerobic (hypoxia) conditions.

171 Using anaerobic in vitro reconstitution, we establish that a s

172 easuring gas production in vitro during 48-h anaerobic incubation with healthy fecal samples.

173 mammalian guts, SCFAs are mostly produced by anaerobic intestinal microbiota through the fermentation

174 ion by an aerobic fungus next to facultative anaerobic lactic acid bacteria and the product-forming a

175 g factor in the transitions to an obligately anaerobic lifestyle.

176 oxygen gradient from the mucus layer to the anaerobic lumen [L.

177 achnospiraceae family are abundant, obligate anaerobic members of the microbiota in healthy humans.

178 biofouling constitutes a great challenge in anaerobic membrane bioreactor (AnMBR).

179 Anaerobic membrane bioreactors (AnMBRs) are in use at th

180 Anaerobic membrane bioreactors (AnMBRs) can significantl

181 of their hosts, these parasites use unusual anaerobic metabolism - this requires rhodoquinone (RQ),

182 ergy-regenerating mechanism, which activates anaerobic metabolism and autophagy-mediated macromolecul

183 e results highlight the interconnectivity of anaerobic metabolism and importance of community dynamic

184 olved in metal transport (feoA, mntH, sirA), anaerobic metabolism genes (adhE, pflA, nrdDG) and a lar

185 the alcohol dehydrogenase (ADH) and greater anaerobic metabolism in comparison with DCA - CF (chloro

186 oretical maximum rate of biomass production, anaerobic metabolism requires import of additional compo

187 Greater anaerobic metabolism resulted in lower ethylene producti

188 n activity was closely tied to S. oneidensis anaerobic metabolism through specific extracellular elec

189 hat an oxygen-sensitive RBP cluster controls anaerobic metabolism to confer hypoxia tolerance.

190 integrates upstream mRNA signals to activate anaerobic metabolism.

191 y transition from an aerobic to an exclusive anaerobic metabolism.

192 s and radical-based mechanisms that optimize anaerobic metabolism; therefore, committed anaerobes hav

193 gene-inferred aerobic, microaerophilic, and anaerobic metabolisms are likely supported by shallower

194 rowth conditions, including both aerobic and anaerobic metabolisms.

195 elsewhere are characterized predominately by anaerobic metabolisms.

196 Our findings link anaerobic methane metabolism and dissimilatory sulfur re

197 ence of aerobic methane oxidation (MOx)- and anaerobic methane oxidation (AOM)-related lipid biomarke

198 pling anammox with nitrite/nitrate-dependent anaerobic methane oxidation (n-DAMO) microorganisms, at

199 ion (anammox) with nitrite/nitrate-dependent anaerobic methane oxidation (n-DAMO), up to 85% of disso

200 (mu-NO)](2+) core is potentially relevant to anaerobic methane oxidation observed in methanotrophic a

201 ity for DNRA, anammox, and nitrite-dependent anaerobic methane oxidation.

202 Nitrate-dependent denitrifying anaerobic methane oxidizing archaea (n-damo) oxidize met

203 About 20 years ago anaerobic methane-oxidizing archaea (ANME) were discover

204 philes that are thought to have evolved from anaerobic methanogens.

205 (MAGs) belonging to potential methanogenic, anaerobic methanotrophic and short-chain alkane-oxidizin

206 re of marker genes specific to methanogenic, anaerobic methanotrophic and short-chain alkane-oxidizin

207 Anaerobic methanotrophic archaea (ANME) consume methane

208 , preceding increased relative abundances of anaerobic methanotrophs ANME-1 within communities.

209 rd that represent geochemical horizons where anaerobic methanotrophy is expected to be active, previo

210 cycle responds, further metabolic evolution (anaerobic methanotrophy) may feed back to the atmosphere

211 storage via aggregation and/or formation of anaerobic (micro)sites that protect residual soil C from

212 In contrast, anaerobic microbes were only minimally revived from this

213 are common sites of active Hg methylation by anaerobic microbes; however, the amount of methylmercury

214 ng as a key process for electron transfer in anaerobic microbial communities, both between species an

215 Recent work has shown that the anaerobic microbial conversion of mercury (Hg) to MeHg r

216 difficult chemical reactions in a variety of anaerobic microbial metabolic pathways.

217 fected birds transplanted with DCA-modulated anaerobic microbiota.

218 orter genes to study molecular mechanisms in anaerobic microorganisms has been hampered by the lack o

219 The recent discovery that anaerobic microorganisms make the same metabolite using

220 The anaerobic microorganisms presented high resistance to As

221 emical form of Hg and its bioavailability to anaerobic microorganisms that can methylate Hg.

222 methylating communities dominated by diverse anaerobic microorganisms that do not reduce sulfate can

223 coal and oil, can be degraded by aerobic or anaerobic microorganisms.

224 are prevalent in a number of other strictly anaerobic microorganisms.

225 certain sulfate-reducing bacteria and other anaerobic microorganisms.

226 of organic carbon inputs, the prevalence of anaerobic microsites and delivery of nutrients to microo

227 The role of anaerobic microsites in well-drained soil on P migration

228 deficient zones (ODZs), and possibly within anaerobic microzones of settling organic matter, but MeH

229 hases are preferentially reduced, increasing anaerobic mineralization of DOM and SOM by 74% and 32-41

230 These anaerobic multi-carbon alkane-oxidizing archaea (ANKA) u

231 criptions of novel Corynebacteriaceae and an anaerobic mycolic acid-producing bacterium in the subord

232 2)) concentration gradient, which reconciles anaerobic N(2) fixation with O(2)-rich atmosphere.

233 erimental tool for gaining insights into the anaerobic naphthalene oxidation pathway from an energeti

234 mechanisms are possibly an adaptation to the anaerobic nature of eubacterial cells with poor toleranc

235 elatively constant ratio between aerobic and anaerobic oil decomposition rates even after prolonged a

236 mples indicated strong enrichment toward the anaerobic order of Clostridia.

237 y relevant activity against Gram-positive or anaerobic organisms.

238 thus is fundamentally different from that in anaerobic organisms.

239 acetogenic and methanogenic branches of many anaerobic organisms.

240 to the reductive evolution of peroxisomes in anaerobic organisms.

241 the expression of recombinant proteins from anaerobic origin or those with cell wall binding profile

242 Anaerobic oxidation of methane (AOM) and methanogenesis

243 mprising microbial communities mediating the anaerobic oxidation of methane are rare.

244 uld facilitate exergonic, sulfite-dependent, anaerobic oxidation of methane to methanol; alternativel

245 verged from those of aerobic and facultative anaerobic pathogenic bacteria.

246 the remote site in 3 facilitates an unusual anaerobic pathway for phenol nitration.

247 The enzymes and transporters in these anaerobic pathways expand our understanding of microbial

248 identified a subclass of peroxisomes, named "anaerobic" peroxisomes that shift the current paradigm a

249 5 in both the initial aerobic and subsequent anaerobic phases of S-deprivation.

250 Our work provides evidence for an anaerobic process in which plasmalogens are formed from

251 antly anoxic Earth surface conditions, where anaerobic processes controlled bioessential element cycl

252 e belt, and demonstrate that elements key to anaerobic prokaryotic molecular nanomachines, including

253 lenges, we have used sequence alignments, an anaerobic purification method, iron quantification, and

254 However, through the use of anaerobic reaction techniques, both one- and two-electro

255 e study employed effluent from a pilot-scale anaerobic reactor and soluble microbial products (SMPs)

256 We examined sludges from full-scale anaerobic reactors for sulfur-reducing activity at pH 2.

257 times higher in aerobic reactors relative to anaerobic reactors, and protozoa numbers significantly i

258 -type cytochromes, many of which function as anaerobic reductases.

259 aeruginosa and is required for growth under anaerobic respiration (i.e. denitrification).

260 rgano-metal complexes, as well as C loss via anaerobic respiration by Fe-reducing bacteria.

261 Waterlogged soil incubations confirmed that anaerobic respiration comobilizes Mn and P and that this

262 o be used as terminal electron acceptors for anaerobic respiration in sulfate- and sulfite-reducing b

263 n of about 100 cytochromes could support the anaerobic respiration of a Shewanella cell.

264 erobic respiration of glucose in freshwater, anaerobic respiration of acetate in marine sediment, hyd

265 Fumarate, an electron acceptor in anaerobic respiration of Escherichia coli, has an additi

266 olically adaptable and can harvest energy by anaerobic respiration using microbiota-derived hydrogen

267 plasm from excessive nitrite toxicity during anaerobic respiration with abundant nitrate.

268 e top-enriched among up-regulated genes, and anaerobic respiration, nitrate metabolism and aromatic a

269 all, multiple lines of evidence confirm that anaerobic respiration, sparked by labile organic matter,

270 ransmembrane enzymes involved in aerobic and anaerobic respiration.

271 cceptors, generating electrical current from anaerobic respiration.

272 MK and DMK function predominantly in anaerobic respiratory chains, whereas UQ is the major el

273 richia coli reprograms host regulation of an anaerobic respiratory system, thereby inhibiting a bet h

274 Surprisingly, we found this anaerobic route to provide a substantial fraction of iso

275 bset of prokaryotes via distinct aerobic and anaerobic routes.

276 sed of Na(+) Here, we show that the strictly anaerobic rumen bacterium Pseudobutyrivibrio ruminis pos

277 ircuit for Na(+) bioenergetics in a strictly anaerobic rumen bacterium.

278 Our implementation of (19)F NMR in anaerobic samples is applicable to other two-component f

279 henotyped under different screening methods (anaerobic screenhouse, anaerobic tray, and aerobic scree

280 comprising six 10 L leach beds and an upflow anaerobic sludge blanket reactor treating the leachate,

281 r results reveal the potential of mesophilic anaerobic sludges as seed material for sulfur-reducing b

282 The suitability of mesophilic anaerobic sludges as the inoculum for sulfur-reducing bi

283 Biosolarization and anaerobic soil disinfestation, developed to manipulate s

284 l layers (0-40 cm) but slightly decreased in anaerobic soil layers (40-100 cm).

285 n enhance germination and seedling growth in anaerobic soils.

286 Our work suggests that an initial anaerobic step in wastewater treatment can reduce the co

287 hypersaline stratum (likely involved in the anaerobic steps of carbon- and sulphur-cycling); and (iv

288 FMT protocols involving anaerobic stool processing methods may enhance microbial

289 s at 30 degrees C were dominated by strictly anaerobic, sulfate-reducing, and spore-forming microorga

290 ical energy and likely evolved from a simple anaerobic system now represented by hydrogen gas-evolvin

291 llus spp. depletion and presence of specific anaerobic taxa including Megasphaera, Prevotella timonen

292 Anaerobic technologies have been proposed as a promising

293 between groups, 1.8 mL.kg(-)1.min(-)1), the anaerobic threshold (0.28 L/min), the peak expiratory fl

294 The anaerobic threshold (AT) remains a widely recognized, an

295 essed as the slope pre- and post-ventilatory anaerobic threshold (VE/VCO2(pre-VATslope), VE/VCO2(post

296 ed on the Vo(2)peak values (25% versus 15%), anaerobic threshold, peak expiratory flow, and muscular

297 Here, we investigated whether microbial anaerobic transformation can contribute to the removal o

298 nt screening methods (anaerobic screenhouse, anaerobic tray, and aerobic screenhouse) to establish th

299 Transitioning to anaerobic treatment could recover energy while reducing

300 urvive vertical migration into saturated and anaerobic zones of peatlands where environmental conditi