ライフサイエンスコーパス: anaerobic

1 rogenase-driven TCA cycle that could support anaerobic acetate oxidation coupled to metal reduction i

2 Microbial populations coupling anaerobic acetate oxidation to Mn(3+) reduction, however

3 In contrast, anaerobic activation of naphthalene by a carboxylation-l

4 onor amendments, different redox conditions (anaerobic, aerobic, sequential anaerobic-aerobic), and t

5 x conditions (anaerobic, aerobic, sequential anaerobic-aerobic), and the extracellular oxidoreductase

6 conventional culture techniques (aerobic and anaerobic agars and thioglycolate broth) compared to ino

7 and the diversity of the key marker gene for anaerobic alkane cycling and outline the need for greate

8 Anaerobic ammonia oxidation (anammox) combined with part

9 ially mediated processes denitrification and anaerobic ammonium oxidation (anammox) affects ecosystem

10 Microbial communities mediating anaerobic ammonium oxidation (anammox) represent one of

11 dative and nitrosative stress resistance and anaerobic ammonium oxidation, a process responsible for

12 Anaerobic ammonium oxidizing (anammox) bacteria own a ce

13 2OH by only three electrons to NO under both anaerobic and aerobic conditions.

14 or bacterial identification after culture in anaerobic and aerobic conditions.

15 nt employing the simultaneous application of anaerobic and aerobic microorganisms on AC could be an e

16 the master regulator for the switch between anaerobic and aerobic respiration in Escherichia coli an

17 presumably the pathway, are widespread among anaerobic and facultatively anaerobic bacteria from soil

18 Many of the disease-initiating bacteria are anaerobic and include organisms such as Porphyromonas gi

19 Methanogens are antibiotic-resistant anaerobic archaea that escape routine detection in clini

20 ardnerella vaginalis predominated with other anaerobic bacteria (40.8%)-were identified in 688 women

21 d CVM predominantly comprised either diverse anaerobic bacteria (n = 39 [42%]), Lactobacillus iners (

22 acterized by a reduced abundance of obligate anaerobic bacteria and an expansion of facultative Prote

23 me plays a central role in the metabolism of anaerobic bacteria and archaea, catalyzing the reversibl

24 amixicile is an effective inhibitor of oral anaerobic bacteria and as such, is a good candidate for

25 also cause non-oxidative cell death because anaerobic bacteria are also killed.

26 widespread among anaerobic and facultatively anaerobic bacteria from soil and freshwater environments

27 osis was observed in Gas6(-/-) mice, because anaerobic bacteria largely expanded by using inflammator

28 , the specific labelling of live endogenous, anaerobic bacteria within the mammalian host.

29 on containing enzymes that are widespread in anaerobic bacteria, archaea, and protozoa, serving as th

30 Anaerobic bacteria, such as Clostridium and Salmonella,

31 have CVM dominated by L. iners or by diverse anaerobic bacteria, than by L. crispatus.

32 These complexes were first described in anaerobic bacteria, where species-specific dockerin doma

33 vely correlating with G. vaginalis and other anaerobic bacteria, which depleted tenofovir by metaboli

34 In general, PFOR is present in all obligate anaerobic bacteria, while oral commensal aerobes, includ

35 Metabolites from anaerobic bacterial fermentation may, therefore, increas

36 ding Clostridiales year round, suggests that anaerobic bacterial processes are common in these dynami

37 ncover a family of polyketides native to the anaerobic bacterium Clostridium acetobutylicum, an organ

38 The strictly anaerobic bacterium Geobacter metallireducens uses the c

39 Fibrobacter succinogenes is an anaerobic bacterium naturally colonising the rumen and c

40 Fusobacterium necrophorum, an obligate anaerobic bacterium, was recently reported to be an impo

41 f acai pulp, and a subsequent pH-controlled, anaerobic, batch-culture fermentation model reflective o

42 The unexpected anaerobic bioavailability of negatively charged halocomp

43 time, dual C-Cl isotope fractionation during anaerobic biodegradation of 1,2-dichloroethane (1,2-DCA)

44 sotope fractionation during both aerobic and anaerobic biodegradation of 1,2-dichloroethane (1,2-DCA)

45 nalysis to differentiate between aerobic and anaerobic biodegradation pathways of 1,2-DCA in the fiel

46 heat sources include energy from aerobic and anaerobic biodegradation, anaerobic metal corrosion, ash

47 Blood was added to paired aerobic or anaerobic bottles, with the volume in each bottle in eac

48 In anaerobic bottom waters, the natural tracer radon ((222)

49 - 3 per thousand and -77 +/- 9 per thousand (anaerobic C-Cl bond cleavage via reductive dihaloelimina

50 Temperature sensitivity of anaerobic carbon mineralization in wetlands remains poor

51 Key enzymes of such anaerobic catabolic pathways are corrinoid and Fe-S clus

52 action included taxa known to be aerobic and anaerobic chemoorganotrophs.

53 and experimental approaches with a synthetic anaerobic coculture pairing fermentative Escherichia col

54 Although obligate anaerobic commensal bacteria have been associated with c

55 ither simultaneously or individually in live anaerobic commensal bacteria.

56 e causes a systemic dysbiosis of aerobic and anaerobic commensal bacteria.

57 Methanogens belong to the anaerobic community responsible for brain abscess, and M

58 ypothesized that methanogens are part of the anaerobic community that cause brain abscess.

59 We found an anaerobic component at each velocity tested.

60 in PAO1) on C1018 carbon steel in a strictly anaerobic condition.

61 electrochemical sensor, we found that under anaerobic conditions aliphatic and aromatic thiols (as w

62 ntial for phototrophic growth under strictly anaerobic conditions and appeared to play a role in reve

63 ter capable of functioning under aerobic and anaerobic conditions and exhibiting no physiological lim

64 ellular, labile Fe(2+) pool was higher under anaerobic conditions compared with aerobic conditions, s

65 e c, but an acceptor that can function under anaerobic conditions has not been identified.

66 The increased activity of Fur under anaerobic conditions led to a decrease in expression of

67 included organism factors (lack of growth in anaerobic conditions obscuring plate contamination), hum

68 at their base by incoming stormwater before anaerobic conditions rapidly re-established, although ex

69 of enolase in the RNase E/degradosome under anaerobic conditions regulates cell morphology, resultin

70 ination to young seedlings under aerobic and anaerobic conditions revealed 82% similarity in the tran

71 Under anaerobic conditions the first-order oxidation rate cons

72 te with differences between cell elongation (anaerobic conditions) versus cell division (aerobic cond

73 Under anaerobic conditions, a rate of approximately 4.0 s(-1)

74 ized Fur-mediated repression of feoABC under anaerobic conditions, allowing ferrous transport to incr

75 Under anaerobic conditions, cultures grown on rich media suppl

76 Under anaerobic conditions, enolase bound to the RNase E/degra

77 lines under elevated moisture and associated anaerobic conditions, leading to soil C accumulation.

78 nd transcriptional repression increase under anaerobic conditions, suggesting that Fur is controlled

79 Under anaerobic conditions, we observed complete removal of AE

80 on of (14)C-DNAN occurred at higher rates in anaerobic conditions, with a moderate increase when pyru

81 erns under aerobic to diffuse patterns under anaerobic conditions.

82 al cell filamentation during infection under anaerobic conditions.

83 iverse species of bacteria under aerobic and anaerobic conditions.

84 biofilm reactors operated under aerobic and anaerobic conditions.

85 treated with trimethoprim under aerobic and anaerobic conditions.

86 re physiological relevant ferrous iron under anaerobic conditions.

87 ging byproducts of nitrate respiration under anaerobic conditions.

88 making disulfide bonds (dsb(-) ) exposed to anaerobic conditions.

89 xylamine (NH2OH) quantitatively to N2O under anaerobic conditions.

90 signals at 1mM of glucose were 17.9muA under anaerobic conditions.

91 nd triclinic birnessite) at pH 4 and 7 under anaerobic conditions.

92 tance to trimethoprim under both aerobic and anaerobic conditions.

93 C. guilliermondii grows poorly under anaerobic conditions.

94 e that seems to function in both aerobic and anaerobic conditions.

95 ng between the aerobic surface layer and the anaerobic core in nitrite-rich anoxic marine zones (AMZs

96 genomic sequencing with standard aerobic and anaerobic culture in 97 sonication fluid samples from pr

97 erval {CI}, 1.2-15.4] for women with diverse anaerobic CVM and OR, 4.4 [95% CI, 1.3-15.6], for women

98 ence spectra were measured over a five weeks anaerobic dark incubation period.

99 rbours different populations responsible for anaerobic DCM and CM metabolism, and further imply that

100 n identified as metabolite in the pathway of anaerobic degradation of naphthalene by sulfate-reducing

101 ios that rely on excess capacity at existing anaerobic digester (AD) and solid biomass combustion fac

102 rce recovery facilities that already combust anaerobic digester biogas for energy since it may be pos

103 , promise to be an innovative technology for anaerobic digester biogas upgrading.

104 de of interspecies electron exchange in some anaerobic digesters converting wastes to methane.

105 After propagation in laboratory-scale anaerobic digesters, community composition (determined f

106 ously been used to improve CH4 production in anaerobic digesters, has not been explored in methanogen

107 Anaerobic digestion (AD) has been shown to have the biol

108 kg of carbon dioxide equivalents (CO2e) for anaerobic digestion (AD) to 0.38 kg of CO2e for landfill

109 amples from seven WWTPs in Ireland which use anaerobic digestion (AD), thermal drying (TD), or lime s

110 lular polysaccharide (EPS) production during anaerobic digestion (AD).

111 Anaerobic digestion is a widely used organic waste treat

112 Two-phase anaerobic digestion of oil refinery waste activated slud

113 was focused on determining the influence of anaerobic digestion on the speciation of copper and zinc

114 Anaerobic digestion results demonstrated that MW-A pretr

115 ecreased in all microcosms, but thermophilic anaerobic digestion, alkaline stabilization, and pasteur

116 mesophilic anaerobic digestion, thermophilic anaerobic digestion, pasteurization, and alkaline stabil

117 s (air drying, aerobic digestion, mesophilic anaerobic digestion, thermophilic anaerobic digestion, p

118 bal carbon cycle and in the biotechnology of anaerobic digestion.

119 g to incineration, and separated organics to anaerobic digestion.

120 in 2010, with the largest contribution from anaerobic digestion; the effects on NH3 emissions were s

121 more research is needed before recommending anaerobic disposal intended to promote arsenic volatiliz

122 ported for nitrite oxidation, as well as for anaerobic dissimilatory nitrate reduction and sulfate re

123 Prokaryotes have aerobic and anaerobic electron acceptors for oxidative folding of pe

124 and its flux rate approximates flow to other anaerobic electron acceptors.

125 es-specific; only two showed accumulation of anaerobic end products and three exhibited the classical

126 abolic alterations increase both aerobic and anaerobic energy expenditure.

127 homeostasis that regulates both aerobic and anaerobic energy metabolism.

128 f gender and prior experience on aerobic and anaerobic energy systems contributions, and the activity

129 ity compared to real sport, both aerobic and anaerobic energy systems should be considered in the eva

130 crobial peroxide producing cell (MPPC) as an anaerobic energy-conversion technology for converting pr

131 methylation in metabolically versatile mixed anaerobic enrichments from a Mekong Delta paddy soil.

132 rther, the host cell cytosol may resemble an anaerobic environment, with tissue-specific variations i

133 s in the presence of a ROS quencher or in an anaerobic environment.

134 tance of DIET to carbon and electron flow in anaerobic environments, and the biochemistry and physiol

135 cell growth and tolerance of nutrient-poor, anaerobic environments.

136 rtant for carbon cycling in nutrient-limited anaerobic environments.

137 s sulfate as sulfur sources further indicate anaerobic ethylene production from 2-(methylthio)ethanol

138 bon is produced predominantly as a result of anaerobic eukaryotic metabolic activity.

139 Anaerobic explosion could be particularly beneficial in

140 ce n-butyric acid and n-caproic acid via the anaerobic fermentation of human fecal material.

141 Net CO2 production was much greater in anaerobic fermentation stage than in initial aerobic pha

142 to use the high thermodynamic efficiency of anaerobic fermentation to convert organic biomass or org

143 mediated directly via the parasite's unique anaerobic fermentative metabolism or indirectly via para

144 oplasma-like organism was predicted to be an anaerobic fermenter associated to some jellyfish cells,

145 s in aerobic Proteobacteria and decreases in anaerobic Firmicutes and Melainabacteria in the murine f

146 er 72 hours of incubation in an experimental anaerobic flow chamber model compared with titanium impl

147 72 hours of incubation was assessed using an anaerobic flow chamber model.

148 ulture, E. coli and R. palustris resemble an anaerobic food web by cross-feeding essential carbon (or

149 mic and the extent of its involvement in the anaerobic formation and degradation of hydrocarbons.

150 However, the biocatalytic activity of anaerobic fungal cellulosomes is expanded by the inclusi

151 ared to the commercial cocktail CTec2, these anaerobic fungal cocktails provided comparable or slight

152 High-quality genomes of the anaerobic fungi Anaeromyces robustus, Neocallimastix cal

153 To this end, anaerobic fungi in the rumen have been identified as a p

154 , analogous structures have been reported in anaerobic fungi, which are known to assemble by sequence

155 y sealed reactors and constant flushing with anaerobic gases.

156 y time on many of the induced ergosterol and anaerobic gene promoters, increases its association with

157 in transcription, including a coinduction of anaerobic genes and ergosterol biosynthesis genes, biosy

158 ible to submergence and also fails to induce anaerobic genes at the level of the wild type.

159 induction of alcohol dehydrogenase and other anaerobic genes.

160 acid beta-oxidation, as confirmed by reduced anaerobic glycolysis and an increased oxygen consumption

161 P production relied proportionally more upon anaerobic glycolysis and oxidative phosphorylation, and

162 Here, we report that CDK4 promotes anaerobic glycolysis and represses fatty acid oxidation

163 that: intermittent exercise relies less upon anaerobic glycolysis for ATP provision than continuous e

164 ation drives energy production by regulating anaerobic glycolysis in cancer cells, suggesting a route

165 ted glucose metabolism in hypoxic cells from anaerobic glycolysis to oxidative phosphorylation (OXPHO

166 Both showed typical features of anaerobic glycolysis, which were paralleled by increased

167 expression of HIF-1alpha targets involved in anaerobic glycolysis.

168 compromise microcirculatory flow, leading to anaerobic glycolysis.

169 covered a role for this factor in regulating anaerobic glycolysis.

170 xidative ( approximately 10 mm min(-1) ) and anaerobic glycolytic ( approximately 1 mm min(-1) ) comp

171 Up-regulation of the anaerobic glycolytic pathway in the muscle of fast-growi

172 ccharolytic anaerobic Gram-positive rods and anaerobic Gram-negative rods, which were not frequently

173 ctivity against parasites, mycobacteria, and anaerobic Gram-positive and Gram-negative bacteria.

174 lso colonized by uncultivable asaccharolytic anaerobic Gram-positive rods and anaerobic Gram-negative

175 microorganisms, uncultivable asaccharolytic anaerobic Gram-positive rods and other uncultivable Gram

176 About 167 genes required for anaerobic growth on acetate in light were identified, 35

177 Anaerobic growth on nitrate confirms the O2-dependence o

178 eria gonorrheae norB-aniA cassette promoting anaerobic growth.

179 ulpturing force of community assembly within anaerobic gut microbial communities.

180 r intestine in mammals, yet no mechanism for anaerobic heme degradation has been reported.

181 al sampling revealed C. guilliermondii in an anaerobic holding jar in the clinical microbiology labor

182 that increased significantly during dark and anaerobic incubation matching three components previousl

183 prevalence and particular landscape of mixed anaerobic infection in HS, paving the way for rationale

184 s study was to characterize the landscape of anaerobic infections in HS using high-throughput sequenc

185 mmenced quickly but continued throughout the anaerobic interevent period and lacked clear relationshi

186 Although C. difficile is strictly anaerobic, it survives in aerobic environments and trans

187 nd in the stomach and small intestine, while anaerobic Lachnospiraceae and Ruminococcaceae, fermentin

188 The microbiome of 80 anaerobic lesions was compared to that of 88 control sam

189 t least formate or hydrogen as donor (in the anaerobic lumen) or oxygen as acceptor (near the epithel

190 mplete tricarboxylic acid (TCA) cycle in the anaerobic mammalian gut.

191 An oxygen-tolerant TCA cycle supporting anaerobic manganese reduction is thus a new connection i

192 An anaerobic membrane bioreactor was retrofitted with polyv

193 croalgae, which as eukaryotes have different anaerobic metabolic pathways to prokaryotes such as bact

194 uring anoxia, the naked mole-rat switches to anaerobic metabolism fueled by fructose, which is active

195 demonstrate that the switch from aerobic to anaerobic metabolism is brought about by changes in the

196 J- or U-shaped metabolism-speed curves; (ii) anaerobic metabolism is involved at all swimming speeds

197 tained higher flesh firmness and reduced the anaerobic metabolism, although it decreased fruit qualit

198 Products of bacterial anaerobic metabolism, like butyrate and other short-chai

199 ction of genes encoding enzymes required for anaerobic metabolism.

200 hey cannot meet cellular energy demands with anaerobic metabolism.

201 Model predictions indicate that both anaerobic metal corrosion and ash hydration/carbonation

202 y from aerobic and anaerobic biodegradation, anaerobic metal corrosion, ash hydration and carbonation

203 coveries have shown that the marker gene for anaerobic methane cycling (mcrA) is more widespread in t

204 dization analysis revealed that denitrifying anaerobic methane oxidation (DAMO) archaea, Anammox bact

205 DIET may also have a role in anaerobic methane oxidation coupled to sulfate reduction

206 rs of epsilonC = 3 and epsilonD = 54 suggest anaerobic methane oxidation is partly responsible for th

207 sible for the utilization of methane through anaerobic methane oxidation.

208 oenzyme M reductase (MCR), found in strictly anaerobic methanogenic and methanotrophic archaea, catal

209 The finding of an abundance of anaerobic methanogens enriched at the surface where oxyg

210 ethyl-coenzyme M reductase from unculturable anaerobic methanotrophs for capturing methane and secret

211 plain the subsistence of these facultatively anaerobic microbes whose stratigraphy follows changing p

212 )) is transformed to methylmercury (MeHg) by anaerobic microbes.

213 ctor, and examined the effects of NZVI/PS on anaerobic microbial communities during the treatment pro

214 (SCFAs), such as butyrate, produced through anaerobic microbial metabolism represent a major energy

215 OM) affects mercury (Hg) redox reactions and anaerobic microbial methylation in the environment.

216 s of bioavailable organic carbon that fueled anaerobic microbial respiration and stabilized U(IV).

217 fluence on the endogenous rate of aerobic or anaerobic microbial respiratory activity.

218 In this study, anaerobic microbial thiosulfate conversion to sulfide in

219 Indeed, mixed anaerobic microbiota are associated with a majority of H

220 flammation in CKD, we eradicated facultative anaerobic microbiota with antibiotics.

221 Among these, a special group of anaerobic microorganisms was discovered that could conse

222 In anaerobic microorganisms, most monocyclic aromatic growt

223 Anaerobic microscale thermophoresis results indicate tha

224 Here, we show that anaerobic microsites are important regulators of soil ca

225 driven by aerobic respiration; the impact of anaerobic microsites prevalent even within well-drained

226 gene deletion strains demonstrated that this anaerobic MSP functions via sequential action of MTA pho

227 re, we report the presence of an exclusively anaerobic MSP that couples MTA metabolism to ethylene fo

228 h the existence of a functional, exclusively anaerobic MSP, but they also suggest a possible route by

229 the activity will help us better understand anaerobic MTBE degradation processes in the field and de

230 out of 18 patients (41%) had either obligate anaerobic (n = 5) or microaerophilic (n = 4, one of whom

231 s close to the theoretical stoichiometry for anaerobic naphthalene degradation by a sulfate-reducing

232 for conversion in cell free extracts of the anaerobic naphthalene degraders Desulfobacterium strain

233 For this strictly anaerobic, obligate fermentative bacterium, we propose t

234 the reduced mitoNEET [2Fe-2S] clusters under anaerobic or aerobic conditions.

235 mily of polyketides has been identified from anaerobic organisms.

236 activities and converts to methylmercury by anaerobic organisms.

237 lic model of Ca Entotheonella as facultative anaerobic, organotrophic organisms with the ability to u

238 chemistry, as well as the important role of anaerobic oxidation in controlling the fate of dissolved

239 Anaerobic oxidation of methane (AOM) is an important pro

240 Anaerobic oxidation of methane (AOM) was shown to reduce

241 hanoperedens spp. archaea thought to perform anaerobic oxidation of methane linked to iron reduction

242 ion could not be fully explained by complete anaerobic oxidation of the ZVI and utilization of produc

243 elevated microbial P compounds stocks under anaerobic paddy-rice management.

244 9 bottle sets (52.5% aerobic pairs and 47.5% anaerobic pairs), 430 (7.5%) were positive for bacterial

245 PFOR is present in these anaerobic pathogenic bacteria and thus we hypothesized t

246 penem-resistant Enterobacteriaceae, and most anaerobic pathogens.

247 Anaerobic pathway accounted for 8.9 +/- 5.6% of total en

248 observed that growth of the PFOR-containing anaerobic periodontal pathogens, grown in both monospeci

249 IET can serve as the source of electrons for anaerobic photosynthesis further broadens its potential

250 Syntrophic anaerobic photosynthesis is therefore a carbon cycling p

251 aerobic respiration that we call 'syntrophic anaerobic photosynthesis'.

252 Thus, we postulate that anaerobic plates became intermittently contaminated.

253 Passaging from intermittently contaminated anaerobic plates to primary quadrants of aerobic media d

254 the clinical microbiology laboratory, where anaerobic plates were prereduced and held before inocula

255 l inflammation, and they are also part of an anaerobic polymicrobial consortium responsible for endod

256 for anammox, real municipal wastewater after anaerobic pretreatment was treated by enriched ammonium

257 ification within the oxic surface layer fuel anaerobic processes in the anoxic core of AMZs, where 30

258 easurement of VFA levels during AD and other anaerobic processes.

259 In our experiments, anaerobic production of dissolved inorganic carbon was c

260 ore the emergence of PSII, as found today in anaerobic prokaryotic organisms that use carbon monoxide

261 henotrophs in the sediments were facultative anaerobic Proteobacteria capable of coping with OAI-asso

262 reductions were observed in the abundance of anaerobic, proteolytic bacteria such as Peptostreptococc

263 ehyde as intermediate and play a key role in anaerobic redox balance in many fermenting bacteria.

264 out the sediment column indicating that both anaerobic reductive dechlorination and aerobic degradati

265 ded via coexisting aerobic ethenotrophic and anaerobic reductive dechlorination pathways.

266 t is due to biodegradation, and particularly anaerobic reductive dechlorination.

267 wer abundances of fungal C decomposition and anaerobic-related genes.

268 For the anaerobic remineralization of organic matter in marine s

269 cells to rely more on fatty acid oxidation, anaerobic respiration and fermentation for ATP productio

270 ssociated with oxidative/nitrosative stress, anaerobic respiration and lactate metabolism.

271 t RavA-ViaA are functionally associated with anaerobic respiration in Escherichia coli through intera

272 We probe anaerobic respiration of bacteria in the presence of con

273 abolism linking anoxygenic photosynthesis to anaerobic respiration that we call 'syntrophic anaerobic

274 like function for RavA-ViaA during bacterial anaerobic respiration with fumarate as the terminal elec

275 fting microbial metabolism to less efficient anaerobic respiration, and selectively protecting otherw

276 including pathways for CO2 and N2 fixation, anaerobic respiration, sulfur oxidation, fermentation an

277 xpanded by using inflammatory byproducts for anaerobic respiration.

278 both proteins are co-expressed with multiple anaerobic respiratory genes, many of which are regulated

279 Comparison between aerobic and anaerobic results showed that ferrihydrite promoted 2,6-

280 Two gram-negative anaerobic rod taxa, Prevotella and Porphyromonas, predom

281 ires" to reduce Mn(IV) and Fe(III) oxides in anaerobic sediments.

282 esults were replicated in the laboratory via anaerobic selenate-reducing enrichment cultures.

283 gradation of brilliant red X-3B in an upflow anaerobic sludge blanket (UASB) reactor, and examined th

284 te nitrogen removal from partially nitrified anaerobic sludge digestion liquor through the use of a m

285 increasingly used for nitrogen removal from anaerobic sludge digestion liquor.

286 This enteric pathogen colonizes the anaerobic space of the lower intestine in mammals, yet n

287 pths, PA taxa were primarily affiliated with anaerobic sulfate ( SO42-)-reducing lineages.

288 might reflect ADHE-mediated anticipation of anaerobic survival.

289 gh-diversity (n = 41) mCTs with abundance of anaerobic taxa.

290 Further, shifting from anaerobic to aerobic conditions leads to a 10-fold incre

291 donana, and an investigation of a shift from anaerobic to aerobic growth for the bacterium Escherichi

292 ry genes, many of which are regulated by the anaerobic transcriptional regulator Fnr.

293 mbining and extending the Wastewater Aerobic/anaerobic Transformations in Sewers (WATS) model and Act

294 anure, and the effect of the pretreatment on anaerobic treatment and biogas production was evaluated

295 contained higher levels of etheneotroph and anaerobic VC-dechlorinator functional genes and transcri

296 We conclude that both etheneotrophs and anaerobic VC-dechlorinators have the potential to simult

297 be mediated by three major bacterial guilds: anaerobic VC-dechlorinators, methanotrophs, and ethene-o

298 SA and FA Plus (aerobic) and SN and FN Plus (anaerobic), was performed in a clinical setting with pat

299 genome-resolved metagenomics to characterize anaerobic wastewater treatment sludge enrichments perfor

300 ickly increase dissolved oxygen to extremely anaerobic water in the initial 40 min until the CaO2 she