ライフサイエンスコーパス: nitrogen source

1 cost methodology and allocated by municipal nitrogen source.

2 rol strain when melamine was supplied as the nitrogen source.

3 rograms are strikingly similar regardless of nitrogen source.

4 arginine, glutamate, or proline) is the sole nitrogen source.

5 ating the use of aromatic amino acids as the nitrogen source.

6 ut remains capable of utilizing nitrite as a nitrogen source.

7 is scarce, with protein being available as a nitrogen source.

8 O-benzoylhydroxylamines as the electrophilic nitrogen source.

9 on source and ethylene diamine acting as the nitrogen source.

10 y generation using histidine as a carbon and nitrogen source.

11 and amination reactions using azides as the nitrogen source.

12 ly available hydroxylamine derivative as the nitrogen source.

13 methylamine as a carbon source but not as a nitrogen source.

14 B (AsnB) that uses glutamine or ammonia as a nitrogen source.

15 ining d-glucosaminate as the sole carbon and nitrogen source.

16 assed the Haber-Bosch process in providing a nitrogen source.

17 ved to live on caffeine as a sole carbon and nitrogen source.

18 glycosides uses alkyl and aryl azides as the nitrogen source.

19 of substrate and a convenient phenol-derived nitrogen source.

20 reductase, did not grow on nitrate as a sole nitrogen source.

21 able to utilize glycine but not alanine as a nitrogen source.

22 is capable of growth on cyanide as the sole nitrogen source.

23 ved using either glutamine or ammonia as the nitrogen source.

24 major transporter for putrescine as the sole nitrogen source.

25 reagent as an oxidant and bistosylimide as a nitrogen source.

26 om soil microcosms containing NQ as the sole nitrogen source.

27 o prevent growth with putrescine as the sole nitrogen source.

28 rbon source and with [(1)(5)N]NH(4)Cl as the nitrogen source.

29 alyst and N,N-di-t-butyldiaziridinone (1) as nitrogen source.

30 d dienes using di-tert-butyldiaziridinone as nitrogen source.

31 unable to utilize GABA as a sole carbon and nitrogen source.

32 ted by another growth limiting nutrient, the nitrogen source.

33 chia coli K-12 to grow on uracil as the sole nitrogen source.

34 o survive in acidic environments and/or as a nitrogen source.

35 n external (AS-B) or internal (CPS, beta-LS) nitrogen source.

36 ent reaction, in which ammonia serves as the nitrogen source.

37 mmonia, urea, and arginine over nitrate as a nitrogen source.

38 talyst and di-tert-butyldiaziridinone as the nitrogen source.

39 efins with 1,3-di-tert-butyldiaziridinone as nitrogen source.

40 ize carbamoyl phosphate using glutamine as a nitrogen source.

41 pport bacterial growth on ammeline as a sole nitrogen source.

42 in response to the addition of nitrate as a nitrogen source.

43 2C to detoxify and assimilate AC as its sole nitrogen source.

44 s essential role in alanine utilisation as a nitrogen source.

45 he enzymes for utilizing purines as the sole nitrogen source.

46 s catalyst and di-tert-butyldiaziridinone as nitrogen source.

47 containing l-arginine as the sole carbon and nitrogen source.

48 growth rate of the cells was limited by the nitrogen source.

49 on medium containing l-glutamine as the sole nitrogen source.

50 npr1Delta occurred only with ammonia as the nitrogen source.

51 of cells to utilize ammonia as a repressive nitrogen source.

52 ng amino acids into yeast cells for use as a nitrogen source.

53 vity enabled growth on ornithine as the sole nitrogen source.

54 ing 14N and 15N ammonium sulfate as the sole nitrogen source.

55 ior of the full NCR circuit under changes in nitrogen source.

56 methylamine, nor use monomethylamine as sole nitrogen source.

57 unusual ability to use L- or D-alanine as a nitrogen source.

58 tivity and could not use nitrate as the sole nitrogen source.

59 anol as a carbon source and methylamine as a nitrogen source.

60 duced in good yields when using DABCO as the nitrogen source.

61 llylbenzene derivatives, using azides as the nitrogen source.

62 s not confer growth advantages on l-Arg as a nitrogen source.

63 lized by the algal endosymbiont as a primary nitrogen source.

64 waste streams is typically considered as the nitrogen source.

65 ther, trimethylsilyl bromide and N(2) as the nitrogen source.

66 ron), and porous g-C3N4 as both template and nitrogen source.

67 mal medium containing polyamines as the sole nitrogen source.

68 lls and medium, and prevented use of OP as a nitrogen source.

69 owth when cultured with ammonium as the sole nitrogen source.

70 solution, or upon addition of an assimilable nitrogen source.

71 one-pot protocol, whereas TMSN3 is used as a nitrogen source.

72 mine as a carbon and energy source or just a nitrogen source.

73 , confirming the suitability of the low-cost nitrogen source.

74 rides of serine, threonine, and cystine as a nitrogen source.

75 here NH3 serves as both activating agent and nitrogen source.

76 nitrate assimilation in response to various nitrogen sources.

77 and (15)N-labeled yeast extract as the only nitrogen sources.

78 ed in the utilization of selected carbon and nitrogen sources.

79 sustained TORC1 activity in response to good nitrogen sources.

80 e, and hydroxyproline as the sole carbon and nitrogen sources.

81 of acrylates is reported using sulfamates as nitrogen sources.

82 ilize methylated amines (MAs) as alternative nitrogen sources.

83 ssing the quantity and quality of carbon and nitrogen sources.

84 genes required for utilization of alternate nitrogen sources.

85 Cad), and spermidine (Spd), as carbon and/or nitrogen sources.

86 itrogen (ammonia, nitrate) or amino acids as nitrogen sources.

87 whose products are required to utilize poor nitrogen sources.

88 or energy, signal transduction pathways, and nitrogen sources.

89 revisiae, to the availability and quality of nitrogen sources.

90 ln3, NCR gene activation, and growth in poor nitrogen sources.

91 ar emphasis on those sensitive to carbon and nitrogen sources.

92 re likely parallel responses to derepressive nitrogen sources.

93 mechanisms that enable growth on suboptimal nitrogen sources.

94 nts, and plants frequently make use of these nitrogen sources.

95 lates in the presence of specific carbon and nitrogen sources.

96 od (glutamine or ammonia) and poor (proline) nitrogen sources.

97 pared to ammonium; and (iv) co-metabolism of nitrogen sources.

98 d evaluate the record in terms of changes in nitrogen sources.

99 ethods targeting agricultural and stormwater nitrogen sources.

100 r colonies when grown on different inorganic nitrogen sources.

101 nsequently, for using nitrate and nitrite as nitrogen sources.

102 he most attractive and industrially relevant nitrogen sources.

103 nity and allowing the host to access diverse nitrogen sources.

104 ulfonyl-substituted amine (H(2)NTces) as the nitrogen source, a diacyloxyiodobenzene as the oxidant,

105 investigated, where modification to both the nitrogen source, a sulfamate ester, and substrate are sh

106 l species we examined changed their dominant nitrogen source abruptly, and in unison, in response to

107 M. tuberculosis utilizes nitrate as the sole nitrogen source, albeit at lower efficiency than asparag

108 rent chemical nature in carbon substrates or nitrogen sources; all of these parameters can have profo

109 in minimal medium with glutamate as the sole nitrogen source, although they grew slowly with ammonium

110 The alternative nitrogen source ammonia can simulate TORC1 activity to s

111 The impact of the nitrogen source (ammonium sulfate, urea, or sodium nitra

112 The manifold uses amidines as the nitrogen source and activated skipped diynes as the elec

113 aminated using di-tert-butyldiaziridinone as nitrogen source and chiral N-heterocyclic carbene-Pd(0)

114 Thus, the nitrogen source and Gtr/Rag activate TORC1 via different

115 e investigate the activation of TORC1 by the nitrogen source and how this might be related to TORC1 a

116 s reaction utilizes acetonitrile as a single nitrogen source and involves the formation of two new C-

117 Ammonium serves as key nitrogen source and metabolic intermediate, yet excess c

118 ion process using di-t-butyldiaziridinone as nitrogen source and N-heterocyclic carbene-Pd(0) complex

119 using di-tert-butyldiaziridinone (5) as the nitrogen source and Pd(PPh(3))(4) (1-10 mol %) as the ca

120 se soils were capable of using RDX as a sole nitrogen source and possessed the genes xplB and xplA as

121 duce algae with NO from flue gas as the sole nitrogen source and reduces the NOx content in the exhau

122 failed to use uridine or uracil as the sole nitrogen source and that the parental strain could use t

123 s in response to variations in the available nitrogen source and to different concentrations of ammon

124 scens SBW25 to use beta-cyano-L-alanine as a nitrogen source and to tolerate toxic concentrations of

125 the adaptation to rapid changes in available nitrogen sources and concentrations.

126 sitive to growth on organic versus inorganic nitrogen sources and hypo-osmotic stress and limited gro

127 ved in utilization of alternative carbon and nitrogen sources and in mobilizing energy reserves.

128 ated in multiple ways in response to varying nitrogen sources and levels.

129 They also serve as microbial carbon and nitrogen sources and ligands for cell recognition during

130 ve growth of DeltaptsN mutants on amino acid nitrogen sources and other nutrient combinations.

131 lucan masking, whereas other inputs, such as nitrogen sources and quorum sensing molecules, exert lim

132 Escherichia coli to scavenge for alternative nitrogen sources and requires the global transcriptional

133 re spatially decoupled but that nevertheless nitrogen sources and sinks appear to be balanced over th

134 Low temperature, rich nitrogen sources and the Crl and NarP transcription fact

135 vert preQ(0)-tRNA to G(+)-tRNA using several nitrogen sources and to do so in an ATP-independent proc

136 ives from catechols, ammonium acetate as the nitrogen source, and aldehydes (nontoxic and cheap alter

137 of ald was induced when alanine was the sole nitrogen source, and higher levels of Ald enzyme were me

138 ene expression by iron and copper nutrition, nitrogen source, and hydrogen peroxide stress.

139 -limiting chemostat conditions regardless of nitrogen source, and in these conditions, only 34 transc

140 urces, readily prepared azidoformates as the nitrogen sources, and 4-dimethylaminopyridine (DMAP) and

141 lebsiella pneumoniae is able to utilize many nitrogen sources, and the utilization of some of these n

142 ement for Gln3 nuclear localization was both nitrogen source- and strain-dependent.

143 The nitrogen sources applied to Tempranillo grapevines were

144 red analysis allocating replacement costs by nitrogen source, aquaculture-based removal of 14 006 kg

145 ression (NCR) sensitive genes when preferred nitrogen sources are absent or limiting.

146 nsiveness to Msx addition and growth in poor nitrogen sources are distinct from those needed for rapa

147 Many species can also fix N2 when reduced nitrogen sources are scarce.

148 growth on the same assortment of carbon and nitrogen sources as the wild type.

149 The quality of the nitrogen source, as defined by its ability to promote gr

150 ocalization in response to the nature of the nitrogen source available.

151 and energy source for biofilm dispersal once nitrogen sources became available.

152 Anthropogenic nitrogen sources become more important in lower section

153 ine, and 7-methylxanthine as sole carbon and nitrogen sources but also theophylline and 3-methylxanth

154 oorganisms may also utilize methylamine as a nitrogen source, but little is known about their diversi

155 form NO2(-) and NO3(-) that can be used as a nitrogen source by algae.

156 CBB5, utilize caffeine as a sole carbon and nitrogen source by degrading it through sequential N-dem

157 hway utilization with putrescine as the sole nitrogen source by examining mutants with defects in bot

158 release of (15) N ammonium that was used as nitrogen source by other microorganisms not directly usi

159 Growth on L-lysine as a nitrogen source can also be enhanced when the aruH gene

160 ess the uniform phenotype for all repressive nitrogen sources characteristic of ure2Delta.

161 nd in many cases remineralization of a heavy nitrogen source consistent with wastewater nitrogen.

162 igestion of various carbon substrates and/or nitrogen sources could alter monomeric saccharide compos

163 This Sit4 activity masked nitrogen source-dependent changes in Gln3-Myc(13) phosph

164 els in wild type cells do not correlate with nitrogen source-determined intracellular Gln3-Myc13 loca

165 Organisms that use ammonium as the sole nitrogen source discriminate between [(15)N] and [(14)N]

166 ator Mpa was unable to use nitrate as a sole nitrogen source due to a specific failure in the pathway

167 nesis and that histidine serves as a crucial nitrogen source during infection.

168 ially important role for exogenous urea as a nitrogen source during the 2014 event.

169 The use of N(2) versus ammonium as nitrogen source during the enrichment process resulted i

170 Strain PK could ferment complex organic nitrogen sources (e.g. yeast extract, peptone, tryptone)

171 In sugar mixtures with these nitrogen sources, E. coli still consumes glucose first,

172 Other good nitrogen sources, e.g. glutamine, serine, or asparagine,

173 When rapidly utilized, "good" nitrogen sources, e.g., glutamine, are plentiful, Gln3 i

174 nes required to scavenge alternative, "poor" nitrogen sources, e.g., proline.

175 etabolic utilisation of preferred carbon and nitrogen sources, encountered in a host niche-dependent

176 saturated calomel electrode [SCE]), no added nitrogen source except the lysozyme itself, and long rea

177 NO is a poor nitrogen source for algae cultivation because of its low

178 re widespread in the ocean and are important nitrogen source for bacteria.

179 NEG could serve as the sole nitrogen source for E. coli when grown on M9 glucose med

180 rotic processes; the need for glutamine as a nitrogen source for generation of biomass; and the disti

181 have evolved to use DMF as a sole carbon and nitrogen source for growth via degradation by a dimethyl

182 (NAS) can use nitrate or nitrite as the sole nitrogen source for growth when ammonium is limited.

183 . coli was shown to use 3-nitrotyramine as a nitrogen source for growth, conditions which partially i

184 can use ammonia, alanine, or dinitrogen as a nitrogen source for growth.

185 amine is a significant additional carbon and nitrogen source for infecting E. coli strains.

186 ning [ (15)N]-labeled asparagine as the sole nitrogen source for labeling the proteins synthesized up

187 he degradation of osmolytes, could provide a nitrogen source for marine microbes.

188 al for using nitrogen gas (N(2)) as a direct nitrogen source for MP production by hydrogen-oxidizing

189 Arginine is the sole nitrogen source for nitric oxide (NO) synthesis.

190 source for TCA cycle intermediates and as a nitrogen source for nucleotide biosynthesis.

191 ose for carbon, aspartate is predominantly a nitrogen source for nucleotide synthesis.

192 NH3 is an essential molecule as a nitrogen source for prebiotic amino acid syntheses such

193 ne, a polyamine that is not a sole carbon or nitrogen source for R. solanacearum, was enriched 76-fol

194 n consumed, suggesting cheese whey is a good nitrogen source for S. zooepidemicus production of HA.

195 tin decomposition and serves as an important nitrogen source for soil microorganisms.

196 y of 75% in identifying potential carbon and nitrogen sources for K. pneumoniae and of 99% in predict

197 reorganizing the usage of organic carbon and nitrogen sources for protein synthesis and acetyl-coenzy

198 Eight of these could serve as sole carbon or nitrogen sources for R. solanacearum.

199 the other hand, increasing the amount of the nitrogen source from 1.2 to 2-3 equiv was discovered to

200 na572 always selected only one sugar and one nitrogen source from the available alternatives, and fai

201 n = 156) to explanatory variables describing nitrogen sources, geology, and soil and catchment charac

202 s with amino acid and peptide derivatives as nitrogen source giving unique structures.

203 ytoplasmic in cells cultured with repressive nitrogen sources (Gln) and nuclear with derepressive one

204 Addition of either the preferred nitrogen source, glutamine, or the nonpreferred nitrogen

205 w on trimethylamine N-oxide (TMAO) as a sole nitrogen source; however, the molecular and biochemical

206 wed them to effectively barter a specialized nitrogen source (i.e. insects) with host plants for phot

207 luenced by (I) the contribution of different nitrogen sources, (II) by variable environmental conditi

208 utilisation of different amino acids as sole nitrogen sources; (iii) improved nitrogen utilisation fr

209 symbiosis reveals a previously unrecognized nitrogen source in neotropical ecosystems.

210 iability in mineral-associated proteins as a nitrogen source in soils and that only a fraction of the

211 Proteins are a substantial nitrogen source in soils provided that they can be hydro

212 inside the cells was induced by a lack of a nitrogen source in the feed medium.

213 nf2, which is expressed independently of the nitrogen source in the medium.

214 ust be converted to glutamine, the preferred nitrogen source in yeast, to sustain TORC1 activity.

215 n cells growing in the presence of different nitrogen sources in batch cultures.

216 llowing utilization of intestinal carbon and nitrogen sources in particular genes involved in propane

217 n amine protecting groups serve as preformed nitrogen sources in the intermolecular osmium-catalyzed

218 lise nitrate and ammonium, the two principal nitrogen sources in the rhizosphere, is variable and man

219 s to actively discriminate between different nitrogen sources in the soil, with the preferred nitroge

220 osynthesis and the availability of inorganic nitrogen sources in the surface oceans is shifting with

221 such as scopolamine, from simple carbon and nitrogen sources in yeast (Saccharomyces cerevisiae).

222 growth advantage with particular carbon and nitrogen sources, including amino acids, in part due to

223 toca uses a variety of inorganic and organic nitrogen sources, including purines, nitrogen-rich compo

224 ant transformants grown with nitrate as sole nitrogen source (inducing for nitA) were tested for Cas9

225 ries that can efficiently convert carbon and nitrogen sources into a large diversity of intracellular

226 ation of various alkenes using FmocNHCl as a nitrogen source is reported.

227 ria to live on caffeine as a sole carbon and nitrogen source is unknown.

228 Starving microalgae for nitrogen sources is commonly used as a biotechnological

229 ources, and the utilization of some of these nitrogen sources is dependent on the nitrogen assimilati

230 Gcn2p activation upon shifting to secondary nitrogen sources is suggested to occur by means of a dua

231 ies revealed that, in addition to the common nitrogen sources (L-Gln and free amine) of class II glut

232 f Synechocystis sp. PCC 6803 under different nitrogen sources, light intensities, and CO2 concentrati

233 to utilize ethanolamine (EA) as a carbon and nitrogen source may confer an advantage for survival, co

234 utilization of ethanolamine as a carbon and nitrogen source may provide a survival advantage to bact

235 h they grew slowly with ammonium as the sole nitrogen source (MN medium) and were unable to fix N(2).

236 compromised when ammonium served as the sole nitrogen source, mostly due to an extreme imbalance of c

237 These findings suggest that the nitrogen source must be converted to glutamine, the pref

238 ogen sources in the soil, with the preferred nitrogen source, nitrate, acting to suppress primary roo

239 s were carried out to examine the effects of nitrogen source on nitrogen incorporation into cyanophyc

240 influence of foliar application of different nitrogen sources on grape amino acid content.

241 owth-limiting nutrient is the carbon source, nitrogen source or iron.

242 o show that D. vulgaris can use nitrite as a nitrogen source or terminal electron acceptor for growth

243 Exposure of yeast cells to poor nitrogen sources or treatment with the Tor kinase inhibi

244 Addition of organic carbon and nitrogen sources partly alleviated the defects of the mu

245 vitro activities of pathway enzymes, carbon/nitrogen source phenotypes, and/or transcriptomic studie

246 oduction makes one expect that the important nitrogen source precursors of amino acids were obtained

247 important role of AAP1 for efficient use of nitrogen sources present in the rhizosphere.

248 rogen source, glutamine, or the nonpreferred nitrogen source, proline, to cells growing in nitrogen-l

249 2 months of growth on 14N- and 15N-enriched nitrogen sources, proteins were extracted from four dist

250 ons can completely overwhelm its response to nitrogen source quality or inhibitor-generated disruptio

251 vironmental challenge, and diverse watershed nitrogen sources require multifaceted management approac

252 )N ammonium chloride, as the sole carbon and nitrogen sources, respectively.

253 media supplemented with different carbon and nitrogen sources resulted in changes in the pyrazine pro

254 umulated 5-CHO-THF and, with glycine as sole nitrogen source, showed a growth defect; both phenotypes

255 hese conditions, only 34 transcripts exhibit nitrogen source-specific differential gene expression.

256 d uptake systems exist, including carbon and nitrogen source-specific sensors and transporters, that

257 Poor nitrogen sources stimulate rapid but transient Sch9 phos

258 Preferred nitrogen sources stimulate rapid, sustained Sch9 phospho

259 Both nitrogen sources stimulated bulk phytoplankton, bacteria

260 nuclear in cells growing with a derepressive nitrogen source such as proline or those treated with ra

261 s required for the assimilation of secondary nitrogen sources such as gamma-aminobutyric acid (GABA).

262 ytoplasmic in cells provided with repressive nitrogen sources such as glutamine and is nuclear in cel

263 expressed in the presence of a nonpreferred nitrogen source, such as proline, which supports a slowe

264 mes, allowing them greater access to organic nitrogen sources than arbuscular mycorrhizal (AM) fungi.

265 ecreted waste product but also a fundamental nitrogen source that can support tumor biomass.

266 acid [Neu5Ac]) is a bioavailable carbon and nitrogen source that is abundant on mucosal surfaces and

267 c transcripts in the presence of a preferred nitrogen source that supports a fast growth rate, such a

268 abled by the reactivity of thianthrene-based nitrogen sources that can be prepared from primary amine

269 ng O-benzoyl hydroxylamines as electrophilic nitrogen sources that may be accessed in one step.

270 tions directly, then the ability of all good nitrogen sources to restrict Gln3 to the cytoplasm shoul

271 ation, with special attention to alternative nitrogen sources, to address the question of whether nit

272 sides ammonium also glutamine can serve as a nitrogen source under these conditions.

273 rbohydrates (glucose, sucrose, fructose) and nitrogen sources (urea, NH4Cl) at various concentrations

274 cterium tuberculosis utilises amino acids as nitrogen sources, using a combination of bacterial physi

275 dy represents the first in-depth analysis of nitrogen source utilisation by M. tuberculosis and revea

276 es glucose-6-phosphate (G6P) metabolism with nitrogen source utilisation, and thereby regulates the a

277 ptsN gene product does not regulate organic nitrogen source utilization as previously proposed.

278 The evidence for regulation of organic nitrogen source utilization by ptsN is based primarily o

279 ap1Delta and caf20Delta cells have different nitrogen source utilization defects, implying different

280 ptsN has been purported to regulate organic nitrogen source utilization in Escherichia coli K-12.

281 a decreased expression of genes involved in nitrogen source utilization.

282 In yeast, TORC1 responds to the nitrogen source via a poorly understood mechanism.

283 ino-2-deoxy-d-gluconic acid) as a carbon and nitrogen source via a previously uncharacterized mannose

284 ation rate, and additions of carbon sources, nitrogen sources, vitamins and minerals on production of

285 ryl sp(2) C-H bonds using nitroarenes as the nitrogen source was achieved using Mo(CO)6 as the reduct

286 and a specific set of D-amino acids as sole nitrogen sources was abolished in the dadA mutant and/or

287 as well as the effect of external carbon and nitrogen sources, was thereafter verified.

288 assessing M. tuberculosis growth in several nitrogen sources, we found that a mutant strain lacking

289 ile variations in the chemical nature of the nitrogen source were overlooked.

290 anisms that enriched using ATO as carbon and nitrogen source were Terrimonas spp., Ramlibacter-relate

291 wn in a minimal medium with (15)NH4Cl as the nitrogen source were watered onto plants growing in sand

292 Dissolved organic nitrogen sources were dominated by bacterially-derived n

293 Moreover, new carbon and nitrogen sources were predicted and experimentally valid

294 BCAAs into tissue protein and use BCAAs as a nitrogen source, whereas PDAC tumors have decreased BCAA

295 ol, could also grow on thymidine as the sole nitrogen source, whereas strains with lesions in the b10

296 puuP mutant failed to use putrescine as the nitrogen source, which implies one major transporter for

297 e during growth with methylamine as the sole nitrogen source, which we demonstrate is especially true

298 phenylethylamine can be used as a carbon and nitrogen source, while tyramine and dopamine can be used

299 tivation using di-tert-butyldiaziridinone as nitrogen source with a catalyst generated from Pd2(dba)3

300 nesulfonyl), Ns (p-nitrobenzenesulfonyl)] as nitrogen source, with the amination products isolated in