ライフサイエンスコーパス: nitrogen source

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

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

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

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

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

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

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

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

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

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

11 major transporter for putrescine as the sole nitrogen source.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

28 ize carbamoyl phosphate using glutamine as a nitrogen source.

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

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

31 2C to detoxify and assimilate AC as its sole nitrogen source.

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

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

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

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

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

37 mal medium containing polyamines as the sole nitrogen source.

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

39 npr1Delta occurred only with ammonia as the nitrogen source.

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

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

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

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

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

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

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

47 methylamine, nor use monomethylamine as sole nitrogen source.

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

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

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

51 NH(4)(+) or PabA + glutamine is used as the nitrogen source.

52 midotransferase) + glutamine are used as the nitrogen source.

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

54 cytoplasm when cells are returned to a good nitrogen source.

55 cid using either glutamine or ammonia as the nitrogen source.

56 e mutant enzyme when glutamine was used as a nitrogen source.

57 in on ethanolamine as a carbon and energy or nitrogen source.

58 tivity when external ammonia was used as the nitrogen source.

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

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

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

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

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

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

65 rograms are strikingly similar regardless of nitrogen source.

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

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

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

69 O-benzoylhydroxylamines as the electrophilic nitrogen source.

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

71 and amination reactions using azides as the nitrogen source.

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

73 r colonies when grown on different inorganic nitrogen sources.

74 of acrylates is reported using sulfamates as nitrogen sources.

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

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

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

78 genes required for utilization of alternate nitrogen sources.

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

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

81 whose products are required to utilize poor nitrogen sources.

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

83 he most attractive and industrially relevant nitrogen sources.

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

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

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

87 re likely parallel responses to derepressive nitrogen sources.

88 mechanisms that enable growth on suboptimal nitrogen sources.

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

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

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

92 y of the organism to use L- and D-alanine as nitrogen sources.

93 M. maripaludis vary with growth on different nitrogen sources.

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

95 utant was impaired on medium containing poor nitrogen sources.

96 )CH(2)CH(2)CN) were employed as nucleophilic nitrogen sources.

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

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

99 ethods targeting agricultural and stormwater nitrogen sources.

100 sustained TORC1 activity in response to good nitrogen sources.

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

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

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

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

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

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

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

108 ild type on solid medium containing the rich nitrogen source ammonium, the growth of the mutant was i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 The nitrogen sources applied to Tempranillo grapevines were

137 f nitrogen catabolic pathways when preferred nitrogen sources are absent or limiting, a phenomenon kn

138 gh when only poor (e.g. proline) or limiting nitrogen sources are available.

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

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

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

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

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

144 ed deinduction of Ntr gene expression when a nitrogen source became available.

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

146 Anthropogenic nitrogen sources become more important in lower section

147 hat rapamycin treatment and growth with poor nitrogen sources bring about nuclear accumulation of Gln

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

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

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

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

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

153 s ensures efficient utilization of available nitrogen sources by fungi.

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

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

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

157 In an effort to define how different nitrogen sources control Gap1p sorting, we find that mut

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

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

160 slightly hypersensitive to diamide, which is nitrogen source-dependent, and minimally if at all hyper

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

162 On solid growth media with limiting nitrogen source, diploid budding-yeast cells differentia

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

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

165 its Saccharomyces cerevisiae to utilize good nitrogen sources (e.g. glutamine and ammonia) in prefere

166 -sensitive, i.e. expression is low with good nitrogen sources (e.g. glutamine) and high when only poo

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

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

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

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

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

172 Growth of the mutant with poor nitrogen sources eliminated both the arginine uptake and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

190 ) was found to be an effective electrophilic nitrogen source for the direct diamination of alpha,beta

191 use of diazo and azide functional groups as nitrogen sources for carbon radicals.

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

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

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

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

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

197 Secondly, when cultured on a secondary nitrogen source, gat1Delta mutants were unable to activa

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

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

200 vation or growth in medium containing a poor nitrogen source, Gln3 is nuclear and NCR-sensitive trans

201 cells are transferred from a good to a poor nitrogen source (glutamine to proline) or treated with r

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

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

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

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

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

207 in the NTD that were able to grow on a poor nitrogen source in the absence of phosphorylation by the

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

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

210 rge quantities of CAR1 RNA regardless of the nitrogen source in the medium.

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

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

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

214 romyces cerevisiae selectively utilizes good nitrogen sources in preference to poor ones by down-regu

215 nd to the quantity and quality of carbon and nitrogen sources in the environment both by adjusting th

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

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

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

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

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

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

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

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

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

225 c pathways for its utilization as carbon and nitrogen sources is of particular interest as the model

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

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

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

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

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

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

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

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

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

235 termine the effects of glucose and inorganic nitrogen source on gene expression on a global scale in

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

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

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

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

240 es in the nuclei of cells provided with poor nitrogen sources or during nitrogen starvation has led t

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

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

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

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

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

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

247 2 months of growth on 14N- and 15N-enriched nitrogen sources, proteins were extracted from four dist

248 tent way with the quality or quantity of the nitrogen source provided, the intracellular localization

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

250 ene expression should respond in parallel to nitrogen sources, ranging from those that highly repress

251 monia and alpha-ketoglutarate generated by a nitrogen source rather than the severity of NCR it elici

252 ion in response to the quality of carbon and nitrogen sources, respectively.

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

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

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

256 , AtSOX enhanced growth on sarcosine as sole nitrogen source, showing that it has SOX activity in viv

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

258 Thus, the ast operon exhibits nitrogen source-specific induction that is unique for an

259 GabC is proposed to reduce nitrogen source-specific modulation of expression.

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

261 Poor nitrogen sources stimulate rapid but transient Sch9 phos

262 Preferred nitrogen sources stimulate rapid, sustained Sch9 phospho

263 Both nitrogen sources stimulated bulk phytoplankton, bacteria

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

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

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

267 mutant was grown in medium containing a good nitrogen source, such as asparagine.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

292 o utilize external ammonia as an alternative nitrogen source when glutamine is absent.

293 ing proteins that transport and degrade poor nitrogen sources when excess nitrogen is available.

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