ライフサイエンスコーパス: methylamine

1 ydrazine has a reactivity similar to that of methylamine.

2 his enzyme is not essential for oxidation of methylamine.

3 times, including the first monoarylation of methylamine.

4 after treatment with a lysosomal inhibitor, methylamine.

5 ely 50% of each cofactor form at 0.8 or 2 mM methylamine.

6 ved with sodium periodate in the presence of methylamine.

7 n was irradiated (365 nm) in the presence of methylamine.

8 al environment that assimilate nitrogen from methylamine.

9 ted a 1000-fold increase in the Km value for methylamine.

10 fld1 host by selection on plates containing methylamine.

11 adily penetrate germinated spores, including methylamine.

12 rting methyl-Arg to citrulline and releasing methylamine.

13 , none is required for growth on methanol or methylamine.

14 dergo conformational change by reaction with methylamine.

15 otrophs and non-methylotrophs, to metabolize methylamine.

16 isible transmittance) due to dissociation of methylamine.

17 e by other microorganisms not directly using methylamine.

18 sialic acids by covalent derivatization with methylamine.

19 cid into the corresponding N-protected alpha-methylamine.

20 ld during the growth of M. extorquens PA1 on methylamine.

21 tance of yeast to the toxic transport analog methylamine.

22 yl-dH(4)MPT accumulation, enhances growth on methylamine.

23 own pathways by which methane is formed from methylamines.

24 thylamine:CoM methyl transfer from all three methylamines.

25 ved; and 6) mutual counteraction by urea and methylamines.

26 genesis in Methanosarcina barkeri growing on methylamines.

27 transferase specific for methanogenesis from methylamines.

28 tant generally is reduced by urea and/or the methylamines.

29 80 degrees C, or <1 h in ammonium hydroxide/methylamine (1:1) (AMA) at 80 degrees C).

30 ed an increase in growth factors for glyoxal-methylamine (19% by vol) and methylglyoxal-methylamine (

31 h a homologous series of amines or alcohols (methylamine, 2-methyl-2-aminopropane, methanol, or 2-met

32 Dansylcadaverine (20 microM), methylamine (20 mM), and bacitracin (2 mg/ml) prevented

33 ) and three isomeric 15,16-bisnorpimarenyl-N-methylamines (26a-c) were synthesized and evaluated as a

34 g [ZnTe] slabs and terminal hydrazine (2) or methylamine (3) molecules.

35 Unexpectedly, N-benzyl-N-cyclopropyl-N-methylamine (4) was found not to inactivate P450 and not

36 l-methylamine (19% by vol) and methylglyoxal-methylamine (8% by vol) aerosol, indicating that unusual

37 l permeability to the ammonia analog [(14) C]methylamine (+80%, P < 0.05).

38 n base treatment, this second species formed methylamine, a breakdown product characteristic of symme

39 also, for the first time, hepcidin bound to methylamine-activated alpha2M (alpha2M-MA).

40 iments on glycolaldehyde- and hydroxyacetone-methylamine aerosol found that the aerosol particles wer

41 Glyoxal- and methylglyoxal-methylamine aerosol particles shattered in Raman microsc

42 The utilization of (15) N methylamine also led to the release of (15) N ammonium t

43 four different amines: N,N-dimethylamine, N-methylamine, ammonia, and morpholine.

44 -rice showed an excellent gas-sensitivity to methylamine among the four natural pigments sensitized f

45 nted for by interactions between the preQ(1) methylamine and base G5 of the aptamer.

46 covalent incorporation of (14)C from [(14)C]methylamine and benzylamine into PSII subunits has been

47 ture to form MA(1-) (x) DMA(x) PbI(3) (MA is methylamine and DMA is dimethylamine) are defect density

48 cleaved with the small-molecule nucleophiles methylamine and histamine, but when Spy0125 was mechanic

49 ce is evident under conditions of saturating methylamine and oxygen with D319E.

50 The D319E mutant catalyzes the oxidation of methylamine and phenethylamine, but not that of benzylam

51 Methylamine and phenylethylamine were not determined in

52 Labeling of CP47, D2, and D1 with methylamine and phenylhydrazine approached a one-to-one

53 epend on ion concentration, pH, the specific methylamine and substrate, and identity of even a single

54 but the BL group had reduced urine levels of methylamines and aromatic amino acids metabolites.

55 y, secondary and tertiary amines including N-methylamines and molecules used in life science applicat

56 , secondary and tertiary amines as well as N-methylamines and more complex drug targets.

57 clusion that inhibition by dansylcadaverine, methylamine, and bacitracin is not due to an alkalinizat

58 nd indoxyl sulfate, but levels of hippurate, methylamine, and dimethylamine were not significantly lo

59 ith similarity to the methanogenic methanol, methylamine, and methanethiol methyltransferases and to

60 yl)furfuryl alcohol, N,N-dimethylthiophene-2-methylamine, and N,N-dimethylbenzylamine.

61 osine, arginine dipeptides, gamma-D-Glu-Gly, methylamine, and others.

62 ses initiate methanogenesis from the various methylamines, and these enzymes are encoded by genes wit

63 The protein contents in methylamine- and methanol-grown cells showed a significa

64 Methylamine- and pyridine-treated films are also p-type.

65 ormyl-4-methylphenol and bis(2-aminoethyl)-N-methylamine) are described.

66 y = N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine) are investigated in comparison to those of

67 hydrazine) and [ZnTe(ma)] (3; ma = MeNH(2) = methylamine) are two-dimensional (2-D) layered structure

68 AAmRe(O)(X)] DAAm = N,N-bis(2-arylaminoethyl)methylamine; aryl = C6F5 (X = Me, 1, COCH3, 2, Cl, 3) as

69 hylotrophs that have to switch between using methylamine as a carbon and energy source or just a nitr

70 n order to use the NMG pathway for growth on methylamine as a carbon and energy source.

71 lamide synthetase is essential for growth on methylamine as a carbon source but not as a nitrogen sou

72 s that can grow on one-carbon compounds, use methylamine as a carbon source.

73 thylotrophic microorganisms may also utilize methylamine as a nitrogen source, but little is known ab

74 pastoris on methanol as a carbon source and methylamine as a nitrogen source.

75 only when cells are grown in the presence of methylamine as a sole carbon source and is repressed by

76 ables rapid growth on high concentrations of methylamine as the primary carbon and energy substrate,

77 hway plays a pivotal role during growth with methylamine as the sole nitrogen source, which we demons

78 grow on reduced single-carbon compounds like methylamine as the sole source of carbon and energy.

79 he primary C-H bonds in linear- and branched-methylamines, as well as secondary C-H bonds in higher d

80 a novel cobalt(III) Schiff base complex with methylamine axial ligands, and we present both computati

81 glycolamine (DGA), and N,N-bis(3-aminopropyl)methylamine (BAPMA) as a function of temperature and ami

82 The structures of the molecules methylamine-borane, MeH(2)N.BH(3), and dimethylamine-bor

83 talytic dehydrocoupling/dehydrogenation of N-methylamine-borane, MeNH(2).BH(3) (7), to yield the solu

84 The synthesis and biological activity of a methylamine-bridged enkephalin analogue (MABE) is presen

85 port an association of LysRS1 with growth on methylamine, but not an essential role for LysRS1/LysRS2

86 carbonyl cyanide m-chlorophenylhydrazone and methylamine, but not by spermine, consistent with an act

87 pt levels were also high in media with CO or methylamines, but much lower with methanol.

88 erent substrates (72, 190, and 162 s(-1) for methylamine, butylamine, and benzylamine, respectively).

89 observed, respectively, for the reactions of methylamine, butylamine, and benzylamine.

90 counteraction of urea effects on enzymes by methylamines can depend on ion concentration, pH, the sp

91 we report the effects of 1, 3-cyclohexanebis(methylamine) (CBM) on secretion in vivo, a compound chos

92 Methylamine (CH(3)NH(2))-mediated deacylation has previo

93 We report herein the discovery of methylamine (CH3NH2) induced defect-healing (MIDH) of CH

94 vitro ATP-dependent reductive activation of methylamine:CoM methyl transfer from all three methylami

95 SIP experiments using (15) N methylamine combined with metagenomics and metaproteomic

96 After cooling, the methylamine complex is re-formed, returning the absorber

97 layer-composed of a metal halide perovskite-methylamine complex-from a transparent state (68% visibl

98 e, but not other common C1 compounds such as methylamine, could support growth.

99 ny of the persisting organisms play roles in methylamine cycling, ultimately supporting methanogenesi

100 nding character of the adjacent C9-O2 to the methylamine (Cys69 backbone).

101 Methylamine dehydrogenase (MADH) and amicyanin form a ph

102 pared with the complex of the TTQ-containing methylamine dehydrogenase (MADH) and the cupredoxin amic

103 s for methylamine oxidation: the periplasmic methylamine dehydrogenase (MaDH) and the cytoplasmic N-m

104 tryptophylquinone (TTQ) in substrate-reduced methylamine dehydrogenase (MADH) by amicyanin is known t

105 Methylamine dehydrogenase (MADH) catalyzes the oxidative

106 Methylamine dehydrogenase (MADH) contains the protein-de

107 The biosynthesis of methylamine dehydrogenase (MADH) from Paracoccus denitri

108 The biosynthesis of methylamine dehydrogenase (MADH) from Paracoccus denitri

109 Methylamine dehydrogenase (MADH) has been immobilized in

110 factor tryptophan tryptophylquinone (TTQ) in methylamine dehydrogenase (MADH) involves the post-trans

111 Methylamine dehydrogenase (MADH) is a tryptophan tryptop

112 Methylamine dehydrogenase (MADH) is a tryptophan tryptop

113 Paracoccus denitrificans methylamine dehydrogenase (MADH) is an enzyme containing

114 Methylamine dehydrogenase (MADH) may be immobilized in a

115 Methylamine dehydrogenase (MADH) possesses an alpha(2)be

116 The biosynthesis of methylamine dehydrogenase (MADH) requires formation of s

117 in that mediates electron transfer (ET) from methylamine dehydrogenase (MADH) to cytochrome c-551i.

118 he diheme enzyme MauG and different forms of methylamine dehydrogenase (MADH) were subjected to kinet

119 The scheme is based on the use of methylamine dehydrogenase (MADH) which converts primary

120 Contrary to the TTQ-containing subunit of methylamine dehydrogenase (MADH), which is catalytically

121 yptophan tryptophylquinone (TTQ) cofactor of methylamine dehydrogenase (MADH).

122 inone (TTQ), the protein-derived cofactor of methylamine dehydrogenase (MADH).

123 tural electron acceptor for the quinoprotein methylamine dehydrogenase (MADH).

124 tural electron acceptor for the quinoprotein methylamine dehydrogenase (MADH).

125 nal modification of the precursor protein of methylamine dehydrogenase (preMADH) to complete biosynth

126 ional modification of a precursor protein of methylamine dehydrogenase (preMADH) to complete the bios

127 ation of a biosynthetic precursor protein of methylamine dehydrogenase (PreMADH) with partially synth

128 rent from those for the related quinoprotein methylamine dehydrogenase and its associated redox prote

129 ese data in which the reduction of Cu(2+) by methylamine dehydrogenase is a true ET reaction while th

130 talyzes posttranslational modifications of a methylamine dehydrogenase precursor protein to generate

131 -studied aerobic methylotroph, a periplasmic methylamine dehydrogenase that catalyzes the primary oxi

132 ectron transfer (ET) reactions from O-quinol methylamine dehydrogenase to oxidized native and mutant

133 tophylquinone (TTQ), the prosthetic group of methylamine dehydrogenase, is formed by post-translation

134 or the ET reactions from another TTQ enzyme, methylamine dehydrogenase, to amicyanin.

135 related to M. extorquens AM1 but is lacking methylamine dehydrogenase, to dissect the genetics and p

136 pyruvate:ferredoxin oxidoreductase, and the methylamine dehydrogenase-amicyanin complex.

137 Within the methylamine dehydrogenase-amicyanin-cytochrome c-551i co

138 tryptophan tryptophylquinone cofactor within methylamine dehydrogenase.

139 n tryptophylquinone, the prosthetic group of methylamine dehydrogenase.

140 es, methylotrophy is enabled by methanol and methylamine dehydrogenases and their specific electron t

141 Experiments with methylamine demonstrated that ozonation converts methyla

142 n of Tmm and DMS oxidation in R. pomeroyi is methylamine-dependent and regulated at the post-transcri

143 ergy barrier for the ET from copper to heme, methylamine-dependent reduction of heme by the three-pro

144 try of IPA/NO, we prepared the corresponding methylamine derivative as a sodium salt that was highly

145 yrene-maleic acid (SMA) polymers including a methylamine derivative facilitated gentle release of the

146 Interestingly, its methylamine derivative, 49, displayed good enzyme inhibi

147 We find that methylamine, dimethylamine, and trimethylamine undergo m

148 small numbers of water molecules to ammonia, methylamine, dimethylamine, and trimethylamine, and thei

149 eration is found to increase the basicity of methylamine, dimethylamine, benzylamine, and N,N-dimethy

150 eration is found to increase the basicity of methylamine, dimethylamine, benzylamine, N,N-dimethylani

151 reports have shown that the organic cations methylamine, dimethylamine, ethylamine, and trimethylami

152 tion of the omega-bromo groups with ammonia, methylamine, dimethylamine, or trimethylamine provided p

153 tal structures have also been determined for methylamine-, dimethylamine-, and trimethylamine-borane,

154 Whereas the poorly nucleophilic ammonia and methylamine do not react, hydroxylamine, methoxylamine,

155 Ozonation of N-methylamine drugs ubiquitously formed nitromethane, typi

156 compound, N, N-bis (5-ethyl-2-hydroxybenzyl) methylamine (EMD), and present evidence demonstrating it

157 compound, N, N-bis (5-ethyl-2-hydroxybenzyl) methylamine (EMD), in targeting c-Myc in several lung ca

158 values are affected by the degree of excess methylamine employed.

159 (Arg), and several primary amines including methylamine, ethylamine, n-propylamine, n-butylamine, an

160 from uric acid, glucose, ammonia, caffeine, methylamine, ethylenediamine, hydroxylamine, n-butylamin

161 f homologous nucleophiles (e.g., ammonia and methylamine) facilitates recognition and identification

162 (13)C-labeled glucose by derivatization with methylamine followed by multiple reaction monitoring sca

163 onothio-1,3-diketones with alpha-substituted methylamines, followed by their alpha-nitrosation with s

164 ines as functional groups (e.g., secondary N-methylamines) formed chloropicrin at high yields, likely

165 The usual explanation is that the methylamines found in the renal medulla, namely glycerop

166 t a very mild synthesis of N-protected alpha-methylamines from the corresponding amino acids.

167 These drugs all feature N-methylamine functional groups, and certain N-alkylamines

168 ssay conditions (pH and salt concentration), methylamines (glycerophosphocholine, betaine, and trimet

169 terium extorquens AM1, MaDH is essential for methylamine growth, but the NMG pathway has no known phy

170 ne > pyridine > triethylamine > ethylamine > methylamine > diethylamine > tert-butylamine > ammonia.

171 and N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine, has been proposed to attack C-H bonds by an

172 ylglyoxal and the primary amines glycine and methylamine have been determined.

173 However, urea and methylamines have the similar (not counteracting) effect

174 t (4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)methylamine hydrobromide (TCB-2) enhanced C-fiber-evoked

175 s (4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)methylamine hydrobromide (TCB-2).

176 st 4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)methylamine hydrobromide, binds less to the mGlu2 promot

177 5,5-bis-(4-fluorophenyl)tetrahydrofuran-2-yl]methylamine hydrochloride, NCC1048) in a model of hypoxi

178 respect to nucleophilic addition to ammonia, methylamine, hydroxylamine, methoxylamine, and hydrazine

179 Increasing vesicular pH with internal methylamine in hair cells also abolished the transient b

180 rom the dark reactions of methylglyoxal with methylamine in simulated evaporated cloud droplets.

181 In HPAO-2, an inflated (D)k(cat)/K(m)(methylamine) in relation to (D)k(cat)/K(m)(benzylamine)

182 C3), we coupled the free sulfhydryl group of methylamine-inactivated C3 to a thiolSepharose matrix.

183 A total of >30 structurally diverse N-methylamines, including bioactive compounds, were select

184 [(14)C]Methylamine incorporation showed the k(cat)/K(m)((app))

185 The K(m) for methylamine increases from 9 microM to 15 mM.

186 Methylamine-induced thin-film transformation at room-tem

187 ion in the adenine base to incorporate [(3)H]methylamine into the synthesis of [(3)H]MRS2279 to high

188 In HPAO-1, the k(cat)/K(m) for methylamine is 330-fold greater than for benzylamine, wh

189 kcat/Km for methylamine is found to be 80-fold reduced compared to t

190 Archaeal methane formation from methylamines is initiated by distinct methyltransferases

191 is(2-[2-(N',N'-4-dimethylamino)pyridyl]ethyl)methylamine) is described, to model aspects of the chemi

192 (N4Py: N,N-bis(2-pyridylmethyl)bis(2-pyridyl)methylamine), is the least basic oxidant.

193 ve results acquired from peptide mapping and methylamine labeling.

194 The method employs neutron encoded (NeuCode) methylamine labels ((13)C or (15)N enriched) that are af

195 nd the second a bis-tert-butyl-substituted N-methylamine ligand.

196 -N-(2,2,2-trifluoroethylsulfonyl)-pyrid-3-yl methylamine (LY487379) is a selective positive allosteri

197 id (OxA) on NPF from the reaction of MSA and methylamine (MA) at 1 atm and 294 K in the presence and

198 rimethylamine (TMA), dimethylamine (DMA) and methylamine (MA) in fish.

199 RhAG also conferred resistance to methylamine (MA), a toxic analog of ammonium, and expres

200 h trimethylamine (TMA), dimethylamine (DMA), methylamine (MA), and ammonia over the range of 21-28 de

201 with the primary and secondary alkylamines: methylamine (MA), dimethylamine (DMA), and ethylamine (E

202 th the radioactive analog of ammonium [(14)C]methylamine (MA), had an apparent EC(50) of 1.6 mm and a

203 c biosensors (ABSs) for primary alcohols and methylamine (MA).

204 mtaCB3 fusions was delayed, suggesting that methylamines may repress their expression.

205 No measurable amounts of cadaverine (CAD) or methylamine (MEA) were found, showing no spoilage sympto

206 (tfepma = (bis[bis(trifluoroethoxy)phosphino]methylamine, MeN(P[OCH2CF3]2)2), have been prepared by t

207 l2CN(t)Bu (9) (dfpma = bis(difluorophosphino)methylamine, MeN(PF2)2).

208 type of DeltappylT reveals the deficiency in methylamine metabolism expected of a Methanosarcina spec

209 ysine derivative encoded by the UAG codon in methylamine methyltransferase genes of Methanosarcina ba

210 Each methylamine methyltransferase methylates a cognate corri

211 is encoded by a single amber (UAG) codon in methylamine methyltransferase transcripts.

212 Genes encoding methanogenic methylamine methyltransferases all contain an in-frame a

213 vealed only four protein families, including methylamine methyltransferases and transposases.

214 have been characterized previously, a set of methylamine methyltransferases in which Pyl is assumed t

215 Only methylamine methyltransferases matched the Pyl trait and

216 codon in genes encoding proteins such as the methylamine methyltransferases present in some Archaea a

217 etry in A. arabaticum proteins including two methylamine methyltransferases.

218 rtion of pyrrolysine into the active site of methylamine methyltransferases.

219 were comparable with those determined using methylamine-modified alpha(2)M, suggesting that higher-o

220 enriched in prion assemblies captured by the methylamine-modified copolymer.

221 n the presence of excess substrate, the next methylamine molecule initiates a nucleophilic attack of

222 pe, the DeltappylT strain cannot grow on any methylamine, nor use monomethylamine as sole nitrogen so

223 anomalous basicity effect of ammonia and the methylamines on going from the gas phase to aqueous solu

224 d two analogs of ammonium (hydroxylamine and methylamine) on ANR activity in soil slurries.

225 atial arrangement, namely to the interior of methylamine or ammonia-treated alpha(2)M and to the exte

226 prepared from nitrophenyl carbamate 14a and methylamine or directly from 5-aminoimidazole-4-carboxam

227 Aminolyses of these isoquinolinediones with methylamine or ethanolamine produced the isoquinolinedio

228 he compound 3 reacts at normal pressure with methylamine or ethylamine, forming N-alkylpyridinium sal

229 In contrast, methylamine or the inhibitor of macroautophagy, 3-methyl

230 In carbonyl compound reactions with AS, methylamine, or AS/glycine mixtures, product absorbance

231 ature experiments, regardless of whether AS, methylamine, or glycine was present.

232 pheric aldehydes with ammonium sulfate (AS), methylamine, or glycine.

233 lly or chemically in solutions of hydrazine, methylamine, or pyridine to produce electronically coupl

234 Native MADH exhibits a strong preference for methylamine over longer carbon chain amines.

235 nPtRu) coupled with alcohol oxidase (AO) and methylamine oxidase (AMO) were chosen to construct amper

236 kcat for D319E methylamine oxidase is reduced 200-fold compared to that

237 Profiles for WT-catalyzed methylamine oxidation and Y305A-catalyzed ethylamine oxi

238 mutation had no effect on the parameters for methylamine oxidation by MADH, but significantly affecte

239 ection of proteins for the N-methylglutamate methylamine oxidation pathway that appears to be auxilia

240 omparable, while profiles of Y305A-catalyzed methylamine oxidation suggest the pH-dependent build-up

241 ination of the steady state species of D319E methylamine oxidation, in combination with the kinetic d

242 actor to yield a mature enzyme competent for methylamine oxidation.

243 , such as the N-methylglutamate pathway, for methylamine oxidation.

244 cally relevant N-methylglutamate pathway for methylamine oxidation.

245 cterium extorquens AM1 encode two routes for methylamine oxidation: the periplasmic methylamine dehyd

246 hotoactive layers rapidly decompose yielding methylamine, PbI2 , and I2 as products.

247 c amine permeases and may therefore encode a methylamine permease.

248 Ammonium transporter/methylamine permease/rhesus (AMT/Mep/Rh) transporters ar

249 Ammonium transporters (AMT), methylamine permeases (Mep), and the more distantly rela

250 led that aniline and aliphatic amines (e.g., methylamine) prefer to attack C8 of intermediate 4a, aff

251 Methanogenesis from methylamines, probably stemming from degradation of bact

252 ing at approximately 40% RH for all aldehyde-methylamine products.

253 shown that an mtdB mutant is able to grow on methylamine, providing a system to study the role of Mtd

254 ns,trans,trans-[Pt(N3 )2 (OH)2 (MA)(Py)] (MA=methylamine, Py=pyridine).

255 t linearly with increasing concentrations of methylamine (r=0.931).

256 Methylamine reduction at acidic or neutral pH has reveal

257 However, methylamine reduction at pH 8.5 has revealed a copper-li

258 The studies with hydroxylamine and methylamine showed that both of these ammonium analogs i

259 hyltransferase activity, including MtbA, the methylamine-specific CoM methylase and the pyl operon re

260 acetivorans C2A encode putative methanol- or methylamine-specific MT2 enzymes.

261 comes significantly depleted compared to the methylamine starting material.

262 volatile nucleophiles including hydrazines, methylamine, t-butyl hydroperoxide, N-hydroxylamine, alp

263 ion of Km of wild-type enzyme by urea and/or methylamines that is partially additive, whereas at the

264 omotropic weak bases (NH4Cl, chloroquine, or methylamine) that increased lysosomal pH and sensitized

265 For t-butylamine and methylamine, the amount of labeling increased when PSII

266 es in aquatic habitats on the utilization of methylamine, the simplest methylated amine, have mainly

267 pid immobility in and the slow permeation of methylamine through the inner membrane of dormant spores

268 sintegration, either by serum treatment with methylamine to block C4 and C3 split product binding or

269 MADH) catalyzes the oxidative deamination of methylamine to formaldehyde and ammonia.

270 cterium extorquens AM1 oxidizes methanol and methylamine to formaldehyde and subsequently to formate,

271 nase that catalyzes the primary oxidation of methylamine to formaldehyde has been examined in great d

272 ylamine demonstrated that ozonation converts methylamine to nitromethane at approximately 100% yield.

273 ion and (b) S(N)2 substitution reaction with methylamine to provide diamine 14 with inversion of conf

274 laterally separated by 120 A, whereas in the methylamine-transformed alpha2M, the epitopes are at the

275 Hypochlorite oxidation of methylamine-treated alpha2M (alpha2M*), an analogue of t

276 The most significant drop in methylamine uptake was seen for the ump2 and the ump1ump

277 while ump1 disruption only slightly reduced methylamine uptake.

278 tory and assimilatory modules suggested that methylamine use via the N-methylglutamate pathway requir

279 B-like and sox-like genes play a key role in methylamine utilization and encode N-methylglutamate syn

280 ded by the amber codon in genes required for methylamine utilization by members of the Methanosarcina

281 rrectly assembled MADH, eight genes from the methylamine utilization gene cluster of P. denitrificans

282 lete genome of a model obligate methanol and methylamine utilizer, Methylobacillus flagellatus (strai

283 The draft genomes of two methylamine utilizers were obtained and their metabolism

284 teomics facilitated identification of active methylamine-utilizing Alpha- and Gammaproteobacteria.

285 re firstly exposed to atmospheres containing methylamine vapours with concentrations over the range 2

286 ibition of ANR activity by hydroxylamine and methylamine was due to formation of the glutamine analog

287 btained and their metabolism with respect to methylamine was examined.

288 yano-induced cleavage of cysteinyl proteins, methylamine was found to be superior to ammonia for cyan

289 With FXIIIa or tTG catalysis, [(14)C]methylamine was incorporated into Q2A-alpha(2)AP, indica

290 participating in coenzyme M methylation with methylamines, was not inhibited by dimethylsulfide and d

291 he improved NPF descriptions for ammonia and methylamines, we placed special focus on the potential t

292 series of N-substituted (2-phenylcyclopropyl)methylamines were designed and synthesized, with the aim

293 able Ru(II) arene complexes and chiral alpha-methylamines were employed as highly enantioselective ca

294 l reacted (presumably on chamber walls) with methylamine with a rate constant k = (9 +/- 2) x 10(-17)

295 Both forms are rapidly reduced by substrate methylamine with a rate constant of 199 s(-1) but behave

296 mann-type coupling reactions of methanol and methylamine with iodobenzene by beta-diketone- and 1,10-

297 uctive amination of an epoxy aldehyde with N-methylamine with subsequent intramolecular oxirane ring

298 ethanosarcina spp. begin methanogenesis from methylamines with methyltransferases made via the transl

299 ion showed highest reporter gene activity on methylamines with much lower expression on CO or methano

300 f lysK or lysS grew normally on methanol and methylamines with wild-type levels of monomethylamine me