ライフサイエンスコーパス: arabinose

1 concentrated acid were rhamnose, mannose and arabinose.

2 se, while the R analogue was obtained from L-arabinose.

3 tion with 2,3,5-tri-O-benzyl-D-ribose and -D-arabinose.

4 llulose, which is composed of d-xylose and l-arabinose.

5 se, galactose, lactose, fructose, ribose and arabinose.

6 uires the binding of one or two molecules of arabinose.

7 rabinose and the other subunit does not bind arabinose.

8 for pairs of DNA half-sites is controlled by arabinose.

9 r controls antigen gene expression by adding arabinose.

10 d magnitude (K(d)=0.37 mM) in the absence of arabinose.

11 protein and thereby induce CDI by removal of arabinose.

12 in response to the absence or presence of l-arabinose.

13 ossible contribution of the alpha-anomer for arabinose.

14 and not in response to its native effector L-arabinose.

15 on of psl could be controlled by addition of arabinose.

16 uced substantial biofilms in the presence of arabinose.

17 sis of cell wall-building components such as arabinose.

18 sound-induced whey protein (WP) glycation by arabinose.

19 We have found that arabinose, 2'F-arabinose, and ribose substitutions stabi

20 ctin is including galacturonic acid (66.0%), arabinose (26.2%), galactose (3.7%), rhamnose (2.7%) and

21 DO8P) synthase catalyzes the condensation of arabinose 5-phosphate (A5P) and phosphoenolpyruvate (PEP

22 incubated with phosphoenolpyruvate (PEP) and arabinose 5-phosphate (A5P) shows the formed product, 3-

23 the conversion of ribulose 5-phosphate into arabinose 5-phosphate (A5P), the first committed step in

24 Arabinose 5-phosphate isomerase (API), encoded by Y. pes

25 combinant c3406 protein, found it to possess arabinose 5-phosphate isomerase activity, and characteri

26 nt homology to the sugar isomerase domain of arabinose 5-phosphate isomerases but lacking the tandem

27 ine beta-synthase domains found in the other arabinose 5-phosphate isomerases of E. coli.

28 following monosaccharides: glucose (82.51%), arabinose (5.32%) and xylose (12.17%).

29 Arabinose-5-phosphate isomerases (APIs) catalyze the int

30 s, pyrophosphate, a TK cofactor analog and d-arabinose-5-phosphate, a substrate analog.

31 erconversion of d-ribulose-5-phosphate and D-arabinose-5-phosphate, the first step in the biosynthesi

32 n fluorescent proteins, rhamnose, ribose and arabinose, all of which could be related to cellular and

33 se; however, a small amount of xylobiose and arabinose also confirmed the presence of xylosidase and

34 he nucleobases, and instead proceeds through arabinose amino-oxazoline and anhydronucleoside intermed

35 ost of ignoring ribose aminooxazoline, using arabinose aminooxazoline instead.

36 by their resistance to the nonmetabolizable arabinose analog, d-fucose.

37 Polymer-bound galacturonate, xylose, arabinose and apiose residues (all produced via UDP-gluc

38 allographic structures of the complexes with arabinose and cellotriose reveal the important role of s

39 [structures: see text] D-Arabinose and D-glucose are transformed into the identic

40 xperiments involved reactions of d-xylose, d-arabinose and d-ribose with glycine, alpha-l- or beta-al

41 Transcription of the genes required for l-arabinose and d-xylose consumption is regulated by the s

42 li can rapidly switch to the metabolism of l-arabinose and d-xylose in the absence of its preferred c

43 rabinoxylan and catabolism of the released l-arabinose and d-xylose.

44 The polysaccharide rich in arabinose and galactose (39-54%) and mannoproteins (38-5

45 Mannoproteins and polysaccharides rich in arabinose and galactose (PRAG) were poor foam formers bu

46 II (RG-II), but only Polysaccharides Rich in Arabinose and Galactose (PRAGs) were considered in the f

47 d that the cell walls are highly enriched in arabinose and galactose, two major residues of arabinoga

48 sted mainly of galacturonic acid followed by arabinose and galactose.

49 iffusion of L-glutamine, the monosaccharides arabinose and glucose, and the tetrasaccharide stachyose

50 iffusion of L-glutamine, the monosaccharides arabinose and glucose, the disaccharide sucrose, and eve

51 ncipally of neutral oligosaccharides rich in arabinose and glucose.

52 d xylan lacks acetylation but is modified by arabinose and MeGlcA.

53 d to activate transcription in response to D-arabinose and not in response to its native effector L-a

54 ively charged substituents 4-amino-4-deoxy-L-arabinose and phosphoethanolamine respectively.

55 Sugars turanose, trehalose, arabinose and raffinose, elements Ba, Sr, P, Cd and Se,

56 tified the residues involved in binding of L-arabinose and recognition of DNA.

57 odel with different carbon sources, glucose, arabinose and rhamnose, were used to support fungal grow

58 s in which one subunit is capable of binding arabinose and the other subunit does not bind arabinose.

59 -epimerase gene correlated with increases in arabinose and uronic acid content in seedling cell walls

60 ), Tyr(92), or Asn(139), which interact with arabinose and xylose side chains at the -2* subsite, abr

61 Arabinose and xylose were the most present NS with more

62 The total monosaccharide (glucose, arabinose and xylose) levels in the glycosides were dete

63 r of magnitude faster than its diastereomers arabinose and xylose.

64 tivities, from (+)-dehydroisoandrosterone, l-arabinose, and D-xylose on gram scale.

65 e utilization, fermentation of salicin and d-arabinose, and expression of beta-glucosidase activity,

66 ngs cooperatively incorporated xylose (Xyl), arabinose, and glucuronic acid residues from their corre

67 We have found that arabinose, 2'F-arabinose, and ribose substitutions stabilize the propel

68 ctose, and mannose), three pentoses (xylose, arabinose, and ribose), two deoxyhexoses (fucose and rha

69 ce the response of the reported mutants to D-arabinose, and the mutants are not induced by other suga

70 ted to UDP-galacturonic acid (UDP-GalA), UDP-arabinose, and UDP-xylose.

71 the toolkit, particularly those recognizing arabinose- and/or galactose-containing structures, are p

72 l-Arabinose (Ara) is a constituent of several cell wall po

73 In plants, L-arabinose (Ara) is a key component of cell wall polymers

74 luding unique Hep and 4-amino-4-deoxy-beta-L-arabinose (Ara4N) monosaccharides and branched Hep-Hep d

75 e positively charged sugar 4-amino-4-deoxy-l-arabinose (Ara4N) to lipid A in their outer membrane.

76 decaprenyl phosphate-alpha-4-amino-4-deoxy-l-arabinose arabinosyl transferase).

77 e arms and reduce the stability of the minus-arabinose arm structure.

78 achieved using cheap and readily available l-arabinose as a chiral pool.

79 aining why the enzyme can utilize xylose and arabinose as specificity determinants.

80 the program functions as a multiplexer with arabinose as the selector.

81 L-arabinose binding induces movement of wHTH domains, resu

82 strate specificity is conferred by a shallow arabinose binding pocket adjacent to the deep active sit

83 er oxidative stress conditions, preventing L-arabinose binding.

84 ive subsites in the catalytic cleft and an l-arabinose-binding pocket at the bottom of the cleft.

85 namics that accompany the interaction of the arabinose-binding protein (ABP) with its ligand, d-galac

86 redox state of the single cysteine of the L-arabinose-binding protein AraF.

87 The l-arabinose biosensor presented in this study proves the p

88 lved the crystal structures of the apo and L-arabinose-bound BtAraR proteins, as well as the complex

89 sis of truncated LAM, which appeared to lack arabinose branching.

90 ching angiosperms and eudicot xylan, lacking arabinose but possessing acetylation on alternate xylosy

91 e-Drosophila melanogaster prefers D- over L- arabinose, but forms long-term memories of L-arabinose m

92 reduced alpha1-2-mannose side chains and no arabinose caps.

93 into fuels and chemicals using the fungal l-arabinose catabolic pathway.

94 genes, many of which are involved in xylose, arabinose, cellobiose, and hemicellulose metabolism.

95 ective in arabinosyltransferases that extend arabinose chains, indicating that CLV3 must be fully ara

96 e co-utilized and utilization of mannose and arabinose commences before glucose and xylose are exhaus

97 system, which positively reacts to rising l-arabinose concentrations.

98 pendency was detectable over a wide range of arabinose concentrations.

99 Furthermore, enhanced deposition of arabinose-containing carbohydrate was detected in the ki

100 fically hydrolyze non-reducing residues from arabinose-containing polysaccharides.

101 ium smegmatis resulted in a reduction of the arabinose content of both AG and LAM that accompanied th

102 by this strain was linearly dependent on the arabinose content of the medium.

103 position of the NTP, including 2',3'-ddCTP, arabinose-CTP, and 2'-O-methyl-CTP, inhibit polymerase,

104 with a wide range of substrates, including L-arabinose, D-fucose, D-galactose, D-glucose, and D-xylos

105 hamnose) and complex combinations thereof (l-arabinose, d-gluconate).

106 xylose, d-galactose, d-mannose, d-glucose, d-arabinose, d-rhamnose and d-glucuronic acid.

107 Understanding the l-arabinose/d-xylose regulatory network is key for such bi

108 GH43 enzymes, suggesting that the extensive arabinose decorations appended to pectins and xylans may

109 action to other components of xylan, such as arabinose decorations of glucuronoarabinoxylan.

110 At3g57630 was named Extensin Arabinose Deficient transferase, ExAD, accordingly.

111 rate, comparable to the recently described L-arabinose degradation pathway of Azospirillum brasilense

112 rmediates to catabolize L-arabinose via an L-arabinose dehydrogenase, AraA(At), encoded at the Atu111

113 cassette, so that the expression of rpoS was arabinose dependent.

114 M by AraC, in contrast to the well-described arabinose-dependent activation of other target genes.

115 ive rfaH promoter with the tightly regulated arabinose-dependent araC P(BAD) promoter so that rfaH ex

116 med studies where YidC was depleted using an arabinose-dependent expression system.

117 chi8937(pYA3681) exhibits arabinose-dependent growth.

118 by cloning the eilA gene under control of an arabinose-dependent promoter.

119 rsinia pseudotuberculosis mutant strain with arabinose-dependent regulated and delayed shutoff of crp

120 Our results demonstrate that arabinose-dependent regulated crp expression is an effec

121 s KIM5+, a Deltacrp mutant and a mutant with arabinose-dependent regulated delayed-shutoff crp expres

122 We demonstrate arabinose-dependent repression of ydeNM by AraC, in cont

123 is described starting from D-mannnose and L-arabinose derivatives for the D- and L-series, respectiv

124 lly pure 1 is described, starting from the l-arabinose derived chiron ent-6.

125 lective 1,3-dipolar cycloadditions between d-arabinose-derived nitrones and d-mannitol-derived trans-

126 siological recordings indicate that L- and D-arabinose differentially activate Gr43a-expressing neuro

127 The presence of 100 mM L-arabinose does not influence the response of the reporte

128 reorient DPA to the periplasm, allowing this arabinose donor to then be used in the buildup of the ar

129 Mutations in decaprenylphosphoryl-beta-D-arabinose (DPA) biosynthetic and utilization pathway gen

130 ormation of decaprenyl-monophosphoryl-beta-D-arabinose (DPA) in the genome of M. tuberculosis led us

131 sweet and chemically similar sugars-L- and D-arabinose-Drosophila melanogaster prefers D- over L- ara

132 s composed of glucose, galacturonic acid and arabinose; for amaranth, xylose was also a major constit

133 Upon invasion of host tissues, an arabinose-free environment, transcription of asdA, murA,

134 Arabinose from arabinogalactan side chains was hypothesi

135 ,(1 --> 4)-beta-D-glucans, a gradual loss of arabinose from glucuronoarabinoxylans, and an increase i

136 decaprenyl phosphate-4-amino-4-deoxy-alpha-l-arabinose from undecaprenyl phosphate-4-deoxy-4-formylam

137 The most abundant sugars were xylose, arabinose+fructose and sucrose, presenting dried samples

138 both E. coli EDL933 and E. coli MG1655 used arabinose, fucose, and N-acetylglucosamine in the intest

139 d structurally related carbohydrates such as arabinose, fucose, methyl galacturonate and N-acetylgala

140 lbatana terroirs wines, and it modified the (Arabinose+Galactose)/Rhamnose ratio in Canada Judio, Alb

141 y and fraction 10R was composed of rhamnose, arabinose, galactose and uronic acid in 2.8:65.8:28.5:3M

142 Fraction 50R was composed of rhamnose, arabinose, galactose and uronic acid in 4.3:56.2:37.4:2M

143 th was mainly composed of galacturonic acid, arabinose, galactose, xylose and glucose.

144 he most abundant monosaccharide present with arabinose, galactose, xylose and mannose as minor consti

145 The use of commercial enzyme modified the Arabinose/Galactose and the Rhamnose/Galacturonic acid r

146 Behavioral assays indicate that L-arabinose-generated memories require sugar receptor Gr43

147 n the extracted polysaccharides, followed by arabinose, glucose, galacturonic acid, rhamnose, mannose

148 termined monosaccharides (fucose, galactose, arabinose, glucose, rhamnose, xylose, mannose, fructose

149 Fucose, galactose, arabinose, glucose, sucrose, rhamnose, xylose, mannose,

150 We show that hemicellulose branches of arabinose, glucuronic acid, and especially glucuronate s

151 by total acid hydrolysis, resulting in a Xyl:arabinose:glucuronic acid molar ratio of approximately 1

152 array analysis shows that AftD binds complex arabinose glycans.

153 evidence for a diversity of chlorogenic acid-arabinose hybrids formed during roasting, opening new pe

154 (1) was synthesized from readily available d-arabinose in 11% overall yield and >99.5/0.5 dr (diaster

155 enyl phosphate-4-deoxy-4-formylamino-alpha-l-arabinose in polymyxin-resistant strains of E. coli and

156 ransporter in E. coli enabled induction by D-arabinose in the 0.1 mM range.

157 urn was dependent on the amount of available arabinose in the medium.

158 in the pentose ring, which is epimerized to arabinose in the minor product.

159 y sulfated 3-linked beta-arabinan (Ab1) with arabinose in the pyranose form was obtained from green s

160 One involved the arabinose-induced expression of plasmid-encoded sigma(28

161 in aerobic and anaerobic conditions with an arabinose-inducible expression system.

162 The complete genetic program containing an arabinose-inducible FimE controlling CheW/CheW* (and con

163 he oriV origin, this vector is capable of an arabinose-inducible increase in plasmid copy number.

164 c Salmonella vaccine strains with or without arabinose-inducible LacI synthesis.

165 (P(R)), which is negatively regulated by an arabinose-inducible P22 c2 gene located on both the plas

166 ked to MG_454, we cloned this gene behind an arabinose-inducible PBAD promoter in plasmid pHERD20T an

167 ENTR/SD/D-TOPO and transferred to a low copy arabinose-inducible pBAD/Myc-HisA expression plasmid con

168 cells carrying adrA under the control of an arabinose-inducible promoter produced substantial biofil

169 H15) containing surA under the control of an arabinose-inducible promoter restored in vivo binding an

170 f DeltadspI in trans under the control of an arabinose-inducible promoter.

171 sses Cre recombinase under the control of an arabinose-inducible promoter.

172 An arabinose-inducible, rapidly folding OmpA-GFP chimera wa

173 Arabinose induction of a single-copy YpTOP-D117N mutant

174 drolyzable branched RNA analogues containing arabinose instead of ribose at the branchpoint junction

175 ment of recombinant organisms that convert l-arabinose into fuels and chemicals using the fungal l-ar

176 ral small molecules (glucarate, acrylate and arabinose) into the production of green fluorescent prot

177 l-Arabinose is a common constituent of plant cell wall tha

178 tically different structure of this arm when arabinose is absent.

179 ndicated that its cleavage pattern producing arabinose is associated with the chemical recognition of

180 arm of the AraC gene regulatory protein when arabinose is bound to the protein and the dramatically d

181 Escherichia coli L-arabinose isomerase (ECAI; EC 5.3.1.4) catalyzes the iso

182 In this work, we study Lactobacillus sakei L-arabinose isomerase (LsLAI) for D-galactose to D-tagatos

183 Starting from l-arabinose, key functionalized l- glycero- and l- erythro

184 onic substituents, such as 4-amino-4-deoxy-L-arabinose (L-Ara4N) and phosphoehthanolamine (pEtN) at t

185 m (TCS) directly activates 4-amino-4-deoxy-l-arabinose (l-Ara4N) biosynthesis to result in cationic a

186 cation of lipid A with the 4-amino-4-deoxy-L-arabinose (L-Ara4N) moiety is required for resistance to

187 ated that incorporation of 4-amino-4-deoxy-l-arabinose (l-Ara4N) to the lipid A moiety of lipopolysac

188 as mainly composed of D-galacturonic acid, L-arabinose, L-rhamnose, D-galactose and D-glucose.

189 In the presence of arabinose LacI is produced, which binds to Ptrc, blockin

190 High arabinose level suggests that long arabinan side-chains

191 ll walls of other organs and cells had lower arabinose levels in roots and pollen tubes, but no diffe

192 omers, including the d and l enantiomers for arabinose, lyxose, ribose, xylose, ribulose, and xylulos

193 A gguC deletion affected growth only on L-arabinose medium, suggesting that gguC encodes an enzyme

194 ng that gguC encodes an enzyme specific to L-arabinose metabolism, and this gene was renamed araD1.

195 , only ytfQ has an established connection to arabinose metabolism, suggesting that AraC has a broader

196 transcription activator of genes involved in arabinose metabolism.

197 d resistance to killing is 4-amino-4-deoxy-l-arabinose modification of lipid A.

198 ze ester bonds between ferulic acid (FA) and arabinose moieties in arabinoxylans.

199 response of AraC requires the binding of two arabinose molecules.

200 arabinose, but forms long-term memories of L-arabinose more reliably.

201 idopsis (Arabidopsis thaliana) low cell wall arabinose mutant murus5 (mur5) encodes a defective allel

202 t alleles of RGP2, a gene that encodes a UDP-arabinose mutase that interconverts UDP-arabinopyranose

203 rabinofuranosidase that hydrolyses O3-linked arabinose of doubly substituted xylans, a feature of the

204 There is a decrease in 2- and 3-linked arabinose oligosaccharides, that contributes to around a

205 protein, which regulates expression of the l-arabinose operon in Escherichia coli, is a dimer whose D

206 onstructed a new strain containing a tunable arabinose operon promoter PBAD to quantitatively control

207 etween two domains of the Escherichia coli L-arabinose operon regulatory protein AraC.

208 cell cultures were incubated with l-[1-(3)H]arabinose or (E)-[U-(14)C]cinnamate (radiolabelling the

209 minaceous monocots, over the O-2 position of arabinose or the O-6 position of galactose residues.

210 on the dimerization domain's ability to bind arabinose or to dimerize the protein or on the DNA-bindi

211 n free energy of transfer between ribose and arabinose or xylose are attributed, at least in part, to

212 ransport shows interesting overlaps to the D-arabinose pathway, representing another example for path

213 alactan and EmbC is involved in transferring arabinose, perhaps in the early stage of arabinan synthe

214 arabinofuranose, exhibited the low cell wall arabinose phenotype.

215 In vivo, an arabinose-poor environment, the concentration of LacI de

216 t of most carbohydrates; although ribose and arabinose produced more PhIP (44-46 pmol of PhIP/mumol o

217 were inserted between the Escherichia coli l-arabinose promoter and bgaB (beta-galactosidase from Bac

218 trepII-tagged beta under the control of an l-arabinose promoter were constructed.

219 ter or on a plasmid under the control of the arabinose promoter.

220 at expression of these genes is dependent on arabinose provided during growth.

221 ession was dependent on exogenously supplied arabinose provided during in vitro growth.

222 There are residues of mannose, the arabinose, pyranose predominantly, is terminal and 2-O-l

223 ll on a variety of carbon sources, including arabinose, pyruvate, succinate, and malate, but, unlike

224 sory neurons communicate information about L-arabinose quality and concentration-features relevant fo

225 mal repressor gene, lacI, expressed from the arabinose-regulated araC PBAD promoter.

226 An arabinose-regulated c2 gene is present in the chromosome

227 m strain chi8937, with deletions of asdA and arabinose-regulated expression of murA, two genes requir

228 By using an arabinose-regulated expression system, the essentiality

229 hat encodes a domain that contributes to the arabinose-regulated lysis phenotype but has a eukaryotic

230 component is plasmid pYA3681, which encodes arabinose-regulated murA and asdA expression and C2-regu

231 o the presence of its cognate sugar than the arabinose-regulated promoter ParaBAD and provided tighte

232 ersions of this strain and compared with the arabinose-regulated T7 expression system.

233 The differential loss of arabinose relative to mannose was observed indicating th

234 the main monosaccharide of oligo-RG I, while arabinose represented 0.0-12.1%.

235 In particular, the position of the arabinose residue in the arabinoxylan of the switchgrass

236 wed that Rv3792 gene product can transfer an arabinose residue to the C-5 position of the internal 6-

237 ylated species modified with 4-amino-4-deoxy-arabinose residues at both terminal phosphate groups.

238 known mechanisms, such as those occurring in arabinose residues of coffee arabinogalactan side chains

239 anosidase, removing single terminally-linked arabinose residues, decreased the extent of B cell activ

240 , these results show the relevance of single arabinose residues, present at the non-reducing end of p

241 rulic acid esterified to the O-5 position of arabinose residues, typical of graminaceous monocots, ov

242 ometrically substituted with 4-amino-4-deoxy-arabinose residues.

243 partate in the absence or in the presence of arabinose, respectively.

244 e have addressed the question of whether the arabinose response of AraC requires the binding of one o

245 We found that the normal arabinose response of AraC requires the binding of two a

246 al analysis revealed a dramatic reduction of arabinose resulting in a novel truncated AG structure po

247 molecular weight of 2720kDa, are composed of arabinose, rhamnose, glucose, fructose, galactose and xy

248 ncluding selectivity toward pentoses such as arabinose, ribose, and xylose to the exclusion of the ex

249 made up approximately 40-60% of the SDF and arabinose-rich pectic polysaccharides represented approx

250 ermentabilities in human faecal cultures and arabinose-rich POS2 had the greatest prebiotic potential

251 s high in IL 6-3, IL 7-2 and IL 6-2, whereas arabinose showed a low content in IL 10-2, IL 6-3 and IL

252 s showed that this strain could use both the arabinose side chains and xylose backbones up to xylotet

253 The arabinoxylan backbone is decorated with arabinose side chains that may be substituted with ferul

254 rhamnogalacturonan I blocks, branching with arabinose side chains, and with 1,5-, 1,3,5-arabinan and

255 In the presence of arabinose, SLT16 (pCZ1) expressed both the homologous an

256 logous O-antigens, whereas in the absence of arabinose, SLT16 (pCZ1) mainly expressed the heterologou

257 wt% aldose (for example, glucose, xylose or arabinose) solution with a 4:1 aldose:sodium tetraborate

258 An arabinose specific xylanase from glycoside hydrolase fam

259 independently of the commonly used IPTG and arabinose strategies.

260 ve site are solvent exposed, indicating that arabinose substituents can be accommodated in the glycon

261 The arabinose substituents have been introduced in one high-

262 the product profile showed that it produced arabinose substituted oligosaccharides (AXOS) having 2-1

263 d different requirements for the lengths and arabinose substitution pattern of the oligosaccharides t

264 2'F-arabinose substitution provides the greatest stabilizati

265 ease to be synthesized due to the absence of arabinose such that attenuation is gradually manifest in

266 plant-specific glycosyltransferases that add arabinose sugars to diverse proteins including cell wall

267 rates with 2'-azido, 2'-chloro, 2'-amino, or arabinose sugars.

268 osition, mainly constituted of galactose and arabinose, suggesting the presence of arabinogalactans a

269 sbauer analysis on cells induced with 0.5 mM arabinose supports high iron loading in beta.

270 Galactose and arabinose, the predominant constituents of polysaccharid

271 inans releasing arabino-oligosaccharides and arabinose, the second most abundant pentose in nature.

272 Addition of arabinose to chemoautotrophic cultures of B. japonicum d

273 raC gene no longer require the presence of l-arabinose to convert AraC from its repressing to its ind

274 EC 5.3.1.4) catalyzes the isomerization of L-arabinose to L-ribulose in vivo.

275 the enzyme that transfers 4-amino-4-deoxy-l-arabinose to lipid A in polymyxin-resistant strains.

276 ment of the cationic sugar 4-amino-4-deoxy-l-arabinose to lipid A, a reaction catalyzed by the integr

277 eterminants responsible for isomerization of arabinose to ribulose in vivo and galactose to tagatose

278 ecular weights of 620,000 and 470,000Da with arabinose to xylose ratio of 0.7 and 0.6, respectively.

279 had lower endoxylanase activities and higher arabinose-to-xylose ratios of WU-AX than those of corres

280 -lipid glycosyltransferase 4-amino-4-deoxy-L-arabinose transferase (ArnT).

281 iaceae comprised of 10 genes associated with arabinose transport and metabolism.

282 e to encode for the physiologically relevant arabinose transporter in Neurospora.

283 BtAraR) as a novel regulator controlling the arabinose utilization genes.

284 selectable markers (sacB, pheS, gat and the arabinose-utilization operon) and lambda-Red mutant prot

285 Using these constructs and with [ l-arabinose] varying from 0 to 0.5 mM in the growth medium

286 phosphorylated intermediates to catabolize L-arabinose via an L-arabinose dehydrogenase, AraA(At), en

287 L-arabinose was confirmed to be a negative effector of BtA

288 colonization of host lymphoid tissues, where arabinose was not available, the P(BAD) promoter was no

289 tant harboring pHERDMG454, when induced with arabinose, was able to reverse its sensitivity to organi

290 Upon addition of arabinose, we detected a weaker and unexpected interacti

291 utilization of glucose, xylose, fucose, and arabinose, which are also substrates for the ChvE-MmsAB

292 ctions as a replicon only in the presence of arabinose, which is not present in significant levels in

293 The absence of arabinose, which is unavailable in vivo, triggers replic

294 including glucose, galactose, xylose, and L-arabinose, with a requirement for the glucose stereo con

295 However, the absence of arabinose within the mouse bladder resulted in depletion

296 e profile of the wheat bran was dominated by arabinose, xylose, and glucose, whereas mannose and gala

297 Arabinose, xylose, mannose, galactose and glucose were t

298 s based on the simultaneous determination of arabinose, xylose, xylo-oligosaccharides (XOS), and AXOS

299 he Lewis acid mediated reduction of ribose-, arabinose-, xylose-, and lyxose-derived methyl and pheny

300 Sugar complex structures with l-arabinose, xylotriose, and xylohexaose revealed five sub