ライフサイエンスコーパス: arabinose

1 ine 5'-diphospho-beta-(4-deoxy-4-formamido-L-arabinose).

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

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

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

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

6 rabinose and the other subunit does not bind arabinose.

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

8 r controls antigen gene expression by adding arabinose.

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

10 protein and thereby induce CDI by removal of arabinose.

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

12 ossible contribution of the alpha-anomer for arabinose.

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

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

15 uced substantial biofilms in the presence of arabinose.

16 thiazole addition chemistry, starting from L-arabinose.

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

18 concentrated acid were rhamnose, mannose and arabinose.

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

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

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

22 Addition of 4-amino-4-deoxy-l -arabinose (4-aminoarabinose) moieties to the phosphate r

23 pyruvate (PEP) and the corresponding aldose: arabinose 5-phosphate (A5P) and erythrose 4-phosphate (E

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

25 KDO8P synthase catalyzes the condensation of arabinose 5-phosphate (A5P) and phosphoenolpyruvate (PEP

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

27 densation of phosphoenolpyruvate (PEP) and D-arabinose 5-phosphate (A5P) to produce KDO8P and inorgan

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

29 between D-ribulose 5-phosphate (Ru5P) and D-arabinose 5-phosphate (A5P).

30 quence similarity between GutQ and KdsD, a D-arabinose 5-phosphate isomerase (API) from the 3-deoxy-D

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

64 Arabinose and xylose were the most present NS with more

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

116 chi8937(pYA3681) exhibits arabinose-dependent growth.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

133 Arabinose from arabinogalactan side chains was hypothesi

134 ,(1 --> 4)-beta-D-glucans, a gradual loss of arabinose from glucuronoarabinoxylans, and an increase i

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

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

137 iety of sugars, including sucrose, dextrose, arabinose, fructose, and maltose.

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 e binding preference to be ribose > lyxose > arabinose > xylose.

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 en added by loxP/Cre recombination using the arabinose inducible cre gene in the EL350 bacteria.

162 s cloned and placed under the control of the arabinose-inducible ara promoter and transformed into a

163 the hypoxia-responsive fdhF promoter, or the arabinose-inducible araBAD promoter, the bacteria invade

164 SW105 and SW106 cells in addition carry l-arabinose-inducible Cre or Flp genes, respectively.

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

166 The screen relied on FACS and an arabinose-inducible hrpL sigma factor to automate the id

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

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

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

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

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

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

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

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

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

176 uction of Dam in A. hydrophila SSU, using an arabinose-inducible, P(BAD) promoter-based system, reduc

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

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

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

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

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

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

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

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

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

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

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

188 ontaining residues such as 4-amino-4-deoxy-l-arabinose (l-Ara4N) and phosphoethanolamine (pEtN) to Es

189 the addition of the sugar 4-amino-4-deoxy-L-arabinose (L-Ara4N) is a strategy adopted by pathogenic

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

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

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

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

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

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

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

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

198 transcription activator of genes involved in arabinose metabolism.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

215 arabinofuranose, exhibited the low cell wall arabinose phenotype.

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

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

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

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

220 misL gene was driven by the Escherichia coli arabinose promoter, MisL could be detected in the S. Typ

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 c growth chamber or in the presence of 0.02% arabinose, respectively.

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

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

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

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

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

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

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

252 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

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

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

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

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

263 2'F-arabinose substitution provides the greatest stabilizati

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

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

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

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

268 Decaprenylphosphoryl-d-arabinose, the lipid donor of mycobacterial d-arabinofur

269 Galactose and arabinose, the predominant constituents of polysaccharid

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

286 evented the excess DNA replication only when arabinose was added to the medium to induce the synthesi

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