ライフサイエンスコーパス: barrel

1 he thalamus (barreloids), and the neocortex (barrels).

2 y particles (RPs) to one or both ends of the barrel.

3 3b and includes part of the N-terminal beta-barrel.

4 en oil is $100 per barrel but not at $60 per barrel.

5 ing price is competitive with oil at $60 per barrel.

6 ity via the triose-phosphate isomerase (TIM) barrel.

7 lded either as alpha-helical hairpin or beta-barrel.

8 s, including a catalytic TIM (alpha/beta)(8) barrel.

9 substrate are assembled inside the BamA beta-barrel.

10 hat has a central role in folding other beta-barrels.

11 out alone disrupts TCA organization in adult barrels.

12 grappa is often refined by ageing in wooden barrels.

13 hey are all six-stranded, anti-parallel beta-barrels.

14 y interaction networks in transmembrane beta-barrels.

15 d by a major capsid protein bearing two beta-barrels.

16 amic acid, are found in wines aged in wooden barrels.

17 g in wines after differing ageing periods in barrels.

18 d a pH-ISFET, and can be easily installed in barrels.

19 ng the final colour of different batches and barrels.

20 of prodelphinidins after long-term aging in barrels.

21 In addition to control barrels (3 years old), three bending/toasting protocols,

22 phenotypes and suggests that the double beta-barrel, a common feature of the abeta-PFTs, may be an im

23 composed of three domains: a (beta/alpha)(8) barrel, a trimerization domain, and a beta-sandwich doma

24 Barrel activity increased significantly within 500 ms of

25 ; when we controlled for movement amplitude, barrel activity was again greater after a twitch than a

26 500 ms by whisker movements: at least 55% of barrel activity was attributable to sensory feedback fro

27 d without movement were compared, 70%-75% of barrel activity was movement related.

28 s to assess the likelihood that increases in barrel activity were preceded within 500 ms by whisker m

29 litude movements were more likely to trigger barrel activity; when we controlled for movement amplitu

30 conducted under conditions commonly found in barrel aged beer production: different pitching rates, h

31 y, is a decisive factor for the quality of a barrel-aged wine, in this experiment, the structural cha

32 Maintaining wine oxidative stability during barrel ageing and shelf life storage remains a challenge

33 ized by a high alcohol content and a minimum barrel ageing of 10 years.

34 te biological modifications occurring during barrel ageing of beer, in controlled fermentation proces

35 celerated fermentation process for mimicking barrel ageing transformations.

36 Malolactic fermentation (MLF) and oak barrels aging are two oenological processes which modify

37 the Yersinia pestis outer transmembrane beta-barrel Ail as a model, we delineated how a single-residu

38 e new possibility of choosing the OTR of the barrel allows the winemaker to globally control the agei

39 l component of the complex, is itself a beta-barrel and is proposed to play a central role in assembl

40 Sheet/barrel and mixed-alpha/beta proteins exhibit more conven

41 nsertion utilizes aspects of both the hybrid barrel and passive models.

42 amber defined by the top of the designed TIM barrel and the bottom of the ferredoxin dimer.

43 The cachaca was aged in an Amburana barrel and the samples were analyzed with a traditional

44 High SO(2) concentration during aging in barrels and bottles delayed typical phenolic changes and

45 ct of oxygen on wine colour during ageing in barrels and bottles during different times.

46 ied to colour modifications during ageing in barrels and bottles.

47 olic and in-mouthfeel sensory development in barrels and furthermore in bottles.

48 enation conditions throughout the process in barrels and its later evolution in bottles.

49 sampling the entire energy landscape of TIM barrels and offer the possibility of a molecular-level u

50 quired in the cortex for L4 aggregation into barrels and thalamocortical afferent (TCA) segregation.

51 compares, the effect of traditional (wooden barrel) and alternative system (stainless steel tank wit

52 ect of MLF-container (stainless steel tanks, barrels) and barrel toasting (T1, T2, T3) on ellagitanni

53 of the somatosensory cortical map, affecting barrel, and septal areas.

54 n the cost and difficulty in handling wooden barrels, and as an alternative being able to select from

55 Here we introduce a modular barrel architecture, and demonstrate hierarchical assemb

56 tics have increased our understanding of how barrels are constructed and revealed the interplay of th

57 beta-Barrels are sheets of beta-strands wrapped into a cylind

58 ng processes of distillates for which cherry barrels are still not used (e.g., brandy and whisky).

59 -shaped subfield containing approximately 24 barrels, arranged in eight mediolateral rows and a barre

60 Using barrels as MLF-containers i) did not change the aroma pe

61 s assembly of OM proteins (OMPs) by the beta-barrel assembly machine (BAM complex).

62 The beta-barrel assembly machine (Bam) complex in Gram-negative b

63 folded and inserted into the OM by the beta-barrel assembly machine (BAM) complex, which in E. coli

64 In Gram-negative bacteria, the beta-barrel assembly machine (BAM) consists of the beta-barre

65 OMPs are assembled into the OM by the beta-barrel assembly machine (BAM), which is composed of one

66 nt that is inserted into the membrane by the barrel assembly machinery (Bam) complex by an unknown me

67 the outer membrane are mediated by the beta-barrel assembly machinery (BAM) complex.

68 this process, which is mediated by the beta-barrel assembly machinery (BAM) in Gram-negative bacteri

69 OMPs are then offloaded to the beta-Barrel Assembly Machinery (BAM) in the outer-membrane fo

70 The beta-barrel assembly machinery (BAM) is a conserved multicomp

71 outer membrane (OM) is catalysed by the beta-barrel assembly machinery (BAM).

72 due to its genetic interaction with the beta-barrel assembly machinery complex as well as its ability

73 y a mechanism potentially involving the beta-barrel assembly machinery.

74 of BamA acts as a chaperone to catalyze beta-barrel assembly.

75 nal lectin domain of LPHN3 binds to the TEN2 barrel at a site far away from the alternatively spliced

76 h conventional jet fuel when oil is $100 per barrel but not at $60 per barrel.

77 rences between wines aged in control and new barrels, but less clear-cut differences within wines age

78 embrane integration of partially folded beta-barrels by a 'swing' mechanism.

79 losteric pathway mutations at one end of the barrel can be evaluated at the distal end.

80 ch claims that a lateral gate in BamA's beta-barrel can serve as a template for incoming OMPs, and th

81 PolD contains a unique two-barrel catalytic core absent from all other DNA polymera

82 rough the evolution of an ancestral RNAP two-barrel catalytic core.

83 ults, which may be a general feature of beta-barrel channel gating, suggest either an entropy-driven

84 We identified SP2, an Omp85-type beta-barrel channel of the OEM, and CDC48, a cytosolic AAA+ (

85 rial outer membrane and an archetypical beta-barrel channel.

86 enance of projection topology from different barrel columns in the BC, albeit with target-specific pr

87 a single bound CDTa in the prepore and beta-barrel conformations of CDTb.

88 containing a 16-stranded transmembrane beta-barrel connected to two periplasmic domains.

89 the amino terminus of ExsD and the ExsA beta barrel constitute a pivotal part of the ExsD-ExsA interf

90 g wine cellars, where hundreds of individual barrels containing almost finished wines should be monit

91 th apo and holo MtNifB contain a partial TIM barrel core, but unlike apo MtNifB, holo MtNifB is fully

92 ouse anterior lateral motor cortex (ALM) and barrel cortex (S1) upon PV photostimulation in vivo.

93 ep neurons in deprived primary somatosensory barrel cortex (S1BC) has previously been detected.

94 Mouse primary somatosensory barrel cortex (wS1) processes whisker sensory informatio

95 n summary, locomotion significantly enhances barrel cortex activity across layers with L5 neurons mai

96 imaging to assess tactile defensiveness and barrel cortex activity in young and adult Fmr1 knock-out

97 widespread activation of midline and lateral barrel cortex areas following a vibration cue and delaye

98 al and disrupted development of microglia in barrel cortex by chronically depriving sensory signals v

99 in number across brain regions and stable in barrel cortex despite whisker trimming-induced sensory d

100 ptic innervation pattern of GIN cells in the barrel cortex in a layer-specific manner.

101 ial pressure (PO(2)) and flow in the whisker barrel cortex in awake mice.

102 the expected activation of the contralateral barrel cortex in lightly sedated mice, while interhemisp

103 arvalbumin (PV)-positive interneurons in the barrel cortex in vivo and recording three distinct (two

104 e reveal complementary circuits in the mouse barrel cortex involving genetically distinct SST subtype

105 The barrel cortex is within the primary somatosensory cortex

106 nisms underlying sensory processing in mouse barrel cortex L1.

107 e., spindle bursts) and unit activity in the barrel cortex of 5-day-old rats with whisker movements d

108 specific manipulation of L2/3 neurons in the barrel cortex of actively sensing mice (of either sex) t

109 t opposite ends of a microelectrode array in barrel cortex of anesthetized rats.

110 and vascular dynamics simultaneously in the barrel cortex of awake mice under whisker stimulation, w

111 ) and hemodynamic responses were assessed in barrel cortex of awake wild-type or eNMDAR loss-of-funct

112 For half a century now, the barrel cortex of common laboratory rodents has been an e

113 Calcium imaging of layers 2-4 of the barrel cortex revealed maps of object-angle tuning befor

114 ectrophysiology demonstrated that the intact barrel cortex selectively strengthens callosal synapses

115 y and sharpen the response of neurons in the barrel cortex to incoming sensory input signals.

116 ronal activity in layer 2/3 (L2/3) and L5 of barrel cortex using calcium imaging in mice running in a

117 ted activity in GABAergic cells of the mouse barrel cortex using in vivo calcium imaging.

118 patterns of defined types of neurons in the barrel cortex while mice performed an active, whisker-de

119 ensembles of L2/3 pyramidal neurons in mouse barrel cortex while simultaneously recording local netwo

120 Combining tetrode recording in SI barrel cortex with controlled psychophysics, we found a

121 ed a broad remodeling of the proteome in the barrel cortex.

122 vel-dependent fMRI response in somatosensory barrel cortex.

123 hibition reduces activity in the ipsilateral barrel cortex.

124 g in layer 2/3 of the primary somatosensory "barrel" cortex (S1bf) revealed that, in well-trained ani

125 ication of the penile cortex and the whisker-barrel-cortex systems.

126 nd the oxygen transmission rate (OTR) of the barrel define the final wine.

127 V2(17), V2(18)) and larger (V2(20), V2(21)) barrel diameters.

128 with RTX, revealing CD20 as a compact double-barrel dimer bound by two RTX antigen-binding fragments

129 sted in the refolding of the antigen 43 beta-barrel domain and protected it from added protease.

130 suggests that a well-ordered C-terminal beta-barrel domain is not required for TerS(P76-26) to carry

131 of Latrophilin bind across a spiraling beta-barrel domain of Teneurin, the YD shell.

132 ate genes include Dead box helicase 1, a Tim Barrel domain protein and the eukaryotic translation ini

133 al BAM subunit (BamA) itself contains a beta-barrel domain that is essential for OM protein biogenesi

134 ructure lacked the conserved C-terminal beta-barrel domain used by other TerS proteins for binding Te

135 43 was substantially decreased and its beta-barrel domain was undetectable in the outer membrane of

136 t a site located between the lipoyl and beta-barrel domains of AcrA.

137 A putative TIM-barrel enzyme and other newly identified apicoplast biog

138 e or octane occur through restructuring of a barrel extension formed by the extracellular loops.

139 When comparing both MLF-modalities, barrel-fermented wines exhibited greater amounts of vani

140 ) resulted in an increased septa area in the barrel field map.

141 hiskers in the primary somatosensory cortex (barrel field) of adult mice with different cell type spe

142 peptidase I cleavage site, a predicted beta-barrel fold, and cross-phylogroup homology.

143 flexible unstructured loops, such as the TIM-barrel fold.

144 n that adopts an unusual eight-stranded beta-barrel fold.

145 a previously unidentified superfamily of TIM-barrel-fold enzymes for metal-dependent dioxygen activat

146 ire of nonheme diiron monooxygenases and TIM-barrel-fold enzymes.

147 d the molecular mechanisms that control beta-barrel folding and release.

148 quences with 3alpha, 4beta + alpha, and beta-barrel folds, respectively.

149 r 15 months in used and new French 225 L oak barrels, followed by a period of 3 months in bottle.

150 Selecting the appropriate type of barrel for wine maturation but also deciding on the opti

151 ording to their OTR, which are used to build barrels for wine ageing.

152 ronment by embedding within a 26 strand beta-barrel formed by MtrB.

153 of a laterally 'open' form of the BamA beta-barrel forms a rigid interface with the C-terminal beta-

154 with the characteristic capsid protein beta-barrels found in all the viruses in the Picornavirales o

155 s, arranged in eight mediolateral rows and a barrel-free zone capping the anterior border.

156 The barrel-free zone receives topographically ordered input

157 an oak, French oak, Spanish oak and chestnut barrels in order to determine the suitability of alterna

158 y and the ability to form aggregates such as barrels in rodent somatosensory cortex.

159 nterior of the C-terminal transmembrane beta-barrel (inter-N-C).

160 m, where each nascent betaOMP forms a hybrid-barrel intermediate with BAM/SAM in route to its biogene

161 Wine ageing in barrels is conditioned, among other factors, by the amou

162 ng exception to all known transmembrane beta-barrels is the unique odd-stranded, i.e. 19-stranded, st

163 embedded peptide forms 6- or 8-stranded beta-barrel like structures.

164 of four stacked heptameric rings that form a barrel-like structure, sequestering proteolytic sites in

165 Pentamerization forms a barrel lined with charged residues mediating pH-responsi

166 It can be aged in barrels made from different types of wood, similar to ot

167 lign the physiological map to the underlying barrel map.

168 from the thermodynamic analysis of the PagP barrel may explain why cysteine, despite possessing a po

169 The 8-stranded barrels may conduct Ca(2+) ions through an inner cavity,

170 During beer ageing, endogenous barrel microbes grow spontaneously and transform wort/be

171 this process have been put forth: the hybrid barrel model, which claims that a lateral gate in BamA's

172 This barrel (MV) is found to be a potential molecular vessel

173 uble [8+4] self-assembled M(8)L(4) molecular barrel (MV).

174 The platform was integrated into a double-barrel nanoprobe combining pH sensing with feedback-cont

175 and has a 180- angstrom long, 24-strand beta barrel narrow stem tube that undergoes conformational ch

176 CP assembly; Ump1 that helps connect CP half-barrels; Nas2, Nas6, and Hsm3 that assist in RP assembly

177 avity, whereas the tightly packed 6-stranded barrels need to assemble into supramolecular structures

178 asic (b) motifs shared across the entire two-barrel nucleotide polymerase superfamily, and a nucleoti

179 rminal residues of CsgF bind inside the beta-barrel of the pore, forming a defined second constrictio

180 cal assembly of a 100 megadalton DNA-origami barrel of ~90 nm diameter and ~250 nm height, that provi

181 oil spill released approximately 4.9 million barrels of crude oil into the northern Gulf of Mexico in

182 In 2010, 4.9 million barrels of crude oil were released into the northern Gul

183 Transmembrane beta-barrels of eukaryotic outer mitochondrial membranes (OMM

184 of oil sands (OS) generates over one million barrels of heavy oil each day in the Alberta Oil Sands R

185 ) and production volume from active wells in barrels of oil equivalent (BOE) (no BOE, 1-100 BOE/day,

186 structures predominate, but off-pathway beta-barrel oligomers are also predicted.

187 Off-pathway beta-barrel oligomers are also suggested to occur in coassemb

188 proteins and PG, with tethering of the beta-barrel OM protein BbpA becoming most abundant in the sta

189 coproteomic analysis of PG to show that beta-barrel OM proteins are covalently attached to PG in seve

190 description of four putative treponemal beta-barrel OMPs that exhibit the characteristics of multispe

191 Consistent with their classification as beta-barrel OMPs, circular-dichroism spectroscopy revealed th

192 ging method, use of different types of aging barrels) on several parameters: color, non-enzymatic bro

193 Structural analysis shows how the Sam50 beta-barrel opens a lateral gate to accommodate its substrate

194 Interestingly, barrel organization also degrades with age in wildtype m

195 ha-helical sensory rhodopsin II and the beta-barrel outer membrane protein W have been investigated i

196 Integral beta-barrel outer membrane proteins (OMPs) function to establ

197 mplex responsible for the biogenesis of beta-barrel outer membrane proteins (OMPs) in Gram-negative b

198 beta-Barrel outer membrane proteins (OMPs) represent the majo

199 bacteria, the folding and insertion of beta-barrel outer membrane proteins (OMPs) to the outer membr

200 ated Treponema phylogroups for putative beta-barrel outer membrane proteins and considered their pote

201 In mitochondria, beta-barrel outer membrane proteins mediate protein import, m

202 outer membrane populated with a host of beta-barrel outer-membrane proteins (betaOMPs).

203 The major constituent - hydrophobic beta-barrel Outer-Membrane Proteins (OMPs) - are first secret

204 utational strategy on the transmembrane beta-barrel PagP to examine the membrane depth-dependent ener

205 strand insertion inside the nanopore's beta-barrel past the constriction site, its complete unzip fr

206 cheeses in goat's skin bag (GST) or plastic barrel (PBT) were investigated.

207 ecular dynamics simulations, we show how the barrel pore is primed for CdiA toxin secretion.

208 bserved in the transition of prepore to beta-barrel pore, although we also observe a single bound CDT

209 t enable conversion from a prepore to a beta-barrel pore.

210 protein toxin that forms transmembrane beta-barrel pores in host cell membranes.

211 rane and the assembly of outer membrane beta-barrel precursors were severely compromised in CL-lackin

212 ne-shaped tip of a largely hydrophobic helix barrel, prepared for membrane penetration.

213 for three months in high and low oxygenation barrels presents different characteristics.

214 s clear-cut differences within wines aged in barrels produced with the different bending/toasting pro

215 ry neurons of the primary somatosensory (S1) barrel, project only ipsilaterally.

216 assembly machine (BAM) consists of the beta-barrel protein BamA, and four lipoproteins(5-8).

217 n a topology-dependent manner, with the beta-barrel protein being the most robust.

218 ethod to trap a native Escherichia coli beta-barrel protein bound stably to BamA at a late stage of a

219 tional robustness of the folding of the beta-barrel protein is underpinned by its conformationally re

220 res are described, including porins and beta-barrel protein nanopores, aquaporins and related polar s

221 One subunit of the machines is itself a beta-barrel protein that has a central role in folding other

222 including a triosephosphate isomerase (TIM)-barrel protein that likely derived from a core metabolic

223 nged in two-fold symmetry: pore-forming beta-barrel protein Tom40 and four auxiliary alpha-helical tr

224 envelope membranes (TOC/TIC), only one beta-barrel protein, Toc75, has been shown to use this pathwa

225 hat assemble as a 1:1:1 complex to fold beta-barrel proteins and insert them into the mitochondrial o

226 s served as a paradigm for the study of beta-barrel proteins for several decades.

227 Triosephosphate isomerase (TIM) barrel proteins have not only a conserved architecture t

228 The integration of beta-barrel proteins into the bacterial outer membrane (OM) i

229 olysaccharides (LPS), lipoproteins, and beta-barrel proteins to the OM have been identified, but very

230 The route other beta-barrel proteins use has remained unresolved.

231 tivity within the diverse and widespread TIM barrel proteins, targeting murine adenosine deaminase (m

232 established, it can be challenging for beta-barrel proteins, which are important in cellular transpo

233 ing on-line pepsin digestion of soluble beta-barrel proteins.

234 roplasts fold and insert outer membrane beta-barrel proteins.

235 t outer membranes contain transmembrane beta-barrel proteins.

236 ion based on several factors as fermentation barrel, raw material, distillation method and aging.

237 LJBSF barrels receive topographically ordered barrel-specific

238 generating more peptides from the rigid beta-barrel regions, without compromising the ability to pred

239 st inherent of ageing wine spirits in wooden barrels, research has sought to develop more sustainable

240 NDs and SUVs were similar and indicated beta-barrel secondary structure.

241 brane proteins (OMPs) contain a unique "beta barrel" segment that is inserted into the membrane by th

242 ssemble in biological membranes to form beta-barrel shaped oligomeric pores that induce cell leakage.

243 At the heart of the proteasome is the barrel-shaped 20S core particle (CP), which contains two

244 Gynecologic exam revealed a 3-cm barrel-shaped cervix with friability at the os and no ap

245 ery consisting of two oligomeric segments, a barrel-shaped heterotetradecameric protease core compris

246 The range of barrel-shaped proteins found in the outer membrane of ce

247 he three I-domains share a six-stranded beta-barrel skeleton, there are differences (i) in structure

248 JBSF barrels receive topographically ordered barrel-specific input from individual vibrissa and micro

249 rage of chloroalkane metabolism in the giant barrel sponge, Xestospongia muta.

250 toinhibited (alpha-hairpin) and active (beta-barrel) states and plausible refolding pathways have bee

251 tions, making the pores intermediate between barrel stave and toroidal.

252 by stabilizing toroidal pores but disrupting barrel-stave pores.

253 nprecedented triosephosphate isomerase (TIM) barrel structural fold for this class of enzymes and pos

254 may be accompanied by opening of the P2 beta-barrel structure and ligand exchange with the apposing b

255 picomplexans is the conoid, a hollow tapered barrel structure composed of tubulin fibers.

256 lutamine-rich motif on the conserved VP beta-barrel structure of variants incompatible with AAP2 crea

257 ary Proteins (MUPs) contain a conserved beta-barrel structure with a characteristic central hydrophob

258 outer membrane contains proteins with a beta-barrel structure(1,2).

259 ss sections in agreement with a general beta-barrel structure.

260 xcitonic coupling, is limited by the FP beta-barrel structure.

261 Ste24 possesses a novel "alpha-barrel" structure, consisting of a ring of seven transme

262 Although the lower jaw barrel subfield (LJBSF) is a likely source of the input,

263 Barrel subfields in rodent primary somatosensory cortex

264 d to play a central role in assembling other barrel substrates.

265 c ferredoxin fold and a de novo designed TIM barrel-such that their symmetry axes are aligned to crea

266 layer membranes reveals that the 19-stranded barrel surprisingly holds modest to low stability in a l

267 barrel temperature (BT: 60-80 degrees C), screw speed (S

268 The impact of extrusion at different barrel temperature and screw speed on the hempseed hull

269 cus indole-3-glycerol phosphate synthase TIM barrel that appears within 50 mus and must at least part

270 show that the pore is most probably a helix barrel that contains eight D4 peptides arranged in paral

271 ves; each half assembles as an alpha-helical barrel that could potentially serve as a proton conducti

272 the N-terminal domain, into an unbound beta-barrel that interacts with the ribosome.

273 Our results additionally indicate that beta-barrels that do not use transit peptides also enter the

274 ms aged longer, especially those aged in oak barrels that had previously contained Bourbon or wine, s

275 nic cyclic form, while in the absence of the barrel the same DASA exist in cyclic zwitterionic form i

276 domain of OmpA, not with the N-terminal beta-barrel, thus implying that RcsF does not reach the bacte

277 The largest transfer of compounds from the barrel to the whisky was observed around twelve years of

278 the flow of transfer of compounds from wood barrels to distillates is not constant and homogeneous o

279 ntainer (stainless steel tanks, barrels) and barrel toasting (T1, T2, T3) on ellagitannin concentrati

280 Barrel toasting had higher impact on ellagitannin conten

281 uctural detail of medin pores with the CNpNC barrel topology and diameters comparable to values estim

282 Grappa variety, ethanol content and barrel type strongly affected the volatiles profile of t

283 or commonly produces tri/tetra- or hexagonal barrel-type structures.

284 -driven forces shape the structure through a barreling-type instability.

285 ate-limiting step in the closing of the beta-barrel underscore the value of combining simulation and

286 d in the new barrels), were more affected by barrel use (new versus neutral) than by bending/toasting

287 r a ceramide binding site on one side of the barrel wall.

288 Finally, wines storage in barrels were differentiate by Na and Cs concentration.

289 We present a historical perspective on how barrels were discovered, and how thereafter, they became

290 he samples that had been aged in Spanish oak barrels were getting more similar to those aged in Frenc

291 ic pigments (higher in wines aged in the new barrels), were more affected by barrel use (new versus n

292 nucleus most densely innervates layer 4 (L4) barrels, whereas the higher-order posterior thalamic nuc

293 s separate and the CTD refolds into the beta-barrel, which recruits a ribosome, activating translatio

294 icro-pillars on B2 phase deformed by plastic barreling while L1(2) micro-pillars showed high density

295 LF-tank wines, and higher nuts aroma for MLF-barrel wines.

296 is then applied to VDAC, a 19-stranded beta-barrel with 283 residues, for which 67% of the detergent

297 Sam50 forms a 16-stranded transmembrane beta-barrel with a single polypeptide-transport-associated (P

298 amA catalyst forms an asymmetric hybrid beta-barrel with the BamA substrate.

299 Wines aged in barrels with a high oxygenation rate showed greater avid

300 The use of barrels with different and known rates of oxygenation al

301 As different types of barrel woods emerge, it is of great importance for a gui