ライフサイエンスコーパス: phenylpropanoid

1 combined use enhanced the solubility of this phenylpropanoid.

2 iochemical flux toward coumarins and general phenylpropanoids.

3 ion of phenylalanine for the biosynthesis of phenylpropanoids.

4 enzymes, consequently altering the levels of phenylpropanoids.

5 cause dwarfing and decreased accumulation of phenylpropanoids.

6 various classes of 4-O- and 9-O-hexosylated phenylpropanoids.

7 be largely due to the expressed toxicity of phenylpropanoids.

8 MED5 results in increased concentrations of phenylpropanoids.

9 as being involved in binding CoA-conjugated phenylpropanoids.

10 five phenolic compounds, one new acyclic bis phenylpropanoid (1) and four previously known phenolic c

11 cal basil volatiles with very low amounts of phenylpropanoids (1-2%).

12 The phenylpropanoid 3,4-(methylenedioxy)cinnamic acid (MDCA)

13 noid biosynthetic pathway and restoration of phenylpropanoid accumulation in a ref5-1 med5a/b triple

14 a subsequent metabolite negatively influence phenylpropanoid accumulation in ref5 and more importantl

15 independent lines that restore growth and/or phenylpropanoid accumulation in the ref4-3 background.

16 a screen for plants with defects in soluble phenylpropanoid accumulation, has a missense mutation in

17 ors restore growth without restoring soluble phenylpropanoid accumulation, indicating that the growth

18 of the pathway, leading to decreased soluble phenylpropanoid accumulation, reduced lignin content and

19 defects in glucosinolate biosynthesis and in phenylpropanoid accumulation.

20 lts in dwarfism and constitutively repressed phenylpropanoid accumulation.

21 , MED5a and MED5b, results in an increase in phenylpropanoid accumulation.

22 Apigenin C-glycosides and phenylpropanoids acids were identified in all fractions

23 e processes involving amino acids, different phenylpropanoid, alkaloid and terpenoid classes, and fer

24 ghts vital roles of SGAs as phytoalexins and phenylpropanoids along with lignin accumulation unreveal

25 flavonoid, organic acid, sugar, fatty acid, phenylpropanoid and amino acid metabolic pathways indica

26 that MDCA triggers a cross talk between the phenylpropanoid and auxin biosynthetic pathways independ

27 However, few were linked to loci involved in phenylpropanoid and cellulose synthesis or vegetative ph

28 The expression of relevant genes of the phenylpropanoid and ethylene biosynthetic pathways durin

29 tion were up-regulated and genes involved in phenylpropanoid and flavonoid biosynthesis, pentose and

30 to D. rosae was detected for genes from the phenylpropanoid and flavonoid pathways and for individua

31 12 genes that encoded enzymes in the general phenylpropanoid and isoflavonoid pathways.

32 eaves and an increase in the accumulation of phenylpropanoid and lignin biosynthetic gene transcripts

33 long to lipids and lipid-like molecules, and phenylpropanoid and polyketides.

34 r, transcript accumulation of key genes from phenylpropanoid and SGA pathways along with WRKY and MYB

35 many plant species supplied with Si have the phenylpropanoid and terpenoid pathways potentiated and h

36 ytokinins, auxin and synthesis of flavonoid, phenylpropanoids and cell wall.

37 tic compounds from various sources including phenylpropanoids and flavonoids that are abundant in soi

38 e taken into consideration, namely iridoids, phenylpropanoids and flavonoids.

39 s, including sugars; phenolic compounds like phenylpropanoids and flavonoids; alkaloids and glycoside

40 Phenylpropanoids and glucosinolates are two classes of s

41 4CL required for the synthesis of precursor phenylpropanoids and styrylpyrone synthase (SPS), integr

42 are used for the extraction of oxyprenylated phenylpropanoids and the corresponding extract analyzed

43 Our results suggest that phenylpropanoids and their derivatives play an important

44 s to reconstruct plant isoprenoid, alkaloid, phenylpropanoid, and polyketide biosynthetic pathways in

45 most prominent groups being glucosinolates, phenylpropanoids, and dipeptides, the latter of which is

46 rophyll and the biosynthesis of carotenoids, phenylpropanoids, and flavonoids were identified.

47 Phenylpropanoids are phenylalanine-derived specialized m

48 Besides, phenylpropanoids are predominant in winter and flavonoid

49 anine degradation, which may help counteract phenylpropanoid-based defenses before leaf entry.

50 zed in petunia, a plant with flowers rich in phenylpropanoid/benzenoid volatile compounds.

51 owers emit a total of 43 VOCs including nine phenylpropanoids/benzenoids, such as 2-phenylethanol (2P

52 n pathways associated with oxidative stress, phenylpropanoid biosynthesis (including scopoletin), the

53 e-phosphate pathway in primary metabolism to phenylpropanoid biosynthesis by controlling TRANSKETOLAS

54 sight into the transcriptional regulation of phenylpropanoid biosynthesis by the Mediator complex.

55 infected with P. palmivora fail to activate phenylpropanoid biosynthesis gene expression and display

56 onding trend was exhibited by most of tested phenylpropanoid biosynthesis genes.

57 resence of 229 and 943 genes involved in the phenylpropanoid biosynthesis in leaf and root tissues re

58 Phenylpropanoid biosynthesis in plants engenders a vast

59 atly reduced levels of HCEs, suggesting that phenylpropanoid biosynthesis may be repressed in respons

60 e regions with plausible candidate genes for phenylpropanoid biosynthesis or its regulation, includin

61 nalysis showed that KEGG enrichment included phenylpropanoid biosynthesis pathway among group I, grou

62 e genes have putative roles connected to the phenylpropanoid biosynthesis pathway and 17 relate to he

63 actors correlated with downregulation of the phenylpropanoid biosynthesis pathway have been identifie

64 lyase, which catalyzes the first step of the phenylpropanoid biosynthesis pathway.

65 that Arabidopsis SnRK1 negatively regulates phenylpropanoid biosynthesis via a group of Kelch domain

66 tudy reveals that SnRK1 negatively regulates phenylpropanoid biosynthesis, and KFB(PALs) act as regul

67 , particularly those acting in flavonoid and phenylpropanoid biosynthesis, as well as in the regulati

68 ssion of a large number of genes involved in phenylpropanoid biosynthesis, especially between 0 and 1

69 in deposition, from fatty acid metabolism to phenylpropanoid biosynthesis, in sugarcane internodes.

70 Phenylpropanoid biosynthesis, known to be elicited by Co

71 d increased gene expression in shikimate and phenylpropanoid biosynthesis, secondary metabolite syste

72 nriched in six metabolism pathways including phenylpropanoid biosynthesis, sesquiterpenoid and triter

73 genesis and its use in modulating lignin and phenylpropanoid biosynthesis.

74 ormal stature and have no apparent defect in phenylpropanoid biosynthesis.

75 e red pigments of Marchantia are formed by a phenylpropanoid biosynthetic branch distinct from that l

76 petunia (Petunia hybrida) repressed general phenylpropanoid biosynthetic genes and selectively reduc

77 , results in enhanced expression of multiple phenylpropanoid biosynthetic genes, as well as increased

78 phenolic compounds and the expression of the phenylpropanoid biosynthetic genes, was genotype-depende

79 known role in transcriptional regulation of phenylpropanoid biosynthetic genes.

80 is inhibition impacts the early steps of the phenylpropanoid biosynthetic pathway and restoration of

81 The phenylpropanoid biosynthetic pathway that generates lign

82 metabolites) from phenylalanine through the phenylpropanoid biosynthetic pathway.

83 ode enzymes involved in aromatic amino acid, phenylpropanoid, camalexin, and sphingolipid metabolism.

84 p (residues 208-231) conferring affinity for phenylpropanoid-CoA thioesters.

85 ), paying particular attention to changes in phenylpropanoids compared to controls.

86 gene source for the engineering of specific phenylpropanoid components.

87 d carbon is directed toward lignin and other phenylpropanoid compounds for which hydroxycinnamoyl-coe

88 reases in the levels of a specific subset of phenylpropanoid compounds.

89 Phenylpropanoids comprise an important class of plant se

90 3-acetaldoxime (IAOx), and we found that the phenylpropanoid content of cyp79b2 cyp79b3 and ref5-1 cy

91 velopment, along with a strong alteration of phenylpropanoid contents, resulting in accumulation of p

92 ental evidence for the antioxidant role of a phenylpropanoid coupling product in planta.

93 ts and the disruption of these KFBs restores phenylpropanoid deficiency in the mutants.

94 economically important compounds, including phenylpropanoid derivatives and terpenoids.

95 identified where lipid-derived volatiles and phenylpropanoid derivatives were the major components of

96 repressed limonene catabolism and triggered phenylpropanoid derivatives-related changes, which incre

97 Phenylpropanoid-derived compounds represent a diverse fa

98 s and are key regulators of the synthesis of phenylpropanoid-derived compounds.

99 Lignin is a phenylpropanoid-derived heteropolymer important for the

100 n of grass cell walls is esterified with the phenylpropanoid-derived hydroxycinnamic acids ferulic ac

101 The flavonoids are phenylpropanoid-derived metabolites that are ubiquitous

102 ) is the first enzyme in the biosynthesis of phenylpropanoid-derived plant compounds such as flavonoi

103 n Russia and Baltic countries is a source of phenylpropanoid-derived styrylpyrone polyphenols that ca

104 gest that the function of PCBER is to reduce phenylpropanoid dimers in planta to form antioxidants th

105 ential role of steroidal glyco-alkaloids and phenylpropanoids during early blight resistance.

106 A substantial portion of phenylpropanoids (e.g. flavonols) produced by pollen gra

107 to the quantitative variation of four simple phenylpropanoids, eight stilbenes, nine flavonoids, six

108 arieties still maintained very low levels of phenylpropanoids even after UV elicitation, they might b

109 d selection of Strecker aldehydes, terpenes, phenylpropanoids, fatty acid derivatives and carotenoid

110 gerprinting enabled selection of terpenoids, phenylpropanoids, fatty acid derivatives, Strecker aldeh

111 B transcription factor MpMyb14 in activating phenylpropanoid (flavonoid) biosynthesis during oomycete

112 criptomic analysis revealed the induction of phenylpropanoid, flavonoid and isoflavonoid metabolic pa

113 The expression of genes related to phenylpropanoid/flavonoid biosynthesis clearly distingui

114 nes encoding enzymes involved in the general phenylpropanoid/flavonoid pathway and the PA-specific br

115 patterns associated with the accumulation of phenylpropanoids, flavonoids, and anthocyanins in strawb

116 metabolic pathways, including terpenoids and phenylpropanoids/flavonoids.

117 soluble solids - Brix %, phenolic compounds, phenylpropanoids, flavonols, anthocyanins and carotenoid

118 is not limiting for HCE accumulation, nor is phenylpropanoid flux diverted to the synthesis of cell w

119 'Mitchell Diploid' floral volatile benzenoid/phenylpropanoid (FVBP) biosynthesis ultimately produces

120 by products of the floral volatile benzenoid/phenylpropanoid (FVBP) metabolic pathway.

121 ing seed maturation result in an increase in phenylpropanoid gene expression in seeds and that this c

122 owed that maximal expression of 10 out of 17 phenylpropanoid genes analysed occurred at 48h post-inoc

123 lyzed transcript abundances of scent-related phenylpropanoid genes in flowers.

124 tion factors implicated in the regulation of phenylpropanoid genes in maize.

125 that syntelogs of MYB31 and MYB42 do bind to phenylpropanoid genes that function in all stages of the

126 Expression of scent-related phenylpropanoid genes was not affected.

127 lve flavonoids, three phenolic acids and one phenylpropanoid glucoside were identified in the decocti

128 g various phenolic glycosides, a new dimeric phenylpropanoid glucoside, saponins, and fatty acids wer

129 The responses were dominated by changes in phenylpropanoid, glucosinolate, and fatty acid metabolis

130 Salidroside is a phenylpropanoid glycoside isolated from the medicinal pl

131 e compounds such as steroids, flavonoids and phenylpropanoid glycosides etc.

132 plex, and for Mediator in the maintenance of phenylpropanoid homeostasis.

133 or tail subunit, is required for maintaining phenylpropanoid homeostasis.

134 exhibiting significant activity toward other phenylpropanoid hydroxycinnamaldehydes.

135 induced secondary metabolites, belonging to phenylpropanoid, hydroxycinnamic acid (HCAA) and jasmoni

136 ng isomeric variation in the accumulation of phenylpropanoid hydroxycitric acid esters to a single li

137 hesis of volatile terpenoids and nonvolatile phenylpropanoids in ECs (when compared with parenchyma c

138 tresses enhanced the accumulation of various phenylpropanoids in stems of field-grown plants; gas chr

139 Based on the observed interactions of phenylpropanoids in the active site and analysis of kine

140 e harnessed to engineer high levels of novel phenylpropanoids in tomato fruit, offering an effective

141 However, phenylpropanoids, including scoparone, were not critical

142 an elaborate biosynthetic architecture where phenylpropanoid intermediates have to be transported fro

143 indicated that the synthesis of flavins and phenylpropanoids is tightly linked to and putatively cor

144 oach, offers a novel strategy for modulating phenylpropanoid/lignin biosynthesis to improve cell wall

145 f maize phenolic compounds including general phenylpropanoids, lignins, and flavonoids.

146 Isoflavonoids are a class of phenylpropanoids made by legumes, and consumption of die

147 ased levels of these human nutrition-related phenylpropanoids may be desirable, there were no increas

148 ral pathogen deterrence strategy centered on phenylpropanoid-mediated biochemical defenses.

149 Our study suggests that glucosinolate/phenylpropanoid metabolic crosstalk involves the transcr

150 sis, and provide critical insight for future phenylpropanoid metabolic engineering strategies.

151 Mapping of the changed metabolites onto the phenylpropanoid metabolic network revealed partial redir

152 responsive genes that include members of the phenylpropanoid metabolic pathway.

153 lowing photosynthesis for protein formation, phenylpropanoid metabolism (i.e. lignins), and other met

154 triad and structural genes from primary and phenylpropanoid metabolism and compare this mechanism wi

155 Growth inhibition and suppression of phenylpropanoid metabolism can be genetically separated

156 The modulation of phenylpropanoid metabolism clearly distinguished the beh

157 Phenylpropanoid metabolism has to direct up to 30% of th

158 roteins and their roles in the regulation of phenylpropanoid metabolism in plants.

159 context of both our current understanding of phenylpropanoid metabolism in Solanaceous species, and e

160 , Petunia hybrida ODORANT1, to alter Phe and phenylpropanoid metabolism in tomato (Solanum lycopersic

161 The global regulators of phenylpropanoid metabolism may include MYB transcription

162 ter understand the impact of perturbation of phenylpropanoid metabolism on plant growth, we generated

163 Phenylpropanoid metabolism represents a substantial meta

164 thesis by directing carbon flux from general phenylpropanoid metabolism to flavonoid pathway.

165 We identified metabolic pathways such as phenylpropanoid metabolism, and biological processes suc

166 been used to upregulate-specific branches of phenylpropanoid metabolism, but by far the most effectiv

167 Enhancement of phenylpropanoid metabolism, characterized by a restricte

168 ompound fraction and the enzymes involved in phenylpropanoid metabolism.

169 opsis have overlapping yet distinct roles in phenylpropanoid metabolism.

170 ral players in the homeostatic repression of phenylpropanoid metabolism.

171 port of MYB4, a transcriptional repressor of phenylpropanoid metabolism.

172 ting a redirection of metabolite flow within phenylpropanoid metabolism.

173 of PALs, thus posttranslationally regulating phenylpropanoid metabolism.

174 ion of one or more genes encoding enzymes in phenylpropanoid metabolism.

175 rom phenylalanine through the early steps of phenylpropanoid metabolism.

176 tent in source leaves and stems, and altered phenylpropanoid metabolism.

177 tes cinnamic acid to form 4-coumaric acid in phenylpropanoid metabolism.

178 K1-mediated sugar signaling pathway controls phenylpropanoid metabolism.

179 nols and hydroxycinnamic acids are important phenylpropanoid metabolites in plants.

180 chemical classes, including volatile esters, phenylpropanoid metabolites, 1-octen-3-ol, hexanal, and

181 Moreover, comparison of SSR-based data with phenylpropanoid molecules exhibited a statistically sign

182 fy representatives of all known genes in the phenylpropanoid-monolignol biosynthesis pathway.

183 gy-dense, heterogeneous polymer comprised of phenylpropanoid monomers used by plants for structure, w

184 ants in common gardens for 46 phytochemical (phenylpropanoid), morphological and growth traits, and u

185 The results of further GSL analyses in other phenylpropanoid mutants and benzoate feeding experiments

186 fins has been exploited for the synthesis of phenylpropanoid natural products.

187 is showed that the most relevant increase in phenylpropanoids occurred in scoparone, which markedly i

188 undergo oxidative coupling with neighboring phenylpropanoids on glucuronoarabinoxylan and lignin.

189 The phenylpropanoid p-coumarate and structurally related aro

190 -CoA O-methyltransferase associated with the phenylpropanoid pathway and lignin production, is the ge

191 dentification of 35 compounds related to the phenylpropanoid pathway and monolignol biosynthesis.

192 evels of lignin and other metabolites of the phenylpropanoid pathway and regulation of programmed cel

193 sufficient to up-regulate late steps of the phenylpropanoid pathway and to induce PA biosynthesis.

194 DART analysis revealed the activation of phenylpropanoid pathway by chitosan molecule, targeting

195 lencing increased fluxes through the general phenylpropanoid pathway by upregulating the expression o

196 ase (PAL) is the first enzyme of the general phenylpropanoid pathway catalyzing the nonoxidative elim

197 s the study on impact of elicitation and the phenylpropanoid pathway feeding on the nutritional quali

198 OBII plays a regulating role in the volatile phenylpropanoid pathway gene expression that gives rise

199 trus callus caused a down-regulation of many phenylpropanoid pathway genes and reduced the contents o

200 that CsMYBF1 activated several promoters of phenylpropanoid pathway genes in tomato and citrus.

201 nts were essential for CsMYBF1 in activating phenylpropanoid pathway genes.

202 acid and catechin) and in the expression of phenylpropanoid pathway genes.

203 r closely related to known regulators of the phenylpropanoid pathway in other species.

204 investigate the putative involvement of the phenylpropanoid pathway in the defence of citrus fruit,

205 Here, we investigated the involvement of the phenylpropanoid pathway in the induction of resistance i

206 CA is the photo-isomerization product of the phenylpropanoid pathway intermediate trans-CA (t-CA).

207 yme channels metabolic flux from the general phenylpropanoid pathway into benzenoid metabolism.

208 The phenylpropanoid pathway is a major global carbon sink an

209 The phenylpropanoid pathway is responsible for the biosynthe

210 e homologs were found for all enzymes in the phenylpropanoid pathway leading to lignin biosynthesis,

211 n biosynthesis and the stunted growth of the phenylpropanoid pathway mutant reduced epidermal fluores

212 pread changes in gene expression seen in the phenylpropanoid pathway mutant ref8, without restoring t

213 nd enhances our understanding of dwarfing in phenylpropanoid pathway mutants.

214 U46, is not implicated in either the general phenylpropanoid pathway or in the lignification of stems

215 The study revealed phenylpropanoid pathway overexpression resulting in incr

216 The plant phenylpropanoid pathway produces an array of metabolites

217 CINNAMATE 4-HYDROXYLASE, a key enzyme of the phenylpropanoid pathway synthesizing the building blocks

218 are synthesized by a specific branch of the phenylpropanoid pathway that has previously been reporte

219 ouble function for FLESHY in channelling the phenylpropanoid pathway to either lignin or flavour/arom

220 ript accumulation analysis demonstrated core phenylpropanoid pathway transcripts and cell wall modifi

221 sting that the metabolic perturbation of the phenylpropanoid pathway underlies the activation of the

222 the hypothesis that the up-regulation of the phenylpropanoid pathway upon abiotic stress greatly enha

223 characterize the metabolic flux through the phenylpropanoid pathway via the characterization and che

224 The expression of genes in the phenylpropanoid pathway was studied at transcription lev

225 s study, expression of genes involved in the phenylpropanoid pathway was studied in the flavedo (oute

226 Other glucosylated compounds of the phenylpropanoid pathway were also deregulated in these m

227 tic compound vanillylamine (derived from the phenylpropanoid pathway) with a branched-chain fatty aci

228 genes involved in primary metabolism and the phenylpropanoid pathway, and induced a strong accumulati

229 e upregulation of negative regulators of the phenylpropanoid pathway, and that the suppressors revers

230 ive efflux transporter for products from the phenylpropanoid pathway, compromised iron uptake from an

231 icolor) participates in an early step of the phenylpropanoid pathway, exchanging coenzyme A (CoA) est

232 Cysteine appears to influence the phenylpropanoid pathway, favoring the accumulation of po

233 As a result of the phenylpropanoid pathway, many Brassicaceae produce consi

234 atalyzes the first rate-limiting step in the phenylpropanoid pathway, which controls carbon flux to a

235 one biosynthesis, response to stress and the phenylpropanoid pathway, while the genes down-regulated

236 pression levels of the genes involved in the phenylpropanoid pathway.

237 yanins are natural pigments derived from the phenylpropanoid pathway.

238 oA LIGASE (4CL), a key enzyme of the general phenylpropanoid pathway.

239 share the first three enzymatic steps of the phenylpropanoid pathway.

240 d late biosynthetic genes from the flavonoid/phenylpropanoid pathway.

241 monolignols, which are synthesized from the phenylpropanoid pathway.

242 but also in carbohydrate metabolism and the phenylpropanoid pathway.

243 , which catalyzes the second reaction in the phenylpropanoid pathway.

244 implies a novel branch point of the general phenylpropanoid pathway.

245 vonoids and one group of end products of the phenylpropanoid pathway.

246 o regulate various branches of the intricate phenylpropanoid pathway.

247 ) related to anthocyanins content, explained phenylpropanoid pathway.

248 nts as regulators of structural genes of the phenylpropanoid pathway; therefore, we hypothesized that

249 upregulated the shikimate, methyl-donor, and phenylpropanoid pathways (i.e., the pathways supplying t

250 the associated genes of the phenolamide and phenylpropanoid pathways as well as the nicotine biosynt

251 Quantitative proteomics data from ethene and phenylpropanoid pathways indicate additional gene candid

252 re, many genes involved in the flavonoid and phenylpropanoid pathways were highly expressed in Virofl

253 e mevalonate, methylerythritol phosphate and phenylpropanoid pathways.

254 transporters, wall modification, defense and phenylpropanoid pathways.

255 nt-related genes from both the shikimate and phenylpropanoid pathways.

256 e cytosolic and plastidic isoprenoid and the phenylpropanoid pathways.

257 cking leaf herbivore-induced changes in root phenylpropanoid patterns.

258 Importantly, the phenylpropanoid perturbation is not alleviated in gir1 r

259 ase after 36 h, particularly for terpenoids, phenylpropanoids, phytoalexins and fatty acids in the 60

260 esis and serves as the precursor of abundant phenylpropanoid plant natural products.

261 te (pCA) that acylate the side-chains of the phenylpropanoid polymer backbone.

262 Lignin is an abundant phenylpropanoid polymer produced by the oxidative polyme

263 Lignin is a phenylpropanoid polymer produced in the secondary cell w

264 Lignins are complex phenylpropanoid polymers mostly associated with plant se

265 Lignins are phenylpropanoid polymers, derived from monolignols, comm

266 Because of the vast range of functions that phenylpropanoids possess, their synthesis requires preci

267 ostability and antifungal activities of some phenylpropanoids (PPs) were investigated.

268 Stilbenes are a small family of phenylpropanoids produced in a number of unrelated plant

269 lation of glucosinolate intermediates limits phenylpropanoid production in a Mediator Subunit 5 (MED5

270 estor of Plantae, allowing efficient Phe and phenylpropanoid production via arogenate in plants today

271 ay-regulating MYB factor ODORANT1 (ODO1) and phenylpropanoid scent-related structural genes.

272 gars increased significantly, where specific phenylpropanoids showed increment up to 137% and several

273 -amino group was transferred to Cbeta of the phenylpropanoid skeleton with retention of configuration

274 The modulation of genes related to phenylpropanoid/stilbene metabolism highlighted the dist

275 ion of biosynthetic genes acting in the core phenylpropanoid, suberin, lignin, and lignan pathways.

276 eight flavonol glycosides (11-18), and three phenylpropanoid-substituted catechins (19-21).

277 Overall, the flavonol glycosides and phenylpropanoid-substituted catechins showed superior an

278 Additionally, despite the presence of other phenylpropanoid substrates in vivo, sinapaldehyde is the

279 riboflavin biosynthesis in M. truncatula and phenylpropanoid synthesis in Arabidopsis upon iron defic

280 e levels of proteins involved in melanin and phenylpropanoids synthesis, among others.

281 ssociated with the metabolism of jasmonates, phenylpropanoids, terpenoids and L-phenylalanine were mo

282 Eugenol is a volatile phenylpropanoid that contributes to flower and ripe frui

283 Caffeic acid is a natural phenylpropanoid that exhibits various health benefits.

284 rs of genes related to terpene and benzenoid/phenylpropanoid (the main floral scent volatiles) biosyn

285 bic bacteria remove the acyl side chain from phenylpropanoids to leave an aromatic aldehyde, which th

286 Despite the importance of Phe and phenylpropanoids to plant and human health, the pathway

287 termination of eight free phenolic acids and phenylpropanoid vanillin using high performance liquid c

288 tified an R2R3-MYB-like regulatory factor of phenylpropanoid volatile biosynthesis acting downstream

289 1/nsgt1 background, further glycosylation of phenylpropanoid volatile diglycosides does not occur, th

290 PH4 resulted in a marked decrease in floral phenylpropanoid volatile emission, with a concurrent inc

291 o associations involved in fruit acidity and phenylpropanoid volatile production.

292 Phenylpropanoid volatiles are responsible for the key to

293 cleavable diglycosides of the smoky-related phenylpropanoid volatiles into noncleavable triglycoside

294 The mechanism underlying the emission of phenylpropanoid volatiles is poorly understood.

295 copy for quantification of two laserine-type phenylpropanoids was investigated but failed due to low

296 most of the naturally occurring terpenes and phenylpropanoids were better preserved in HPHT treated s

297 ated with SA, while soluble sugars and other phenylpropanoids were inversely correlated.

298 Primary aldehydes and phenylpropanoids were most closely related to green and

299 rotenoids, carbohydrates, polyacetylenes and phenylpropanoids with high bioactive potential was inves

300 has the ability to oxidize a broad range of phenylpropanoids with rather similar efficiencies, which