ライフサイエンスコーパス: phenylpropanoid

1 ion of phenylalanine for the biosynthesis of phenylpropanoids.

2 enzymes, consequently altering the levels of phenylpropanoids.

3 cause dwarfing and decreased accumulation of phenylpropanoids.

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

5 tabolites such as alkaloids, terpenoids, and phenylpropanoids.

6 as being involved in binding CoA-conjugated phenylpropanoids.

7 iochemical flux toward coumarins and general phenylpropanoids.

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

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

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

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

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

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

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

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

16 defects in glucosinolate biosynthesis and in phenylpropanoid accumulation.

17 s not responsive to stresses that stimulated phenylpropanoid accumulation.

18 lts in dwarfism and constitutively repressed phenylpropanoid accumulation.

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

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

21 Increased glucosylation of other phenylpropanoids also occurred in plants overexpressing

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

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

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

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

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

27 12 genes that encoded enzymes in the general phenylpropanoid and isoflavonoid pathways.

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

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

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

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

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

33 at Botrytis also has variable sensitivity to phenylpropanoids and glucosinolates.

34 es, and negatively correlated with levels of phenylpropanoids and phenylalanine ammonia lyase activit

35 4CL required for the synthesis of precursor phenylpropanoids and styrylpyrone synthase (SPS), integr

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

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

38 herbivory through the induction of volatile, phenylpropanoid, and protease inhibitor defenses.

39 vancements in the production of isoprenoids, phenylpropanoids, and alkaloids were made possible by ut

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

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

42 The phenylpropanoids, and the related plant polyketides, hav

43 A, a branch point metabolite from which many phenylpropanoids are made.

44 Phenylpropanoids are phenylalanine-derived specialized m

45 Besides, phenylpropanoids are predominant in winter and flavonoid

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

47 l scent volatiles fall into the terpenoid or phenylpropanoid/benzenoid classes of compounds.

48 alyze the formation of volatile terpenoid or phenylpropanoid/benzenoid compounds, have now been used

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

50 ADT activity, levels of Phe, and downstream phenylpropanoid/benzenoid volatiles.

51 iverse metabolisms of essential amino acids, phenylpropanoids, benzenoids, and fatty acids.

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

53 sis roots may provide new insights into both phenylpropanoid biosynthesis and light signaling in plan

54 Defects in phenylpropanoid biosynthesis arising from deficiency in

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

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

57 Phenylpropanoid biosynthesis in plants engenders a vast

58 Phenylpropanoid biosynthesis in plants engenders a vast

59 wild-type genes are required to repress root phenylpropanoid biosynthesis in the absence of light.

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

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

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

63 most likely TTEs) targeted genes involved in phenylpropanoid biosynthesis, consistent with the abroga

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

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

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

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

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

69 posed to occur at the entry point into plant phenylpropanoid biosynthesis.

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

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

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

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

74 The phenylpropanoid biosynthetic pathway that generates lign

75 metabolites) from phenylalanine through the phenylpropanoid biosynthetic pathway.

76 Plants produce large amounts of phenylpropanoids, both in terms of molecular diversity a

77 soil-grown plants contain almost no soluble phenylpropanoids, but exposure to light leads to the acc

78 e confirmed circadian regulation of P450s in phenylpropanoid, carotenoid, oxylipin, glucosinolate, an

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

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

81 gene source for the engineering of specific phenylpropanoid components.

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

83 ris emit a mixture of volatile benzenoid and phenylpropanoid compounds that include isoeugenol and eu

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

85 Phenylpropanoids comprise an important class of plant se

86 3-acetaldoxime (IAOx), and we found that the phenylpropanoid content of cyp79b2 cyp79b3 and ref5-1 cy

87 its root-to-shoot translocation, and Phe and phenylpropanoid contents were unaltered in pig1-1, indic

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

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

90 economically important compounds, including phenylpropanoid derivatives and terpenoids.

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

92 rance is comprised of 13 volatile benzenoids/phenylpropanoids derived from the aromatic amino acid ph

93 Lignin forms from the polymerization of phenylpropanoid-derived building blocks (the monolignols

94 Phenylpropanoid-derived compounds represent a diverse fa

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

96 Lignin is a phenylpropanoid-derived heteropolymer important for the

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

98 The flavonoids are phenylpropanoid-derived metabolites that are ubiquitous

99 truncatula with activity towards a number of phenylpropanoid-derived natural products including the f

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

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

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

103 d F5H, the lycophyte Selaginella employs one phenylpropanoid dual meta-hydroxylase to bypass several

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

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

106 sed conversion of these compounds into other phenylpropanoid end products.

107 eased levels of several different classes of phenylpropanoid end-products, and exhibit reduced lignin

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

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

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

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

115 metabolic pathways, including terpenoids and phenylpropanoids/flavonoids.

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

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

118 esis of individual floral volatile benzenoid/phenylpropanoid (FVBP) compounds, i.e. at the end of the

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

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

121 analysis of root cell walls and analysis of phenylpropanoid gene expression suggest that coniferin a

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

123 Experiments have shown that many phenylpropanoid genes are highly expressed in light-grow

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

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

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

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

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

129 Salidroside is a phenylpropanoid glycoside isolated from the medicinal pl

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

131 exhibiting significant activity toward other phenylpropanoid hydroxycinnamaldehydes.

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

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

134 The presence of phenylpropanoids in etiolated roots of cop (constitutive

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

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

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

138 syltransferases shown to glucosylate several phenylpropanoids in vitro, including monolignols, hydrox

139 However, phenylpropanoids, including scoparone, were not critical

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

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

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

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

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

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

146 in, through the action of a dual specificity phenylpropanoid meta-hydroxylase, Sm F5H.

147 ch syringyl lignin biosynthesis requires two phenylpropanoid meta-hydroxylases C3'H and F5H, the lyco

148 anoid O-methyltransferase that can methylate phenylpropanoid meta-hydroxyls at both the 3- and 5-posi

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

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

151 The plant-specific phenylpropanoid metabolic pathway produces as some of it

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

153 The data demonstrate the plasticity of phenylpropanoid metabolism and the important role that g

154 Phenylpropanoid metabolism begins with the amino acid ph

155 are consistent with modulation of defensive phenylpropanoid metabolism by M. grisea and the inabilit

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

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

165 Enhancement of phenylpropanoid metabolism, characterized by a restricte

166 agreement with the early position of C4H in phenylpropanoid metabolism, ref3 mutant plants accumulat

167 Brown midrib6 (bmr6) affects phenylpropanoid metabolism, resulting in reduced lignin

168 opsis have overlapping yet distinct roles in phenylpropanoid metabolism.

169 ral players in the homeostatic repression of phenylpropanoid metabolism.

170 ting a redirection of metabolite flow within phenylpropanoid metabolism.

171 of PALs, thus posttranslationally regulating phenylpropanoid metabolism.

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

173 rom phenylalanine through the early steps of phenylpropanoid metabolism.

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

175 associated with secondary wall formation or phenylpropanoid metabolism.

176 romoters for the core and lignin sections of phenylpropanoid metabolism.

177 ompound fraction and the enzymes involved in phenylpropanoid metabolism.

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

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

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

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

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

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

184 COMT is a bifunctional phenylpropanoid O-methyltransferase that can methylate p

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

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

187 the first committed step in the formation of phenylpropanoids, only a few prokaryotic PALs have been

188 The phenylpropanoid p-coumarate and structurally related aro

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

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

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

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

193 AP1 Myb suggested that genes from the entire phenylpropanoid pathway are targets of regulation by Myb

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 The initial reactions of the phenylpropanoid pathway convert phenylalanine to p-couma

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

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

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

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

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

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

204 d non-P450 genes in the many branches of the phenylpropanoid pathway have similar circadian patterns

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

206 The phenylpropanoid pathway in plants leads to the synthesis

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

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

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

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

211 The phenylpropanoid pathway is a major global carbon sink an

212 The phenylpropanoid pathway is responsible for the biosynthe

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

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

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

216 he epistatic relationship of mdr4 to the tt4 phenylpropanoid pathway mutation.

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

218 The plant phenylpropanoid pathway produces an array of metabolites

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

220 alcone isomerases (CHIs), key enzymes in the phenylpropanoid pathway that produces flavonoids and iso

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

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

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

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

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

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

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

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

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

230 enesis-related genes and most members of the phenylpropanoid pathway, and several other genes that ma

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

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

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

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

235 the upstream and downstream segments of the phenylpropanoid pathway, reflecting the plasticity of pl

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

237 -lyase (PAL) catalyzes the first step of the phenylpropanoid pathway, which produces precursors to a

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

239 monolignols, which are synthesized from the phenylpropanoid pathway.

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

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

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

243 ng Populus, SA is derived primarily from the phenylpropanoid pathway.

244 entified induced levels of components of the phenylpropanoid pathway.

245 ols could influence flux through the soluble phenylpropanoid pathway.

246 tose phosphate pathway, and into the general phenylpropanoid pathway.

247 of isoflavone biosynthesis from the general phenylpropanoid pathway.

248 yanins are natural pigments derived from the phenylpropanoid pathway.

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

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

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

252 ed and accumulates reduced quantities of all phenylpropanoid-pathway end products.

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

254 ol 4-phosphate (MEP)/terpenoid and shikimate/phenylpropanoid pathways appears to play an important ro

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

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

257 e mevalonate, methylerythritol phosphate and phenylpropanoid pathways.

258 e cytosolic and plastidic isoprenoid and the phenylpropanoid pathways.

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

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

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

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

263 The presence of the phenylpropanoid polymer lignin in plant cell walls imped

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

265 Lignins are complex phenylpropanoid polymers mostly associated with plant se

266 Lignins are phenylpropanoid polymers, derived from monolignols, comm

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

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

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

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

271 ous for ref4 exhibit intermediate growth and phenylpropanoid-related phenotypes, suggesting that thes

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

273 implies the importance of jasmonic acid and phenylpropanoid signaling pathways locally at the site o

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

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

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 gal activity relative to other M. truncatula phenylpropanoids tested but has not been reported in thi

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

283 Sinapoylmalate is a major phenylpropanoid that is accumulated in Arabidopsis.

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

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

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

287 le for controlling the overall production of phenylpropanoid versus terpenoid constituents in the gla

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 This suggested that phenylpropanoids with an ortho-diphenyl structure such a

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

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