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phenylpropanoid metabolism

9928 relationships annotated with this phrase. Showing first 500 of 9928.
Source entity Relationship Target entity Species
p-coumaroyl putrescine is reduced by less than 45% in (COI1, AT2G39940) mutants compared with WT plants after BPH elicitation Oryza sativa
method developed in this study can potentially facilitate studies of phenylpropanoid metabolism
CaMYB12-like overexpressing tomato fruits showed small, significant change in expression of some phenylpropanoid genes Solanum lycopersicum
metabolomic changes upon agroinfiltration include high levels of chlorogenic acid derivates Nicotiana benthamiana
phenylpropene biosynthetic enzymes are closely related to NADPH-dependent reductases
p-coumarate esters were accumulated in all rosette leaves of (CYP98A3, REF8, AT2G40890) pOpON plants Arabidopsis thaliana
various nonlignin phenylpropanoids are produced through phenylpropanoid pathway
p-coumarate esters were near to or below limits of detection in wild type Arabidopsis thaliana
oldest leaves of dexamethasone (dex)-treated (CYP98A3, REF8, AT2G40890) pOpON contained relatively unchanged levels of flavonoids and sinapoylmalate even 6 days after dexamethasone (dex) application Arabidopsis thaliana
cinnamyl alcohol dehydrogenase (ATCAD8, CAD-B2, ELI3, ELI3-2, AT4G37990) is expressed at lower levels in (XLG2, AT4G34390) mutant Arabidopsis thaliana
phenylpropanoids play important roles in plant growth and development
(ATPAL1, PAL1, AT2G37040) (PHENYLALANINE AMMONIA LYASE1) expression is higher in transgenic plants Solanum tuberosum
deficiency or accumulation of nonlignin phenylpropanoids may contribute to alteration of plant growth
reduced epidermal fluorescence8 (CYP98A3, REF8, AT2G40890) plants exhibits hyperaccumulation of p-coumarate esters Arabidopsis thaliana
flavonoid and sinapoylmalate accumulation is more sensitive to induction of C3′H expression in young leaves than in older leaves Arabidopsis thaliana
phenylalanine downstream metabolism is targeted toward generating phenylpropanoid and phenylpropanoid acetate metabolites
reduced epidermal fluorescence8 (CYP98A3, REF8, AT2G40890) plants exhibits hyperaccumulation of flavonoids Arabidopsis thaliana
reduced flux of carbon into phenylpropanoids mediated by (ATMYB4, MYB4, AT4G38620) is imposed on (ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) mutant Arabidopsis thaliana
sub-optimal photosynthesis when plants are stressed causes low concentration of shikimate pathway intermediates to re-direct entire phenylpropanoid pathway towards production of phytoalexins, volatiles, flavonoids, and anthocyanins
enrichment in phenolics in H12 cell walls was bound to a global induction of phenylpropanoid genes involved in the synthesis of these compounds Zea mays
C3'H deficiency results in multiple changes in phenylpropanoid metabolism Arabidopsis thaliana
flavonoid accumulation in ref8* myb4-1 and ref8* gir1-1 showed similar levels of flavonoid accumulation in ref8* Arabidopsis thaliana
genes downregulated in (AtC3H66, TZF9, AT5G58620) mutant are enriched for phenylpropanoid metabolism and biosynthesis Arabidopsis thaliana
LG8763094 is annotated as hydroxycinnamoyl-CoA quinate hydroxycinnamoyl transferase (HQT) like protein Lactuca sativa
phenylpropanoid metabolism genes are among highest differentially expressed in ABA-treated control cells Vitis vinifera
phenylpropanoid signaling pathway induces accumulation of flavonol glycosides
tyrosine ammonia lyase (TAL) catalyzes non-oxidative deamination of tyrosine
(CCoAOMT1, AT4G34050) is involved in various pathways, including sinapoylmalate formation, scopoletin biosynthesis, and methylation of acylspermidine precursors
effective protection and channeling of reactive catechol moiety is explanation for fuzzy and apparently complicated meta-hydroxylation
NO donors triggered expression of phenylalanine-ammonia lyase (PAL) potato
pigmented layer or endothelium produces proanthocyanidins Arabidopsis thaliana
C3'H deficiency causes hyperaccumulation of p-coumarate esters Arabidopsis thaliana
uninduced (CYP98A3, REF8, AT2G40890) pOpON rosette leaves show hyperaccumulation of flavonoids Arabidopsis thaliana
dexamethasone (DEX) induction substantially reverts metabolic phenotype of (CYP98A3, REF8, AT2G40890) pOpON Arabidopsis thaliana
uninduced (CYP98A3, REF8, AT2G40890) pOpON rosette leaves show accumulation of p-coumarate esters Arabidopsis thaliana
treatment of 35S::VvABF2 cells by ABA up-regulated secondary metabolism and, more particularly, the first steps of the phenylpropanoid pathway (PAL and cinnamic acid 4-hydroxylase) Vitis vinifera
transgenic lines show significant increase in total phenolic compound levels Solanum tuberosum
dexamethasone (dex)-induced expression of C3′H substantially restores soluble phenylpropanoid metabolite content of (CYP98A3, REF8, AT2G40890) pOpON Arabidopsis thaliana
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) ProSNBE lines did not lower general ferulic acid levels
MYB proteins play important role in control of phenylpropanoid metabolism
C3'H induction revealed selective turnover of different phenylpropanoid metabolite pools Arabidopsis thaliana
Cinnamate 4-hydroxylase (NbC4H) is one of the first two enzymes downstream of PAT in channeling phenylalanine toward secondary metabolites Nicotiana benthamiana
genes involved in the phenylpropanoid pathway were particularly observed for enhanced response in ABA-treated VvABF2-overexpressing cells Vitis vinifera
ir-ztl plants do not differ from EV plants in caffeoylputrescine levels Nicotiana attenuata
incorporation of radioactivity from [14C]cinnamate occurred first into hydroxycinnamoyl–CoA Zea mays
gene expression changes in phenylpropanoid genes did not lead to significant effect on phenylpropanoid levels Capsicum annuum; Solanum lycopersicum
targeted and non-targeted approaches enabled identification of participating enzymes of phenylpropanoid biosynthetic machinery
metabolic fluxes within a complex pathway can be redirected towards pool of soluble metabolites
three candidate genes are related to quinate metabolite Lactuca sativa; Lactuca serriola
R2R3 MYBs have been implicated in the regulation of phenylpropanoid metabolism
(ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) mutant may attempt to compensate for lack of sinapoyl malate and sinapoyl glucose by up-regulating (BRT1, UGT84A2, AT3G21560) and (UGT84A3, AT4G15490) Arabidopsis thaliana
LG5482522 (encoding coumarate 3-hydroxylase) identified as candidate gene that affects quinate and chlorogenic acid levels Lactuca serriola
general phenylpropanoid pathway is not restricted to common lignin or flavonoid biosynthesis
versatile metabolic control for channeling of shikimate pathway intermediates is explanation for fuzzy and apparently complicated meta-hydroxylation
natural variation of phenylpropanoid metabolism is surveyed in leaf sinapate ester profiles in 96 accessions Arabidopsis thaliana
ref8* plants have presence of p-coumarate esters Arabidopsis thaliana
(ATMYB4, MYB4, AT4G38620) is transcriptional repressor of phenylpropanoid metabolism Arabidopsis thaliana
StWRKY1 activates 4CL Solanum tuberosum
higher phenylalanine levels in plant leaves lead to enhanced accumulation of phenylalanine-derived phenylpropanoids Arabidopsis thaliana; Solanum lycopersicum; Petunia hybrida
fine regulation of the early steps of phenylpropanoid metabolism revealed in comparing B+ Myc and B− Myc with the NoMyc condition Lotus japonicus
initial three steps of the pathway catalyzed by PAL, cinnamate 4-hydroxylase, and 4-coumaroyl CoA-Ligase are mandatory and provide basis for all subsequent branches and resulting metabolites
4-hydroxylation of trans-cinnamate to 4-coumarate is encoded by single gene (ATC4H, C4H, CYP73A5, REF3, AT2G30490) encoding Arabidopsis thaliana
ccc flowers displays presence of feruloyl malate
ccc triple mutant stems displays dramatically increased flavonol glycosides content
ref8* gir1-1 plants has similar profile to (CYP98A3, REF8, AT2G40890) Arabidopsis thaliana
Treatment with 36 mM Phe caused significant increase in cinnamic acid levels Chrysanthemum morifolium
Phe treatment causes increase in levels of 3-phenyllactic acid
caffeoyl phenyl lactic acid (rosmarinic acid) is predominant soluble phenylpropanoid in Lamiales
decarboxylation catalyzed by phenylacetaldehyde synthase is catalyzed by PHENYLACETALDEHYDE SYNTHASE
sinapoyl glucose (M10) has decreased content in (ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) mutant Arabidopsis thaliana
general phenylpropanoid pathway feeds into hydrolyzable tannins
phenylpropanoid metabolism receives up to 40% of the C in a plant plant carbon
monolignols are synthesised via phenylpropanoid pathway in cytoplasm
four additional Pna lines accumulate sinapoylglucose Arabidopsis thaliana
ccr1g flowers displays reduced level of sinapoyl esters
StWRKY1 activation of phenylpropanoid genes affects deposition of hydroxycinnamic acid amides Solanum tuberosum
feruloyl malate is found in substantial amounts in (ATCAD4, CAD, CAD-C, CAD4, AT3G19450) c d mutant stems
phenylpropanoid metabolism starts with deamination of phenylalanine
mutations in (ATC4H, C4H, CYP73A5, REF3, AT2G30490) result in accumulation of cinnamoylmalate Arabidopsis thaliana
ccc plantlets displays similar reduction in sinapoyl esters
ccc plantlets displays presence of feruloyl malate
feruloyl malate is increased in ccr1g flowers
recombinant mammalian NOS injection triggered expression of phenylalanine-ammonia lyase (PAL) tobacco
ccr1g rosette leaves displays presence of feruloyl malate
shikimate pathway provides core unit for phenylpropanoid metabolism
subsequent methylation by CCoAOMT is consequence of effective protection and channeling of reactive catechol moiety
ccc flowers displays reduced level of sinapoyl esters
phenylpropanoid metabolism starts with decarboxylation catalyzed by phenylacetaldehyde synthase
phenylpropanoid genes involved in this metabolic pathway were repressed in stationary phase Zea mays
caffeoyl quinate (chlorogenic acid) is predominant soluble phenylpropanoid in Solanaceae
ZmCCoAOMT seems to be the main methyl-transferase in control cells Zea mays
tissue-specific expression of GhnsLTPs coordinates disease and insect resistance by regulating metabolic flux redirection in phenylpropanoid pathway Gossypium hirsutum
GhnsLTPsA10 overexpression promotes phenylpropanoid metabolic flux from flavonoid biosynthesis pathway to lignin pathway
sinapate ester accumulation in ref8* myb4-1 and ref8* gir1-1 showed similar levels of sinapate ester accumulation in ref8* Arabidopsis thaliana
GhnsLTPsA10 mediates phenylpropanoid metabolism Gossypium hirsutum; Arabidopsis thaliana
tissue-specific expression of GhnsLTPsA10 coordinates by redirecting metabolic flux in phenylpropanoid pathway
redundant gene and enzyme pattern is required for functional integrity and plasticity of phenylpropanoid biosynthetic pathways
phenylpropanoid perturbation is not alleviated in (GIR1, AT5G06270) (CYP98A3, REF8, AT2G40890) double mutant Arabidopsis thaliana
phenylalanine ammonia lyase (PAL) catalyzes deamination of phenylalanine
Phenylalanine ammonia lyase 1 (AevPAL1)-silenced plants show significantly decreased expression of cinnamyl alcohol dehydrogenase (AevCAD) Aegilops variabilis
glycosylation of p-coumaric acid and ferulic acid by (UGT73C7, AT3G53160) results in significant effect on phenylpropanoid metabolism Arabidopsis thaliana
uninduced (CYP98A3, REF8, AT2G40890) pOpON rosette leaves show decrease of sinapate esters Arabidopsis thaliana
central phenylpropanoid pathway has multiple downstream branches including lignin and flavonoid pathways
phenylpropanoid metabolism pathway genes are induced after inoculation with J2 cereal cyst nematodes (CCNs) Aegilops variabilis
(UGT73C7, AT3G53160) mediates redirection of phenylpropanoid metabolism Arabidopsis thaliana
anthocyanin levels in petunia petals did not correlate with volatile emission petunia
identification of metabolite pattern and elucidation of structural genes and enzymes will provide tremendous challenge to understand phenylpropanoid metabolism Arabidopsis thaliana
135 Pna lines were analyzed for leaf sinapate ester profiles Arabidopsis thaliana
feruloyl malate is increased in ccr1g leaves
free p-coumaric acid and ferulic acid levels were affected by (UGT73C7, AT3G53160) overexpression Arabidopsis thaliana
mutation in (ATC4H, C4H, CYP73A5, REF3, AT2G30490) in -3 plants disturbs dynamic changes of phenylpropanoid pathway Arabidopsis thaliana
phenylpropanoid polyamine conjugate biosynthesis occurs in Arabidopsis tapetum Arabidopsis thaliana
SABATH-family of enzymes are implicated in phenylpropanoid volatile formation
feruloyl malate is increased in ccr1g stems
proanthocyanidins condense into tannins Arabidopsis thaliana
StWRKY1 activates THT Solanum tuberosum
(UGT73C7, AT3G53160) is important regulator that adjusts phenylpropanoid metabolism Arabidopsis thaliana
Phenylalanine ammonia lyase 1 (AevPAL1)-silenced plants show no differences in expression of cinnamate-4-hydroxylase (AevC4H) Aegilops variabilis
leaf phenolic content is analysed for relationship with plant growth Populus
ferulic acid is upstream metabolite in phenylpropanoid pathway Arabidopsis thaliana
(UGT73C7, AT3G53160) redirects phenylpropanoid metabolic pathway
(UGT73C7, AT3G53160) could glycosylate p-coumaric acid
AevPAL1 affects synthesis of downstream secondary metabolites Aegilops variabilis
AevPAL1 alters downstream secondary metabolites Aegilops variabilis
Phenylalanine ammonia lyase 1 (AevPAL1)-silenced plants show significantly lower content of N-caffeoyl putrescine Aegilops variabilis
(UGT73C7, AT3G53160) mediates redirection of phenylpropanoid pathway Arabidopsis thaliana
phenylpropanoid metabolic flux redirection leads to biosynthesis of coumarins
p-coumaric acid and ferulic acid glycosides were observed to accumulate significantly in (UGT73C7, AT3G53160) OE plants Arabidopsis thaliana
cinnamate-4-hydroxylase (ATC4H, C4H, CYP73A5, REF3, AT2G30490) provides precursors for lignin, flavonoid and coumarin synthesis Arabidopsis thaliana
PRODUCTION OF ANTHOCYANIN PIGMENT 1 positively affects scent and pigmentation
gibberellin induces anthocyanins
phenylalanine ammonia lyase (PAL) initiates phenylpropanoid pathway
phenylpropanoid pathway produces lignin Oryza sativa
cis-ferulic acid was significantly affected by Silicon treatment Vigna unguiculata
PfaGT1-316 overexpression had little effect on PGs (phenolic glycosides) and lignin content and S/G ratio Populus tremula × alba
Phenylalanine ammonia lyase 1 (AevPAL1) is induced by cereal cyst nematode (CCN) inoculation Aegilops variabilis
phenylpropanoid biosynthesis related to coumarin and lignin production Lotus japonicus
phenylpropanoid metabolism regulates transcription of (BAL, SNC1, AT4G16890) Arabidopsis thaliana
Mycorrhizal colonization by Gigaspora margarita modulated phenylpropanoid biosynthesis Lotus japonicus; Gigaspora margarita
phenylpropanoids were localized in outer tissues Zea mays
change in one of the metabolic branches of phenylpropanoid pathway will inevitably lead to redistribution of metabolic flux in the whole pathway
function and impact of all members of a gene family remain to be completely established comprehensive understanding of phenylpropanoid biosynthesis
Arabidopsis (ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) knockout mutants display enhanced pool of feruloyl malate at the expense of sinapoyl malate accumulation Arabidopsis thaliana
lignin pathway was promoted in transgenic Arabidopsis Arabidopsis thaliana
phenylalanine ammonia lyase 1 (ATPAL1, PAL1, AT2G37040) encodes AevPAL1 Aegilops variabilis
Phenylalanine ammonia lyase 1 (AevPAL1)-silenced plants show significantly reduced content of sinapinaldehyde Aegilops variabilis
(UGT73C7, AT3G53160) H19L and Q398N showed no reaction products towards p-coumaric and ferulic acid
anthocyanin accumulation levels in corolla epidermis are inverse of VOC emission levels Petunia × hybrida
phenylpropanoid pathway disruption suppressed UGT73C7-promoted (BAL, SNC1, AT4G16890) expression Arabidopsis thaliana
R2R3-MYBs are positive and negative regulators of biosynthetic enzymes required for the production of phenylpropanoids
H2O2 was shown to induce (ATPAL1, PAL1, AT2G37040) gene expression in Arabidopsis Arabidopsis thaliana
phenylpropanoid metabolism redistribution by (UGT73C7, AT3G53160) affected (BAL, SNC1, AT4G16890) activity and plant immunity Arabidopsis thaliana
CYP79-catalyzed aldoximes operate as negative regulators of phenylpropanoid biosynthesis
ZmPALa and ZmPALb genes seemed to be involved in short-term response Zea mays
ccr1g plantlets displays similar reduction in sinapoyl esters
C'3H enzyme uses products of (HCT, AT5G48930) /HQT as substrates
ir-PhMYB4 increases transcript levels of CINNAMATE-4-HYDROXYLASE (PhC4H1 and PhC4H2) Petunia×hybrida
1-aminobenzotriazole (ABT) at 10–20 μM inactivates cinnamic acid 4-hydroxylase (ATC4H, C4H, CYP73A5, REF3, AT2G30490)
foliar non-structural phenylpropanoid derivative (NSP) accrual is promoted in Populus grown under high light Populus species
biosynthesis of non-structural phenylpropanoid derivative (NSP) is metabolically costly in terms of C use Populus species
changed metabolite profile suggests chalcone synthase down-regulation Fragaria × ananassa
PAL transcript is elevated in inoculated compared with control plants at Sevin wheat cultivar at 13–15 dai Triticum aestivum
PAL activity unmodified after 15 h treatment in contrast with stimulation caused by chitosan Beta vulgaris
Populus UGT84A17 exhibits broad in vitro activities toward various hydroxylated and/or methoxylated cinnamic and benzoic acids Populus
Populus GT1-316a is Potri.009G095300 Populus trichocarpa
4-coumarate-CoA ligase transcript is upregulated in TR185 mutant
p-coumaric acid and ferulic acid glycosides in (UGT73C7, AT3G53160) knockout plants were obviously lower than those in wild-type plants Arabidopsis thaliana
peak 4 is tentatively identified as Feruloyl-O-pentoside malonate Lotus corniculatus
CaPAL1 acts via its enzymatic activity in phenylpropanoid pathway Capsicum annuum; Arabidopsis thaliana
PAL activity is the first committed step of this biosynthetic pathway Arabidopsis thaliana
phenylpropanoids are further transformed into anthocyanins, lignins, flavonoids and phytoalexins
phenylpropanoid-derived condensed tannins (CTs) have substantial biosynthetic costs
expression of upstream phenylalanine ammonia-lyase (PAL) gene remained relatively constant Populus species
tomato fruits contain phenolics Solanum lycopersicum
feruloyl-CoA was redirected to soluble feruloyl malate Arabidopsis thaliana
slow-growing clone has comparatively high condensed tannin (CT) and phenolic glycoside (PG) accrual in leaves Populus
silicic acid treatment significantly regulates transcript abundance of 4-coumarate-CoA ligase (LOC_Os01g67540) Oryza sativa
cinnamoyl-CoA-reductase expression level remained low in woolly peaches after ripening Prunus persica
p-coumaric acid and ferulic acid are upstream metabolites in the phenylpropanoid pathway
GST-UGT73C7 fusion protein could glucosylate ferulic acid
Phenylalanine ammonia lyase 1 (AevPAL1)-silenced plants show significantly lower content of feruloylcholine Aegilops variabilis
foliar production of phenylpropanoid defence chemicals was not the primary cause of reduced plant growth in the slow-growing clone Populus
wounding probably potentiated lignin production Triticum aestivum
fluorescence may be due to enhanced synthesis of flavanones betagarin and betavulgarin Beta vulgaris
PhMYB4 functions in repression of (ATC4H, C4H, CYP73A5, REF3, AT2G30490) transcription Petunia×hybrida
phenylalanine is present in only spurious amounts in all samples Solanum tuberosum subsp. tuberosum
PtMYB8 have been linked to phenylpropanoid metabolism Pinus taeda
compound 4 consists of ferulic acid linked to malonated pentose sugar Lotus corniculatus
elevated hydroxycinnamoyl-glucose accumulation was driven by PfaGT1-316 overexpression and redirection of phenylpropanoid pathway intermediates Populus tremula × alba
SlAREB1 overexpression fruits at red ripe stage showed reduced content of rutin Solanum lycopersicum
phenylalanine ammonia-lyase (PAL) can be affected by light through non-transcriptional mechanism
PtMYB1 or PtMYB8 overexpression is congruent with decrease of low molecular weight phenolic compounds Picea glauca
C from acetate groups is sufficient to sustain flavonoid biosynthesis Salix (willow)
clone PP_LEa0008K15f encodes a 323 amino acid peptide that showed 75% identity to putative CCR of Arabidopsis thaliana Arabidopsis thaliana
phenylalanine and tyrosine are amino acid precursors for the phenylpropanoid pathway Solanum tuberosum subsp. tuberosum
TET did not induce alterations in contents of 5-caffeoylquinic acid Solanum lycopersicum
foliar non-structural phenylpropanoid derivative (NSP) accrual is promoted in Populus grown under low N Populus species
ABA partially represses PAL activity Solanum lycopersicum
lignin production accumulated in the presence of the pathogen Triticum aestivum; Septoria tritici
petunia (ATC4H, C4H, CYP73A5, REF3, AT2G30490) transcript accumulation is consistent with increased requirement for phenylpropanoid metabolites after anthesis Petunia
Pv (ATCRR2, CCR2, AT2G39180) prefers caffeoyl-CoA as substrate Panicum virgatum
As(V)-responsive genes are predominantly down-regulated in phenylpropanoid metabolism Oryza sativa
cluster B is represented by phenylalanine (Phe) Arabidopsis thaliana
Phe is the key substrate for many secondary plant metabolites including anthocyanins and lignin Zea mays
defence-related genes are involved in phenylpropanoid pathway Oryza sativa
ABT induces significant decreases in levels of dicaffeoylquinic acid Solanum lycopersicum
down-regulation of CCR might cause variations in the flux through the pathway
foliar non-structural phenylpropanoid derivative (NSP) accrual is promoted in Populus grown under elevated carbon dioxide levels Populus species
(ATMYB4, MYB4, AT4G38620) regulates one of the first steps of the phenylpropanoid pathway, controlled by the CYNAMATE-4-HYDROXYLASE (ATC4H, C4H, CYP73A5, REF3, AT2G30490) enzyme Arabidopsis thaliana
transgenic strawberry shows increased accumulation of ferulate derivatives Fragaria × ananassa
PAL transcript is reduced in inoculated compared with control plants at Sevin wheat cultivar at 9–11 dai Triticum aestivum
UGT84A17 plays an important role in phenylpropanoid metabolism Populus
Arabidopsis (UGT84A3, AT4G15490) utilize multiple hydroxycinnamate substrates in vitro Arabidopsis thaliana
overexpression of Populus UGT84A17 in transgenic Populus led to hyperaccumulation of hydroxycinnamate glucose esters Populus
phenylpropanoid metabolism-related genes were significantly induced by herbicidal concentrations of 2,4-Dichlorophenoxyacetic acid (2,4-D) Triticum aestivum
UGT84A17 responds to developmental and environmental cues Populus
Arabidopsis (BRT1, UGT84A2, AT3G21560) is best characterized member of UGT84A subfamily Arabidopsis thaliana
VIT_12s0057g00420 is co-expressed with genes enriched in Ammonia-lyase activity Vitis vinifera
CCR is the first enzyme in lignin branch of the phenylpropanoid pathway
chalcone synthase (ATCHS, CHS, TT4, AT5G13930) uses same precursor metabolites as stilbene synthase (STS)
232 candidate genes involved in phenylpropanoid metabolism Arabidopsis thaliana
SlAREB1 overexpression fruits at red ripe stage showed reduced content of isoquercitrin Solanum lycopersicum
phenylpropanoid 2,3-dioxygenase acts on ferulic acid
abcg29-1 and abcg29-2 had reduced levels in roots of sinapoyl malate and sinapoyl glucose Arabidopsis thaliana
PtMYB1 and PtMYB8 overexpression affects upstream and downstream biosynthetic pathways linked to phenylpropanoid metabolism Picea glauca
p-coumaric acid showed no changes in abundance in each of the comparisons Vigna unguiculata
anthocyanins and phytoalexins are synthesized through phenylpropanoid pathway
PAL transcript shows no significant difference between inoculated and control plants at Stakado wheat cultivar at remaining time points Triticum aestivum
various branches of the phenylpropanoid pathway are closely linked
some MYB factors possess repressor activities and inhibit phenolic compound synthesis
chitosan activates phenylpropanoid pathway
caffeic acid shows higher levels in drought-stressed than in well-watered plants Solanum tuberosum subsp. tuberosum
infiltration solution had clear impact on p-hydroxybenzoic acid, p-coumaric acid, and trans-sinapic acid Vigna unguiculata
feruloyl tyramine is reduced by less than 45% in (COI1, AT2G39940) mutants compared with WT plants after BPH elicitation Oryza sativa
MYB12-like VIGS silenced pepper fruit showed small, significant change in expression of some phenylpropanoid genes Capsicum annuum
(ATC4H, C4H, CYP73A5, REF3, AT2G30490) (cinnamate 4-hydroxylase) is cinnamate 4-hydroxylase
(UGT84A1, AT4G15480) catalyses formation of hydroxycinnamate glucose esters Arabidopsis thaliana
phenylalanine ammonia lyase (PAL) was induced by herbicidal concentrations of 2,4-Dichlorophenoxyacetic acid (2,4-D) Triticum aestivum
ORF JF799117 expressed in Escherichia coli exhibits equal activity toward feruloyl CoA and p-coumaroyl CoA Escherichia coli
anthocyanins belong to phenylpropanoid secondary metabolites
PtMYB1 is involved in phenylpropanoid metabolism Pinus taeda
salicin-containing phenolic glycosides (PGs) commonly comprise 1 to >25% of leaf dry weight in Populus Populus species
di-feruloyl spermidine is significantly reduced in coi2 mutants compared with WT plants after BPH elicitation Oryza sativa
repression of IbMYB1 family genes affects metabolic flux in the phenylpropanoid pathway Ipomoea batatas
XM_004491570.2 gene encodes phenylalanine ammonia-lyase 3
hydroxycinnamates are precursors to flavonoids
oilseed rape UGT84A10 utilize multiple hydroxycinnamate substrates in vitro Brassica napus
expanding leaves (LPI-5) of PfaGT1-316 transgenic plants accumulated ~15-fold higher levels of caffeoyl-glucose Populus tremula × alba
phenylpropanoids act as precursors for cell-wall formation
key genes and metabolites are predominantly involved in phenylpropanoid pathway Brassica napus
NtWRKY41a overexpression repressed flavonoid accumulation Nicotiana tabacum
flavonol synthases are up-regulated in (H3.3, HTR8, AT5G10980) K27A lines Arabidopsis thaliana
phenylpropene biosynthetic enzymes and NADPH-dependent reductases constitute PIP family
sinapoyl-malate is major soluble phenylpropanoid in Brassicaceae
UGT84A clade includes members known to catalyse formation of hydroxycinnamate glucose esters
PtMYB1 activates transcription through specific binding to AC motifs from promoters of phenylpropanoid pathway genes Pinus taeda
phenylpropanoid pathway genes were downregulated phosphorus depletion Medicago truncatula
Populus is known for large and diverse reserves of phenylpropanoids Populus
six glucose esters (caffeoyl-, 4-coumaroyl-, 4-hydroxybenzoyl-, feruloyl-, cinnamoyl-, and benzoyl-glucose) were more abundant in transgenic plants than in WT across all tissues and N regimes Populus tremula × alba
phenylpropanoid genes (PAL, 4CL, and CCOMT isoforms) showed no transgenic effects PfaGT1-316 overexpression Populus tremula × alba
caffeic acid is higher in SUL than in NOJ Solanum tuberosum subsp. tuberosum
down-regulation of CCR in tomato through RNAi strategy leads to quantitative and qualitative changes in soluble phenolic content Solanum lycopersicum
comparative, whole-plant approach was employed for analysis of phenylpropanoid metabolism and its possible effects on growth Populus species
(ABCD1, ACN2, AtABCD1, CTS, PED3, PXA1, AT4G39850) (condensed tannins) were largely unaffected by PfaGT1-316 overexpression Populus tremula × alba
tyrosine and phenylalanine are essential for many phenylpropanoid compounds
GT1s catalyze formation of hydroxycinnamoyl-glucose esters
in vitro PfaGT1-316 glycosylation products of naringenin and kaempferol were not detected in Populus tissues Populus tremula × alba
PtMYB4 activates transcription through specific binding to AC motifs from promoters of phenylpropanoid pathway genes Pinus taeda
umbelliferone occupies pivotal position in plant phenylpropanoid network
phenylpropanoid derivatives significantly affected by GT1-316 overexpression were also significantly changed by N stress in wild types Populus
overexpression of Populus UGT84A17 in transgenic Populus led to hyperaccumulation of cinnamoyl-glucose esters Populus
upregulation of PAL expression was accompanied by presence of soluble and wall-bound phenolic compounds Prunus armeniaca; Prunus domestica
UGT84A6 (FaGT2) catalyses formation of hydroxycinnamate glucose esters Fragaria × ananassa
benzoic acid decreased in infected berries Vitis vinifera
(ALDH1A, ALDH2C4, REF1, AT3G24503) encodes coniferaldehyde dehydrogenase Arabidopsis thaliana
(ATMYB75, AtPAP1, MYB75, PAP1, PAP1-D, SIAA1, AT1G56650) is activator for flavonoid biosynthesis and repressor for lignin biosynthesis Arabidopsis thaliana
cinnamoyl-CoA-reductase expression level in cold-stored peaches is lower than in juicy fruit Prunus persica
CCR is responsible for conversion of hydroxycinnamic acid CoA esters to their corresponding hydroxycinnamaldehydes
chalcone synthase shows decreased transcript levels in transgenic strawberry Fragaria × ananassa
GT1-316 overexpression decreased levels of kaempferol-3-O-rutinoside Populus
sinapoyl-choline accumulates at high levels in seed of Brassicaceae species
phenylpropanoid pathway may be more active in rosette leaves than in cotyledons Arabidopsis thaliana
phenylpropanoid pathway activation leads to synthesis of different phenolics
PAL expression was down-regulated in SlAREB1 antisense lines Solanum lycopersicum
soluble phenylpropanoids such as dehydrodiconiferyl alcohol glycosides might contribute to growth defects of plants with perturbed phenylpropanoid metabolism
Phenylalanine ammonia lyase (NbPAL) is one of the first two enzymes downstream of PAT in channeling phenylalanine toward secondary metabolites Nicotiana benthamiana
phenylpropanoid signaling pathway induces accumulation of anthocyanin derivates
Arabidopsis (BRT1, UGT84A2, AT3G21560) and Brassica napus UGT84A9 produce sinapoyl-glucose Arabidopsis thaliana; Brassica napus
overexpression of Populus UGT84A17 in transgenic Populus led to hyperaccumulation of 4-coumaroyl-glucose esters Populus
dexamethasone (dex) application to (CYP98A3, REF8, AT2G40890) pOpON caused p-coumarate ester content in all rosette leaves to drop significantly after 3 days and reach wild-type levels within 6 days p-coumarate ester content Arabidopsis thaliana
transcriptome analysis found 7 phenylpropanoid-related differentially expressed genes (DEGs) between WT and NtWRKY41a-OE plants Nicotiana tabacum
PAL activity induction significantly higher in CaPAL1-OX leaves by Hpa Noco2 infection than in WT leaves Arabidopsis thaliana
cinnamyl alcohol dehydrogenase-like is expressed at lower levels in (XLG2, AT4G34390) mutant Arabidopsis thaliana
feruloyl tyramine is significantly reduced in coi2 mutants compared with WT plants after BPH elicitation Oryza sativa
di-feruloyl spermidine shows no difference in levels in (COI1, AT2G39940) mutants compared with WT plants Oryza sativa
NADPH-dependent reductases act on phenylpropanoid-derived substrates
ferulate 5-hydroxylase uses NADPH-CPR-cytochrome b5 (CB5) electron transfer chain Arabidopsis thaliana
phenylpropene volatiles rely on precursors shared with monolignol biosynthesis Petunia hybrida
altered profiles of non-lignin phenylpropanoid metabolites may be associated with dwarfism in lignin-altered transgenics and mutants
disruption of microsomal CB5 gene resulted in reduction of sinapoyl malate in leaf Arabidopsis thaliana
disruption of all microsomal CB5 member resulted in none or only limited additive effect on S-lignin monomer and sinapoyl ester synthesis Arabidopsis thaliana
mutations in (SCPL19, SNG2, AT5G09640) dramatically alter soluble phenylpropanoid pools Arabidopsis thaliana
phenylpropanoid signaling pathway induces accumulation of chlorogenic acid
(BZO1, AT1G65880) displays significantly greater turnover for cinnamate Arabidopsis thaliana
metabolic response of N-replete GT1-316 overexpression transgenic plants overlapped with metabolic response of N-stressed wild types Populus
sinapoyl-glucose is acyl donor for biosynthesis of sinapoyl-malate and sinapoyl-choline
UGT84A-mediated hydroxycinnamate glycosylation plays an important role in phenylpropanoid metabolism during Populus stress response Populus tremula × alba
KEGG (Kyoto Encyclopedia of Genes and Genomes) analysis indicated changes in metabolism of phenylpropanoids Arabidopsis thaliana
(BZO1, AT1G65880) shows activity toward caffeate Arabidopsis thaliana
SCPL acyltransferases synthesize sinapoylated metabolites Arabidopsis thaliana
phenylpropanoid pathway comprises syntheses of flavonoid and lignin
phenylpropanoid derivatives are found ubiquitously across plant kingdom
Artemisia annua ecotypes accumulate varying amounts of scopolin Artemisia annua
root exudates of Arabidopsis include phenylpropanoids Arabidopsis thaliana
feruloyl-CoA was redirected to cell wall-bound ferulate esters Arabidopsis thaliana
Ta-CCR1 and Ta-CCR2 recombinant enzymes could use sinapoyl-CoA as substrate Triticum aestivum
phenylpropanoid pathway produces phytoalexin Oryza sativa
phenylpropanoid pathway leads to production of lignin
GRMZM2G466833 is associated with caffeic_acid_trans metabolite level Zea mays
decrease in ferulate in prolonged night and in (ATPGMP, PGM, PGM1, STF1, AT5G51820) mutant could not be related to any clear change at the level of transcripts for genes involved in ferulate synthesis
GT1s that catalyze formation of hydroxycinnamoyl-glucose esters belong to UGT84A subfamily of group L of plant GT1 proteins
UGT84A9 (oilseed rape BnSGT1) catalyses formation of sinapate glucose esters Brassica napus
UGT84A10 catalyses formation of hydroxycinnamate glucose esters Brassica napus
(BZO1, AT1G65880) shows highest activity toward cinnamate Arabidopsis thaliana
higher UV absorbance in ccr1g and ccc mutant pollen may be explained by accumulation of feruloyl malate and feruloyl glucose in the anthers Arabidopsis thaliana
(BRT1, UGT84A2, AT3G21560) is involved in biosynthesis of UV filter sinapoyl malate Arabidopsis thaliana
phenylalanine ammonia lyase (PAL) catalyzes non-oxidative deamination of phenylalanine to trans-cinnamate
C3'H deficiency causes hyperaccumulation of flavonoids Arabidopsis thaliana
SUB most likely regulates phenolic pathway Arabidopsis thaliana; Nicotiana benthamiana
aromatic part of piperine is likely derived from phenylpropanoid metabolism Piper nigrum
phenylpropanoid pathway is responsible for biosynthesis of flavonoids Arabidopsis thaliana
4-coumaroyl CoA represents most important branchpoint within central phenylpropanoid biosynthesis
ccc triple mutant stems displays increased level of feruloyl malate
tannins oxidize, giving brown color to mature seeds Arabidopsis thaliana
p-coumarate is phenylalanine-derived phenylpropanoid with anti-fungal activity
MYB194 overexpression causes repression of phenylpropanoid enzyme genes Populus
PhTE1 downregulation results in increase of feruloyl-CoA levels Petunia hybrida
caffeic acid minor activity detected in presence of Md CNL Malus domestica
low-artemisinin ecotype GS produces higher amount of scopolin Artemisia annua
phenylpropanoid metabolic pathway genes are regulated in both OsCOI1 and OsCOI2 lines Oryza sativa
DMGs with evening-phased H3K9ac and H3K27ac are enriched with phenylpropanoid metabolism Petunia hybrida
4CL (4-coumarate:CoA ligase) is 4-coumarate:CoA ligase
Pna-10 accession accumulates sinapoylglucose Arabidopsis thaliana
C3'H deficiency causes blocked sinapate ester biosynthesis Arabidopsis thaliana
PAL is starting point to produce flavonols and anthocyanins Salvia miltiorrhiza
p-coumaroyl putrescine is significantly reduced in coi2 mutants compared with WT plants after BPH elicitation Oryza sativa
transgenic approaches used to reveal insights into apparently redundant gene and enzyme pattern required for functional integrity and plasticity of phenylpropanoid biosynthetic pathways
second PAL-gene in poplar is specifically targeted to condensed tannin formation Populus trichocarpa
(HCT, AT5G48930) down-regulation results in significant increase in caffeoylquinate esters in stems
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) mutant displays high perturbations of sinapate esters pool
feruloyl malate is found in substantial amounts in (ATCAD4, CAD, CAD-C, CAD4, AT3G19450) c d mutant leaves
(ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) mutant re-directs part of the carbon flux within the phenylpropanoid pathway towards flavonoid biosynthesis Arabidopsis thaliana
4-coumaroyl CoA is direct precursor for flavonoid or H-lignin biosynthesis
NO stimulated increase in PAL level Solanum lycopersicum
Caffeoyl Coenzyme A 3-O-methyltransferase 1 (CCoAOMT 1) is involved in formation of sinapoyl malate Arabidopsis thaliana
XM_004507487.2 gene encodes 4-coumarate-CoA ligase 1-like
(BZO1, AT1G65880) may function as cinnamoyl CoA ligase Arabidopsis thaliana
phenylpropanoid metabolic space comprises interconnected metabolic branches
SCT can generate benzoylcholine (BC) Arabidopsis thaliana
4-coumaric acid is substrate for Md CNL Malus domestica
representative phenylpropanoid genes (PAL, 4CL, and CCOMT isoforms) showed N-sensitive expression responses in an isoform- and tissue-dependent manner N stress Populus tremula × alba
insect attack triggers major rewiring of gene networks associated with phenylpropanoid metabolism
irCDPK4/5 stems contain chlorogenic acid (CGA) Nicotiana attenuata
120 cDNA fragments preferentially expressed in red perilla encode proteins related to phenylpropanoid-derived metabolism Perilla frutescens
root exudates of Arabidopsis include hydroxycinnamic acids Arabidopsis thaliana
irCDPK4/5 stems contain 12-fold higher cryptochlorogenic acid (CCA) content than WT Nicotiana attenuata
phenylpropanoid metabolism is involved in synthesis of sporopollenin Arabidopsis thaliana
interconnected metabolic branches contribute to biosynthesis of compounds with functions in plant development and stress adaptation
PAL (phenylalanine ammonium lyase) is phenylalanine ammonium lyase
(ATMYB71, MYB305, MYB71, AT3G24310) regulates transcription of phenylpropanoid genes Nicotiana tabacum
phenylpropanoid metabolism could be perturbed not only at biosynthesis level, but also by modification of monolignol transport
(UGT73C7, AT3G53160) catalyzes glycosylation of p-coumaric acid and ferulic acid to form glycosides Arabidopsis thaliana
rapid reconfiguration of gene expression allows prioritized production of metabolites that help the plant solve ecological problems
higher levels of anthocyanins and phenolic compounds in transgenic plants explain higher levels of anthocyanins and phenolic compounds in transgenic potato plants Solanum tuberosum
SUB-OX N. benthamiana leaves accompanied by accumulation of phenylpropanoid-associated transcripts Nicotiana benthamiana
LG5482522 encodes coumarate 3-hydroxylase (C'3H), a P450-dependent monooxygenase Lactuca sativa
Phenylalanine ammonia lyase 1 (AevPAL1)-silenced plants show significantly decreased expression of chalcone synthase (AevCHS) Aegilops variabilis
cell wall-bound HCA levels in (UGT73C7, AT3G53160) knockout lines were reduced in (UGT73C7, AT3G53160) knockout lines Arabidopsis thaliana
prioritisation for phenylalanine biosynthesis may reflect feed defence-associated biosynthesis of phenylpropanoids and flavonoids Nicotiana tabacum
C3′H deficiency in (CYP98A3, REF8, AT2G40890) blocks formation of sinapate esters Arabidopsis thaliana
p-coumarate esters and flavonoids are hyperaccumulated in (CYP98A3, REF8, AT2G40890) mutants Arabidopsis thaliana
NbPAL and NbC4H expression was clearly reduced in plants silenced for NbPAT Nicotiana benthamiana
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) plays dual role in plants: is important for lignin biosynthesis Arabidopsis thaliana
flavonoids are phenylpropanoid and phenylpropanoid acetate metabolites
plants overexpressing (AtMYB62, BW62B, BW62C, MYB62, AT1G68320) accumulate anthocyanins Arabidopsis thaliana
dexamethasone application substantially reverses biochemical phenotypes of (CYP98A3, REF8, AT2G40890) plants Arabidopsis thaliana
yield penalty of (ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) mutants is not caused by ferulic acid accumulation Arabidopsis thaliana
salicylate is phenylalanine-derived phenylpropanoid with anti-fungal activity
ferulate is phenylalanine-derived phenylpropanoid with anti-fungal activity
root exudates of Arabidopsis include coumarins Arabidopsis thaliana
perturbation of phenylpropanoid metabolism influences plant growth and development Arabidopsis thaliana
sinapate esters such as sinapoylmalate have decreased content in (CYP98A3, REF8, AT2G40890) mutants Arabidopsis thaliana
dexamethasone (dex) treatment of (CYP98A3, REF8, AT2G40890) pOpON plants restores to wild-type levels sinapoylmalate content Arabidopsis thaliana
phenylpropanoid signaling pathway activates expression of specific enzymes
chlorogenic acid and quercetin glycoside metabolites accumulation is higher in transgenic plants Solanum tuberosum
phenylpropanoid metabolic pathway produces hydroxycinnamate amides
one of the drought-responsive phenylpropanoid pathway products was mapped to same SNP marker as the root PAL
dexamethasone (dex) treatment of (CYP98A3, REF8, AT2G40890) pOpON plants significantly decreases p-coumarate ester accumulation Arabidopsis thaliana
genes representing phenylpropanoid pathway and flavonoid/anthocyanin biosynthesis or modification enzymes were observed in Class 2+3
old leaves of C3′H-induced (CYP98A3, REF8, AT2G40890) pOpON plants undergo selective turnover of leaf soluble phenylpropanoid metabolites Arabidopsis thaliana
depletion of other phenylpropanoid-related metabolites could be cause for yield penalty of lignin-modified plants
phenylpropanoid pathway is responsible for biosynthesis of lignin Arabidopsis thaliana
young and newly emerging leaves of dexamethasone (dex)-treated (CYP98A3, REF8, AT2G40890) pOpON show decrease in flavonoids and increase in sinapoylmalate levels within 3 days of dexamethasone (dex) application Arabidopsis thaliana
one insertion line showing severe symptoms of Fe deficiency turned out to carry a deletion in a gene involved in the phenylpropanoid pathway Arabidopsis thaliana
phenylpropanoid metabolism results in production of anthocyanin
functional HPL significantly reduces levels of enhanced anthocyanins in response to waterlogging
(ATMYB4, MYB4, AT4G38620) represses 4CL Arabidopsis thaliana
MYB194 overexpression results in greatly reduced accumulation of phenolic glycosides Populus
PhTE1 downregulation results in increase of cinnamoyl-CoA levels Petunia hybrida
trans-cinnamate production is first and pivotal step in phenylpropanoid metabolism pathway
Phenylalanine ammonia lyase 1 (AevPAL1)-silenced plants show significantly decreased content of flavonoid (flavonol, flavone and derivatives) Aegilops variabilis
p-coumaric acid and ferulic acid are important precursors for biosynthesis of phenylpropanoid metabolites Arabidopsis thaliana
metabolic flux of phenylpropanoid pathway is redistributed to biosynthesis of HCAs and coumarins Arabidopsis thaliana
NO GAMETOPHORES2/HYDROXYCINNAMOYL-CoA:SHIKIMATE HYDROXYCINNAMOYL TRANSFERASE (NOG2/ (HCT, AT5G48930) ) is component of phenylpropanoid pathway Physcomitrium
suppression of F5H-mediated 5-hydroxylation of phenolic results in redirection of carbon flux to guaiacyl derivative Arabidopsis thaliana
7-hydroxy-6-methoxycoumarin (scopoletin) is phenylpropanoid compound
Disruption of AtCB5D resulted in reduction of 5-hydroxylated phenolic esters in Arabidopsis leaves Arabidopsis thaliana
IbMYB1 family genes play dual roles as activators to stimulate flavonoid biosynthesis and repressors to reduce lignin synthesis Ipomoea batatas
mis-accumulated phenol-related molecules in (H3.3, HTR8, AT5G10980) K27A show great enrichment in phenylpropanoids Arabidopsis thaliana
lignin is synthesized through phenylpropanoid pathway
dexamethasone (dex) treatment of (CYP98A3, REF8, AT2G40890) pOpON plants restores to wild-type levels flavonoid content Arabidopsis thaliana
G×E clusters featured genes representing general phenylpropanoid pathway Vitis vinifera
Md CNL has higher affinity for cinnamic acid Malus domestica
Md CNL has higher turnover number for cinnamic acid Malus domestica
redirection of metabolic flux toward scopoletin biosynthesis rather than toward biosynthesis of monolignols Arabidopsis thaliana
vast variety of aromatic compounds includes proanthocyanidins
loss of CB5 exhibited no impairment on seed coat ferulate synthesis Arabidopsis thaliana
nuclear translocation of PAL reduces enzymatic activity of PAL Arabidopsis thaliana
PhTE1 downregulation resulted in increased pools of lignin Petunia hybrida
catalytic efficiency (kcat/Km) for cinnamic acid is 44 times that for 4-coumaric acid Malus domestica
differential requirement of electron transfer system offers powerful tool to manipulate phenolic synthesis in tissue-specific manner Arabidopsis thaliana
biosynthetic enzyme CCoAOMT3 exhibits significant reduction in evening induction when treated with MB-3 Petunia hybrida
cinnamic acid originates from L-phenylalanine
caffeic acid O -methyltransferase is protein exhibiting strong G×E interactions
ethephon treatment increases hydroxycinnamic acid concentrations by >20% in line NB-R Daucus carota
PhTE1 downregulation results in increase of p-coumaric acid levels Petunia hybrida
cinnamic acid 4-hydroxylase ( (ATC4H, C4H, CYP73A5, REF3, AT2G30490) ) catalyzes 4-hydroxylation of the first aromatic compound cinnamic acid Arabidopsis thaliana
phenylpropanoid metabolic pathway produces lignin
phenylpropanoid pathway leads to synthesis of wide range of secondary metabolites
PhTE1 downregulation leads to increased production of anthocyanins Petunia hybrida
Md CNL-catalysed reaction with cinnamic acid product identified as cinnamoyl-CoA Malus domestica
NADH-CBR1-CB5 pathway dominates seed sinapoyl ester biosynthesis Arabidopsis thaliana
phenylpropanoid metabolism branch is likely tightly controlled
benzoic acid no enzyme activity observed in presence of Md CNL Malus domestica
P450s are crucial to biosynthesis and metabolism of phenylpropanoids
vast variety of aromatic compounds includes lignin
disruption of (AR2, ATR2, AT4G30210) affected leaf sinapoyl malate accumulation Arabidopsis thaliana
Phi application at 24 h post-application induces genes involved in phenylpropanoid pathway Panicum virgatum
C6-C3 core structure elaborates vast variety of aromatic compounds
(ATATR, ATR, ATR-2, ATRAD3, AT5G40820) mutant does not perturb leaf sinapoyl ester accumulation Arabidopsis thaliana
phenylpropanoid metabolic pathway produces flavonoids
HCAs were present in both L er and (ATCHS, CHS, TT4, AT5G13930) Arabidopsis thaliana
cryptochlorogenic acid (CCA) levels do not differ between irCDPK4/5 and irCDPK4/5 × irMYB8 stem tissue Nicotiana attenuata
NtWRKY41a knockout promoted scopoletin accumulation Nicotiana tabacum
(ATMYB12, MYB12, PFG1, AT2G47460) overexpression increases production of phenylpropanoids Solanum lycopersicum
(ATPAL1, PAL1, AT2G37040) (F6'H1, AT3G13610) (ATCHS, CHS, TT4, AT5G13930) (ATFLS1, FLS, FLS1, AT5G08640) and (F3'H, F3H, TT6, AT3G51240) genes had higher transcript abundance in root after shift from low (0.5% w/v) to high (3% w/v) sucrose regime in wild type Arabidopsis thaliana
Pp-inoculated Arabidopsis non-host shows induction of phenylpropanoid metabolism-associated genes Arabidopsis thaliana
vast variety of aromatic compounds includes hydroxycinnamate esters
disruption of (ATCBR, CBR, CBR1, AT5G17770) yielded much severer depletion on seed soluble sinapate Arabidopsis thaliana
ccc triple mutant stems displays dramatically increased sinapoyl malate
LG8763094 (encoding hydroxycinnamoyl-CoA quinate hydroxycinnamoyl transferase) identified as candidate gene that affects quinate and chlorogenic acid levels Lactuca serriola
overexpression of the StMtf1-MYB-transcription factor achieved overproduction of chlorogenic acid specifically in potato tubers Solanum tuberosum
lignan is rich in sesame seeds Sesamum indicum L.
divergent tissue expression in roots and leaves coordinates via redirection of metabolic flux
aromatics in suberin principally comprise ferulic acid, coumaric acid, and cinnamic acid
hindering one branch of phenylpropene biosynthesis results in enhanced metabolic flux to other branch of phenylpropanoid metabolism petunia
transcriptional regulators modulate phenylpropanoid accumulation
(CYP84A1, F5H, FAH1, AT4G36220) gene knockdown reveals pleiotropic changes in Arabidopsis metabolome Arabidopsis thaliana
ZmCOMT partially replaced ZmCCoAOMT when DCB was present in the culture media Zea mays
61 genes enriched in phenylpropanoid metabolic process and secondary metabolite biosynthetic process Brassica napus
feruloyl malate is found in substantial amounts in (ATCAD4, CAD, CAD-C, CAD4, AT3G19450) c d mutant flowers
HPLC analysis analyzed leaf soluble phenylpropanoid metabolites Arabidopsis thaliana
phenylpropanoids are class of compounds derived from phenylalanine
organ and developmentally specific pattern of metabolites is characteristic for each plant species
entry step of the phenylpropanoid pathway in Solanaceae is represented by estimated 20 putative PAL-genes Lycopersicon esculentum
phenylalanine ammonia lyase (PAL) directs carbon flow from shikimate pathway to various branches of general phenylpropanoid metabolism
artichoke HQT gene catalyzes synthesis of quinate esters of p-coumaroyl and caffeoyl from p-coumaroyl-CoA and caffeoyl-CoA Cynara cardunculus subsp. scolymus
C'3H enzyme catalyzes synthesis of shikimate and quinate esters of caffeoyl
targeted and non-targeted approaches revealed numerous genes, enzymes, and metabolites essential for regulation and compartmentation
Phe treatment causes increase in levels of benzaldehyde
(AR2, ATR2, AT4G30210) mutants show increased abundance of benzenoids Arabidopsis thaliana
(ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) mutant exhibits perturbation in phenylpropanoid composition
general phenylpropanoid pathway feeds into coumarins
small subset of phenylpropanoids like coumaroyl- and caffeoyl CoA esters diversification achieved by array of subsequent oxygenases, reductases, and transferases
generation of Ery4P in the Calvin–Benson cycle restricts flux through phenylpropanoid pathway
p-coumarate ester accumulation in ref8* myb4-1 and ref8* gir1-1 showed similar levels of p-coumarate ester accumulation in ref8* Arabidopsis thaliana
central phenylpropanoid pathway is catalysed by PAL, (ATC4H, C4H, CYP73A5, REF3, AT2G30490) and 4CL
general phenylpropanoid pathway feeds into phenolic volatiles
diversification of phenylpropanoids by oxygenases, reductases, and transferases results in observed complexity and heterogeneity of plant phenylpropanoid metabolite profiles
several phenylpropanoid genes involved in the synthesis of hydroxycinnamates resulting in a strong increase in these compounds in the cell wall Zea mays
phenylpropanoid metabolism in ref8* myb4-1 was not upregulated in ref8* myb4-1 compared with ref8* Arabidopsis thaliana
differential expression of LG8763094 and LG5482522 consequently leads to differential accumulation of quinate and chlorogenic acid between wild and cultivated lettuce Lactuca sativa; Lactuca serriola
PhTE1 downregulation results in increase of cinnamic acid levels Petunia hybrida
NADPH-CPR-cytochrome b5 (CB5) electron transfer chain supports benzene ring 5-hydroxylation Arabidopsis thaliana
lignin pathway was significantly inhibited in silenced cotton plants
phenylalanine ammonia lyase knockout mutants increase susceptibility to virulent strain of the bacterial pathogen Pseudomonas syringae Arabidopsis thaliana
(UGT73C7, AT3G53160) is responsible for glucosylation of p-coumaric acids and ferulic acids in plant cells Arabidopsis thaliana
p-coumaric acid and ferulic acid synthesis is initiated by cinnamate-4-hydroxylase (ATC4H, C4H, CYP73A5, REF3, AT2G30490) Arabidopsis thaliana
ccr1g flowers displays presence of feruloyl malate
ccc rosette leaves displays presence of feruloyl malate