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secondary metabolism

36744 relationships annotated with this phrase. Showing first 500 of 36744.
Source entity Relationship Target entity Species
Nicotiana benthamiana accumulates pyridine alkaloids Nicotiana benthamiana
light wavelength is critical for production of different metabolites
I3M (indol-3-ylmethyl glucosinolate) is most abundant indole glucosinolate Arabidopsis thaliana
Phosphocreatine is one of key components enriched by intercropping
secondary metabolites from plant-beneficial fungi include antimicrobial substances
ADB-resistant ashes showed 16% higher verbascoside levels
Fusarium graminearum fgrdrp2 knock-out strain exhibited decreased mycotoxin production Fusarium graminearum
GmHAD1-2 regulates lateral root length mainly through affecting flavonoid synthesis in roots Glycine max
(AT1G10585) shows correlated expression with (UGT76E12, AT3G46660) (JAO4, JOX4, AT2G38240) (ATST2A, ST2A, AT5G07010) (ATJRG21, JAO3, JOX3, JRG21, AT3G55970) and TERPENE SYNTHASE04 expression Arabidopsis thaliana
members within antagonistic taxa often possess metabolic capability to produce antimicrobial substances
bacterial cyclic lipopeptides (CLiPs) are produced by Streptomyces
orfamide A is secreted by Pseudomonas protegens Pf-5 Pseudomonas protegens
aromatic O-methyltransferases (OMT) methylate benzylisoquinoline alkaloids
hemolytic activity of the dinoflagellate Karenia mikimotoi is initiated by light Karenia mikimotoi
soyasapogenol B is one of key components enriched by intercropping
mycorrhizal fungi regulate flavonoid biosynthesis Populus
arbuscular mycorrhizal fungi (AMF) inoculation modified concentrations of plant secondary chemicals
chicory tissues contained 114 terpenoids Cichorium intybus
transcriptomic and metabolomic analyses allowed correlation of newly discovered phenotypes to defective biosynthetic pathways Arabidopsis thaliana
RL22 showed high content of phenolics guaiacol and eugenol Solanum melongena
Fusarium graminearum fgrdrp3 knock-out strain exhibited decreased mycotoxin production Fusarium graminearum
bracts of heat-treated plants contained less neoglucobrassicin than bracts of non-treated plants Brassica rapa
plants synthesize volatile organic compounds (VOCs)
Albugo genome does not encode key secondary metabolites potentially responsible for negative correlations with other microbes
jazD plants accumulate elevated levels of Trp-derived defense compounds Arabidopsis thaliana
MsOMT1 did not show activity with p-coumaric acid Mitragyna speciosa
red light regulated synthetase gene clusters (mcyB and mcyD) related to microcystin Microcystis aeruginosa
(PRK, AT1G32060) (PGK, PGK3, PGKc, AT1G79550) and RuBP enzymes in P. globosa responded clearly to low level of HA in green light Phaeocystis globosa
aromatic amino acids (AAAs) are precursors for specialized compounds that mediate plant interactions with other organisms
ACT catalyzes rate-limiting step in HCAA biosynthesis Arabidopsis thaliana
chestnut tea system exhibits higher levels of allantoic acid
jasmonic acid (JA) or methyl jasmonate (MJ) treatment simultaneously activate ascorbate biosynthetic pathway Arabidopsis thaliana
structural and biosynthetic properties of compounds inform about biosynthetic (in)dependence of compounds
upregulation of GAPDH and TK genes may affect hemolytic metabolites Phaeocystis globosa
photosynthetic dark reaction (Calvin cycle) is involved in toxin metabolism
5-MT resistance in j1256 is not associated with increased production of I3M (indole glucosinolate) Arabidopsis thaliana
MsOMT1 did not show activity with gallic acid Mitragyna speciosa
hemolytic activity (HA) of Heterosigma akashiwo decreased when light intensity exceeded or fell below optimal light intensity (100 μmol m −2 s −1 ) Heterosigma akashiwo
bacterial cyclic lipopeptides (CLiPs) are produced by cyanobacteria
mis-accumulation of phenol-related molecules confirms effect of identified transcriptomic mis-regulation on production of plant metabolic components Arabidopsis thaliana
light regime varied significantly with hemolytic activity (HA) of P. globosa Phaeocystis globosa
energy distribution alters metabolic production
effect of ROS in P. globosa could be excluded as responsible for hemolytic effect Phaeocystis globosa
HCAA accumulation in jazD and j1256 leaves is greater than WT by more than 14-fold Arabidopsis thaliana
loss of histone acetylation marks at night possibly shuts down carbon flow into the specialized metabolic network Petunia hybrida
metabolism of three and five-carbon sugars (GAP and Ru5P) corresponding to production of glycolipid-like hemolysin in P. globosa Phaeocystis globosa
feruloylagmatine is hydroxycinnamic acid amide Arabidopsis thaliana
SABATH family methyltransferases methylate salicylic acid
MsOMT1 did not show activity with caffeic acid Mitragyna speciosa
red and green light stimulated toxin production of Mycrocystis aeruginosa Microcystis aeruginosa
evidence of glycolipids or glycoside-like hemolytic substances in P. globosa lead to hypothesis that hemolytic compounds may be involved in the dark reaction Phaeocystis globosa
tryptophan (Trp) is precursor of protective compounds
acetyltransferase gene knockout results in over-accumulation of catechol glucoside Zea mays
camalexin is major Arabidopsis phytoalexin Arabidopsis thaliana
ability to moonlight in production of dicaffeoylquinic acids (diCQAs) may be limited to hydroxycinnamoyl-Coenzyme A:quinate hydroxycinnamoyl transferase (HQT) enzymes from Solanaceous species with His residue Solanaceae
L. leucocephala leaves may have similar enzymes for conversion of 3H4P to useable compounds during stress conditions Leucaena leucocephala
other metabolites were also consistently induced in all analyzed tissues Solanum lycopersicum
ADT-deficient Arabidopsis mutants had significantly reduced lignin contents Arabidopsis thaliana
three putative galactolipids were detected in Arabidopsis extracts Arabidopsis thaliana
Group 3 metabolites were absent from Pinot Noir berries
biosynthesis pathway of hemolytic components in P. globosa appears to be associated with Calvin cycle Phaeocystis globosa
chemotypes differ in relative composition of glucosinolates
direct targets are most likely related to maturation-related genes like secondary metabolism related genes
elevated temperature influenced glucosinolates Brassica rapa
reduced glucosinolate biosynthesis affects phenylpropanoid production Arabidopsis thaliana
flavonoids and terpenoids were most represented biochemical class among annotated markers Atriplex imbricata
poplar mutants are affected exclusively in suberin biosynthesis Populus trichocarpa
SCPL proteins involved in secondary metabolism
jasmonic acid (JA) or methyl jasmonate (MJ) treatment simultaneously activate jasmonate biosynthetic pathway Arabidopsis thaliana
chicory is rich in sesquiterpene lactones Cichorium intybus
Amaryllidaceae and Asparagaceae produce fructans with internal glucose residue, including neo-inulin type
SABATH family methyltransferases methylate jasmonic acid
p-coumaroylagmatine is hydroxycinnamic acid amide Arabidopsis thaliana
SCPL proteins can be carboxypeptidases or acyltransferases
(IAA26, PAP1, AT3G16500) (AtMYB47, MYB47, AT1G18710) (ERF113, RAP2.6, AT1G43160) and (AT1G10585) can be target points by JAMs to regulate JA-responsive metabolic genes Arabidopsis thaliana
related measures of phytochemical dissimilarity do not take into account biosynthetic properties of compounds
heat-treated plants contained more gluconapin than non-treated plants Brassica rapa
Plant O-methyltransferases (OMTs) allow plants to synthesize a series of economically and pharmaceutically valuable compounds
OMTs are important group of enzymes involved in synthesis of various useful secondary metabolites in medicinal plants
bacterial cyclic lipopeptides (CLiPs) are produced by Bacillus
lycorine is one of key components enriched by intercropping
heat-treated plants contained more total glucosinolates than non-treated plants Brassica rapa
single-species inocula had stronger effects on plant secondary chemistry
pleiotropic drug resistance protein may be involved in camalexin secretion Arabidopsis thaliana
glandular trichomes produce large amounts of volatile organic compounds (VOCs) Solanum lycopersicum
light spectra shift from green to red light or from red to green light HA responded significantly within a few minutes hemolytic activity (HA) of P. globosa Phaeocystis globosa
upregulation of GAPDH and TK genes ultimately affecting glycolipid-like hemolytic substances in P. globosa Phaeocystis globosa
vertical transformation of P. globosa would ultimately lead to variation in hemolytic activity variation Phaeocystis globosa
two classes of antifungal defense compounds, camalexin and HCAAs were more abundant in j1245 Arabidopsis thaliana
LjMYB36 affects isoflavonoid metabolism Lotus japonicus
repellent biosynthesis gene is present in Himalayan eggplant variety Solanum melongena
calceolarioside and ligustroside levels did not differ between ADB-resistant and ADB-susceptible ashes
MsOMT1 did not show activity with trans-cinnamic acid Mitragyna speciosa
(AtJAZ1, JAZ1, TIFY10A, AT1G19180) /2/5/6 repress production of anti-fungal metabolites Arabidopsis thaliana
j1256 leaves have unchanged level of bulk indole glucosinolates (IGs) Arabidopsis thaliana
metabolic pathways of (E)-2-decenal could be deciphered future research Aristolochia delavayi
glucosinolate composition and quantities varied largely between leaf, bract and floral tissues Brassica rapa
secondary metabolites show differential mycorrhizal responses between wild and domesticated rice genotypes Oryza sativa; Oryza rufipogon
flavonoids were among the phenolics depleted in nia1nia2 and (ARAPPT, CUE1, NOX1, PPT, AT5G33320) compared with other genotypes Arabidopsis thaliana
OMTs from Scutellaria baicalensis are involved in biosynthesis of anticancer methoxylated 4′-deoxyflavones Scutellaria baicalensis
response of pigments and HA indicates that HA may interfere or bypass the biosynthesis of Diad or Fuco Phaeocystis globosa
catechol is converted to catechol glucoside Zea mays
chicory genome contained six biosynthetic gene clusters (BGCs) Cichorium intybus
ERM fungi produce tissue rich in melanin
mixed-strain inoculation treatment had generally weaker effects on plant secondary chemistry
jasmonic acid (JA) or methyl jasmonate (MJ) treatment simultaneously activate anthocyanin biosynthetic pathway Arabidopsis thaliana
DEGP group SpR was enriched for esterase activity and acyltransferase activity Schrenkiella parvula
3-hydroxy-4-pyridone (3H4P) may be degraded further by other plant enzymes Leucaena leucocephala
uridine diphosphate glycosyltransferase (UGT) mediate glycosylation of secondary metabolites
increased endogenous jasmonic acid (JA) regulates plant secondary metabolism Oryza sativa
monomeric phenylpropanoids in triple and quadruple knockouts had amounts reduced by approximately 25% and 20% in NA and DA plants respectively relative to wild type Arabidopsis thaliana
metabolite classes detected showed largest reductions in multiple ADT knockout mutants Arabidopsis thaliana
stress-induced increase in secondary metabolites is indicative of diverse roles these molecules play in protecting the cell
hemolytic components in P. globosa could be easily destroyed or transformed depending on light conditions Phaeocystis globosa
(AtJAZ1, JAZ1, TIFY10A, AT1G19180) /2/5/6 repress biosynthesis of select amino-acid-derived defense compounds Arabidopsis thaliana
flavonoids represented most negatively correlated metabolites in Maihueniopsis camachoi Maihueniopsis camachoi
Solanum lycopersicum hydroxycinnamoyl-Coenzyme A:quinate hydroxycinnamoyl transferase (SlHQT) acts as CCT in absence of aromatic acyl-CoA donors Solanum lycopersicum
phenylpropanoid-derived metabolites corresponded to monomeric or dimeric (lignan) phenylpropanoid metabolites Arabidopsis thaliana
intraspecific chemical diversity of organic compounds has been termed chemodiversity
flowers of heat-treated plants contained more total glucosinolates than flowers of non-treated plants Brassica rapa
anthocyanins accumulate in young leaves and senescing leaves Hypoxis prostrata
PIFs (PHYTOCHROME INTERACTING FACTORS) control biosynthesis of anthocyanin Arabidopsis thaliana
PAs turn brown as they oxidize Arabidopsis thaliana
altered ADT activity reveals profound effects on secondary metabolites Arabidopsis thaliana
ferulic acid conjugates were observed as down-regulated in root tissue Solanum lycopersicum
ADT mutants revealed significantly increased apocarotenoids contents Arabidopsis thaliana
Phe metabolism reveals profound effects on secondary metabolites Arabidopsis thaliana
known polar secondary metabolites in Arabidopsis include flavonoids, phenylpropanoids, benzenoids, and glucosinolates Arabidopsis thaliana
flavonoid reduction levels in (ADT3, PD1, AT2G27820) /4/5/6 under short-day conditions were just over half of those observed for long-day-grown plant lines Arabidopsis thaliana
different scion-rootstock combinations could have influenced overall accumulation of secondary metabolites Vitis vinifera
cytochrome P450 family proteins encoded more than half of genes in heme binding Gene Ontology term Arabidopsis thaliana
control cells secrete different amounts of each stilbene in culture medium Vitis vinifera
three putative galactolipids were annotated previously in Arabidopsis based on comparison of high-resolution tandem mass spectrometry (MS/MS) spectra Arabidopsis thaliana
MEKK1-MAPKKKα/MKK4-MKK5/MPK3-MPK6 module mediates synthesis of camalexin Arabidopsis thaliana
3′-phosphoadenosine 5′-phosphosulfate (PAPS) is a donor of sulfate groups in secondary metabolism
alfalfa (Medicago sativa) contains almost no proanthocyanidins (PA) in leaves and stems Medicago sativa
secondary metabolism enzymes are regulated by VvABF2 Vitis vinifera
galactolipids and putative apocarotenoids is associated with (ADT3, PD1, AT2G27820) /4/5/6 Arabidopsis thaliana
flavonoids are produced by plants
tyrosine (Tyr) may serve as precursor of phenylpropanoids
biosynthesis of secondary metabolites is embedded into cellular ultrastructures
triterpenoids were typically detected in leaf tissue of accessions
Crude extracts of yam presented range of triterpenoids, including cholesterol
tomato seed extract contains 14 flavonoids Solanum lycopersicum
eriodictyol-hexose has 10 QTL Solanum lycopersicum; Solanum pennellii
S27 displayed anthocyanin accumulation Arabidopsis thaliana
flavonoids are synthesized by general phenylpropanoid pathway
chlorogenate:chlorogenate transferase (CCT) activity is irreversible chlorogenate:chlorogenate transferase (CCT) reaction Solanum lycopersicum
biosynthesis of phenylpropanoids, flavonoids, and anthocyanins significantly overrepresented among up-regulated genes Solanum lycopersicum
dark-brown phenotype is tightly associated with serotonin level Oryza sativa
six flavonoids in wild type consisted of four kaempferol glycosides and two quercetin derivatives Arabidopsis thaliana
lignans in (ADT4, AT3G44720) /5 showed slightly lower reductions of approximately 58% for NA plants and 55% for DA plants Arabidopsis thaliana
flavonoids are remarkably diverse group of secondary products Arabidopsis thaliana
chlorogenic acid in root tissue increase was only observed after 24 h in root tissue Solanum lycopersicum
(AtROS1, DML1, ROS1, AT2G36490) /DEL expression in contrast to Nicotiana no major changes in nonflavonoid metabolites could be observed in tomato root and shoot Solanum lycopersicum
Brassicaceae metabolites is characteristic of Arabidopsis Arabidopsis thaliana
P. trichocarpa and F. sachalinensis possess CYPs belonging to large and functionally diverse (AtCYP71, CYP71, AT3G44600) family Populus trichocarpa; Fallopia sachalinensis
trans-piceid in nontreated VvABF2-overexpressing cells is present at lower concentration than trans-piceid in nontreated control cells Vitis vinifera
ABA treatment of control cell suspensions maintains trans-piceid amount Vitis vinifera
ADT mutants revealed reduced glucosinolate contents Arabidopsis thaliana
flavonoids in (ADT3, PD1, AT2G27820) /4/5/6 showed significant changes in levels with reductions of approximately 40% and 30% in NA and DA plants compared with wild-type plants Arabidopsis thaliana
Solanum lycopersicum hydroxycinnamoyl-Coenzyme A:quinate hydroxycinnamoyl transferase (SlHQT) moonlights by participating in dicaffeoylquinic acid (diCQA) synthesis in vacuole Solanum lycopersicum
brown color of PAs imparts color to Arabidopsis seeds Arabidopsis thaliana
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) mutants show significantly increased glucosinolates Arabidopsis thaliana
metabolomics analyses focused on non-targeted (polar) secondary metabolites Arabidopsis thaliana
altered ADT activity affects secondary metabolism Arabidopsis thaliana
partial blockage of Phe biosynthetic pathway has significant and widespread metabolic effects Arabidopsis thaliana
variety-specific metabolomic differences impact on quality traits Vitis vinifera (Pinot Noir and Cabernet Sauvignon)
tyrosine serves as precursor for secondary metabolites
chloroplast hosts secondary metabolism
licorice, Dioscorea polystachya, Wolfiporia extensa, and Polyporus umbellatus are rich sources of triterpenes
overlapping DEGs were significantly enriched in KEGG pathways of 'phenylpropanoid biosynthesis', 'glutathione metabolism', and 'cytochrome P450 involved metabolism' Triticum aestivum
isoflavone is produced by Glycine max (L.) Merr. Glycine max
Strobilanthes cusia contains new indole alkaloids Strobilanthes cusia
(BGLU21, AT1G66270) (BGLU22, AT1G66280) and (BGLU23, LEB, PSR3.1, PYK10, AT3G09260) hydrolyze scopolin Arabidopsis thaliana
Increased levels of Phe in plant leaves lead to accumulation of numerous derived phenolics and phenylpropanoids
Phe pre-treatment prevented decrease in levels of Phe and Phe-derived volatiles Chrysanthemum morifolium
BAHD activity of Solanum lycopersicum hydroxycinnamoyl-Coenzyme A:quinate hydroxycinnamoyl transferase (SlHQT) is freely reversible BAHD acyl transfer reaction Solanum lycopersicum
steviol originates from plastid-localized precursors
ADT mutants revealed significantly increased putative galactolipids contents Arabidopsis thaliana
young Hakea prostrata leaves showed lower anthocyanin concentrations Hakea prostrata
genetic manipulations included reductions in glucosinolate and phenolic glucoside contents Arabidopsis thaliana
FAD-binding motif is present in reticuline oxide precursor Oryza sativa
chlorogenate:glucarate caffeoyltransferase catalyzes transfer of caffeoyl moiety of chlorogenic acid (CGA) Solanum lycopersicum
substrate starvation of the shikimate pathway prevents anthocyanin biosynthesis in response to drought Kalanchoë fedtschenkoi
glucosinolates is family of C/S-containing defense compounds Arabidopsis thaliana
Solanum lycopersicum hydroxycinnamoyl-Coenzyme A:quinate hydroxycinnamoyl transferase (SlHQT) could act as BAHD acyl transferase at pH 6 to 7 in cytoplasm Solanum lycopersicum
genes in cluster C12 were enriched mainly in secondary metabolite biosynthetic process Triticum aestivum
Cytochrome P450 mono-oxygenase (CYP71B34, AT3G26300) (HORVU7Hr1G096560) showed higher expression levels in transgenic compared to null segregants Hordeum vulgare
vacuolar localization of chlorogenate:chlorogenate transferase (CCT) activity would favor dicaffeoylquinic acid (diCQA) biosynthesis Solanum lycopersicum
trans-piceid content in 35S::VvABF2 cells is multiplied by maximal factor of 2.5 upon ABA treatment Vitis vinifera
chlorogenic acid levels did not differ significantly from control after 5 d or 14 d in root tissue Solanum lycopersicum
transcriptomics data suggest positive link between anthocyanins' biosynthesis and cuticular wax biosynthesis Solanum lycopersicum
metabolic adjustments are associated with synthesis of bioenergetic, redox, and secondary signaling molecules
pipecolate accumulation shows no significant correlation with dark-brown color phenotype Oryza sativa
ADT isoform deficiencies caused stronger reductions in lignin contents Arabidopsis thaliana
ADT mutants revealed reduced phenylpropanoid contents Arabidopsis thaliana
wild type had detected six flavonoids Arabidopsis thaliana
chlorogenic acid (CGA) can accumulate only if sequestered in vacuoles of cells Solanum lycopersicum
seven genes such as ROMT1 and (HAT14, AT5G06710)
Stilbenes (resveratrol and its oligomers pallidol and viniferin) were much more abundant in Pinot Noir berries than in Cabernet Sauvignon berries Vitis vinifera (Pinot Noir and Cabernet Sauvignon)
three CYP706 members from other plant species have been functionally characterized previously and demonstrated to catalyze oxygenation reactions Gossypium arboruem; Callitropsis nootkatensis; Erigeron breviscapus
(CCL, AT3G26740) (CCR-LIKE) is chloroplast phosphoprotein Arabidopsis thaliana
diversity of plant-microbe interactions has been suggested as driving force behind diversity in plant secondary metabolites
(AQC1, HPS7, TPST, AT1G08030) mutant exhibits overproduction of anthocyanin Arabidopsis thaliana
safranal gives saffron its distinct aroma Crocus sativus
root application of ABA reduced isoflavonoid levels Glycine max
nitrogen starvation is tightly linked to anthocyanin biosynthesis Arabidopsis thaliana
tyrosine (Tyr) serves as precursor of isoquinoline alkaloids
proline is involved in synthesis of secondary metabolites
dicaffeoylquinic acid (diCQA) synthesis in coffee is proposed to occur via uncharacterized activity of hydroxycinnamoyl-Coenzyme A transferase (HCT, AT5G48930) on chlorogenic acid (CGA) and Coenzyme A (CoA) Coffea arabica
alternative routes for dicaffeoylquinic acid (diCQA) formation may have arisen by convergent evolution in different families of plants
metabolomic analysis significantly increased understanding of the effects of ADT modulation in Arabidopsis Arabidopsis thaliana
Metabolites related to Pinot Noir berries (Group 2) included amino acids (l-Met, Ser, and Ala), saccharide sugars (1-methylgalactose and β-gentiobiose), stilbenes (resveratrol and the associated oligomers pallidol and viniferin), and flavonoids (taxifolin and peonidin-3-glucoside)
stilbenes accumulated specifically in Pinot Noir Vitis vinifera (Pinot Noir)
binding of the aldoxime nitrogen to the heme allows for charge transfer from Fe(II) to the aldoxime C=N bond
Oleuropein levels were 28% lower in ADB-resistant ashes
light stress induced expression of genes involved in O-glycan biosynthesis Phaeocystis globosa
variation in hemolytic activity resulting in massive fish-killing effects in surface coastal ocean waters Phaeocystis globosa
acd6-1 mutant accumulates high levels of camalexin Arabidopsis thaliana
Differential sugar-sugar modification of phytochemicals may impact taste quality and intensity
catecholamine dopamine was vastly more abundant in Musa
Burkholderia can produce phytohormones and vitamins
GO term oxidoreductase activity was found exclusively in callus Solanum lycopersicum
The glycosidases catalyzing this reaction have not been identified Crocus sativus
Phe-derived compounds, phenolic glucosides, and glucosinolates is characteristic of wild type Arabidopsis thaliana
hydroxycinnamoyl-Coenzyme A:quinate hydroxycinnamoyl transferase (HQT) binds chlorogenic acid (CGA) Solanum lycopersicum
site-directed mutagenesis of Solanum lycopersicum hydroxycinnamoyl-Coenzyme A:quinate hydroxycinnamoyl transferase (SlHQT) confirmed role of His-276 in chlorogenate:chlorogenate transferase (CCT) reaction Solanum lycopersicum
trans-resveratrol content in 35S::VvABF2 cells is multiplied by maximal factor of 6.2 upon ABA treatment Vitis vinifera
HFL rice shows beneficial effect of high accumulation of serotonin Oryza sativa
four other putative lignans had no precise structure being determined due to lack of sufficient material for unambiguous structure determination Arabidopsis thaliana
co-expression analysis and metabolite profiling integration reveals novel components in secondary metabolism
acarbose is synthesized in Actinoplanes sp. SE50/110 Actinoplanes sp. SE50/110
meta-Tyrosine (m-Tyr) is naturally synthesized in fescue grasses Festuca spp.
JA and SA regulate biosynthesis of anthraquinones
indican, indigo and indirubin are main active materials in Strobilanthes cusia Strobilanthes cusia
naringenin chalcone accumulates in epidermis Solanum lycopersicum
Solyc12g096870 and Solyc12g098600 were subjected to phylogenetic analysis Solanum lycopersicum; Solanum pennellii
quercetin-3-O-sophoroside-O-rhamnoside is seed- and Solanum pennellii -specific compound Solanum pennellii
tyrosine (Tyr) serves as precursor of plastoquinones
profiling of specialized metabolites in seeds identified 338 putative metabolite quantitative trait loci (mQTL) Solanum pennellii; Solanum lycopersicum
caffeoyl-hexoside I was 4.3-fold increased or decreased in IL1-3 compared with M82 Solanum lycopersicum; Solanum pennellii
Tie-dyed2 mutant exhibits anthocyanin increases correlating with elevated carbohydrates Zea mays
Hydrophobic phytochemicals undergo glycosylation
salvianolic acids (SalAs) is group of secondary metabolites in Salvia miltiorrhiza Salvia miltiorrhiza
FACT may have function in suberin biosynthesis Arabidopsis thaliana
glycoalkaloid derivative m/z = 1081.6 showed significant changes in 17 introgression lines compared with M82 Solanum lycopersicum; Solanum pennellii
gene expression of all candidates in RNA-seq data from M82 and S. pennellii showed no expression for Solyc12g096820 and Solyc12g098590 Solanum lycopersicum; Solanum pennellii
quercetin-3-O-sophoroside-O-rhamnoside specifically accumulated in wild species Solanum pennellii (LA0716) compared with other wild species and cultivated varieties Solanum pennellii; Solanum lycopersicum
beneficial interactions between Brassicaceae plants and fungal endophytes appear tightly regulated by tryptophan-derived secondary metabolite pathway
PAL pathway shares common precursors for biosynthesis of phytoalexins Populus; Oryza sativa
side-chain modifications of methionine-derived glucosinolates contribute to structure diversity of glucosinolates Arabidopsis thaliana
metabolic pathways for sulfur assimilation required for production of downstream sulfur-containing compounds
unknowns that could be assigned to compound class were predominantly secondary metabolites
GABA is involved in synthesis of secondary metabolites
rutin apioside is major flavonoid derivative Solanum lycopersicum
Treatment with 36 mM Phe caused significant increase in 3-phenyllactate levels Chrysanthemum morifolium
sinapate esters is UV-absorbent aromatic secondary metabolites
genes and enzymes controlling aromatic amino acid (AAA) biosynthesis require identification of cross-regulatory interactions with genes and enzymes controlling conversion of aromatic amino acids (AAA) into secondary metabolites
Isoprenoid/terpenoid sweeteners (licorice glycyrrhizin, stevia rebaudioside, monk fruit mogroside) illustrate impact of differential sugar-sugar modification on taste quality
metabolic QTL (mQTL) analysis found 338 putative mQTL for hydroxycinnamates, flavonol and glycoalkaloid compounds Solanum lycopersicum; Solanum pennellii
kaempferol-3-O-rutinoside has 19 QTL Solanum lycopersicum; Solanum pennellii
five sublines (318-3, 3202-1, 3105-2, 3132-8, 3188-75) displayed same phenotypes with ILs 12-3 and 12-4 Solanum lycopersicum; Solanum pennellii
ILs 7-4 and 7-4-1 and cultivated variety harvested leaves, fruit pericarp, peel and seeds and analyzed specialized metabolite content via LC-MS Solanum lycopersicum; Solanum pennellii
piperine is detected only in minor levels in leaves or shoots Piper nigrum
artificial cold acclimation (CA) commonly enriches secondary metabolism pathway
gene deletions and duplications are mechanisms for diversification of secondary metabolism Arabidopsis thaliana
3′-phosphoadenosine 5′-phosphosulfate (PAPS) is donor of active sulfate for sulfation reactions in secondary metabolism
tyrosine (Tyr) serves as precursor of non-protein amino acids
isoflavones are derived from phenylalanine pathway
Solyc07g043410 in IL7-4 and IL7-4-1 compared with M82 Solanum lycopersicum; Solanum pennellii
two putative mQTL for flavonols cross-validated by evaluation of metabolite content of recombinants Solanum lycopersicum
genomic sequencing of fungi has revealed greater diversity of secondary metabolism
isolation of nuclei allows removal of plant secondary metabolites
wild Erythroxylum plants contain flavonoids Erythroxylum species
Pna-10 accumulates low level of 1,2-disinapoylglucose
cross-talk between Pi-limitation and nitrate-limitation signaling pathways affects anthocyanin synthesis Arabidopsis thaliana
better nutritional balance and flavor could be achieved in current and re- or de novo domesticated crops
sweet potato phenolics many remain structurally elusive
338 putative metabolite quantitative trait loci (mQTL) for flavonoids Solanum pennellii; Solanum lycopersicum
kaempferol accumulates in epidermis Solanum lycopersicum
14 annotated gene models in fine-mapped region includes four UGTs in duplicated genomic regions Solanum lycopersicum
Pna-10 still accumulates significant amount of sinapoylglucose
glandular trichomes produce diverse specialized metabolites Solanum lycopersicum
coding regions of Solyc12g096870 and Solyc12g098600 were very similar between M82 and Solanum pennellii Solanum lycopersicum; Solanum pennellii
SNPs from (ATIPT5, IPT5, AT5G19040) (LOC_Os07g11050) exerted negative allelic effect on pericarp color and catechin content Oryza sativa
tea flavor biosynthetic pathways expand beyond well-characterized tea metabolites such as catechins, l-theanine, and caffeine Camellia sinensis
tea flavor biosynthetic pathways include wide range of other metabolites Camellia sinensis
PLASMODESMAL LIPID-BINDING PROTEIN 5 (HWI1, PDLP5, AT1G70690) overexpression causes accumulation of anthocyanin
146 up-regulated genes were identified during anthocyanin degradation Brunfelsia calycina
theoretical models are good explanation for allocation to secondary metabolites in xylem and phloem
phosphorus availability did not affect concentration of leaf volatile terpene (LVT) Pinus pinaster
enhanced expression of SST leads to alterations in sinapate ester profiles
plant CYP family catalyze extremely diverse reactions with substantially lower sequence identity Strobilanthes cusia
seed-specific flavonol compound was additionally studied across range of wild species of lycopersicum complex Solanum lycopersicum complex
promoter regions of Solyc12g096870 and Solyc12g098600 showed several deletions or insertions in M82 promoter sequences compared with Solanum pennellii promoter sequences Solanum lycopersicum; Solanum pennellii
indigo content in leaf at stage 4 most abundant up to 2000 μg g⁻¹ Strobilanthes cusia
LBD family members are involved in anthocyanin biosynthesis
338 putative metabolite quantitative trait loci (mQTL) for further specialized metabolites Solanum pennellii; Solanum lycopersicum
seed cavity tissues contain phenolic compounds Solanum lycopersicum
Steroidal glycoalkaloids (SGAs) are secondary metabolites
overlapping introgression lines IL12-3 and IL12-4 showed specific changes in four flavonoid compounds Solanum lycopersicum; Solanum pennellii
introgression lines IL12-3 and IL12-4 showed clear changes in three major peaks in LC-MS chromatograms Solanum lycopersicum; Solanum pennellii
gene expression of Solyc12g098600 and Solyc12g096870 higher in seed tissue Solanum lycopersicum; Solanum pennellii
overlapping region of IL7-4 and IL7-4-1 on chromosome 7 is correlated with significantly increased levels of three distinct glycoalkaloid peaks at m/z = 1197.7, m/z = 1065.9 and m/z = 1067.8 Solanum lycopersicum; Solanum pennellii
(ASL39, LBD37, AT5G67420) 38, and 39 repress (IAA26, PAP1, AT3G16500) and (IAA27, PAP2, AT4G29080) Arabidopsis thaliana
Scutellaria baicalensis produces baicalein and related flavonoids
Glycosylation of hydrophobic phytochemicals is mainly mediated by UDP-sugar-dependent glycosyl transferases (UGTs)
protochlorophyllide reductase gene PILA_29041 is involved in secondary metabolism
Three KEGG pathways (KO00904, KO00940, KO00941) belong to secondary metabolism
rice lines with haplotypes 1 and 5 had lower flavonoid and phenolic compound content Oryza sativa
co-expression analysis is integrated with metabolite profiling
resources and energy are diverted into biosynthesis of secondary metabolites
some amino acids are starting point for synthesis of secondary metabolites
isorhamnetin-3-O-sophoroside is seed-specific flavonol-O-sophoroside Solanum lycopersicum
steroidal alkaloid aglycone and sugar moieties yield massive structural diversity of SGAs
14 annotated gene models in fine-mapped region includes two genes (Solyc07g043420: 2-oxoglutarate-dependent dioxygenase and Solyc07g043460: cytochrome P450) Solanum lycopersicum
induction of genes allocated to secondary metabolite biosynthetic pathways indicates diversion of resources into secondary metabolite biosynthesis
peak D (m/z = 625.1) is identified as isorhamnetin-3-diglucoside Solanum lycopersicum; Solanum pennellii
occurrence of quercetin-3-O-sophoroside-O-rhamnoside is found across Solanum pennellii Solanum pennellii
four lines (6428, 6489, 6612 and 6703) exhibited significantly higher levels of glycoalkaloid derivatives (m/z = 1197.7, m/z = 1065.9 and m/z = 1067.8) Solanum lycopersicum; Solanum pennellii
genes encoding secondary metabolite biosynthetic enzymes involved in the same pathway are found in clusters in plant genomes plants
DkMYB14 repressive function and DkMYB14 activator function contribute to elimination of astringency Diospyros kaki Thunb.
glucosinolate biosynthesis is intrically linked with auxin homeostasis Arabidopsis thaliana
oxidations are prerequisite for bioactive compound decoration
modern isotope labelling was successfully applied to nitrogen- and sulphur-containing plant metabolites
Pna-10 was found to have deletion of SMT and SAT genes Arabidopsis thaliana
aromatic amino acids (AAA) serve as precursors for aromatic secondary metabolites plants
rutin was increased or decreased by 4.4 and 0.26 in ILs 1-2 and 12-4 compared with M82 Solanum lycopersicum; Solanum pennellii
peaks D (m/z = 625.1) and E (m/z = 609.1) accumulated to considerable levels in M82 but were undetectable or negligibly present in overlapping ILs 12-3 and 12-4 Solanum lycopersicum; Solanum pennellii
11 mapping sublines sharing same genomic region from cultivated variety had undetectable or neglected amounts of flavonoid triglycosides Solanum lycopersicum; Solanum pennellii
Solyc12g096870 and Solyc12g098600 suggest that Solyc12g096870 and Solyc12g098600 act as either 5GT or 7GT in tomato seeds Solanum lycopersicum
redirection of secondary metabolism caused by GhnsLTPsA10 contributes to insect resistance Gossypium hirsutum
scientific community is just starting to explore the range of specialized metabolites produced in amaranths Amaranthus
plants present major challenge due to propensity for further conversion of desired activated products into conjugates or other derivatives
structural and regulatory genes of superfamilies of enzymes involved in secondary metabolism are direct consequence of complex plant–environment interaction mediated by soluble and insoluble secondary metabolites including phenylpropanoids
sulfur starvation is tightly linked to anthocyanin biosynthesis Arabidopsis thaliana
secondary metabolites relevant to industrial production and therapeutic application
one putative mQTL for steroidal glycoalkaloids cross-validated by evaluation of metabolite content of recombinants Solanum lycopersicum
gene-specific polymerase chain reaction (PCR) primers of all six candidates used to check gene expression using cDNA from fresh seeds Solanum lycopersicum; Solanum pennellii
Solyc12g096870 and Solyc12g098600 showed presence of mRNA only in IL12-3 and IL12-4 seeds Solanum lycopersicum; Solanum pennellii
tissue-specific metabolite analysis revealed higher accumulation of glycoalkaloid derivatives in seed and leaves of ILs 7-4 and 7-4-1 compared with M82 Solanum lycopersicum; Solanum pennellii
metabolic profiling using gas chromatography–time of flight mass spectrometry (GC-TOF-MS) quantified 117 metabolites Oryza sativa
haplotypes 2, 3, and 4 showed higher antioxidant potential in whole-grain and polished white rice Oryza sativa
main flavonols and anthocyanins in red inner tepals of wintersweet are cyanidin-3-O-glucoside, cyanidin-3-O-rutinoside, quercetin-3-O-rutinoside, kaempferol-3-O-rutinoside, and quercetin aglycone Chimonanthus praecox
UDP-glycosyl transferases (UGTs) are involved in the production of defence compounds plants
Proanthocyanidins (PAs) can be classified into soluble and insoluble proanthocyanidins (PAs)
types of colonizing microbes influence tryptophan-derived secondary metabolite pathway
modification of soil microbiota increases pyrrolidine alkaloid concentration Jacobaea vulgaris
extensive repertoire of chemicals in wild Erythroxylum plants could serve as substrates for promiscuous decorative enzymes Erythroxylum species
hydroxycinnamoyl-Coenzyme A:quinate hydroxycinnamoyl transferase (HQT) is candidate for chlorogenate:chlorogenate transferase (CCT) activity Solanum lycopersicum
high vacuolar concentrations of chlorogenic acid (CGA) could promote dicaffeoylquinic acid (diCQA) biosynthesis Solanum lycopersicum
young leaves with increasing inorganic phosphate (Pi) availability had lower anthocyanin Hakea prostrata
secondary metabolism genes in condition 3 are dramatically affected in 35S::VvABF2 cells treated with ABA Vitis vinifera
Abscisic acid glucosyl ester (ABA-GE) originates from plastid-localized precursors
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) mutants show significant accumulation of scopoletin Arabidopsis thaliana
Proanthocyanidins (PAs) are phenolic secondary metabolites
Arabidopsis thaliana secondary metabolites have internal roles within Arabidopsis thaliana Arabidopsis thaliana
epicuticular wax shows considerable variation among natural accessions of Arabidopsis thaliana Arabidopsis thaliana
other enzymes may compete with SST for substrate
phosphorus starvation is tightly linked to anthocyanin biosynthesis Arabidopsis thaliana
triterpenoids constituted source of chemical diversity within RTB crops
unknowns in sweet potato mostly comprise phenolic-derived compounds
flavonoid and carotenoid pathways show cross-talk leading to production of metabolites that share biological role
Solanum pennellii introgression lines used for profiling of specialized metabolites in seeds Solanum pennellii; Solanum lycopersicum
mQTL for glycoalkaloid on chromosome 7 were validated using S. pennellii backcross inbred lines (BILs) and sub-ILs Solanum pennellii
quercetin-3-O-sophoroside-O-rhamnoside negligible or none of this flavonol was detected in peel or fruit pericarp Solanum lycopersicum; Solanum pennellii
overall inhibitory effect on cancer growth may be due to a wide range of bioactive compounds present in haplotype 4 rice lines
superior haplotype selected rice lines contained three times more bound phenolics than the other haplotypes
silencing of AevPAL1 and AevTDC1 largely reduced syringic acid Aegilops variabilis
cluster CBS&M was over-represented in secondary metabolism Oryza sativa
coumarins is one of secondary metabolites of Arabidopsis thaliana Arabidopsis thaliana
oxidations are critical steps for bioactive compound formation
secondary metabolites differ significantly between bryophytes and seed plants
elicitors derived from fungal, bacterial or yeast cell wall extracts used to increase the accumulation of specific metabolites in various plant cell cultures
glycosylation is implicated in increase of solubility of secondary metabolites
phosphorus availability and MeJa induction interaction (P×MeJa) does not affect concentration of leaf volatile terpenes (LVT) Pinus pinaster
absence of induced traumatic resin canals within pine needles limits capacity for greater terpene foliar concentrations Pinus pinaster
Pna-10 accession accumulates sinapoylglucose Arabidopsis thaliana
elicitor-triggered expression of secondary metabolism is linked with far-reaching shifts of gene expression
yeast glycoprotein elicitor can be used to differentiate induction of secondary metabolism
sugars play central role in secondary metabolism
UV-B irradiation might induce accumulation of flavonols and anthocyanins Salvia miltiorrhiza
land plants produce diverse repertoire of specialized metabolites
MEP pathway-derived isopentenyl diphosphate (IDP) and dimethylallyl diphosphate (DMADP) are incorporated into cytosolic terpenoids
soluble proanthocyanidins (PAs) can be converted into insoluble proanthocyanidins (PAs) Diospyros kaki Thunb.
overexpression of strigolactone-associated genes in hairy roots altered bacterial and fungal microbiota Glycine max
secondary metabolism occurs in plant-associated filamentous ascomycetes
bacteria produce abscisic acid (ABA)
helvolic acid is produced by rice sheath rot fungus Sarocladium oryzae
anthocyanin glycosides are widely present in roots, stems, leaves, flowers, fruits, and seeds of plants
contigs annotated as involved in secondary metabolism, lipid metabolism and ascorbate–glutathione (GSH) cycle equally represented regardless of hydration state Craterostigma plantagineum
metabolic systems create complex natural products
maize ZmTTK1 kinase controls anthocyanin biosynthesis Zea mays
barley is without hydroxamic acid pathway
genomic sequencing of fungi has revealed novel taxonomic distributions of known compounds
symbionts contribute bioactive secondary metabolites
JA is known to have a role in production of secondary metabolites
α-copaene is minor part of spectrum of sesquiterpenes produced by some sesquiterpene synthases
general phenylpropanoid pathway leads to biosynthesis of lignans
constitutive overexpression of PtMYB8 in spruce was associated with strong decreases in transcript levels of flavonoid, terpenoid, and benzenoid biosynthesis enzymes Picea glauca
one biosynthetic gene cluster is particularly striking with genes encoding three different types of biosynthetic enzymes conserved across all five Amaranthaceae genomes analysed Amaranthaceae
this gene cluster is hypothesized to play a role in terpene synthesis pathway Amaranthus cruentus
terpene synthesis pathway leads to compounds that may be specific to this lineage Amaranthus cruentus
terpenophenolics, stilbenes, and isoflavonoids are limited to few species only
glucosinolates shows considerable variation among natural accessions of Arabidopsis thaliana Arabidopsis thaliana
tryptophan serves as precursor for secondary metabolites
some transcription factors regulate genes encoding both primary and secondary metabolism associated with aromatic amino acids (AAA)
338 putative metabolite quantitative trait loci (mQTL) for steroidal glycoalkaloids Solanum pennellii; Solanum lycopersicum
seed-specific flavonol compound was additionally studied across several different accessions of S. pennellii Solanum pennellii
Exogenous feeding of Phe leads to accumulation of numerous derived phenolics and phenylpropanoids
haplotype 4 lines contribute to higher antioxidant potential Oryza sativa
jasmonate (JA) is involved in biosynthesis of secondary metabolites
DkMYB14 promotes insolubilization of proanthocyanidins (PAs) Diospyros kaki Thunb.
secondary plant metabolites can be small lipophilic molecules (SLMs)
cis-jasmone induces production of I
microbes produce and secrete abscisic acid (ABA)
endophytes present in leaf-spot-diseased leaves increases cercosporin production by Cercospora sp. JNU001
deuterium atoms transferred via primary metabolites and cofactors such as NAD(P)D leads to incorporation into specialised metabolites such as huperzine A Phlegmariurus tetrastichus
Gln-18:3-specific association mapping result not driven by variation in a single VOC biosynthetic pathway Zea mays
other antifungal metabolites may compensate for Burkholderia ambifaria strains that do not produce cepacin Burkholderia ambifaria
Colletotrichum gloeosporioides positively-regulates SMEs produced by Nigrospora oryzae
phenylalanine ammonia-lyase (PAL) catalyzes first reaction in biosynthesis from L-phenylalanine to natural products based on phenylpropane skeleton
flavonoids are low molecular weight secondary plant metabolites
high pigment-1 mutations (hp-1 and hp-1 w) are characterized by enhanced levels of functional metabolites Solanum lycopersicum
AevPAL1 and AevTDC1 possibly affect downstream metabolites in cereal cyst nematode (CCN) resistance coordinately Aegilops variabilis
P deficiency leads to increasing accumulation of anthocyanin
UDP-glycosyl transferases (UGTs) are involved in the activity and stability of secondary metabolites plants
plant secondary metabolism comprises diverse compounds and enzymes
secondary metabolites isolated from Arabidopsis thaliana Arabidopsis thaliana
(CMU1, KLCR1, AT4G10840) targeting of shikimate pathway channels chorismate into phenylpropanoid pathway Zea mays
(CMU1, KLCR1, AT4G10840) functions as chorismate mutase Ustilago maydis
three-dimensional apical cells is linked with flavonoids bryophytes
(AtJAZ4, JAZ4, TIFY6A, AT1G48500) is involved in secondary metabolite accumulation
tryptophan-derived secondary metabolite pathway specifically developed in Brassicaceae
secondary metabolism related genes are enriched in accessory genome
terpenes are plant compounds with complex structures and biosynthetic origins
stabilization of TmTTK1 controls anthocyanin biosynthesis Zea mays
anthocyanidins are known to be present in maize Zea mays
genes involved in indole biosynthetic pathway had among highest proportion of ZmPep3 DEGs compared to size of the group (62%) Zea mays
anthocyanins are secondary metabolites
secondary metabolism components were more abundant in bundle sheath cells Oryza sativa
abundant proanthocyanidins (PAs) in persimmon fruit cause strong sensation of astringency Diospyros kaki Thunb.
overexpression of strigolactone-associated genes resulted in increased abundances of Rhizobiaceae and Fusarium solani Glycine max
camalexin is representative specialized (secondary) metabolite in Arabidopsis Arabidopsis thaliana
chloroplasts are the source of secondary metabolites
R2R3 MYB TFs main function is to regulate secondary metabolism in plants
plastid HXKs can function in synthesis of erythrose 4-phosphate in secondary metabolism
largest diversity of phenolic compounds was encountered in cassava and sweet potato
JA and SA play important roles in regulation of biosynthesis of secondary metabolites
lines from an independently derived backcross inbred line population used for analysis of mQTL for flavonols Solanum lycopersicum
184 QTL are for 27 annotated metabolites Solanum lycopersicum; Solanum pennellii
11 mapping sublines sharing same genomic region from cultivated variety had substantially higher levels of flavonoid diglycosides Solanum lycopersicum; Solanum pennellii
four genes (Solyc07g043410, Solyc07g043490, Solyc07g043420 and Solyc07g043460) were found to be significantly more highly expressed in leaves of overlapping ILs 7-4 and 7-4-1 Solanum lycopersicum; Solanum pennellii
metabolite classes majority belonging to flavone, organic acids and flavone C-glycosides Oryza sativa
resolved genomes have enabled deeper understanding of glucosinolate diversity Brassicales
(PLD, PLDALPHA1, AT3G15730) activity stimulation associated with silymarin production Silybum marianum
fragrant benzenoids may be formed from anthocyanin degradation products Brunfelsia calycina
2OG-Fe(II) oxygenase family enzymes in plants catalyze hydroxylation and desaturation steps in the synthesis of gibberellins, anthocyanidins, and flavones Arabidopsis thaliana
six biosynthetic gene clusters showed conserved co-location of biosynthetic enzymes across all five Amaranthaceae genomes Amaranthus cruentus; Amaranthus hypochondriacus; Beta vulgaris; Chenopodium quinoa; Spinacia oleracea
exogenous abscisic acid treatment on tea reduces damage by changing content of metabolites Camellia sinensis
plants secrete secondary metabolites
plants produce specialized metabolites
all strains of Burkholderia ambifaria produce pyrrolnitrin Burkholderia ambifaria
Sphingomonas melonis confers resistance by interfering with production of virulence factor tropolone Oryza sativa
SV-GWAS identified large-effect loci associated with seed glucosinolates, including a candidate gene, BnaA09.GTR2 Brassica napus
tea flavor biosynthetic pathways extend beyond well-characterized tea metabolites Camellia sinensis
SA and scopoletin accumulation in adjacent tissues of tobacco leaf parts infiltrated with a glycoprotein resulted from de novo synthesis rather than from diffusion from infiltrated tissues where HR was occurring Nicotiana tabacum
increased nutrient availability can cause neutral responses in leaf terpene content
bryophyte testbed success will require quantitative knowledge of fluxes facilitating high rates of terpenoid biosynthesis Bryophyta
flavonoids is phenolic secondary metabolites
synapoyl malate slight decline in PI tissues Arabidopsis thaliana
induction of naphthoquinone synthesis by chitin injection into Nepenthes pitchers represents a convenient method of obtaining pure liquid enriched in droserone in planta Nepenthes
addition of Mst to suspensions strongly enhanced silymarin production Silybum marianum
seven proteins were identified during anthocyanin degradation Brunfelsia calycina
glycosylation is implicated in storage and regulation of levels of hormones and signal molecules
different plant species produce distinct arrays of flavonoids
Phenylalanine ammonia lyase (PAL) and tryptophan decarboxylase (TDC) act as first enzymes of phenylpropanoid and tryptophan metabolism
glucosinolate is second major class of specialized metabolites in Arabidopsis Arabidopsis thaliana
capsaicinoids is type of alkaloid in Solanaceae Solanaceae
cytochrome P450 mono-oxygenase CYP72A68 (CYP72A68) down-regulated with fold change of −4.0-fold Glycine max
(CAT2, AT4G35090) deficiency may impact on the distribution of SMs in response to infection Arabidopsis thaliana
subsets of genes displaying repressed expression in both genotypes were involved in biosynthesis of lignin, lipids, sulfolipids, thalianols, and carbohydrates Arabidopsis thaliana
compound B is annotated as isorhamnetin-3-O-sophoroside-O-rhamnoside Solanum lycopersicum; Solanum pennellii
genomic region on chromosome 12 contains nine annotated UDP-glycosyltransferase genes Solanum lycopersicum
southern Solanum pennellii accessions, including LA0716 contained six times higher levels of quercetin-3-O-sophoroside-O-rhamnoside compared with far northern Solanum pennellii accessions Solanum pennellii
wild Erythroxylum plants contain tannins Erythroxylum species
alkaloids have been characterized in medicinal plants
bryophytes are chemically complex
biosynthetic pathways and regulatory mechanisms of pharmacologically active triterpenoids involve organization of metabolic gene clusters for coordinated expression
up-regulated genes in OsWRKY13-overexpressing plants includes genes in GO subcategory secondary metabolism Oryza sativa
cluster C groups secondary metabolites whose accumulation is not induced or repressed in PI tissues Arabidopsis thaliana
phosphorus availability does not affect concentration of total leaf volatile terpenes (LVT) Pinus pinaster
pine leaves are structurally limited in capacity for greater terpene foliar concentrations Pinus pinaster
skin contains substances responsible for flavour and aroma
flavonols are not predominant in Cannabis glands Cannabis sativa
flavonoids (diosmin, etc.) were present at lower levels in shade group
Arabidopsis thaliana secondary metabolites mediate ecological interactions Arabidopsis thaliana
modifications of plant secondary metabolism place only relatively low burden on diverted photosynthate
some species produce hundreds of acylsugars in a single organ