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1 uronic acid methyl ester (3), and (6-trans-p-coumaroyl)-3-O-beta-D-glucopyranosyl-(5-acetyl)-2-deoxy-
2 cluding the new natural compounds (6-trans-p-coumaroyl)-3-O-beta-D-glucopyranosyl-2-deoxy-D-riburonic
3 nosyl-2-deoxy-D-riburonic acid (1), (6-cis-p-coumaroyl)-3-O-beta-D-glucopyranosyl-2-deoxy-D-riburonic
4 yl-2-deoxy-D-riburonic acid (2a), (6-trans-p-coumaroyl)-3-O-beta-D-glucopyranosyl-2-deoxy-D-riburonic
5 production of p-coumaroyl shikimate and of p-coumaroyl 4-hydroxyphenyllactate, respectively, were par
6 ified in basil peltate glands that convert p-coumaroyl 4-hydroxyphenyllactic acid to its caffeoyl der
7 ate as a native acyl acceptor to produce a p-coumaroyl-5-O-shikimate intermediate.
8                                            p-Coumaroyl-6-secologanoside (comselogoside) is a secoirid
9 igher retention coefficient was observed for coumaroyl and acetyl derivatives when compared with the
10 s 3-O-glucosides, as well as their acetyl, p-coumaroyl and caffeoyl ester forms.
11 ular charge transfer excited state for the p-coumaroyl and caffeoyl ester forms.
12 namoyl transferase capable of transferring p-coumaroyl and caffeoyl moieties from their CoA derivativ
13                              We found that 4-coumaroyl and caffeoyl shikimic acids are inhibitors of
14                                            4-Coumaroyl and caffeoyl shikimic acids both act as compet
15                              Inhibition by 4-coumaroyl and caffeoyl shikimic acids may play significa
16 vatives, HCT2 favors transfer to malate of p-coumaroyl and feruloyl moieties over caffeoyl moieties b
17 ida KT2440 was engineered to convert mixed p-coumaroyl- and coniferyl-type LRCs to beta-ketoadipic ac
18 y release of cell-wall derived feruloyl- and coumaroyl-arabinose.
19 oumarate:CoA ligase (4CL), which generates p-coumaroyl CoA and caffeoyl CoA from their respective aci
20 propanoid pathway convert phenylalanine to p-coumaroyl CoA, a branch point metabolite from which many
21 oA ligase (4CL) catalyzes the formation of 4-coumaroyl CoA, a precursor of both flavonoids and monoli
22  the role of pCA in maize development, the p-coumaroyl CoA:hydroxycinnamyl alcohol transferase (pCAT)
23 mega-hydroxyacids using both feruloyl- and p-coumaroyl- CoA as the acyl donors.
24 imer bound two molecules of the catabolite p-coumaroyl-CoA (Kd = 11 +/- 1 muM).
25 nt retained a relatively high affinity for p-coumaroyl-CoA (Kd = 89 +/- 6 muM).
26 T showed a preference in enzyme assays for p-coumaroyl-CoA and benzoyl-CoA as acyl donor substrates a
27 yme A (CoA) ligation of 4-coumaric acid to 4-coumaroyl-CoA and caffeic acid to caffeoyl-CoA.
28 ic acid strongly inhibits the formation of 4-coumaroyl-CoA and caffeoyl-CoA.
29            Based on the exact chemistry of p-coumaroyl-CoA and shikimic acid in the active site and a
30 n of the phenylpropanoid chalcone from one p-coumaroyl-CoA and three malonyl-coenzyme A (CoA) thioest
31                                       With p-coumaroyl-CoA as a starter molecule, the G256A and G256V
32 g of SbHCT should occur sequentially, with p-coumaroyl-CoA binding prior to the acyl acceptor molecul
33 by the addition of nanomolar quantities of p-coumaroyl-CoA but not by p-coumarate.
34 tein of Arabidopsis thaliana (thale cress) 4-coumaroyl-CoA ligase (At4CL1) and Vitis vinifera (grape)
35                           Both HCT and the 4-coumaroyl-CoA ligase relocalized closer to the membrane
36  It is interesting that the Pt4CL2 product p-coumaroyl-CoA predominated in assays with developing lea
37                                   The CouR-p-coumaroyl-CoA structure revealed two ligand molecules bo
38  SbCCR2, displayed greater activity toward p-coumaroyl-CoA than did SbCCR1, which could imply a role
39 played higher affinity for caffeoyl-CoA or p-coumaroyl-CoA than for feruloyl-CoA, the enzyme showed s
40  is involved in the transesterification of p-coumaroyl-CoA to p-coumaroyl shikimate, one of the key s
41 ively, and formed naringenin chalcone when 4-coumaroyl-CoA was used as starter molecule.
42 one, benzophenone, and phloroglucinol from 4-coumaroyl-CoA, benzoyl-CoA, and hexanoyl-CoA, respective
43                            The presence of p-coumaroyl-CoA, but neither p-coumarate nor CoASH, abroga
44  to synthesize cinnamoyl-coenzyme A (CoA), p-coumaroyl-CoA, feruloyl-CoA, caffeoyl-CoA, and benzoyl-C
45 orm and ternary complex with shikimate and p-coumaroyl-CoA, which was converted to its product during
46 tal structures of ligand-free CouR and its p-coumaroyl-CoA-bound form showed no significant conformat
47 ikimic acid inhibits only the formation of 4-coumaroyl-CoA.
48  in production of naringenin chalcone from p-coumaroyl-CoA.
49 nt analyses suggested a requirement of the p-coumaroyl-CoA:agmatine N4-p-coumaroyl transferase ACT fo
50                  An acyltransferase, named p-coumaroyl-CoA:monolignol transferase (OsPMT), that could
51 tion of monolignol conjugates assembled by p-coumaroyl-CoA:monolignol transferase (PMT) enzymes, memb
52 eruloyl CoA, but CCR2 prefers caffeoyl and 4-coumaroyl CoAs, exhibits sigmoidal kinetics with these s
53 sion profiles of relevant genes, including p-coumaroyl coenzyme A 2'-hydroxylases, flavone synthases,
54 s simulations suggested that SvBAHD05 is a p-coumaroyl coenzyme A transferase (PAT) mainly involved i
55     These results suggest that OsAT10 is a p-coumaroyl coenzyme A transferase involved in glucuronoar
56 rmed on monolignols under the catalysis of p-coumaroyl-coenzyme A monolignol transferase (PMT).
57                    The rice (Oryza sativa) p-COUMAROYL-Coenzyme A MONOLIGNOL TRANSFERASE gene was int
58                      Plants expressing the p-COUMAROYL-Coenzyme A MONOLIGNOL TRANSFERASE transgene ca
59 e (HCT) capable of utilizing shikimate and p-coumaroyl-coenzyme A to generate p-coumaroyl shikimate.
60 functional analysis of LAP5 and LAP6 using 4-coumaroyl-coenzyme A yielded bis-noryangonin (a commonly
61 :shikimic acid p-coumaroyl transferase and p-coumaroyl-coenzyme A:4-hydroxyphenyllactic acid p-coumar
62 isrupting genes encoding CAld5H along with p-COUMAROYL-COENZYME A:MONOLIGNOL TRANSFERASE (PMT), a gra
63                                            p-Coumaroyl-coenzyme A:shikimic acid p-coumaroyl transfera
64             Two distinct acyltransferases, p-coumaroyl-coenzyme A:shikimic acid p-coumaroyl transfera
65                                As results, p-coumaroyl conjugates with tartaric, sinapic and ferulic
66  respectively, while it was much lower for p-coumaroyl derivatives (7-100% and 14-31%, respectively).
67 hat the antioxidant activity, the content in coumaroyl derivatives of anthocyanins and the vitisins A
68 4-hydroxylases (PtrC4H1 and PtrC4H2) and a p-coumaroyl ester 3-hydroxylase (PtrC3H3) are the enzymes
69 s found for the PtrC4H1/C4H2/C3H3-mediated p-coumaroyl ester 3-hydroxylation.
70 e (HCT) capable of forming caffeoyl and/or p-coumaroyl esters with malate.
71 observed with the donors feruloyl-glucose, 4-coumaroyl-glucose, and sinapoyl-glucose, which are known
72 oside, peonidin 3-rutinoside, petunidin 3-(6-coumaroyl)-glucoside and cyanidin 3-(6-coumaroyl)-glucos
73 at 60% ethanol concentration except the 3-(6-coumaroyl)-glucoside of cyanidin and petunidin whose max
74  3-(6-coumaroyl)-glucoside and cyanidin 3-(6-coumaroyl)-glucoside.
75 (2.18 +/- 1.01 mg/100 g), peonidin 3-O-(6"-p-coumaroyl-glucoside (1.06 +/- 0.81 mg/100 g), fertaric a
76  such as 3-methylcatechol, cyanidin 3-O-6"-p-coumaroyl-glucoside, delphinidin 3-O-glucoside, querceti
77      Anthocyanins acylated with feruloyl and coumaroyl glycosides were the most stable carrot pigment
78 , a substrate similar to FAX(3) but with a p-coumaroyl group instead of a feruloyl moiety was hydroly
79 rst report of chicoric, caffeoyl-hexaric and coumaroyl-hexaric acids and some glycosylate derivatives
80 te profiling identified elevated levels of p-coumaroyl hexose, caffeic acid hexoside and ferulic acid
81 nolic acids, protocatechuic acid hexoside, p-coumaroyl hexoside, and 5-O-p-coumaroylquinic acid, and
82 s the RpaI signal synthase, which produces p-coumaroyl-homoserine lactone (pC-HSL) and RpaR, which is
83 eumoniae, that produces the small molecule p-coumaroyl-homoserine lactone (pC-HSL) when the output of
84 the RpaI-synthesized quorum-sensing signal p-coumaroyl-homoserine lactone (pC-HSL).
85 izobia, direct production of the aryl-HSLs p-coumaroyl-HSL and cinnamoyl-HSL, respectively.
86 stris uses an acyl-HSL synthase to produce p-coumaroyl-HSL by using environmental p-coumaric acid rat
87                         We also found that p-coumaroyl-HSL is made by other bacteria including Bradyr
88  fatty acyl-HSL receptors that responds to p-coumaroyl-HSL to regulate global gene expression.
89  that it produces and detects an aryl-HSL, p-coumaroyl-HSL, and signal production requires an exogeno
90 m malate to CoA) by HCT2 was observed with p-coumaroyl-malate but not phaselic acid.
91 he HCT2-silenced plants, phaselic acid and p-coumaroyl-malate levels were reduced to <5% that of wild
92     Interestingly, apart from feruloyl and p-coumaroyl modifications on arabinose, putative caffeoyl
93 malate, whereas HCT2 transfers caffeoyl or p-coumaroyl moieties from a coenzyme A-thiolester to malat
94 i indicate that HCT1 transfers caffeoyl or p-coumaroyl moieties from a coenzyme A-thiolester to shiki
95 ived from malonyl-CoA decarboxylation to a p-coumaroyl moiety attached to an active site cysteine.
96 merization of the vinyl-double bond in the p-coumaroyl moiety occurred when the extract was exposed t
97                                     HA and p-coumaroyl putrescine were identified as shoot-specific a
98 ty to hydroxylate 4-coumaroyl shikimate or 4-coumaroyl quinate to generate caffeoyl shikimate or CGA.
99  acid, di-caffeoyl quinic acid, quinic acid, coumaroyl quinic acid as polar constitutes in coffee oil
100     The major peaks in the juice belonged to coumaroyl-quinic acid, chlorogenic acid, procyanidin B2,
101                           Petunidin-3-(trans-coumaroyl)-rutinoside-5-glucoside and delphinidin-3-(tra
102 ncluding two new anthocyanins [malvidin-3-(p-coumaroyl)-rutinoside-5-glucoside and malvidin-3-(ferulo
103 inoside-5-glucoside and delphinidin-3-(trans-coumaroyl)-rutinoside-5-glucoside were the most abundant
104 troscopy to be delphinidin-3-(4'''-O-trans-p-coumaroyl)-rutinoside-5-O-glucoside and petunidin-3-(4''
105 -O-glucoside and petunidin-3-(4'''-O-trans-p-coumaroyl)-rutinoside-5-O-glucoside.
106        We also characterized two switchgrass coumaroyl shikimate 3'-hydroxylase (C3'H) enzymes (PvC3'
107 mate hydroxycinnamoyl transferase (HCT) or p-coumaroyl shikimate 3'-hydroxylase (C3'H) lead to reduce
108  defective in a lignin biosynthetic enzyme p-coumaroyl shikimate 3'-hydroxylase (C3'H), exhibits seve
109 sferase, responsible for the production of p-coumaroyl shikimate and of p-coumaroyl 4-hydroxyphenylla
110                   The shikimate residue in p-coumaroyl shikimate is released in later steps, and the
111 vailable again for the biosynthesis of new p-coumaroyl shikimate molecules.
112 rome P450s had the capacity to hydroxylate 4-coumaroyl shikimate or 4-coumaroyl quinate to generate c
113  transesterification of p-coumaroyl-CoA to p-coumaroyl shikimate, one of the key steps in the biosynt
114 ome P450 CYP98A13, which meta hydroxylates p-coumaroyl shikimate, were isolated and found to be highl
115 ate and p-coumaroyl-coenzyme A to generate p-coumaroyl shikimate.
116 enzymes were found to be very specific for p-coumaroyl shikimate.
117                                            4-Coumaroyl shikimic acid strongly inhibits the formation
118 cid to caffeic acid and the other converts p-coumaroyl shikimic acid to caffeoyl shikimic acid.
119 id is essential for the 3-hydroxylation of 4-coumaroyl shikimic acid.
120 yl spermidine, and N(1),N(5),N(10)-tri-p-(E)-coumaroyl spermidine amides.
121   Kaempferol-O-neohesperidoside and N,N,N,-p-coumaroyl spermidine were characteristic safflower metab
122 idine, N(10)-(E)-caffeoyl-N(1),N(5)-di-p-(E)-coumaroyl spermidine, and N(1),N(5),N(10)-tri-p-(E)-coum
123  to be N(1),N(10)-di-(E)-caffeoyl-N(5)-p-(E)-coumaroyl spermidine, N(1)-(E)-caffeoyl-N(5),N(10)-di-p-
124 idine, N(1)-(E)-caffeoyl-N(5),N(10)-di-p-(E)-coumaroyl spermidine, N(10)-(E)-caffeoyl-N(1),N(5)-di-p-
125 irement of the p-coumaroyl-CoA:agmatine N4-p-coumaroyl transferase ACT for the biosynthesis and of th
126 ases, p-coumaroyl-coenzyme A:shikimic acid p-coumaroyl transferase and p-coumaroyl-coenzyme A:4-hydro
127       p-Coumaroyl-coenzyme A:shikimic acid p-coumaroyl transferase is expressed in basil peltate glan
128 royl-coenzyme A:4-hydroxyphenyllactic acid p-coumaroyl transferase, responsible for the production of
129 amine conjugates, feruloyl-tyramine (FT) and coumaroyl-tyramine (CT).

 
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