ライフサイエンスコーパス: indole-3-acetic acid

1 as induced in the presence of 2,4-D and IAA (indole-3-acetic acid).

2 ed for polar transport of the hormone auxin (indole-3-acetic acid).

3 e gut microbiome (e.g., CMPF, phenylsulfate, indole-3-acetic acid).

4 play an important role in converting IPA to indole-3-acetic acid.

5 hydrogen peroxide, abscisic acid (ABA), and indole-3-acetic acid.

6 pression in response to exogenously supplied indole-3-acetic acid.

7 e-3-butyric acid (IBA) to the active hormone indole-3-acetic acid.

8 ecific for the carboxyl-bearing phytohormone indole-3-acetic acid.

9 duced conversion of indole-3-butyric acid to indole-3-acetic acid.

10 ty was enhanced by ethylene and inhibited by indole-3-acetic acid.

11 s was increased by treatment with 0.1 microM indole-3-acetic acid.

12 ction of the microbial tryptophan metabolite indole-3-acetic acid.

13 ven by the bacterially-produced phytohormone indole-3-acetic acid.

14 d response of the apx6 mutants to ABA and to indole-3-acetic acid.

15 Indole-3-acetic acid (1 microm, 10 microm, 0.1 mm, and 1

16 m was 5-methoxy-2-methyl-1-(phenylmethyl)-1H-indole-3-acetic acid (13a).

17 A mutant version of Auxin/Indole-3-Acetic Acid 16 (AUX/IAA16; a gene previously im

18 ntrations of isolated uremic solutes such as indole-3-acetic acid (3.5 mug/mL), indoxyl sulfate (25 m

19 arable to that of oxindole-3-acetic acid and indole-3-acetic acid (62 picomoles per shoot).

20 seedlings to 2,3-dihydro-7-hydroxy-2-oxo-1H indole-3-acetic acid-7'-O-beta-D-glycopyranoside with th

21 e intake resulted in reduced serum levels of indole-3-acetic acid, a microbial tryptophan metabolite,

22 d seedlings treated with different hormones (indole-3-acetic acid, abscisic acid, gibberellin, methyl

23 alicylic acid, cinnamic acid, jasmonic acid, indole-3-acetic acid, abscisic acid, unsaturated C(18) f

24 indole-3-aspartic acid (an indicator of high indole-3-acetic acid accumulation, which inhibits lettuc

25 n and that these mutants show reduced auxin (indole-3-acetic acid) accumulation and auxin responses c

26 ce that OsbZIP49 activates the expression of indole-3-acetic acid-amido synthetases OsGH3-2 and OsGH3

27 Abscisic acid and indole-3-acetic acid-amino acid conjugates accumulated i

28 d was partially characterized as an ester of indole-3-acetic acid and a desoxyaminohexose.

29 endogenous hormones measured in leaves, both indole-3-acetic acid and abscisic acid contents were dec

30 nutrient acquisition and the accumulation of indole-3-acetic acid and antioxidants in tissues, are al

31 Bacterial production of indole-3-acetic acid and attachment to algae are signifi

32 etics and thermodynamics of the oxidation of indole-3-acetic acid and derivatives and of phenols by h

33 bolic branch point between the primary auxin indole-3-acetic acid and indole glucosinolate biosynthes

34 Finally, it was found that the auxins indole-3-acetic acid and indole-3-acetamide, which were

35 that neither the naturally occurring auxins indole-3-acetic acid and indole-3-butyric acid, nor the

36 ts respond normally to the endogenous auxins indole-3-acetic acid and indole-butyric acid.

37 as purified and characterized as an ester of indole-3-acetic acid and myo-inositol.

38 fate, while for weakly bound toxins, namely, indole-3-acetic acid and p-cresyl glucuronide, an increa

39 second compound was found to be an ester of indole-3-acetic acid and the disaccharide rutinose (gluc

40 Indole-3-acetic acid and tryptophan serve as signalling

41 s (sirtinol, 2,4-dichlorophenoxyacetic acid, indole-3-acetic acid) and a host of pleiotropic phenotyp

42 ation of COR, salicylic acid, jasmonic acid, indole-3-acetic acid, and abscisic acid illustrate the p

43 l analysis of salicylic acid, jasmonic acid, indole-3-acetic acid, and abscisic acid is typically ach

44 osine, kynurenic acid, indole-3-lactic acid, indole-3-acetic acid, and betaine were observed than in

45 cussed to be involved in the biosynthesis of indole-3-acetic acid, and Cytochrome P450 (CYP) 71B6 wer

46 ds including indole-3-butyric acid, 4-chloro-indole-3-acetic acid, and indole-3-propionic acid.

47 itination at baseline and that uremic serum, indole-3-acetic acid, and indoxyl sulfate significantly

48 ibution of total radioactivity, radiolabeled indole-3-acetic acid, and radiolabeled ester conjugated

49 wards small substrates including the natural indole-3-acetic acid, and the synthetic auxin 2,4-dichlo

50 t one route to produce another phytohormone, indole-3-acetic acid, and thus, AOs play important roles

51 ulation of FQR1 mRNA begins within 10 min of indole-3-acetic acid application and reaches a maximum o

52 Free indole-3-acetic acid applied to the endosperm supplies s

53 f other plant hormones, including zeatin and indole-3-acetic acid, are observed in BGL-1 lines.

54 Overexpression of BADC1 in wri1-1 decreased indole-3-acetic acid-Asp content and partially rescued i

55 th reduction in root length and elevation of indole-3-acetic acid-Asp levels relative to the wild typ

56 oxIAA) and increases in the conjugated forms indole-3-acetic acid aspartic acid (IAA-Asp) and indole-

57 ifically, elevated levels of auxin conjugate indole-3-acetic acid-aspartic acid (IAA-Asp) were observ

58 tors are repressed by interaction with AUXIN/INDOLE 3-ACETIC ACID (Aux/IAA) proteins.

59 auxin-transcription activators, while auxin/indole-3-acetic acid (Aux/IAA) are auxin-transcription r

60 ved Arabidopsis (Arabidopsis thaliana) Auxin/indole-3-acetic acid (Aux/IAA) family member.

61 The AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) genes encode short-lived

62 Auxin/indole-3-acetic acid (Aux/IAA) genes encode short-lived

63 Auxin/indole-3-acetic acid (Aux/IAA) proteins function as repr

64 xin-responsive degradation of multiple auxin/indole-3-acetic acid (Aux/IAA) proteins is essential for

65 BIF1 and BIF4 encode AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) proteins, which are key c

66 pivots on the interaction between the AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) repressor proteins and th

67 tical model revealed the centrality of auxin/indole-3-acetic acid (Aux/IAA) transcriptional corepress

68 Auxin induces the degradation of AUXIN/INDOLE-3-ACETIC ACID (AUX/IAA) transcriptional repressor

69 In the presence of auxin, AUXIN/INDOLE-3-ACETIC ACID (AUX/IAA) transcriptional repressor

70 )/AUXIN SIGNALING F-BOX protein and an AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) transcriptional repressor

71 y two counteracted teams including (1) auxin/indole-3-acetic acid (AUX/IAA)-histone deacetylase (HDA)

72 y two counteracted teams including (1) auxin/indole-3-acetic acid (AUX/IAA)-histone deacetylase (HDA)

73 by facilitating proteolytic removal of auxin/indole-3-acetic acid (AUX/IAA)-inducible repressors, whi

74 n auxin response is the degradation of Auxin/Indole-3-Acetic Acid (Aux/IAA, referred to hereafter as

75 and their interaction with the plant hormone indole-3-acetic acid (auxin).

76 es encode enzymes that convert tryptophan to indole-3-acetic acid (auxin): iaaM (tryptophan mono-oxyg

77 using alpha-(2,4-dimethylphenylethyl-2-oxo)-indole-3-acetic acid (auxinole), alpha-(phenylethyl-2-ox

78 conversion of indole-3-butyric acid (IBA) to indole-3-acetic acid, because ech2 seedlings have altere

79 d metabolism and transport, and key steps in indole-3-acetic acid biosynthesis, catabolism, and trans

80 afb5-5, that responds to conventional auxin (indole-3-acetic acid) but has a strongly diminished resp

81 laced these CCMTs into a clade that includes indole-3-acetic acid carboxyl methyltransferases and a l

82 mice confirmed that B. ovatus could elevate indole-3-acetic acid concentrations in vivo.

83 o lead to a sustained elevation of leaf free indole-3-acetic acid content relative to untreated contr

84 reover, cu-3 mutants retained sensitivity to indole-3-acetic acid, cytokinins, gibberellin, and absci

85 acteria raise the question as to whether the indole-3-acetic acid degradation pathway is present in h

86 , gravity affects the steady state amount of indole-3-acetic acid derived from indole-3-acetyl-myo-in

87 Asymmetric distribution of [3H]indole-3-acetic acid, derived from the applied [3H]indol

88 l defects that can be ascribed to changes in indole-3-acetic acid distribution.

89 auxin antagonist alpha-(phenyl ethyl-2-one)-indole-3-acetic acid enhanced ABA-regulated stomatal mov

90 g abscisic acid, gibberellin, jasmonic acid, indole-3-acetic acid, etc.

91 it is the same as IAA7, a member of the IAA (indole-3-acetic acid) family of auxin-inducible genes.

92 ate flux near neuronal cells; and endogenous indole-3-acetic acid flux near the surface of Zea mays r

93 nphysiological concentrations of ethylene or indole-3-acetic acid for protracted periods (more than 2

94 eta-oxidation enzymes as in the synthesis of indole-3-acetic acid from indole-3-butyric acid.

95 a photooxidation product of the plant auxin indole-3-acetic acid, functions as an affinity label of

96 rolactone, three urolithin glucuronides, and indole-3-acetic acid glucuronide.

97 le-3-acetic acid aspartic acid (IAA-Asp) and indole-3-acetic acid glutamic acid (IAA-Glu) of 438- and

98 y for indole-3-acetic acid in Zea seedlings: Indole-3-acetic acid --> Oxindole-3-acetic acid --> 7-Hy

99 preference for the naturally occurring auxin indole 3-acetic acid (IAA) and is important for coordina

100 epicotyls were loaded symmetrically with 3H-indole 3-acetic acid (IAA) or 45Ca2+, then subjected to

101 We investigated whether the uremic solute indole-3 acetic acid (IAA) predicts clinical outcomes in

102 Indole-3 acetic acid (IAA)-induced changes in gene expre

103 years of evidence showing a pivotal role for indole-3-acetic acid (IAA or auxin) in plant development

104 m segments have implicated the plant hormone indole-3-acetic acid (IAA or auxin) in the regulation of

105 The plant hormone indole-3-acetic acid (IAA or auxin) mediates the elongat

106 Second, a transient gradient of free indole-3-acetic acid (IAA) across the pulvinus was appar

107 Exogenous indole-3-acetic acid (IAA) also elevated flavonoid accum

108 Indole-3-acetic acid (IAA) and 1-aminocyclopropane-1-car

109 ompared with the control group and decreased indole-3-acetic acid (IAA) and abscisic acid (ABA) conce

110 than the wild type at low concentrations of indole-3-acetic acid (IAA) and also under low nutrient c

111 tophan (Trp), including the growth regulator indole-3-acetic acid (IAA) and defense compounds against

112 binding properties of indoxyl sulfate (IS), indole-3-acetic acid (IAA) and hippuric acid (HIPA) and

113 y metabolites including the growth regulator indole-3-acetic acid (IAA) and indole glucosinolate defe

114 The auxins indole-3-acetic acid (IAA) and naphthaleneacetic acid st

115 Indole-3-acetic acid (IAA) and other hormones were quant

116 auxin biology include synthesis of the auxin indole-3-acetic acid (IAA) and production of virulence f

117 Gretchen Hagen 3.5 (AtGH3.5) conjugates both indole-3-acetic acid (IAA) and salicylic acid (SA) to mo

118 s have suggested that AtGSTF2 interacts with indole-3-acetic acid (IAA) and the auxin transport inhib

119 the auxin precursor IBA and the active auxin indole-3-acetic acid (IAA) and those with restored respo

120 s of indole-3-acetyl-1-O-beta-D-glucose from indole-3-acetic acid (IAA) and uridine diphosphoglucose

121 mal cells under control conditions and after indole-3-acetic acid (IAA) application.

122 h plants regulate levels of the phytohormone indole-3-acetic acid (IAA) are complex and not fully und

123 Amide-linked conjugates of indole-3-acetic acid (IAA) are putative storage or inact

124 owever, the expression of genes encoding the indole-3-acetic acid (IAA) biosynthesis enzyme TRYPTOPHA

125 Plants can regulate levels of the auxin indole-3-acetic acid (IAA) by conjugation to amino acids

126 -butyric acid (IBA) is converted into active indole-3-acetic acid (IAA) by peroxisomal beta-oxidation

127 acid (IBA) is converted to the active auxin indole-3-acetic acid (IAA) by removal of two side-chain

128 Amide-linked indole-3-acetic acid (IAA) conjugates constitute approxi

129 The formation and hydrolysis of indole-3-acetic acid (IAA) conjugates represent a potent

130 by formation and hydrolysis of amide-linked indole-3-acetic acid (IAA) conjugates.

131 IBA treatments locally increased endogenous indole-3-acetic acid (IAA) content, whereas the combinat

132 Exogenous indole-3-acetic acid (IAA) enhances the constitutive exp

133 s thaliana, cotyledons and leaves synthesize indole-3-acetic acid (IAA) from tryptophan through indol

134 ence indicates that amino acid conjugates of indole-3-acetic acid (IAA) function in auxin homeostasis

135 Furthermore, homologous members of the AUX/indole-3-acetic acid (IAA) gene family mediate the actio

136 tural auxins indole-3-butyric acid (IBA) and indole-3-acetic acid (IAA) has been described in Arabido

137 Most indole-3-acetic acid (IAA) in higher plants is conjugate

138 BA), which is apparently shortened to active indole-3-acetic acid (IAA) in peroxisomes by a process s

139 The bulk of indole-3-acetic acid (IAA) in plants is found in the for

140 be the coupling between the concentration of indole-3-acetic acid (IAA) in the cambial region of a tr

141 n induces an asymmetric distribution of free indole-3-acetic acid (IAA) in the cortex-epidermis of th

142 iments show that afb4-2 is hypersensitive to indole-3-acetic acid (IAA) in the hypocotyl, indicating

143 To date, the role of the auxin indole-3-acetic acid (IAA) in this context is not well u

144 84B1, whose recombinant product glucosylated indole-3-acetic acid (IAA) in vitro.

145 PLC-ESI-MS/MS analysis showed that levels of indole-3-acetic acid (IAA) increased and levels of absci

146 ACC and indole-3-acetic acid (IAA) increased the abundance of tr

147 olated pea (Pisum sativum L.) seedlings with indole-3-acetic acid (IAA) induced within 15 min an incr

148 We show that indole-3-acetic acid (IAA) inhibition of abscisic acid (

149 Indole-3-acetic acid (IAA) is a primary phytohormone tha

150 Polar transport of the natural auxin indole-3-acetic acid (IAA) is important in a number of p

151 We further found that the free indole-3-acetic acid (IAA) level in hypocotyl regions be

152 .F.W. Meyer ecotype had significantly higher indole-3-acetic acid (IAA) levels than a UV-sensitive ec

153 nel mass and a recently reported decrease in indole-3-acetic acid (IAA) levels throughout kernel deve

154 Whereas indole-3-acetic acid (IAA) levels were elevated in young

155 tant phenotypes were rescued when endogenous indole-3-acetic acid (IAA) levels were increased by grow

156 Increasing indole-3-acetic acid (IAA) levels, either in stem tissue

157 have developed a high-throughput screen for indole-3-acetic acid (IAA) levels.

158 leaves is paralleled by an increase in free indole-3-acetic acid (IAA) levels.

159 Indole-3-acetic acid (IAA) methyltransferase (IAMT) is a

160 Either 5-[3H]indole-3-acetic acid (IAA) or 5-[3H]indole-3-acetyl-myo-

161 Furthermore, exogenous application of indole-3-acetic acid (IAA) or auxin analogues might effe

162 Cuttings treated with indole-3-acetic acid (IAA) or subjected to salt stress s

163 est that the enzymatic reactions involved in indole-3-acetic acid (IAA) production via IPyA are diffe

164 Indole-3-acetic acid (IAA) promotes ethylene biosynthesi

165 es facilitates ubiquitination of auxin (aux)/indole-3-acetic acid (IAA) repressor proteins in the pre

166 although AgNO(3) dramatically decreased root indole-3-acetic acid (IAA) responsiveness in inhibition

167 ized carrier proteins to transport the auxin indole-3-acetic acid (IAA) to target tissues.

168 first enzyme-catalyzed reaction leading from indole-3-acetic acid (IAA) to the myo-inositol esters of

169 companied by a rapid increase in radioactive indole-3-acetic acid (IAA) transport and its accumulatio

170 mutation significantly enhance radiolabeled indole-3-acetic acid (IAA) transport in both the acropet

171 Root basipetal and acropetal indole-3-acetic acid (IAA) transport increase with ACC t

172 were to determine whether both polarities of indole-3-acetic acid (IAA) transport occur in roots of A

173 Indole-3-acetic acid (IAA) was identified in F. distichu

174 the promotion of lateral root initiation by indole-3-acetic acid (IAA) was reduced as the IAA concen

175 Indole-3-acetic acid (IAA), a major plant auxin, is prod

176 of bacterial cultures and the production of indole-3-acetic acid (IAA), a ubiquitous plant hormone t

177 onversion of indole-3-pyruvic acid (IPyA) to indole-3-acetic acid (IAA), acting downstream of CKRC1/T

178 The auxin, indole-3-acetic acid (IAA), and auxin efflux inhibitors,

179 rabidopsis genes were specifically active on indole-3-acetic acid (IAA), and one was active on both I

180 ant-associated microbes synthesize the auxin indole-3-acetic acid (IAA), and several IAA biosynthetic

181 In addition to MeJA and indole-3-acetic acid (IAA), axr1-24 had decreased sensit

182 synthesis and degradation of the main auxin, indole-3-acetic acid (IAA), by sugars requires changes i

183 hey were also screened for the production of indole-3-acetic acid (IAA), hydrogen cyanide (HCN), ammo

184 IBA is converted to the more abundant auxin, indole-3-acetic acid (IAA), in a mechanism that parallel

185 l mechanisms to regulate levels of the auxin indole-3-acetic acid (IAA), including the formation and

186 The native auxin, indole-3-acetic acid (IAA), is a major regulator of plan

187 A plant growth-promoting substance, such as indole-3-acetic acid (IAA), known to be produced by G. d

188 nscripts that were consistently regulated by indole-3-acetic acid (IAA), partitioning into 60 cluster

189 stasis of the major form of auxin in plants, indole-3-acetic acid (IAA), remains unclear.

190 Indole-3-acetic acid (IAA), the main naturally occurring

191 an antagonistic manner to that of the auxin indole-3-acetic acid (IAA), the mechanism by which remai

192 Levels of indole-3-acetic acid (IAA), the primary auxin, are tight

193 When combined with plant auxin, indole-3-acetic acid (IAA), the SPE fraction shows a syn

194 airway lactobacilli associated with reduced indole-3-acetic acid (IAA), which was in turn linked to

195 changes in auxin metabolism, mediated by the indole-3-acetic acid (IAA)-amido synthetase Gretchen Hag

196 Conjugation to amino acids by indole-3-acetic acid (IAA)-amido synthetases is an impor

197 ulation of a conjugated form of the hormone, indole-3-acetic acid (IAA)-Asp, to promote disease devel

198 We show that the expression of an indole-3-acetic acid (IAA)-modified protein from bean se

199 a that are resistant to growth inhibition by indole-3-acetic acid (IAA)-phenylalanine have been isola

200 al root primordia; decreased auxin maxima in indole-3-acetic acid (IAA)-treated root apical meristems

201 s peroxisomal beta-oxidation to release free indole-3-acetic acid (IAA).

202 The most abundant natural auxin is indole-3-acetic acid (IAA).

203 ly via its conversion to the principal auxin indole-3-acetic acid (IAA).

204 r 2,4-dichlorophenoxyacetic acid (2,4-D) and indole-3-acetic acid (IAA).

205 estigated the sensitivity of rhd1-4 roots to indole-3-acetic acid (IAA).

206 remain sensitive to the more abundant auxin indole-3-acetic acid (IAA).

207 didate precursor of the plant growth hormone indole-3-acetic acid (IAA).

208 logical responses like the endogenous auxin, indole-3-acetic acid (IAA).

209 or produces high concentrations of the auxin indole-3-acetic acid (IAA).

210 nt hormone, usually occurring in the form of indole-3-acetic acid (IAA).

211 30 specifically transports picloram, but not indole-3-acetic acid (IAA).

212 nclude camalexin, indole glucosinolates, and indole-3-acetic acid (IAA); however, the steps in their

213 ynthesis pathway and increases in the auxin [indole-3-acetic acid (IAA)] biosynthesis pathway.

214 static regulation of the phytohormone auxin [indole-3-acetic acid (IAA)] is essential to plant growth

215 Spatial regulation of the plant hormone indole-3-acetic acid (IAA, or auxin) is essential for pl

216 The Trp conjugate with indole-3-acetic acid (IAA-Trp) produced a similar respon

217 sion of GRETCHEN HAGEN3.2 (ZmGH3.2, encoding indole-3-acetic acid [IAA] deactivating enzyme), and inc

218 he biosynthesis of the main auxin in plants (indole-3-acetic acid [IAA]) has been elucidated recently

219 The plant hormone auxin (indole-3-acetic acid [IAA]) is found both free and conju

220 The phytohormone auxin (indole-3-acetic acid [IAA]) plays a fundamental role in

221 rile (IAN; a possible precursor of the auxin indole-3-acetic acid [IAA]) was carried out under mild c

222 (1-NAA); however, traditional auxins (e.g., indole-3-acetic acid [IAA], 2,4-D, 1-NAA) have no effect

223 IAR3 hydrolyzes an inactive form of auxin (indole-3-acetic acid [IAA]-alanine) and releases bioacti

224 er to survey the entire literature on auxin (indole-3-acetic acid, IAA) action in all plants, with sp

225 The phytohormone auxin (indole-3-acetic acid, IAA) is a small organic molecule t

226 indole-3-butyric acid (IBA) to active auxin (indole-3-acetic acid; IAA) modulates lateral root format

227 ycerol and each of two inhibitors of hKAT I: indole-3-acetic acid (IAC) and Tris.

228 The polar movement of [(3)H]indole-3-acetic acid in both hypocotyl sections and prim

229 s roots and increases the retention of [(3)H]indole-3-acetic acid in root tips of maize.

230 pplied to the endosperm supplies some of the indole-3-acetic acid in the mesocotyl but essentially no

231 induction of primary auxin response genes by indole-3-acetic acid in the presence of growth-inhibitor

232 bution and chemical form of the radiolabeled indole-3-acetic acid in the shoot depending upon whether

233 ic acid-glucoside is a natural metabolite of indole-3-acetic acid in Z. mays seedlings.

234 route as the principal catabolic pathway for indole-3-acetic acid in Zea seedlings: Indole-3-acetic a

235 etic acid, and radiolabeled ester conjugated indole-3-acetic acid, in the shoots was then determined.

236 ns of auxin response factors (ARF) and auxin/indole 3-acetic acid inducible proteins regulate transcr

237 ly of transcription factors as well as AUXIN/INDOLE-3-ACETIC ACID INDUCIBLE (AUX/IAA) proteins that r

238 analyses revealed that expression of several indole-3-acetic acid-inducible genes, including Aux/IAA,

239 P, and the auxin-inducible genes MONOPTEROS, INDOLE-3-ACETIC ACID INDUCIBLE1 (IAA1), and IAA19.

240 /SL signaling, D14-LIKE2, KAR-UP F-BOX1, and INDOLE-3-ACETIC ACID INDUCIBLE1, is rescued in smax1 max

241 t increases in the expression of some genes (INDOLE-3-ACETIC ACID-INDUCIBLE1 and PHYTOCHROME B ACTIVA

242 ated tissues and others through signaling of INDOLE-3-ACETIC ACID INDUCIBLE28 (IAA28), CRANE (IAA18),

243 The auxin indole-3-acetic acid is a key plant hormone essential fo

244 Indole-3-acetic acid is oxidized to oxindole-3-acetic ac

245 According to the classic model, the auxin indole-3-acetic acid is produced in the shoot tip and tr

246 We propose that the level of indole-3-acetic acid is regulated by the flux of indole-

247 We also show that the widespread auxin, indole-3-acetic acid, is synthesized by a parallel pathw

248 In particular, indole-3-acetic acid levels declined after ABA treatment

249 ed within 12 h of increasing the R:FR, while indole-3-acetic acid levels did not change.

250 of this enzyme in the homeostatic control of indole-3-acetic acid levels in Zea mays is discussed.

251 Jasmonic acid and indole-3-acetic acid levels were also found to increase

252 hypocotyls contained considerably lower free indole-3-acetic acid levels when compared with wild-type

253 nhibitor response1/auxin-related f-box-auxin/indole-3-acetic acid-mediated auxin-signaling machinery

254 ft1-2, and 35S:PFT1 seedlings in response to indole-3-acetic acid, naphthaleneacetic acid, and the po

255 uding a number of transcripts encoding Auxin/Indole-3-Acetic Acids, negative regulators of auxin sign

256 ere fully assigned as tetrahydropentoxyline, indole-3-acetic-acid-O-glucuronide, p-cresol glucuronide

257 pe dilution, accounting for 19% of the ester indole-3-acetic acid of the shoot.

258 id in the shoot depending upon whether 5-[3H]indole-3-acetic acid or 5-[3H]indole-3-acetyl-myo-inosit

259 d an auxin-inhibitor (a-(phenyl ethyl-2-one)-indole-3-acetic acid (PEO-IAA)), together with the MIR17

260 c acid (auxinole), alpha-(phenylethyl-2-oxo)-indole-3-acetic acid (PEO-IAA), and 5-fluoroindole-3-ace

261 Indole-3-acetic acid (plant auxin) has low toxicity but

262 atranscriptome analyses that show widespread indole-3-acetic acid production by Sulfitobacter-related

263 se and indoleacetamide hydrolase can enhance indole-3-acetic acid production by up to ninefold.

264 Auxin/indole-3-acetic acid protein (Aux/IAA) luciferase (LUC)

265 ene family products, together with the AUXIN/INDOLE-3-ACETIC ACID proteins, regulate auxin-mediated t

266 All 16 maize auxin/indole-3-acetic acid repressor proteins were degraded in

267 intermediate indole-3-pyruvic acid (IPA) and indole-3-acetic acid rescues the tir2 short hypocotyl ph

268 sitivity to reactive oxygen species, reduced indole-3-acetic acid secretion, reduced biofilm and pell

269 This compound was also formed from labeled indole-3-acetic acid supplied to intact seedlings and ro

270 m cell division via secretion of the hormone indole-3-acetic acid, synthesized by the bacterium using

271 se mutant, but it also is less responsive to indole-3-acetic acid, synthetic auxins, auxin transport

272 1 seedlings accumulate nearly threefold more indole-3-acetic acid than the wild type.

273 oxygenases participates in converting IPA to indole-3-acetic acid, the main auxin in plants.

274 Indole-3-acetic acid, the major form of auxin in higher

275 unds related to the biosynthetic pathways of indole-3-acetic acid, the primary growth regulator in pl

276 trations but maintain wild-type responses to indole-3-acetic acid, the principle active auxin.

277 dehydrogenase to synthesize the phytohormone indole-3-acetic acid to elude host responses.

278 tration of the in vitro enzymic oxidation of indole-3-acetic acid to oxindole-3-acetic acid in higher

279 tic acid in the mesocotyl but essentially no indole-3-acetic acid to the coleoptile or primary leaves

280 perm provides both free and ester conjugated indole-3-acetic acid to the mesocotyl and coleoptile.

281 nositol and 1 picomole per plant per hour of indole-3-acetic acid to the shoot and thus is comparable

282 with auxin-regulated proteolysis of an auxin/indole-3-acetic acid transcription factor, and two impar

283 Basipetal indole-3-acetic acid transport and gravitropism are redu

284 The are mutant has increased indole-3-acetic acid transport and greater sensitivity t

285 We demonstrate that 2,4-D, but not indole-3-acetic acid transport is affected by mutations

286 avitropic response, a reduction in basipetal indole-3-acetic acid transport, and a delay in the asymm

287 Y6) mutant makes no flavonoids, has elevated indole-3-acetic acid transport, and exhibits a delayed g

288 ings exhibit increased and reduced basipetal indole-3-acetic acid transport, respectively.

289 function inhibits gravitropism and basipetal indole-3-acetic acid transport.

290 Cel1 and Cel5 mRNA decreased 99% when indole-3-acetic acid was added during ethylene treatment

291 contrast, Cel6 mRNA increased slightly when indole-3-acetic acid was added.

292 m was applied unilaterally to the cap and 3H-indole-3-acetic acid was applied to the basal cut surfac

293 Indole-3-acetic acid was detectable in D. dichotoma germ

294 noyl-Ile, salicylic acid, abscisic acid, and indole-3-acetic acid were compromised due to PAE9 loss o

295 m mass spectrometry and larger quantities of indole-3-acetic acid were detected.

296 Esters of indole-3-acetic acid were extracted and purified from th

297 l as enzymes that act upon jasmonic acid and indole-3-acetic acid were identified.

298 homolog RAMOSA1 ENHANCER LOCUS2, maize auxin/indole-3-acetic acids were able to repress AUXIN RESPONS

299 nd 3-mercaptopropionate, and the plant auxin indole 3-acetic acid, were released by S. elongatus at m

300 eld [3H]indole-3-acetyl-myo-inositol and [3H]indole-3-acetic acid which were then transported to the