ライフサイエンスコーパス: petunia

1 igated in plants of the South American genus Petunia.

2 ORISMATE MUTASE (PhCM1 and PhCM2) cDNAs from petunia.

3 omologous to those activating PH1 and PH5 in petunia.

4 sponsible for synthesis of methylbenzoate in petunia.

5 40 h in snapdragon and approximately 32 h in petunia.

6 es the flavonols required for germination in petunia.

7 eens of pollen/pollen tube cDNA libraries of petunia.

8 d to illustrate PhHCT and PhCSE functions of petunia.

9 required for pollen germination in maize and petunia.

10 element may have utility for gene tagging in petunia.

11 ome of different inbred lines and species of Petunia.

12 assembly is not conserved between tomato and petunia.

13 t, and the economically important ornamental petunia.

14 ODO1 and other FVBP genes to the evening in Petunia.

15 l in leaves but not flowers of nontransgenic petunias.

16 A-CoA) have previously been characterized in petunia, a plant with flowers rich in phenylpropanoid/be

17 Similarly, petunia acylsugars lack an acyl group at the R3' positio

18 Of the three identified petunia ADTs, expression of ADT1 was the highest in petu

19 such as tomato, pepper, tobacco, potato, and Petunia, all belonging to the Solanaceae family.

20 Like PH3, TTG2 can bind to petunia AN11 and the Arabidopsis homolog TTG1, complemen

21 f sequences of floral MADS-box proteins from petunia and found that the rate differences for 14 pairs

22 ontrolling crop timing and quality traits in Petunia and highlight the power of using multiple inters

23 attempted bulk isolation from protoplasts of Petunia and oat (Avena sativa).

24 logy to restorers in distantly related taxa (petunia and rice) than to PPRs elsewhere in the Mimulus

25 Petunia and snapdragon both synthesize methylbenzoate fr

26 n shown to enhance expression variegation in petunia and tobacco and to carry a hot spot for de novo

27 resent in tomato, potato, eggplants, pepper, petunia and tobacco can be inhibited by Avr2 with the ex

28 y increases zeatin levels, Sho expression in petunia and tobacco especially enhances the levels of ce

29 s resembling those of the Solanaceae species petunia and tobacco.

30 fingers similar to zinc finger proteins from petunia and wheat.

31 a, and Proliferating cell factor) genes from petunia, and have identified that these TCP-type transcr

32 , a regulator of anthocyanin biosynthesis in petunia, and more distantly related to those of the beta

33 Arabidopsis homolog TTG1, complement ph3 in petunia, and reactivate the PH3 target gene PH5.

34 d define aleurain homologues in Arabidopsis, Petunia, and tobacco cell extracts.

35 teins ANTHOCYANIN11 (AN11) (Petunia hybrida [petunia]) and TRANSPARENT TESTA GLABRA1 (TTG1) (Arabidop

36 nown to regulate anthocyanin accumulation in petunia anthers.

37 Genetically, the comparable step in the petunia anthocyanin pathway is controlled by the Anthocy

38 In turn, the four members of the petunia AP1/SQUA subfamily redundantly are required for

39 In turn, we demonstrate that the petunia AP2-type REPRESSOR OF B-FUNCTION (ROB) genes rep

40 s regulatory network in the Asterid model of petunia are similar to those in the Rosid model of Arabi

41 y genome sequences will enhance the value of Petunia as a model system for research on unique biologi

42 In Petunia, as in tobacco, fed radioactive Spd is bound to

43 na in the proximal-distal transcriptome, the Petunia axillaris fused and proximal corolla tube expres

44 a emit mostly benzaldehyde, while flowers of Petunia axillaris subsp. axillaris emit a mixture of vol

45 in a natural population of self-incompatible Petunia axillaris subsp. axillaris, and found that all t

46 a and the S(N) -haplotype of self-compatible Petunia axillaris, but not in the S-locus remnants of se

47 ce suppression of Ph-4CL1 did not affect the petunia benzenoid scent profile, whereas downregulation

48 In petunia, both the nuclear Rf gene and mitochondrial CMS-

49 s are similar to a pollen-expressed RLK from petunia, but they are expressed later during pollen deve

50 s involved transformation of tomato with the Petunia chi-a gene encoding chalcone isomerase.

51 In Petunia, constitutive expression of PhLHY depressed the

52 te and phenylethyl benzoate, both present in petunia corollas, with similar catalytic efficiencies.

53 no acid identity and are highly expressed in petunia corollas.

54 s for post-pollination ethylene synthesis in petunia corollas.

55 esis and sensitivity and ABA accumulation in petunia corollas.

56 ated in snapdragon cv Maryland True Pink and petunia cv Mitchell flowers using a volatile ester, meth

57 ethanol benzoyltransferase was isolated from petunia cv Mitchell using a functional genomic approach.

58 Transcripts for petunia cyclotides and acyclotides encode the shortest k

59 rsor structure, their sequences suggest that petunia cyclotides mature via the same biosynthetic rout

60 which is moderately to highly repetitive in petunia, does not predominantly localise to constitutive

61 RNA is spatially and temporally regulated in petunia during plant development.

62 ly (snapdragon) and nocturnally (tobacco and petunia) emitting plants.

63 We recently reported the identification of a petunia enzyme, isoeugenol synthase 1 (PhIGS1) that cata

64 acid sequence is most similar to that of the petunia Epf1 protein, they possess an interfinger linker

65 g that Pszf1 may be the pea homologue of the petunia Epf1 zinc finger gene.

66 cide resistance by stable integration of the petunia EPSPS gene into the tobacco chloroplast genome u

67 In petunia, expression of the gene responsible for methylbe

68 d floral color in the hummingbird-pollinated Petunia exserta (Solanaceae) from a colorless ancestor.

69 in addition to 29-32 kDa aleurain homologs, Petunia extracts contain a protein of approximately 50 k

70 nd PhPHB2, sequences that we identified in a petunia floral expressed sequence tag (EST) database, sh

71 R (BEN) confines the C-function to the inner petunia floral whorls, in parallel with the microRNA BLI

72 Petunia flower petals emit large amounts of isoeugenol,

73 Interestingly, ODO1-silenced transgenic petunia flowers accumulated higher EOBI transcript level

74 ntrations of supplied phenylalanine (Phe) in petunia flowers and capture flux redistributions caused

75 We also found that petunia flowers contain an enzyme, PhEGS1, that is highl

76 plant system, we simultaneously decreased in petunia flowers expression of all three Phe ammonia lyas

77 rom atomistic simulations and emissions from petunia flowers indicates that the role of the plant cut

78 Floral scent emission of petunia flowers is regulated by light conditions, circad

79 Down-regulation of PhCHD expression in petunia flowers resulted in reduced CHD enzyme activity,

80 sotope labeling, and transient expression in petunia flowers reveal that BALDH is capable of oxidizin

81 near least squares optimization of data from petunia flowers supplied with either 75 or 150 mm(2)H(5)

82 e to the formation of benzenoid compounds in petunia flowers.

83 ing interspecific variation in the styles of Petunia flowers.

84 entification and characterization of a novel petunia gene encoding an enzyme belonging to the BAHD ac

85 onal genomics approach, we have identified a petunia gene encoding cinnamoyl-CoA hydratase-dehydrogen

86 with TRV containing CHS and a fragment of a petunia gene encoding for 1-aminocyclopropane-1-carboxyl

87 acco rattle virus (TRV) bearing fragments of Petunia genes resulted in systemic infection and virus-i

88 The petunia genome contains a gene encoding a 9,10(9',10') c

89 ry and differential screening to identify 22 petunia germinating pollen clones.

90 cific glycine-rich proteins (GRP) related to petunia GRP1 (ptGRP1) was examined in three species of m

91 Simple leaves, such as those of petunia, have a single unit of blade, whereas compound l

92 in regulatory proteins ANTHOCYANIN11 (AN11) (Petunia hybrida [petunia]) and TRANSPARENT TESTA GLABRA1

93 By characterization of a Petunia hybrida adenosine triphosphate-binding cassette

94 ML2 and two MIXTA-related genes, PhMYB1 from Petunia hybrida and AtMYB16 from Arabidopsis thaliana, i

95 nalyses of CCRs from Medicago truncatula and Petunia hybrida and of an atypical CAD (CAD2) from M. tr

96 SBP1 from Petunia hybrida and Solanum chacoense is a putative E3 u

97 We have isolated and characterized Petunia hybrida cv. Mitchell phenylacetaldehyde synthase

98 Petunia (Petunia hybrida cv. Mitchell) flowers, which emit large

99 The Sho gene from Petunia hybrida encodes an enzyme responsible for the sy

100 l cuticle based on the epicuticular waxes of Petunia hybrida flower petals was formulated to test the

101 t a mixture of eugenol and isoeugenol, while Petunia hybrida flowers emit mostly isoeugenol with smal

102 Here, we used Petunia hybrida flowers, which are rich in Phe-derived v

103 A repetitive DNA sequence (RPS) from Petunia hybrida had previously been shown to enhance exp

104 The Petunia hybrida HAIRY MERISTEM (HAM) gene, a member of t

105 Petunia hybrida is a popular bedding plant that has a lo

106 ic expression of a MYB transcription factor, Petunia hybrida ODORANT1, to alter Phe and phenylpropano

107 gene PhGATA19, resulted in reduced fusion of Petunia hybrida petals, with silencing of both PhGATA19

108 ith high homology to the recently identified Petunia hybrida phenylacetaldehyde synthase involved in

109 Here, a gene encoding a Petunia hybrida plastidial cationic amino-acid transport

110 ation of a spontaneous mutable Hf1 allele in Petunia hybrida provided an opportunity to isolate and c

111 ind with a high degree of specificity to the Petunia hybrida S-ribonuclease.

112 ding Protein1 (Pi SBP1), almost identical to Petunia hybrida SBP1, which interacts with Pi SLFs, S-RN

113 with 59 to 61% sequence identity to petunia (Petunia hybrida) and potato (Solanum tuberosum) FLS.

114 proteins ANTHOCYANIN11 (AN11) from petunia (Petunia hybrida) and TRANSPARENT TESTA GLABRA1 (TTG1) fr

115 eas of star-type bicolour petals of petunia (Petunia hybrida) are caused by post-transcriptional gene

116 Using petunia (Petunia hybrida) as a model for vegetative branching, we

117 We show that the petunia (Petunia hybrida) C-clade genes PETUNIA MADS BOX GENE3 an

118 s tested by RNAi suppression of the petunia (Petunia hybrida) cinnamoyl-CoA reductase 1 (PhCCR1), whi

119 vestigate the metabolic pathways in petunia (Petunia hybrida) cv Mitchell leading from Phe to benzeno

120 s MYB99, a putative ortholog of the petunia (Petunia hybrida) floral scent regulator ODORANT1 (ODO1),

121 ropenes (isoeugenol and eugenol) in petunia (Petunia hybrida) flowers have the precursor 4-coumaryl c

122 nalysis of the benzenoid network in petunia (Petunia hybrida) flowers revealed that both pathways yie

123 Here, we show that in petunia (Petunia hybrida) flowers, which typically produce high p

124 olated in a genetic mutant screen a petunia (Petunia hybrida) Gibberellic Acid Insensitive, Repressor

125 regulates anthocyanin synthesis in petunia (Petunia hybrida) has been characterized.

126 he AIS1 protein is 59% identical to petunia (Petunia hybrida) isoeugenol synthase 1 and displays appa

127 We have isolated a cDNA from petunia (Petunia hybrida) leaves encoding a putative protein of 2

128 fied two potential CoA-ligases from petunia (Petunia hybrida) petal-specific cDNA libraries.

129 Agrobacterium-mediated infection of petunia (Petunia hybrida) plants with tobacco rattle virus (TRV)

130 Experiments with germinating petunia (Petunia hybrida) pollen and boronate-affinity chromatogr

131 Petunia (Petunia hybrida) pollen requires flavonols (Fl) to germi

132 xpression of VvMYB4a and VvMYB4b in petunia (Petunia hybrida) repressed general phenylpropanoid biosy

133 is a glutathione S-transferase from petunia (Petunia hybrida) required for efficient anthocyanin expo

134 s, tobacco (Nicotiana tabacum), and petunia (Petunia hybrida) resulted in plants with GA deficiency a

135 we show that in the asterid species petunia (Petunia hybrida), AP2B/BLIND ENHANCER (BEN) confines the

136 In petunia (Petunia hybrida), EMISSION OF BENZENOIDS II (EOBII) cont

137 ragrance in many flowers, including petunia (Petunia hybrida).

138 snapdragon (Antirrhinum majus), and petunia (Petunia hybrida).

139 Flowers of the artificial hybrid Petunia hybrida, a cross between P. integrifolia and P.

140 ajus, Epilobium hirsutum, Nicotiana tabacum, Petunia hybrida, and the cereal crop Setaria italica to

141 lyses of genomic DNA from the progenitors of Petunia hybrida, as well as from Nicotiana tabacum, indi

142 repetitive hypermethylated DNA fragment from Petunia hybrida, attracts DNA methylation when transferr

143 In Petunia hybrida, SL transport within the plant and towar

144 In Petunia hybrida, volatile emissions are dominated by pro

145 s to be the orthologous gene of PhEOBII from Petunia hybrida, which contributes to the regulation of

146 ed in estolide biosynthesis in the stigma of Petunia hybrida.

147 ity with the flavonoid-3',5'-hydroxylases of Petunia hybrida.

148 anum lycopersicum; SlpreproHypSys), petunia (Petunia hybrida; PhpreproHypSys), potato (Solanum tubero

149 extensions, faba bean [Vicia faba], petunia [Petunia hybrida], and tobacco [Nicotiana tabacum]).

150 Genetic analysis in petunia identified two vacuolar P-ATPases, PH1 and PH5,

151 rt Mosaic Virus promoter was introduced into petunia in the sense and antisense orientations using Ag

152 erization of PiSLF, an S-locus F-box gene of Petunia inflata (Solanaceae).

153 d genetic and physical map of the S locus of Petunia inflata and identify any additional genes locate

154 sed S2 -SLF1 (SLF1 with an S2 -haplotype) of Petunia inflata for co-immunoprecipitation (Co-IP) and m

155 19 S haplotypes from a natural population of Petunia inflata in Argentina, used reverse transcriptase

156 Here, we show that SLF1 of Petunia inflata is itself subject to degradation via the

157 y of the 20 lysine residues in S(3)-RNase of Petunia inflata might be targets for ubiquitination.

158 Petunia inflata possesses S-RNase-based self-incompatibi

159 Petunia inflata S-locus F-box (Pi SLF) is thought to fun

160 ng that non-self interactions between PiSLF (Petunia inflata SLF) and S-RNase are stronger than self-

161 on and characterization of PiORP1, an ORP of Petunia inflata that interacts with the cytoplasmic kina

162 lination-induced petal senescence process in Petunia inflata using a number of cell performance marke

163 Mb of the S(2) -haplotype of the S-locus in Petunia inflata using bacterial artificial chromosome cl

164 n-expressed receptor-like kinase of petunia (Petunia inflata), named PRK1, and we have shown by the a

165 calmodulin-like domain protein kinases from Petunia inflata, CALMODULIN-LIKE DOMAIN PROTEIN KINASE1

166 tdInsP2)-cleaving phospholipase C (PLC) from Petunia inflata, named Pet PLC1.

167 To identify the pollen S gene of Petunia inflata, we had previously used mRNA differentia

168 ity) locus regulates self-incompatibility in Petunia inflata; the S-RNase regulates pistil specificit

169 Flowers of Petunia integrifolia emit mostly benzaldehyde, while flo

170 Self-incompatibility in Petunia is controlled by the polymorphic S-locus, which

171 total FVBP emission in PhCM1 RNAi knockdown petunias is reduced by approximately 60-70%, and total c

172 spatial distribution of cyclotides within a petunia leaf section by MALDI imaging and observed that

173 tion tagging experiment we have identified a petunia line that showed CK-specific effects including e

174 The genomes reveal that the Petunia lineage has experienced at least two rounds of h

175 ounts of unedited RPS12 protein in different petunia lines correlate with the abundance of unedited t

176 Conversely, transgenic petunia lines expressing VvMYBC2-L1 and VvMYBC2-L3 showe

177 Additionally, in the Petunia lines in which PhLHY expression was reduced, the

178 Different petunia lines were found vary in the extent of rps12 tra

179 ionone synthesis in the corollas of selected petunia lines, indicating a significant role for this en

180 In petunia, loss-of-function nam mutants result in embryos

181 the petunia (Petunia hybrida) C-clade genes PETUNIA MADS BOX GENE3 and FLORAL BINDING PROTEIN6 (FBP6

182 aditional model systems such as Arabidopsis, Petunia, maize or rice.

183 Petunia may have evolved at least two types of SLF prote

184 GS) approach to knock down PH4 expression in petunia, measured volatile emission and internal pool si

185 (PhCCoAOMT1) from the petals of the fragrant petunia 'Mitchell'.

186 iple forms of RPS12 proteins are produced in petunia mitochondria as a result of partial editing, we

187 ibosomal protein S12 are partially edited in petunia mitochondria.

188 nedited-specific antibodies are present in a petunia mitochondrial ribosome fraction.

189 osttranscriptional C-repression mechanism in petunia, most likely not existing in Arabidopsis.

190 Both maize and petunia mutants are self-sterile due to a failure to pro

191 tivity has a pleiotropic effect in maize and petunia mutants: pollen fertility as well as flavonoid s

192 Here, we reveal the involvement of PH4, a petunia MYB-R2R3 transcription factor previously studied

193 This gene is a member of the NAC domain [petunia NAM (no apical meristem) and Arabidopsis ATAF1,

194 rch has revealed that stress-responsive NAC (petunia NAM and Arabidopsis ATAF1, ATAF2, and CUC2) tran

195 main transcription factor, homologous to the Petunia NAM and Arabidopsis CUC proteins.

196 The petunia NAM and ArabidopsisATAF1 and CUC2 genes define t

197 cyclic peptides we called "acyclotides" from petunia of the agronomically important Solanaceae plant

198 tracts DNA methylation when transferred into Petunia or other species.

199 gene, STENOFOLIA (STF), and its orthologs in Petunia, pea, and Nicotiana sylvestris are required for

200 ADTs, expression of ADT1 was the highest in petunia petals and positively correlated with endogenous

201 s synthesized predominantly via arogenate in petunia petals and uncover a novel posttranscriptional r

202 hat cell layer-specific homeotic activity in petunia petals differently impacts tube and limb develop

203 ADT1 suppression via RNA interference in petunia petals significantly reduced ADT activity, level

204 In petunia petals, AN11 and the bHLH protein AN1 activate,

205 ed Phe ((2)H(5)-Phe) was supplied to excised petunia petals.

206 alcohol, for which activity was detected in petunia petals.

207 t cell layers in the modular architecture of petunia petals.

208 Petunia (Petunia hybrida cv. Mitchell) flowers, which em

209 protein with 59 to 61% sequence identity to petunia (Petunia hybrida) and potato (Solanum tuberosum)

210 The WD40 proteins ANTHOCYANIN11 (AN11) from petunia (Petunia hybrida) and TRANSPARENT TESTA GLABRA1

211 White areas of star-type bicolour petals of petunia (Petunia hybrida) are caused by post-transcripti

212 Using petunia (Petunia hybrida) as a model for vegetative bran

213 We show that the petunia (Petunia hybrida) C-clade genes PETUNIA MADS BOX

214 thesis was tested by RNAi suppression of the petunia (Petunia hybrida) cinnamoyl-CoA reductase 1 (PhC

215 sed to investigate the metabolic pathways in petunia (Petunia hybrida) cv Mitchell leading from Phe t

216 rabidopsis MYB99, a putative ortholog of the petunia (Petunia hybrida) floral scent regulator ODORANT

217 e phenylpropenes (isoeugenol and eugenol) in petunia (Petunia hybrida) flowers have the precursor 4-c

218 ic flux analysis of the benzenoid network in petunia (Petunia hybrida) flowers revealed that both pat

219 Here, we show that in petunia (Petunia hybrida) flowers, which typically produ

220 e have isolated in a genetic mutant screen a petunia (Petunia hybrida) Gibberellic Acid Insensitive,

221 work that regulates anthocyanin synthesis in petunia (Petunia hybrida) has been characterized.

222 The AIS1 protein is 59% identical to petunia (Petunia hybrida) isoeugenol synthase 1 and disp

223 We have isolated a cDNA from petunia (Petunia hybrida) leaves encoding a putative pro

224 we identified two potential CoA-ligases from petunia (Petunia hybrida) petal-specific cDNA libraries.

225 Agrobacterium-mediated infection of petunia (Petunia hybrida) plants with tobacco rattle vir

226 Experiments with germinating petunia (Petunia hybrida) pollen and boronate-affinity c

227 Petunia (Petunia hybrida) pollen requires flavonols (Fl)

228 itutive expression of VvMYB4a and VvMYB4b in petunia (Petunia hybrida) repressed general phenylpropan

229 AN9 is a glutathione S-transferase from petunia (Petunia hybrida) required for efficient anthocy

230 rabidopsis, tobacco (Nicotiana tabacum), and petunia (Petunia hybrida) resulted in plants with GA def

231 Here, we show that in the asterid species petunia (Petunia hybrida), AP2B/BLIND ENHANCER (BEN) con

232 In petunia (Petunia hybrida), EMISSION OF BENZENOIDS II (EO

233 tant to fragrance in many flowers, including petunia (Petunia hybrida).

234 haliana, snapdragon (Antirrhinum majus), and petunia (Petunia hybrida).

235 mato (Solanum lycopersicum; SlpreproHypSys), petunia (Petunia hybrida; PhpreproHypSys), potato (Solan

236 tly pollen-expressed receptor-like kinase of petunia (Petunia inflata), named PRK1, and we have shown

237 To gain a better understanding of EIN2, a petunia (Petunia x hybrida cv Mitchell Diploid [MD]) hom

238 sion of alpha-Gal was modified in transgenic petunia (Petunia x hybrida cv Mitchell).

239 We transformed petunia (Petunia x hybrida cv V26) with P(SAG12)-IPT.

240 Here, we studied petunia (Petunia x hybrida) petals that form a limb and

241 nsitive tomato (Lycopersicon esculentum) and petunia (Petunia x hybrida) plants were conducted to det

242 In many flowering plants, such as petunia (Petunia x hybrida), ethylene produced in floral

243 P1/SQUA genes in the distant asterid species petunia (Petunia x hybrida).

244 e sheath extensions, faba bean [Vicia faba], petunia [Petunia hybrida], and tobacco [Nicotiana tabacu

245 The basil and petunia phenylpropene-forming enzymes belong to a struct

246 ified and characterized the phylogenetics of petunia PIF family members (PhPIFs).

247 ction of chalcone synthase A transgenes into petunia plants can result in degradation of chalcone syn

248 action of PPR genes, we generated transgenic petunia plants expressing a functional tagged version of

249 red to wild-type MD and ethylene-insensitive petunia plants expressing the Arabidopsis etr1-1 gene fo

250 was validated using flowers from transgenic petunia plants in which benzyl CoA:benzyl alcohol/phenyl

251 est this hypothesis, we generated transgenic petunia plants in which the expression of BPBT, the gene

252 Transgenic petunia plants with reduced PhEIN2 expression were compa

253 vity also affected the overall morphology of petunia plants, resulting in larger flowers and leaves,

254 observed in ethylene-insensitive transgenic petunia plants.

255 ower abscission when expressed in tomato and petunia plants.

256 flowers and a vein-clearing symptom in aged petunia plants.

257 peptide fragments of F3GalTase purified from petunia pollen were used to isolate a full-length cDNA c

258 Petunia possesses self-incompatibility, by which pistils

259 e polymorphisms (SNPs) for the interspecific Petunia recombinant inbred line (RIL) population - P. ax

260 D APICAL DOMINANCE 1 (DAD1) genes of pea and petunia, respectively, are orthologous to MAX4 and funct

261 The Petunia restorer of fertility gene product is a mitochon

262 Down-regulating alpha-Gal in petunia results in an increase in freezing tolerance at

263 later during pollen development than is the petunia RLK.

264 using a cross-species method by hybridizing petunia samples to a 4 x 44 K Agilent tomato array.

265 and II, which together with ODO1 coregulate petunia scent biosynthesis genes.

266 d metabolism and compare this mechanism with petunia scent control.

267 and higher order mutants, we report that the petunia SEP1/SEP2/SEP3 orthologs together with AGL6 enco

268 nation functions, with a master role for the petunia SEP3 ortholog FLORAL BINDING PROTEIN2 (FBP2).

269 pressed Cullin1 gene with high similarity to Petunia SI factors interacts genetically with a gene at

270 sympetaly in the asterid core eudicot genus Petunia (Solanaceae), we carried out global and fine-sca

271 Reciprocal transfer of traits between Petunia species now shows that colour and scent are equa

272 The element is named Petunia Spm-like (Psl).

273 Petunia spp. synthesize acylsugars that are structurally

274 ermination-inducing constituent in wild-type petunia stigma extracts.

275 cylglycerol-based estolide polyesters in the petunia stigma.

276 The peptides were active in a petunia suspension culture bioassay at nanomolar concent

277 ene insensitive (44568) and Mitchell Diploid petunias, that multiple components of emission of volati

278 In Petunia, the polymorphic S-locus determines self/non-sel

279 ps of ASATs are predicted between tomato and petunia, these are not supported by biochemical assays.

280 way, have been isolated and characterized in petunia through reverse genetic and biochemical approach

281 itial events enable the SL receptor DAD2 (in petunia) to interact with the F-box protein PhMAX2A of t

282 roduction, we cloned and characterized three petunia transcripts with high similarity to p-coumarate

283 lcone synthase (chs) co-suppression among 47 Petunia transformants.

284 topic labeling experiments were performed in petunia transgenic lines.

285 ty in the regulatory circuitry that controls petunia vacuolar acidification and Arabidopsis hair deve

286 we focused on an endogenous pararetrovirus, petunia vein clearing virus (PVCV), because this virus m

287 SV), Tobacco vein clearing virus (TVCV), and Petunia vein clearing virus (PVCV), can generate episoma

288 oate emission, with minimal changes in other petunia VOCs.

289 d to the Trans Proteomic Pipeline project's 'Petunia' web interface, but can also be run as a command

290 Petunia x hybrida cv 'Mitchell Diploid' floral volatile

291 n a better understanding of EIN2, a petunia (Petunia x hybrida cv Mitchell Diploid [MD]) homolog of t

292 lpha-Gal was modified in transgenic petunia (Petunia x hybrida cv Mitchell).

293 We transformed petunia (Petunia x hybrida cv V26) with P(SAG12)-IPT.

294 In Petunia x hybrida cv. 'Mitchell Diploid' floral fragranc

295 to the synthesis of FVBPs in the corolla of Petunia x hybrida cv. 'Mitchell Diploid'.

296 Recently an R2R3-MYB was identified in Petunia x hybrida line P720 to have a role in the transc

297 Here, we studied petunia (Petunia x hybrida) petals that form a limb and tube thro

298 omato (Lycopersicon esculentum) and petunia (Petunia x hybrida) plants were conducted to determine if

299 In many flowering plants, such as petunia (Petunia x hybrida), ethylene produced in floral organs a

300 enes in the distant asterid species petunia (Petunia x hybrida).