ライフサイエンスコーパス: Petunia hybrida

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

21 In Petunia hybrida cv. Mitchell flowers, the biosynthesis a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

41 This redundancy is lost in Petunia hybrida, not because of the inability of PhCUL1-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

59 In Petunia hybrida, volatile emissions are dominated by pro

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