Flower Color Development and Nano-Science

ChemInform ◽  
2004 ◽  
Vol 35 (40) ◽  
Author(s):  
Kumi Yoshida ◽  
Kin-ichi Oyama ◽  
Tadao Kondo
2004 ◽  
Vol 62 (5) ◽  
pp. 490-499 ◽  
Author(s):  
Kumi Yoshida ◽  
Kin-ichi Oyama ◽  
Tadao Kondo

Life ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 113
Author(s):  
Xueqiang Cui ◽  
Jieling Deng ◽  
Changyan Huang ◽  
Xuan Tang ◽  
Xianmin Li ◽  
...  

Dendrobium nestor is a famous orchid species in the Orchidaceae family. There is a diversity of flower colorations in the Dendrobium species, but knowledge of the genes involved and molecular mechanism underlying the flower color formation in D. nestor is less studied. Therefore, we performed transcriptome profiling using Illumina sequencing to facilitate thorough studies of the purple color formation in petal samples collected at three developmental stages, namely—flower bud stage (F), half bloom stage (H), and full bloom stage (B) in D. nestor. In addition, we identified key genes and their biosynthetic pathways as well as the transcription factors (TFs) associated with purple flower color formation. We found that the phenylpropanoid–flavonoid–anthocyanin biosynthesis genes such as phenylalanine ammonia lyase, chalcone synthase, anthocyanidin synthase, and UDP-flavonoid glucosyl transferase, were largely up-regulated in the H and B samples as compared to the F samples. This upregulation might partly account for the accumulation of anthocyanins, which confer the purple coloration in these samples. We further identified several differentially expressed genes related to phytohormones such as auxin, ethylene, cytokinins, salicylic acid, brassinosteroid, and abscisic acid, as well as TFs such as MYB and bHLH, which might play important roles in color formation in D. nestor flower. Sturdy upregulation of anthocyanin biosynthetic structural genes might be a potential regulatory mechanism in purple color formation in D. nestor flowers. Several TFs were predicted to regulate the anthocyanin genes through a K-mean clustering analysis. Our study provides valuable resource for future studies to expand our understanding of flower color development mechanisms in D. nestor.


2019 ◽  
Vol 20 (19) ◽  
pp. 4743 ◽  
Author(s):  
Hongli Liu ◽  
Qian Lou ◽  
Junren Ma ◽  
Beibei Su ◽  
Zhuangzhuang Gao ◽  
...  

Grape hyacinth (Muscari spp.) is a popular ornamental plant with bulbous flowers noted for their rich blue color. Muscari species have been thought to accumulate delphinidin and cyanidin rather than pelargonidin-type anthocyanins because their dihydroflavonol 4-reductase (DFR) does not efficiently reduce dihydrokaempferol. In our study, we clone a novel DFR gene from blue flowers of Muscari. aucheri. Quantitative real-time PCR (qRT-PCR) and anthocyanin analysis showed that the expression pattern of MaDFR had strong correlations with the accumulation of delphinidin, relatively weak correlations with cyanidin, and no correations with pelargonidin. However, in vitro enzymatic analysis revealed that the MaDFR enzyme can reduce all the three types of dihydroflavonols (dihydrokaempferol, dihydroquercetin, and dihydromyricetin), although it most preferred dihydromyricetin as a substrate to produce leucodelphinidin, the precursor of blue-hued delphinidin. This indicated that there may be other functional genes responsible for the loss of red pelargonidin-based pigments in Muscari. To further verify the substrate-specific selection domains of MaDFR, an assay of amino acid substitutions was conducted. The activity of MaDFR was not affected whenever the N135 or E146 site was mutated. However, when both of them were mutated, the catalytic activity of MaDFR was lost completely. The results suggest that both the N135 and E146 sites are essential for the activity of MaDFR. Additionally, the heterologous expression of MaDFR in tobacco (Nicotiana tabacum) resulted in increasing anthocyanin accumulation, leading to a darker flower color, which suggested that MaDFR was involved in color development in flowers. In summary, MaDFR has a high preference for dihydromyricetin, and it could be a powerful candidate gene for genetic engineering for blue flower colour modification. Our results also make a valuable contribution to understanding the basis of color variation in the genus Muscari.


2006 ◽  
Vol 67 (10) ◽  
pp. 992-998 ◽  
Author(s):  
Kumi Yoshida ◽  
Sayoko Kitahara ◽  
Daisuke Ito ◽  
Tadao Kondo

2020 ◽  
Author(s):  
Jianjun Li ◽  
Chenglin Ye ◽  
Jingxiao Ma ◽  
Ting Cheng ◽  
Yan Lv ◽  
...  

Abstract Background:‘Yujin 2’ is new variety of Lonicera japonica Thunb and its flower color can change from red to yellow; hence, it is a good model for investigating flower color development mechanisms. Results:High throughput transcriptome sequencing of seven flower development stages of Yujin No.2 was carried out, and 133,487 unigenes were annotated, among which 73,088 were differentially expressed. Then the real-time PCR analysis was carried out. Further, the number of up-regulated DEGs was higher than those that were down-regulated. Of these annotated DEGs, plant hormone signal transduction, phenylpropanoid biosynthesis, and flavonoid biosynthesis were active throughout the flowering process during each stage, whereas carotenoid biosynthesis was inactive in the S1-6 stages. Furthermore, phenylalanine synthesis was enhanced in the S1 phase; however, anthocyanin synthesis was weakened in the S5 and S6 phases, which may be consistent with the changes in petal color of ‘Yujin 2’ from red (S1) to white (S5) and gold (S6). The results showed that 114 unigenes were associated with anthocyanin metabolism, and 72 were significantly upregulated or downregulated. According to the analysis of TFs in anthocyanin metabolism, we obtained 47 transcription factors, which belonged to 18 families. The LjDFR, LjABCB1, LjMYC6, LjDDB2, and LjANS genes rapidly increased during the first three stages. However, only LjF3'5'H expression was significantly down-regulated at S5, which was consistent with anthocyanin accumulation. Conclusions:This study developed a transcriptome profile of flower color generation for L. japonica as well as annotated unigene sets of seven anthesis phases, thereby providing possibilities for improving the germplasm of L. japonica with genetic engineering technologies and cultivating new varieties of different colors.


1996 ◽  
Vol 54 (1) ◽  
pp. 42-53 ◽  
Author(s):  
Tadao KONDO ◽  
Minoru UEDA ◽  
Kumi YOSHIDA

HortScience ◽  
1991 ◽  
Vol 26 (9) ◽  
pp. 1215-1216 ◽  
Author(s):  
David B. Rubino

Fifteen cultivated genotypes of Exacum affine Balf. were evaluated for flower development and for flower and leaf color at 0 days (marketable stage, ≈ 25% of plant canopy covered with flowers), and after 14 and 28 days of maintenance in a low-irradiance environment (≈ 1 μmol·m-2·s-1 photosynthetically active radiation from cool-white fluorescent lights for 12 hours daily). Flowering and flower color development were reduced, but leaf color improved during maintenance under low irradiance. Variability was observed among the 15 genotypes for flower bud and flower color development in a low-irradiance environment.


Weed Science ◽  
1980 ◽  
Vol 28 (3) ◽  
pp. 347-351 ◽  
Author(s):  
M. K. McCarty ◽  
H. J. Gorz ◽  
F. A. Haskins

Four flower-color phenotypes were observed in a population of musk thistle (Carduus thoermeri Weinm.). This plant has been commonly referred to as C. nutans L. The four phenotypes were: purple corolla and purple pollen, pink corolla and white pollen, white corolla and purple pollen, and white corolla and white pollen. In four generations, 177 self-pollinated individuals of these four phenotypes produced 2123 progeny plants that were classified. Results support the hypothesis that three independent gene pairs were involved in determining the four flower phenotypes. The gene pairs have been designated P/p, W/w, and Pi/pi. It was postulated that all three dominant alleles, P, W, and Pi, must be present to produce both purple corollas and purple pollen. The p allele prevents color development in both corollas and pollen; the w allele eliminates color in corollas but does not affect pollen color; and the pi allele dilutes corolla color from purple to pink and eliminates pollen color. Height measurements of progenies of self-pollinated plants indicated that decreased plant height was associated with inbreeding. On the basis of the evidence presented, the musk thistle plants used in these experiments appear to belong to a single species.


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