Petal Pigmentation Research Articles

Methylation Modification in Ornamental Plants: Impact on Floral Aroma and Color.

Methylation represents a crucial class of modification that orchestrates a spectrum of regulatory roles in plants, impacting ornamental characteristics, growth, development, and responses to abiotic stress. The establishment and maintenance of methylation involve the coordinated actions of multiple regulatory factors. Methyltransferases play a pivotal role by specifically recognizing and methylating targeted sites, which induces alterations in chromatin structure and gene expression, subsequently influencing the release of volatile aromatic substances and the accumulation of pigments in plant petals. In this paper, we review the regulatory mechanisms of methylation modification reactions and their effects on the changes in aromatic substances and pigments in plant petals. We also explore the potential of methylation modifications to unravel the regulatory mechanisms underlying aroma and color in plant petals. This aims to further elucidate the synthesis, metabolism, and regulatory mechanisms of various methylation modifications related to the aroma and color substances in plant petals, thereby providing a theoretical reference for improving the aroma and color of plant petals.

Characterization of key genes in anthocyanin and flavonoid biosynthesis during floral development in Rosa canina L.

This study investigates the transition of Rosa canina L. petals from pink to white, driven by genetic and biochemical factors. It characterizes the expression of ten key genes involved in anthocyanin and flavonoid biosynthesis across five developmental stages, correlating gene expression with flavonoid and anthocyanin concentrations and colorimetric changes. Initially, the petals exhibit a rich flavonoid profile, dominated by Rutin and Kaempferol derivatives. The peak anthocyanin concentration, corresponding to the deepest color saturation, occurs in the subsequent stage. Advanced chromatographic analyses identify key flavonoids persisting into the final white petal stage. Notably, the ANS gene shows a dramatic 137.82-fold increase in expression at the final stage, indicating its crucial role in petal color maturation despite the absence of visible pigmentation. The study provides a comprehensive characterization of the genetic and biochemical mechanisms underlying petal pigmentation, suggesting that reduced anthocyanin synthesis and increased flavonol concentration led to white petals. It also highlights the roles of other genes such as PAL, CCD1, FLS, CHI, CHS, UFGT, F3H, DFR, and RhMYB1, indicating that post-translational modifications and other regulatory mechanisms may influence anthocyanin stability and degradation.

Exploring the Mechanisms Underlying Petal Pigmentation Differences in Two Cultivars of Physalis philadelphica Based on HPLC and NGS

Exploring the Mechanisms Underlying Petal Pigmentation Differences in Two Cultivars of Physalis philadelphica Based on HPLC and NGS

Preharvest calcium application boosts the biostimulatory effect of protein hydrolysate by improving the postharvest life of gerbera cut flower

Among the various categories of plant biostimulants currently available on the market, protein hydrolysates, primarily composed of a heterogeneous mixture of peptides and amino acids, have gradually gained prominence. Nevertheless, the positive effects of these products on the production and longevity of cut flowers are still not well-explored. The purpose of this research was thus to fill this gap by assessing the impacts of a plant-derived protein hydrolysate, with and without the addition of calcium (PH and PH+Ca), on the growth, quality, and vaselife of two cultivars of gerbera with different pigmentation (Brunello and Tommy, red and yellow, respectively). Regardless of cultivar, foliar application of PH improved growth, flower production, absorption of key nutrients, and photosynthetic performance, compared to the control. On the other hand, the PH+Ca treatment exhibited the best results during vaselife. For both cultivars, the application of PH+Ca increased the durability of gerbera flowers, reducing the weight loss by an average of 19 % on day 10 compared to untreated flowers. Although cultivar-dependent, the positive effects of the PH+Ca biostimulant were also observed on petal pigmentation during vase life. For the Tommy cultivar, for instance, the Chroma values of treated flowers remained unchanged during the post-harvest period, unlike what was observed for untreated flowers. Therefore, considering the positive effects resulting from the use of PH and PH+Ca on gerbera, it would be interesting to further investigate the use of biostimulants in floriculture to increase the sustainability of the sector and especially with regard to cut flower production, without reducing or even improving the performance that is conventionally achieved.

Functional redundancy of R2R3-MYB transcription factors involved in anthocyanin biosynthesis is manifested in anther pigmentation in petunia.

Accumulation of anthocyanin provides pigmentation in plant tissues. In petunia, gene expression profiles that lead to anthocyanin production have been extensively characterized in terms of pigmentation in flower petals. Anthers are also pigmented, but the transcriptional control of the genes for anthocyanin biosynthesis in anthers has not been fully characterized. Here we addressed this issue by analyzing the expression of structural genes and genes encoding transcription factors (TFs) of the pathway. Ectopic expression of the PURPLE HAZE (PHZ) gene encoding an R2R3-MYB activator induced pigmentation in anthers. The pigmentation was accompanied by an increase in mRNA levels of AN1, MYB27 and MYBx among the genes encoding TFs. Among the structural genes, mRNA levels of four late biosynthetic genes (LBGs) were higher in the transformants than in the wild type. Analyses of gene expression profile using commercial varieties indicated that mRNA levels of MYB27, MYBx and LBGs and of AN4, responsible for anther pigmentation, were higher in pigmented anthers than in nonpigmented. Differences in the gene expression profile between pigmented anthers induced by ectopic PHZ expression and their nonpigmented control and those between pigmented anthers and nonpigmented anthers of existing varieties were thus remarkably similar. These observations suggest that a high level of expression of the LBGs is characteristic of pigmented anthers and that ectopic PHZ expression in the an4 - genetic background induced changes in the transcriptional network toward the state established in pigmented anthers, which is intrinsically brought about by the function of AN4.

FaMYB6-like negatively regulates FaMYB10-induced anthocyanin accumulation during strawberry fruit ripening

Anthocyanins are one of the essential compounds affecting the quality of strawberry fruit. Several R2R3-MYB transcription factors have been well characterized as the anthocyanin activators in strawberry. However, we still lack valuable information on how R2R3-MYB repressors regulate strawberry anthocyanin accumulation. Here, we cloned a novel R2R3-MYB gene, FaMYB6-like, and characterized its repressive role during anthocyanin accumulation. FaMYB6-like encodes a nuclear localization protein, which was clustered into the FaMYB1-like type repressor clade in phylogenetic analysis. FaMYB6-like showed high expressions in anthocyanin-accumulating fruit and low transcript abundance in flowers, vegetative tissues, and early development stages of fruit. Transient overexpression of FaMYB6L-like repressed the expression of anthocyanin biosynthetic and transport genes, and reduced anthocyanin content in postharvest strawberry fruit. Transgenic tobacco lines overexpressing FaMYB6-like displayed a reduction in petal pigmentation. Overexpression of FaMYB6L-like in white-fleshed strawberry inhibited anthocyanin accumulation induced by FaMYB10. Protein interaction and promoter activation assays revealed that FaMYB6-like repressed the activation of target gene promoters by FaMYB10-FabHLH3 activation complex via its interaction with FabHLH3. Additionally, FaMYB6-like promoter activity can be activated by FaMYB10-FabHLH3 complex. Taken together, our study revealed that FaMYB6-like acted as a transcriptional repressor involved in an ‘activator-and-repressor’ feedback regulation mechanism for maintaining the balance of anthocyanin concentrations.

Selection and Validation of qRT-PCR Internal Reference Genes to Study Flower Color Formation in Camellia impressinervis.

Real-time quantitative PCR (qRT-PCR) is a pivotal technique for gene expression analysis. To ensure reliable and accurate results, the internal reference genes must exhibit stable expression across varied experimental conditions. Currently, no internal reference genes for Camellia impressinervis have been established. This study aimed to identify stable internal reference genes from eight candidates derived from different developmental stages of C. impressinervis flowers. We employed geNorm, NormFinder, and BestKeeper to evaluate the expression stability of these candidates, which was followed by a comprehensive stability analysis. The results indicated that CiTUB, a tubulin gene, exhibited the most stable expression among the eight reference gene candidates in the petals. Subsequently, CiTUB was utilized as an internal reference for the qRT-PCR analysis of six genes implicated in the petal pigment synthesis pathway of C. impressinervis. The qRT-PCR results were corroborated by transcriptome sequencing data, affirming the stability and suitability of CiTUB as a reference gene. This study marks the first identification of stable internal reference genes within the entire genome of C. impressinervis, establishing a foundation for future gene expression and functional studies. Identifying such stable reference genes is crucial for advancing molecular research on C. impressinervis.

DcbHLH1 interacts with DcMYB1 and DcMYB2 to dynamically regulate petal pigmentation in Dianthus caryophyllus

The carnation (Dianthus caryophyllus L.) is a beloved and widely embraced ornamental flower worldwide, celebrated for vibrant hues, delightful fragrance, and prolonged blooming season. Within the petals of carnation blooms, anthocyanins, natural pigments, are responsible for the diverse range of captivating colors they display. However, the intricate molecular processes orchestrating the synthesis of these anthocyanins in carnations remain unclear. This study unveils DcbHLH1 as a pivotal regulator actively participating in anthocyanin biosynthesis within carnation flowers. Y1H and dual-LUC provided evidences that DcbHLH1 exhibited direct binding to the promoters of DcCHS and DcDFR, consequently leading to the activation of their gene expressions. In the earlier stages (S2 and S3) of blooming, DcMYB1 synergistically enhances the transcriptional activation capacity of DcbHLH1 through their collaborative interaction. As the flower matures into the later stages (S4 and S5), DcMYB1 expression exhibited a rapid decline. Concurrently, the repressor gene, DcMYB2, experienced a swift upsurge in expression, ultimately inhibiting anthocyanin biosynthesis and curtailing the transcriptional activation activity of DcbHLH1 through direct interaction with DcbHLH1. Our results show a narrative of the dynamic interplay between DcbHLH1-DcMYB1 and DcbHLH1-DcMYB2, unveiling their roles in orchestrating the array of hues that adorn carnation petals over various flowering stages. These findings offer novel insights into the regulatory mechanisms influencing anthocyanin biosynthesis in ornamental plants.

Cell layer-specific expression of the homeotic MADS-box transcription factor PhDEF contributes to modular petal morphogenesis in petunia.

Floral homeotic MADS-box transcription factors ensure the correct morphogenesis of floral organs, which are organized in different cell layers deriving from distinct meristematic layers. How cells from these distinct layers acquire their respective identities and coordinate their growth to ensure normal floral organ morphogenesis is unresolved. Here, we studied petunia (Petunia × hybrida) petals that form a limb and tube through congenital fusion. We identified petunia mutants (periclinal chimeras) expressing the B-class MADS-box gene DEFICIENS in the petal epidermis or in the petal mesophyll, called wico and star, respectively. Strikingly, wico flowers form a strongly reduced tube while their limbs are almost normal, while star flowers form a normal tube but greatly reduced and unpigmented limbs, showing that petunia petal morphogenesis is highly modular. These mutants highlight the layer-specific roles of PhDEF during petal development. We explored the link between PhDEF and petal pigmentation, a well-characterized limb epidermal trait. The anthocyanin biosynthesis pathway was strongly downregulated in star petals, including its major regulator ANTHOCYANIN2 (AN2). We established that PhDEF directly binds to the AN2 terminator in vitro and in vivo, suggesting that PhDEF might regulate AN2 expression and therefore petal epidermis pigmentation. Altogether, we show that cell layer-specific homeotic activity in petunia petals differently impacts tube and limb development, revealing the relative importance of the different cell layers in the modular architecture of petunia petals.

Seleção de acessos de rosa-do-deserto com alto potencial ornamental

Abstract Adenium obesum belongs to the Apocynaceae family and is characterized as a succulent shrub with a multitude of botanical and morphological features of ornamental interest. The aim of this study was to evaluate the genetic dissimilarity of 28 accessions of A. obesum using morphological descriptors and multivariate techniques with the aim of pre-selecting the genotypes with the greatest ornamental potential. The distribution of the number of flowers throughout the year showed two flowering peaks in January and September. Twenty-one petal pigmentation patterns were identified, and 50% of the accessions had double-petal arrangement. The Gower’s algorithm and the UPGMA-generated dissimilarity matrix indicated the formation of three groups. While Tocher’s clustering method separated the accessions into eight groups showing greater ability to distinguish the evaluated genotypes. In conclusion, the multivariate analyses applied were effective in accessing the genetic diversity among the 28 accessions evaluated. The accessions ICA001, ICA005, ICA006, ICA018, ICA019, and ICA027 were preselected to compose the germplasm collection due to their high ornamental potential.

Sunflower physiological adjustments to elevated CO2 and temperature do not improve reproductive performance and productivity

High levels of carbon dioxide (eCO2) and temperature (eT) affect the physiological performance of sunflowers, but the full extent of their influence on productivity and floral traits remains to be disclosed. Here, we show that eT increased the maximum rate of carboxylation, maximum electron transport capacity, and net rate of triose-phosphate production, indicating enhanced carbon fixation. Although eT increased reactive oxygen species (ROS) concentration in the leaves, no signs of lipid peroxidation in cellular membranes were detected, and plants activated antioxidant systems to counteract the increase in ROS. Moreover, under eT, sunflower pollen exhibited higher amounts of Fe and Zn but also experienced reduced development and productivity due to increased production of empty seeds. In response to eCO2, sunflowers reduced stomatal conductance, limiting water loss, contributing to increased water use efficiency and enhanced photosynthesis. Additionally, under eCO2, sunflowers displayed pollen with higher levels of P, increased biomass gain, and productivity. Lastly, the isolated effects of eCO2 and eT had contrasting impacts on inflorescence size, but the combination of these factors did not result in changes compared to current conditions. However, both factors contributed to increased carotenoid content in ray florets. In contrast, the eCO2eT combination enhanced photosynthesis, flavonoid production in ray florets, and reduced the amount of K and Cu in pollen. In conclusion, eCO2eT improved the physiological performance of sunflowers, but this was not accompanied by increased growth and productivity. The reduction in seed production in sunflowers can have negative impacts on ecology, genetic diversity, and agricultural economy. While eCO2eT did not affect sunflower inflorescence size, they did affect petal pigmentation and pollen quality, which can have significant implications for pollinator health. Understanding the full extent of eCO2eT effects poses a challenge for developing effective mitigation strategies and optimizing agricultural sustainability in the face of climate change.

A novel transcription factor PsMYBM enhances the biosynthesis of anthocyanins in response to light in tree peony

Light is a vital environmental factor that affects the biosynthesis of anthocyanin, and the ornamental and economic value of ornamental plants can be improved by properly regulating the conditions of light for their growth. Tree peony (Paeonia suffruticosa Andrews), “the king of flowers” in China, is popular in the whole country and contributes to cultivar breeding throughout the world. In the tree peony industry, light affects not only flower color and quality when the cultivation of flowers is forced but also its ornamental value in specific gardens and fields. However, the molecular mechanism on how light regulates the biosynthesis of anthocyanin is unclear. In this study, darkness was found to decrease the pigmentation of flower petals in the tree peony cultivar ‘Higurashi’. The differentially expressed genes responsible for anthocyanin biosynthesis were obtained through a comparative transcriptome analysis of flower petals under light/dark conditions. This led to the identification of an R2R3-MYB transcription factor designated PsMYBM. The transient silencing of PsMYBM reduced the biosynthesis of anthocyanins in the petals, while its overexpression promoted the formation of various colors in organs in transgenic tobacco (Nicotiana tabacum cv. Nc89) plants. In addition, it has been demonstrated that PsMYBM can directly activate the promotors of PsCHS and PsF3H. Moreover, light-responsive elements were also identified in the PsMYBM promoter, which could be directly bound by the light signal factor PsHY5. This study illuminates the mechanism of anthocyanin biosynthesis in response to light in tree peony, which could be applied to other woody ornamental plants. It also provides key gene resources to improve the flower color and germplasm innovation.

Analysis of Physiological and Biochemical Factors Affecting Flower Color of Herbaceous Peony in Different Flowering Periods

Herbaceous peony (Paeonia lactiflora Pall.) is a famous ornamental plant, and the study of its flower color is of great significance for cultivating new flower varieties. To explore the factors driving the formation and change of herbaceous peony flower color, we selected five herbaceous peony varieties at four flowering stages to determine the change in flower color, petal area, and microstructure. We also examined the composition and content of petal pigments, soluble sugar and soluble protein content, pH value of cell fluid, and water content. Finally, we analyzed the correlations between each factor. We found that Pn3G5G, Pg3G5G, and Cy3G5G were the main anthocyanin components in red and purple petals. Qu3G, Qu7G, Is3G, and lutein play important roles in yellow petal formation. The change in herbaceous peony flower color during the flowering process is directly caused by changes in the anthocyanin and carotenoid content in petals. In addition, changes in other physiological indices also influence the change in flower color. This study explored the physiological and biochemical factors affecting the color of herbaceous peony petals, which has an important practical significance for studying the physiological mechanism of herbaceous peony flower color formation and color breeding of new flowers.

Functional identification of anthocyanin glucosyltransferase genes: a Ps3GT catalyzes pelargonidin to pelargonidin 3-O-glucoside painting the vivid red flower color of Paeonia.

Glycosylation from an anthocyanidin 3-O-glucosyltransferase Ps3GT (PsUGT78A27) facilitates the accumulation of pelargonidin 3-O-glucoside, which defines the vivid red flower color and occurs only in specific peony tree cultivars. Although tree peony cultivars of Chinese and Japanese both originated from China, vivid red color is only found in flowers of Japanese cultivars but not of Chinese cultivar groups. In this study, a Japanese tree peony cultivar 'Taiyoh' with vivid red petals and a Chinese tree peony cultivar 'Hu Hong' with reddish pink petals were chosen as the experimental materials. Flavonoids profiling indicated that pelargonidin 3-O-glucoside (Pg3G) detected only in Japanese cultivar contributed to vivid red color of tree peony petals, while pelargonidin 3,5-di-O-glucoside (Pg3G5G) found in both of Japanese and Chinese cultivars was responsible for pink flower color. Through the integration of full-length transcriptome sequencing and in vitro enzymatic activity analysis, two anthocyanin glucosyltransferase genes PsUGT78A27 and PsUGT75L45 were isolated from the petals of tree peony, and their encoding products exhibited enzymatic activities of pelargonidin 3-O-glucosyltransferase and anthocyanin 5-O-glucosyltransferase, respectively. Further quantitative real-time PCR revealed that PsUGT78A27 displayed high expression in petals of both cultivars and PsUGT75L45 was expressed at high levels in cultivar 'Hu Hong' only. Using a gene gun technique, the GFP fusion proteins of PsUGT78A27 and PsUGT75L45 were visualized to be cytoplasmic and nuclear localization in the epidermal cells of tree peony petals, and the glucosylation function of PsUGT78A27 and PsUGT75L45 to alter petal color of tree peony and herbaceous peony had been directly validated in vivo. These results demonstrated that PsUGT78A27 and PsUGT75L45 are key players for the presence or absence of vivid red flower color in tree peony cultivars. Our findings further elucidated the chemical and molecular mechanism of petal pigmentation of Paeonia and could help breed the Paeonia cultivars possessing novel flower colors.

Anthocyanin metabolism in Nelumbo: translational and post-translational regulation control transcription

BackgroundLotus (Nelumbo Adans.) is used as an herbal medicine and the flowers are a source of natural flavonoids. ‘Da Sajin’, which was firstly found in the plateau area, is a natural mutant in flower color with red streamers dyeing around white petals.ResultsThe LC–MS-MS results showed that eight anthocyanin compounds, including cyanidin 3-O-glucoside, cyanidin 3-O-galactoside, malvidin 3-O-galactoside, and malvidin 3-O-glucoside, were differentially enriched in red-pigmented tissues of the petals, whereas most of these metabolites were undetected in white tissues of the petals. Transcriptome profiling indicated that the relative high expression levels of structural genes, such as NnPAL, NnF3H, and NnANS, was inconsistent with the low anthocyanin concentration in white tissues. Members of the NnMYB and NnbHLH transcription factor families were presumed to play a role in the metabolic flux in the anthocyanin and proanthocyanidin biosynthetic pathway. The expression model of translational initiation factor, ribosomal proteins and SKP1–CUL1–F-box protein complex related genes suggested an important role for translational and post-translational network in anthocyanin biosynthesis. In addition, pathway analysis indicated that light reaction or photo destruction might be an important external cause for floral color determination in lotus.ConclusionsIn this study, it is supposed that the natural lotus mutant ‘Da Sajin’ may have originated from a red-flowered ancestor. Partial loss of anthocyanin pigments in petals may result from metabolic disorder caused by light destruction. This disorder is mainly regulated at post translation and translation level, resulting in a non-inherited phenotype. These results contribute to an improved understanding of anthocyanin metabolism in lotus, and indicate that the translational and post-translational regulatory network determines the metabolic flux of anthocyanins and proanthocyanidins under specific environmental conditions.

A glutathione S-transferase GhTT19 determines flower petal pigmentation via regulating anthocyanin accumulation in cotton.

Anthocyanin accumulations in the flowers can improve seed production of hybrid lines, and produce higher commodity value in cotton fibre. However, the genetic mechanism underlying the anthocyanin pigmentation in cotton petals is poorly understood. Here, we showed that the red petal phenotype was introgressed from Gossypium bickii through recombination with the segment containing the R3 bic region in the A07 chromosome of Gossypium hirsutum variety LR compared with the near-isogenic line of LW with white flower petals. The cyanidin-3-O-glucoside (Cy3G) was the major anthocyanin in red petals of cotton. A GhTT19 encoding a TT19-like GST was mapped to the R3 bic site associated with red petals via map-based cloning, but GhTT19 homologue gene from the D genome was not expressed in G. hirsutum. Intriguingly, allelic variations in the promoters between GhTT19LW and GhTT19LR , rather than genic regions, were found as genetic causal of petal colour variations. GhTT19-GFP was found localized in both the endoplasmic reticulum and tonoplast for facilitating anthocyanin transport. An additional MYB binding element found only in the promoter of GhTT19LR , but not in that of GhTT19LW , enhanced its transactivation by the MYB activator GhPAP1. The transgenic analysis confirmed the function of GhTT19 in regulating the red flower phenotype in cotton. The essential light signalling component GhHY5 bonded to and activated the promoter of GhPAP1, and the GhHY5-GhPAP1 module together regulated GhTT19 expression to mediate the light-activation of petal anthocyanin pigmentation in cotton. This study provides new insights into the molecular mechanisms for anthocyanin accumulation and may lay a foundation for faster genetic improvement of cotton.

Eco-Evo-Devo of petal pigmentation patterning.

Colourful spots, stripes and rings decorate the corolla of most flowering plants and fulfil important biotic and abiotic functions. Spatial differences in the pigmentation of epidermal cells can create these patterns. The last few years have yielded new data that have started to illuminate the mechanisms controlling the function, formation and evolution of petal patterns. These advances have broad impacts beyond the immediate field as pigmentation patterns are wonderful systems to explore multiscale biological problems: from understanding how cells make decisions at the microscale to examining the roots of biodiversity at the macroscale. These new results also reveal there is more to petal patterning than meets the eye, opening up a brand new area of investigation. In this mini-review, we summarise our current knowledge on the Eco-Evo-Devo of petal pigmentation patterns and discuss some of the most exciting yet unanswered questions that represent avenues for future research.

Glucose Supply Induces PsMYB2-Mediated Anthocyanin Accumulation in Paeonia suffruticosa 'Tai Yang' Cut Flower.

Tree peony (Paeonia suffruticosa) is a well-known Chinese ornamental plant with showy flower color. However, the color fading problem during vase time seriously blocks its development in the cut flower market. In this study, we found that exogenous glucose supply improved the color quality of P. suffruticosa ‘Tai Yang’ cut flowers with increased total soluble sugar and anthocyanin contents of petals. Besides, the promotion effect of glucose was better than the osmotic control of 3-O-methylglucose (3OMG) treatment and the glucose analog mannose treatment. The structural genes, including PsF3H, PsF3′H, PsDFR, PsAOMT, and PsUF5GT, were remarkably upregulated under glucose treatment. Meanwhile, the regulatory genes, including PsbHLH1, PsbHLH3, PsMYB2, PsWD40-1, and PsWD40-2, also showed a strong response to glucose treatment. Among these five regulatory genes, PsMYB2 showed less response to 3OMG treatment but was highly expressed under glucose and mannose treatments, indicating that PsMYB2 may have an important role in the glucose signal pathway. Ectopic overexpression of PsMYB2 in Nicotiana tabacum resulted in a strong pigmentation in petals and stamens of tobacco flowers accompanied with multiple anthocyanin biosynthetic genes upregulated. More importantly, the overexpression of PsMYB2 enhanced the ability of glucose-induced anthocyanin accumulation in Arabidopsis thaliana seedlings since PsMYB2-overexpressing Arabidopsis showed higher expression levels of AtPAL1, AtCHS, AtF3H, AtF3′H, AtDFR, and AtLDOX than those of wild type under glucose treatment. In summary, we suggested that glucose supply promoted petal coloration of P. suffruticosa ‘Tai Yang’ cut flower through the signal pathway, and PsMYB2 was a key component in this process. Our research made a further understanding of the mechanism that glucose-induced anthocyanin biosynthesis of P. suffruticosa cut flowers during postharvest development, laying a foundation for color retention technology development of cut flowers.

Comparative Transcriptome Analysis of Anthocyanin Biosynthesis in Pansy (Viola × wittrockiana Gams.)

Pansy (Viola × wittrockiana Gams.) is an important and attractive ornamental plant with a wide variety of flower colors. To date, the molecular genetic understanding of its colorful petal pigment patterns remains largely unknown. In this study, we analyzed the bicolor petals of “Mengdie” in cytological, physiological, and transcriptomic aspects. Results showed that the difference of flower colors was mainly determined by the pigment distribution in the epidermal cells. Pigment analysis indicated that anthocyanins had strong correlations with color parameters, which acted as the main factor in flower coloration. Comparative transcriptome analysis found a total of 43,908 unigenes with the mean length of 682 bp. There were 24,323, 16,668, 8507, and 7680 unigenes annotated in the Nr, Swiss-Prot, KOG, and KEGG databases, respectively. Differential expression genes (DEGs) showed that the expression of anthocyanin late biosynthesis genes (LBGs), VwF3′H, VwF3′5′H, and VwUFGT, would be likely to play a major role in the color formation of pansy. The expression patterns of selected DEGs were verified by qRT-PCR. This study contributes an excellent insight into molecular mechanism of pigment biosynthesis and provides some useful information for flower color modification in pansy.

Quercetin-derivatives painting the yellow petals of American lotus (Nelumbo lutea) and enzymatic basis for their accumulation

American lotus (Nelumbo lutea) is one of the two species in Nelumbo and has only yellow flower. Identification of total flavonoids showed wild American lotus contained almost only flavonols with quercetin 3-O-glucuronide to be the dominant pigment. The variation tendency of the total flavonol content was coincident with yellow color variation of petals during flower development. To understand the mechanism of accumulation and constituent of pigments in petals, three pivotal genes, NlFLS1, NlFLS2 and NlFLS3, which were predicted to encode flavonol synthases were isolated and characterized by analyses of basic bioinformatics, temporal and spatial expression patterns and enzymatic activity. Their temporal expression levels showed the same variation tendency, which was also consistent with the development-dependent variation of total flavonol content. Spatial expression patterns indicated the three genes should function in petals. All the three proteins were demonstrated to be bifunctional dioxygenase, possessing both flavonol synthase activity and flavanone 3-hydroxylase activity. Besides, other flavonol biosynthesis related genes were also investigated on their expression levels to give more clues on the mechanism. Substrate preferences of the three FLSs, substrate competitions between the FLSs and other flavonol biosynthesis related enzymes, and the greatly differential expression levels between F3’H (flavonoid 3′-hydroxylase) and F3’5’H (flavonoid 3′,5′-hydroxylase) contributed to the flavonol constituent in the petals of America lotus, namely abundant quercetin-derivatives while very few kaempferol-derivatives and myricetin-derivatives.