Gentian is an important ornamental flower in Japan. The corolla of the majority of cultivated Japanese gentians have green spots, which are rarely encountered in flowers of other angiosperms. Little information is available on the functional traits of the green spots. In this study, we characterized the green spots in the Japanese gentian corolla using a number of microscopic techniques. Opto-digital microscopy revealed that a single visible green spot is composed of approximately 100 epidermal cells. The epidermal cells of a green spot formed a dome-like structure and the cell lumen contained many green structures that were granular and approximately 5 μm in diameter. The green structures emitted red autofluorescence when irradiated with 488 nm excitation light. Transmission electron microscopy revealed that the green structures contained typical thylakoids and grana, thus indicating they are chloroplasts. No grana were observed and the thylakoids had collapsed in the plastids of epidermal cells surrounding green spots. To estimate the rate of photosynthetic electron transfer of the green spots, we measured chlorophyll fluorescence using the MICROSCOPY version of an Imaging-PAM (pulse-amplitude-modulated) fluorometer. Under actinic light of 449 μmol m−2 s−1, substantial electron flow through photosystem II was observed. Observation of green spot formation during corolla development revealed that immature green spots formed at an early bud stage and developed to maturity associated with chloroplast degradation in the surrounding epidermal cells. These results confirmed that the Japanese gentian corolla contains functional chloroplasts in restricted areas of epidermal cells and indicated that a sophisticated program for differential regulation of chloroplast formation and degradation is operative in the epidermis.
Citation: Takahashi S, Ozawa S, Sonoike K, Sasaki K, Nishihara M (2020) Morphological and cytological observations of corolla green spots reveal the presence of functional chloroplasts in Japanese gentian. PLoS ONE 15(8): e0237173. https://doi.org/10.1371/journal.pone.0237173
Editor: Hiroshi Ezura, University of Tsukuba, JAPAN
Received: June 3, 2020; Accepted: July 21, 2020; Published: August 26, 2020
Copyright: © 2020 Takahashi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: This study was financially supported by the Iwate prefectural government. This work was supported by the Ministry of Education, Culture, Sports, Science and Technology (MEXT) [Grant-in-Aid for Scientific Research on Innovative Areas Nos. JP16H06552 and JP16H06553 to K.S.] The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: BEC, blue epidermal cell; GEC, green epidermal cell; PAM, pulse-amplitude-modulated; PAR, photosynthetically active radiation; PG, plastoglobule; PSI, photosystem I; PSII, photosystem II; SEM, scanning electron microscope; TEM, transmission electron microscopy; ΦII, quantum yield of photosystem II
Angiosperms have evolved a variety of flower traits, such as diverse colors, patterns, shapes, and scents, to attract pollinators for efficient sexual reproduction [1, 2]. Among angiosperms, Gentiana is a genus of flowering plants belonging to the gentian family (Gentianaceae). More than 400 species are classified in this cosmopolitan genus and are specially distributed in alpine areas . In Japan, gentians are important ornamental plants grown as a cut flower or a flowering potted plant. Furthermore, the roots and rhizomes of gentians are used in traditional medicine for skin diseases caused by wind-heat or damp-heat . To date, more than 300 gentian cultivars derived from G. scabra, G. triflora, and their hybrids have been bred and selected for ornamental purposes . Generally, Japanese cultivated gentians have green spots on the corolla adaxial surface, irrespective of flower color (S1 Fig). Previous molecular biological studies have investigated diverse characteristics of Japanese gentians, which include not only flower color (detailed in latter part) but also flower shape [6, 7], flowering time , overwintering , and floral odor .
The vivid blue color of the corolla of Japanese gentians is conferred by gentiodelphin, a polyacylated anthocyanin . The structure of other delphinidin derivatives has also been characterized . Several Japanese gentians produce pink or white flowers (S1 Fig). Previous research revealed that disruption of the gene encoding flavonoid 3′,5′-hydroxylase (GtF3′5′H), a crucial enzyme for delphinidin biosynthesis, results in development of a pink corolla in the mutant [13, 14]. In a similar manner, disruption of the genes that encode anthocyanidin synthase (GtANS) and a R2R3-MYB transcription factor (GtMYB3) regulating expression of genes associated with flavonoid biosynthesis leads to a white-corolla phenotype [15, 16]. Using this information, molecular DNA markers to distinguish individuals with pink or white corollas from genotypes with blue-pigmented corollas have been developed [17, 18]. Recently, novel technologies, such as radiation with heavy ion beams and genome editing using the clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (CRISPR/Cas9) system, have been applied to induce novel flower colors in gentian [19, 20].
In contrast to the studies of flower color, no scientific research has been conducted previously on the green spots of the Japanese gentian corolla to the best of our knowledge. On the other hand, in other plant families, several studies on the formation of petal spots have been performed and are well summarized in a review by Davies et al. . For instance, in Iris japonica, the accumulation of carotenoids, anthocyanins or both in epidermal cells form spots. In Asiatic hybrid lilies (Lilium spp.; Liliaceae), splatter-type spots are formed via anthocyanin accumulation regulated by LhMYB12-Lat expression . In Clarkia gracilis (Onagraceae), the anthocyanin biosynthetic pathway is regulated to form sector-type spots . Swertia bimaculata (Gentianaceae) possesses nectaries, with a flat spot-like shape and yellow-green color, that are located in the middle of the corolla lobe; it is reported that the nectaries function as pollinator manipulators .
The presence of green spots on the corolla is an important factor that determines the commercial value of Japanese gentians. Green spots are usually an undesirable trait and breeders select lines with few green spots on the corolla. The size and number of the green spots vary among cultivars, and are barely noticeable in some cultivars. Japanese gentians generally do not bloom in the year of planting, therefore molecular markers are extremely useful to expedite gentian breeding [5, 24]. Accurate prediction of the presence or absence of green spots before flowering using DNA markers will greatly improve breeding efficiency. To this purpose, we aim to develop DNA markers for green spots. However, limited information on corolla green spots in gentian is available and detailed observation has not been conducted. In this study, we focused on green spots of the gentian corolla and aimed to characterize their properties using a variety of microscopic techniques. We determined that the cells in green spots retain functional chloroplasts, unlike the surrounding epidermal cells. This is the first report describing the traits of green spots on the corolla of Japanese gentians.
Materials and methods
The Japanese gentian breeding line ‘Bzc-1’  was used in this study. The plants were grown in soil in pots under natural daylight in a greenhouse at the Iwate Agricultural Research Center (S2 Fig).
The epidermis and cross-sections of the ‘Bzc-1’ corolla with green spots were observed with an opto-digital microscope (DSX500, Olympus Co., Tokyo, Japan). The cross-sections were cut by hand to 300 μm thickness with a razor blade. A digital microscopy image of the corolla used for SEM analysis was taken by Leica MZ16 FA (Leica microsystems, Wetzlar, Germany) with DIGITAL SIGHT DS-5Mc (Nikon, Kawasaki, Japan).
Scanning electron microscopy
Fresh corollas (without fixation) with green spots sampled from ‘Bzc-1’ were subjected to scanning electron microscopy (SEM) analysis. The SEM images shown in Fig 1 were acquired using a JCM-6000 NeoScope (JEOL Ltd, Tokyo, Japan) at an acceleration voltage of 15 kV. The SEM images shown in Fig 4 were captured using a Miniscope TM4000 (Hitachi High-Tech Co., Tokyo, Japan) at an acceleration voltage of 15 kV.
(A) Flower morphology, (B) adaxial surface of the corolla, (C) high-magnification image of the adaxial surface of the corolla, (D) high-magnification image of a green spot, (E) green epidermal cells (GECs), (F) cross-section of a corolla, (G) cross-section of a green spot, (H) cross-section of GECs. (I–L) Confocal laser micrographs of green spots. The images in (I), (J), and (K) correspond to a Nomarski differential interference contrast image, autofluorescence, and the merged image, respectively. Autofluorescence of GECs is shown in (L). (M) A digital microscopy image of the corolla used for SEM analysis, (N) SEM image of the adaxial surface of the corolla, (O) SEM image of the adaxial surface of a green spot.
Confocal laser scanning microscopy
Fresh corollas sampled from ‘Bzc-1’ were observed with a FLUOVIEW FV1000 confocal laser scanning microscope (Olympus Co., Tokyo, Japan). Fluorescence images were acquired using a 650–750 nm long-pass filter after excitation with an Ar laser (λex = 488 nm).
Transmission electron microscopy
Fresh corollas sampled from ‘Bzc-1’ were fixed with 2% paraformaldehyde and 2% glutaraldehyde in 0.05 M cacodylate buffer (pH 7.4) at 4°C overnight. After fixation, the samples were washed three times with 0.05 M cacodylate buffer for 30 min each, and were postfixed with 2% osmium tetroxide in 0.05 M cacodylate buffer at 4°C for 3 h. Subsequently, the samples were dehydrated in a graded ethanol series (50%, 70%, 90%, and 100%). The dehydrated samples were infiltrated with propylene oxide (PO) twice for 30 min each and were placed into a 70:30 mixture of PO and resin (Quetol-651, Nisshin EM Co., Tokyo, Japan) for 1 h. Subsequently, the tube cap was opened and PO was volatilized overnight. The samples were transferred to fresh 100% resin and were polymerized at 60°C for 48 h. The polymerized resin blocks were ultra-thin-sectioned (80 nm) with a diamond knife using an Ultracut UCT ultramicrotome (Leica, Vienna, Austria). The sections were mounted on copper grids, stained with 2% uranyl acetate at room temperature for 15 min, washed with distilled water, then secondary-stained with Lead stain solution (Sigma-Aldrich Co., Tokyo, Japan) at room temperature for 3 min. The grids were observed using a transmission electron microscope (JEM-1400Plus, JEOL Ltd, Tokyo, Japan) at an acceleration voltage of 100 kV. Digital images were captured with a CCD camera.
Imaging pulse-amplitude-modulated (PAM) chlorophyll fluorescence
Chlorophyll fluorescence imaging was performed using the MICROSCOPY version of Imaging-PAM (Heinz Walz, Effeltrich, Germany) fluorometer with a microscope (Axioscope with 10× objective lens, Carl Zeiss, Germany) and ImagingWinGigE software (Heinz Walz). A blue LED lamp (IMAG-L470M, Heinz Walz) was used for measurements or as an actinic light source. A small piece (about 1 cm2) of ‘Bzc-1’ corolla with green spots was placed on a microscope slide and dark-acclimated for 5 min at room temperature. Subsequently, images of ΦII, a parameter that represents photosynthetic yield (effective quantum yield of photosynthetic electron transfer), were obtained under actinic light at 449 μmol m–2 s–1.
Structure of green spots on corolla
The breeding line ‘Bzc-1’, a typical Japanese gentian (producing flowers with a blue corolla and green spots), was selected as the study material (Fig 1A and 1B). ‘Bzc-1’ bears dozens of green spots per corolla. The green spots are present in the corolla lobe but not in the paracorolla. Surface images of a green spot acquired with an opto-digital microscope are shown in Fig 1C–1E. A green spot was composed of approximately 100 epidermal cells (Fig 1D). Furthermore, the epidermal cells forming a green spot contained many green objects (Fig 1E). To clarify the cell types that constituted the green spots, we prepared cross-sections of the ‘Bzc-1’ corolla and observed that the green spots were composed solely of epidermal cells (Fig 1F). The green objects had a granular structure approximately 5 μm in diameter (Fig 1G and 1H). Hereafter, the epidermal cells forming a green spot are referred to as green epidermal cells (GECs).
Next, the corolla of ‘Bzc-1’ was observed using a confocal laser microscope (Fig 1I–1L). Under 488 nm blue excitation light, the green spot emitted red autofluorescence (Fig 1J). In contrast, epidermal cells other than GECs did not autofluoresce (Fig 1J). Hereafter, epidermal cells other than GECs are referred to as blue epidermal cells (BECs) designated after the vivid blue pigmentation. Observation of the GECs at higher magnification revealed that the granular structures emitted red fluorescence (Fig 1L).
To reveal the surface structure of GECs and BECs, we next performed SEM analysis. Recently, Bailes and Glover classified the protruding parts of epidermal cell morphology of Vicia faba L. by perimeter shape, projection, and cell surface micromorphology . According to their classification method, perimeter shape, projection, and cell surface micromorphology of GECs and BECs were categorized into papillose, conical and striate, respectively (Fig 1M–1O). In addition, a green spot formed a dome-like structure. Other than the formation of a dome, the surface structure of GECs and BECs did not differ. The physiological function of the dome is uncharacterized to date and may be a crucial feature to elucidate the role of green spots.
GECs contain chloroplasts
Given that the green granules in the GECs were approximately 5 μm in diameter and emitted red autofluorescence upon excitation with blue light, we speculated that the structures were chloroplasts. However, it is generally accepted that chloroplasts are absent in epidermal cells. Transmission electron microscopy (TEM) analysis was performed to observe the detailed structure of the green granules in GECs. Fig 2 shows TEM images of cross-sections of the ‘Bzc-1’ corolla. The GECs were elongated in shape, with vacuoles in the upper part of the cell lumen and numerous chloroplasts observed in the lower part of the cell lumen (Fig 2A). The BECs also were elongated in shape similar to GECs, but the cell lumen was mostly occupied by vacuoles and contained plastids instead of chloroplasts (Fig 2B). In addition, observation of the boundary region between GECs and BECs revealed that both cell types were clearly distinguished and no cells of intermediate morphology were observed (Fig 2C and 2D). Fig 2E shows the chloroplast structure of GECs. The chloroplasts contained thylakoids and developed grana, similar to the chloroplasts typically present in the leaves of higher plants. In contrast, in the plastid of BECs, the thylakoids were collapsed and no grana were observed (Fig 2F). In addition, the number of plastoglobules (PGs) was higher in plastids of BECs than those of GECs (Fig 2E and 2F). Elevation in PG number and size is observed during chloroplast degradation under leaf senescence . Therefore, the plastids of BECs are not considered to be chromoplasts associated with flower color but plastid forms after chloroplast degradation. Corolla mesophyll cells showed an elliptic shape, and the cell lumen was almost entirely occupied by vacuoles (Fig 2G). In addition, the plastids of corolla mesophyll cells contained larger PGs (Fig 2H).
(A) Cross-section of green epidermal cells (GECs; upper side) and corolla mesophyll cells (lower side), (B) cross-section of blue epidermal cells (BECs) and corolla mesophyll cells, (C, D) cross-section of GECs and BECs. The letters G and B denote GEC and BEC, respectively. Black arrows indicate the boundary between GECs and BECs. (E) Chloroplasts in GECs, (F) plastids in BECs, (G) cross-section of corolla mesophyll cells, (H) plastids in a corolla mesophyll cell.
Photosynthesis of the green spots
Next, we examined the function of the chloroplasts in GECs. Given that the size of the green spot was quite small, photosynthetic yield of chloroplasts in GECs was determined using the MICROSCOPY version of an Imaging-PAM fluorometer. One to two green spots were obtained from three independent corollas and measured at a total of five points. Under actinic light of 449 μmol m−2 s−1, which is comparable to the photon flux density in the greenhouse for growing ‘Bzc-1’, areas corresponding to green spots showed relatively uniform and high ΦII, a parameter representing the relative yield of photosynthetic electron transport (Fig 3). Photosynthetic activity was not detected in the parts outside of the green spots. The mean ΦII was 0.50 ± 0.01 for the five green spots. This value is comparable to those of Arabidopsis thaliana leaves  or Hibiscus rosa-sinensis , indicating that the functioning of photosystem II (PSII) and photosystem I (PSI) is intact in the chloroplasts in GECs.
ΦII of green spots and neighboring cells was determined under actinic light of 449 μmol photons m−2 s−1 at room temperature and is shown as a pseudo-color image.
If these chloroplasts are active in photosynthesis, carbon dioxide should be taken up from the atmosphere into chloroplasts. We observed that stomata were present on the abaxial surface of the corolla but not on the adaxial surface (Fig 4). These results supported the conclusion that the green spots of the ‘Bzc-1’ corolla are photosynthetically active.
Chloroplast development and degradation in corolla
The results thus far revealed that the green spots on the ‘Bzc-1’ corolla were composed of GECs containing functional chloroplasts. It is widely accepted that chloroplasts are absent in epidermal cells except for guard cells in plant leaves. No chloroplasts were observed in epidermal cells of ‘Bzc-1’ leaves (S2 Fig), implying that green spots are formed in the epidermis of the corolla in developing buds after the plant switches from vegetative to reproductive growth. To determine when green spots develop in the ‘Bzc-1’ corolla, the floral bud epidermis at three developmental stages (stages 1, 2, and 3) was observed (Fig 5A). Stage 3 buds possessed well-developed green spots, whereas stage 1 buds showed no green spots. Stage 2 buds had developing green spots consisting of approximately 10 GECs. This observation revealed that green spots developed during bud growth and arose independently of each other.
(A) Developmental status of green spots in floral buds at three developmental stages. (B) Chlorophyll autofluorescence from the green spot and epidermal cells of buds (stage 3).
In stage 3 buds, we detected chlorophyll autofluorescence not only in green spots but also in surrounding epidermal cells (Fig 5B). The size of granules emitting chlorophyll autofluorescence observed in the surrounding epidermal cells was distinctly smaller than GEC chloroplasts. In Arabidopsis thaliana, chloroplasts in the corolla are converted to leucoplasts during corolla development . Therefore, during bud development, it is suggested that chloroplast degradation is promoted in epidermal cells except GECs. No chlorophyll fluorescence was observed in BECs (Fig 1J), suggesting that chloroplast degradation was completed in the corolla of fully opened flowers. In addition, we observed chloroplasts in mesophyll cells of stage 3 buds (S2 Fig). Given that chloroplasts are not observed in the corolla mesophyll cells of a fully opened flower (Figs 1E and 2G), it is suggested that these chloroplasts are degraded during development from the bud to anthesis.
In the present study, we revealed that green spots on the ‘Bzc-1’ corolla have functional chloroplasts and perform photosynthesis (Figs 2 and 3). Interestingly, the greens spots were composed of only epidermal cells (Figs 1 and 2). Furthermore, we observed that the ‘Bzc-1’ corolla bears stomata on the abaxial surface (i.e., the opposite surface to that of the green spots) (Fig 4). In leaves, stomata are involved not only in gas exchange with the atmosphere during photosynthesis, but also play a role in lowering the leaf temperature that has risen owing to strong sunlight during transpiration. Previous studies have been conducted on stomata in corollas, focusing on transpiration [30, 31], but to our knowledge no information on photosynthesis is available. The presence of stomata in the ‘Bzc-1’ corolla is suggested to aid in the continued photosynthesis of the green spots. The green spots develop during floral bud growth (Fig 5). The corolla contains two types of epidermal cells: GECs that develop and maintain chloroplasts, and BECs in which chloroplasts are degraded. These findings are apparently unique and Japanese gentian may prove to be ideal material for studying plastid dedifferentiation.
It is an unusual phenomenon that functional chloroplasts are formed and maintained in epidermal cells. In contrast to gentian, green-flowered chrysanthemum (Chrysanthemum morifolium) accumulated chloroplasts in mesophyll cells but not in epidermal cells (S3 Fig). It is proposed that green-flowered mutants, such as the green-flowered chrysanthemum, if they arose in nature, may soon disappear because the green flower trait is undesirable for reproduction . However, green spots are considered to perform a function because they are often present in wild-type gentian flowers of various Gentiana species [3, 33] and are independent of the corolla color (S1 Fig). Previous studies have noted the existence of chloroplasts in the epidermal pavement cells of Arabidopsis thaliana [34–37]. However, the chloroplasts described in these studies are smaller than mesophyll chloroplasts, indicating that these chloroplasts are not equivalent to GEC chloroplasts.
Generally, the energy that supports plant life is provided by photosynthesis in the leaves . On the other hand, it has been reported that photosynthesis performed in tissues other than leaves, in green non-leaf organs (e.g., wheat ear, sycamore seed pods, tomato fruit, strawberry fruit, greengage, cherries and apples), contributes to yield . One possibility is that green spots on the corolla of Japanese gentian contribute to extension of the flower life. However, because the area of green spots on the corolla is small, their importance as a site for energy production must be considered with caution.
An additional possibility is to consider the biological function of the green spots as a floral pattern. It is widely accepted that flower patterns, including spots, act as a nectar guide to attract pollinators [40–42]. In Asiatic hybrid lilies and Clarkia gracilis, anthocyanin accumulation is regulated to form splatter-type spots and sector-type spots, respectively [21, 22]. However, it must be taken into account that the green spots of Japanese gentian are dependent on chlorophyll and show different optical properties from spots composed of anthocyanins. Swertia bimaculata, a member of the Gentianaceae, uses nectaries of a flat, yellow-green, spot-like form located in the middle of the corolla lobe to attract pollinators . However, compared with the green spots of Japanese gentian, the nectaries of S. bimaculata are relatively large, few in number (two per corolla lobe), and their location is limited. Therefore, it is unlikely that green spots of Japanese gentians serve the same function. A field investigation is required to evaluate the function of the green spots of Japanese gentians in pollination, e.g., as a possible guide to attract pollinators.
The color of the green spots is derived from chlorophyll. Chlorophyll has a photosensitizing effect, thus it requires a functional chloroplast for safe accumulation. In Japanese gentian, the GECs possessed functional chloroplasts (Figs 2A, 2E and 3). In leaves, two transcription factor families, namely the GATA NITRATE-INDUCIBLE CARBON-METABOLISM-INVOLVED (GNC) family and the GOLDEN TWO-LIKE (GLK) family, play a central role in chloroplast development . In chrysanthemum, expression levels of genes encoding critical enzymes (glutamyl-tRNA reductase, Mg-protoporphyrin IX chelatase, Mg-protoporphyrin IX monomethylester cyclase, and protochlorophyllide oxidoreductase) for chlorophyll synthesis are strongly correlated with chlorophyll content and flower color . Analysis of the expression profiles of these genes in gentian is required in a future study. Elucidation of the regulatory mechanism of plastid differentiation in GECs and BECs is predicted to reveal a novel regulatory system for plastid differentiation. The master regulator of chloroplast development in corolla will be useful for development of molecular markers for green spots in Japanese gentian in the future.
S1 Fig. Flower variation of Japanese gentian cultivated at the Iwate Agricultural Research Center.
S2 Fig. Morphology of Japanese gentian ‘Bzc-1’.
(A) Plant morphology of ‘Bzc-1’ grown in a pot in the greenhouse. (B) Cross-sections of a leaf and a floral bud.
We thank R. Washiashi and Y. Kurokawa at the Iwate Biotechnology Research Center for technical assistance. We thank Robert McKenzie, PhD, from Edanz Group (www.edanzediting.com/ac), for editing a draft of this manuscript.
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