Genetic engineering of yellow betalain pigments beyond the species barrier


Betalains are one of the major plant pigment groups found in some higher plants and higher fungi. They are not produced naturally in any plant species outside of the order Caryophyllales, nor are they produced by anthocyanin-accumulating Caryophyllales. Here, we attempted to reconstruct the betalain biosynthetic pathway as a self-contained system in an anthocyanin-producing plant species. The combined expressions of a tyrosinase gene from shiitake mushroom and a DOPA 4,5-dioxygenase gene from the four-o'clock plant resulted in successful betalain production in cultured cells of tobacco BY2 and Arabidopsis T87. Transgenic tobacco BY2 cells were bright yellow because of the accumulation of betaxanthins. LC-TOF-MS analyses showed that proline-betaxanthin (Pro-Bx) accumulated as the major betaxanthin in these transgenic BY2 cells. Transgenic Arabidopsis T87 cells also produced betaxanthins, but produced lower levels than transgenic BY2 cells. These results illustrate the success of a novel genetic engineering strategy for betalain biosynthesis.


The coloration of flowers and fruits is due to the accumulation of pigments such as flavonoids (including anthocyanins), carotenoids and betalains1,2. Anthocyanins and carotenoids are widely distributed in angiosperms, whereas betalains are water-soluble nitrogenous pigments found only in some plants in the order Caryophyllales (but not in the families Caryophyllaceae and Molluginaceae)3 and in some higher fungi, such as fly agaric (Amanita muscaria)4. Although betalains have functions analogous to those of anthocyanins as pigments, anthocyanins and betalains are mutually exclusive pigments in plants3. This raises the taxonomic mystery of why betalains cannot be produced in any plants outside of the order Caryophyllales5,6.

Betalains, which include the red-violet betacyanins and the yellow betaxanthins, are biosynthesized from the amino acid tyrosine by several enzymatic and spontaneous chemical steps (Fig. 1)7. The first step is the conversion of tyrosine to dihydroxyphenylalanine (L-DOPA) by uncharacterized enzyme(s) with tyrosine-hydroxylating activity. L-DOPA is converted to betalamic acid (BA), which is an important precursor of betalain biosynthesis, by DOPA 4,5-dioxygenase (DOD)8. In addition, L-DOPA is also converted to cyclo-DOPA by a cytochrome P450 enzyme9. BA conjugates with an amino acid or amine to form yellow betaxanthins. This condensation of BA with amino acids is considered as a spontaneous non-enzymatic reaction10. There are two pathways postulated for betacyanin biosynthesis (Fig. 1). Namely, glycosylation steps occur at the precursor molecule, cyclo-DOPA, or after the condensation of cyclo-DOPA with BA to form betanidin. Both betanidin 5-O-glucosyltransferase (betanidin 5GT) and cyclo-DOPA 5-O-glucosyltransferase (cDOPA 5GT) have been identified11,12. Both betacyanins and betaxanthins accumulate in the vacuole, like anthocyanins2. As described above, the first enzymatic step in betalain biosynthesis is the formation of L-DOPA from tyrosine, which involves a hydroxylation step (Fig. 1). In plants, tyrosine-hydroxylating activity has mainly been attributed to tyrosinase, but has also been attributed to tyrosine hydroxylase13,14,15,16. However, the involvement of either enzyme has not been shown conclusively, nor has any gene encoding a product with this activity been yet identified in betalain-producing plants. In contrast, the tyrosinase involved in the formation of melanin, the brown pigment produced during development and post-harvest storage of mushrooms, has been well studied and characterized17.

Figure 1

Betalain biosynthetic pathway.

Thick arrows show enzymatic reactions, dotted arrows show spontaneous reactions. I, enzyme with tyrosine-hydroxylating activity (LeTYR in this study); II, L-DOPA oxidase; III, DOPA 4,5-dioxygenase (MjDOD in this study); IV, betanidin 5-O-glucosyltransferase; V, cyclo-DOPA 5-O-glucosyltransferase. Enzymes used for betaxanthin engineering in this study are shown in red font.

Schliemann et al.18 proposed that the concerted action of two enzymes, DOD from A. muscaria and DOPA oxidase from Portulaca grandiflora, synthesized betanidin, one of the betacyanins, in vitro. Feeding of betalamic acid to broad bean (Vicia faba L.) seedlings, which do not synthesize betaxanthins, resulted in the formation of dopaxanthin10. More recently, Harris et al.19 reported that transgenic Arabidopsis expressing the DOD gene from the fungus A. muscaria produced betaxanthin and betacyanin when supplied with the substrate L-DOPA. However, there are no reports on production of betalain pigments in non-betalain producing plants in vivo without feeding of the pathway intermediates.

In this study, we have shown that production of betaxanthin pigments without exogenous substrates is possible in suspension-cultured cells of both tobacco and Arabidopsis. We demonstrated that the combined expressions of a fungal tyrosinase gene and a plant DOD gene made a successful heterologous expression system for production of betaxanthins in these cultured cells. This is the first report of a self-contained betalain biosynthetic system in plant species outside of the order Caryophyllales.


Establishment of transgenic BY2 suspension cells for production of betaxanthins

To produce betalain pigments in anthocyanin-producing plant species outside of the order Caryophyllales, we first selected tobacco (Nicotiana tabacum), which belongs to the family Solanaceae, as the transformation host. The tobacco BY-2 cell line is the most popular suspension cell line in plant research and its rapid growth characteristics make it an ideal experimental material20. We produced transgenic tobacco BY2 cells expressing tyrosinase from shiitake mushroom (Lentinula edodes, LeTYR)21 and/or MjDOD from the four-o'clock plant (Mirabilis jalapa)22 under the control of the cauliflower mosaic virus 35S promoter (35Sp). Calli expressing both 35Sp-LeTYR and 35Sp-MjDOD showed bright yellow coloration (Fig. 2a). Transgenic calli expressing 35Sp-LeTYR or 35Sp-MjDOD showed no color change compared with those of the vector control and untransformed wild-type (Fig. 2a).

Figure 2

Analyses of transgenic tobacco BY2 calli.

(a) Images of typical transgenic BY2 calli. WT, wild-type; VC, vector control (pIG121-Hm); TYR, 35Sp-LeTYR line no. 3; DOD, 35Sp-MjDOD line no. 3; TYR/DOD, 35Sp-LeTYR/35Sp-MjDOD line no. 3. (b) Northern blot analysis. Total RNAs were isolated from wild-type (WT) and transgenic BY2 including vector control (VC) and three independent transgenic lines 35Sp-LeTYR (TYR), 35Sp-MjDOD (DOD) and 35Sp-LeTYR/35Sp-MjDOD (TYR/DOD). Total RNAs (5 μg) were separated on an agarose gel and then transferred to a nylon membrane and hybridized with LeTYR or MjDOD probes. Ethidium bromide staining of rRNA bands shows quality and loading controls. (c) Tyrosine-hydroxylating activity and accumulation of LeTYR proteins in transgenic BY2 calli. The activity was determined by CE-MS analysis as described in Materials and methods. Western blot analysis was performed using anti-LeTYR antibody21.

Expression and enzymatic activity analysis of transgenic tobacco BY2 cells

We analyzed transgene expressions in each of the three transgenic BY2 lines by northern blot analysis (Fig. 2b). The expressions of LeTYR were detected in both 35Sp-LeTYR and 35Sp-LeTYR/35Sp-MjDOD transgenic BY2 calli. However, the expression levels of LeTYR in 35Sp-LeTYR/35Sp-MjDOD lines were higher than those in 35Sp-LeTYR lines (Fig. 2b). In addition, we detected degraded and aberrant LeTYR transcripts in transgenic BY2 calli. These degraded and aberrant transcripts of LeTYR were also observed in the fruiting body of shiitake mushroom21. There were similar expression levels of MjDOD in 35Sp-MjDOD and 35Sp-LeTYR/35Sp-MjDOD lines, except for 35Sp-MjDOD line no. 1. Western blot analysis of the tyrosinase protein with an anti-LeTYR polyclonal antibody was performed for transgenic BY2 calli (Fig. 2c). In the crude protein extracts from shiitake mushroom, there were two bands corresponding to the premature 68-kDa and mature 45-kDa proteins, as reported by Sato et al.21. In transgenic BY2 calli with 35Sp-LeTYR or 35Sp-LeTYR/35Sp-MjDOD, premature 68-kDa signals were detected, but mature 45-kDa signals were scarcely detected. The 68-kDa signals in 35Sp-LeTYR lines were much weaker than those in 35Sp-LeTYR/35Sp-MjDOD co-expressing lines (Fig. 2c). The results of western blot analysis were largely consistent with the expression levels determined by northern blot analysis (Figs. 2b, c).

Next, we investigated tyrosine-hydroxylating activities in 35Sp-LeTYR and 35Sp-LeTYR/35Sp-MjDOD transgenic BY2 cell lines. The crude proteins extracted from transgenic BY2 lines showed no DOPA oxidase activity in the 3-methyl-2-benzothiazolinone hydrazone hydrochloride (MBTH) assay (data not shown). Thus, the tyrosine-hydroxylating activity, which synthesizes L-DOPA from tyrosine, was compared among the transgenic BY2 cell lines (Fig. 2c). No tyrosine-hydroxylating activity was detected in wild-type, the vector control, or 35Sp-MjDOD lines. Among the three 35Sp-LeTYR lines, line no. 3, which showed the strongest 68-kDa signal in the western blot analysis, showed tyrosine-hydroxylating activity of 1.2 nmol L-DOPA h−1 mg protein−1. The 35Sp-LeTYR/35Sp-MjDOD lines showed tyrosine-hydroxylating activities comparable to, or 3-fold higher than, that of 35Sp-LeTYR line no. 3. These tyrosine-hydroxylating activities were largely consistent with the expression levels determined by northern blot and western blot analyses.

LC-TOF-MS analyses of betaxanthins in transgenic BY2 cells

Pigments accumulated in transgenic BY2 calli were investigated by LC-TOF-MS. We detected BA (m/z = 212.056, λmax = 425 nm), the precursor of betaxanthin, in 35Sp-LeTYR/35Sp-MjDOD transgenic cell lines, but not in the vector control, 35Sp-LeTYR, or 35Sp-MjDOD lines. Therefore, the combined expression of LeTYR and MjDOD was essential for accumulation of betalamic acid in tobacco BY2 cells.

35Sp-LeTYR/35Sp-MjDOD transgenic BY2 lines nos. 1, 2 and 3 accumulated 1.16 ± 0.13, 1.69 ± 0.18 and 1.67 ± 0.05 μmole betaxanthins/g dry weight, respectively, as calculated from the molar extinction coefficient for betaxanthins. When 4-week-old calli were compared, transgenic line no. 3 showed the most stable proliferation and vivid yellow color among the three transgenic lines (Fig. 3a, Supplementary Fig. S1). The accumulation of betaxanthins started to increase at 4 weeks after subculture and reached the maximum at 8 weeks, thereafter decreasing rapidly (Fig. 3b). However, their calli turned brown after 5 weeks subculture and became stunted (Fig. 3a, Supplementary Fig. S1). Therefore, 4-week-old calli of 35Sp-LeTYR/35Sp-MjDOD line no. 3 were used for further analyses.

Figure 3

Betaxanthin accumulation in 35Sp-LeTYR/35Sp-MjDOD transgenic BY2 cells.

(a) Typical phenotypes of vector control (VC) and 35Sp-LeTYR/35Sp-MjDOD line no. 3 (TYR/DOD no. 3) calli after 4- and 8-weeks subculture. (b) Change in betaxanthin concentration over time in transgenic calli line no. 3 after subculture. Betaxanthins were extracted in 80% (v/v) methanol containing 0.04% (v/v) HCl and concentration was calculated from absorbance at 480 nm. (c) Identification of betaxanthins by LC-TOF-MS in 35Sp-LeTYR/35Sp-MjDOD transgenic BY2 cells. Chromatography profiles of extracts from vector control (dashed line) and 35Sp-LeTYR/35Sp-MjDOD line no.3 (thick line). Peak 1, retention time 23.8 min, m/z = 340.114, λmax = 470 nm, Glutamine-Bx (Vulgaxanthin I); Peak 2, 27.4 min, m/z = 313.104, λmax = 470 nm, Threonine-Bx; Peak 3, 41.3 min, m/z = 309.1084, λmax = 480 nm, Proline-Bx (Indicaxanthin).

HPLC analysis detected one major and some minor peaks at 470 nm (Fig. 3c). There was no clear peak in the vector control, 35Sp-LeTYR, or 35Sp-MjDOD transgenic BY2 calli. The major peak (retention time 41.3 min, m/z = 309.108, λmax = 480 nm) was assigned to proline-Bx (Pro-Bx, indicaxanthin; Fig. 1) by comparison with synthesized betaxanthin standards. The 35Sp-LeTYR/35Sp-MjDOD transgenic BY2 line no. 3 accumulated a maximum of 3.3 μmoles Pro-Bx/g dry weight (Fig. 3c, peak 3), based on synthetic authentic Pro-Bx as the standard. The other minor peaks 1 (23.8 min, m/z = 340.114, λmax = 470 nm) and 2 (27.4 min, m/z = 313.104, λmax = 470 nm) were assigned to glutamine-Bx (Gln-Bx, vulgaxanthin I) and threonine-Bx (Thr-Bx), respectively (Fig. 3c). Accumulation of betaxanthins was also detected in other 35Sp-LeTYR/35Sp-MjDOD transgenic BY2 lines.

Production of betaxanthins in Arabidopsis T87 cells

In addition to tobacco BY2 cells, we produced 35Sp-LeTYR/35Sp-MjDOD transgenic calli of Arabidopsis T87 cells. We obtained 40 independent transgenic calli with 35SpLeTYR/35SpMjDOD and selected two transgenic calli lines that showed high expression levels of both LeTYR and MjDOD genes in a northern blot analysis (Fig. 4a). Western blot analysis detected 68-kDa signals of the LeTYR protein in both transgenic lines, like in transgenic BY2 calli (Fig. 4a). The wild-type Arabidopsis T87 cells were also yellow when cultured in darkness; therefore, we did not observe a marked difference in color phenotype between the vector control and the transgenic lines (Fig. 4b). However, the aqueous extracts from transgenic lines were slightly yellow, whereas that from the vector control was colorless (Fig. 4c). HPLC analysis detected some very weak peaks in Arabidopsis transgenic line no. 1, but we could not identify specific betaxanthins.

Figure 4

Analysis of 35Sp-LeTYR/35Sp-MjDOD transgenic Arabidopsis T87 cells.

(a) Analyses of LeTYR and MjDOD transcripts and LeTYR protein accumulation. VC, vector control pIG121Hm; TD1 and TD2, independent 35Sp-LeTYR/35Sp-MjDOD transgenic T87 cell lines. (b) Images of typical transgenic T87 calli. (c) Aqueous extracts from transgenic T87 calli.

These results indicated that the combined expressions of LeTYR and MjDOD could induce the accumulation of betaxanthins in cultured cells of non-Caryophyllales plants, but the specific components and amounts of betalains produced differed between tobacco and Arabidopsis.


Betalains are Caryophyllales-specific plant pigments that are responsible for the red-violet and yellow coloration instead of anthocyanins in some plants in the order Caryophyllales. The betalain biosynthetic pathway in plants was deduced from genetic and metabolite analysis of P. grandiflora mutants23 and then the genes encoding DOD, betanidin 5GT and cDOPA5GT were identified from plants in the Caryophyllales8,11,22,24. More recently, CYP76AD1 encoding L-DOPA oxidase was identified from Beta vulgaris and it was revealed that the oxidation of L-DOPA to cyclo-DOPA was catalyzed by this enzyme in betacyanin biosynthesis9. It was suggested that this cytochrome P450, CYP76AD1, may have tyrosine-hydroxylating activity to synthesize L-DOPA from tyrosine9, although further confirmation is necessary. Thus, the gene encoding an enzyme with tyrosine-hydroxylating activity, which is responsible for the crucial first step in betalain biosynthesis, was not identified, although the enzyme had been partially purified in earlier works13,14. The results of those previous studies strongly suggested that a tyrosinase belonging to the copper protein polyphenol oxidase (PPO) family is the tyrosine-hydroxylating enzyme involved in betalain biosynthesis, although it has never been proven conclusively. Most plant PPOs have a plastid transit peptide at the N-terminal17. Although PPO genes have been cloned from pokeweed (Phytolacca americana), it is not certain whether they actually function in betalain biosynthesis25. Müeller et al.26 reported the purification of tyrosinase from the betalain-containing pileus of the mushroom Amanita muscaria, but no additional experiments had been conducted until now.

In previous studies, broad bean and DOD-expressing Arabidopsis produced betalains when fed with betalamic acid and L-DOPA, respectively10,19. These results suggested that anthocyanin-producing plant species have the potential to produce betalains if they are provided with suitable precursors for betalain biosynthesis. However, a betalain-specific gene that encodes an enzyme with tyrosine-hydroxylating activity, whether from higher plants or fungi, was not available for combining with DOD to complete the biosynthetic pathway. We considered that mushroom tyrosinases linked to the synthesis of melanin pigments have been well characterized17 and might be used to reconstruct betalain biosynthesis. In fact, LeTYR from shiitake mushroom resulted in accumulation of L-DOPA in BY2 cells; that is, the foreign LeTYR protein showed tyrosine-hydroxylating activity in cultured plant cells (Fig. 2c). Thereafter, MjDOD protein could convert L-DOPA produced by LeTYR into betalamic acid, leading to the formation of yellow betaxanthins in transgenic tobacco BY2 cells expressing both MjDOD and LeTYR genes (Fig. 2a; Fig. 3). The betaxanthin accumulation peaked at 8 weeks after subculture, even though the transgenic calli turned brown in prolonged culture after 5 weeks (Figs. 3a,b, Supplemental Fig. S1). This suggested that there was accumulation of other metabolites as a result of the foreign tyrosinase activity. Since the browning also occurred in transgenic BY2 cells expressing LeTYR only, these were not betalain-derived compounds. This browning was considered to represent accumulation of L-DOPA-derived (but not betaxanthin-derived) metabolites via dopaquinone that might be toxic to plant cells. One strategy to reduce or eliminate browning is to convert the metabolites to nontoxic compounds by introducing other detoxifying enzymes. If successful, this may result in more effective accumulation of betaxanthins in transgenic BY2 cells. We also produced a transgenic Arabidopsis T87 cell line by introducing the same constructs (Fig. 4). However, betaxanthin accumulated to lower levels in T87 transgenic cells than in BY2 transgenic cells and the coloration of Arabidopsis transgenic cells could not be observed visually (Fig. 4b). It is unknown why the amount of heterologous betaxanthin produced differed among the plant species used as transformation hosts, but there are several possible explanations: the transport efficiency of BA may differ between tobacco and Arabidopsis, and/or there may be differences in tyrosine availability or in competing endogenous reactions that use tyrosine and/or the L-DOPA substrate. Further research is required to elucidate the precise reason(s).

The condensation of BA with amino acids in planta is a spontaneous reaction10. Pro-Bx accumulated preferentially in transgenic BY2 cells, reaching a concentration of 3.3 μmoles/g dry weight (Fig. 3c). Pro-Bx (indicaxanthin) accumulated as a major pigment in Opuntia ficus-indica27 and Mirabilis jalapa28. The yellow callus from B. vulgaris produced 4.2 μmoles/g dry weight of total betaxanthin29. Therefore, the amounts of betaxanthins accumulated in transgenic BY2 cells were similar to those reported in calli and roots from plants in the Caryophyllales. When BA was fed to broad bean, the major betaxanthin was dopaxanthin10. In that case, amino acid analysis of the hypocotyl extract of broad bean seedlings revealed that L-DOPA was the most abundant amino acid present. However, the accumulation levels of amino acids are not the only factors influencing condensation reactions with BA30. Further studies are necessary to clarify the mechanisms of accumulation of specific betaxanthins in plant cells.

We transformed 35Sp-LeTYR/35Sp-MjDOD transgenic BY2 calli with a cDOPA5GT gene from M. jalapa24. However, none of the transgenic cell lines accumulated betacyanins. This indicated that cyclo-DOPA, which is the substrate of cDOPA5GT, was not abundantly accumulated, probably because of deficient or low L-DOPA oxidase activity. It is noteworthy that C-terminal processing of tyrosinase has been reported in several fungi31,32,33. Processing of tyrosinase is catalyzed by endogenous proteases such as the serine proteases and this proteolytic cleavage plays a critical role in enzyme activity. For example, analysis of a recombinant tyrosinase from Pholiota microspora revealed that the latent 67-kDa premature form did not have catalytic activity but the C-terminal cleaved 44-kDa mature form was catalytically active33, although the analysis did not distinguish between monophenolase and diphenolase activities. In transgenic BY2 calli expressing LeTYR, the premature 68-kDa LeTYR was detected from the early growth stages but the mature 45-kDa LeTYR appeared at later growth stages (Fig. 2c, Supplementary Fig. S2). It is unknown why LeTYR was not efficiently processed, but it is likely that plant proteases could not efficiently process the fungal tyrosinase protein because of its low expression level at the early growth stages of BY2 cells. In light of these facts, it is most likely that the unprocessed LeTYR accumulated in BY2 cells had only tyrosine-hydroxylating activity and not DOPA oxidase activity. However, betacyanins were not accumulated even at later growth stages when the mature 45-kDa LeTYR appeared, suggesting that the enzymatic activity of the shiitake tyrosinase expressed in BY2 calli was insufficient for efficient production of cyclo-DOPA. Therefore, the additional expression of CYP76AD1 might induce betacyanin accumulation in transgenic BY2 calli. Moreover, Goldfeder et al.34 demonstrated that the amino acid residue at position 218 influenced the monophenolase/diphenolase activity ratio of a bacterial tyrosinase by affecting the positioning of substrates within the active site. Protein engineering of a fungal tyrosinase involved in enzymatic activity or C-terminal processing might be also useful for the effective production of betalains in plant cells.

In conclusion, our results demonstrated that it is possible to engineer betalain biosynthesis in a heterologous expression system without extraneous substrate feeding. A fungal tyrosinase was able to substitute for the tyrosine-hydroxylating enzyme of betaxanthin-accumulating plants to accumulate L-DOPA in plant cells. Betalains are naturally limited to the order Caryophyllales in higher plants, but genetic engineering can now overcome the species barrier. As betalain pigments have beneficial properties for human nutrition and plant coloration, our approach may contribute to the development of genetically modified crops in the future.


Vector construction and BY2 transformation

The coding region sequences (CDS) of L. edodes tyrosinase (LeTYR, accession number AB027512)21 and M. jalapa DOPA 4,5-dioxygenase (MjDOD, AB435372)22 were used to replace the GUS gene in the binary vector pBI121 (kanamycin resistance) and pEBisHR (hygromycin resistance), respectively. pBI121-35Sp-LeTYR and pEBisHR-35Sp-MjDOD binary vectors were transformed into Agrobacterium tumefaciens EHA105 or EHA101.

The transformation of BY2 cells was performed following the procedure of An35. Transgenic calli were selected on medium containing 200 mg l−1 kanamycin or 20 mg l−1 hygromycin B and 500 mg l−1 carbenicillin and were subcultured every 2 weeks. A. thaliana ecotype Columbia suspension-cultured T87 cells36 were obtained from the RIKEN BioResource Center. T87 cells were transformed by an Agrobacterium-mediated method as described by Ogawa et al.37.

Expression analysis

Total RNAs were isolated from 200 mg (fresh weight) transgenic calli using a Fast RNA pro GREEN Kit (MP Bio Japan, Tokyo, Japan). Total RNAs (5 μg) were separated on a 1% agarose gel and then transferred onto a Hybond N+ membrane (GE healthcare, Little Chalfont, UK). The probes for LeTYR and MjDOD genes were labeled using a DIG-PCR labeling Kit (Roche Applied Sciences, Indianapolis, IN, USA). The hybridization and detection procedures were performed using the DIG Luminescent Detection Kit for Nucleic Acids (Roche) according to manufacturer's instructions.

Western blot analysis of LeTYR protein

Tissues (1 g fresh weight) of the transgenic BY2 and Arabidopsis T87 cell lines were lyophilized and crude proteins were extracted using 400 μl 50 mM HEPES buffer [pH 7.0]. Protein concentration was measured as described by Bradford38. For each transgenic callus, 10 μg crude protein was separated by SDS-PAGE (10% acrylamide) and transferred onto a polyvinylidene difluoride (PVDF) membrane. The membrane was blocked by blocking buffer (phosphate buffered saline [PBS] plus 5% skimmed milk and 0.3% Tween-20) for at least 12 h and then probed with a rabbit polyclonal antibody raised against LeTYR21. After extensive washing, membranes were incubated with the goat anti-rabbit IgG secondary antibody conjugated to alkaline phosphatase (Bio-Rad Laboratories, Hercules, CA, USA) and detected using an Immun-Blot Assay Kit (Bio-Rad).

Tyrosine-hydroxylating activity assay

To investigate tyrosine-hydroxylating activity, crude proteins were extracted from freeze-dried transgenic BY2 cells at 4 weeks after subculture using 400 μl 50 mM HEPES buffer [pH 7.0]. After centrifugation at 20,000 × g at 4°C for 10 min, the supernatants were collected and protein concentrations were measured as described above. Then, 25 μl crude extract containing 150 μg protein was mixed with 25 μl 2 mM tyrosine and incubated at 30°C for 30 min. The reaction was terminated by incubating the mixture at 95°C for 3 min. Boiled crude extracts were also assayed as the control. The mixture was centrifuged at 20,000 × g for 5 min and the supernatants were subjected to further analysis. The synthesized L-DOPA was quantified by capillary electrophoresis-mass spectrometry (CE-MS; Agilent Technologies, Santa Clara, CA, USA) according to the method of Takahashi et al39. The activities were represented by the amount of newly synthesized L-DOPA (nmol h−1 mg−1 protein). The MBTH assay was also performed to detect diphenolase activity as described by Rodriguez-Lopez et al.40.

Metabolite analysis

Transgenic BY2 cells (100 mg fresh weight) were powdered using a Micro Smash M100 (TOMY) and homogenized with 200 μl 1% (v/v) formic acid. After centrifugation, the supernatant was filtered through a Millipore 5-kDa-cutoff filter (Millipore) and the filtrates were used for analysis. Betaxanthins were analyzed by Agilent 6520 Accurate-Mass quadrupole time-of-flight liquid chromatography/mass spectrometry (Q-TOF LC/MS; Agilent Technologies). Separation was performed on a Develosil PRAQUEOUS-AR-5 column (4.6 mm × 250 mm; Numura Chemical Co., Seto, Japan) with a gradient elution of 3–20% (v/v) acetonitrile containing 0.1% (v/v) formic acid for 60 min, followed by 20–60% (v/v) for 30 min at a flow rate of 0.25 ml min 1−1 at 30°C. Absorbance at 470 nm was monitored by an Agilent 1200 Diode-Array Detector SL (Agilent Technologies). The total concentration of betaxanthin was calculated using the molar extinction coefficient (480 nm, ε = 48,000)29. Pro-Bx was quantified based on the area on the HPLC chromatogram monitored at 470 nm using synthetic authentic Pro-Bx as the standard. The HPLC separation was performed as described previously41.


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We thank Dr. Toshitsugu Sato, Kitami Institute of Technology, for providing the shiitake tyrosinase gene and for helpful discussions. The authors thank Dr. Ikuo Nakamura, Chiba University, for providing the pEBis binary vector. We thank the RIKEN BioResource Center for providing Arabidopsis thaliana T87 cells.

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T.N. and M.N. designed research, T.N., E.Y., H.T., T.I., N.S., M.S., I.T., M.S., Y.S. and M.N. performed research, T.N., H.T., N.S., Y.O. and M.N. analyzed data and T.N. and M.N. wrote the paper.

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Nakatsuka, T., Yamada, E., Takahashi, H. et al. Genetic engineering of yellow betalain pigments beyond the species barrier. Sci Rep 3, 1970 (2013).

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