Nucleoside 5′-Phosphoramidates Control the Phenylpropanoid Pathway in Vitis vinifera Suspension-Cultured Cells

It is known that cells contain various uncommon nucleotides such as dinucleoside polyphosphates (NpnN’s) and adenosine 5′-phosphoramidate (NH2-pA) belonging to nucleoside 5′-phosphoramidates (NH2-pNs). Their cellular levels are enzymatically controlled. Some of them are accumulated in cells under stress, and therefore, they could act as signal molecules. Our previous research carried out in Arabidopsis thaliana and grape (Vitis vinifera) showed that NpnN’s induced the expression of genes in the phenylpropanoid pathway and favored the accumulation of their products, which protect plants against stress. Moreover, we found that NH2-pA could play a signaling role in Arabidopsis seedlings. Data presented in this paper show that exogenously applied purine (NH2-pA, NH2-pG) and pyrimidine (NH2-pU, NH2-pC) nucleoside 5′-phosphoramidates can modify the expression of genes that control the biosynthesis of both stilbenes and lignin in Vitis vinifera cv. Monastrell suspension-cultured cells. We investigated the expression of genes encoding for phenylalanine ammonia-lyase (PAL1), cinnamate-4-hydroxylase (C4H1), 4-coumarate:coenzyme A ligase (4CL1), chalcone synthase (CHS1), stilbene synthase (STS1), cinnamoyl-coenzyme A:NADP oxidoreductase (CCR2), and cinnamyl alcohol dehydrogenase (CAD1). Each of the tested NH2-pNs also induced the expression of the trans-resveratrol cell membrane transporter VvABCG44 gene and caused the accumulation of trans-resveratrol and trans-piceid in grape cells as well as in the culture medium. NH2-pC, however, evoked the most effective induction of phenylpropanoid pathway genes such as PAL1, C4H1, 4CL1, and STS1. Moreover, this nucleotide also induced at short times the accumulation of N-benzoylputrescine (BenPut), one of the phenylamides that are derivatives of phenylpropanoid and polyamines. The investigated nucleotides did not change either the lignin content or the cell dry weight, nor did they affect the cell viability throughout the experiment. The results suggest that nucleoside 5′-phosphoramidates could be considered as new signaling molecules.


Introduction
Continuing our long-lasting studies on uncommon nucleotides, over a decade ago [1][2][3][4][5][6], we began to investigate the biochemistry of a rather neglected nucleotide, adenosine 5phosphoramidate (NH 2 -pA), since it appeared to be a very good substrate of Fhit (for fragile histidine triad) proteins [7]. Much earlier, this compound was detected among cellular nucleotides purified from the alga Chlorella pyrenoidosa [8]. It is known that in various organisms including plants, NH 2 -pA can be synthesized [5,9] and degraded [7,10,11] by various enzymes, and it is considered as an enzymatic mechanism controlling the concentration of this nucleotide in cells. Its synthesis proceeds according to the reaction SO 4 -pA + NH 4 + → NH 2 -pA + SO 4 2− + 2H + catalyzed by adenylyl sulfate:ammonia adenylyltransferase (EC 2.7.7.51) (Figure 1). This activity was found in the algae Chlorella pyrenoidosa and Euglena gracilis, the amoeba Dictyostelium discoideum, the bacterium Escherichia coli, and the higher plants Hordeum vulgare, Spinacia oleracea [8], and Lupinus luteus [5]. In the latter organism, this transferase activity proved to be an inherent property of dinucleoside triphosphatase, the Fhit protein [5]. So far, various enzymes have been shown to catalyze the degradation of NH 2 -pA, in most cases by hydrolysis to ammonia and AMP [10][11][12][13][14][15], and in a few cases to ammonia and ADP by phosphorolysis [14]. Interestingly, Fhits, regardless of their origin, are able to catalyze both the synthesis and cleavage of NH 2 -pA [5]. Our recent studies on in vitro cultivated Arabidopsis seedlings showed that exogenous NH 2 -pA induced the expression of genes of the general phenylpropanoid pathway such as PAL1, PAL2, PAL3, PAL4, C4H, 4CL1, 4CL2, and 4CL3. Moreover, it was also observed that induction of CCR2, CHS, and ICS2 expression caused the accumulation of lignins, anthocyanins, and salicylic acid, respectively [4], which protect cells against various types of stresses. Other compounds that are involved in plant defenses against abiotic and biotic stresses are phenylamides, also termed as phenolamides or hydroxycinnamic acid amides [16]. The phenylamides arise from phenolic moieties, hydrocinnamic and benzoic acids, covalently linked through amide bonds to an aromatic monoamine or an aliphatic polyamine. Their synthesis is positioned at the crossroads of the phenylpropanoid pathway and the metabolism of amines [16] and can be used in the cross-linking of cell wall components in plants ( Figure 2) [17,18]. An elevated concentration of phenylamides has been reported in a wide range of plant species, and it can play a protective role against biotic stresses [19][20][21]. This is why we decided to check whether the NH 2 -pNs also affect the metabolism of those compounds.
Although it is not known whether any of the NH 2 -pNs accumulates in response to environmental stresses, according to our earlier observation of the induction of the phenylpropanoid pathway in Arabidopsis thaliana seedlings by NH 2 -pA [4], it seems plausible that biotic and abiotic environmental factors do affect the accumulation of this nucleotide, the putative regulatory molecule. The signaling transduction pathways underlying both abiotic and biotic stresses mediating the regulation of cellular responses are still intensively studied by many researchers. One of the defense strategies in higher plants under abiotic and biotic stresses is an activation of the phenylpropanoid pathway [22]. This pathway occurs widely in plant species, conferring adaptive advantages to diverse ecosystems. Its activation leads to the enhanced production of various phenylpropanoid compounds such as flavonoids [23,24], lignins [25], anthocyanins [26], salicylic acid [27], and stilbenes [28]. These metabolites reduce the adverse effects caused by stress-induced oxidative damage. One of the most studied stilbenes is trans-resveratrol. This compound is especially involved in plant-pathogen interactions [28] and plays an important role in plant responses to cadmium [29]. Besides the phenylpropanoid-based mechanism of plant responses to various biotic and abiotic stresses, another mechanism is the regulation of the ratio of S-containing compounds such as methionine, glutathione, phytochelatins, and glucosinolates by the activity of ATP-sulfurylase [30]. Through these S-compounds, that enzyme is involved in the plant tolerance of several biotic and abiotic stresses. For example, glutathione can control the gene expression of antioxidant enzymes such as superoxide dismutase or glutathione reductase as well as enzymes of the phenylpropanoid pathway (e.g., chalcone synthase and phenylalanine ammonia-lyase) under cadmium stress [31]. ATP-sulfurylase catalyzes the activation of SO 4 2− , yielding high-energy adenosine-5 -phosphosulfate (APS) [30]. It is known that in plants, APS can be converted into NH 2 -pNs by ammonolysis catalyzed by adenylylsulfate-ammonia adenylyltransferase [9] and Fhit proteins [5]. Moreover, Fhit can degrade NH 2 -pA, releasing AMP and NH 3 [7,10,15]. The main goal of our research was to learn how NH 2 -pA as well as other NH 2 -pNs including NH 2 -pG (guanosine 5 -phosphoramidate), NH 2 -pC (cytidine 5 -phosphoramidate), and NH 2 -pU (uridine 5 -phosphoramidate) regulate the metabolism of phenylpropanoids and biosynthesis of phenylamides in grape cells. Moreover, we wanted to determine how these uncommon nucleotides impact the expression of the gene coding for the VvABCG44 transporter, which was proven to be involved in the transport (export) of trans-resveratrol in Vitis vinifera. This paper describes the results of experiments conducted on a Vitis vinifera cv. Monastrell suspension cell culture and presents a hypothesis concerning links between NH 2 -pNs and the production of trans-resveratrol.

Results
In this study, we used a suspension cell culture (SCC) of the grape cell cultivar Monastrell, which is a very convenient model. First, because of the equal distribution of molecules studied as effectors among the cells, and second, this particular variety of the grape effectively synthesizes the phenylpropanoid molecule trans-resveratrol. The analysis of gene expression and accumulation of different products of the phenylpropanoid pathway was carried out as described in our earlier studies [3,4,6]. For details, see Section 4. In our earlier studies on the effect of NH 2 -pA on the expression of the genes coding for phenylalanine ammonia-lyase (PAL) and 4-coumarate:coenzyme A ligase (4CL) in Arabidopsis seedlings, we found that of the concentrations tested in the 0.05-25 µM range, 5 µM NH 2 -pA appeared to be the most effective [4]. In addition, in the experiments on the grape suspension cells described here, this relatively low concentration of NH 2 -pA evoked marked effects. Therefore, each of the investigated NH 2 -pNs was applied to the cells at a fixed 5 µM concentration. Based on previous studies [3,4,6,[32][33][34], we chose the following genes: PAL1, C4H1, 4CL1, STS1, CAD1, and CCR2. In addition, we selected the time points of the experiment based on our previous works [3,6]. The expression of the CHS1, the branch point of flavonoid biosynthesis, was evaluated at the same time points as other gene expressions were analyzed in this study, but it was not detected. The same results were observed in the grape suspension cell culture in our previous studies [3,6] and by Lijavetzky and coworkers [32]. These data strongly suggest that flavonoids are not synthesized in the dark in cells of this plant species.

Effect of Exogenous NH 2 -pNs on the Expression of Genes of the General Phenylpropanoid Pathway
Expression of the three genes PAL1, C4H1, and 4CL1 was analyzed in the cells collected between 6 and 72 h of growth after elicitation. The results of these experiments are summarized in Figure 3a-c. A marked increase in the expression of the studied genes was observed in the grape cells collected after 72 h. Interestingly, NH 2 -pC evoked the most significant effect of the analyzed compounds, with an approximately 8-fold increase in PAL1. It was over 2-fold higher in comparison to the effect exerted by NH 2 -pG and NH 2 -pU and about 4-fold higher than that caused by NH 2 -pA. Additionally, the expression of 4CL1 was induced much more effectively by NH 2 -pC than by the other tested NH 2 -pN, and it reached about a 10-fold increase with respect to the controls. Effects evoked by 5 µM NH 2 -pG, NH 2 -pA, or NH 2 -pU were less spectacular, with only 4-, 3.2-, and 3-fold increases compared to the control, respectively. The expression of PAL1 and 4CL1 after 6 and 24 h of elicitation by each of the tested nucleotides did not change. In the case of C4H1 expression, we observed an inhibitory effect evoked by NH 2 -pU, NH 2 -pA, and NH 2 -pG at 72 h. It was about 2-to 3-fold lower than in the control. In cells treated with NH 2 -pC, the expression of C4H1 increased up to 2.5-fold. However, it was 5-to 8-fold higher than in cells treated with other nucleotides (Figure 3a-c). Total RNA was reverse-transcribed into cDNA and used as a template for real-time quantification PCR reaction as described in the Section 4. Specific primers were designed for PAL1, C4H1, 4CL1, and EFα1 (elongation factor 1-alpha, which was used as an endogenous control). The expression level of PAL1, C4H1, and 4CL1 in the control cells (no nucleotide added) was set to 1. Values represent the mean ± standard deviation of the three replicates. Values without a common letter were significantly different according to the analysis of variance (ANOVA) and Tukey's honestly significant difference (HSD) multiple range test (p ≤ 0.05).

Effect of Exogenous NH 2 -pNs on Stilbene Synthase Gene (STS1) Expression and Stilbene Accumulation in Grape Cells
All of the tested NH 2 -pNs increased the expression of STS1 about 2-fold after 24 h, but only NH 2 -pG, NH 2 -pC, and NH 2 -pU also increased the expression of STS1 in 72 h. At this time point, the most effective was NH 2 -pC, even causing a 13-fold higher expression than in the control (Figure 4a). Such a spectacular effect inspired us to investigate how this induction of STS1 expression affects the accumulation of the related stilbene compounds (i.e., trans-resveratrol and its glycoside -trans-piceid). In the cells collected after 6 and 12 h, no significant effect of the tested nucleotides on trans-resveratrol content was found. However, after 24 h of elicitation with any of the investigated NH 2 -pNs, a dramatic increase in the level of this secondary metabolite was observed ( Figure 4b). The most significant effect was evoked by NH 2 -pA and NH 2 -pU at 24 h. In their presence, the accumulation of trans-resveratrol in the grape cells reached 961 µg g −1 dry weight (DW) and 821 µg g −1 DW, respectively, and it was about 1.7-and 1.5-fold higher than in the control cells ( Figure 4b).
We did not observe statistically significant changes in trans-resveratrol accumulation in the presence of NH 2 -pG compared with the control cells. However, in grape cells treated with the pyrimidine nucleotide, NH 2 -pC, the accumulation of trans-resveratrol only reached 76 µg g −1 DW, and it was 7-fold lower than in the control cells. In the cells collected after 48 h, the trans-resveratrol content was much lower than that at 24 h of the experiment, and in those collected after 72 h, it was as low a level as in the cells collected after 6 and 12 h of elicitation ( Figure 4b). The trans-piceid content, similar to trans-resveratrol, was low at 6 and 12 h, irrespective of the nucleotide treatment ( Figure 4c). The content of trans-piceid was clearly elevated after 24 h of elicitation including in the control cells, but it was dramatically decreased in the cells treated with NH 2 -pG, being 13-fold lower than in the control cells and reached only 183 µg g −1 DW (Figure 4c). Interestingly, however, after 48 h, the accumulation of trans-piceid reached a maximum. At this time, in cells treated with NH 2 -pA or NH 2 -pC, the level of this stilbene was over 2-fold higher than in the control cells. Similar to the trans-resveratrol content, the level of trans-piceid decreased dramatically after 72 h of elicitation and reached a level comparable to that observed after 6 and 12 h of the experiment (Figure 4c). (c) accumulation of trans-piceid. Total RNA was reverse-transcribed into cDNA and used as a template for real-time quantification PCR reaction as described in the Section 4. Specific primers were designed for STS1 and EFα1 (elongation factor 1-alpha, which was used as an endogenous control). The expression level of STS1 in the control cells (no nucleotide added) was set to 1. Values represent the mean ± standard deviation of the three replicates. Accumulation of transresveratrol and trans-piceid was determined using the HPLC method as described in the Section 4. Values without a common letter are significantly different according to ANOVA and Tukey's HSD multiple range test (p ≤ 0.05).

Expression of the Gene Coding for the Resveratrol Transporter VvABCG44 (ATP-Binding Cassette Transporter) and Stilbene Content in the Spent Media
It is known that treatment of cultured grape cells with an elicitor, cyclodextrin, causes the accumulation of trans-resveratrol and induction of gene expression of the full-size ABCG transporter, which is associated with the transport of this stilbene compound in plants [35]. Therefore, we also analyzed the effects of NH 2 -pNs on the expression of the VvABCG44 gene. As shown in Figure 5a, each of the investigated nucleoside phosphoramidates evoked around a 3-fold increase of the gene expression, and it was already observed after 6 h of elicitation. Then, this gene expression declined at 24 and 72 h. An exception was observed in cells treated with NH 2 -pG at 72 h, since the increase in the gene expression was still 2-fold higher than in the controls. The time-course of trans-resveratrol and trans-piceid accumulation in the spent medium in response to NH 2 -pNs are shown in Figure 5b,c, respectively. Intensive export of these compounds from the cells to the media occurred, and it was observed just after 6 h of elicitation. The concentration of trans-resveratrol after 6 h of NH 2 -pG application really reached 9.5 µM (Figure 4b), but the concentration of trans-piceid after 6 h of NH 2 -pC reached less than 2 µM (Figure 5c). In the spent medium in which the cells were treated with NH 2 -pA, we observed a gradual increase in trans-resveratrol content up to 48 h. Then, the level of this stilbene drastically decreased (Figure 5b). At 72 h of the experiment, the concentration of trans-resveratrol was at the same level as in the control media. The highest accumulation of trans-piceid in the spent media caused by nucleotides was observed at 24 h, and for NH 2 -pA, NH 2 -pC, NH 2 -pG, and NH 2 -pU, it was 12-, 9-, 7-, and 5-fold higher than in the control media, respectively; however, only the 12-fold increase was statistically significant (Figure 5c). (c) accumulation of trans-piceid. Total RNA was reverse-transcribed into cDNA and used as a template for real-time quantification PCR reaction as described in the Section 4. Specific primers were designed for VvABCG44 and EFα1 (elongation factor 1-alpha, which was used as an endogenous control). The expression level of VvABCG44 in the control cells (no nucleotide added) was set to 1. Accumulation of trans-resveratrol and trans-piceid was determined using the HPLC method as described in the Section 4. Values are the mean ± standard deviation of the three replicates. Values without a common letter were significantly different according to ANOVA and Tukey's HSD multiple range test (p ≤ 0.05).

Cell Viability
Because we observed, both in the cells and in the spent media, a considerable decrease in the content of trans-resveratrol and trans-piceid at 72 h of the experiment, and due to the fact that at this time there was no effect of nucleotides on the content of these two stilbenes, we assessed the cell viability and cell growth (expressed as dry weight content) to exclude the possibility of cell death caused by the exogenous application of nucleotides. As shown in Figure 6, no losses in cell viability were observed by fluorescent microscopy at 72 h of treatment with the nucleotides. We also analyzed changes in the cell dry weight throughout the experiment. As shown in Figure 7, the nucleotide-treated cells displayed a similar biomass increase (from 10 to over 29 g DW L −1 ), and therefore cell growth as the control (i.e., untreated cells).

Expression of Genes Encoding for Enzymes of Monolignol Biosynthesis and Lignin Content
We tested both the expression of genes involved in lignin biosynthesis and the accumulation of lignin, one of the main products of the phenylpropanoid pathway. CCR2 gene encodes cinnamoyl-CoA reductase, which is the first step in monolignol biosynthesis. As can be seen in Figure 8a, the expression of CCR2 was induced by nucleotides only at 6 h of treatment, and for NH 2 -pU, NH 2 -pA, NH 2 -pC, and NH 2 -pG, it was 1.8-, 2-, 2.2-and 2.9-fold higher than in the control, respectively. Then, a reduced expression of CCR2 was observed, being at 72 h 2-fold lower in all nucleotide treatments than in the control (i.e., untreated cells) (Figure 8a). , cinnamyl alcohol dehydrogenase (c) lignin content. Total RNA was reverse-transcribed into cDNA and used as a template for real-time quantification PCR reaction as described in the Section 4. Specific primers were designed for CCR2, CAD1, and EFα1 (elongation factor 1-alpha, which was used as an endogenous control). The expression level of CCR2 and CAD1 in the control cells (no nucleotide added) was set to 1. The lignin content was determined as described in the Section 4. Values represent the mean ± standard deviation of the three replicates. Values without a common letter were significantly different according to ANOVA and Tukey's HSD multiple range test (p ≤ 0.05). CAD1 gene expression, encoding cinnamyl alcohol dehydrogenase, was also assessed. Expression of this gene increased up to 2.7-fold in cells treated with 5 µM NH 2 -pC at 72 h. At this time point, all other tested nucleotides evoked only a 2-fold higher effect than in the control cells (Figure 8b).
On the other hand, the nucleotides investigated in this study during the experiments had no effect on the lignin content, and its level was similar to that found in control cells (Figure 8c).

Effect of Exogenous NH 2 -pNs on the Content of Phenylamides in Both Cells and the Spent Media
Among the twenty-five phenylamides tested (Supplementary Materials (Methods S2)), only N-benzoylputrescine (BenPut) was accumulated in grape cells. The content of this phenylamide depended on the NH 2 -pN nature and treatment time (Figure 9). Interestingly, at 6 h of treatment, NH 2 -pC evoked induction of accumulation of BenPut. Its content reached 0.32 µg g −1 DW, and its level hardly changed throughout the experiment. In the case of other NH 2 -pNs, BenPut was not detected at 6 h. At 24 h, an accumulation of BenPut was observed in cells treated with NH 2 -pA, NH 2 -pG, and NH 2 -pC. At the further time points of the experiment, both in the controls and cells treated with nucleotides, the level of BenPut was similar and remained stable. To our knowledge, this is the first time detecting the accumulation of phenylamides in Vitis vinifera. On the other hand, we did not observe the accumulation of any of the twenty-five tested phenylamides in the spent media.

Discussion
This study demonstrated that the uncommon nucleotide NH 2 -pA, naturally occurring in organisms, applied to a cell suspension of Vitis vinifera, induced the expression of genes that control both the biosynthesis of stilbenes (Figures 4a and 5a) and lignins (Figure 8a,b). This induction caused a transient accumulation of trans-resveratrol and trans-piceid, both in the cells and spent media (Figures 4b,c and 5b,c), respectively. Another purine nucleotide, NH 2 -pG, also induced the gene expression of resveratrol-cell-membranetransporter throughout the experiment (Figure 5a). In fact, three canonical congeners of NH 2 -pA: NH 2 -pG, NH 2 -pC, and NH 2 -pU, which have not been so far identified as natural metabolites in any organism, also affected the expression of the aforementioned genes and accumulation of stilbene compounds. Although all the tested nucleoside phosphoramidates acted as elicitors, some differences in effectiveness were observed among them. In fact, NH 2 -pA (purine nucleotide) proved to be the most effective in inducing VvABCG44 gene expression as well as in trans-resveratrol and trans-piceid accumulation. Additionally, NH 2 -pC (pyrimidine nucleotide) turned out to be quite effective in inducing genes of the phenylpropanoid pathway in Vitis vinifera. However, during a short exposure time (6 h), NH 2 -pG evoked the most significant effect on the expression of VvABCG44 (Figure 5a) and trans-resveratrol accumulation in the spent medium (Figure 5b) among all investigated NH 2 -pNs. The level of trans-resveratrol and trans-piceid decreased at 72 h of the experiment both in the medium and cells (Figure 4b,c and Figure 5b,c, respectively). As the cell suspension of Vitis vinifera remains alive at the end of the treatment with these nucleotides (Figure 6), it is plausible to think that trans-resveratrol and its glucoside, trans-piceid could be transformed by the action of cellular or extracellular peroxidases into other more complex stilbenes (such as viniferins) [36]. Results obtained from this study together with those previously carried out in Arabidopsis seedlings treated with NH 2 -pA [4] suggests that the investigated nucleotides can act as signal molecules in plants. Moreover, our earlier studies showed that any common nucleotides such as AMP, GMP, UMP, and CMP that could be a product of degradation of NH 2 -pNs did not evoke the accumulation of stilbenes in Vitis vinifera suspension cell culture [6].
We also investigated whether exogenously applied NH 2 -pNs affected in grape cells the biosynthesis of lignin -other compounds derived from the phenylpropanoid pathway, known to be accumulated in plant tissues in response to abiotic or biotic stresses [25]. It was found, however, that the nucleotides used substantially modified neither the lignin content nor the cell growth (assessed as cell dry weight). Still, it should be kept in mind that both lignin biosynthesis and dry weight accumulation are long-term processes, and 72 h of treatment might not be sufficient to observe this effect on the accumulation of lignin and cell dry weight. These results nevertheless suggest that NH 2 -pNs would be involved in the early signaling stages in response to environmental stimuli.
Considering the signaling role of the investigated nucleotides, the question is: what is the target of NH 2 -pA, or generally, all NH 2 -pNs? To answer this question, we postulate that in the control of gene expression by NH 2 -pNs, the HIT proteins, which catalyze the cleavage of the phosphoramide bond in these nucleotides, are involved. As mentioned earlier, hydrolysis of the P-N bond liberates more energy than splitting the phosphate anhydride (P-O) bond; −38 kJ/mol versus −34 kJ/mol, respectively [9]. Whether the postulated signal transduction mediated by NH 2 -pNs causes the adenylation, or generally the nucleotidylation, of the hypothetical target molecule, or causes only its conformational changes is another intriguing question awaiting elucidation. Speculating further, we suggest that, in plant cells, there is a link between the metabolism of sulfur and NH 2 -pAs: first, by the double role of Fhit protein, which can act as an adenylylsulfate:ammonia adenylyltransferase, and as nucleoside phosphoramidase [5]; and second, by the known activation of sulfate metabolic pathways under biotic and abiotic stresses in plants [30].
Based on our previous studies on the effect of NH 2 -pA on phenylpropanoid metabolism in Arabidopsis seedlings [4], a fact considered in our literature review [37], and the results presented here, we postulate that NH 2 -pNs are involved in the plant response to environmental stresses via induction of the phenylpropanoid pathway. In Figure 10, we summarize the knowledge about the pathway of NH 2 -pA metabolism and its effect on the phenylpropanoid pathway. Although our results indicate that another NH 2 -pN (i.e., NH 2 -pC) exerts impressive effects on the same genes of the phenylpropanoid pathway (Figures 3 and 4), we do not know if this compound occurs in nature and what enzymatic reaction might be responsible for its biosynthesis. We trust that our findings open new avenues that will be followed by different 'omic' studies that will shed more light on physiological functions of these nucleotides.

Plant Materials
Vitis vinifera L. cv. Monastrell calli were established as described by Calderon et al. [38] and maintained at 25 • C in darkness in 250 mL flasks containing 100 mL of fresh culture medium (Gamborg B 5 , Duchefa, The Netherlands). Monastrell SCC was initiated by inoculating friable callus pieces in 250 mL Erlenmeyer flasks containing 100 mL of liquid Gamborg B 5 medium (pH 6.0) at 25 • C in the dark and were routinely maintained by periodic subcultures every 14-16 days as described by Belchí-Navarro et al. [39] and Almagro et al. [40].

Elicitor Treatment
Elicitation experiments were carried out in triplicate using 10-day-old Monastrell SCC. At that stage of cell development, 3 g of fresh weight of cells was washed with cold distilled water, transferred into 50 mL flasks, suspended in 15 mL of fresh Gamborg B 5 medium supplemented with 5 µM NH 2 -pN (NH 2 -pA, NH 2 -pG, NH 2 -pU, or NH 2 -pC), and incubated for 72 h at 25 • C in the dark on a rotary shaker (110 rpm). Control samples, without elicitors, were always run in parallel. The cells were harvested after 6, 24, 48, and 72 h, separated from the culture medium by filtration under a gentle vacuum, rapidly washed with cold distilled water, frozen in liquid nitrogen, and kept at −80 • C until use. The spent culture media were also frozen and stored at −20 • C until use.

NH 2 -pNs Chemical Synthesis
Details of the chemical synthesis of NH 2 -pA, NH 2 -pG, NH 2 -pU, and NH 2 -pC, and their characterization by HRMS, 1 H NMR, 13 C NMR, and 31 P NMR are given in the Supplementary Materials (Methods S2).

Lignin Determination
Lignin content was measured based on the method described by Syros et al. [41]. The harvested cells were air-dried at 70 • C, and 0.1 g dry mass was subjected to triple ethanol extraction at 80 • C. Each time, 3 mL of 80% (v/v) ethanol was added, and after the incubation, it was precisely discarded. The first extraction lasted for 1.5 h, the second, and the third for 1 h. Subsequently, 3 mL of chloroform was added, and the samples were heated to 62 • C. After 1 h, chloroform extract was removed, and samples were air-dried in an oven at 50 • C. Dried cells were digested at 70 • C in 2.6 mL of a solution of 25% (v/v) acetyl bromide in acetic acid containing 2.7% (v/v) perchloric acid. After 1 h of incubation, 100 µL of each sample was added to 580 µL of a solution of 2 N sodium hydroxide and acetic acid. The reaction was terminated by adding 20 µL of 7.5 M hydroxylamine hydrochloride. Then, the samples were filled up to 2 mL with acetic acid, and the absorbance at 280 nm was measured. Lignin content was expressed as mg g −1 DW, using a linear calibration curve with a commercial lignin alkali standard (Sigma, St. Louis, MO, USA).

Determination of Phenylamide Content in Cells and Spent Media
Phenylamide analysis was performed according to Morimoto et al. [19]. The grape cells were air-dried at 70 • C, then phenylamides were extracted with 10 mL of 80% methanol. For concentration, the samples were dried on a SpeedVac, and suspended in 300 µL of methanol. To extract phenylamides from the spent media, solid-phase extraction (SPE) (Superclean ENVI-18 SPE Tubes, Supelco, Bellefonte, PA, USA) was applied. The compounds from the SPE columns were eluted with 80% methanol and concentrated by drying on a SpeedVac, and suspending in 300 µL of methanol. Then, the samples were subjected to LC-MS/MS analysis. More details are given in the Supplementary Materials (Methods S2).

Cell Viability
Cell viability was evaluated using the Plant Cell Viability Assay Kit (Sigma-Aldrich) according to the manufacturer's instructions. The cells were incubated for 1-2 min in fresh Gamborg medium, then 10 µL of the assay kit diluted in 1 M PBS pH 7.4 was added to 90 µL of cell suspension and mixed by gently tapping the tube. Fluorescence was monitored with an AxioVert 200 Carl Zeiss microscope using a Zeiss filter (FS09 exc = 495 nm, emi = 517 nm and FS15exc = 538 nm, emi = 617 nm).

Genes Expression Analyses
Total RNA was extracted from 200 mg of Monastrell frozen cells using the RNeasy Plant Minikit (Qiagen, Hilden, Germany) according to the supplier's recommendations as previously described [3,6]. The concentration of each RNA sample was measured using a NanoDrop 2000 spectrophotometer (Thermo Scientific, Waltham, MA, USA). Only the RNA samples with a 260/280 ratio between 1.9 and 2.1 were used for the analysis. The integrity of RNA samples was also assessed by agarose gel electrophoresis and purity was confirmed by PCR using EFα1-specific primers. Then, 3 µg of total RNA was used for cDNA synthesis with oligo(dT) 20 (50 µM) primers and the Superscript III Reverse Transcriptase Kit (Invitrogen). A quantitative real-time PCR reaction was carried out using a CFX96 Real-Time PCR Detection System (Bio-Rad) and iTaq Universal SYBR Green Supermix (Bio-Rad), and the specific primers for Monastrell genes (PAL1, C4H1, 4CL1, CHS1, STS1, VvABCG44, CCR2, CAD1, and EFα1). The comparative C T method for relative quantification was used with EFα1 as an endogenous control. The amount of target, normalized to an endogenous reference and relative to a calibrator, is given by 2 −∆∆CT [42]. Primer sequences and GenBank accession numbers are presented in the Supplementary Materials (Table S1).

Statistical Analysis
Data concerning mRNA level and concentrations of stilbenes, lignin, phenylamide and dry weight are the means of three independent replicates ± standard deviation. The statistical significance of the differences between averages was determined by ANOVA using Tukey's HSD multiple range test at p ≤ 0.05.

Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Not applicable.

Data Availability Statement:
The data that support the findings of this study are available from the corresponding author upon reasonable request.