taxonID	type	format	identifier	references	title	description	created	creator	contributor	publisher	audience	source	license	rightsHolder	datasetID
03AE2D4F0B50615EFCD4F9D6FBF47632.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/10491348/files/figure.png	https://doi.org/10.5281/zenodo.10491348	Fig. 2. LC–ESI–MS chromatogram of the MeOH extract of a P.lanceolata callus grown on medium 10(0.33) (25 mg dry wt./ml, total ion chromatogram in negative ion mode). Note that in this injection, the area under curve of plantamajoside was beyond the linear range of determination, and thus, major NPs were quantified in the 100-fold dilution, and not from the chromatogram presented here.Main peaks are marked with the metabolite numbers used in text, see Table 1 for putative identification.NPs compared with standards are marked with an asterisk. For m/z values, and putative identification, see Table 1. Abbreviations: AC, acteoside; PM, plantamajoside.	Fig. 2. LC–ESI–MS chromatogram of the MeOH extract of a P.lanceolata callus grown on medium 10(0.33) (25 mg dry wt./ml, total ion chromatogram in negative ion mode). Note that in this injection, the area under curve of plantamajoside was beyond the linear range of determination, and thus, major NPs were quantified in the 100-fold dilution, and not from the chromatogram presented here.Main peaks are marked with the metabolite numbers used in text, see Table 1 for putative identification.NPs compared with standards are marked with an asterisk. For m/z values, and putative identification, see Table 1. Abbreviations: AC, acteoside; PM, plantamajoside.	2014-10-31	Gonda, Sándor;Kiss-Szikszai, Attila;Szucs, Zsolt;Máthé, Csaba;Vasas, Gábor		Zenodo	biologists	Gonda, Sándor;Kiss-Szikszai, Attila;Szucs, Zsolt;Máthé, Csaba;Vasas, Gábor			
03AE2D4F0B50615EFCD4F9D6FBF47632.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/10491350/files/figure.png	https://doi.org/10.5281/zenodo.10491350	Fig. 3. Proposed fragmentation pattern of plantamajoside, the main phenylethanoid glycoside of the P. lanceolata callus extract in negative mode LC–ESI–MS3. The main fragmentation route is highlighted with bold arrows and bold font.	Fig. 3. Proposed fragmentation pattern of plantamajoside, the main phenylethanoid glycoside of the P. lanceolata callus extract in negative mode LC–ESI–MS3. The main fragmentation route is highlighted with bold arrows and bold font.	2014-10-31	Gonda, Sándor;Kiss-Szikszai, Attila;Szucs, Zsolt;Máthé, Csaba;Vasas, Gábor		Zenodo	biologists	Gonda, Sándor;Kiss-Szikszai, Attila;Szucs, Zsolt;Máthé, Csaba;Vasas, Gábor			
03AE2D4F0B50615EFCD4F9D6FBF47632.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/10491346/files/figure.png	https://doi.org/10.5281/zenodo.10491346	Fig. 1. Selected phenylethanoid glycosides detected from the MeOH extracts of P. lanceolata calli by LC–ESI–MS3. Plantamajoside, R 1 = Glc, R 2 = H; Acteoside, R 1 = Rha, R2 = H; Desrhamnosyl-acteoside, R1 = R2 = H; Lavandulifolioside, R1 = Ara(1->2)Rha, R2 = H; Leucosceptoside A, R1 = Rha, R2 = Me. For details of identification, see text and Table 1. Abbreviations: Ara, arabinose; Glc, glucose; Rha, rhamnose.	Fig. 1. Selected phenylethanoid glycosides detected from the MeOH extracts of P. lanceolata calli by LC–ESI–MS3. Plantamajoside, R 1 = Glc, R 2 = H; Acteoside, R 1 = Rha, R2 = H; Desrhamnosyl-acteoside, R1 = R2 = H; Lavandulifolioside, R1 = Ara(1->2)Rha, R2 = H; Leucosceptoside A, R1 = Rha, R2 = Me. For details of identification, see text and Table 1. Abbreviations: Ara, arabinose; Glc, glucose; Rha, rhamnose.	2014-10-31	Gonda, Sándor;Kiss-Szikszai, Attila;Szucs, Zsolt;Máthé, Csaba;Vasas, Gábor		Zenodo	biologists	Gonda, Sándor;Kiss-Szikszai, Attila;Szucs, Zsolt;Máthé, Csaba;Vasas, Gábor			
03AE2D4F0B50615EFCD4F9D6FBF47632.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/10491354/files/figure.png	https://doi.org/10.5281/zenodo.10491354	Fig. 4. Principal component (PC) analysis score plot of the scaled, centered and per-composition averaged natural product abundance dataset. The plot shows the effect of media composition on the metabolome as a whole. The NP abundances were measured by LC–ESI–MS3 from MeOH extracts of P. lanceolata calli grown on media with different N source compositions. For more details, see text. Subplots: (a) Pseudo-3D score plot of PCs 1–3. PC2 and PC3 scores are plotted on axes x and y, respectively, while PC1 is made proportional to point size (see legend). Media codes are as follows: N concentration (mM), followed by NH + /NO – ratio (ratio of NH + in the total N source) in 4 3 4 parentheses. The NH + concentration in the media is coded by color (see legend). Abbreviations: NSC, N source concentration. (b), Loading plot for the first three PCs showing 4 contribution of the 89 individual metabolites to the PC scores. The order of NPs was obtained from hierarchical cluster analysis of the NP abundances.	Fig. 4. Principal component (PC) analysis score plot of the scaled, centered and per-composition averaged natural product abundance dataset. The plot shows the effect of media composition on the metabolome as a whole. The NP abundances were measured by LC–ESI–MS3 from MeOH extracts of P. lanceolata calli grown on media with different N source compositions. For more details, see text. Subplots: (a) Pseudo-3D score plot of PCs 1–3. PC2 and PC3 scores are plotted on axes x and y, respectively, while PC1 is made proportional to point size (see legend). Media codes are as follows: N concentration (mM), followed by NH + /NO – ratio (ratio of NH + in the total N source) in 4 3 4 parentheses. The NH + concentration in the media is coded by color (see legend). Abbreviations: NSC, N source concentration. (b), Loading plot for the first three PCs showing 4 contribution of the 89 individual metabolites to the PC scores. The order of NPs was obtained from hierarchical cluster analysis of the NP abundances.	2014-10-31	Gonda, Sándor;Kiss-Szikszai, Attila;Szucs, Zsolt;Máthé, Csaba;Vasas, Gábor		Zenodo	biologists	Gonda, Sándor;Kiss-Szikszai, Attila;Szucs, Zsolt;Máthé, Csaba;Vasas, Gábor			
03AE2D4F0B50615EFCD4F9D6FBF47632.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/10491356/files/figure.png	https://doi.org/10.5281/zenodo.10491356	Fig. 5. Abundance of selected natural products from extracts of P. lanceolata calli grown on media with different N source concentrations and NH + /NO – ratios (ratio of NH + in 4 3 4 the total N source).Color is proportional to the abundance (area under curve) for the given NPs, quantified in extracted ion chromatograms (a, b, c, e), or content of dry weight expressed as percent (d, f) Subplots: (a), 22, putatively identified as desrhamnosyl-acteoside, cluster 1; (b), 49, a plantamajoside isomer, cluster 2; (c), 8, putatively identified as a plantamajoside hexoside, cluster 3; (d), 18, plantamajoside (plantamajoside), cluster 4; (e), 65, putatively identified as a dimethyl-acetyl acteoside, cluster 4; (f), 27, acteoside, cluster 6.	Fig. 5. Abundance of selected natural products from extracts of P. lanceolata calli grown on media with different N source concentrations and NH + /NO – ratios (ratio of NH + in 4 3 4 the total N source).Color is proportional to the abundance (area under curve) for the given NPs, quantified in extracted ion chromatograms (a, b, c, e), or content of dry weight expressed as percent (d, f) Subplots: (a), 22, putatively identified as desrhamnosyl-acteoside, cluster 1; (b), 49, a plantamajoside isomer, cluster 2; (c), 8, putatively identified as a plantamajoside hexoside, cluster 3; (d), 18, plantamajoside (plantamajoside), cluster 4; (e), 65, putatively identified as a dimethyl-acetyl acteoside, cluster 4; (f), 27, acteoside, cluster 6.	2014-10-31	Gonda, Sándor;Kiss-Szikszai, Attila;Szucs, Zsolt;Máthé, Csaba;Vasas, Gábor		Zenodo	biologists	Gonda, Sándor;Kiss-Szikszai, Attila;Szucs, Zsolt;Máthé, Csaba;Vasas, Gábor			
