taxonID	type	format	identifier	references	title	description	created	creator	contributor	publisher	audience	source	license	rightsHolder	datasetID
2812FE14FA2AAC2FFCDBFB69FC7AF9BC.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/10481560/files/figure.png	https://doi.org/10.5281/zenodo.10481560	Fig. 2. The content changes of Praeruptorin A, Praeruptorin B and Imperatorin. A. The content of three coumarin compounds in different tissues (Root, Stem and Leaf). B. The content changes of three coumarin compounds under MeJA elicitation. C. The content changes of three coumarin compounds under H2O2 treatment. D. The content changes of three coumarin compounds under UV elicitation. E. The content changes of three coumarin compounds under cold treatment. F. The content changes of three coumarin compounds under heat treatment. Values represent means ± SD (n = 3).	Fig. 2. The content changes of Praeruptorin A, Praeruptorin B and Imperatorin. A. The content of three coumarin compounds in different tissues (Root, Stem and Leaf). B. The content changes of three coumarin compounds under MeJA elicitation. C. The content changes of three coumarin compounds under H2O2 treatment. D. The content changes of three coumarin compounds under UV elicitation. E. The content changes of three coumarin compounds under cold treatment. F. The content changes of three coumarin compounds under heat treatment. Values represent means ± SD (n = 3).	2019-02-28	Sui, Ziwei;Luo, Jun;Yao, Ruolan;Huang, Chuanlong;Zhao, Yucheng;Kong, Lingyi		Zenodo	biologists	Sui, Ziwei;Luo, Jun;Yao, Ruolan;Huang, Chuanlong;Zhao, Yucheng;Kong, Lingyi			
2812FE14FA2AAC2FFCDBFB69FC7AF9BC.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/10481562/files/figure.png	https://doi.org/10.5281/zenodo.10481562	Fig. 3. Subcellular localization of PpPAL in Arabidopsis protoplasts. Green panels show GFP fluorescence, red panels show mCherry fluorescence and chloroplast autofluorescence is shown in blue panels. Merged panels represent combined fluorescence from GFP, mCherry and chloroplasts. Arabidopsis protoplasts containing GFP were used as a blank control and AtGAPC1-mCherry was used as a positive control for cytosol localization. Bars = 20 μm. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)	Fig. 3. Subcellular localization of PpPAL in Arabidopsis protoplasts. Green panels show GFP fluorescence, red panels show mCherry fluorescence and chloroplast autofluorescence is shown in blue panels. Merged panels represent combined fluorescence from GFP, mCherry and chloroplasts. Arabidopsis protoplasts containing GFP were used as a blank control and AtGAPC1-mCherry was used as a positive control for cytosol localization. Bars = 20 μm. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)	2019-02-28	Sui, Ziwei;Luo, Jun;Yao, Ruolan;Huang, Chuanlong;Zhao, Yucheng;Kong, Lingyi		Zenodo	biologists	Sui, Ziwei;Luo, Jun;Yao, Ruolan;Huang, Chuanlong;Zhao, Yucheng;Kong, Lingyi			
