taxonID	type	format	identifier	references	title	description	created	creator	contributor	publisher	audience	source	license	rightsHolder	datasetID
24402D474367FFEF087E916AFB66F923.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/8292674/files/figure.png	https://doi.org/10.5281/zenodo.8292674	Fig. 1. The GC-MS oxylipin profiles of P. patens (A, B) and M. polymorpha (C, D). A and C, the profiles of endogenous oxylipins (Me/TMSi), the mixed ion current chromatograms (m/z 149, 177, 210, 225, 238, 278, 306, 308, 311). B and D, profiles of oxylipins (Me/TMSi) biosynthesized upon the in vitro preincubations of P. patens and M. polymorpha with α linolenic acid. The experimental details are described under “Experimental”.	Fig. 1. The GC-MS oxylipin profiles of P. patens (A, B) and M. polymorpha (C, D). A and C, the profiles of endogenous oxylipins (Me/TMSi), the mixed ion current chromatograms (m/z 149, 177, 210, 225, 238, 278, 306, 308, 311). B and D, profiles of oxylipins (Me/TMSi) biosynthesized upon the in vitro preincubations of P. patens and M. polymorpha with α linolenic acid. The experimental details are described under “Experimental”.	2020-12-31	Mukhtarova, Lucia S.;Lantsova, Natalia V.;Khairutdinov, Bulat I.;Grechkin, Alexander N.		Zenodo	biologists	Mukhtarova, Lucia S.;Lantsova, Natalia V.;Khairutdinov, Bulat I.;Grechkin, Alexander N.			
24402D474367FFEF087E916AFB66F923.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/8292676/files/figure.png	https://doi.org/10.5281/zenodo.8292676	Fig. 2. The electron impact mass spectra and fragmentation schemes (insets) for products 1 (A), 2 (B), and 3 (C).	Fig. 2. The electron impact mass spectra and fragmentation schemes (insets) for products 1 (A), 2 (B), and 3 (C).	2020-12-31	Mukhtarova, Lucia S.;Lantsova, Natalia V.;Khairutdinov, Bulat I.;Grechkin, Alexander N.		Zenodo	biologists	Mukhtarova, Lucia S.;Lantsova, Natalia V.;Khairutdinov, Bulat I.;Grechkin, Alexander N.			
24402D474367FFEF087E916AFB66F923.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/8292678/files/figure.png	https://doi.org/10.5281/zenodo.8292678	Fig. 3. The proposed pathways of biosynthesis of major cyclopentenones in P. patens and M. polymorpha. β oxn, β oxidation.	Fig. 3. The proposed pathways of biosynthesis of major cyclopentenones in P. patens and M. polymorpha. β oxn, β oxidation.	2020-12-31	Mukhtarova, Lucia S.;Lantsova, Natalia V.;Khairutdinov, Bulat I.;Grechkin, Alexander N.		Zenodo	biologists	Mukhtarova, Lucia S.;Lantsova, Natalia V.;Khairutdinov, Bulat I.;Grechkin, Alexander N.			
24402D474364FFEE0B289420FD9BF8CC.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/8292674/files/figure.png	https://doi.org/10.5281/zenodo.8292674	Fig. 1. The GC-MS oxylipin profiles of P. patens (A, B) and M. polymorpha (C, D). A and C, the profiles of endogenous oxylipins (Me/TMSi), the mixed ion current chromatograms (m/z 149, 177, 210, 225, 238, 278, 306, 308, 311). B and D, profiles of oxylipins (Me/TMSi) biosynthesized upon the in vitro preincubations of P. patens and M. polymorpha with α linolenic acid. The experimental details are described under “Experimental”.	Fig. 1. The GC-MS oxylipin profiles of P. patens (A, B) and M. polymorpha (C, D). A and C, the profiles of endogenous oxylipins (Me/TMSi), the mixed ion current chromatograms (m/z 149, 177, 210, 225, 238, 278, 306, 308, 311). B and D, profiles of oxylipins (Me/TMSi) biosynthesized upon the in vitro preincubations of P. patens and M. polymorpha with α linolenic acid. The experimental details are described under “Experimental”.	2020-12-31	Mukhtarova, Lucia S.;Lantsova, Natalia V.;Khairutdinov, Bulat I.;Grechkin, Alexander N.		Zenodo	biologists	Mukhtarova, Lucia S.;Lantsova, Natalia V.;Khairutdinov, Bulat I.;Grechkin, Alexander N.			
