taxonID	type	format	identifier	references	title	description	created	creator	contributor	publisher	audience	source	license	rightsHolder	datasetID
03D06A6DFFE6FFB0FFD5A409FD9AD394.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/8259766/files/figure.png	https://doi.org/10.5281/zenodo.8259766	Fig. 1. An archetypic glucosinolate-myrosinase system, leading to an isothiocyanate (A) and an oxazolidine-2-thione (B) from myrosinase-catalyzed hydrolysis of two ancient glucosinolates, 11 and 31. The hydrolysis reactions are unbalanced; water is an additional reactant and glucose, sulfate and hydrogen ion are also released during the myrosinase-catalyzed hydrolysis. A rearrangement precedes the formation of isothiocyanate (Blaˇzevi´c et al., 2020).	Fig. 1. An archetypic glucosinolate-myrosinase system, leading to an isothiocyanate (A) and an oxazolidine-2-thione (B) from myrosinase-catalyzed hydrolysis of two ancient glucosinolates, 11 and 31. The hydrolysis reactions are unbalanced; water is an additional reactant and glucose, sulfate and hydrogen ion are also released during the myrosinase-catalyzed hydrolysis. A rearrangement precedes the formation of isothiocyanate (Blaˇzevi´c et al., 2020).	2021-05-31	Agerbirk, Niels;Hansen, Cecilie Cetti;Kiefer, Christiane;Hauser, Thure P.;Ørgaard, Marian;Lange, Conny Bruun Asmussen;Cipollini, Don;Koch, Marcus A.		Zenodo	biologists	Agerbirk, Niels;Hansen, Cecilie Cetti;Kiefer, Christiane;Hauser, Thure P.;Ørgaard, Marian;Lange, Conny Bruun Asmussen;Cipollini, Don;Koch, Marcus A.			
