Plant peroxisomes have the capacity to generate different reactive oxygen and nitrogen species (ROS and RNS), such as H 2 O 2 , superoxide radical (O 2 Ă Ă ), nitric oxide and peroxynitrite (ONOO -). These organelles have an active nitrooxidative metabolism which can be exacerbated by adverse stress conditions. Hydrogen sulfide (H 2 S) is a new signaling gasotransmitter which can mediate the posttranslational modification (PTM) persulfidation. We used Arabidopsis thaliana transgenic seedlings expressing cyan fluorescent protein (CFP) fused to a canonical peroxisome targeting signal 1 (PTS1) to visualize peroxisomes in living cells, as well as a specific fluorescent probe which showed that peroxisomes contain H 2 S. H 2 S was also detected in chloroplasts under glyphosate-induced oxidative stress conditions. Peroxisomal enzyme activities, including catalase, photorespiratory H 2 O 2 -generating glycolate oxidase (GOX) and hydroxypyruvate reductase (HPR), were assayed in vitro with a H 2 S donor. In line with the persulfidation of this enzyme, catalase activity declined significantly in the presence of the H 2 S donor. To corroborate the inhibitory effect of H 2 S on catalase activity, we also assayed pure catalase from bovine liver and pepper fruit-enriched samples, in which catalase activity was inhibited. Taken together, these data provide evidence of the presence of H 2 S in plant peroxisomes which appears to regulate catalase activity and, consequently, the peroxisomal H 2 O 2 metabolism. . In plant systems, several enzymes are capable of generating H 2 S, which is part of the cysteine (Cys) metabolism. These enzymes, including L-and D-cysteine desulfhydrase (L-DES/D-DES), sulfite reductase (SiR), cyano alanine synthase (CAS) and cysteine synthase (CS) (Li et al. 2013; Calderwood and Kopriva 2014; Hancock and Whiteman 2014), are present in different subcellular compartments, such as cytosol, chloroplasts