Plant Peroxisomes: A Factory of Reactive Species

Corpas, Francisco J.; González-Gordo, Salvador; Palma, José M.

doi:10.3389/fpls.2020.00853

REVIEW article

Front. Plant Sci., 03 July 2020

Sec. Plant Physiology

Volume 11 - 2020 | https://doi.org/10.3389/fpls.2020.00853

This article is part of the Research Topic Subcellular Compartmentalization of Plant Antioxidants and ROS Generating Systems View all 9 articles

Plant Peroxisomes: A Factory of Reactive Species

$\r\nFrancisco J. Corpas*$ Francisco J. Corpas^*

Salvador González-Gordo $Jos M. Palma\r\n$ José M. Palma

Group of Antioxidants, Free Radicals and Nitric Oxide in Biotechnology, Food and Agriculture, Department of Biochemistry, Cell and Molecular Biology of Plants, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas (CSIC), Granada, Spain

Plant peroxisomes are organelles enclosed by a single membrane whose biochemical composition has the capacity to adapt depending on the plant tissue, developmental stage, as well as internal and external cellular stimuli. Apart from the peroxisomal metabolism of reactive oxygen species (ROS), discovered several decades ago, new molecules with signaling potential, including nitric oxide (NO) and hydrogen sulfide (H₂S), have been detected in these organelles in recent years. These molecules generate a family of derived molecules, called reactive nitrogen species (RNS) and reactive sulfur species (RSS), whose peroxisomal metabolism is autoregulated through posttranslational modifications (PTMs) such as S-nitrosation, nitration and persulfidation. The peroxisomal metabolism of these reactive species, which can be weaponized against pathogens, is susceptible to modification in response to external stimuli. This review aims to provide up-to-date information on crosstalk between these reactive species families and peroxisomes, as well as on their cellular environment in light of the well-recognized signaling properties of H₂O₂, NO and H₂S.

Introduction

For many years, peroxisomes in higher plants have been given different names, such as glyoxysomes during seed germination and leaf senescence, as well as leaf, root and fruit peroxisomes according to their presence in different organs and at different physiological stages (Tolbert and Essner, 1981; Palma et al., 2018). This is explained by the presence of metabolic pathways which appear to be specific to each type of peroxisome. However, peroxisomes, which share a number of metabolites and enzymes common to all types of peroxisome, is now the preferred term regardless of their specific metabolic characteristics (Pracharoenwattana and Smith, 2008). The most noteworthy metabolites and enzymes include H₂O₂ and catalase, which are directly involved in the metabolism of reactive oxygen species (ROS) (Su et al., 2018; Sousa et al., 2019).

Peroxisomes have a simple morphological constitution composed of a single membrane surrounding an amorphous matrix. Over the last 30 years, an increasing number of new and often unexpected components and processes in these organelles have been identified (Bueno and del Río, 1992; del Río et al., 1992; Corpas et al., 1994, 2001, 2017a, 2019a, Barroso et al., 1999; Reumann et al., 2009; Clastre et al., 2011; Simkin et al., 2011; Chowdhary et al., 2012; Guirimand et al., 2012; Oikawa et al., 2015; Reumann and Bartel, 2016; Kao et al., 2018; Pan et al., 2018, 2020; Borek et al., 2019), indicating that the plant peroxisomal metabolism and consequently peroxisomal enzymatic and non-enzymatic components are more diverse than previously predicted. The diverse complementary range of experimental approaches used to identify these new peroxisomal constituents includes: (i) the biochemical, proteomic and molecular analysis of purified peroxisomes combined with bioinformatics methodologies and (ii) cell biology studies of features such as immune localization with the aid of electron microscopy and specific fluorescent probes with appropriated controls. Although the model plant Arabidopsis thaliana has increased our knowledge of plant peroxisomes, it should be pointed out that studies of peroxisomes from other plant species have been essential, as the peroxisomal metabolism can be modulated depending on the plant organ, development time and plant species involved. Therefore, this review principally aims to provide an update of research on the metabolism of reactive species associated with oxygen, nitrogen and, more recently, sulfur, as well as to outline new challenges and possible future research perspectives regarding crosstalk between peroxisomes and other subcellular compartments such as oil bodies, mitochondria and plastids which are closely related both biochemically and structurally (Palma et al., 2006; Oikawa et al., 2019). Information on plant peroxisomes could also be useful in relation to peroxisome research into other organisms and vice versa.

Peroxisomal ROS Metabolism

Reactive oxygen species (ROS) are produced by a series of single-electron reductions in molecular oxygen which sequentially form superoxide (O₂^•–), hydrogen peroxide (H₂O₂) and hydroxyl (HO^•) radicals and ultimately ending in water (Figure 1). It is worth noting that the term peroxisomes, formerly known as microbodies, originates from their high H₂O₂ content (De Duve and Baudhuin, 1966; Corpas, 2015). Plant peroxisomes contain a significant number of enzymatic systems capable of generating H₂O₂ such as glycolate oxidase (GOX), acyl-CoA oxidase (AOX), urate oxidase (UO), polyamine oxidase, copper amine oxidase (CuAO), sulfite oxidase (SO), sarcosine oxidase (SOX), or superoxide dismutase (SOD) (Hauck et al., 2014; Corpas et al., 2017a and references therein). These H₂O₂-generating enzymes are involved in multiple biochemical pathways which are essential not only for the endogenous metabolism of plant peroxisomes but also for their interactions with other subcellular compartments such as plastids, mitochondria, cytosols, oil bodies and nuclei. In these subcellular interconnections, H₂O₂ itself plays a highly important role as a signal molecule in crosstalk between organelles in order to coordinate cell function.

FIGURE 1

Figure 1. Reactive oxygen species (ROS) produced from a sequential one-electron reduction from oxygen.

Photorespiration has been estimated to be responsible for 70% of total H₂O₂ generated mainly from peroxisomal GOX in photosynthetic tissues (Noctor et al., 2002). Zhang et al. (2016) have described an elegant dynamic physical GOX-catalase association-dissociation mechanism that fine-tunes peroxisomal H₂O₂ in rice plants. Although peroxisomal H₂O₂ is kept under control when GOX and catalase are associated, under stress conditions and when mediated by salicylic acid (SA), this complex GOX-catalase dissociation mechanism inhibits catalase activity, leading to an increase in cellular H₂O₂ which acts as a signaling molecule (Zhang et al., 2016; Kohli et al., 2019). Another sophisticated mechanism, involving the interaction of the γb protein from the barley stripe mosaic virus with GOX, has been reported to inhibit GOX and to facilitate infection with the virus (Yang et al., 2018). More recently, Yamauchi et al. (2019) observed a connection between the H₂O₂-generating GOX and catalase, which is required in the stomatal movement. Thus, when there is an increase of oxidized peroxisomes they were removed by pexophagy allowing an increase in H₂O₂ in guard cells which mediated the stomatal closure. This mechanism of ROS homeostasis in guard cells seems to be relevant in response to environmental changes. On the other hand, the new peroxisomal small heat shock protein Hsp17.6CII, capable of increasing catalase activity especially under stress conditions, has been reported to be present in Arabidopsis plants (Li et al., 2017).

Acyl-CoA oxidase is another key peroxisomal H₂O₂-generating enzyme involved in fatty acid β-oxidation which, in collaboration with lipid bodies, enables triacylglyceride mobilization especially during seed germination and is also involved in the synthesis of signal molecules such as jasmonic acid (Baker et al., 2006; Chen et al., 2019b; Wang X. et al., 2019; Xin et al., 2019). However, under stress conditions such as salinity, ROS generated by peroxisomal fatty acid β-oxidation have a negative impact and contribute to oxidative damage (Yu et al., 2019).

Polyamines such as putrescine, spermidine and spermine are well known to be involved in multiple physiological processes, as well as mechanisms of response to various stress conditions (Wuddineh et al., 2018; Chen et al., 2019a; Wang W. et al., 2019). Several enzymes involved in the catabolism of polyamine, including H₂O₂-producing polyamine oxidase (PAO) and copper amino oxidase (CuAO), have been reported to be present in plant peroxisomes (Moschou et al., 2008; Kusano et al., 2015). These enzymes are also involved in the γ-aminobutyric acid (GABA) biosynthesis signaling pathway (Zarei et al., 2015; Corpas et al., 2009b).

In addition, peroxisomal xanthine oxidoreductase (XOR) and superoxide dismutase (SOD), key enzymes in O₂^•– and H₂O₂ metabolism, can be regulated by stress conditions such as salinity, heavy metal and ozone stress (Corpas et al., 1993, 2008; Ueda et al., 2013).

Although catalase is the principal antioxidant enzyme in the matrix of all types of peroxisome (Mhamdi et al., 2010, 2012; Palma et al., 2020 and references therein), other enzymatic antioxidants are present in both the matrix and the membrane. It is also important to highlight the role of SOD isozymes, which differ according to peroxisomal origin (del Río et al., 2018). Thus, peroxisomes of watermelon cotyledons have two SOD isoenzymes, a CuZn-SOD located in the matrix and a Mn-SOD that is bound to the membrane (Bueno and del Río, 1992; Rodríguez-Serrano et al., 2007); pea leaf peroxisomes have a Mn-SOD present in the matrix; sunflower cotyledon peroxisomes have only a CuZn-SOD which is also located in the matrix (Corpas et al., 1998); carnation petal and pepper fruit peroxisomes have a Mn- and an Fe-SOD (Droillard and Paulin, 1990; Palma et al., 2018); and olive fruits peroxisomes contain four SOD isozymes, an Fe-SOD, two CuZn-SOD and a Mn-SOD (López-Huertas and del Río, 2014). Therefore, it could be hypothesized that the presence of two or more types of SOD in peroxisomes must have some physiological advantages. Thus, one of the SOD isozymes could be constitutive while the other one could be inducible under environmental or physiological stimuli such as seedling development, leaf senescence or fruit ripening.

In addition, it is worth noting the role of ascorbate-glutathione cycle components, including ascorbate peroxidase (APX), monodehydroascorbate reductase (MDAR), dehydroasrcorbate reductase (DAR) and glutathione reductase (GR) (Jiménez et al., 1998; Romero-Puertas et al., 2006; López-Huertas and del Río, 2014; Corpas et al., 2017a). While MDAR is present in both matrix and membrane (Leterrier et al., 2005; Lisenbee et al., 2005; Eastmond, 2007), APX is exclusively located in the membrane (Corpas et al., 1994; Yamaguchi et al., 1995; Bunkelmann and Trelease, 1996). With its high affinity for H₂O₂ (low Km value around 74 μM), membrane-bound APX appears to have fine-tuned control of H₂O₂ (Ishikawa et al., 1998) as compared to catalase, which, with a Km value in the mM range, is less efficient at low concentrations of H₂O₂ (Huang et al., 1983; Mhamdi et al., 2010). The Km values for plant catalase are reported to vary quite considerably, with, for example, a Km of 50 mM in Beta vulgaris (Dinçer and Aydemir, 2001), 100 mM in rice (Ray et al., 2012) and 190 mM in pea (del Río et al., 1977). Peroxisomal APX appears to be critical in a diverse range of processes such as seedling development (Corpas and Trelease, 1998) and leaf senescence (Ribeiro et al., 2017). To maintain the ascorbate-glutathione cycle at the GR level, NADPH needs to be supplied by NADP-dependent endogenous dehydrogenases including glucose-6-phosphate dehydrogenase (G6PDH), 6-phosphogluconate dehydrogenase (6PGDH) and isocitrate dehydrogenase (NADP-ICDH) (Leterrier et al., 2016; Corpas and Barroso, 2018b and references therein). In addition, Corpas et al. (2017b) have reported the presence of a protein immunologically related to plant peroxiredoxins, whose expression is differentially modulated under oxidative stresses such as those induced by CdCl₂ and the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D); however, further research is necessary to clarify this phenomenon. Figure 2 shows a working model of the ROS metabolism and its interaction with other reactive species, including NO and H₂S, which modulate the activity of peroxisomal enzymes through posttranslational modifications (PTMs), events which will be further discussed below.

FIGURE 2

Figure 2. Simple model of the global metabolism of reactive oxygen/nitrogen/sulfur species in plant peroxisomes. Peroxisomes have an important battery of H₂O₂-generating enzymes, being the photorespiratory glycolate oxidase (GOX) one of the most relevant. Peroxisomal xanthine oxidoreductase (XOR) activity generates uric acid which the concomitant generation of superoxide radical (O₂^•–) which is dismutated to H₂O₂ by superoxide dismutase (SOD). All three SOD types have been described in plant peroxisomes from different origin, CuZ-SOD, Mn-SOD, and Fe-SOD. The H₂O₂ pool is mainly decomposed by catalase (CAT) but also by the membrane-bound ascorbate peroxidase (APX). An L-arginine (L-Arg) and Ca²⁺ dependent NOS-like activity generates NO which can react chemically with O₂^– to produce peroxynitrite (ONOO^–), a nitrating molecule that facilitates PTMs such as tyrosine nitration. NO can also interact with reduced glutathione (GSH) to form S-nitrosoglutathione (GSNO), a NO donor which mediates S-nitrosation. GSH is regenerated by glutathione reductase (GR) which requires NADPH supplied by several NADPH-generating enzymes (NADPH-ICDH, G6PDH, and 6PGDH). Uric acid is a ONOO^– scavenger, this being a mechanism of peroxisomal auto-regulation. With all these components, and according to reported data, the peroxisomal targets of NO-derived PTMs identified so far are CAT, CuZn-SOD, and monodehydroascorbate reductase (MDAR) which can undergo an inhibitory effect either by nitration or S-nitrosation. Additionally, CAT and GOX can be inhibited by hydrogen sulfide (H₂S), and CAT is also inhibited by carbonylation. The H₂O₂-generating sulfite oxidase (SO) converts sulfite (SO₃^2–) to sulfate (SO₄^2–), which is a mechanism of protection because sulfite inhibits catalase activity. Red line denotes inhibition effect.

Given the capacity of ROS to mediate several PTMs, particularly carbonylation and S-sulfenylation, certain amino acid residues, especially arginine, lysine, threonine and proline, are carbonylated, which affects target protein function in many cases (Debska et al., 2012; Lounifi et al., 2013). Several studies have identified peroxisomal proteins, such as catalase, malate synthase and the fatty acid β-oxidation multifunctional protein AIM1, which undergo carbonylation (Nguyen and Donaldson, 2005; Anand et al., 2009; Mano et al., 2014; Rodríguez-Ruiz et al., 2019). On the other hand, H₂O₂ can oxidize specific protein cysteine thiols to sulfenic acid (SOH), a process known as S-sulfenylation, which usually results in enzymatic inactivation. Using proteomic techniques, approximately 2% of peroxisomal proteins have been reported to be susceptible to S-sulfenylation (Akter et al., 2017; Huang et al., 2019). This PTM has been observed to occur with respect to fatty acid β-oxidation acyl-coenzyme A oxidase 1, the multifunctional proteins MFP2, and AIM1, as well as amine oxidase, phosphomevalonate kinase, MDAR and NADP-ICDH. Table 1 shows a summary of peroxisomal enzymes targeted by carbonylation and S-sulfenylation, as well as other PTMs mediated by RNS and RSS, a subject which will be discussed below.

TABLE 1

Table 1. Peroxisomal enzymes target of diverse posttranslational modifications (PTMs) whose activities are affected by either ROS, RNS, or RSS.

Given growing awareness of the important role of ROS peroxisomal metabolism in combating biotic stress, the expression of genes encoding for peroxisomal proteins involved in their biogenesis, fatty acid catabolism and the H₂O₂-generating glyoxylate cycle have been reported to increase during interactions between the pathogen Sclerotinia sclerotiorum and rapeseed (Brassica napus), thus facilitating pathogen cell wall degradation and metabolism detoxification (Chittem et al., 2020). On the other hand, using the Arabidopsis nca1 mutant with no catalase activity 1, containing residual activity of the three catalase isozymes, Hackenberg et al. (2013) identified a link between catalase and ROS production as autophagy-dependent cell death progresses. Table 2 shows some functional implications of peroxisomal H₂O₂ and other signal molecules generated in this organelle.

TABLE 2

Table 2. Signal molecules generated in plant peroxisomes during different processes and their functional implications.

The generation of singlet oxygen (¹O₂) has always been associated with chloroplasts, particularly in photosystem II, responsible for various types of photo-damage which triggers distinct cellular responses (Wagner et al., 2004; Rosenwasser et al., 2011; Chen and Fluhr, 2018; Dogra et al., 2018). Using the green fluorescence probe to detect ¹O₂, peroxisomes, mitochondria and nuclei have been shown to be either the origin or target of ¹O₂, suggesting that this ROS is generated in a light-independent manner (Mor et al., 2014). These findings open up new questions about the importance of ¹O₂ in the mechanism of response to plant stress in which several subcellular compartments including peroxisomes are involved.

Peroxisomal Reactive Nitrogen Species (RNS)

Nitric oxide (NO) metabolism has a significant impact on cellular metabolisms due to its involvement in the important plant physiological processes of seed and pollen germination, root development, stomatal closure, senescence and fruit ripening, as well as in the mechanism of response to many environmental stresses including salinity, drought, heavy metals and extreme temperature (Neill et al., 2008; León et al., 2014; Begara-Morales et al., 2018; Kolbert et al., 2019; Wei et al., 2020). NO belongs to a family of related molecules called reactive nitrogen species (RNS), with peroxynitrite (ONOO^–) and S-nitrosogluthione (GSNO) being the most studied. Using various experimental approaches including electron paramagnetic resonance (EPR) spectroscopy, as well as biochemical and cellular biology, some RNS including NO, ONOO^– and GSNO have been detected in plant peroxisomes (Barroso et al., 2013; Corpas and Barroso, 2014b; Corpas et al., 2019). Identification of peroxisomal proteins undergoing PTMs mediated by these NO-derived species is strong evidence of an active RNS metabolism in peroxisomes. Figures 3A–H shows in vivo images of NO and ONOO^– in Arabidopsis guard cell peroxisomes detected by confocal laser scanning microscopy (CLSM) and specific fluorescent probes.

FIGURE 3

Figure 3. Representative images illustrating the CLSM in vivo detection of nitric oxide (NO) and peroxynitrite (ONOO^–), peroxisomes (red) and chloroplasts (blue) in guard cells of transgenic Arabidopsis seedlings expressing CFP-PTS1. (A,E) Fluorescence punctate (red) attributable to CFP-PTS1, indicating the localization of peroxisomes in guard cells. (B,F) Fluorescence punctate (green) attributable to the detection in the same guard cells of NO and ONOO^–, respectively. (C,G) Chlorophyll autofluorescence (blue) attributable to the detection of chloroplasts. (D,H) Merged images for corresponding panels. Reproduced with permission from Corpas et al. (2017a) provided by Elsevier.

ONOO^– results from a reaction between NO with O₂^•–, considered one of the fastest chemical reactions with a rate constant (k) of 1.9 × 10¹⁰ M^–1 s^–1 (Kissner et al., 1997). ONOO^–, a strong oxidant and nitrating molecule involved in protein tyrosine nitration (NO₂-Tyr), modifies protein function, mostly through inhibition (Corpas et al., 2009a; Mata-Pérez et al., 2016). This NO-derived PTM involves the covalent oxidative addition of a nitro group (-NO₂) to tyrosine residues, a highly selective process which depends on factors such as the protein environment of the Tyr and the nitration mechanism (Bartesaghi and Radi, 2018). Table 1 shows some nitrated proteins identified in plant peroxisomes and how their function is affected. Interestingly, some of the proteins affected are directly involved in the ROS metabolism, indicating a close metabolic interconnection between both families of reactive species.

The antioxidant glutathione (GSH), a tripeptide (γ-Glu-Cys-Gly), undergoes S-nitrosation in order to generate GSNO, a low-molecular-weight NO reservoir, through a covalent addition of NO to the thiol group of Cys residues in order to form S-nitrosothiol (SNO) (Airaki et al., 2011). GSNO is a key molecule given its dynamic interaction with free cysteines, GSH and proteins through processes such as S-nitrosation, S-transnitrosation and S-glutathionylation (Broniowska et al., 2013; Corpas et al., 2013a, b). GSNO is enzymatically decomposed by GSNO reductase (GSNOR; Leterrier et al., 2011), an enzyme susceptible to S-nitrosation and consequently inhibition (Guerra et al., 2016). An increase in Tyr nitration, an irreversible process, is usually associated with nitro-oxidative stress; however, protein S-nitrosation, a reversible process, is a regulatory protein mechanism that occurs under physiological and stress conditions. Table 1 shows some peroxisomal proteins targeted by S-nitrosation, as well as proteins involved in ROS metabolism which are targeted by these NO-mediated PTMs.

The number of peroxisomal proteins targeted by NO-mediated PTMs is growing continuously. Using the biotin-switch technique and liquid chromatography/mass spectrometry/mass spectrometry (LC-MS/MS), several more S-nitrosated peroxisomal proteins have been identified during adventitious root growth induced by treatment with NO (Niu et al., 2019). These proteins include the peroxisomal LON2 protease, which is necessary for matrix protein import into peroxisomes (Lingard and Bartel, 2009); isocitrate lyase (ICL), involved in the glyoxylate cycle; and the multifunctional AIM1-like isoform, involved in fatty acid β-oxidation.

However, the source of enzymatic NO, as yet unelucidated, is currently the most controversial aspect of NO metabolism in higher plants (Kolbert et al., 2019). Two main candidates have been proposed: nitrate reductase (NR) (Mohn et al., 2019) and L-arginine-dependent NO synthase-like activity (Corpas et al., 2017a). Although no evidence of NR has been found in plant peroxisomes, NO synthase-like activity has been found and characterized in peroxisomes purified from pea leaves (Barroso et al., 1999). Though as yet unidentified, this protein is called NOS-like activity, as peroxisomal NO generation requires NOS proteins similar to those found in animals, including L-arginine, NADPH, FMN, FAD, tetrahydrobiopterin, calcium, and calmodulin (Corpas and Barroso, 2017b; Corpas et al., 2019). The protein responsible for NO generation is imported by a type 2 peroxisomal targeting signal involving a process dependent on calmodulin and calcium (Corpas and Barroso, 2014a, 2018a).

Peroxisomal NO metabolism is involved in processes such as pollen tube germination (Prado et al., 2004), lateral root formation (Schlicht et al., 2013), and leaf senescence (Corpas et al., 2019), as well as in responses to environmental and heavy metal stresses such as salinity (Corpas et al., 2009b), lead (Corpas and Barroso, 2017a), and cadmium (Corpas and Barroso, 2014b; Piacentini et al., 2020).

Reactive Sulfur Species (RSS) in Plant Peroxisomes

Reactive sulfur species (RSS) are chemically comparable to ROS (Olson, 2019) and can be generated from hydrogen sulfide (H₂S), some of these species are thiyl radical (HS^•), hydrogen persulfide (H₂S₂), persulfide radical (HS₂^•–), sulfite (SO₃^2–) or sulfate (SO₄^2–) among others (Gruhlke and Slusarenko, 2012; Ono et al., 2014; Mishanina et al., 2015; Park et al., 2015; Schöneich, 2016). However, the biochemistry of H₂S in cells, given its multiple interactions with other reactive species, is more complex than previously thought (see Filipovic et al., 2018 for a more in-depth review); for example, protein thiyl radicals are generated during the reaction of H₂O₂ with heme proteins, possibly inducing protein degradation (Schöneich, 2016).

Different molecules and enzymes, such as GSH (Müller et al., 2004), glutathione reductase (Romero-Puertas et al., 2006), and sulfite oxidase (Nowak et al., 2004; Hänsch and Mendel, 2005), involved in sulfur metabolism, are present in plant peroxisomes. Sulfite oxidase (SO) catalyzes the conversion of sulfite to sulfate by producing H₂O₂. The functional relevance of this enzyme is that it can protect catalase activity since sulfite, at low concentration, has the capacity to inhibit catalase activity (Veljovic-Jovanovic et al., 1998). Nevertheless, despite the greater importance attributed to peroxisomal SO in a recent study, mitochondrial SO in animal cells has the capacity to generate NO from nitrite (Bender et al., 2019), while NO enzymatic generation from SO in plant peroxisomes remains to be proven. An earlier study confirmed the important role played by the peroxisomal RSS metabolism (Corpas and Barroso, 2015).

H₂S has recently been proven to be present in plant peroxisomes (Corpas et al., 2019a). Figures 4A–G shows representative images of H₂S in peroxisomes from the root tips and guard cells of Arabidopsis seedlings detected by in vivo CLSM and a specific fluorescent probe. Using proteomic techniques, some peroxisomal enzymes have been identified as targets of persulfidation (Aroca et al., 2015, 2017). On the other hand, in vitro analysis shows that catalase activity from Arabidopsis and sweet pepper fruits is inhibited in the presence of H₂S (Corpas et al., 2019a). Although, to our knowledge, the enzymatic source of peroxisomal H₂S remains unknown, previous studies have proposed some potential candidates. For example, catalase, which functions as a sulfide oxidase or sulfur reductase, is capable of oxidizing or generating H₂S (Olson et al., 2017). SOD has also been reported to have the capacity to catalyze the reaction between O₂ and H₂S to generate persulfide (Olson et al., 2018). In a previous study by Corpas and Barroso (2015), the presence of these enzymatic and non-enzymatic components in plant peroxisomes indicates that, in addition to ROS and RNS, these organelles also have an active RSS metabolism.

FIGURE 4

Figure 4. Representative images illustrating the CLSM in vivo detection of H₂S (red color) and peroxisomes (green color) in root tips (A–C) and guard cells (D–G) of 10 days old Arabidopsis seedlings expressing CFP-PTS1. (A,D) Fluorescence puncta (green) attributable to CFP-PTS1, indicating the localization of peroxisomes. (B,E) Fluorescence punctate (red) attributable to H₂S detection in the same area. (C) Merged image of (A,B) showing colocalized fluorescence punctate (yellow). (F) Chlorophyll autofluorescence (blue) demonstrating location of chloroplasts. (G) Merged images of (D–F). H₂S (red color) was detected by using 5 mM WSP-5, a fluorescence probe for H₂S. Arrows indicate representative punctate spots corresponding to the colocalization of H₂S with peroxisomes. Asterisks indicate localization of H₂S in the cytosol. Reproduced with permission from Corpas et al. (2019a) provided by John Wiley and Sons.

Crosstalk Between Peroxisomal Reactive Species

Functional interactions and inter-regulation through PTMs in these families of reactive species are shown in Figure 2. In this working model, under physiological conditions, catalase, the main antioxidant enzyme, regulates levels of H₂O₂ generated by different pathways, principally photorespiratory glycolate oxidase (GOX) (Noctor et al., 2002). On the other hand, peroxisomal xanthine oxidoreductase (XOR) activity involved in purine catabolism generates uric acid, with the concomitant formation of the O₂^•– (Corpas et al., 1997, 2008; Zarepour et al., 2010), which, in turn, is dismutated to H₂O₂ by SOD. The pool of H₂O₂ is mainly decomposed by catalase (CAT) and also by membrane-bound ascorbate peroxidase (APX). L-Arg-dependent NOS-like activity generates NO (Corpas et al., 2019) which chemically reacts with O₂^•– to produce peroxynitrite (ONOO^–), a nitrating molecule that facilitates PTMs such as tyrosine nitration. NO also interacts with reduced glutathione (GSH) to form S-nitrosoglutathione (GSNO), a NO donor that mediates S-nitrosation. Uric acid is a physiological ONOO^– scavenger (Alamillo and García-Olmedo, 2001) involved in endogenous peroxisomal auto-regulation. Thus, the peroxisomal enzymes targeted by NO-derived PTMs, catalase (CAT), CuZn-SOD, and monodehydroascorbate reductase (MDAR), are inhibited by nitration and S-nitrosation. Both CAT, and GOX are inhibited by H₂S; the former is also inhibited by carbonylation when H₂O₂ is overproduced. In addition, H₂O₂-generating sulfite oxidase (SO) is involved in the conversion of sulfite to sulfate which, given sulfite’s ability to inhibit SO, has been reported to be a catalase protection mechanism. These interconnections highlight the biochemical complexity of this self-regulated plant peroxisome network, in which the antioxidant catalase is one of the most regulated peroxisomal enzymes (Palma et al., 2020).

Conclusion

Much of our knowledge of reactive species metabolism in plant peroxisomes is now well established. The three molecular families ROS, RNS, and RSS are present in plant peroxisomes, which are considered to be potential producers of reactive species and to play an important role in the cell signaling network. However, our limited knowledge of reactive species families needs to be expanded by identifying new peroxisomal protein targets. We also need to determine the effect of the different PTMs, carbonylation, S-sulfenylation, S-nitrosation, tyrosine nitration, and persulfidation, on target protein function and peroxisomal metabolism. In addition, interactions with other subcellular compartments which share biochemical pathways such as photorespiration, fatty acid β-oxidation, isoprenoid biosynthesis and purine and polyamine metabolism (Clastre et al., 2011; Guirimand et al., 2012; Corpas et al., 2019b) should be investigated. Similarly, the relationship between reactive species and complex peroxisomal biogenesis, division and matrix/membrane protein import mechanisms (Reumann and Bartel, 2016; Kao et al., 2018) has been underexplored (López-Huertas et al., 2000). Further research should also be carried out to identify the proteins responsible for endogenous peroxisomal generation of NO and H₂S. This would increase our knowledge of how organelle biochemistry is modulated within the framework of the whole cell metabolism. This research could lead to biotechnological applications given the important role of peroxisomes in many physiological processes and in responses to biotic and abiotic stresses. Furthermore, in addition to harboring reactive species, with their known signaling properties, peroxisomes are a source of other signaling molecules such as jasmonic acid and γ-aminibutic acid (GABA), which extends the functional role of plant peroxisomes. Table 2 shows signaling molecules generated in the plant peroxisomal metabolism and some examples of their role in various plant processes.

Author Contributions

Authors have made a collaborative, direct and intellectual contribution to the work, and have approved it for publication.

Funding

This work was supported by the European Regional Development Fund co-financed grant from the Ministry of Economy and Competitiveness (AGL2015-65104-P and PID2019-103924GB-I00), the Plan Andaluz de Investigación, Desarrollo e Innovación (P18-FR-1359), and the Junta de Andalucía (group BIO192), Spain.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

SG-G acknowledges a “Formación de Personal Investigador” contract (BES-2016-078368) from the Ministry of Economy and Competitiveness, Spain.

References

Airaki, M., Sánchez-Moreno, L., Leterrier, M., Barroso, J. B., Palma, J. M., and Corpas, F. J. (2011). Detection and quantification of S-nitrosoglutathione (GSNO) in pepper (Capsicum annuum L.) plant organs by LC-ES/MS. Plant Cell Physiol. 52, 2006–2015. doi: 10.1093/pcp/pcr133

PubMed Abstract | CrossRef Full Text | Google Scholar

Akter, S., Carpentier, S., Van Breusegem, F., and Messens, J. (2017). Identification of dimedone-trapped sulfenylated proteins in plants under stress. Biochem. Biophys. Rep. 9, 106–113. doi: 10.1016/j.bbrep.2016.11.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Alamillo, J. M., and García-Olmedo, F. (2001). Effects of urate, a natural inhibitor of peroxynitrite-mediated toxicity, in the response of Arabidopsis thaliana to the bacterial pathogen Pseudomonas syringae. Plant J. 25, 529–540. doi: 10.1046/j.1365-313x.2001.00984.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Anand, P., Kwak, Y., Simha, R., and Donaldson, R. P. (2009). Hydrogen peroxide induced oxidation of peroxisomal malate synthase and catalase. Arch. Biochem. Biophys. 491, 25–31. doi: 10.1016/j.abb.2009.09.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Aroca, A., Benito, J. M., Gotor, C., and Romero, L. C. (2017). Persulfidation proteome reveals the regulation of protein function by hydrogen sulfide in diverse biological processes in Arabidopsis. J. Exp. Bot. 68, 4915–4927. doi: 10.1093/jxb/erx294

PubMed Abstract | CrossRef Full Text | Google Scholar

Aroca, Á, Serna, A., Gotor, C., and Romero, L. C. (2015). S-sulfhydration: a cysteine posttranslational modification in plant systems. Plant Physiol. 168, 334–342. doi: 10.1104/pp.15.00009

PubMed Abstract | CrossRef Full Text | Google Scholar

Baker, A., Graham, I. A., Holdsworth, M., Smith, S. M., and Theodoulou, F. L. (2006). Chewing the fat: beta-oxidation in signalling and development. Trends Plant Sci. 11, 124–132. doi: 10.1016/j.tplants.2006.01.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Barroso, J. B., Corpas, F. J., Carreras, A., Sandalio, L. M., Valderrama, R., Palma, J. M., et al. (1999). Localization of nitric-oxide synthase in plant peroxisomes. J. Biol. Chem. 274, 36729–36733.