Original Research ARTICLE
From Cyanobacteria to Human, MAPEG-Type Glutathione-S-Transferases Operate in Cell Tolerance to Heat, Cold, and Lipid Peroxidation
- Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, University of Paris-Sud, Université Paris-Saclay, Gif-sur-Yvette, France
The MAPEG2 sub-family of glutathione-S-transferase proteins (GST) has been poorly investigated in vivo, even in prokaryotes such as cyanobacteria the organisms that are regarded as having developed glutathione-dependent enzymes to protect themselves against the reactive oxygen species (ROS) often produced by their powerful photosynthesis. We report the first in vivo analysis of a cyanobacterial MAPEG2-like protein (Sll1147) in the model cyanobacterium Synechocystis PCC 6803. While Sll1147 is dispensable to cell growth in standard photo-autotrophic conditions, it plays an important role in the resistance to heat and cold, and to n-tertbutyl hydroperoxide (n-tBOOH) that induces lipid peroxidation. These findings suggest that Sll1147 could be involved in membrane fluidity, which is critical for photosynthesis. Attesting its sensitivity to these stresses, the Δsll1147 mutant lacking Sll1147 challenged by heat, cold, or n-tBOOH undergoes transient accumulation of peroxidized lipids and then of reduced and oxidized glutathione. These results are welcome because little is known concerning the signaling and/or protection mechanisms used by cyanobacteria to cope with heat and cold, two inevitable environmental stresses that limit their growth, and thus their production of biomass for our food chain and of biotechnologically interesting chemicals. Also interestingly, the decreased resistance to heat, cold and n-tBOOH of the Δsll1147 mutant could be rescued back to normal (wild-type) levels upon the expression of synthetic MAPEG2-encoding human genes adapted to the cyanobacterial codon usage. These synthetic hmGST2 and hmGST3 genes were also able to increase the Escherichia coli tolerance to heat and n-tBOOH. Collectively, these finding indicate that the activity of the MAPEG2 proteins have been conserved, at least in part, during evolution from (cyano)bacteria to human.
Glutathione, the highly abundant (1–10 mM) tripeptide L-glutamyl-L-cysteinyl-L-glycine (Lu, 2013), plays an important role in the protection against oxidative and metabolic stresses in most organisms. The reduced (major) form (GSH) of glutathione maintains reduced state of the intracellular compartment(s) and donates electrons to various enzymes (Fahey, 2013; Lu, 2013), such as the glutathione-S-transferases (GST) that operate in the detoxification of reactive oxygen species (ROS), xenobiotics, and/or heavy metals (Yadav, 2010; Noctor et al., 2012). The resulting oxidized form of glutathione, the dimeric disulfide form (GSSG), is then reduced back to GSH by various factors, such as the NADPH-using enzyme glutathione reductase (GR) that occurs in many (Couto et al., 2016), but not all organisms such as the presently studied model cyanobacterium Synechocystis sp. PCC 6803 (Marteyn et al., 2009; Naraimsamy et al., 2013). The superfamily of GSTs enzymes (EC 184.108.40.206) can be divided in three categories: the cytosolic GSTs, the mitochondrial GSTs and the microsomal GSTs also designated as MAPEGs (membrane-associated proteins involved in ecosanoïd and glutathione metabolism) (Oakley, 2011).
Mammalian membrane-associated proteins involved in ecosanoïd and glutathione metabolisms have different functions and low sequence similarities. They define six types of proteins namely: (i) mGST1, (ii) mGST2 and (iii) mGST3, (iv) the 5-lipoxygenase-activating protein (FLAP), (v) the prostaglandin E synthase (PGES) and (vi) the leukotriene C4 (LTC4) synthase, which can be grouped in two families: MAPEG1 (mGST1/PGES) and MAPEG2 (mGST2/mGST3/FLAP/LTC4 synthase) (for reviews see Jakobsson et al., 2000; Bresell et al., 2005; Pearson, 2005; Deponte, 2013). MAPEG homologs identified in insects (Drosophila melanogaster, and Anopheles gambiae) can be placed in the MAPEG1 family (Bresell et al., 2005), while MAPEG homologs found in fungi (Aspergillus nidulans) and plants (Arabidopsis thaliana, Oryza sativa, and Ricinus communis) belong to MAPEG2 (Bresell et al., 2005). MAPEG1 and MAPEG2 members were found in prokaryotes but not in archae (Bresell et al., 2005; Pearson, 2005).
Membrane-associated proteins involved in ecosanoïd and glutathione metabolism proteins are not merely “membrane associated” proteins as proposed by their acronym, but in fact integral membrane proteins (Deponte, 2013). They contain 4 transmembranes helices as was suggested by their hydropathy plots (Jakobsson et al., 1999; Bresell et al., 2005) and verified in the X-ray crystallography of the mammalian proteins: mGST1 (Holm et al., 2002, 2006), LTC4 synthase (Ago et al., 2007) and PGES (Sjögren et al., 2013). Furthermore, the trimeric state was revealed by X-ray crystallography for mGST1 (Hebert et al., 1995; Ålander et al., 2009). Each monomer were found to bind on GSH molecule but only one subunit is catalytically active in both rat mGST1 and human mGST2 (Ålander et al., 2009; Ahmad et al., 2015).
Mammalian MAPEGs use a GSH-dependent isomerase activity to operate in the biosynthesis of leukotrienes (FLAP and LTC4 synthase) or prostaglandin E (PGES) (Morgenstern et al., 2011), (GPI) (Deponte, 2013) that are required for allergic (Ago et al., 2007) and inflammatory (Sjögren et al., 2013) responses. MAPEGs also play a role in detoxification (Johansson et al., 2010), using a GSH-transferase activity (Deponte, 2013) as well as the GSH-dependent reduction of organic fatty acid and lipid hydroperoxides through their peroxidase activity (Mosialou et al., 1995; Johansson et al., 2010; Deponte, 2013; Zhang et al., 2017).
Unlike the human mGST1 (hmGST1), which operates in lipid peroxidation (Johansson et al., 2010) and tumorigenesis and drug resistance (for review see Morgenstern et al., 2011), the precise in vivo role of (human) hmGST2 and hmGST3 is not well described though they could be interesting targets for drug development. Very interestingly, hmGST2 and hmGST3 share amino-acids sequence homology with MAPEG-like proteins from simple and fast growing prokaryotes, such as Escherichia coli and the model cyanobacterium Synechocystis PCC 6803. These E. coli and Synechocystis PCC 6803 MAPEG-like genes were cloned in an E. coli expression vector, and the MAPEG-like proteins were purified (partially in the case of the Synechocystis PCC 6803 protein) and appeared to catalyze the conjugation of 1-chloro-2,4-dinitrobenzene (CDNB) with GSH, thereby showing that GST activity can be regarded as a common denominator for a majority of MAPEG members throughout the kingdoms of life (Bresell et al., 2005). These findings are interesting because cyanobacteria are attractive organisms to study the role of GSTs and their selectivity/redundancy. They are regarded as the inventor of the oxygenic photosynthesis (Archibald, 2009; William Schopf, 2011) and of the GSH synthesis and dependent enzymes to protect themselves against the ROS they (often) produce when their active photosynthesis is altered by stresses (light, temperature, and metals) (William Schopf, 2011).
In the frame of our long-term interest in stress responses in cyanobacteria (for a review see Cassier-Chauvat and Chauvat, 2014) we carried out the first (to our knowledge) in vivo analysis, of the MAPEG protein of Synechocystis sp. PCC 6803 (hereafter Synechocystis). We report that the Synechocystis MAPEG protein (designated Sll1147 in CyanoBase) plays a prominent role in the cell tolerance to heat- and cold-temperatures and the protection against lipid peroxidation. The Δsll1147 deletion mutant lacking Sll1147 undergoes a transient sequential accumulation of peroxidized lipids and then of GSH and GSSG. We also demonstrate that the stress-tolerance of the Δsll1147 mutant can be restored following the production of hmGST2 and hmGST3 the human MAPEG counterparts of Sll147. This finding shows that (at least some) MAPEG functions have been conserved throughout evolution and can be (easily) studied in Synechocystis.
The Sll1147 MAPEG-Like GST Is Dispensable for the Photoautotrophic Growth of Synechocystis
To analyze in vivo the role of the Sll1147 GST, we constructed the Δsll1147:Kmr deletion mutant, using the standard gene replacement procedure that comprises three main steps. First, the DNA region containing sll1147 surrounded by its 300 bp flanking DNA regions was amplified by PCR using specific oligonucleotides primers (Supplementary Table S1). Second, the sll1147 protein-coding sequence was replaced by a transcription-terminator-less kanamycin resistance (Kmr) gene for selection, while preserving the 300 bp of sll1147 flanking DNA regions for homologous recombination that mediate targeted gene replacement upon transformation to Synechocystis (Labarre et al., 1989). Third, the resulting deletion cassette (Supplementary Table S2) was introduced in Synechocystis by transformation (Labarre et al., 1989). A few Kmr transformants were selected and analyzed by PCR with specific oligonucleotide primers (Figures 1A,B and Supplementary Table S1) to verify that the Kmr marker gene had properly replaced sll1147 in the Synechocystis chromosome, thanks to homologous DNA recombination occurring in the 300-bp sll1147-flanking DNA region shared by the Δsll1147:Kmr incoming DNA and the Synechocystis recipient chromosome which is polyploid [it occurs at about ten copies per cell (Labarre et al., 1989)].
Figure 1. The sll1147 gene is dispensable for the photoautotrophic growth of Synechocystis. (A) PCR analysis of the sll1147 chromosome locus in Synechocystis WT strain and the Δsll1147:Kmr mutant constructed in this study. The genes are represented by colored arrows (sll1147+, blue; Kmr, green) pointing into the direction of their transcription. The same color code is used to represent the PCR oligonucleotides primers (dotted arrows, see Supplementary Table S1 for their sequence) and the corresponding PCR products (double arrows) typical of the presence of WT (sll1147+ and KmS) or mutant (Δsll1147: Kmr) chromosome copies. (B) Typical UV-light image of the agarose gel showing the PCR products corresponding to the genes sll1147+ (PCR2, blue) or Kmr (PCR1, green) generated from WT and Δsll1147: Kmr cells grown in absence (MM) or presence (Km) of the selective antibiotic. M (marker DNA) stands for the GeneRuler 1 kb Plus DNA Ladder (Thermo Fisher Scientific). Note that WT cells harbor only WT chromosomes while Δsll1147:Kmr mutant cells possess only Δsll1147:Kmr chromosomes. (C) Typical growth curves of the WT strain and sll1147 mutant growing under standard photoautotrophic conditions.
All Δsll1147:Kmr transformants growing in standard photoautotrophic conditions in the presence of kanamycin possessed only Δsll1147:Kmr chromosomes (Figure 1B, see the presence of the 941 bp PCR product characteristic of Δsll1147:Kmr chromosomes) but no WT chromosomes [Figure 1B, see the absence of a 355 bp PCR band typical of WT (sll1147+) chromosomes]. The absence of WT chromosome copies (sll1147+, i.e., KmS) in the Δsll1147:Kmr mutant was confirmed by growing it for multiple generations in absence of Km to stop counter-selecting possible WT (sll1147+ and KmS) chromosome copies, which could have escape detection, prior to the PCR assays. Again the Δsll1147:Kmr mutant possessed only Δsll1147:Kmr chromosomes (Figure 1B, see the presence of the 941 bp PCR product and the absence of a 355 bp PCR band). Together, these data demonstrate that sll1147 is non-essential for the standard photoautotrophic growth of Synechocystis.
The Sll1147 MAPEG-Like GST Operates in the Tolerance of Synechocystis to n-tertbutyl Hydroperoxide
Recently, we showed that the Sll1545 and Slr0236 GSTs, distantly related to the presently studied MAPEG-like GST Sll1147, operate (negatively) in the tolerance to hydrogen peroxide (Kammerscheit et al., 2019) a ROS frequently generated by the cell metabolism (Imlay, 2013). Consequently, having a strong interest in the selectivity/redundancy of the role of GSH-dependent enzymes (Picciocchi et al., 2007; Michaut et al., 2008; Marteyn et al., 2009, 2013), we have tested the influence of hydrogen peroxide (H2O2) and n-tertbutyl hydroperoxide (n-tBOOH), which induces lipid peroxidation (Andrade et al., 2018), on the fitness of the Synechocystis WT strain and the Δsll1147:Kmr mutant. Both the growth and survival of the Δsll1147:Kmr mutant (hereafter Δsll1147) were decreased by n-tBOOH (Figures 2B,C) and H2O2 (Supplementary Figure S1), as compared to the WT strain. Collectively, these data suggest that Sll1147 operates in the protection against the two peroxides H2O2 and n-tBOOH.
Figure 2. The Δsll1147 mutant is sensitive to n-tertbutyl hydroperoxide. (A) Ten milliliters of mid-log-phase cultures (initial OD580nm = 0.1) were incubated for 72 h in liquid mineral medium (MM) under standard photoautotrophic conditions with or without the indicated concentrations of n-tBOOH, prior to transfer in spectrophotometric cuvette and photography. (B) Typical growth curve of the WT strain and Δsll1147 mutant incubated in liquid MM containing 10 μM n-tBOOH. (C) Typical survival of WT and Δsll1147 cells exposed for 72 h to various n-tBOOH concentrations. Data shown in (B,C) are expressed as the mean ± standard deviation (SD) of three experiments.
In Response to n-tertbutyl Hydroperoxide (n-tBOOH), the Δsll1147 Sensitive Mutant Transiently Accumulates Peroxidized Lipids and Then Glutathione
To analyze the influence of n-tBOOH on the Δsll1147 sensitive mutant and the WT control strain, we measured the malondialdehyde (MDA) content as a marker of lipid peroxidation, using the standard thiobarbituric acid reactive substances (TBARS) assay (Zeb and Ullah, 2016). As GSTs are generally involved in glutathione-dependent reactions, we also measured the levels of the reduced, oxidized and total glutathione (GSH, GSSG, and GStotal = GSH + GSSG) using the relevant standard assay (Akerboom and Sies, 1981) as we previously described (Kammerscheit et al., 2019).
In the WT strain, the level of MDA was almost unaffected by (18.75 μM) n-tBOOH (Figure 3B) while GSH and GSSG were weakly (about twofold) and transiently increased at 1 h (GSH) and 3 h (GSSG), before returning to their normal levels at 24 h (Figures 3F,H). These data are consistent with the WT strain being little affected by n-tBOOH [it was resistant up to 25 μM; (Figure 2)]. By contrast, the Δsll1147 mutant challenged by n-tBOOH highly and rapidly accumulated MDA (within 1 h), the level of which decreased down to the unstressed level (at 8 h, Figure 3B). Concomitantly to the MDA decline (between 1 and 3 h), the mutant Δsll1147 strongly accumulated both GSH and GSSG (up to 25 and 10 mM, respectively), that subsequently returned to the unstressed level (at 24 h, Figures 3B,F,H). The strong and sequential accumulation of the stress indicator MDA (at 1 h) and then (at 8 h) of GSH (detoxification) and GSSG (generated upon the GSH-mediated detoxification) are consistent with the high sensitivity of the Δsll1147 mutant to n-tBOOH (Figure 2). Altogether, these findings indicate that Sll1147 normally operates in the protection against peroxidized lipids elicited by n-tBOOH, using a process that transiently accelerates the synthesis of reduced glutathione (GSH) which is subsequently oxidized in glutathione disulfide (GSSG). In contrast, Δsll1147 cells challenged by H2O2 did not significantly modify their level of GSH and GSSG as compared to WT cells (Supplementary Figure S2), indicating that the Sll1147 and glutathione-dependent response is somehow more “specific” to peroxidized lipids than to other kind of ROS, as observed with mGST1 substrates (Mosialou et al., 1995).
Figure 3. The Δsll1147 sensitive mutant challenged by n-tBOOH, transiently accumulates peroxidized lipids and then glutathione. Kinetic analysis of the influence of n-tertbutyl hydroperoxide (n-tBOOH) on the abundance of peroxidized lipids, measured as the MDA content (A,B), total glutathione (C,D), GSH (E,F), and GSSG (G,H) in Synechocystis WT and Δsll1147 cells. The data are expressed as the mean ± SD of three assays and ∗ indicates significant difference between mutant and WT (t-test, P < 0.05).
The Sll1147 MAPEG-Like GST Operates in the Tolerance of Synechocystis to Both Heat and Cold Stresses
Several lines of evidence prompted us to test the influence of the presence (WT) and absence of Sll1147 (Δsll1147 mutant) on the tolerance of Synechocystis to high and low temperatures. Like other photosynthetic organisms, cyanobacteria are frequently exposed to fluctuations in temperatures triggered by the alternation of seasons, the day-night cycles, and the passages of clouds that filter sunlight. Furthermore, it is known that (i) temperature stress can trigger lipid peroxidation; (ii) mutant impaired in the defense against lipid peroxidation are temperature sensitive, and (iii) glutathione operates in the resistance to temperature stress and lipid peroxidation (Hasanuzzaman et al., 2017). Consequently, we have tested and compared the influence of high (39°C) and low (4°C) temperatures on the growth and/or survival of the WT and Δsll1147 strains of Synechocystis. The fitness of the two strains was similar at 30°C (the standard growth temperature of Synechocystis) and 34°C (Figures 4C,D). As compared to the WT strain, the growth and survival of the Δsll1147 mutant were decreased by high temperatures (Figures 4E,F). These data showed that Sll1147 is required for the tolerance to heat. We also found that the survival of the Δsll1147 mutant was strongly decreased after a 48 h exposure at 4°C (Figures 4G,H), showing that Sll1147 is also involved in the tolerance to low temperatures. To our knowledge this is the first evidence that a cyanobacterial GST (the MAPEG-like Sll1147 protein) operates in the protection against heat and cold stresses.
Figure 4. The Sll1147 MAPEG-like GST is involved in the Synechocystis tolerance to high and low temperatures. Ten milliliters of mid-log-phase cultures (initial OD580nm = 0.1) were incubated in liquid MM for 24 h under standard light (2500 lux; 31.25 μE.m– 2.s–1) at the indicated temperatures, prior to photographing the culture flasks (A) and survival analysis (B). (C–F) Growth curves of WT and Δsll1147 strains incubated in liquid MM under standard light (2500 lux; 31.25 μE.m–2.s–1) at various temperatures: 30°C (C), 34°C (D), 36.5°C (E), and 39°C (F). (G) Ten milliliters of mid-log-phase cultures (initial OD580nm = 0.1) were incubated in liquid MM for 48 h under standard light (2500 lux; 31.25 μE.m–2.s–1) at 4°C and then 24 h at 30°C for recovery, before photographing the culture flasks. (H) Survival of WT strain and Δsll1147, Δsll1147:pRmGST2, Δsll1147:pRmGST3, and Δsll1147:pRsll0067 mutants exposed for 48 h to 4°C. Data shown in (B–F,H) are expressed as the mean ± SD of three experiments.
The Heat-Sensitive Mutant Δsll1147 Exposed to a High Temperature Transiently Accumulates Peroxidized Lipids and Then Glutathione
Heat is an important environmental stressor known to elicit lipid peroxidation in photosynthetic organisms where it leads to the formation of the secondary product, MDA that can be detected by TBARS assay [for example see, (Prasad et al., 2016) and references therein]. Thus, to analyze the influence of heat in Synechocystis WT strain and Δsll1147 mutant we measured in each strain the MDA content and the levels of the reduced and oxidized glutathione (GSH, GSSG and total glutathione). In accordance with its heat sensitivity the Δsll1147 mutant incubated at 39°C rapidly (within 1 h) accumulated MDA, which decreased down to the unstressed level (at 8 h, Figure 5A). Concomitantly to the MDA decline (particularly between 3 and 8 h), the Δsll1147 mutant accumulated both GSH and GSSG (up to about 20 and 5 mM, respectively), which remained high (GSH, Figure 5C) or decreased down to the unstressed level (at 24 h, GSSG, Figure 5D). Collectively, these data indicate that Sll1147 normally operates in the detoxification of peroxidized lipids elicited by heat, using a redox process that transforms reduced glutathione (GSH) in oxidized glutathione (GSSG).
Figure 5. The Δsll1147 heat sensitive mutant challenged by heat transiently accumulates peroxidized lipids, GSH, and GSSG. Kinetic analysis of the influence of high temperature exposure (39°C) on the abundance of peroxidized lipids measured as MDA content (A), total glutathione (B), GSH (C), and GSSG (D) in Synechocystis WT and mutant Δsll1147. Data are expressed as the mean ± SD of three assays and ∗ indicates significant difference between mutant and WT (t-test, P < 0.05).
The Cold-Sensitive Mutant Δsll1147 Exposed to a Low Temperature Transiently Accumulates Peroxidized Lipids and Then Glutathione
We also analyze the influence of cold in Synechocystis WT strain and Δsll1147 mutant on the level of reduced and oxidized glutathione (GSH and GSSG) and on the MDA content, because cold treatment modifies the content of total glutathione and increases ROS (H2O2 and O2–) and malondialdehyde levels (MDA) (Hasanuzzaman et al., 2017). In agreement with its cold sensitivity the Δsll1147 mutant incubated at 4°C rapidly (within 1 h) accumulated MDA which peaked at 3 h (up to 10 mM) and subsequently decreased down to the WT level (at 8 h, Figure 6A). The Δsll1147 mutant accumulated both GSH and GSSG (up to about 16 and 3 mM, respectively), which remained high (for both GSH and GSSG, Figures 6C,D) compared to the WT levels. Collectively, these data indicate that Sll1147 normally operates in the detoxification of peroxidized lipids elicited by heat, using a redox process that transforms reduced glutathione (GSH) in oxidized glutathione (GSSG).
Figure 6. In response to cold, the Δsll1147 sensitive mutant transiently accumulates peroxidized lipids, GSH and GSSG. Kinetic analysis of the influence of cold temperature exposure (4°C) on the abundance of peroxidized lipids measured as MDA content (A), total glutathione (B), GSH (C), and GSSG (D) in Synechocystis WT and mutant Δsll1147. Data are expressed as the mean ± SD of three assays and ∗ indicates significant difference between mutant and WT (t-test, P < 0.05).
The Human hmGST2 and hmGST3 MAPEG Proteins, but Not the Unrelated Sll0067 Synechocystis GST Protein, Can Restore the Cell Tolerance to n-tBOOH and Heat of the Synechocystis Mutant Lacking the Sll1147 MAPEG-Like Protein
Previous bioinformatic studies showed that the cyanobacterial Sll1147 protein shares common features (amino-acid sequences and hydropathy plots) with the human mGST2 and mGST3 MAPEGs (hereafter hmGST2 and hmGST3) (Jakobsson et al., 1999). As the role of these hmGST2 and hmGST3 proteins in cell physiology is poorly understood, we tested whether they can operate in the tolerance to temperature and lipid peroxidation stresses, like their “(cyano)bacterial ancestor” Sll1147. Practically, we tested whether the hmGST2 and/or hmGST3 proteins can restore the tolerance to heat, cold and n-tertbutyl hydroperoxide (n-tBOOH) in the Synechocystis Δsll1147 mutant lacking Sll1147. Therefore, we constructed the gene-complementation DNA cassettes that contain the following parts (Supplementary Table S2 and Supplementary Figure S3). A synthetic version of the hmGST2 or hmGST3 genes adapted to the cyanobacterial codon usage and expressed from the efficient pR promoter (Mermet-Bouvier and Chauvat, 1994). Downstream of these recombinant genes, pR-hmGST2 and pR-hmGST3, we placed an antibiotic-resistance marker gene (Smr/Spr) for selection. Finally, these cassettes were flanked by sll1147-surrounding Synechocystis DNA regions to serve as platform of homology for genetic recombination mediating the integration of each DNA cassettes (Δsll1147:pR-hmGST2-Smr/Spr and Δsll1147:pR-hmGST3-Smr/Spr) at the sll1147 locus upon transformation in Synechocystis. Similarly, the Δsll1147:pR-sll0067-Kmr control DNA cassette was constructed (Supplementary Table S2 and Supplementary Figure S3) to test the influence of the Sll0067 GST unrelated to Sll1147 [they share a small amino-acids sequence identity percentage (14.4%)] on the presently studied stresses.
The Δsll1147:pR-hmGST2-Smr/Spr and Δsll1147:pR-hmGST3-Smr/Spr cassettes were transformed in the Δsll1147:Kmr selecting for the Smr/Spr (Kms) phenotype. In each case several transformant clones were analyzed by PCR and DNA sequencing (Supplementary Figure S3) to verify that they contained the complementation DNA-cassette Δsll1147:pR-hmGST2-Smr/Spr or Δsll1147:pR-hmGST3-Smr/Spr integrated in place of the Δsll1147:Kmr locus in all Synechocystis chromosome copies, as expected.
The Δsll1147:pR-hmGST2-Smr/Spr and Δsll1147:pR-hmGST3-Smr/Spr reporter strains grew as healthy as the Synechocystis WT strain and the Δsll1147:Kmr mutant under standard condtions (30°C, Figures 7A,C). Interestingly, the growth of these reporter strains was less affected by the heat (39°C) and n-tBOOH (10 μM) stresses than those the Δsll1147:Kmr mutant (Figures 7A,B). These data indicate that the hmGST2 and hmGST3 human proteins can rescue the tolerance to heat and n-tBOOH that are low in the Δsll1147:Kmr mutant due to its lack of Sll1147 (Figure 7D). To confirm that the higher resistance to n-tBOOH and heat of the Δsll1147:pR-hmGST3-Smr/Spr reporter strain was due to the expression of the pR-hmGST3 gene, not an adventitious selection of a suppressor mutation somewhere in the Synechocystis genome, we transformed the Δsll1147:pR-hmGST3-Smr/Spr cells with the Δsll1147:pR-sll0067-Kmr cassette to substitute the pR-hmGST3 gene by the pR-sll0067 gene encoding the Sll0067 GST unrelated to the MAPEG proteins hmGST3, hmGST2, and Sll1147/. We verified by PCR and DNA sequencing (Supplementary Figure S3) that the resulting Δsll1147:pR-sll0067-Kmr reporter cells harbored the pR-sll0067 gene in place of the pR-hmGST3 gene in every chromosome copy, and that these cells remained as sensitive to n-tBOOH and heat as the Δsll1147 mutant (Figure 7B), as expected. These data confirmed that the absence of the MAPEG-like Sll1147 protein decreases the tolerance to n-tBOOH and heat, which can be rescued by the human orthologs hmGST2 and hmGST3, but not the unrelated cyanobacterial GST Sll0067. Collectively, these finding indicate that MAPEG enzymes, but not all GSTs, play an important role in the cellular resistance to heat and lipid peroxidation, which has been conserved, at least in part, during evolution.
Figure 7. The human hmGST2 and hmGST3 proteins can restore the Δsll1147 tolerance to heat and n-tBOOH. (A,B) Growth curve of Synechocystis WT and relevant reporter strains (initial OD580nm = 0.02) incubated in liquid MM under standard light (2500 lux; 31.25 μE.m–2.s–1) and temperature (30°C), without (A) or with n-tBOOH 10 μM (B). (C,D) Growth curve of WT and relevant reporter strains (initial OD580nm = 0.1) incubated in liquid MM under standard light (2500 lux; 31.25 μE.m–2.s–1) at 30°C (C) or 39°C (D). Data shown in all panels are expressed as the mean ± SD of three experiments.
The Human hmGST2 and hmGST3 MAPEG Proteins Cannot Rescue the Cell Tolerance to Cold, in the Synechocystis Mutant Lacking the Sll1147 MAPEG-Like Protein
The same genetic complementation strategy was used to test whether the human hmGST2 and hmGST3 proteins, and the other Synechocystis GST protein Sll0067, are able to rescue the cold tolerance of the Synechocystis Δsll1147:Kmr mutant. The survival of the reporter strains Δsll1147:pR-sll0067 strain was similarly as the Δsll1147:Kmr deletion mutant suggesting that Sll0067 does not play a role in cold tolerance. The survival of the reporter strains Δsll1147:pR-hmGST2 and Δsll1147:pR-hmGST3 were even lower (10-fold) than that of the deletion mutant Δsll1147:Kmr (Figure 4H) suggesting that both hmGST2 and hmGST3 might play a negative influence on resistance to cold.
The Human hmGST2 and hmGST3 MAPEG Proteins, but Not the Unrelated Sll0067 Synechocystis GST Protein, Can Increase the E. coli Tolerance to n-tBOOH and Heat
We also evaluated the influence of the studied protein on the survival of E. coli to n-tBOOH or high temperatures (Figure 8). As observed in Synechocystis, the human MAPEG proteins hmGST2, hmGST3 but not the unrelated cyanobacterial protein Sll0067 could increase the E. coli resistance to lipid peroxidation (n-tBOOH) and heat. Together the findings in Synechocystis and E. coli suggest that the MAPEG GSTs play arole in membrane fluidity that has been conserved, at least in part (tolerance to heat and n-tBOOH, but not cold) during evolution.
Figure 8. The production of hmGST2 and hmGST3 increase the Escherichia coli survival to n-tBOOH and heat. Survival of E. coli TOP 10 strains harboring, or not (WT control strain) one of the studied GST-producing plasmid challenged for 2 h (initial OD600nm = 0.1) by the indicated temperatures (A) or n-tBOOH concentration (B). Data shown in all panels are expressed as the mean ± SD of three experiments.
We presently report the first in vivo analysis of a MAPEG2-type GST protein, i.e., the protein designated as Sll147 in CyanoBase (see text footnote 1) of the well-studied unicellular cyanobacterium Synechocystis PCC 6803 (Synechocystis). The motivations for this study are as followins. First, the MAPEG2 sub-family of “Membrane-Associated Proteins involved in Ecosanoïd and Glutathione metabolism” proteins has been poorly studied in vivo, even though (i) the human MAPEG2 proteins hmGST2 and hmGST3 are regarded as biomarker for tumorigenesis, and (ii) MAPEG2 proteins are also present in basic easily manipulable organisms like bacteria. Second, only two glutathione transferases (GSTs) have so far been studied in vivo in cyanobacteria (Kammerscheit et al., 2019), even though these environmentally crucial prokaryotes are regarded as having developed glutathione (GSH) and GSH-dependent enzymes, such GSTs, to protect themselves against the toxic ROS often produced by their powerful photosynthesis (William Schopf, 2011). These Synechocystis Sll1145 and Slr0236 GSTs, unrelated to Sll1147, were shown in vivo to play a prominent role in the resistance to photo-oxidative stress (Kammerscheit et al., 2019). Third, Sll1147 and other prokaryotic and eukaryotic MAPEG enzymes produced from recombinant E. coli strains were only shown to have the classical in vitro GST activity, which is the conjugation of GSH with the standard 1-chloro-2,4-dinitrobenzene (CDNB) exogenous agent (Bresell et al., 2005). Fourth, the analysis of the selectivity/redundancy of GSTs is bound to be easier in a well-studied basic organism such as Synechocystis than in higher eukaryotes that possess (i) various tissues (Morgenstern et al., 2011), (ii) complex developmental processes (Björkhem-Bergman et al., 2014) and (iii) large enzyme families. For example, 27 GST encoding genes were identified in human and classified into 7 classes (Alpha, Mu, Pi, Theta, Omega, Zeta, Kappa, and MAPEG) (Nebert and Vasiliou, 2004) whereas Synechocystis possesses only six GSTs including Sll1147.
We presently report that the MAPEG-2 type Sll1147 protein is dispensable to the growth of Synechocystis in standard photo-autotrophic conditions (Figure 1), whereas it is an important player in cell tolerance heat (Figures 4A–F) and cold (Figures 4G,H), two inevitable environmental stresses for cyanobacteria elicited by the alternation of seasons, the day-night cycles, and the passages of clouds filtering sunlight, which limit their production of biomass that is crucial for our food chain. Using relevant assays, we showed that Sll1147 operates in the protection against peroxidized lipids elicited by heat and cold stresses, using a redox process that transforms reduced glutathione (GSH) in oxidized glutathione (GSSG) (Figures 5, 6). These findings are welcome for the following reason. Though it is known that cold generates a decrease in membrane fluidity, which can be compensated by the desaturation of membrane lipids by fatty acid desaturases, whereas heat causes fluidization of the membranes, which can be compensated by the replacement of unsaturated fatty acids in membrane lipids by newly synthesized saturated fatty acids, these processes are poorly described in cyanobacteria (Maksimov et al., 2017; Pittera et al., 2018). Indeed, to our knowledge, no GST has been proposed to operate in protection against temperature stress in cyanobacteria, yet. Furthermore, cyanobacteria have valuable biotechnological potentials (ecological production of chemicals) that are often hampered by our limited knowledge of their responses to stresses (Jones, 2014; Cassier-Chauvat et al., 2016). Most cyanobacterial species that are being used for chemical production grow optimally between 25 and 35°C, while temperatures in outdoor photobioreactors can be greater than 40°C in subtropical zones. Furthermore, culturing in elevated temperatures can be beneficial in reducing the potential for microbial contamination (Kitchener and Grunden, 2018). Thus, it is important to get a good understanding of heat tolerance in cyanobacteria in the future view order to select or generate strains capable to flourish under high temperatures.
We also showed that Sll1147 is involved in the tolerance to n-tertbutyl hydroperoxide (n-tBOOH), which elicits peroxidized lipids (Johansson et al., 2010), using a redox process that transforms GSH in GSSG (Figures 2, 3), again possibly to restore membrane fluidity. These data are consistent with previous observations that (i) the human hmGST1 protein is active (in vitro) on various oxidized lipids (Mosialou et al., 1995); (ii) cancer cells overproducing hmGST1 are more resistant to n-tBOOH than their control counterpart (no overproduction of mGST1) (Johansson et al., 2010); and (iii) the sea cucumber mGST1 is also involved in the tolerance to lipid peroxidation (Zhang et al., 2017).
Sll1147 was also found to be required for the tolerance to hydrogen peroxide (H2O2) (entary Supplementary Figure S1) similarly to what found for the Sll1145 GST (Kammerscheit et al., 2019), unrelated to Sll1147. However, the H2O2 protection process involving Sll1147 is not accompanied by change in glutathione status (Supplementary Figure S2), unlike what found in the case of Sll1145 (Kammerscheit et al., 2019). Together, these findings emphasize on the selectivity of cyanobacteria GSTs, a poorly investigated field so far.
Finally, as a previous phylogenetic analysis has shown that Sll1147 resembles the human MAPEG hmGST2 and hmGST3 (Bresell et al., 2005), we tested whether the expression of synthetic hmGST2 and hmGST3 genes, adapted to the cyanobacterial codon usage, could restore the tolerance to n-tBOOH, and heat in the Synechocystis mutant lacking Sll1147 (Δsll1147). Indeed, these complementation tests were positive, whereas the control test performed with the other Synechocystis GST Sll0067, unrelated to Sll1147, was negative, as expected (Figure 7). Similar findings were observed when these cyanobacterial and human genes were expressed in E. coli (Figure 8). Collectively, these findings indicate that the activity of the MAPEG2 proteins have been conserved, at least in part, during evolution from (cyano)bacteria to human. In this context it is important to note that human MAPEG proteins play a role in inflammation and fever (Sjögren et al., 2013; Bankova et al., 2016, 99) that should be fully investigated. Also interestingly, these human MAPEGs appeared to be able to restore the tolerance of the SynechocystisΔsll1147 mutant to heat but not cold, which increases or decrease the fluidization of cell membranes, respectively. These findings suggest that depending on their amino-acids sequence MAPEG protein can differently influence some players operating in the signaling of and/or protection against heat but not cold.
Materials and Methods
Bacterial Strains, Growth, and Stress Assays
Escherichia coli TOP10 (Invitrogen) used for gene manipulation was grown on LB at 37°C. Antibiotic selections were performed with ampicillin (Amp) 100 μg.mL–1, kanamycine (Km) 50 μg.mL–1 or both streptomycin (Sm) 25 μg.mL–1 and spectinomycin (Sp) 75 μg.mL–1. For survival analysis, cells challenged by the indicated treatments were plated on Difco LB agar and incubated one day before counting the surviving colonies.
Synechocystis PCC 6803 (Synechocystis) was grown at 30°C in liquid mineral medium (MM), i.e., BG11 medium (Rippka et al., 1979) enriched with 3.78 mM Na2CO3 (Jittawuttipoka et al., 2013), under continuous agitation (140 rpm) and white light (2500 lux; 31.25 μE.m–2.s–1) at 30°C unless stated otherwise. Antibiotic selections were performed with Km 50 μg.mL–1 or both Sm 5 μg.mL–1 and Sp 5 μg.mL–1. For growth analysis mid-exponential phase cultures (OD580nm = 0.3 to 0.8) were adjusted to OD580nm = 0.02 (5.105 cells.mL–1) and subsequently incubated in liquid MM containing (or not) the indicated agents, under the indicated temperatures, prior to measuring OD580 or photographing the flasks culture. For growth analysis, or OD580nm = 0.1 (2.5 × 106 cells.mL–1) for survival analysis, For survival analysis mid-exponential phase cultures were adjusted to OD580nm = 0.1 (2.5 × 106 cells.mL–1) before the indicated challenges. Then cells were serially diluted in MM, spread on MM solidified with 1% agar (Difco) and incubated during 5–7 days under standard conditions (2500 lux; 31.25 μE.m–2.s–1; 30°C) before counting the surviving colonies.
Construction of the DNA Cassette for Targeted Deletion of the sll1147 Gene, and Its Substitution by Recombinant Genes Encoding Other GSTs
The two Synechocystis DNA regions (about 300 bp in length each) flanking the sll1147 protein coding sequence (CS) were independently amplified by PCR, using specific oligonucleotides primers (Supplementary Table S1). Then, these two DNA regions were joined by standard PCR-driven overlap extension (Heckman and Pease, 2007) in a single DNA segment harboring a SmaI restriction site in place of the sll1147 CS. After cloning in pGEMt (Promega), the resulting plasmid pGEMT-ABsll1147 (Supplementary Table S2) was opened at the unique SmaI site where we cloned the Kmr cassette (a HincII fragment of the commercial pUC4K plasmid, Pharmacia) in the same orientation as the sll1147 CS it replaced. The Δsll1147:Kmr cassette was transformed (Labarre et al., 1989) to Synechocystis wild-type (WT) strain, generating the Δsll1147:Kmr deletion mutant. The Δsll1147:Kmr deletion cassette was verified by PCR and nucleotide sequencing (Mix2Seq Kit, Eurofins Genomics) before and after propagation in Synechocystis.
We also cloned in the SmaI site of pGEMT-ABsll1147 various DNA cassettes that were assembled using NEBuilder HiFi DNA Assembly Master Mix (New England BioLabs) from relevant DNA sequences. These DNA cassette comprises (from 5′ terminus to 3′ end) the very active lambda phage pR promoter and cro ribosome binding site (Mermet-Bouvier and Chauvat, 1994) we routinely used for high-level gene expression [see (Ortega-Ramos et al., 2014) and references therein]. These pR promoter and cro RBS direct the expression of the synthetic genes (adapted to the Synechocystis codon usage for efficient translation) encoding either the human hmGST2 or hmGST3 proteins (Uniprot-ID: Q99735; O14880) or the Synechocystis Sll0067 (Uniprot-ID: Q55139) protein. Each recombinant gene was followed by an antibiotic resistant marker gene Kmr (originating from pUC4K, Pharmacia) or Smr/Spr [originating from our pFC1 plasmid (Mermet-Bouvier and Chauvat, 1994)]. All DNA cassettes were verified by PCR and nucleotide sequencing (Mix2Seq Kit, Eurofins Genomics) before and after propagation in Synechocystis. The Δsll1147:Kmr deletion mutant was used as the recipient strain for the transformation by the DNA cassettes required to test the heterologous complementation by the human proteins hmGST2 and hmGST3. The Δsll1147:pR-sll0067-Kmr cassette used to test the possible complementation by Sll0067 was transformed into the Δsll1147:pR-hmGST3-Smr/Spr mutant.
Cell Culture and Assay of the Reduced (GSH) and Oxidized (GSSG) Forms of Glutathione
All reagents were purchased from Sigma-Aldrich. Fifty milliliters of exponentially-growing cultures were diluted twofold down to OD580 = 0.4, and incubated for various durations under white light (2500 lux; 31.25 μE.m–2.s–1) in the presence of the indicated agents. Cells were rapidly collected by filtration on a 0.45 μm cellulose membrane (Millipore) under light; re-suspended in 1 mL of acidic extraction phosphate buffer [100 mM KH2PO4/K2HPO4; 1 mM EDTA; 5% (w/v) 5-sulfosalicylic acid (SSA)]; disrupted by a three freezing-thawing cycles in liquid nitrogen and hot water bath, and strong mixing (Vibrax VXR, Ika) for 10 min at 4°C; prior to centrifugation (14,000 rpm, 4°C, 5 min) to eliminate unbroken cells and membranes. Cell extracts were purified by a 20 min centrifugation at 14,000 rpm at 4°C through a filter (Amicon Ultra – 0.5 mL 30K; Millipore) to eliminate proteins larger than 30 kDa, and stored at −80°C until use. Before GSSG assay, 100 μL of filtrate were treated with 2 μL of neat 2-vinylpyridine for 1 h on ice to block reduced glutathione (GSH) and then with 2 μL of fourfold diluted triethanolamine solution. For assays, 10 μL untreated filtrate samples (total glutathione assay) and 20 μL treated samples (oxidized GSSG assay) were loaded on a UV-compatible 96-well plate (Greiner bio-one). A first reaction mixture containing yeast GR at final concentration 1.25 U/mL in phosphate buffer (100 mM KH2PO4/K2HPO4 buffer and 1 mM EDTA, pH 7.5) was prepared and distributed to each well. A second reaction mixture containing 0.2 mM DTNB [5,5′-dithiobis-(2-nitrobenzoic acid)] and 0.3 mM NADPH in phosphate buffer was automatically added in each well by a microplate reader (ClarioStar; BMG Labtech). The reaction was immediately followed by measuring for 1 min at 30°C the absorption at 412 nm of the yellow TNB (5′-thio-2-nitrobenzoic acid) product (Akerboom and Sies, 1981). Standard curves prepared with various concentrations of GSH or GSSG were used to calculate the GSSG (oxidized) and total glutathione (GSSG + reduced GSH) using the Synechocystis cell volume value of 1.2.10–11 mL (Mazouni et al., 2004). The GSH content was calculated by subtracting the GSSG content from the total glutathione content.
Estimation of the Peroxidized Lipids by TBARS Assay
The determination of TBARS as a marker of lipid peroxidation is based on the reaction of MDA and thiobarbituric acid (TBA) in acidic medium at high temperature (Zeb and Ullah, 2016). All chemicals (butylated hydroxytoluene BHT, MDA, and thiobarbituric acid TBA) were purchased from Sigma-Aldrich. 100 mL of exponentially growing cultures were diluted twofold down to OD580 = 0.5, and incubated under white light (2500 lux; 31.25 μE.m–2.s–1) in the indicated conditions. Cells were rapidly collected by filtration as described above and re-suspended in 1 mL of glacial acetic acid supplemented with 0.5 mM BHT (butylated hydroxytoluene BHT) to prevent any further oxidation. MDA extraction was performed as described above for the glutathione assay thanks to: (i) freeze-thaw cycle (liquid nitrogen-hot water), (ii) strong mixing for 10 min at 4°C (Vibrax VXR, Ika) and (iii) centrifugation (14,000 rpm, 4°C, 5 min) to eliminate unbroken cells and membranes. Cells extracts containing MDA were then purified by a 20 min centrifugation at 14,000 rpm at 4°C through a filter (Amicon Ultra – 0.5 mL 30K; Millipore) to eliminate proteins and avoid cross reaction. Filtrates were stored at −80°C until assays in the presence of 100 μL of 4 mM TBA. The absorbance of this mixture was measured at 532 nm using the above-mentioned microplate reader prior to the formation of the MDA-TBA adducts that begins at high temperature (A532nm before). Then, the reaction mixture was heated at 50°C for 3 h and subsequently cooled at room temperature. The absorbance at 532 nm was measured after the reaction (A532nm after) to determine ΔA532nm = A532nm after – A532nm before as the absorbance only due to MDA absorption at 532 nm. In parallel, MDA standard curve was prepared and used to calculate the MDA content using the above-mentioned Synechocystis cell volume.
Data Availability Statement
All datasets generated for this study are included in the manuscript/Supplementary Files.
CC-C and FC conceived the project. XK, CC-C, and FC conceived the experiments, analyzed the data, and wrote the manuscript. XK performed the experiments. CC-C agreed to serve as the author responsible for contact and ensures communication.
This work was partly supported by the CEA-DRF Remember project. XK received a Ph.D. fellowship from the MENESR.
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.
We thank Mathias Raguin for help in performing glutathione assays.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2019.02248/full#supplementary-material
Ago, H., Kanaoka, Y., Irikura, D., Lam, B. K., Shimamura, T., Austen, K. F., et al. (2007). Crystal structure of a human membrane protein involved in cysteinyl leukotriene biosynthesis. Nature 448, 609–612. doi: 10.1038/nature05936
Ahmad, S., Thulasingam, M., Palombo, I., Daley, D. O., Johnson, K. A., Morgenstern, R., et al. (2015). Trimeric microsomal glutathione transferase 2 displays one third of the sites reactivity. Biochim. Biophys. Acta 1854, 1365–1371. doi: 10.1016/j.bbapap.2015.06.003
Ålander, J., Lengqvist, J., Holm, P. J., Svensson, R., Gerbaux, P., van den Heuvel, R. H. H., et al. (2009). Microsomal glutathione transferase 1 exhibits one-third-of-the-sites-reactivity towards glutathione. Arch. Biochem. Biophys. 487, 42–48. doi: 10.1016/j.abb.2009.04.009
Andrade, N., Silva, C., and Martel, F. (2018). The effect of oxidative stress upon intestinal sugar transport: an in vitro study using human intestinal epithelial (Caco-2) cells. Toxicol. Res. 7, 1236–1246. doi: 10.1039/C8TX00183A
Bankova, L. G., Lai, J., Yoshimoto, E., Boyce, J. A., Austen, K. F., Kanaoka, Y., et al. (2016). Leukotriene E4 elicits respiratory epithelial cell mucin release through the G-protein–coupled receptor, GPR99. Proc. Natl. Acad. Sci. U.S.A. 113, 6242–6247. doi: 10.1073/pnas.1605957113
Björkhem-Bergman, L., Johansson, M., Morgenstern, R., Rane, A., and Ekström, L. (2014). Prenatal expression of thioredoxin reductase 1 (TRXR1) and microsomal glutathione transferase 1 (MGST1) in humans. FEBS Open Bio 4, 886–891. doi: 10.1016/j.fob.2014.10.005
Bresell, A., Weinander, R., Lundqvist, G., Raza, H., Shimoji, M., Sun, T.-H., et al. (2005). Bioinformatic and enzymatic characterization of the MAPEG superfamily. FEBS J. 272, 1688–1703. doi: 10.1111/j.1742-4658.2005.04596.x
Cassier-Chauvat, C., Veaudor, T., and Chauvat, F. (2016). Comparative genomics of DNA recombination and repair in Cyanobacteria: biotechnological implications. Front. Microbiol. 7:1809. doi: 10.3389/fmicb.2016.01809
Couto, N., Wood, J., and Barber, J. (2016). The role of glutathione reductase and related enzymes on cellular redox homoeostasis network. Free Radic. Biol. Med. 95, 27–42. doi: 10.1016/j.freeradbiomed.2016.02.028
Hasanuzzaman, M., Nahar, K., Anee, T. I., and Fujita, M. (2017). Glutathione in plants: biosynthesis and physiological role in environmental stress tolerance. Physiol. Mol. Biol. Plants Int. J. Funct. Plant Biol. 23, 249–268. doi: 10.1007/s12298-017-0422-2
Holm, P. J., Bhakat, P., Jegerschöld, C., Gyobu, N., Mitsuoka, K., Fujiyoshi, Y., et al. (2006). Structural basis for detoxification and oxidative stress protection in membranes. J. Mol. Biol. 360, 934–945. doi: 10.1016/j.jmb.2006.05.056
Holm, P. J., Morgenstern, R., and Hebert, H. (2002). The 3-D structure of microsomal glutathione transferase 1 at 6 A resolution as determined by electron crystallography of p22(1)2(1) crystals. Biochim. Biophys. Acta 1594, 276–285.
Jakobsson, P. J., Morgenstern, R., Mancini, J., Ford-Hutchinson, A., and Persson, B. (1999). Common structural features of MAPEG – a widespread superfamily of membrane associated proteins with highly divergent functions in eicosanoid and glutathione metabolism. Protein Sci. Publ. Protein Soc. 8, 689–692. doi: 10.1110/ps.8.3.689
Jakobsson, P. J., Morgenstern, R., Mancini, J., Ford-Hutchinson, A., and Persson, B. (2000). Membrane-associated proteins in eicosanoid and glutathione metabolism (MAPEG). A widespread protein superfamily. Am. J. Respir. Crit. Care Med. 161, S20–S24. doi: 10.1164/ajrccm.161.supplement_1.ltta-5
Jittawuttipoka, T., Planchon, M., Spalla, O., Benzerara, K., Guyot, F., Cassier-Chauvat, C., et al. (2013). Multidisciplinary evidences that Synechocystis PCC6803 exopolysaccharides operate in cell sedimentation and protection against salt and metal stresses. PloS One 8:e55564. doi: 10.1371/journal.pone.0055564
Johansson, K., Järvliden, J., Gogvadze, V., and Morgenstern, R. (2010). Multiple roles of microsomal glutathione transferase 1 in cellular protection: a mechanistic study. Free Radic. Biol. Med. 49, 1638–1645. doi: 10.1016/j.freeradbiomed.2010.08.013
Kammerscheit, X., Chauvat, F., and Cassier-Chauvat, C. (2019). First in vivo evidences that glutathione-S-transferase operates in photo-oxidative stress in Cyanobacteria. Front. Microbiol. 10:1899. doi: 10.3389/fmicb.2019.01899
Kitchener, R. L., and Grunden, A. M. (2018). Methods for enhancing Cyanobacterial stress tolerance to enable improved production of biofuels and industrially relevant chemicals. Appl. Microbiol. Biotechnol. 102, 1617–1628. doi: 10.1007/s00253-018-8755-5
Labarre, J., Chauvat, F., and Thuriaux, P. (1989). Insertional mutagenesis by random cloning of antibiotic resistance genes into the genome of the Cyanobacterium Synechocystis strain PCC 6803. J. Bacteriol. 171, 3449–3457.
Maksimov, E. G., Mironov, K. S., Trofimova, M. S., Nechaeva, N. L., Todorenko, D. A., Klementiev, K. E., et al. (2017). Membrane fluidity controls redox-regulated cold stress responses in Cyanobacteria. Photosynth. Res. 133, 215–223. doi: 10.1007/s11120-017-0337-3
Marteyn, B., Domain, F., Legrain, P., Chauvat, F., and Cassier-Chauvat, C. (2009). The thioredoxin reductase-glutaredoxins-ferredoxin crossroad pathway for selenate tolerance in Synechocystis PCC6803. Mol. Microbiol. 71, 520–532. doi: 10.1111/j.1365-2958.2008.06550.x
Marteyn, B., Sakr, S., Farci, S., Bedhomme, M., Chardonnet, S., Decottignies, P., et al. (2013). The Synechocystis PCC6803 MerA-like enzyme operates in the reduction of both mercury and uranium under the control of the glutaredoxin 1 enzyme. J. Bacteriol. 195, 4138–4145. doi: 10.1128/JB.00272-13
Mazouni, K., Domain, F., Cassier-Chauvat, C., and Chauvat, F. (2004). Molecular analysis of the key cytokinetic components of Cyanobacteria: FtsZ, ZipN and MinCDE. Mol. Microbiol. 52, 1145–1158. doi: 10.1111/j.1365-2958.2004.04042.x
Mermet-Bouvier, P., and Chauvat, F. (1994). A conditional expression vector for the cyanobacteria Synechocystis sp. strains PCC6803 and PCC6714 or Synechococcus sp. strains PCC7942 and PCC6301. Curr. Microbiol. 28, 145–148.
Michaut, M., Kerrien, S., Montecchi-Palazzi, L., Chauvat, F., Cassier-Chauvat, C., Aude, J.-C., et al. (2008). InteroPORC: automated inference of highly conserved protein interaction networks. Bioinforma. Oxf. Engl. 24, 1625–1631. doi: 10.1093/bioinformatics/btn249
Mosialou, E., Piemonte, F., Andersson, C., Vos, R. M., van Bladeren, P. J., and Morgenstern, R. (1995). Microsomal glutathione transferase: lipid-derived substrates and lipid dependence. Arch. Biochem. Biophys. 320, 210–216.
Naraimsamy, K., Marteyn, B., Sakr, S., Cassier-Chauvat, C., and Chauvat, F. (2013). Genomics of the pleïotropic glutathione system in Cyanobacteria. Adv. Bot. Res. 65, 157–188. doi: 10.1016/B978-0-12-394313-2.00005-6
Noctor, G., Mhamdi, A., Chaouch, S., Han, Y., Neukermans, J., Marquez-Garcia, B., et al. (2012). Glutathione in plants: an integrated overview. Plant Cell Environ. 35, 454–484. doi: 10.1111/j.1365-3040.2011.02400.x
Ortega-Ramos, M., Jittawuttipoka, T., Saenkham, P., Czarnecka-Kwasiborski, A., Bottin, H., Cassier-Chauvat, C., et al. (2014). Engineering Synechocystis PCC6803 for hydrogen production: influence on the tolerance to oxidative and sugar stresses. PloS One 9:e89372. doi: 10.1371/journal.pone.0089372
Pearson, W. R. (2005). “Phylogenies of Glutathione Transferase Families,” in Methods in Enzymology Gluthione Transferases and Gamma-Glutamyl Transpeptidases, eds H. Sies, and L. Packer (Cambridge, MA: Academic Press), 186–204. doi: 10.1016/S0076-6879(05)01012-8
Picciocchi, A., Saguez, C., Boussac, A., Cassier-Chauvat, C., and Chauvat, F. (2007). CGFS-type monothiol glutaredoxins from the Cyanobacterium Synechocystis PCC6803 and other evolutionary distant model organisms possess a glutathione-ligated [2Fe-2S] cluster. Biochemistry 46, 15018–15026. doi: 10.1021/bi7013272
Pittera, J., Jouhet, J., Breton, S., Garczarek, L., Partensky, F., Maréchal, É., et al. (2018). Thermoacclimation and genome adaptation of the membrane lipidome in marine Synechococcus. Environ. Microbiol. 20, 612–631. doi: 10.1111/1462-2920.13985
Rippka, R., Deruelles, J., Waterbury, J. B., Herdman, M., and Stanier, R. Y. (1979). Generic assignments, strain histories and properties of pure cultures of Cyanobacteria. Microbiology 111, 1–61. doi: 10.1099/00221287-111-1-1
Sjögren, T., Nord, J., Ek, M., Johansson, P., Liu, G., and Geschwindner, S. (2013). Crystal structure of microsomal prostaglandin E2 synthase provides insight into diversity in the MAPEG superfamily. Proc. Natl. Acad. Sci. U.S.A. 110, 3806–3811. doi: 10.1073/pnas.1218504110
Yadav, S. K. (2010). Heavy metals toxicity in plants: an overview on the role of glutathione and phytochelatins in heavy metal stress tolerance of plants. South Afr. J. Bot. 76, 167–179. doi: 10.1016/j.sajb.2009.10.007
Zeb, A., and Ullah, F. (2016). A simple spectrophotometric method for the determination of thiobarbituric acid reactive substances in fried fast foods. J. Anal. Methods Chem. 2016:9412767. doi: 10.1155/2016/9412767
Keywords: Synechocystis PCC 6803, microsomal glutathione transferase, mGST2, mGST3, temperature stresses, heterologous complementation, knockout mutant, membrane stress
Citation: Kammerscheit X, Chauvat F and Cassier-Chauvat C (2019) From Cyanobacteria to Human, MAPEG-Type Glutathione-S-Transferases Operate in Cell Tolerance to Heat, Cold, and Lipid Peroxidation. Front. Microbiol. 10:2248. doi: 10.3389/fmicb.2019.02248
Received: 13 August 2019; Accepted: 13 September 2019;
Published: 27 September 2019.
Edited by:Wendy Schluchter, University of New Orleans, United States
Reviewed by:Dmitry A. Los, Timiryazev Institute of Plant Physiology (RAS), Russia
Lou Sherman, Purdue University, United States
Qingfang He, University of Arkansas at Little Rock, United States
Copyright © 2019 Kammerscheit, Chauvat and Cassier-Chauvat. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.