Characterization of Tetrathionate Hydrolase from Acidothermophilic Sulfur-oxidizing Archaeon Metallosphaera cuprina Ar-4

1. Introduction

Reduced inorganic sulfur compounds (RISCs) are widely distributed in hot springs, sedimentary mud, volcanic craters, and acidic wastewater [1-3]. The dissimilatory sulfur oxidation of RISC is a significant geochemical process, which is carried out exclusively by prokaryotes, and the energy generated during this process is coupled with photosynthesis and respiratory processes [4, 5]. Metallosphaera cuprina, a member of the Sulfolobales order within the archaeal domain, was isolated from the sediment of an acidic hot spring in Tengchong County, Yunnan Province, China. This organism thrives at temperatures ranging from 55 to 75°C and a pH range of 2.5-5.5. M. cuprina is a facultative chemoautotroph that oxidizes S⁰, pyrite, and tetrathionate to produce sulfuric acid under aerobic conditions while also capable of chemoheterotrophically growing with yeast extract [6-8]. The members of Sulfolobales shows great potential for bioleaching [9, 10].

Archaea with sulfur oxidizing function have been widely observed in the Sulfolobales order [11]. Among the Sulfolobales members, Metallosphaera [12], Acidianus [13], and Sulfolobus [14] are representative sulfur-oxidizing archaea found in high temperature and acidic environments. These species are capable of metabolizing various sulfur compounds, as well as exhibiting heterotrophic and other physiological characteristics that enhance their adaptability to local environments. Previous research on thermophilic archaea has primarily focused on studying enzymes involved in the sulfur oxidation process, resulting in the discovery of a series of enzymes, such as Sulfur Oxygenase Reductase (SOR), Sulfide:Quinone Oxidoreductase (SQR), Sulfite-acceptor Oxidoreductases (SAOR), Thiosulfate:Quinone Oxidoreductase (TQO), and Tetrathionate Hydrolase (TTH) in Acidianus brierleyi (Ac. brierleyi) and Acidianus ambivalens (Ac. ambivalens) [11, 15].

Meanwhile, there have been numerous studies on the well-established sulfur-oxidizing systems from bacteria [16-18] such as Acidithiobacillus ferrooxidans (At. ferrooxidans), Acidithiobacillus caldus (At. caldus), Acidiphilium acidophilum (Ap. acidophilum). The enzyme-catalyzed reactions in these bacteria are most suitable at pH levels between 2.0–4.0. Studies have reported that TTH of At. ferrooxidans and At. caldus are both located in the periplasmic space of cells [19, 20]. The TTH of At. ferrooxidans hydrolyzes S₄O₆^2- into S₂O₃^2-, S⁰ and SO₄^2-, while the TTH of At. caldus produces S₂O₃^2-, S₅O₆^2- and SO₄^2- [19-22]. In Thermithiobacillus tepidarius (former Thiobacillus tepidarius), the TTH was supposed to locate either on or inside the cytoplasmic membrane, oxidize tetrathionate to S⁰, SO₃^2- and other polythionates [23]. In archaea, the TTH of Ac. ambivalens is located in the pseudo-periplasmic space of the cell and is connected to the outer membrane of the cell membrane, displaying optimal activity at pH 1.0 and 95°C or above [15]. TTH of Acidianus hospitalis (Ac. hospitalis) is found in extracellular proteins [24, 25]. When exposed to ultraviolet rays and mitogen C stress, the extracellular secretion of Ac. hospitalis TTH was promoted [24].

Kanao et al. utilized Western Blot to examine the regulation of TTH in Acidithiobacillus thiooxidans in the presence of different substrates. The expression of TTH was significantly higher when cultured with S₄O₆^2- as substrate compared to that with S⁰ and S₂O₃^2- as substrates. At. ferrooxidans cultured with S₄O₆^2- expressed the tth gene while did not express it when iron was used as the substrate [26, 27]. Through transcriptomic and proteomic analyses, it was observed that At. caldus expressed the TTH gene when cultured with S₄O₆^2- as the substrate, but did not when cultured with S⁰ alone [20]. Results from RT-qPCR indicated that the expression level of TTH with S₄O₆^2- as the substrate in At. caldus was about 200 times higher than that with S⁰ as the substrate [28]. Protze's Northern Blot experiment demonstrated that when Ac. ambivalens was cultured with S₄O₆^2- as the substrate, the transcription level of TTH RNA was significantly higher compared to when cultured with S⁰ as the substrate [15]. Furthermore, TTH activity with cyanolysis could only be detected when S₄O₆^2- was used as the substrate [15]. Researches on TTH in archaea primarily focused on the genus Acidianus. Although high homologous TTH gene sequences have also been identified in the genome of the genus Metallosphere, they have not been identified in the proteome or extensively studied in the field of biochemistry and molecular biology.

In this study, we present evidence that M. cuprina Ar-4 cultured with S₄O₆^2- displays higher TTH expression level compared with S⁰ as the sole sulfur source. Additionally, we demonstrate that the TTH protein of M. cuprina Ar-4 mainly present in cytoplasm and periplasm and exhibits an optimum activity at pH of 6.0, distinguishing it from other TTH proteins, which show their activity at pH 1.0–4.0 and exist solely in the periplasm or cytoplasm or extracellular.

2. Results

2.1. Gene Sequence Analysis and Structure Prediction of Tetrathionate Hydrolase of M. cuprina

Based on the genome analysis, it is supposed that mcup_1281 of M. cuprina Ar-4 might encode a homologous protein of the TTH1 of Ac. ambivlaens. Further analysis conducted using the ExPASy ProtParam tool and determined that mcup_1281 encoded an open reading frame (ORF) consisting of 537 amino acid residues. The protein did not contain any disulfide bonds and only had one cysteine residue in the sequence. The presumed molecular weight was around 57.4 kDa. Further analysis of the protein’s secondary structure predicted the presence of a transmembrane region. These findings suggest that Mcup_1281 is likely located in the extracellular space and is associated with the cell membrane.

AlphaFold2 was used to predict the three-dimensional model. The Mcup_1281 monomer structure appeared to be mainly consisted of beta strands and coil structures and exhibited an eight-bladed β-propeller motif with each blade (I–VIII) consisting of average four antiparallel β-strands. Five α-helices were located outside the β-propeller region. Two of these α-helices (α2-α3) were suggested to participate in dimerization (19). No c-type cytochrome domain was identified in Mcup_1281, unlike the nitrite reductase (Nir PDB 1QKS with RMSD 2.9 Å). The tryptophan residues in the Mcup_1281 were predominantly located within the beta strands region similar to the TTH of At. ferrooxidans (PDB 6L8A with RMSD 1.5 Å) (Figure S1).

2.2. The TTH Gene is Expressed BOTH in Tetrathionate and S⁰ Grown Cells of M. cuprina

To analyze the transcriptional expression of mcup_1281, total RNA from cells cultured in different mediums (5 g S⁰, 5 mmol/L K₂S₄O₆, or 2 g/L yeast extract) was extracted respectively. The transcription levels of mcup_1281 under different culture conditions were detected via RT-qPCR, and the 16S rRNA gene was used as the reference gene. The results showed that the transcription level of mcup_1281 increased by 5.4-fold and 4-fold when K₂S₄O₆ and S⁰ were used as energy sources compared to the control group (yeast extract as energy source) (Figure 1). Therefore, we propose that Mcup_1281 plays an important role in the sulfur metabolism of M. cuprina, and define the Mcup_1281 as TTH_Mc.

2.3. Preliminary Study on TTH Activity of M. cuprina

The different cell lysates of Metallosphaera cuprina Ar-4 grown aerobically using three different mediums (Basic Salts Medium added 5 g/L S⁰, 5 mmol/L K₂S₄O₆, or 2 g/L yeast extract separately [6, 14], see details at methods section 4.1) were respectively detected by the continuous enzyme activity assay method (detailed as 4.6) [29]. One unit enzyme activity (U) was defined as the increase of absorbance at 290 nm per minute (∆A₂₉₀ min^-1) of cell lysates. When using 1 mmol/L K₂S₄O₆ as the substrate and incubating reaction mixture at 65°C and pH 3.0, the specific enzyme activity (activity of per mg protein) was 0.60 U/mg protein and 0.29 U/mg protein for cells grown on 5 mmol/L K₂S₄O₆ and 5 g/L S⁰, respectively. The TTH_Mc activity with K₂S₄O₆ as the energy source was almost 2 times higher than that with S⁰. However, TTH_Mc activity was not detected in the cell lysate cultured in yeast extract (Figure 2). The results were in line with the transcription results of Figure 1.

2.4. Tetrathionate Hydrolase Primarily Located in Cytoplasm and Periplasm

Discontinuous method (see 4.6.2) [30] was used to detect the tetrathionate hydrolase (TTH) activity of Mcup_1281 in various cell fractions, including cell-free culture supernatant, cytoplasm, periplasm, and membrane fraction. Pyrophosphatase, as the cytoplasm marker, was used for identified different cell fractions. TTH activity was found in the cell-free culture supernatant, while its activity did not increase when cells were stressed with 5% mitomycin C, different from TTH of Acidianus hospitalis [24]. The cytoplasm, periplasm, and membrane proteins presented 1.172 U, 0.391 U, and 0.059 U of TTH activity respectively, which accounted for 72.26%, 24.05%, and 3.70% of the total TTH activity. The specific activity of the periplasmic fraction was 7.727 U/mg, of the cytoplasmic fraction was 0.526 U/mg, and 0.01 U/mg for the membrane at pH 3.0 and 0.009 U/mg for the membrane at pH 7.0 (Figure 3). The higher specific activity of the periplasmic indicated that less amount TTH in periplasm than cytoplasm, while the least TTH activity and the specific activity supported that TTH did not locate on membrane. The results indicated that TTH_Mc was primarily located in the cytoplasm with less amount presence in the periplasm and barely any in the membrane (Table S1).

2.5. Purification of the Tetrathionate Hydrolase from Whole Cell

Silver-stained SDS gels of different purification steps confirmed the presence of TTH band at about 54 kDa in M. cuprina Ar-4 (Figure S2). The specific activity of TTH in the total cell extract of M. cuprina Ar-4 grown on 5 mmol/L K₂S₄O₆ was found to be 0.724 U/mg. After four chromatographic purification steps including DEAE anion exchange column chromatography, hydrophobic chromatography, size exclusion chromatography, and Q-sepharose chromatography, the specific activity increased to 11.67 U/mg protein, representing a 26.70-fold purification with 1.24% recovery (Table 1 & Figure S3).

2.6. Tetrathionate Hydrolase of M. cuprina is an Acid Resisting Thermophilic Enzyme

The enzyme activity of TTH_Mc was tested under different temperature and pH conditions. As the temperature increased, the enzymatic efficiency increased almost linearly. The specific activity remained at approximately 30 U/mg at 95 ºC (Figure 4A). However, the maximal and optimum temperature of TTH_Mc could not be determined due to the inability to reach a higher temperature range. The pH experiment showed that the maximum activity occurred at pH 6.0; specific activity of TTH_Mc increased from 9.54 ± 0.17 U/mg at pH 1.0 to 39.44 ± 1.75 U/mg at pH 6.0, then decreased at pH 7.0 (Figure 4B). 0.01 mol/L Magnesium greatly stimulated the enzyme activity, while 0.01 mol/L calcium seriously inhibited the enzyme activity. Other divalent metal ions such as Fe²⁺, Zn²⁺, Mn²⁺, and Ni²⁺ had less effect on the specific activity of the enzyme (Table 2 & Figure S4).

The reaction process of tetrathionate catalyzed by TTH_Mc followed a Michaelis-Menten curve; the substrate hydrolysis velocity (V) was influenced by the enzyme as well as substrate concentration. When the enzyme concentrations were 1.15 μg/L and 2.30 μg/L, the half-lives of the substrates were 55.12 min and 27.36 min respectively. The reaction rate constants corresponding to the half-life were K_1.15μg=0.01258 mmol/L·min and K_2.30μg=0.02533 mmol/L·min respectively and the enzyme concentration showed inversely proportional to the half-life (Figure S5). The kinetic parameters of TTH activity were measured at a temperature of 95°C and pH of 6.0 with 1.15 µg TTH_Mc. The apparent K_m value for tetrathionate was determined to be 0.35 mmol/L while the observed V_max was measured as 86.3 μmol/min (Figure 5).

2.7. Hydrolysis Products of Tetrathionate by Tetrathionate Hydrolase

Analysis of the enzymatic reaction mixture by HPLC revealed the presence of four peaks. Besides the peak of tetrathionate at a retention time of 9.5 min, thiosulfate presented at a retention time of 5 min (Figure 6. Retention times of pentathionate and hexathionate were 11.8 min and 21.6 min respectively, which were also identified using standards described by Miura & Kawaoi [29].

3. Discussion

Tetrathionate plays a significant role in the metabolism of acidophilic microorganisms, particularly in the RISC pathway as it serves both as a substrate and as a mesostate [31]. The location in cells and characters of the enzyme responsible for tetrathionate metabolism varies greatly among different species [12, 15, 22]. There is a lack of systematic studies on tetrathionate hydrolase of acidothermophilic sulfur-oxidizing archaeon Metallosphaera genus, another member of the Sulfolobaceae family. In our study, a tetrathionate hydrolase was purified from Metallosphaera cuprina Ar-4, , the main objective of this investigation was to gain a comprehensive understanding of the tetrathionate hydrolase, determine its cellular localization, and characterize its biological properties.

3.1. TTH in Archaea and Bacteria Species

The TTH_Mc encoded by Mcup_1281 (PQQ-binding-like beta-propeller repeat protein) of M. cuprina is clustered to that of other Metallophaera sp. However, it exhibits differences with that of Sulfolobus spp., Acidianus spp., and Sulfurisphaera spp. It has been observed that the TTH cluster is conserved in Metallophaera [12]. Additionally, the region surrounding TTH contains an ABC transporter, a 4Fe-4S cluster domain-containing protein, and a vitamin epoxide reductase family protein (Figure S6). Tetrathionate hydrolases are widely found in sulfur-oxidizing archaea and bacteria, but the number of gene copies and protein location are not consistent across microorganisms [15]. There is no information available on the regulatory system that controls the tetrathionate intermediate pathway in sulfur-oxidizing archaea, such as the two-component system RsrS-RsrR found in Acidithiobacillus species [32]. We hypothesize that sulfur-oxidizing archaea have developed a specialized regulatory system to adapt to challenging environmental conditions.

The top-scoring BLAST entries of TTH_Mc at the Uniprot and NCBI databases (pairwise identity >30%) were highly similar homologs found in acidophilic archaea and bacteria (Figure S7). These homologs belong to the PQQ family proteins and are likely to be authentic tetrathionate hydrolases. The proteins formed separate branches according to their respective species, indicating conservation of tetrathionate hydrolases within the same species. However, there were some variations observed in tetrathionate hydrolases among different species. In addition, it was noted that the Metallosphaera spp. lacked tth2 gene copies of tetrathionate hydrolases found in Acidianus spp.

Unlike the tetrathionate hydrolase of Ac. ambivalens, TTH_Mc can also be detected in cells of M. cuprina Ar-4 grown on S⁰ as the sole energy medium. The transcription level of TTH_Mc is higher in cells grown on K₂S₄O₆ than in cells grown on S⁰. This suggests that the expression of tetrathionate hydrolase varies among different species and that tetrathionate metabolism in M. cuprina Ar-4 is TTH-dependent, similar to sulfur-oxidizing bacteria [33]. We also found the presence of Fe (II) in the broth from tetrathionate- and sulfur-grown M. cuprina Ar-4 cells, through the addition of Fe (III) to the medium, there is a possibility that it came from the contact of tetrathionate hydrolase with ferric reductase, although this was not shown [34].

3.2. TTH is Found in the Cytoplasm and Periplasm of K₂S₄O₆ and S⁰-Grown Cells

It has been suggested that TTH (TTH1) of Ac. ambivlaens is located in the pseudo-periplasmic space [15]. Additionally, it has been stated that TTH of Ac. hospitalis was a secreted protein with a zipper-like shape [24]. However, we found that TTH_Mc is a soluble protein and it has the highest specific activity in periplasm and cytoplasm compared to other fractions. Moreover, the optimal pH of TTH_Mc is 6.0, unlike TTH of other microorganisms. These results indicate that TTH_Mc is located in both the periplasm and the cytoplasm.

A series of purification strategies are based on the chemical properties of protein, such as its hydrophobicity, charge property and molecular weight. In a recent study, tetrathionate hydrolase was purified using four chromatographies [15]. The ion exchange column chromatography process with NaCl concentrations of 150 mM-300 mM resulted in similar charge properties of TTH_Mc as Ac. ambivalens TTH1 [15]. However, the hydrophobicity character differed between TTH1 and TTH_Mc. TTH_Mc precipitated in 2 mol/L (NH₄)₂SO₄. The specific activity consistently increased with each high number of purification steps, but the recovery yield was only 1.24%. This low yield may be attributed to purification steps, as increased steps often lead to a higher protein loss rate. Additionally, metal ions or cofactors like calcium may play a crucial role in stabilizing the protein structure [35].

3.3. Biochemical Properties of Tetrathionate Hydrolase

Some biochemical properties of TTH_Mc of M. cuprina are similar to those of other acidophilic archaea [15]. The optimal temperature for this enzyme is above 95°C, which is much higher than the enzymes from mesophilic species (optimum at 40–65°C), even higher than the optimal growth temperature of M. cuprina [6]. By the protein sequence of the TTH_Mc, we calculated that the isoelectric point (pI) of TTH_Mc is 4.70 by ExPASy ProtParam (https://web.expasy.org/protparam/), different from that of TTH1 of Ac. ambivlaens which is 6.48 [15]. Nevertheless, TTH_Mc exhibited an optimal pH of 6.0, which is higher than the typical pH ranges [1.0-4.0] observed for TTHs from other sulfur-oxidizing bacteria and archaea [15]. This suggests that TTH_Mc is more effective in the intracellular environment. The molecular mass of the enzyme is approximately 57 kDa, however, no homodimer formation was observed. At pH 6.0 and 95°C, the K_m value of TTH_Mc for tetrathionate is 0.35 mmol/L. Reported K_m values for TTH vary widely, suggesting differing substrate affinities across species. Among them, the TTH from Thiobacillus ferrooxidans (Ac. ferrooxidans) stands out with a K_m value of 50 μmol/L, appearing a higher substrate affinity [23].

3.4. Evolutionary Insights of TTHs Functionality

To delve deeper into the evolutionary history of TTHs functionality, we constructed a protein sequence similarity network (SSN) using TTH_Mc as the query [36]. The analysis reveals that TTHs from the Sulfolobaceae family cluster closely with homologs predominantly from other acidophilic sulfur/iron-oxidizing bacterial groups such as the Acidithiobacillaceae, Alicyclobacillaceae, Sulfobacillus, and Leptospirillum. These homologs form a dense cluster on the periphery of the entire SSN (Figure 7A) and maintain few connections with distantly related homologs of unknown function. This pattern supports the occurrence of cross-domain horizontal gene transfer (HGT) of TTH, further corroborated by the unconserved genomic contexts within the Sulfolobaceae strains and the presence of nearby transposase element (Figure S8). Previous studies have shown that an aspartate residue corresponding to Asp353 in TTH_Mc is crucial for the activity of the TTH from Acidithiobacillus ferrooxidans [19]. This aspartate residue is highly conserved within the TTH sub-cluster and is occasionally substituted by another acidic residue, glutamate (Figure 7B). This suggests that this aspartate residue initiates the reaction through protonating the S (alpha) atom of the tetrathionate [19].

Classical molecular dynamics were utilized to explore additional key interacting residues in TTH_Mc (Figure 7C). The analysis identified Arg460, Arg497, and Ala407 as the residues with the highest interaction rates. These residues likely serve as electrostatic stabilizers, forming hydrogen bonds with the terminal oxygen atoms adjacent to the S (alpha) atom of tetrathionate. Furthermore, Gln140, Thr139, Val136, and Arg132 of TTH_Mc, positioned on a helix extending from the narrower propeller side, interact with the substrate via water-mediated bridges.. Within the taxa from the TTH sub-SSN, Arg460 and Arg497 are frequently substituted by another basic residue (lysine) (Figure 7D-E). Additionally, other interacting residues lack aligned counterparts in remote sub-SSNs at equivalent positions, indicating the absence of corresponding structural regions (marked in grey) (Figure S9A-G). Moreover, three methionine residues—Met172, Met238, and Met279—situated near the tetrathionate binding pocket have been identified as putative metal ligands in TTH_Mc (Figure S9H-J). These residues are conserved within the sub-SSN of TTHs, though variations exist such as histidine replacing methionine in some instances. These findings suggest that the presence of these interacting residues likely enhances substrate binding and TTH activity across the TTH protein superfamily.

To further validate the functional significance of TTH-like proteins, future research should focus on functional assays and detailed experimental investigations. Such experiments will aid in confirming the role of these identified residues and their contributions to enzymatic activity. Overall, this study offers significant insights into evolutionary dynamics of TTH_Mc, setting the stage for a deeper understanding of tetrathionate hydrolase activity in related proteins.

4. Materials and Methods

4.1. Strains and Growth Conditions

Metallosphaera cuprina Ar-4^T was cultured at 65 °C in three different mediums described from modifying Allen medium [6, 14]. The BSM (Basic Salts Medium) contained (NH₄)₂SO₄ 1.3 g, K₂HPO₄ 0.28 g, MgSO₄·7H₂O 0.25 g, CaCl₂·2H₂O 0.07 g, FeCl₃·6H₂O 0.02 g, MnCl₂·4H₂O 1.8 mg, Na₂B₄O₇·10H₂O 4.5 mg, ZnSO₄·7H₂O 0.22 mg, CuCl₂·2H₂O 0.05 mg, Na₂MoO₄·2H₂O 0.03 mg, CoSO₄·7H₂O 0.01 mg, VoSO₄·2H₂O 0.03 mg. The initial pH was adjusted to 3.5 with sterile 50% H₂SO₄. About 5 g sterile S⁰ or 5 mmol/L K₂S₄O₆ as sulfur source and 0.2% yeast extract were added in BSM to promote cells growing. 2 g/L yeast extract was added in BSM for heterotrophic culture strains. Cell growth was monitored by optical density at 600 nm.

4.2. Sequence Analysis

The homologous amino acid sequences were searched in Uniprot and NCBI databases with Mcup_1281 as a probe. The multiple alignment (the homologs amino acid sequences from Metallaspahera spp., Acidianus spp., and Acidithiobacillus spp., etc) and a phylogenetic dendrogram were constructed using MAFFT version 7 with the L-INS-I algorithm, the BLOSUM 30 similarity matrix, a gap opening penalty of 1.53, and the offset value of 0.1. Using the ITOL (http://itol.embl) aimed to modifying the phylogenetic tree. The amino sequences of TTH from Metallaspahera, Acidianus, Acidithiobacillus were compared and analyzed by ESPript 3.0 (http://espript.ibcp.fr/ESPript/cgi-bin/ESPript.cgi).

Second structure of Mcup_1281 was predicted by SOPMA (https://npsa.lyon.inserm.fr/cgi-bin/npsa_automat.pl?page=/NPSA/npsa_sopma.html). Prediction of signal sequences and transmembrane domain were done with TMHMM and SignalP (http://www.cbs.dtu.dk/services/). Three-dimensional models of Mcup_1281 were predicted by AlphaFold2 [37] and the template model was quinoprotein alcohol dehydrogenase of Pseudomonas putida (PDB accession number 1kv9). The image of prediction model was shown by Viewer Lite. MD simulations for the protein-ligand complex were performed using the Desmond Molecular Dynamics System version 3.6 (D. E. Shaw Research, New York, NY, 2008) with OPLS_2005 force field.

4.3. RNA Extraction from Cells and Transcription Analysis for Mcup_1281

Cells grown on three different mediums containing 5 g/L S⁰, 5 mmol/L K₂S₄O₆ and 2 g/L yeast extract respectively were harvested by 10000×g centrifugation for 10 min. Total RNA of cells was extracted with E.Z.N.A Total RNA Kit I (Omega). The quantity and quality of the RNA was measured by UV absorption (A260/A280=1.8-2.0) using NanoDrop One (Thermo Fisher Scientific, USA). The RNA was reverse transcribed by HiFi-Script cDNA Synthesis Kit (CWBIO, China). 16S rRNA gene of Ar-4^T was set as the reference gene and the mcup_1281 as target gene. The target DNA fragments used for synthesis were amplified with the primers Real-TTH-F (GCGGGGTTCACAAGTTTGAC) and Real-TTH-R (GCCTGTGCTGGATGATGT), while the reference gene fragments primers were Real-16S rRNA-F (TTGGGATCGAGGGCTGAAAC) and Real-16S rRNA-R (TCCCCTACGGCTACCTTGTT). LightCycler® 480 System (Roche, Switzerland) was used for quantitative PCR and program included: Pre-incubation 95℃ 1 cycle; Amplification; degeneration at 95℃ for 10 s, annealing at 55℃ for 20 s, extension at 72℃ for 40 cycles; Melting curve: 95℃ for 5 s, 55℃ for 1 min, 1 cycle.

4.4. Tetrathionate Hydrolases Purification from Whole Cells

Purification of tetrathionate hydrolases from whole cells was carried out by modifying the method described by Protze (15). 5 g of wet cell was collected from the TT medium or S⁰ medium. Cells were resuspended in 50 mL 40 mmol/L K₃PO₃ buffer (pH 7.0) with 10 mmol/L MgCl₂, 25 μg/mL RNase, 10 μg/mL DNase I and 1 mmol/L phenylmethanesulfonyl fluoride (PMSF). After adding 1 mm glass beads, cells were disrupted three times through a homogenizer (Fast-prep-24, MP, USA) with 6.0 m/s, 30 s. Cell debris and unbroken cells were discarded by centrifugation at 10000×g and 4 °C for 15 min. The soluble fraction and membrane were separated by centrifugation at 140000×g and 4°C for 60 min. The supernatant was dialyzed against 40 mmol K₃PO₃ and 10 mmol/L MgCl₂ (pH 7.0) at 4 °C for 16 h and the membrane was stored at -80 °C with phosphate buffer saline (PBS) (pH 7.2). The dialyzed soluble fraction containing crude enzyme was applied on the DEAE Sepharose fast-flow column (4×5 mL column volume (CV); GE Healthcare) equilibrated with 40 mmol/L K₃PO₃ and 10 mmol/L MgCl₂, pH 7.0. Proteins were eluted by NaCl solution with a linear concentration gradient of 0-0.2 mol/L, 0.2-0.4 mol/L, 0.4-0.6 mol/L, 0.6-0.8 mol/L, and 0.8-1.0 mol/L, each for 5-10 CV. The eluent fraction showing activity of tetrathionate hydrolases were pooled and dialyzed against 50 mmol/L Tris/HCl (pH 8.0) supplemented 1 mol/L (NH₄)₂SO₄ for 16 h at 4 °C. After dialysis, the fraction was centrifugated at 40000×g and 4℃. The supernatant was next applied onto Phenyl-Sepharose Fast-Flow column [5mL column volume (CV); GE Healthcare]. Protein was eluted by 10 CV (NH₄)₂SO₄ with a linear gradient from 1 mol/L to 0 mol/L. Fractions showing tetrathionate hydrolases activity were pooled and concentrated with Centriprep YM-30 centrifugal ultrafiltration tube (15 mL Millipore, USA) and then eluted by 40 mmol/L PBS (pH 7.5) with flow rate of 0.5 mL/min through Superdex 200 size exclusion column (30 mm×600 mm; GE Healthcare). The peak showing the tetrathionate hydrolases activity was applied on the Q-Sepharose-HP column [5 mL column; GE Healthcare]. Protein was eluted by NaCl with a linear gradient from 0.15 mol/L to 0.6 mol/L. Every purification fraction was detected with Silver-stained SDS-PAGE and HPLC enzyme assay to ensure tetrathionate hydrolases activity.

4.5. Cell Fractionation Separation

Cells of M. cuprina Ar-4 were grown to stationary phases and centrifugated at 10000×g for 30 min. The cell-free supernatant was in turn filtered through filters with hole sizes of 2.2 μm, 0.8 μm, and 0.22 μm. The filtrate then was concentrated with Centriprep YM-30 centrifugal ultrafiltration tube (15 mL Millipore, USA) as extracellular protein.

1 g wet cells were washed twice with 10 mmol/L Tris-HCl buffer solution and resuspended with 50 mL 10 mmol/L Tris-HCl buffer solution (pH 7.3), then equivalent volume of 10 mmol/L Tris-HCl buffer containing 40% sucrose was slowly added into and rocked slowly for 30 min at room temperature followed by centrifugation with 10000×g at 4 °C. Then the cells were quickly resuspended with 50 mL 5 mmol/L MgCl₂ at 4 °C and remove spheroplast by centrifugation at 10000×g for 30 min. The supernatant was periplasmic protein [38].

Spheroplast were washed three times with BSM and resuspended with 100 mmol/L Tris-HCl and disrupted by sonication using Vibra Cell, cell debris was removed by 10000×g for 15 min and the soluble fraction was centrifuged by 100000×g for 60 min at 4 °C to separate the membrane (precipitate) and cytoplasmic (supernatant) fraction.

The membrane fraction was washed three times with distilled deionized water, resuspended in an elution buffer, and stayed on ice overnight. The formate buffer (pH 3.0) contained 0.5% (v/v) N-lauroylsarcosine, 1% (v/v) SDS, and 1% (v/v) Triton X-100 or 100 mmol/L Tris-HCl buffer (pH 7.0) contained 0.5% (v/v) Triton X-100, 5 mmol/L EDTA were used as elution buffer [38]. The fraction was centrifuged by 100000×g for 60 min at 4℃ and the soluble fraction was concentrated with Centriprep YM-30 centrifugal ultrafiltration tube (15 mL Millipore, USA) as the membrane protein fraction that was tested for TTH activity.

4.6. Enzyme Characteristic Assay

Tetrathionate hydrolase activity of different fractions was determined by two methods.

4.6.1. Continuous Method of Enzyme Activity Assay

The continuous assay is based on the principle that tetrathionate hydrolases hydrolyze K₂S₄O₆ to produce a series of sulfur-containing compounds which increase absorbance at 290 nm [29]. The reaction mixture (1 mL, pH 3.5) contained 50 mmol/L K₃PO₃, 1 mmol/L K₂S₄O₆, and 25-100 μL cell lysate or distillation water as control. Enzyme activity was detected by full-wavelength scan which was found that the absorption value of the mixture increases from 250 nm to 430 nm. This could represent that tetrathionate hydrolases hydrolyzes K₂S₄O₆. In order to ensure the sensitivity and practicality of the measurement, the change rate of absorbance at 290 nm was selected to define the catalytic efficiency of tetrathionate hydrolases [29]. One unit enzyme activity was defined as the ΔA₂₉₀ min^-1.

Pyrophosphatase activity was detected with the method of Richter and Schäfer to assess the purity of each fraction [15, 39]. 1μg protein from each fraction was incubated with reaction buffer containing 40 mM acetate, 40 mM imidazole, 40 mM Tris, 2.5 mM MgC1₂ and 0.2 mM Ppi (Na₄ P₂ O₇) for 30 mins at 60 °C. The concentration of Ppi was detected by Pyrophosphate Assay Kit (MAK168, Sigma-Aldrich, USA). A unit Pyrophosphatase activity was defined as the amount of protein required for hydrolysis of 1 µmol/L of Ppi in one min. The protein concentration of different fraction of cells was detected by BCA assay.

4.6.2. Discontinuous Method of Enzyme Activity Assay

For understanding the products from tetrathionate hydrolyzation, we used HPLC assays method described by Miura & Kawaoi [29] to detect the sulfur-containing intermediates and quantify the activity of purified tetrathionate hydrolases. The K₂S₄O₆ used in the study was purchased from the Merck KGaA (Germany) and its purity was over 98%. Na₂S₂O₃ was purchased from Sinopharm (China), its purity was over 99%. 1)The determination of optimal temperature of TTH was proceeded in 1mL 50 mmol/L formate buffer (pH 3.0) containing 1-2 mmol/L K₂S₄O₆ and 1 mol/L (NH₄)₂SO₄ (Sigma-Aldrich, USA). The reaction was started by adding 25 μL protein and hatched in water bath from 25 °C to 95 °C with the interval of 10 °C. 2) The determination of optimal pH of TTH carried in the same solution system of temperature test and set pH at 1-7 with the interval of 1.0, hatched at 65 °C. 3) Vmax and Km were detected and calculated at 1.15 µg TTH with different tetrathionate concentration. To stop the enzyme reaction, the sample was rapidly frozen in liquid nitrogen for 3 min and then boiled in boiling water for 5 min, repeated 3 times. The mixture was filtered by 0.22 μm filter of polyethersulfone (SLGP033R, Millipore, USA). The contents of chemical compounds were determined using an Agilent 1290 infinity II (Agilent, Germany) consisting of a binary pump system and auto-sampler. A chromatography separation was achieved with an Agilent Eclipse Plus C18 column (4.6 mm×150 mm, 5 µm) and maintained at 30 °C during the run. The mobile phase was acetonitrile (Thermo Fisher, USA)/water (20:80 V/V) with 6 mmol/L Tetrapropylammonium hydroxide (TPA, Sigma-Aldrich, USA) adjusted pH as 5.0 by acetic acid. The flow rate was 0.8 mL·min^-1 and the UV-detector was set at 230 nm. A unit enzyme activity of tetrathionate hydrolase was defined as the amount of protein required for hydrolysis of 1 µmol/L of S₄O₆^2- in one min. The specific enzyme activity was the activity of per mg TTH.

4.7. Effects of Bivalent Ions on Enzyme Activity

The series of bivalent metal ions almost were metal chlorides, including magnesium chloride, zinc chloride, ferric chloride, nickel chloride, manganese chloride, and calcium chloride. The effects of metal ions on TTH_Mc activity were detected by discontinuous methods of enzyme activity assay with 0.01 mol/L metal ion at 95°C and pH 6.0.

4.8. Statistics

Statistics were performed using Prism 8 (Graphpad). All quantification tests were independently performed for at least three replications. Data were represented as the mean. Significance was determined using one-way ANOVA analysis, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 throughout the manuscript.