A novel subtilase with NaCl-activated and oxidant-stable activity from Virgibacillussp. SK37
© Phrommao et al; licensee BioMed Central Ltd. 2011
Received: 4 February 2011
Accepted: 9 June 2011
Published: 9 June 2011
Microbial proteases are one of the most commercially valuable enzymes, of which the largest market share has been taken by subtilases or alkaline proteases of the Bacillus species. Despite a large amount of information on microbial proteases, a search for novel proteases with unique properties is still of interest for both basic and applied aspects of this highly complex class of enzymes. Oxidant stable proteases (OSPs) have been shown to have a wide application in the detergent and bleaching industries and recently have become one of the most attractive enzymes in various biotechnological applications.
A gene encoding a novel member of the subtilase superfamily was isolated from Virgibacillus sp. SK37, a protease-producing bacterium isolated from Thai fish sauce fermentation. The gene was cloned by an activity-based screening of a genomic DNA expression library on Luria-Bertani (LB) agar plates containing 1 mM IPTG and 3% skim milk. Of the 100,000 clones screened, all six isolated positive clones comprised one overlapping open reading frame of 45% identity to the aprX gene from Bacillus species. This gene, designated aprX-sk37 was cloned into pET21d(+) and over-expressed in E. coli BL21(DE3). The enzyme product, designated AprX-SK37, was purified by an immobilized metal ion affinity chromatography to apparent homogeneity and characterized. The AprX-SK37 enzyme showed optimal catalytic conditions at pH 9.5 and 55°C, based on the azocasein assay containing 5 mM CaCl2. Maximum catalytic activity was found at 1 M NaCl with residual activity of 30% at 3 M NaCl. Thermal stability of the enzyme was also enhanced by 1 M NaCl. The enzyme was absolutely calcium-dependent, with optimal concentration of CaCl2 at 15 mM. Inhibitory effects by phenylmethanesulfonyl fluoride and ethylenediaminetetraacetic acid indicated that this enzyme is a metal-dependent serine protease. The enzyme activity was sensitive towards reducing agents, urea, and SDS, but relatively stable up to 5% of H2O2. Phylogenetic analysis suggested that AprX-SK37 belongs to a novel family of the subtilase superfamily. We propose the name of this new family as alkaline serine protease-X (AprX).
The stability towards H2O2 and moderately halo- and thermo-tolerant properties of the AprX-SK37 enzyme are attractive for various biotechnological applications.
Microbial proteases are one of the most commercially valuable enzymes , of which the largest market share has been taken by subtilases or alkaline proteases of the Bacillus species, which has been extensively studied in terms of both biological properties and applications [1–3]. Subtilase is the superfamily of subtilisin-like serine proteases  in the clan SB of serine peptidases, family S8, according to the MEROPS database . It is one of the biggest clans of serine peptidases and ubiquitously distributed in various organisms, including bacteria, archaea, eukaryotes, and viruses . Based on amino acid sequence similarity, they are classified into six families: subtilisins, thermitase, proteinase K, lantibiotic peptidase, kexin, and pyrolysin . Subtilisins are further classified into six subfamilies namely, true subtilisins, high-alkaline proteases, intracellular proteases , phylogenetically intermediate subtilisins (PISs) [7, 8], high molecular mass subtilisins (HMSs) [9, 10], and oxidant stable proteases (OSPs) [11, 12]. The latter subfamily, OSPs, has been shown to have a wide application in the detergent and bleaching industries and has recently become one of the most attractive enzymes in various biotechnological applications. [8, 11–17].
Despite the tremendous amount of information on microbial proteases, a search for novel proteases with unique properties is still of interest for both basic and applied aspects of these highly complex class of enzymes . In addition to a classical method of screening for a new microorganism harbouring an interesting protease from various environments , different molecular biology techniques, such as directed evolution [18, 19], site directed mutagenesis  and metagenomic analysis , have been used to engineer numerous proteases with improved or novel properties. By applying DNA technology, it is essential that the gene of the protease of interest is cloned, engineered and expressed in an efficient host.
In this research, a genomic library of Virgibacillus sp. SK37, a moderately halophilic bacterium isolated from Thai fish sauce  was constructed and screened for heterologous protease expression in Escherichia coli. After an extensive screening, one open reading frame encoding a gene similar to aprX was obtained. This gene was cloned, over-expressed in E. coli and purified by immobilized metal ion affinity chromatography (IMAC). Biochemical characterization of the purified enzyme revealed that this novel protease was relatively oxidant stable and moderately halo- and thermo-tolerant. This is the first report on the biochemical characterization of the recombinant AprX-related serine protease. In addition, the evolutionary relationship of this enzyme with other AprXs from different bacteria and other enzymes in the subtilases superfamily was studied.
Genomic DNA library construction and screening
Screening of a Virgibacillus sp. SK37 genomic DNA expression library in E. coli DH10B was done on LB-skim milk agar plates as described in the materials and methods section. An enumeration analysis determined the size of the genomic library to be 1.56 × 105 clones with 15% background (blue colonies harboring self-ligated plasmid), yielding 1.33 × 105 clones with inserts. When an average size of 4.4 × 106 bp of bacilli genomic DNA was considered (calculated from whole genome sizes available from the NCBI database), this library theoretically covered the genome size of at least 91 and 302 times (depth of coverage) when the DNA fragments of 3,000 and 10,000 bps, respectively, were taken into account. Of approximately 100,000 clones screened (accounting for more than 68 depth of coverage), six clones showed clear halo zones, indicating the presence of proteolytic activity. The recombinant plasmids were individually extracted from these six clones and their DNA inserts were analyzed. Restriction digestion analysis showed that among these 6 clones, there were four different DNA inserts based upon size: ~ 3,300 bp (1 clone), ~3,800 bp (1 clone), ~4,300 bp (3 clones), and ~5,300 bp (1 clone). Remarkably, nucleotide sequence analysis of these clones indicated that they all shared overlapping nucleotide sequences, resulting in an open reading frame (ORF) of only one putative gene.
Nucleotide and deduced amino acid sequences analysis
Homology analysis of AprX-SK37 and other enzymes in the subtilase superfamily
Bacillus subtilis subsp. subtilis 168
Tritirachium album limber
lantibiotic leader peptidase
Lactobacillus sakei L45
Phylogenetic tree analysis
The subtilase superfamily was phylogenetically grouped into six clusters: subtilisins, thermitase, proteinase K, lantibiotic peptidases, kexin, and pyrolysins (indicated by solid square brackets), which represent subtiliase family S8A, B, C, D, E, and F, respectively, . From our analysis, AprX-SK37 was not categorized into any of these families, but shared the same cluster with other AprXs, which was positioned apart from other subtilase families (dashed square bracket). Notably, within the AprX cluster, AprX-SK37 is relatively distant from other AprXs. Most OSPs that are produced from alkaliphilic bacilli are clustered together in the tree (dashed square bracket), i.e. E-1, LP-Ya, and SD-521 from B. cohnii DSM 6307, NP-1 from B. halmapalus DSM8723, KP-43 from Bacillus sp. KSM-KP43 . However, some of OSPs such as sapB (AM748727) from B. pumilus CBS , LD1 (AB085752) from Bacillus sp. KSM-LD , and I-52 from B. clausii I-52 [16, 25], were not located in the OSPs cluster, but appeared to be members of the subtilisin family.
Over-expression and purification of recombinant VirgibacillusAprX-SK37
Effects of pH and temperature
Effects of NaCl and CaCl2
Proteases produced from Virgibacillus sp. SK37 have been shown to exhibit NaCl- and CaCl2-activated characteristics [26, 27]. Therefore, the effects of NaCl and CaCl2 on the activity of AprX-SK37 were studied. As demonstrated in Figure 5c (diamond, solid line) the activity of AprX-SK37 increased slightly when NaCl was added, and showed maximum activity at 1 M. The activity decreased to 30% at 3 M NaCl. On the contrary, subtilisin A, which was used as a control, did not show NaCl-activated characteristics as indicated by a decrease in activity with increasing concentration of NaCl as shown in Figure 5c (square, solid line). Both AprX-SK37 and subtilisin A appeared to require at least 0.25 M of NaCl to retain their original activities after incubation at 25°C for 24 h (Figure 5c, dashed lines). When the AprX-SK37 enzyme was first pre-incubated with 0.5 - 3 M NaCl for 24 h at 25°C and pH 9.5, the activity was enhanced up to 125% (Figure 5c, diamond, dashed lines). These NaCl-enhancing stability effects could not be observed in subtilisin A (Figure 5c, square, dashed lines).
In addition to NaCl, AprX-SK37 also showed a CaCl2-dependent characteristic as shown in Figure 5d (diamond, solid line). The enzyme was inactive in the absence of Ca2+ and required 15 mM CaCl2 for its maximal activity. This is opposite to the Ca2+ independent charateristic of subtilisin A (Figure 5d, square, solid line). The activities of both AprX-SK37 and subtilisin A gradually decreased when the CaCl2 concentration was higher than 30 mM. The remaining activities of AprX-SK37 and subtilisin A, when CaCl2 reached 100 mM, were 66 and 73%, respectively. Both enzymes showed moderate stability (50% remaining activity) after pre-incubation for 24 h at 25°C.
Effects of reducing agents and various inhibitors
Effects of protease inhibitors and denaturants on recombinant AprX-SK37 activity using azocasein as a substratea
Remaining activity (%)
Serine protease inhibitor
Cysteine protease inhibitor
Aspartic protease inhibitor
Amino peptidase inhibitor
Remaining activity (%)
Effect of oxidizing agent
This research reports the cloning, expression, biochemical characterization, and phylogenetic analysis of a novel intracellular bacterial AprX serine protease. A previous report  of this enzyme from B. subtilis, focusing on bioinformatic analysis and regulation of gene expression, indicated that this enzyme is an intracellular serine protease, which is expressed in the stationary phase and not essential for either growth or sporulation. The AprX-SK37 enzyme in this study was derived from a moderately halophilic bacterium, Virgibacillus sp. SK37, which was isolated from Thai fish sauce that was saturated with 26-28% of NaCl. This bacterium produced numerous NaCl-activated subtilisin-like proteinases, three of them having been partially purified and characterized as extracellular halotolerant bacillopeptidase F-like proteinases . Their activities did not depend on calcium, showed maximum activity at pH 8, 55-60°C, 25-30% NaCl and 70-100 mMol l-1 CaCl2, and stability at 0-30% NaCl and <20 mMol l-1 CaCl2 . The NaCl-activated property of AprX-SK37 was not unexpected as it has been shown that the cell membrane of halophilic bacteria is incapable to completely prevent an increased flux of sodium into the cells . Intracellular Na+ concentrations of moderately halophilic bacteria growing in media containing 2-4 M NaCl were found between 0.13 to 3.52 M with an average of 1.37 M . Our enzyme can be activated and stabilized by 1 M NaCl (5.8% w/v) and tolerate up to 3 M NaCl (17.4% w/v). To the best of our knowledge, this is the first report on a halotolerant intracellular serine protease.
DNA sequence analysis of aprX-sk37 indicated that the gene is regulated by two putative σA promoters (PL and PS), which have been suggested to function as primary and secondary promoters of B. subtilis aprX, respectively . The open reading frame (ORF) of Virgibacillus aprX-sk37 is slightly smaller than that of B. subtilis aprX and lacks the alternative start condon TTG, at position 76-78, Met/Leu26 in AprX numbering of B. subtilis. The predicted MM and pI of AprX-SK37 are in the same range as those of AprXs from Bacillus species (MM of 42.2-48.9 kDa and pI at 4.9-6.1). The key difference between AprX-SK37, other AprXs, and some other intracellular proteases is its N-terminal domain, which showed no similarity to those of known proteins in the database. It has been suggested that the N-terminal domain of subtilases acts as an intramolecular chaperone or pro-peptide that mediates enzyme folding; nevertheless, the role of this domain on AprX-SK37 activity is unclear. The localization of AprX from B. subtilis in cytoplasm has been previously reported . The recombinant AprX-SK37 in this study is found in cytoplasm; however, the precise localization of the wild-type enzyme is unknown. The enzyme appeared to be active without cleavage of any pro-peptide. Its putative function as a chaperone for correct enzyme folding or as a regulatory domain remains to be explored.
The benefit of isolating a novel enzyme from a DNA expression library instead of PCR-cloning using degenerated primers is that the gene encoding active enzyme can be readily obtained. This advantage is very important especially for Bacillus subtilases, which often form inactive, insoluble aggregates when produced in E. coli expression systems [34–36]. The recombinant AprX-SK37 appeared to be located as active soluble protein in the cytosolic compartment; none were found as inactive, insoluble inclusion bodies or secreted into the periplasm or culture media. The fact that the enzyme was first identified from E. coli colonies that showed halo zone during genomic DNA library screening could be the result of membrane leakage after prolonged growth for more than 24 h. Remarkably, despite a thorough screening of the library that covered approx. 70 depth of the library, no other protease genes could be isolated. This could be because other enzymes formed inactive aggregates, are unstable in E. coli, or the enzyme activity may require higher sodium or calcium, which was not included in the screening condition. Moreover, it could be because the active enzymes might need specific post-translational modification, which was lacking in the E. coli expression system and that the substrate in our screening (milk protein) was not an appropriate substrate for certain enzymes. Further modification of screening conditions may lead to the identification of additional active enzymes. pET vector was used to express the recombinant aprX-sk37 gene in this study. This system has been shown to be efficient for the expression of various Bacillus hydrolytic enzymes [37, 38]. The canonical ribosomal binding site in this vector is identical to that of Virgibacillus aprX-sk37. The high level of expression could be because of synonymous codon usage, which leads to a fast translation rate in the E. coli expression system .
Phylogenetic analysis revealed that AprX-SK37 belongs to the superfamily of subtilases or subtilisin-like proteases. This result is consistent with the family analysis of B. subtilis AprX . Moreover, our analysis indicated that the AprXs are clustered in a distinct group, of which AprX-SK37 is relatively different from. This could be because AprX-SK37 possesses unique characteristics of oxidant stability and moderate salt-activation, which are not found in other AprXs. However, according to our phylogenetic tree, AprX-SK37 was not categorized into the OSPs group. Notably, phylogenetic analysis of OSPs reports little evolutionary relationship among this group of enzymes. Our phylogenetic analysis indicated that most OSPs do not belong to any of the subtilisin families previously described in bacteria or fungi, but appear to belong to a different cluster (designated OSP in Figure 3). This finding is similar to the phylogenetic analysis of a subtilisin-like protease gene family in the grass endophytic fungus Epichloë festucae . Hence, OSPs should not be classified as the subfamily of subtilisins as previously suggested [11, 12]. Phylogenetic analysis of various OSPs producers suggested that the sources of OSPs encompass bacilli from diverse taxon, which could be the result of different mechanisms of oxidant stabilization. Taken together the result of phylogenetic analysis as discussed above, we would like to propose a new family of subtilases superfamily, namely alkaline serine protease X (AprX) or subitlase S8G, according to the MEROPS database derived from subtilases classification by Siezen and Leunissen . In addition, we believe that the classification of OSPs has to be re-defined.
Biochemical characterization revealed that recombinant AprX-SK37 is a Ca2+- dependent alkaline serine protease and moderate thermophile with optimal pH and temperature at 9.5 and 55°C, respectively. The enzyme requires calcium to function with maximum activity at 15 mM CaCl2. A Calcium-dependent characteristic is well known for members of the subtilases superfamily, of which conserved calcium binding sites are essential for enzyme stability and/or activity . In nature, calcium may play a physiological role in aprX-sk37 gene regulation as it has been shown that a massive accumulation of calcium during sporulation is found in most bacilli in order to respond to adverse environmental changes . In B. subtilis, AprX is expressed in the late stationary phase under the control of various transition state regulatory genes . The high sensitivity of AprX-SK37 to a reducing agent suggested that disulfide bonds are essential for structural stability. The primary amino acid sequence revealed that AprX-SK37 contains 8 cysteines (Cys). This richness in Cys is unique for enzymes in the AprX family since Cys is usually absent from subtilases in Gram-positive bacteria [4, 29].
In general, subtilases are inactivated by hydrogen peroxide due to the oxidation of methionine (Met), located next to the catalytic serine (Met222 in subtilisin BPN numbering), thus preventing the formation of the tetrahedral intermediate during the transition state of their hydrolytic reaction [42, 43]. AprX-SK37 possesses Met368 next to catalytic Ser367, similar to other subtiliases (Figure 2) and other OSPs [8, 11, 12, 14–16]. The actual mechanism of oxidant stability is still unclear. In the study of KP-43, an OSP enzyme, oxidation of Met was not a fatal modification, but rather altered its substrate specificity . KP-43's crystal structure suggested that the rate of Met-oxidation in KP-43 was lower than those of other subtilases, probably due to the longer distance between the Met residue in the catalytic vicinity and the oxyanion hole . Hence, the oxidant-stable ability is strongly dependent on enzyme conformation and structural integrity, which is intrinsic to each enzyme. The oxidant stability as well as halotolerant and moderately thermophilic properties of AprX-SK37 should make this novel enzyme attractive for biotechnological applications in the future.
A novel oxidant stable, halotolerant and moderately thermophilic alkaline serine protease, named AprX-SK37, has been identified and characterized. Its unique property is attractive for various biotechnological applications.
Restriction endonucleases, T4 DNA ligase, and calf intestinal phosphatase (CIP) were purchased from New England Biolabs (New England Biolabs, Ipswich, MA). Pfu polymerase was obtained from Promega (Promega, Madison, WI). Skim milk was purchased from Merk (MerkKGoA, Darmstadt, Germany). Azocasein and subtilisin A (subtilisin Carlsberg) were purchased from Sigma (Sigma-Aldrich, St. Louis, MO). All other reagents for molecular and biochemical analysis were of molecular and analytical grade, respectively.
Bacterial strains, plasmids, and growth conditions
Virgibacillus sp. SK37 (GenBank/NCBI no. DQ910840) was cultured at 35°C in a modified halophilic medium (1% yeast extract, 0.3% trisodium citrate, 0.2% potassium chloride, 2.5% magnesium sulfate, and 5% NaCl). The pH was adjusted to 7.0 by NaOH. Escherichia coli strain DH5α and DH10B (Mega DH10B™ T1Relectrocomp™, Invitrogen, CA) were used as host strains for cloning and genomic DNA expression, respectively. E. coli BL21(DE3) (Novagen, Madison, WI) was used for enzyme expression. They were grown aerobically at 37°C in Luria-Bertani (LB) medium. Plasmid vector pUC19 (New England Biolabs, Ipswich, MA) and pET21d+ (Novagen, Madison, WI) were used for genomic library construction and over-expression, respectively.
General molecular biology techniques
Cloning, DNA manipulation, and agarose gel electrophoresis were done as previously described . Genomic DNA was isolated from Virgibacillus sp. SK37 using a Wizard® genomic extraction kit (Promega, Madison, WI). Plasmid was isolated with Qiagen plasmid preparation kit (Qiagen, Hilden, Germany). PCR products were separated by gel electrophoresis, and bands of the expected size were isolated from the gel using Qiagen QIAquick gel extraction kit (Qiagen, Hilden, Germany). Automated DNA sequencing was carried out by Macrogen (Seoul, Korea), using the primer-walking technique with pUC/M13 forward/reverse primers for pUC19, and T7/SP6 promoter primers for pET21d+ as initial primers, respectively. Enzymes and reagents were used according to the manufacturer's instructions unless otherwise stated.
Genomic DNA library construction
The genomic DNA of Virgibacillus sp. SK37 was partially digested by incubating with 10 units of BfuCI per 150 μg of genomic DNA at 37°C for 20 min. Fragments ranging in size from 3 to 10 kilobase pairs (kb) were isolated from the agarose gel. The plasmid pUC19 was digested with BamHI and 5'-phosphate groups were removed with calf intestinal phosphatase (CIP, New England Biolabs) prior to gel purification using Qiagen QIAquick gel extraction kit (Qiagen, Hilden, Germany). The genomic BfuCI fragments were ligated with dephosphorylated linearized pUC19 by T4 DNA ligase at a ratio of 3:1. This ligation mixture was precipitated by isopropanol and re-dissolved in 30 μl nuclease-free water prior to transform into competent E. coli DH10B by electroporation (2 mm cuvette, 2500 V, Electroporator 2510, Eppendorf AG, Hamburg, Germany). The transformants were then spread on LBAmp plates containing 2% (w/v) glucose (LBAmp+Glu). The plates were incubated for approx. 14 h at 37°C. Colonies growing on the LBAmp+Glu plates were scraped from the agar surface and transferred into LB broth containing 15% glycerol and kept at -70°C until use. A small aliquot of the transformants were spread onto LBAmp plates supplemented with 1 mM isopropyl-β-D-thiogalactopyranoside (IPTG) and 0.2% (w/v) bromo-chloro-indolyl-galactopyranoside (X-gal) (LBAmp+IPTG+X-gal) for enumeration and determination of percentage of blue white colonies, representing DNA library size and % background.
Screening of protease-producing clones
The clones from genomic DNA library were spread onto LBAmp plates supplemented with 3% (w/v) skim milk powder. The clones were grown at 37°C for 18 h. Positive colonies showing protease activity as indicated by the formation of transparent halo zones around the colonies were selected as positive clones after continual incubation of the plates at 30°C for additional 7 h.
DNA sequence analysis
Plasmid from each protease-positive clone was isolated by Qiagen plasmid preparation kit. Both strands of DNA insert were sequenced by automated DNA sequencing (Macrogen, Korea). The full length DNA insert of each positive-clone, open reading frames (ORFs), and homology of putative coding sequences were analyzed using tools provided by the National Center for Biotechnology Information (NCBI, http://www.ncbi.nlm.nih.gov). Bacterial promoter and transcription termination site of protease coding gene were predicted by Softberry Bioinformatics tools (http://linux1.softberry.com/berry.phtml). Isoelectric point (pI) and molecular mass of deduced amino acid sequence were calculated using software from ExPASy Proteomics server (http://ca.expasy.org/tools/pi_tool.html).
Cloning, over-expression, and purification of the recombinant AprX-SK37
Putative protease gene was amplified by PCR using forward (5'-CTG TGC TCT AGA GCA AAG TAA AAA CAA CTA TTC TAT AAG GAG GAA G-3') and reverse (5'-CTG TGC CTC GAG ATT CAC TTT CTG CAC CTG CTG TAC G-3') primers (the XbaI and XhoI sites are underlined). Thirty-five cycles of PCR were performed in a thermal cycler (MJ Research PCT-200 Thermal Cycler DNA Engine, GMI Inc, Ramsey, MI) using Pfu DNA polymerase. The amplified 1356 bp DNA product flanked by XbaI and XhoI restriction sites was cloned into the corresponding restriction sites of pET21d (+) vector for the expression of C-terminally 6xHis tagged enzyme. The integrity of the construct, designated pET-AprX-SK37, was confirmed by agarose gel electrophoresis followed by automated double-strand DNA sequencing. To express the enzyme, the pET-AprX-SK37 vector was transformed into E. coli BL21 (DE3). A single colony of E. coli BL21 harboring pET-AprX-SK37 (BL21/pET-AprX-SK37) was grown at 37°C in LBAmp until the OD600 reached 0.6-0.7, then 0.1 mM IPTG was added to induce the gene expression. After further incubation at 16°C for 18 h, the cells were harvested and resuspended in lysis buffer (30 mM Tris-HCl, pH 8.0, 0.3 M NaCl, and 10 mM imidazole). Lysozyme was added to a final concentration of 1 mg/ml and incubated on ice for 30 min. Lysozyme-treated cells were broken by sonication on ice for 2 min with a 10 s bursts at 300 W and a 10 s cooling period between each burst. The lysate was clarified by centrifugation at 10,000 × g for 30 min at 4°C. The recombinant 6xHis-tagged enzyme in the cleared lysate was purified using nickel-nitrilotriacetic acid (Ni-NTA) metal affinity chromatography (Qiagen, Hilden, Germany), according to the manufacturer's protocol with some modifications. After the cleared lysate was incubated with Ni-NTA at 4°C for 4 h with rotary shaking, the slurry was loaded into a column and washed with 10 bed volumes of lysis buffer followed by 10 bed volumes of wash buffers (30 mM Tris-HCl, pH 8.0, 1.0 M NaCl) containing 50 and 80 mM imidazole, respectively. The recombinant enzyme was recovered with an elution buffer containing 250 mM imidazole. Protein concentration and purity of the purified protein were analyzed by Bradford method using bovine serum albumin (BSA) as the standard , and SDS-PAGE stained with Coomassie Brilliant blue, respectively.
Amino acid sequence alignment and construction of the phylogenetic tree
Amino acid sequences of proteases similar to the enzyme in this study were retrieved by BLAST search (http://blast.ncbi.nlm.nih.gov/Blast.cgi). Multiple amino acid sequence alignment was done by ClustalX program  using sequences of AprX-related enzymes retrieved from SwissProt database (http://www.isb-sib.ch/services/databases). Sequence identity was calculated by ClustalW2. A phylogenetic tree was constructed from sequences of enzymes representing each member of the subtilase superfamily  and oxidant stable proteases (OSPs), obtained from extensive search of the Pubmed (http://www.ncbi.nlm.nih.gov/pubmed/) and Swiss-Prot (http://www.isb-sib.ch/services/databases) databases. The phylogenetic tree was constructed based on amino acid similarity within catalytic domains as described by Saeki et al , using MEGA version 4 software  and was inferred by the bootstrapping neighbor-joining method , of which sites involving gaps were excluded from the analysis.
Genbank accession number
The accession number of our recently isolated gene from the Virgibacillussp. SK37 is HM587897 and the protein identification number is ADM26217
Determination of protease activity
Protease activity was determined using azocasein as a substrate. The standard assay reaction in 500 μl contained 5 mg/ml azocasein, 100 mM Tris-glycine buffer, pH 9.5, 5 mM CaCl2, and 20 μg/ml of purified recombinant protease. The mixture was incubated at 55°C for 30 min with vigorous shaking. The reaction was stopped by adding 150 μl of 20% trichloroacetic acid (TCA) and kept on ice for 30 min, followed by centrifugation at 12,500 × g for 30 min. Then, the supernatant (250 μl) was mixed with equal volume of 2.5 M NaOH and the absorbance at 405 nm was measured. Specific activity (U/mg) was defined as an increase of 0.01 OD405 units per minute per milligram of enzyme. Protease activity was also analyzed by native-PAGE casein-zymography. Purified protease in a loading buffer without SDS and β-mercaptoethanol was electrophoresed through a 12% polyacrylamide gel under native condition. Subsequently, the gel was submerged in 2% (w/v) casein solution for 30 min at 4°C with gentle shaking. The gel was then transferred into a reaction buffer containing 50 mM Tris-glycine, pH 9.5, 250 mM NaCl, and 5 mM CaCl2 and further incubated at 55°C for 90 min, followed by staining with Coomassie blue. The protease activity was determined as a clear band against a blue background.
Effects of pH and temperature on protease activity
The effect of pH on proteolytic activity was examined in the presence of various 100 mM buffers, namely sodium acetate (pH 5.0-6.0), Tris-Maleate (pH 6.0-7.5), Tris-HCl (pH 7.5-9.0), Tris-glycine (pH 8.5-9.5), and glycine (pH 9.0-11.0), at 55°C and 5 mM CaCl2. To study the effect of temperature, the standard assay was applied using Tris-glycine buffer, pH 9.5 at 25-90°C. Thermostability of the protease was analyzed by incubating the enzyme at various temperatures (25-90°C) for 120 min and residual activity was measured at the standard assay condition (55°C, pH 9.5 and 5 mM CaCl2) and calculated as a percentage of activity of the enzyme prior to incubation.
Effects of NaCl and CaCl2on protease activity
Protease activity at various concentrations of either NaCl (0 to 4.0 M) or CaCl2 (0 to 100 mM) was measured at 55°C and pH 9.5. Subtilisin A was used as a representative of the subtilisin S8A family, and its catalytic activity was determined at its optimum condition at 60°C, in 100 mM Tris-HCl, pH 8.0 in appropriate concentrations of NaCl and CaCl2. The CaCl2 concentration was fixed at 5 mM in all NaCl assays. Maximum activity of each protease was defined as 100%. In enzyme stability studies, the enzymes were pre-incubated in the presence of various concentrations of either NaCl (0 to 4 M) or CaCl2 (0 to 100 mM) at 25°C for 24 h at pH 9.5 or 8.0 for the purified recombinant AprX-SK37 and subtilisin A, respectively. Residual activities were measured at 55 and 60°C for AprX-SK37 and subtilisin A, respectively, and expressed as relative activity compared to the reaction containing appropriate concentrations of NaCl or CaCl2 without pre-incubation.
Effects of NaCl and CaCl2on thermostability
The effects of NaCl and CaCl2 on the thermostability of the recombinant AprX-SK37 was determined by monitoring enzyme activity at moderate (40°C) and high (55°C) inactivation temperatures according to the results from the thermal stability assays. The enzyme was prepared in 100 mM Tris-glycine pH 9.5 containing; (I) 5 mM CaCl2: (II) 5 mM CaCl2 and 1 M NaCl: (III) 15 mM CaCl2: (IV) 15 mM CaCl2 and 1 M NaCl. The reactions were pre-incubated at either 40 or 55°C for up to 4 h and aliquots were withdrawn at various time intervals to measure residual activities at the standard assay condition.
Effects of protease inhibitors and denaturants
The effects of various protease inhibitors and protein denaturants on protease activity were determined using various substances, namely leupeptin, soy-bean trypsin inhibitor (SBTI), L-1-chloro-3-[-4-tosylamido]-7-amino-2-heptanone (TLCK), L-1-chloro-3-[-4-tosylamida]-4-phenyl-2-butane (TPCK), phenylmethanesulfonyl fluoride (PMSF), ethylenediaminetetraacetic acid (EDTA), imidazole, L-histidine, bestatin, pepstatin A, iodoacetic acid (IAA), N-methylmaleimide (NEM), β-mercaptoethanol (BME), dithiothreitol (DTT), E64, urea, and sodium dodecyl sulfate (SDS). Various concentrations of substances used in this study were listed in Table 2. The enzyme was mixed with each substance at room temperature for 30 min before azocasein was added to initiate catalytic reaction under the standard assay condition. Relative activity was calculated using the activity of the enzyme in the absence of these substances as 100%.
Stability towards oxidizing agent
Hydrogen peroxide (H2O2) was used as a representative of the oxidizing agent. Protease activity was measured in the presence of H2O2 at concentrations ranging from 0 to 5% (w/v). Enzyme activity was performed before and after pre-incubation the reaction in the absence of substrate for 30 min at 25°C. The reaction in the absence of H2O2 and without pre-incubation was taken as 100%.
This work was funded by the Royal Golden Jubilee Program (#PHD/0027/2548), the National Center for Genetic Engineering and Biotechnology (BIOTEC) (grant No. BT-B-0-FT-19-5041), and Suranaree University of Technology. The authors would like to thank Glenn Burchette and Erin Witek for kindly English editing this manuscript.
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