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Sci Rep. 2017; 7: 10684.
Published online 2017 September 6. doi:  10.1038/s41598-017-10932-8
PMCID: PMC5587760

Halotolerant aminopeptidase M29 from Mesorhizobium SEMIA 3007 with biotechnological potential and its impact on biofilm synthesis

Abstract

The aminopeptidase gene from Mesorhizobium SEMIA3007 was cloned and overexpressed in Escherichia coli. The enzyme called MesoAmp exhibited optimum activity at pH 8.5 and 45 °C and was strongly activated by Co2+ and Mn2+. Under these reaction conditions, the enzyme displayed Km and kcat values of 0.2364 ± 0.018 mM and 712.1 ± 88.12 s−1, respectively. Additionally, the enzyme showed remarkable stability in organic solvents and was active at high concentrations of NaCl, suggesting that the enzyme might be suitable for use in biotechnology. MesoAmp is responsible for 40% of the organism’s aminopeptidase activity. However, the enzyme’s absence does not affect bacterial growth in synthetic broth, although it interfered with biofilm synthesis and osmoregulation. To the best of our knowledge, this report describes the first detailed characterization of aminopeptidase from Mesorhizobium and suggests its importance in biofilm formation and osmotic stress tolerance. In summary, this work lays the foundation for potential biotechnological applications and/or the development of environmentally friendly technologies and describes the first solvent- and halo-tolerant aminopeptidases identified from the Mesorhizobium genus and its importance in bacterial metabolism.

Introduction

A large diversity of Mesorhizobium species have been identified in different environmental niches, including artic soil1, marine sponge2, semi-arid and saline soil3, and polychlorinated biphenyl (PCB) contaminated soil4. The large distribution of Mesorhizobium sp. suggests that species within this genus have adapted to several eco-climatic conditions because of its heterogeneous and extremely plastic genome. Although knowledge of the role of Mesorhizobium in the nitrogen-fixing process is currently expanding, the potential for its use in biotechnology is still limited, because only a few biomolecules with industrial application have been reported. These enzymes with industrial applications include cyclic β-(1,2)-glucans5, L-ribulose 3-epimerase6, β-transaminase7, cellulase8, L-rhamnose isomerase9 and pyridoxine 4-oxidase10. However, despite the potential industrial relevance and a large database of peptidases [3179 known peptidases, and homologues from 29 Mesorhizobium genomes], there is almost no information concerning the biochemistry of the proteolytic system or any peptidase from the Mesorhizobium genus.

Aminopeptidases (EC 3.4.11) are a diverse group of exopeptidases involved in the catalysis of peptide bond cleavage at the amino-terminus of proteins, releasing amino acids residues, preferably hydrophobic ones. These enzymes are widely distributed in bacteria, fungi, plants and animal tissues with important physiological roles, such as the maturation and degradation of proteins, the regulation of hormonal levels, defence control, hydrolysis of regulatory peptides, regulation of genes expression, support of the amino acids pool11, peptidoglycane metabolism12, nitrogen nutrition and virulence factors13. Aminopeptidases are used extensively in the biopharmaceutical industry to remove N-terminal sequences in the production of anti-hypertensive peptides11 and antiviral compounds14. Additionally, these enzymes have an important role in the food industry by modifying organoleptic characteristics (e.g., texture, bitterness and flavour)15. Furthermore, aminopeptidases can be used with other endopeptidases for wastewater treatment to degrade proteins16.

Over the last years, several types of experiments to improve the physicochemical characteristics of these enzymes have been performed including chemical modification, protein immobilization, protein engineering and directed enzyme evolution. However, if the enzymes are naturally stable and exhibit high activities in the presence of physicochemical factors, such modifications are not necessary. Therefore, it is conceivable that genomic data mining could be used to find an enzyme naturally stable or catalytically efficient enough to optimally fit process requirements that are solely dictated by substrate and product properties. In the era of big data, the genomic resources in various databases are highly valuable, making genomic data mining a growing area with an unprecedented capacity for the discovery of novel enzymes, since a huge abundance of enzymes already exists in these unexplored genomic resources.

In this study, we report the discovery of the mesoamp gene by genomic data mining. The gene shares 54% sequence identity with aminopeptidase T from Thermus thermophilus when analysed with The Peptidase Database (MEROPS). This gene was cloned into an expression vector and the recombinant protein, named MesoAmp, was functionally and physically characterized. Our results show that MesoAmp could be overexpressed in a stable dimeric form and purified without contaminants. The functional characterization of the enzyme showed that it was active in the presence of a high concentration of salt and organic solvents. Taken together, these data demonstrate the interesting features of MesoAmp in bacterial metabolism and support the potential of this enzyme for use in biotechnological processes.

Results

Sixty-eight peptidases were predicted by comparative genomic analysis

The automatic annotation tool identified 101 ORFs that possibly encode peptidases that are similar to the Mesorhizobium genome annotated in MEROPS17. To characterize the proteolytic machinery of the Mesorhizobium genus, the protein sequences of each of the 101 ORFs were subjected to an exhaustive search against the MEROPS peptidase database. Using the comparative database search, we detected a total of sixty-eight peptidases belonging to 26 clans of proteolytic enzymes. These enzymes were distributed into groups based on the catalytic type of the proteolytic mechanism: 6.8% aspartic, 3% glutamic, 2.7% cysteine, 41.1% metallo, 35.6% serine, 4.1% treonin, 4.1% mixed and 5.5% peptidase inhibitors (Table S2). This finding supports our hypothesis that a large number of peptidases with biotechnological potential remain unexplored in the Mesorhizobium genome.

Three peptidases with biotechnological potential were discovered

Considering the physicochemical characteristics of peptidases with similar sequences and biochemical characteristics as pH, temperature and thermostability, we identified three enzymes with potential biotechnological applications (Table S3).

We selected Aminopeptidase T and called the enzyme MesoAmp. We focused on this enzyme for further bioinformatic analysis and biochemical characterization.

Sequence analysis of MesoAmp revealed the amino acid fingerprint of thermophilic metalloproteases

The sequence of MesoAmp consists of 1257 pb (G + C content = 64%) encoding a protein with 418 amino acids. No signal peptide sequence was identified. The comparison of the complete amino acid sequence with the proteins from the database displayed the highest homology (95%) with the aminopeptidase from Mesorhizobium ciceri and another species of Mesorhizobium. MesoAmp has 54% sequence identity with an aminopeptidase T (AmpT) from Thermus thermophilus (MER001285), 40% sequence identity with aminopeptidase S (PepS) (MER005731) and the aminopeptidase S (AmpS) (MER014416) enzymes from Streptococcus thermophilus and Staphylococcus aureus, respectively.

The multiple sequence alignment of the MesoAmp sequence with AmpT, PepS and AmpS revealed an 8 amino acid fingerprint that provides a signature for a thermophilic metalloprotease18, as well as the catalytic amino acid Tyr at position 352 and the metal-binding residues Glu259, Glu325, His354, His387 that are shown in detail in Supplementary Figure S1. The analysis using the ConSurf server revealed that the most conserved amino acids located in the C-terminus of the protein (Supplementary Figure S1).

Dimeric structure of MesoAmp with high degree of conservation

The three-dimensional model of MesoAmp was created using Modeller and validated using ModFold that demonstrated that there was less than a 1:1,000 chance that the models were incorrect. The Ramachandran plots for the models revealed a relatively high number of amino acids in allowed regions (98.08%) that is an indication for further model optimizations. The structural model of MesoAmp superimposed remarkably well with the AmpS structure, displaying a r.m.s.d of 0.508 Å (Fig. 1A and B). The analysis using Z-Dock revealed a homodimer structure with an N-terminal dimerization domain (Fig. 1C). The conserved residues between scarcely conserved clusters located on the surface of the protein (Fig. 1D) are presumably important for the maintenance of the structural integrity of these surface patches19. Buried inside the protein is the highly conserved region constituting the substrate–binding pocket (Fig. 1D and E) and the substrate-binding cavity of 1,780 Å3 (Fig. 1F).

Figure 1
The structural features of the MesoAmp model. (A) The superimposed structures of MesoAmp model (gray) with the structure of Staphylococcus aureus aminopeptidase chain A (blue), revealing the conservation of the alpha/beta fold, with a root mean square ...

MesoAmp was expressed in the soluble fraction and the active enzyme obtained was in a dimeric form

The optimal conditions for the production of the soluble and active form of MesoAmp from E. coli BL21(DE3) were IPTG at a final concentration of 0.1 mM, an induction temperature of 30 °C and 12 h growth under 200 rpm. Under these conditions, the recombinant protein was soluble in the supernatant of the cell lysate that aided further purification. The SDS–PAGE analysis of purified MesoAmp revealed the enzyme was completely purified by affinity chromatography and weighed 45.72 kDa under denaturing conditions (Supplementary Figure S2A) as predicted with ProtParam tool (http://us.expasy.org/tools/protparam.html). The molecular mass of the native enzyme was estimated to be 88.05 kDa by gel filtration (Supplementary Figure S2B). Our results indicate that the enzyme is a homodimer that is highly common for the aminopeptidase M29 family20.

MesoAmp is active in a wide range of pH values and temperatures

The effects of pH and temperature on MesoAmp activity were examined spectrophotometrically using Leu-p-NA as substrate. The pH curve displayed a maximum activity within a narrow pH range from pH 7.5 to 9.0 with no significant difference between these pH values (Fig. 2A). The enzymatic activity was almost completely lost when the pH was lower than 6.5 or higher than 10.0. The experiments subsequently described were carried out in 100 mM bicarbonate sodium-hydroxide buffer at pH 8.5. The purified recombinant MesoAmp exhibited the highest activity at 40 °C. Interestingly, MesoAmp still maintained more than 80% of its activity in the temperature range from 35 to 55 °C (Fig. 2B).

Figure 2
Physicochemical analysis of MesoAmp. (A) The pH effect on the enzymatic activity of MesoAmp in different buffers: McIlvaine buffer ([filled triangle]); Sodium citrate buffer ([increment]); Sodium phosphate buffer (♦); Tris-HCl buffer (•); Bicarbonate-Sodium ...

The CD spectrum of the recombinant protein displayed two negative peaks in the far-UV region at 208 nm and 222 nm, as expected for alpha-beta secondary structure (Supplementary Figure S3A). MesoAmp displayed a melting temperature (Tm) of 53.2 °C in the presence and absence of Co2+ ions. Therefore, the cobalt ion does not change the alpha-beta content in the thermal denaturation assay (data not shown). Temperatures above 40 °C induced the denaturation of the α-helical structure of MesoAmp, showing a transition to the irreversible state (Supplementary Figure S3B). The disruption of its secondary structure begins below 55 °C as indicated by the increase in the unfolded fraction (60% unfolded), whereas the enzymatic activity is not significantly altered up to this point.

Metallopeptidases exhibit a broad range of metal-ion dependencies. The activity of MesoAmp in the presence of different metal ions is shown in Table 1. Approximately 90% of the activity was lost in the presence of Ca2+, Ba2+, Al2+ and Zn2+ ions. Conversely, MesoAmp displayed enhanced catalytic activity in the presence of Co2+ and Mn2+ ions (17-fold and 8-fold, respectively). All other metal ions tested (with a rank order of Mg2+ > Ni2+ > Mg2+ > I2+) had stimulatory effects on the enzymatic activity of MesoAmp.

Table 1
The effect of various divalent cations on the MesoAmp activity.

After determining the optimum temperature and pH, the activity of MesoAmp was tested with Leu-p-NA at pH 8.5, 40 °C in the presence of 3 mM Co2+. The Km, Vmax and Kcat values were calculated to be 0.2364 ± 0.0182 mM, 1.115 ± 0.020 mM.s−1 and 712.1 ± 88.12 s−1 respectively.

Thermal treatment at 45 and 50 °C after 60 min pre-incubation did not influence the activity of the enzyme. However, MesoAmp lost half of its activity when incubated at 55 °C for 15 min, and it was rapidly inactivated when incubated at 70 °C (Supplementary Figure S4). After 5 min incubations at these higher temperatures, the enzymatic activity decreased by approximately 95%.

MesoAmp retains its activity in the presence of organic solvents and at high salt concentrations

PMSF and iodoacetic acid did not influence enzyme activity. However, metal-chelating agents such as EDTA severely inhibited its activity (Table 2) indicating that MesoAmp is a metallopeptidase. We tested the activity of the enzyme in the presence of denaturing agents (Table 2). The MesoAmp activity was very sensitive to concentrations of guanidine-HCl between 0.5 and 2.0 M, indicating a significant disruption in the secondary structure of the protein. However, urea treatment did not substantially affect the activity at concentrations of 0.5 M and 1 M but reduced the activity by half when at 2 M.

Table 2
The effect of inhibitors and denaturing agents on the activity of MesoAmp*.

Zhuo and Dixon21 found that the role of sulfhydryl reagents was to chelate small amounts of metal ions. To prevent this chelating mechanism, we measured the enzymatic activity without metal ions. The role of DTT as a metal chelator makes it unsuitable to use with MesoAmp. As shown in Table 2, the presence of DTT and β-mercaptoethanol considerably decreased the enzymatic activity. On the other hand, NaCl treatment enhanced the activity of MesoAmp (Table 2) by 1.2-fold compared to the enzymatic activity without NaCl.

The presence of non-ionic surfactants, such as Tween (20 and 80) and Triton (X-100 and X-114), slightly decreased the amount of enzymatic activity (Table 3). Nevertheless, ionic and cationic surfactants (SDS and CTAB) resulted in complete loss of MesoAmp activity (data not shown). Previous reports have indicated that the inhibitory effect of SDS or CTAB could be caused by their binding to the enzyme at more than one site, thus modifying the tertiary structure and altering the charge distribution20.

Table 3
The effect of various detergents on the activity of MesoAmp*.

One of the most interesting characteristics of MesoAmp is its stability in the presence of organic solvents, as shown in Fig. 3. Interestingly, the activity of MesoAmp was stable, particularly at 5% and 10% (v/v) concentrations of ethanol, methanol, 2-propanol and hexane, with a slight increase in activity at 20% (v/v) ethanol and methanol. However, at 40% (v/v), the enzyme was completely inactivated. In the presence of acetone, DMSO, chloroform, butanol and heptane at concentrations above 10%, the enzymatic activity decreased by 50% followed by complete inactivation at higher concentrations of these solvents.

Figure 3
The effect of different organic solvents on MesoAmp activity. The remaining enzymatic activity was determined in the aqueous phase without solvent (none) under the standard conditions of the assay. The Log P (logarithm of the partition coefficient of ...

MesoAmp is not required for growth in vitro but is necessary for biofilm production and halotolerance

MesoAmp was responsible for 40% of the intracellular leucine aminopeptidase activity (Fig. 4A). Nevertheless, both strains Mesorhizobium SEMIA3007 and Δmesoamp did not display a significant difference of growth in TY broth (Fig. 4B) suggesting that MesoAmp is not involved in growth in synthetic media. To determine the potential role of peptidases in Mesorhizobium SEMIA3007 metabolism, the halo-tolerance, solvent-tolerance and biofilm production of the [increment]MesoAmp mutant was evaluated.

Figure 4
Aminopeptidase activity and in vitro growth kinetic assay of Mesorhizobium sp SEMIA 3007 and Δmesoamp. (A) Enzymatic activity of Mesorhizobium sp SEMIA 3007 and Δmesoamp strains using Leu-pNA as the substrate in 100 mM bicarbonate sodium-hydroxide ...

Biofilm formation is an important microbial survival strategy. We therefore examined whether the absence of the MesoAmp enzyme had an effect on biofilm formation in Mesorhizobium SEMIA3007. Figure 5A reveals a significant decrease (80%) in the capacity in biofilm formation in PGE broth (glucose as carbon source) and 50% in PGY broth (glycerol as carbon source) for Δmesoamp. The effect of mesoamp gene expression on Mesorhizobium stress tolerance was studied by liquid culture assays. When assayed by the liquid culture method under saline stress conditions, growth of Δmesoamp cells decreased significantly with time compared to Mesorhizobium SEMIA3007 strain (Fig. 5B). Δmesoamp displayed approximately 60 to 80% decreased saline stress tolerance in 0.2 and 0.3 M of NaCl, respectively, and a total loss of tolerance to higher concentrations of salt (0.4 and 0.5 M, respectively). Mesorhizobium SEMIA3007 and Δmesoamp showed tolerance to DMSO and hexane (Figure S5). According to the literature, the mechanisms by which bacteria present solvent tolerance (adaptations such as the efflux pumps, cis-trans fatty acids membrane isomerisation, rapid membrane repair mechanisms and membrane-localized transporters22, 23) are several and complexes, thus cannot be attributed to a single gene.

Figure 5
Biofilm production and halotolerance assay. (A) Effect of salt on growth of Mesorhizobium sp SEMIA 3007 and Δmesoamp strains. Bacteria were inoculated in TY medium containing different salt concentrations. Each point represents the average of ...

Discussion

To date, in addition to the genes observed in bacteria, the ones encoding M29 aminopeptidases have been identified in animals, plants and Archea. However, a highly limited number of aminopeptidases M29 from Thermus aquaticus, Thermus thermophilus, Bacillus stearothermophilus, Streptococcus thermophilus, S. pneumoniae, S. aureus, Borrelia burgdorferi and Listeria monocitogenes have been characterized13, 20, 24, 25. In this study, we present the results of genomic data mining in Mesorhizobium sp., as well as the cloning, overproduction in E. coli, and characterization of a highly halo-tolerant and solvent-tolerant aminopeptidase. This is a promising enzyme with possible applications in the production of debittered hydrolysates, the conversion of L-homophenylalanyl amide into L-homophenylalanine, and the development of flavouring for dairy products20.

The protein encoded by the mesoamp gene possesses only 40%–50% sequence identity with other members of the M29 family of characterized metallopeptidases. It displays a conserved catalytic domain in the C-terminal region and an 8-element fingerprint that provides a signature for thermophilic metalloproteases (Thermoptase) and virtually spans the full alignment length26.

The structural model of MesoAmp displays a long substrate-binding hole in the N-terminal domain that functions to limit the length of the C-terminal side of the substrate. The binding pocket in the C-terminus domain provides the molecular basis for the selectivity of its residues (Fig. 2E)27.

The enzymatic characterization of the MesoAmp indicated that the protein retained 80% of its enzymatic activity in an alkaline pH range of 7.5 to 9.0 with maximal activity at pH 8.5. These results are comparable with those on AmpT (optimal pH between 7.0 and 8.0) and PepS aminopeptidase (optimal pH between 7.5–8.5)28. According to Wang, T, et al.20, there is a substantial decrease in the activity outside the pH range 7.0 to 9.0, and it is primarily due to irreversible changes in the protein structure or to the destabilization by buffer species.

The M29 family is characterized by an optimal temperature between 60 to 70 °C17. In contrast, MesoAmp had its optimal activity at 40 °C and maintained 80% of its activity at 55 °C with a decrease of 50% of its activity at 60 °C. The thermal stability of proteins seems to be a complex phenomenon that can be affected by many factors. In general, proteins can be stabilized by decreases in their entropy of unfolding29. In the primary structure of MesoAmp, the proline residue represents as much as 4.3% of the sequence. At the same time, prolines represent only 5.4% and 4.1% of the residues in the amino acid sequences of Amp T and PePS, respectively. This finding suggests that other factors are responsible for their thermal stability such as the presence of disulfide bonds formed by cysteine residues that stabilize proteins by decreasing the entropy of the protein’s unfolded state30 and/or oligomeric state formation, representing an adaptive advantage relative to their monomeric counterparts24. The ability to act at temperatures over 40 °C is of great biotechnological importance, reducing the risk of contamination by mesophilic microorganisms. In addition, this characteristic favours substrate and product solubility and increases reaction rates for reducing viscosity and for increasing the diffusion coefficients of the substrates31.

Metalloaminopeptidases exhibit a broad range of metal ion dependence, and Zn2+ is the most frequently associated cation. Members of the M29 family from Staphylococcus aureus, B. stearothermophilus and L. monosytogenes have Co2+ and Mg2+ as cofactors. On the other hand, the cofactor for PepS is unknown, but it is unlikely to be Ca2+, Cu2+, Zn2+ Co2+, Mn2+ and Hg2+ because low concentrations of these cations inactivated the enzyme32. MesoAmp displays a high dependence on Co2+ and Mn2+ ions, and the effect of Co2+ on aminopeptidases has been frequently described in the literature. This cation increases the relative activity from 333, 534 to 26 times that of the normal activity35. A study focusing on density functional theory36 determined that the electronic nature of cobalt and manganese ions activates water molecules, thus influencing the generation of the intermediate state (enzyme-substrate), which consequently increases the reaction rate.

MesoAmp exhibited relative resistance in the presence of polar and non-polar solvents, and this phenomenon has been observed in many cases37. Nevertheless, the reason for such tolerance has not been established to date. To a certain extent, this solvent activation imparts conformational flexibility to the protein, causing an increase in activity. Additionally, the relative abundance of hydrophobic residues located on the surface of a molecule plays an important role in the structural stability of proteins37, 38. Salt has several important effects on the stability of proteins, primarily by charge modification on the protein surface or/and alteration of charges between substrate and enzyme31. This effect can subsequently increase enzyme activity. Further studies of the tertiary structure of the aminopeptidase M29 family might clarify the molecular basis of the mechanism of its environmental adaptation at high salt concentrations.

The proteolytic machinery has a functional redundancy between several enzymes. Mesorhizobium sp SEMIA3007 produces enzymes with a similar metabolic function (Table S4) according to the Brenda databases39. In the absence of MesoAmp, the other enzymes with amino peptidase activity can supply the demand for intracellular amino acids required for bacterial development such as protein synthesis. For that reason, in spite of having a decrease of aminopeptidase activity in the absence of MesoAmp, the growth of Mesorhizobium in synthetic media is not affected. However, aminopeptidases may exhibit other functions in addition to the degradation of intracellular peptides and maintenance of the pool of amino acids, such as cell resistance to osmotic stress, biofilm production, and cell invasion4042. To our knowledge, we have characterized aminopeptidase from Mesorhizobium or other rhizobacteria for the first time.

Previous work has reported the multifunctionality of aminopeptidases. In S. typhimurium, peptidases involved in exogenous peptide degradation, protein turnover and degradation of abnormal proteins43. In E. coli, PepA is also endowed with DNA binding activity in regulation of the carAB operon44. In Lactococcus lactis, PepF plays a role in the pyruvate metabolism, cell wall and protein secretion45. In S. thermophilus, PepS aminopeptidase has cellular functions as peptidoglycan metabolism12. Our results suggest that MesoAmp is indispensable for biofilm production and osmotic stress tolerance (Table 4), functions totally undescribed for other aminopeptidases. However, considering that there is no growth defect in the Δmesoamp strain that might account for decreased biofilm production, we suggest that MesoAmp plays a non-nutritional role. The mechanism by which aminopeptidases affect the synthesis of biofilms is not well understood, because their formation and maintenance are multifactorial processes influenced mainly by production and nature of the intra- and extracellular polysaccharides46. For Mesorhizobium, the fact that MesoAmp contributes to biofilm production might be attributed to the ability of this enzyme to catalyse the peptides to release free leucine and other amino acids that serve as a substrate for a variety of catabolic pathways47. In the absence of MesoAmp, the mutant cannot keep that pool of amino acids, thus making it sensitive to osmotic stress. Many species of bacteria have also been shown to increase the proline and leucine pool size and accumulate total free amino acids under osmotic stress contributing to their adaptability to a saline environment4749.

Table 4
Biochemical and physiological properties of the M29 family aminopeptidases.

Conclusions

The major problem of bioprocesses today is the uncompetitive production costs compared to chemical synthesis. High fresh water, energy consuming sterilization, discontinuous fermentation to avoid microbial contamination and the solubility of non-polar substrates50 increase production costs. Enzymes with new physicochemical properties (thermo-, solvent- and halo-tolerance) can reduce economic costs, making these enzymes more profitable for industrial bioprocesses. Our bioinformatics approach can greatly shorten the working time51 resulting in a significant advantage over conventional methods. Furthermore, in certain cases, along with the metagenomic approach29, it is possible to identify new enzymes with high biotechnological potential in a sea of bioinformatics data. Some thermo-tolerant52, solvent-tolerant20 and halo-tolerant53 aminopeptidases have been reported, however, none display all three features simultaneously (see Table 4).

It is very difficult to elucidate the pleiotropic functions of mesoamp, mainly due to the complexity of biological systems. We have increased our knowledge of aminopeptidases in the M29 family and confirmed their involvement in the biofilm synthesis and resistance to osmotic stress, but the precise mechanisms by which it interferes with these cellular functions is still unclear. This situation encourages the development of complex and precise biological models that take into account pleiotropy and the connection of all other cellular functions.

Materials and Methods

The de novo sequencing of Mesorhizobium SEMIA3007 genome used a combined strategy involving Illumina – HiscanSQ. The prediction of ORFs and annotation were performed using the Rast system54 and deposited in the Laboratory of Biochemistry of Microorganisms and Plants (LBMP) database at São Paulo State University, Jaboticabal Campus. The data sets results are available in the NCBI BioProject SRR370304055.

Homology search and comparative sequence analysis

The annotation of the assembled sequence was conducted using RAST (Rapid Annotation Using Subsystem Technology)56. A search for ORFs that encode peptidases was performed, and the selected ORFs were compared individually in the MEROPS peptidase database using the local alignment tool (http://merops.sanger.ac.uk/index.shtml).

mesoamp sequence analysis

Protein signatures and conserved motifs were examined using InterProScan26, and the theoretical physiochemical data were generated with the ProtParam tool from ExPASy (http://www.expasy.org/). To estimate the evolutionary conservation of each amino acid translated from the mesoamp gene, its sequence was aligned with 24 amino acid sequence from the aminopeptidase members of the M29 family (Table S1) using the CLUSTAL W programme57. The alignment was analysed with the ConSurf server58. Additionally, an analysis was performed with the SignalP 4.1 server59 in order to identify possible signal peptides.

Molecular modelling

A search for proteins structurally similar to MesoAmp was performed using BLASTP against the Protein Data Bank (PDB). The molecular models of the enzyme were built using the Modeller 9.10 programme60 with the default parameters based on the structural coordinates of the aminopeptidase PepS from Streptococcus pneumoniae (PDB code: 4ICQ)27, the aminopeptidase T from Thermus thermophilus (PDB code: 2AYI)61 and the aminopeptidase S from Staphyloccus aureus (PDB code: 1ZJC)62. A quality assessment of the models was performed by ModFold63. The scores of the amino acid position conservation displayed by the Consurf server were projected onto the MesoAmp structure. The molecular docking was calculated using M-ZDOCK64. The cavity volumes were calculated by KVfinder65, and the PyMOL software66 was used to visualize the models and to prepare the figures.

DNA cloning, heterologous overexpression and protein purification

Preparation of plasmids, DNA manipulations, and transformation of E. coli BL21(DE3) competent cells were performed as previously described67, 68 using the following synthetic oligonucleotides: Forward 5′ CAGGCATATGATCATGACCACACATTCG 3′ and Reverse 5′ CGAACTCGAGCCCTCAGGCCCACT 3′ that had sites for the restriction enzymes NdeI and XhoI, respectively (underlined). The protein concentration was determined using spectrophotometer analysis with a Nanodrop ND-1000 with the theoretical extinction coefficient (54680 M−1 cm−1) obtained from the ProtParam tool and the Bradford method69 with bovine serum albumin (BSA) as a reference.

Size exclusion chromatography for molecular mass determination

The protein samples were analysed using 10% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The gel was stained with Coomassie Brilliant Blue G-250 and destained with 10% (v/v) acetic acid70. The molecular mass of the native enzyme was estimated by size exclusion chromatography (SEC) using a Hiload16/600 Superdex 200 column (GE Healthcare Bio-Sciences, Uppsala, Sweden) previously equilibrated with purification buffer (100 mM Tris-HCl pH 8.0; 200 mM NaCl; 5% (w/v) glycerol). The calibration curve was obtained using the Protein Standard Mix 15–600 kDa (Sigma-Aldrich, St. Louis, MO.), which contains standard proteins [thyroglobulin bovine (670 kDa); γ-globulins (150 kDa); Albumin (44.3 kDa); Ribonuclease A (13.7 kDa); and P-aminobenzoic acid (pABA) (0.13 kDa)], and then plotting the log of the molecular weight of the protein against the elution volume (ml). From this calibration curve, the molecular weight of MesoAmp was determined. The chromatograms were obtained by measuring the absorbance at 280 nm using an ÄKTA pure system (GE Healthcare) at a flow rate of 0.5 mL min−1. All collected fractions were analysed by SDS-PAGE, and the fraction containing pure MesoAmp was used for further assays.

Kinetic assays

Aminopeptidase activity was measured by spectrophotometric detection via the hydrolysis of L-leucine-p-nitroanilide (Leu-p-NA)20 by continuously monitoring the p-nitrophenol (p-NA) release at 405 nm using the spectrophotometer reader MultiScan Go (Thermo Scientific). The molar extinction coefficient (εpNA = 9,620) was used to calculate the enzymatic activity. Unless otherwise indicated, the reaction was performed using 1 µg of pure MesoAmp in 20 mM Tris-HCl pH 8.0 buffer at room temperature in a final volume of 200 μL. The assays were carried out in triplicate, and a control was performed for each reaction without the enzyme to measure the spontaneous hydrolysis of the substrates. Linear regressions were performed to determine the initial velocity (Vo) of the reaction.

Effect of pH and temperature on enzymatic activity

The effect of pH on MesoAmp activity was determined at 35 °C using the following buffers at 100 mM: McIlvaine (pH 3.0 to 4.5); sodium citrate (pH 4.0 to 6.5); sodium phosphate (6.5 to 8.0); Tris-HCl (pH 7.0 to 8.5); bicarbonate-sodium hydroxide (8.5 to 11.0); glycine-sodium hydroxide (8.5 to 10.5) and monosodium phosphate - sodium hydroxide (11.0 to 12.0). The optimal temperature was determined in the range of 10 to 90 °C using 5 °C or 10 °C steps. After these preliminary experiments, the assays were carried out in 100 mM Tris-HCl buffer pH 8.5 at 40 °C.

To verify the thermostability of MesoAmp, an activity assay was performed under the temperature range of 40 °C to 70 °C by pre-incubating the purified enzyme for 5, 15, 30, 45 or 60 minutes followed by an immediate ice bath at 4 °C for 10 minutes. The residual activity was determined after each incubation time.

Effect of metal ions, peptidase inhibitor agents and detergents on the enzymatic activity

To evaluate the influence of metal ions on MesoAmp activity, 2 mM (final concentration) of K+, Mg2+, Ca2+, Mn2+, Co2+, Cu+2, Fe+2, Ni+2, Al+3, Li+, Zn2+, Hg2+, Cd2+ or Ba2+ was added to the enzyme solution, and the residual activity was measured. A control without metal ions was used to calculate the residual activity.

Specific peptidase inhibitors were added to the enzyme solution (10 mM) including phenylmethylsulfonyl fluoride (PMSF) or iodoacetic acid that inhibit serine protease and cysteine protease, respectively, and ethylenediamine tetraacetic acid (EDTA) (5, 10 and 20 mM), that inhibits metalloproteases.

The effects of detergents on MesoAmp activity was investigated using Tween 20, Tween 80, Triton X-100 and Triton X114 at 0.5%, 1% and 2% (w/v). The enzyme was incubated with each detergent at room temperature for 30 min. The residual activity was determined and compared to the control. The procedure for the analysis of the effects of ionic surfactants was the same as above except that the enzyme was treated with sodium dodecyl sulfate (SDS) or hexadecyl trimethyl ammonium bromide (CTAB) at 1%, 2% and 4% (w/v).

Effect of denaturing agents and organic solvents on the enzymatic activity

The effects of urea, guanidine (0.5, 1 and 2 M), NaCl (0.5, 1, 2, 3 and 4 M), Dithiothreitol (DTT) and β-mercaptoethanol (1, 5 and 10 mM) on the activity of MesoAmp were investigated. Samples were incubated at room temperature for 45 min, and the residual activity was determined and compared to the control.

The stability of MesoAmp in the presence of organic solvents was assessed by measuring the residual activity of the enzyme after incubating it at 4 °C for 45 min with 5, 10, 20, and 40% (v/v) of methanol, ethanol, 2- propanol, acetone, chloroform, butanol, cyclohexane, hexane, heptane or dimethyl sulfoxide (DMSO). The resulting activity was compared to the control.

Kinetic parameters of purified MesoAmp

The Km, Vmax and Kcat parameters were calculated from the initial rates of the hydrolysis of Leu-p-NA in the concentration range of 0.05 to 2.5 mM at the optimal conditions for the enzyme, and the non-linear regression of the data using the Michaelis-Menten equation was performed by GraphPad Prism, Version 5.00 for Windows (GraphPad Software, San Diego California USA, www.graphpad.com).

All data obtained were analysed using the R software. An ANOVA and Tukey’s test at 5% probability were used to compare the treatment methods.

Circular dichroism and thermostability measurements

The circular dichroism (CD) analysis of the purified MesoAmp was performed using a JASCO J-815 spectropolarimeter (Jasco, Tokyo, Japan) linked to a PFD-425S Peltier temperature controller. The enzyme was analysed at 4.4 µmol in 5 mM sodium phosphate, pH 8.0, in the presence and absence of 8.8 µmol Co2+. The average of thirty consecutive scans was recorded over a wavelength range of 200 to 260 nm using a 1 mm cuvette, and for both assays, the buffer baseline was subtracted. The thermostability of the enzyme was verified, and its thermal unfolding was monitored by the changes in ellipticity at 222 nm. The temperature was increased with a heating rate of 1 °C min-1 in the range of 20 to 105 °C. The melting point (Tm) represents the temperature at the midpoint of the unfolding transition71.

Construction of mesoamp deletion mutant

To generate the Δmesoamp allelic replacement plasmid, 510 and 543 bp DNA fragments located upstream and downstream of the mesoamp open reading frame were amplified by PCR and cloned into the nonreplicating vector pNPTS13872. The upstream DNA fragment was amplified using primers P(A)F - 5′ TGCGGATCCTGGCGCAGGAAGTGTT 3′ (BamHI restriction sites are underlined), and P(B)R - 5′ CCTCCCTACGTGGGAATCTGACCCATA 3′. The downstream DNA fragment was PCR amplified using primers P(C)F – 5′ GATTCCCACGTAGGGAGGTCGAATGGC 3′ and P(D)R – 5′ CTGGAATTCGTCGGGGACCGGGTTCTG 3′ (EcoRI restriction sites are underlined). A stable in-frame deletion of mesoamp was generated by homologous recombination and allelic replacement using an SOE-PCR. The DNA fragment, framed by BamHI and EcoRI sites, was cloned into a BamHI and EcoRI-digested pNPTS138 to generate plasmid pJL38Δmesoamp. Mesorhizobium SEMIA3007 electro-competent cells, and electroporation was carried out using the conventional method73. Transformant cells with pJL38Δmesoamp integrated upstream of the mesoamp locus were obtained by selecting for kanamycin resistance. The recombinants were identified as kanamycin-sensitive colonies and confirmed by PCR with primers P(A)F and P(D)R. The resultant in-frame deletion mutant was further verified by DNA sequencing and finally designated Δmesoamp strain.

Growth, biofilm production and halotolerance assay

To determine the potential role of aminopeptidases in Mesorhizobium sp physiology, Δmesoamp mutant was evaluated in conditions of osmotic and thermic stress and in biofilm production. For routine growth, TY broth74 was used. The initial OD600nm of each bacterial suspension was adjusted to 0.05 as a starting time point (0 h). The bacterial cultures were incubated at 30 °C with shaking at 200 rpm and kinetic growth was measured (OD600 nm) at 2 h interval for 96 hours.

For comparative analyses of the biofilm production by the wild-type and mutant strains TY, PSY (K2HPO4 1.4 g−l, KH2PO4 1.0 g−l, MgSO4 0.2 g−l, sucrose 10 g−l, yeast extract 1.0 g−l), PGY (K2HPO4 1.4 g−l, KH2PO4 1.0 g−l, MgSO4 0.2 g−l, glycerol 10 g−l, yeast extract 1.0 g−l) and PGE (K2HPO4 0.5 g−l, MgSO4 0.2 g−l, NaCl 0.1 g−l, yeast extract 3.0 g−l and glucose 10.0 g−l) broth were used, following incubation at 30 °C with shaking at 200 rpm for 144 h. Then, the biofilms were stained by crystal violet methods as previously described75. To investigate halotolerance, Mesorhizobium SEMIA3007 and Δmesoamp strain were inoculated into TY broth for 24 h at 30 °C with constant shaking at 200 rpm until the exponential growth phase was reached. Then, the density was estimated spectrophotometrically to achieve an approximate starting concentration (OD600nm = 0.5). The bacterial cultures were incubated into TY broth containing 0.05, 0.1, 0.2, 0.3, 0.4, 0.5, 0.75, 1.0; 1.25, 1.50 or 2 M of NaCl, at 30 °C with shaking at 200 rpm and the OD600nm was monitored for 72 h every twenty-four hours.

Nucleotide sequence accession number

The DNA sequence of mesoamp gene was deposited at GenBank with the reference code WP_069093355.1.

Electronic supplementary material

Acknowledgements

We would like to thank the Programa de Pós Graduação em Microbiologia Agropecuária, UNESP, Jaboticabal, São Paulo State, Brazil. This work was supported by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq).

Author Contributions

Author Contributions

E.M.S., E.G.M.L. and E.R.M. conception and design of the study; E.M.S., M.R., T.M., E.S.G.-P. and E.G.M.L. analysis and interpretation of data; E.M.S., M.R. and T.M. wrote the manuscript; E.G.M.L. conceived and supervised the study and made manuscript revisions.

Notes

Competing Interests

The authors declare that they have no competing interests.

Footnotes

Electronic supplementary material

Supplementary information accompanies this paper at doi:10.1038/s41598-017-10932-8

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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