l-Asparaginase from Streptomyces griseus NIOT-VKMA29: optimization of process variables using factorial designs and molecular characterization of l-asparaginase gene

Abstract

Marine actinobacteria are known to be a rich source for novel metabolites with diverse biological activities. In this study, a potential extracellular L-asparaginase was characterised from the Streptomyces griseus NIOT-VKMA29. Box-Behnken based optimization was used to determine the culture medium components to enhance the L-asparaginase production. pH, starch, yeast extract and L-asparagine has a direct correlation for enzyme production with a maximum yield of 56.78 IU mL⁻¹. A verification experiment was performed to validate the experiment and more than 99% validity was established. L-Asparaginase biosynthesis gene (ansA) from Streptomyces griseus NIOT-VKMA29 was heterologously expressed in Escherichia coli M15 and the enzyme production was increased threefold (123 IU mL⁻¹) over the native strain. The ansA gene sequences reported in this study encloses several base substitutions with that of reported sequences in GenBank, resulting in altered amino acid sequences of the translated protein.

Introduction

l-Asparaginase is an amidohydrolase which catalyses the hydrolysis of amino acid asparagine into aspartic acid and ammonia. Neoplastic cells cannot synthesize l-asparagine in the absence of l-asparagine synthase; therefore, they should be solely dependent on the circulating sources for l-asparaginase. The commonest therapeutic practice is to inject the l-asparaginase intravenously to decrease concentration of l-asparagine in the blood, thereby selectively affecting the neoplastic cells¹. The asparaginase from Escherichia coli and Erwinia carotovora are currently being used in the treatment of acute lymphoblastic leukaemia. However, the prolonged administration of l-asparaginase, leads to anaphylactic shock in humans. Therefore, there is a continuing need to screen novel organisms that have the potential to produce high levels of l-asparaginase².

Among the actinobacteria, several Streptomyces sp., such as S. karnatakensis, S. venuzuzlae, S. longsporusflavus, S. gulbargensis and marine Streptomyces sp. PDK2 have been explored for l-asparaginase production³. Extracellular asparaginases are more advantagious than intracellular ones as they can be produced in abundance in the culture broth under normal conditions and can be purified economically⁴. The Andaman coast of India is an outsized diverse and unexploited ecosystem, which can be explored for novel actinobacteria with effective bioactive molecules⁵. Marine actinobacteria with high alkalotolerent and halotolerant characteristics from Andaman and Nicobar (A & N) Islands and their pharmaceutical and industrial importance has already been reported by Meena et al.⁵. Microorganisms from these unexplored environments are expected to have proteins with features different from the organisms from other environments. In this study, an attempt was made to optimize the l-asparaginase production with various medium components using Box-Behnken experimental design and for overexpression of the l-asparaginase biosynthesis gene (ansA) from S. griseus NIOT-VKMA29.

Methods

Actinobacterial isolate and growth conditions. The actinobacterial strain,

NIOT-VKMA29 was isolated from the marine sediments of Phoenix Bay in Port Blair, A & N Islands, India and was grown aerobically in the Starch Casein Agar (SCA) supplemented with nalidixic acid (25 μg mL⁻¹, Hi-Media, India) to inhibit the fast growing Gram-negative bacteria.

Identification of the potential actinobacteria

Morphological, biochemical, cultivatory and physiological characterization of the potential isolate was performed as recommended in the International Streptomyces Project (ISP) described by Shirling and Gottileb⁶. Microscopic examination was performed by cover slip culture and cellophane method. Formation of aerial, substrate mycelium and spore arrangements on mycelium were monitored under a phase contrast microscope (Nikon Eclipse E600, USA) at 100× magnification and a scanning electron microscopy (TESCAN VEGA3, Czech Republic). Genomic DNA of actinobacterial strain NIOT-VKMA29 was isolated by following the modified procedure of Kutchma et al.⁷. Amplification of 16S rRNA was performed using universal primers 16Sf (5′ AGAGTTTGATCCTGGCTCAG 3′) and 16Sr (5′ GGTTACCTTGTTACGACTT 3′). Final volume of PCR was 25 μL, which comprised Taq buffer (1×), dNTP’s (200 μM) (MBI Fermentas, USA), forward and reverse primer (0.5 μM), MgCl₂ (1.0 mM), Taq DNA polymerase (1.25 U) (MBI Fermentas), template (1 μL) and for the rest with autoclaved Milli Q water. PCR was performed in the initial denaturation at 98 °C for 3 min, followed by 30 cycles of reaction with denaturation at 94 °C for 1 min; annealing at 53 °C for 1 min; extension at 72 °C; and final extension at 72 °C for 10 min. PCR amplicon was analyzed on 1.5% agarose gel along with DNA molecular weight marker (MBI Fermentas). Positive amplicon as judged by the size were purified using QIAquick PCR purification kit (Qiagen, Germany) and sequenced on an ABI PRISM 377 genetic analyzer (Applied Biosystems, USA).

16S rRNA sequences of the potential strain were aligned manually in the GenBank database with BLAST⁸ and the sequences with 98–100% homology were considered for molecular taxonomy analysis. Multiple alignments of 16S rRNA sequences in this study and the sequences in GenBank database were performed with the CLUSTAL X program⁹. Phylogenetic trees were constructed by using the neighbor-joining and maximum-parsimony methods in Molecular Evolutionary Genetic Analysis (MEGA version 6.0)¹⁰ and bootstrap values based on 1,000 replication¹¹.

Primary screening and submerged fermentation

Primary screening for l-asparaginase production from S. griseus NIOT-VKMA29 was carried out in asparagine dextrose salt medium containing 1.0% l-asparagine (w/v), 0.2% dextrose (w/v), 0.1% K₂HPO₄ (w/v), 0.05% MgSO₄.7H₂O (w/v), 1.5% agar (w/v) supplemented with 0.009% phenol red (v/v) as an indicator¹². Production of l-asparaginase was performed by shake flask method and the medium with culture and control was incubated at 30 °C for 10 days. l-Asparaginase production and the biomass were monitored every 24 h. Cell growth was expressed in dry weight of biomass³.

Determination of l-asparaginase and l-glutaminase activity

l-Asparaginase activity in the culture filtrates of S. griseus NIOT-VKMA29 was determined according to the method of Imada et al.¹³. The rate of hydrolysis of l-asparagine was determined by measuring the ammonia released using Nessler’s reagent. Protein content in the culture filtrate was estimated by the standard protocol of Lowry et al.¹⁴ using bovine serum albumin as standard. Asparaginase activity was calculated and expressed as units/mg protein.

l-Glutaminase assay was carried out as described previously by Imada et al.¹³ using 189 mM l-glutamine as substrate in 50 mM Tris buffer (pH 8.6) and the absorbance was documented at 436 nm. One International Unit (IU) of l-glutaminase activity is defined as the amount of enzyme required to release 1 μmole of ammonia per mL min⁻¹ at pH 8.6 and 37 °C.

Standardization of culture conditions for l-asparaginase production

One hundred millilitre of production medium was inoculated with S. griseus NIOT-VKMA29 and incubated at various pH (5, 6, 7, 8, 9 and 10) and temperature (20, 25, 30, 35, 37, 40, 45 and 50 °C). The pH at which maximum activity occurs is considered the optimum pH and the temperature at which maximum yield of enzyme observed is considered the optimum temperature³.

The effects of different carbon (1%) and nitrogen (1%) sources on cell growth and l-asparaginase production was studied in the basal medium containing K₂HPO₄ (0.05%) and MgSO4.7H2O (0.01%) at pH 8. The effects of different concentrations of l-asparagine (0.5–2.5%) were examined for l-asparaginase production under induced conditions to check for stimulation of l-asparaginase production by following the procedure of Sudhir et al.⁴.

Optimization of l-asparaginase production by Box-Behnken design

Based on the preliminary studies, 4 parameters, viz., concentrations of l-asparagine (A), yeast extract (Y), starch (S) and pH (P) were identified as factors with a strong influence on l-asparaginase production by S. griseus NIOT-VKMA29. A Box-Behnken design (BBD) with a total of 27 experiments consisting of 24 factorial points (−1 and +1) and 3 central points (0, 0) were employed to understand the influence of the 4 selected parameters on l-asparaginase production. Table 1 shows the experimental plan and the levels of independent variables. All variable levels X_i were coded as x_i according to the following equation, so that X₀ corresponded to the central value:

Table 1 Box-Behnken design along with experimental and predicted l-asparaginase activity (IU/mL).

Where x_i = dimensionless value of an independent variable, X_i = real value of an independent variable, X₀ = real value of an independent variable at the central point and ΔX_i = step change.

The obtained data was fitted by a second-order model to correlate the experimental

l-asparaginase activity to the studied variables. The general form of the second-degree polynomial equation is,

Where Y_i = predicted response (l-asparaginase activity), xi & xj = input variables that influence the l-asparaginase production, β₀ = offset term, β_i = i^th linear coefficient, β_ii = i^th quadratic coefficient and e = error.

The analysis of model was carried out in the form of analysis of variance (ANOVA). The R² statistic indicates the percentage of the variability of optimization parameters that were explained by the model. Three-dimensional surface plots were drawn to illustrate the main and interactive effects of the selected variables on l-asparaginase production. The design was analyzed and the coefficients of the model were tested for their significance by linear regression analysis using MATLAB 6.0. All experiments were conducted in triplicate and mean values were used for analysis.

PCR amplification of l-asparaginase biosynthesis gene

l-Asparaginase biosynthesis gene (ansA) of S. griseus NIOT-VKMA29 was PCR amplified by using gene specific primers designed using Primer3 programme available at http://frodo.wi.mit.edu/primer3 (Table 2). PCR was performed in 50 μL of reaction mixture, which contained 50 ng of genomic DNA, 0.5 μM of each primer, 200 μM each of dNTP (MBI Fermentas), 1.25 U of Pfu DNA polymerase (MBI Fermentas), 1× Pfu buffer; 2.5 mM of MgSO₄ and for the rest autoclaved Milli Q water. Amplification was performed in a Master cycler (Eppendorf, Germany) with the following conditions: initial denaturation at 94 °C for 3 min, followed by 30 repeated cycles of 94 °C for 30 s, 52 °C for 1 min, 72 °C for 2 min and final extension at 72 °C for 10 min. PCR amplicons were analyzed on 1.5% agarose gel along with DNA molecular weight marker (MBI Fermentas) and documented in gel documentation system (UVP BioSpectrum Imaging system, USA).

Table 2 Gene specific primers for l-asparaginase gene.

Cloning and sequencing

PCR amplicon of ansA was purified by MinElute Gel purification Kit (Qiagen, Germany) and cloned into pTZ57R/T (MBI Fermentas), according to the manufacturer’s instructions. pTZ57R/T-ansA construct was transformed into competent E. coli JM109 (recA1, endA1, gyrA96, thi-1, hsdR17 (rK–mk+), e14–(mcrA−), supE44, relA1, Δ(lac-proAB)/F’ (traD36, proAB+, lac Iq, lacZ ΔM15) and plated on Luria Bertani (LB) agar containing ampicillin (100 μg mL⁻¹), isopropyl-β-D-thiogalactoside (IPTG, 50 μM) and X-gal (80 μg mL⁻¹) and incubated overnight at 37 °C. White colonies were selected for PCR amplification with vector primers M13f-M13r (MBI Fermentas) and the clones with correct insert as judged by size were sequenced on an ABI PRISM 377 genetic analyzer (Applied Biosystems Inc., USA).

In silico sequence analysis

The obtained nucleotide sequences were compared with database sequences using BLAST provided by NCBI (http://www.ncbi.nlm.nih.gov) and multiple sequence alignment of the blast hits were carried out using Clustal Omega. The output alignments were imported into the GeneDoc program (http://www.psc.edu/biomed/genedoc/) and the version 7.05 of BioEdit program (www.mbio.ncsu.edu/BioEdit/) to calculate the percent identities among the nucleotide and amino acid sequences. The phylogenetic analyses were carried out using MEGA 6.0 program. The molecular masses and theoretical pI values of the polypeptides were predicted using the ProtParam tool (http://www.expasy.org/tools/protparam.html). The sequence generated in this study was deposited in the GenBank database under the accession number KF724083.

Heterologous expression of l-asparaginase biosynthesis gene

The recombinant plasmid pTZ57R/T-ansA cassette was double digested with EcoRI and BamHI (MBI Fermentas) and purified by the MinElute gel purification kit. The purified ansA gene was religated into pQE30 (Qiagen, Germany), which had previously been digested and purified. The resulting recombinant expression vector pQE30-ansA cassette was transformed into the competent E. coli M15. The overexpression of the l-asparaginase gene in the host cell was performed by following the methodology provided in the QIAexpress Type IV Kit (Qiagen). A single colony of the recombinant clone was inoculated into 10 mL of LB broth containing 100 μg mL⁻¹ ampicillin and 25 μg mL⁻¹ kanamycin and incubated overnight at 37 °C. Approximately 5.0 mL of the culture was transferred into 100 mL LB broth containing 100 μg mL⁻¹ ampicillin and 25 μg mL⁻¹ kanamycin and incubated at 37 °C until the OD₆₀₀ value was reached 0.6–0.7. IPTG was then added to the culture broth at the final concentration of 1 mM and was continuously incubated at 37 °C for 4 h. The induced bacterial cells were harvested by centrifugation and resuspended in 1 × SDS-PAGE sample buffer and lysed in boiling water bath for 3 min. The cells were centrifuged at 4,000 × g for 20 min and the supernatant was checked for soluble proteins to study the expression. The expression of target protein was analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) as described by Laemmli,¹⁵. The molecular mass was estimated with the protein ladder (Sigma, USA).

Results and Discussion

Identification of the potent strain

The actinobacterial strain, NIOT-VKMA29 is a Gram-positive, non-acid fast, non-motile, aerobic and filamentous organism, with very long rods, spores on aerial mycelium are rectiflexible chains as observed by cover-slip method and evaluated by phase contrast microscope (Nikon Eclipse E600, USA) and scanning electron microscopy (TESCAN VEGA3, Czech Republic) (Fig. 1a). The 16S rRNA sequences (1,427 bp) generated in this study were deposited in GenBank under the accession number KF031012. Upon analysis with the BLAST program and phylogenetic analysis, it was established that the deduced nucleotide sequences of NIOT-VKMA29 was highly homologous (100%) with the reported 16S rRNA sequences of S. griseus (GenBank accession no. JX007982) (Fig. 1b). Based on the morphological and biochemical characteristics (Table 3) and the phylogenetic analysis, the isolate NIOT-VKMA29 was identified as S. griseus.

Table 3 Phenotypic characteristics of selected actinobacteria.

Figure 1

(a) Scanning electron microscopic image of S. griseus NIOT-VKMA29 (b) Phylogenetic tree based on 16S rRNA sequences using neighbor-joining method for S. griseus NIOT-VKMA29. Branch distances represent nucleotide substitution rate and scale bar represents the number of changes per nucleotide position.

Standardization of culture conditions for l-asparaginase production

The potent strain was subjected to submerged fermentation to determine the production of l-asparaginase. The production medium was inoculated with S. griseus NIOT-VKMA29 and the enzyme activity was analyzed every 24 h of incubation. Production of l-asparaginase started after 24 h of incubation and reached the maximum after 144 h of incubation (6^th day 5.36 IU mL⁻¹). When the production was carried out in ADS broth at pH 7.4 and temperature 37 °C, the l-asparaginase activity reached 5.36 IU mL⁻¹ (Fig. 2) with merely 0.18 IU mL⁻¹ of glutaminase activity. Amena et al.² and Mostafa and Salama¹⁶, reported the maximum l-asparaginase production on 6^th day in Streptomyces gulbargensis and Streptomyces collinus, respectively.

Figure 2

Effect of batch time, pH and temperature (°C) on enzyme activity.

A study of initial pH levels (5–10) on the production of l-asparaginase by S. griseus NIOT-VKMA29 indicated optimum enzyme production at pH 8 (5.97 IU mL⁻¹). It was found that the strain grows well at an alkali pH of 8 and optimum temperature for enzyme production ranged from 30–35 °C in the optimized production medium. Narayana et al.³ also revealed maximum l-asparaginase production at 35 °C by S. albidoflavus. Extreme pH and temperature did not favor cell growth as well as production of l-asparaginase by S. griseus NIOT-VKMA29. The l-asparaginase production was maximum by S. griseus NIOT-VKMA29 in the production medium with optimized initial pH 8 for 144 h at 35 °C (Fig. 2).

Different carbon sources like starch, glycerol, maltose, glucose and lactose were amended in the production medium to determine their impact on l-asparaginase production. As compared to various carbon sources tested, l-asparaginase production was high (8.93 IU mL⁻¹) in the production medium containing starch (1%) as the carbon source (Fig. 3). The production of l-asparaginase was marginally favourable with low cost substrates viz., starch, glycerol and maltose and there is no significant effect with glucose and lactose. Abdel-Fatah¹⁷ also reported starch as the best carbon source for l-asparaginase production in Streptomyces longsporusflavus. The effect of nitrogen compounds on the production of l-asparaginase by strain S. griseus NIOT-VKMA29 was studied using various nitrogen sources such as soya peptone, malt extract, peptone and yeast extract. l-Asparaginase production by S. griseus NIOT-VKMA29 varied with the different nitrogen sources (Fig. 3). Among them, culture medium amended with yeast extract favoured maximum l-asparaginase production (9.27 IU mL⁻¹) followed by peptone. The final pH of fermentation broth consisting of starch, glycerol and maltose developed alkaline conditions, whereas in medium amended with other carbon sources it developed acidic, which may have led to the decline in productivity of l-asparaginase. The acidity of the fermentation medium could inhibit the production of l-asparaginase¹⁸ and because of this nature, glucose is reported to be the repressor for l-asparaginase production¹⁹. Observations are recorded on the enhancement of l-asparaginase synthesis by different concentrations of l-asparagine in the culture medium. This study was carried out based on the earlier reports that a synthetic medium with l-asparagine as nitrogen source stimulated more enzyme production than biologically by Streptomyces sp.¹⁶. Thus, medium containing different concentrations (0.5–2.5%) of l-asparagine were used and the maximum l-asparaginase activity was found to be 11.27 IU mL⁻¹ at 1.5% of l-asparagine (Fig. 3).

Figure 3

Effect of carbon, nitrogen and l-asparagine concentration on enzyme production.

Optimization of l-asparaginase production by Box-Behnken design

The l-asparaginase activity corresponding to the Box-Behnken experimental run was used as a response for analysis. Table 3 shows that the production of l-asparaginase varies from 20.18 to 56.78 (IU mL⁻¹), indicating the dominant role of selected variables and their concentrations on enzyme production by S. griseus NIOT-VKMA29. The low percentage of variation between the observed and predicted values indicates the accuracy of the experiment. From the results it was clear that only the 3^rd run had an error of 11.60%; in all the other runs it was nearer to 5%, which shows the experiments were conducted with precision.

A multiple regression analysis was performed on the obtained data and the accuracy of the data was tested by the regression coefficient (R²). The regression coefficient (R²) was 0.9878, indicating that only 1.22% of the variability in the response could not be explained by the model. The high value of adjusted R² (0.9737) suggested a higher significance of the model. The correlation plot (Fig. 4), obtained a high adjusted R² value of 0.9737, also indicated that the obtained regression model given a good explanation of the relationship between the independent and response variables. In the present experiment, the coefficient of variance (CV) was 5.32%, which implies good precision and reliability. The application of response surface methodology (RSM) yielded the following regression equation, which is an empirical relationship between the selected parameters and l-asparaginase production.

Figure 4

Correlation between the experimental and predicted l-asparaginase activity.

The coefficients were selected based on their corresponding t, F and p-values (Table 4). The overall p-value of the model is <0.0001 and the F-value is 69.89 (model F-value > p-value), implying that the model is significant. Further, to confirm the acceptance of model, a precision test was performed, which measures the signal to noise ratio. The precision value greater than 4 is considered adequate. In the present experiment, a ratio of 28.789 was observed, indicating an adequate signal. The correlation coefficient, model p and F values and an adequate precision value suggest that the proposed model could be used to navigate the design space.

Table 4 ANOVA, main effects and coefficients.

Coefficients which have a low p-value and high F-value are considered as significant terms. Based on this linear term of starch (S), the interaction terms of l-asparagine with yeast extract, starch (A*Y, A*S) and starch vs. pH (S*P) are insignificant terms. The square term of l-asparagine had the highest effect indicating that it was the most important component for l-asparaginase production. The square terms of l-asparagine, starch and yeast extract have a higher effect value than the linear terms, indicating that these variables have more influence on the enzyme production; any alteration in these levels could influence the production in a significant manner.

The regression equation (Eq. 3) developed here was used to generate 3D and 2D surface & contour plots respectively. Using the drawn surface and contour plots’ interactions, selected parameters at different conditions were evaluated. All contours were circular or elliptical in nature, indicating’s that all selected parameters were independent of each other. Figure 5a,c depicts the interaction of l-asparagine with other selected variables; it was observed that l-asparagine concentration was independent of the carbon and nitrogen sources. l-Asparagine at the concentration range of 1.4–1.6% was optimum for effective l-asparaginase production by S. griseus NIOT-VKMA29. Figure 5a,d,e represents the interaction of yeast extract with other parameters. In Fig. 5e, the contour is slightly inclined towards pH indicating that yeast extract concentration has a slight influence on pH of the medium. From Fig. 5a,d,e it can be seen that yeast extract at a concentration range of 1.9–2.1% is optimum. Figure 5d represents the interaction of carbon and nitrogen sources; this contour is elliptical in nature indicating that both were independent of each other. Figure 5e,f indicates that yeast extract and starch have a minimal influence on the culture pH.

Figure 5

Surface and contour plots of the selected parameters interaction:

(a) l-asparagine with yeast extract (b) l-asparagine with starch (c) l-asparagine with pH (d) yeast extract with starch (e) yeast extract with pH (f) starch with pH.

A numerical method given by Myers and Montgomery,²⁰ was used to solve the regression equation. The optimal values of parameters were as follows: l-asparagine concentration 1.53%, yeast extract concentration 2.04%, starch concentration 1.48% and pH 8.04, with corresponding l-asparaginase production at 56.50 (IU mL⁻¹). On conducting the experiments under these conditions, 56.81 IU/mL of enzyme was obtained. Liu and Zajic,²¹ also found that yeast extract stimulates the production of l-asparaginase in Erwinia aroideae. Yeast extract is essential for cell growth and l-asparaginase production but higher concentrations inhibit the production in Streptomyces albidoflavus³. Sahu et al.²² reported that the Streptomyces sp. such as S. aureofasciculus LA-2, S. canus LA-29 and S. olivoviridis LA-35 exhibited optimum growth and l-asparaginase production at pH range of 7–8.

PCR amplification, molecular cloning and in silico analysis of l-asparaginase gene

The asparaginase biosynthesis gene (ansA) of S. griseus NIOT-VKMA29 encodes polynucleotides of 987 bp, composed of 328 amino acids, with a molecular mass of 33721 Da., based on the in silico estimates (http://www.expasy.org/tools/protparam.html). The isoelectric point of the ansA protein was determined as 5.73. The asparaginase gene was cloned in pTZ57R/T and transformed into E. coli JM109. In silico sequence analysis revealed that the amino acid sequences of ansA gene shared a significant similarity to the l-asparaginase sequences from other Streptomyces species (Fig. 6a). Phylogenetic tree analysis also construes the higher level of homology between the sequences (Fig. 6b). The conserved domain (http://www.ncbi.nlm.nih.gov/Structure/cdd) and motif scan (http://myhits.isb-sib.ch/cgi-bin/motif_scan) analysis revealed that the l-asparaginase of S. griseus NIOT-VKMA29 belongs to l-Asparaginase II family and the amino acid sequences were significantly conserved among the previous reports from Streptomyces species.

Figure 6

(a) Multiple sequence alignment of amino acid substitutions of l-asparaginase in S. griseus NIOT-VKMA29 with GenBank reports (b) Phylogenetic tree analysis using neighbour-joining algorithm with 1000 bootstrap replicates depicting the evolutionary relationship between l-asparaginase from other Streptomyces species. (c) SDS-PAGE analyses of the expressed ansA gene of S. griseus NIOT-VKMA29. Lane a, Total protein of the IPTG induced ansA gene cassette; Lane b, Total protein of the uinduced ansA gene cassette; Lane c, Protein molecular mass marker.

Functional characterization of l-asparaginase biosynthesis gene

The recombinant expression vector pQE30-ansA cassette was transformed into E. coli M15(pREP4). The expression of asparaginase biosynthetic gene was confirmed by Nesslerization assay. The enzyme activity in expressed cells was 123 IU mL⁻¹, which was three times more than that of control cells. The asparaginase biosynthesis gene ansA have been functionally characterized in Nocardiopsis alba²³. Expression of the asparaginase gene was analysed by SDS-PAGE electrophoresis. The lysates of induced cells revealed a clear expressed band with molecular mass of 34 kDa that correspond to ansA, which was not present in the uninduced cells (Fig. 6c). Molecular weight of the purified recombinant asparaginase was similar to the asparaginase reported from S. albidoflavus³.

Conclusion

The production of l-asparaginase from S. griseus NIOT-VKMA29 was increased from 5.36 to 56.78 IU mL⁻¹ in 6^th day after optimization using Box-Behnken design with the following conditions; pH 8.04, l-asparagine 1.53%, yeast extract 2.04% and starch 1.48%. Moreover, the engineered E. coli with l-asparaginase biosynthesis gene has the potential pharmaceutical and industrial application, since it can produce the glutaminase free anti-tumour enzyme at high rates and can avoid the complex down streaming process associated with conventional bioprocess.