Abstract
Background: L-asparaginase is one of the most widely used chemotherapeutic agents for
the treatment of a variety of lymphoproliferative disorders and particularly acute lymphoblastic leukemia.
Due to increased applications of L-asparaginase in several industrial fields including food processing
and medical fields, its production needs to be increased to several folds.
Objectives: The aim was (i) to identify the significant factors which affect L-asparaginase production
by Streptomyces fradiae NEAE-82 and (ii) to achieve higher production of L-asparaginase.
Methods: Sixteen assigned factors and three dummy factors were screened using Plackett-Burman experimental
design to determine the most important factors for the production of L-asparaginase by
Streptomyces fradiae NEAE-82.
Results: L-asparagine was determined to be the most significant positive independent factor (P-value
0.0092) affecting L-asparaginase production by Streptomyces fradiae NEAE-82 followed by pH and
NaCl with significant P-values of 0.0133 and 0.0272; respectively. These factors were further optimized
by Box-Behnken experimental design. The optimized fermentation conditions, which resulted in
the maximum L-asparagine activity of 53.572 UmL-1 are g/L: dextrose 4, L-asparagine 15, KNO3 2,
MgSO4.7H2O 0.5, K2HPO4 1, FeSO4.7H2O 0.02, NaCl 0.2, ZnSO4 0.01 and inoculum size 2 %, v/v for
7 days incubation at temperature 37°C, agitation speed 100 rpm, pH 8.5.
Conclusion: A total of 3.41-fold increase in the production of L-asparaginase was achieved in the medium
after statistical improvement (53.572 UmL-1) as compared to the unoptimized basal medium used
prior to the application of Plackett-Burman (15.704 UmL-1).
Keywords:
L-asparaginase production, Streptomyces fradiae NEAE-82, Plackett-Burman, Box-Behnken designs, lymphoblastic
leukemia, lymphocytes.
Graphical Abstract
[2]
Jain R, Zaidi K, Verma Y, Saxena P. L-asparaginase: A promising enzyme for treatment of acute lymphoblastic leukemia. People’s J Sci Res 2012; 5(1): 29-35.
[4]
Kumar K, Verma N. The various sources and application of L-asparaginase. Asian J Biochem Pharm Res 2012; 2: 197-205.
[5]
Savitri AN, Azmi W. Microbial L-asparaginase: A potent antitumour enzyme. Int J Biotechnol 2003; 2: 184-94.
[8]
Reynolds D, Taylor J. The fungal holomorph: A consideration of mitotic, meiotic and pleomorphic speciation Wallingford, UK. Wallingford, UK: CAB International 1993.
[11]
Maysa E, Amira M, Gamal E, Sanaa T, Sayed E. Production, immobilization and anti-tumor activity of L-asparaginase of Bacillus sp. R36. J Am Sci 2010; 6: 157-65.
[13]
Patro KKR, Satpathy S, Gupta N. Evaluation of some fungi for Lasparaginase production. Ind J Fund Appl Life Sci 2011; 1: 219-21.
[15]
El-Naggar NE, Abdelwahed NA. Optimization of process parameters for the production of alkali-tolerant carboxymethyl cellulase by newly isolated Streptomyces sp. strain NEAE-D. Afr J Biotechnol 2012; 11: 1185.
[25]
De jong PJ. L-asparaginase production by Streptomyces griseus. Appl microbial 1972; 23: 1163-4.
[27]
Saxena RK, Sinha U. L-asparaginase and glutaminase activities in the culture filtrates of Aspergillus nidulans. Curr Sci 1981; 50: 218-9.
[38]
Sreenivasulu V, Jayaveera K, Rao PM. Optimization of process parameters for the production of L-asparaginase from an isolated fungus. Res J Pharmaco Phytochem 2009; 1: 30-4.
[39]
Sudhir AP, Dave BR, Trivedi KA, Subramanian RB. Production and amplification of an l-asparaginase gene from actinomycete isolate Streptomyces ABR2 Ann microbial 2012; 62: 1609-14.
[40]
Gurunathan B, Sahadevan R. Design of experiments and artificial neural network linked genetic algorithm for modeling and optimization of L-asparaginase production by Aspergillus terreus MTCC 1782. Biotechnol bioproc Eng 2011; 16: 50-8.
[42]
Pattnaik S, Kabi R, Ram KJ, Bhanot K. L-Asparaginase activity in Aeromonas sp. isolated from freshwater mussel. Indian J Exp Biol 2000; 38: 1143-6.
[43]
Jain P, Pundir R. Effect of fermentation medium, pH and temperature variations on antibacterial soil fungal metabolite production. Agric Technol Thail 2011; 7: 247-69.
[46]
Mathew A, Dhevendaran K, Georgekutty M, Natarajan P. L-asparaginase activity in antagonistic Streptomycetes associated with clam Villorita cyprinoides (Hanley). Indian J Geo-Mar Sci 1994; 23: 204-8.
[47]
Monica T, Lincoln L, Niyonzima F, Sunil S. Isolation, purification and characterization of fungal extracellular L-asparaginase from Mucor Hiemalis. J Biocatal Biotransf 2013; 9: 12-4.
[50]
Nei M, Kumar S. Molecular evolution and phylogenetics. New York: Oxford University Press 2000.
[51]
Fisher SH, Wray LV. Bacillus subtilis 168 contains two differentially regulated genes encoding L-asparaginase. J bacterial 2002; 184: 2148-54.
[55]
Shakambari G, Sumi BM, Ashokkumar B, Palanivelu P, Varalakshmi P. Industrial effluent as a substrate for glutaminase free. Lasparaginase production from Pseudomonas plecoglossicida strain RS1; media optimization, enzyme purification and its characterization RSC Adv 2015; 5: 48729-38.
[57]
Weisberg S. Applied Linear Regression. 2nd ed. New York, USA: John Wiley and Sons 1985.
[58]
Box GEP, Hunter WG, Hunter JS. Statistics for Experiments. New York, USA: John Wiley and Sons Inc. 1978; pp. 291-334.