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Production of Naringinase by Using Amla on Solid State Fermentation


Affiliations
1 Associate Professor, Department of Biotechnology, Nirmala College of Pharmacy, Atmakuru, Mangalagiri, Guntur., India
2 Principal, KVSR Siddhartha College of Pharmaceutical Sciences Vijayawada, Andhra Pradesh., India
3 Principal, Nirmala College of Pharmacy, Atmakur, Andhra Pradesh., India
4 Assistant Professor, KVSR Siddhartha College of Pharmaceutical Sciences, Vijayawada, Andhra Pradesh., India
     

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Microbial enzymes are widely used in different pharmaceutical, textile and in leather industries, mainly because of vast availability of sources. They could be genetically modified and are considered as more economical in comparison to plant and animal enzymes. Production of microbial enzymes by application of fermentation involves microbial propagation like bacteria, mold and yeast to get useful product. There are two methods of fermentation used to produce microbial enzymes called submerged fermentation and solid-state fermentation. Submerged fermentation involves the production of enzymes by using microorganisms in a liquid state nutrient media. Solid-state fermentation is the cultivation of microorganisms in solid substrate. Nutrients containing carbon compounds are broken down by the microorganisms, which produce the enzymes either intracellular or extracellular. Industries that use enzymes generated by fermentation are the brewing, wine making, baking, cheese making, dairy, beverages, and cereals. In the present study Asperigillus Niger strain was used to produce the extra cellular naringinase enzyme in nutrient medium containing Amla as a solid substrate. Amla is the chief material for the production maximum Naringinase enzyme. The study also involved in the optimization of various physical parameters like temperature, PH, incubation period, mass of inoculum. The study concluded that pH -5.5, temperature of 28oc, incubation period of 96 hrs and 20% of inoculums for maximum naringinase production.

Keywords

Naringinase, Amla, Asperigillus Niger, solid state fermentation, Enzymes.
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  • Yusof S. Ghazali HM. King GS. Naringin content in local citrus fruits. Journal of Food Chemistry. 1990: 37(2):113-121.
  • Narendra Kumar G. Karthik Raja S. Arul Luca Sunder Singh R. Production and optimization of extracellular fungal chitinase produced by Metarhizium anisopliae (M) Sorokin through Submerged and solid state fermentation. Research J.Pharm and Tech. 2015:8(3):28-284. doi:10.5958/0974-360X.2015.00047.5
  • Abdel-Fattah Y. Optimization of thermo stable lipase production from a thermophilic Geobacillus sp. using Box–Behnken experimental design. Biotechnology Letter. 2002:24(4): 1217–1222.
  • Abel H, Marie D, Nathalie R, Danielle D, Louis S, Louis C. Purification and characterization of an extracellular lipase from a thermophilic Rhizopus oryzae strain isolated From palm fruit. Enzyme Microbial Technology. 2000:26(4):421–430.
  • Canganella F, Andrade C, Antranikian G. Characterization of amylolytic and pullulytic enzymes from thermophilic archaea and from a new Ferivido bacterium species. Applied Microbiology Biotechnology. 1994:42 (5): 239–245.
  • Bertoldo C, Duffner F, Jorgensen P, Antrakianin G. Pullulanase type I from Ferividobacteriumpennavorans VEN5: cloning, sequencing, expression of the gene and biochemical characterization of the recombinant enzyme. Applied Microbiology Biotechnology. 2012: 65 (5): 2084–2091.
  • Utharalakshmi. N. Ganesh Kumar. A. Narendra kumar.G. Optimization of cellulose producing Aspergillus flavus SB4 by Solid state Fermentation using Response Surface Methodology (RSM)-CCD. Research J. Pharm. and Tech. 2015:8(4): 349-354.
  • Pandey RA, Malhotra S, Tankhiwale A, Pande S, Pathe PP, Kaul SN, Treatment of biological treated distillery effluent – A case study. International Journal of Environmental Studies. 2003: 60(4): 263-275.
  • Saravanan R. Dhachinamoorthi D. Renuga G. Senthil kumar K. Production of L. Aspariginase from Pectbacterium carotovorum (MTCC 1428) and Bacillus circulans (MTTCC1428). Research J. Pharm. and Tech. 2011: 4(8): 1323-1327.
  • Narta UK, Kanwar SS, Azmi W. Pharmacological and clinical evaluation of L- Asparaginase in the treatment of leukemia. Crit Rev Oncol Hematol. 2007; 61(5): 208–221.
  • Magiera S. Kwietniowska E. Fast, Simple and Efficient salting-out assisted liquid-liquid extraction of naringenin from fruit juice samples prior to their enantioselective determination by liquid chromatography. Food Chemistry. 2016; 211(7):227-234.
  • Abeer Nasr Shehata. Abeer Abas Abd El Aty. Optimization of Process Parameters by Statistical Experimental Designs for the Production of Naringinase Enzyme by Marine Fungi International Journal of Chemical Engineering. 2014: 5(7): 232-248 http://dx.doi.org/10.1155/2014/273523.
  • Bram B. Solomon G.L. Production of Naringinase by A.niger, Applied Microbiology. 1965: 13(6): 842–845.
  • Okado j et.al., S.naringinase production by fermentation. Japan patent. 73,06,554(1973).
  • Saravanan R. Dhachinamoorthi D. Renuga G. Senthil Kumar K. Production of L-Asparaginase from Pectobacterium carotovorum (MTCC 1428) and Bacillus circulans (MTCC 1428). Research J. Pharm. and Tech. 2011; 4(8):1323-27.
  • Utharalakshmi N. Ganesh Kumar A. Narendra kumar K. Optimization of Cellulase Producing Aspergillus flavus SB4 by Solid State Fermentation using Response Surface Methodology (RSM)-CCD. Research J. Pharm. and Tech. 2015; 8(4):349-354. doi: 10.5958/0974-360X.2015.00058.X
  • Davis,W. B. 1947 Determination of flavones in citrus fruits anal. Chem. 19:476-478.
  • Supriya C. Hari Priya.K. Abdul tallahat. Production of tannase enzyme by using Aspergillus niger (ATCC1644) strain on solid substrate fermentations. Int. J. Pharm and Ind. Res., 2014; 4 (3):76 – 81.

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  • Production of Naringinase by Using Amla on Solid State Fermentation

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Authors

Supriya Chatla
Associate Professor, Department of Biotechnology, Nirmala College of Pharmacy, Atmakuru, Mangalagiri, Guntur., India
Devalarao Garikapati
Principal, KVSR Siddhartha College of Pharmaceutical Sciences Vijayawada, Andhra Pradesh., India
Abdul Rahaman
Principal, Nirmala College of Pharmacy, Atmakur, Andhra Pradesh., India
Iswarya Obilineni
Assistant Professor, KVSR Siddhartha College of Pharmaceutical Sciences, Vijayawada, Andhra Pradesh., India

Abstract


Microbial enzymes are widely used in different pharmaceutical, textile and in leather industries, mainly because of vast availability of sources. They could be genetically modified and are considered as more economical in comparison to plant and animal enzymes. Production of microbial enzymes by application of fermentation involves microbial propagation like bacteria, mold and yeast to get useful product. There are two methods of fermentation used to produce microbial enzymes called submerged fermentation and solid-state fermentation. Submerged fermentation involves the production of enzymes by using microorganisms in a liquid state nutrient media. Solid-state fermentation is the cultivation of microorganisms in solid substrate. Nutrients containing carbon compounds are broken down by the microorganisms, which produce the enzymes either intracellular or extracellular. Industries that use enzymes generated by fermentation are the brewing, wine making, baking, cheese making, dairy, beverages, and cereals. In the present study Asperigillus Niger strain was used to produce the extra cellular naringinase enzyme in nutrient medium containing Amla as a solid substrate. Amla is the chief material for the production maximum Naringinase enzyme. The study also involved in the optimization of various physical parameters like temperature, PH, incubation period, mass of inoculum. The study concluded that pH -5.5, temperature of 28oc, incubation period of 96 hrs and 20% of inoculums for maximum naringinase production.

Keywords


Naringinase, Amla, Asperigillus Niger, solid state fermentation, Enzymes.

References