Abstract
Aspergillus niger strains 1, 2 and 3 isolated from cassava dumpsites were used for the production of amylase enzyme. The Aspergillus niger strains 1, 2 and 3 had diameter (mm) zone of clearance of 17.0, 23.0 and 8.0 respectively using Potato dextrose agar plates fortified with starch. Studies on the amylase enzyme activity (mg/ml) of Aspergillus niger strains 1 and 2 showed 19,340 and 16,510 respectively. These values were higher than the commercially available amylase enzyme that had an activity of 5,722.2. The protein (mg/ml) and specific activity (units/mg) for amylase from Aspergillus niger strain 1 was 28.39 and 681.23 while 21.76 and 758.73 from Aspergillus niger 2 respectively. Purification using ammonium sulphate (% w/v) at 60, 80 and 100 on amylase enzyme from Aspergillus niger strain 1 for enzyme activity, protein and specific activity was 44405.49, 17.01 and 2610.55, 28949.76, 23.62 and 1225.65, 36220.25, 16.67, and 2172.787 respectively. The microbial production of Amylase enzyme in Nigeria from Cassava peel will reduce cost of production, convert cassava peel from waste condition to wealth, and will boost economy through indigenous industrialization.
References
Anselme P, Jean-Francois PS. Memior on diastase, the principal products of its reactions and their applications to the industrial arts. Annaled de chimie et de physique 1883; 2nd series 53: 73-92.
Dixon M, Webb EC. Enzymes. 2nd edn. Longmans Publishers, London 1964
Forgaty WM, Kelly CT. Recent advances in microbial amylases. In microbial enzymes and Biotechnology 2nd edition. Elsevier Applied Science London 1991; pp. 71-132.
Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951; 193: 265-75.
Okafor N. Patents and free communication in Industrial Microbiology. Industrial Microbiology, University of Ile-Ife Limited, Ile-Ife., 1989.
Orji FA, Dike EN, Lawal AK, et al. Production of Cellulase from Bacillus species using Cellul;ose from Brewers Spent Grain (BSG) as Sole Carbon Source. Asian J Microbiol Biotechnol Environ Sci 2013; 15(4): 839-48.
Ramakrishma SV, Suseela T, Ghilyal NP, et al. Indian J Technol 1982; 20: 476-80.
Miller GL. Use of Dinitrosalicylic Acid reagent for determination of reducing sugars. Anal Chem 1959; 31: 426-28. http://dx.doi.org/10.1021/ac60147a030
Ohimain EI, Izah SC, Jenakumo E. Physico-chemical and Microbial screening of Palm Oil mill effluents for Amylase production. Greener J Biol Sci 2011; 3(8): 307-18.
Nwagwu TN, Okolo BN. Extracellular production of a thermo-tolerant Fusarium species isolated from Eastern Nigeria Soil, Braz Archiv Biol Technol 2011; 5(4): 649-58. http://dx.doi.org/10.1590/S1516-89132011000400002
Akpomie OO, Akponah E, Okorawhe P. Amylase production potentials of bacterial isolates obtained from Cassava root peels. Agric Sci Res J 2012; 2(2): 95-99.
Zadrazil F, Punia AK. Studies on the effect of particle size on solid state fermentation of sugar cane bagasse into animal feed using white rot fungi. Biores Technol 199; 54: 85-97.
Sen S, Veeranki VD, Mandal B. Effect of physical parameters, carbon and nitrogen sources on the production of alkaline protease from a newly isolated Bacillus pseudofirmus SVB1. Ann Microbiol 2009; 59(3): 531-38. http://dx.doi.org/10.1007/BF03175142
Ominyi MC, Ogbonna JC, Nwoba EG, Nwagu KE, Ukachi R. Isolation, and screening of ?-amylase and Glucoamylase producing fungi and their Glucomaylase producing fungi and their application in Bioethanol, production. Int J Sci Nat 2013; 4(1): 44-50.
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Copyright (c) 2014 A.K. Lawal, A.M. Banjoko, S.O. Olatope, F.A. Alebiosu, F.A. Orji, Y.L. Suberu, E.E. Itoandon, K.A. Shittu, O.D. Adelaja, E. Ojo, E.N. Dike, G.N. Elemo