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Open AccessJournal Article

Production of Microbial Protease from Selected Soil Fungal Isolates

O. A. Oseni
- 01 Jan 2011 - 
- Vol. 23
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TLDR
The results of the enzyme activity showed that the organisms; Aspergillus flavus, As pergillus niger, AsPergillus fumigatus and Penicillium italicum produced the protease enzyme maximally between day three and day five of incubation while the effect of temperature and thermal stability on the enzyme production showed temperature optimal for enzyme production was between 30 and 60 0 C.
Abstract
This study was undertaken to monitor the production of protease enzyme from soil fungal isolates obtained from Omo natural forest in Ogun State of Nigeria. The study also sought to determine the kinetic parameters of the enzyme with the aim of establishing the industrial and biotechnological importance of this microbial enzyme. The harvested mycelia of the fungi were separately homogenized in buffered culture medium for five days using shaker incubator in which the protease activity was monitored. The results of the enzyme activity showed that the organisms; Aspergillus flavus, Aspergillus niger, Aspergillus fumigatus and Penicillium italicum produced the protease enzyme maximally between day three and day five of incubation while the effect of temperature and thermal stability on the enzyme production showed temperature optimal for enzyme production was between 30 and 60 0 C and the thermal stability on the enzyme activity was between 30 and 50 0 C. The optimal pH on the enzyme production was observed to be between pH 3.5 and 5.5 for the organisms. Keywords: Soil microorganism, fungal isolate, incubation period, microbial enzyme Nig J. Biotech . Vol. 23 (2011) 28 - 34

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Impact of microbial proteases on biotechnological industries.

TL;DR: Genetically engineered strains or engineered proteases have much more importance over natural isolates/protease in industries due to higher production rate and other advantages.
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Protease production by thermo-alkaliphilic novel gut isolate Kitasatospora cheerisanensis GAP 12.4 from Gryllotalpa africana

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Isolation and Characterization of Neutral Proteases Producing Soil fungus Cladosporium sp PAB2014 Strain FGCC/BLS2: Process Optimization for Improved Enzyme Production

TL;DR: Isolate FGCC/BLS2 showed maximum hydrolysis capacity when compared to wild type positive reference strain Aspergillus flavus and optimum physico-cultural conditions for enhanced protease production from selected isolate were investigated.
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References
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Journal ArticleDOI

Short-term assays of soil proteolytic enzyme activities using proteins and dipeptide derivatives as substrates

TL;DR: The soils investigated exhibited optimal protease activity near pH 8.0 and 60°C, and were consistent in their preferential hydrolysis of dipeptide derivatives containing amino acids with hydrophobic side chains, however, soils varied widely in their relative activities towards a given diPEptide derivative and towards benzoyl arginine amide, a cationic substrate used in the assay of ‘trypsin-like’ enzymes.
Journal ArticleDOI

An overview on fermentation, downstream processing and properties of microbial alkaline proteases

TL;DR: Alkaline proteases useful for detergent applications are mostly active in the pH range 8–12 and at temperatures between 50 and 70°C, with a few exceptions of extreme pH optima up to pH 13 and activity at temperatures up to 80–90°C.
Journal ArticleDOI

Comparative evaluation of neutral protease production by Aspergillus oryzae in submerged and solid-state fermentation

TL;DR: In this article, a comparative study was carried out on the production of neutral protease using agro-industrial residues as substrate in solid-state fermentation (SSF) and submerged fermentation (SmF).
Journal ArticleDOI

Studies on production of thermostable alkaline protease from thermophilic and alkaliphilic Bacillus sp. JB-99 in a chemically defined medium

TL;DR: The thermophilic and alkaliphilic Bacillus sp. JB-99 was isolated from sugarcane molasses and was cultured in 250 ml Erlenmeyer flasks containing 50 ml of synthetic medium consisting of (g/l): citric acid; 10.0, NaNO 3 ; 10.
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