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http://dx.doi.org/10.5352/JLS.2013.23.12.1486

Protease Properties of Protease-Producing Bacteria Isolated from the Digestive Tract of Octopus vulgaris  

Liu, Qing (Department of Food Science and Technology, College of Fisheries Sciences, Pukyong National University)
Ren, Pei (Department of Food Science and Technology, Qingdao Agricultural University)
Piao, Meizi (Department of Food Science and Technology, Qingdao Agricultural University)
Yang, Ji-Young (Department of Food Science and Technology, College of Fisheries Sciences, Pukyong National University)
Publication Information
Journal of Life Science / v.23, no.12, 2013 , pp. 1486-1494 More about this Journal
Abstract
A high protease-producing strain was isolated and identified from the digestive tract of octopus vulgaris by detecting a hydrolysis circle of protease and its activity. The strain was identified by morphology observation, biochemical experiments, and 16S rRNA sequence analysis. The protease obtained from the strain was purified by a three-step process involving ammonium sulfate precipitation, carboxy methyl-cellulose (CM-52) cation-exchange chromatography, and DEAE-Sephadex A50 anion-exchange chromatography. The properties of protease were characterized as well. The strain Bacillus sp. QDV-3, which produced the highest activity of protease, was isolated. On the basis of the phenotypic and biochemical characterization and 16S rRNA gene-sequencing studies, the isolate was identified as follows: domain: Bacteria; phylum: Firmicutes; class: Bacilli; order: Bacillales; family: Bacillaceae; and genus: Bacillus. The isolate was shown to have a 99.2% similarity with Bacillus flexus. A high active protease designated as QDV-E, with a molecular weight of 61.6 kDa, was obtained. The enzyme was found to be active in the pH range of 9.0-9.5 and its optimum temperature was $40^{\circ}C$. The protease activity retained more than 96% at the temperature of $50^{\circ}C$ for 60 min. Phenylmethylsulfonyl fluoride (PMSF) inhibited the enzyme activity, thus confirming that this protease isolated from Bacillus sp. QDV-3 is an alkaline serine protease. Metal ions, $Mn^{2+}$ and $Mg^{2+}$, were determined to enhance the protease activity, whereas $Ba^{2+}$, $Zn^{2+}$, and $Cu^{2+}$ were found to inactivate the enzyme.
Keywords
Identification; intestinal bacteria; octopus vulgaris; protease; purification;
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