OPTIMIZATION OF PROTEASE PRODUCTION FROM BACTERIA ISOLATED FROM SOIL

سال انتشار: 1394
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 367

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شناسه ملی سند علمی:

JR_ARJ-1-7_003

تاریخ نمایه سازی: 26 اسفند 1394

چکیده مقاله:

Microbial proteases contribute nearly 40% of the total worldwide enzyme market. Hence, with the view of this significance, objective of the present study was to isolate and optimize the protease production from soil borne bacteria. Soil is the ideal habitat for many extracellular enzyme producingbacteria therefore soil samples were collected from two different sites of Banasthali University and bacteria were isolated by serial dilution agar platetechnique. Isolated bacteria were screened on gelatin agar medium for proteolytic activity. Based on the results of primary screening 4 bacterialisolates from soil sample 1 and 4 bacterial isolates from soil sample 2 were selected for protease production in production medium. Four bacterialisolates from soil sample 1 were named as AKS-1, AKS-2, AKS-3 and AKS-4, respectively. Four bacterial isolates from soil sample 2 were namedas AKS-5, AKS-6, AKS-7 and AKS-8, respectively. Isolate AKS-4 exhibited maximum protease activity (44.89 U/mL) after 48 h of incubationand isolate AKS-2 was producing minimum protease activity (2.37 U/mL) after 72 h of incubation. Isolate AKS-6 exhibited maximum proteaseactivity (37.94 U/mL) after 3 days of incubation and isolate AKS-8 was producing minimum protease activity (1.22 U/mL) after 3 days ofincubation. Hyper producing isolates (AKS-4 and AKS-6) from both soil samples were selected for optimization study. The optimum conditions for protease production by isolate AKS-4 were found to be at pH 8.5 after 5 days of incubation using glucose as carbon source and casein as nitrogen source. Maximum yield of enzyme was obtained by isolate AKS-6 at pH 10.5 after 5 days of incubation using starch as carbon source and casein as nitrogen source. Among all studied bacterial isolates, the maximum protease activity (52.29 U/mL) was recorded in isolate AKS-4 after optimization of culture conditions.

نویسندگان

Arun Kumar Sharma

Department of Bioscience and Biotechnology, Banasthali University, Rajasthan, India.

Vinay Sharma

Department of Bioscience and Biotechnology, Banasthali University, Rajasthan, India.

Jyoti Saxena

Department of Biochemical Engineering, Bipin Tripathi Kumaon Institute of Technology, Dwarahat, Uttrakhand.

Bindu Yadav

Department of Bioscience and Biotechnology, Banasthali University, Rajasthan, India.