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A Temperature and Salt-Tolerant l-Glutaminase from Gangotri Region of Uttarakhand Himalaya: Enzyme Purification and Characterization
Authors:Lokendra Kumar  Balvinder Singh  Dilip Kumar Adhikari  Joydeep Mukherjee  Debashish Ghosh
Affiliation:(1) Department of Biochemistry, Sardar Bhagwan Singh PG Institute of Biomedical Sciences and Research, Balawala, Dehradun, 248161, India;(2) Department of Biochemistry, Dolphin PG Institute of Biomedical and Natural Science, Dehradun, 248007, India;(3) Biotechnology Area, Indian Institute of Petroleum (CSIR), Dehradun, 248005, India;(4) School of Environmental Studies, Jadavpur University, Kolkata, 700032, India;
Abstract:Purification and characterization of halotolerant, thermostable alkaline l-glutaminase from a Bacillus sp. LKG-01 (MTCC 10401), isolated from Gangotri region of Uttarakhand Himalaya, is being reported in this paper. Enzyme has been purified 49-fold from cell-free extract with 25% recovery (specific activity 584.2 U/mg protein) by (NH4)2SO4 precipitation followed by anion exchange chromatography and gel filtration. Enzyme has a molecular weight of 66 kDa. l-Glutaminase is most active at pH 11.0 and stable in the pH range 8.0–11.0. Temperature optimum is 70 °C and is completely stable after 3 h pre-incubation at 50 °C. Enzyme reflects more enhanced activity with 1–20% (w/v) NaCl, which is further reduced to 80% when NaCl concentration was increased up to 25%. l-Glutaminase is almost active with K+, Zn2+, and Ni2+ ions and K m and V max values of 240 μM and 277.77 ± 1.1 U/mg proteins, respectively. Higher specific activity, purification fold, better halo-tolerance, and thermostability would make this enzyme more attractive for food fermentation with respect to other soil microbe derived l-glutaminase reported so far.
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