Journal
BIORESOURCE TECHNOLOGY
Volume 99, Issue 7, Pages 2544-2551Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.biortech.2007.04.035
Keywords
tannase; Chebulina myrobalan; purification; Penicillium variable
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Tannase from Penicillium variable IARI 2031 was purified by a two-step purification strategy comprising of ultra-filtration using 100 kDa molecular weight cutoff and gel-filtration using Sephadex G-200. A purification fold of 135 with 91% yield of tannase was obtained. The enzyme has temperature and pH optima of 50 degrees C and 5 degrees C, respectively. However, the functional temperature range is from 25 to 80 degrees C and functional pH range is from 3.0 to 8.0. This tannase could successfully be immobilized on Amberlite IR where it retains about 85% of the initial catalytic activity even after ninth cycle of its use. Based on the Michaelis-Menten constant (K-m) of tannase, tannic acid is the best substrate with K-m of 32 mM and V-max of 1.11 mu mol ml(-1) min(-1). Tannase is inhibited by phenyl methyl sulphonyl fluoride (PMSF) and N-ethylmaleimide retaining only 28.1% and 19% residual activity indicating that this enzyme belongs to the class of serine hydrolases. Tannase in both crude and crude lyophilized forms is stable for one year retaining more than 60% residual activity. (C) 2007 Elsevier Ltd. All rights reserved.
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