Abstract

Nichawee Wipusaree1, Prakitsin Sihanonth2, Jittra Piapukiew3, Polkit Sangvanich4and Aphichart Karnchanatat5*

Xylanases are a class of enzymes that degrade -1, 4-xylan, a linear polysaccharide found as hemicellulose in plant cell walls, in xylose. They are one of the most important enzyme groups used in industry and agriculture. Fifty-four endophytic fungi were isolated and examined for xylanase production. Xylanase activity was found in thirty of the isolates in primary screening by growing on solid xylan agar plates. After secondary screening for xylanase activity in xylan liquid culture, the isolate that yielded the highest xylanase-production (PTRa9) was selected for further evaluation. Optimal xylanase production was achieved after 4 days of culture with 2% (w/v) rice bran and 0.1% (w/v) ammonium sulfate as the carbon and nitrogen source respectively. This xylanase was enriched 60.8-fold to apparent homogeneity by sequential ammonium sulphate precipitation, Diethylaminoethyl (DEAE)-cellulose ion exchange and Superdex 75 gel filtration chromatography. The resultant 54.8 kDa protein had a specific activity of 161.1 U/mg protein, an optimal temperature of 45°C, with >90% activity from -20 to 45 oC, a broad pH range of 3.0 to 11.0 (optimal at pH 5.0),and was sensitive to most divalent cations but especially by Hg2+, Cu2+and EDTA. From the kinetic analysis, it had a Kmof 0.421 mg/ml and a Vmaxof 0.826 U/mg protein