Isolation, purification and characterization of the xylanase produced by Arthrobacter sp. MTCC 5214 when grown in solid-state fermentation

• Published in: Enzyme and microbial technology 2006-08, Vol.39 (4), p.732-742
• Main Authors: Khandeparkar, R.D.S., Bhosle, N.B.
• Format: Article
• Language: English
• Subjects: Arthrobacter; Arthrobacter sp; Biological and medical sciences; Biotechnology; Fermentation; Fundamental and applied biological sciences. Psychology; Oryza sativa; Purification; Triticum aestivum; Wheat bran; Xylanase
• ISSN: 0141-0229; 1879-0909
• DOI: 10.1016/j.enzmictec.2005.12.008

Thermoalkalophilic Arthrobacter sp. produced extracellular xylanase, when wheat bran, rice husk, rice bran and bagassae were used as carbon source under solid-state fermentation (SSF). The xylanase enzyme was isolated by ammonium sulfate (80%) fractionation, and purified to homogeneity using size exclusion and ion exchange chromatography. The molecular mass of xylanase was ∼20 kDa. Enzyme retained 100% activity at pH 7 and 8 for 24 h. It was interesting to note that at higher pH such as 9, 10 and 11 the enzyme activity increased over the period of incubation. The optimum temperature for the enzyme activity was 100 °C at pH 9.0. At 80 °C and pH 9, half-life of enzyme was 30 min. Half-life of enzyme at 70 and 60 °C was 18 and 24 h, respectively. While at 50 °C the enzyme retained 79% of activity even after 48 h. For xylan, the enzyme gave a K m value of 0.9 mg/ml, and V max value of 3571 μmol/min/mg when the reaction was carried out at 100 °C and pH 9. In the presence of metal ions such as Co 2+, Zn 2+, Fe 2+, Cu 2+, Mg 2+ and Ca 2+ and metal chelator EDTA the activity of the enzyme increased. Whereas strong inhibition of the enzyme activity was observed in the presence of Hg 2+. These are some novel characteristics that make this enzyme potentially very effective for industrial applications.