Purification of xylanase produced by Bacillus pumilus
Abstract
This study was aimed at purifying xylanase produced by Bacillus pumilus. The spent medium contained 27.9 UmL-1 xylanase activity and 1.5 mgmL-1 protein. The highest specific activity (33.7 Umg-1 protein) was achieved with 50 % (NH4)2SO4 saturation and the xylanase recovery was 94.8 %. The dialyzed and DEAE-Sepharose purified enzyme showed 6.7-fold increase in specific activity with a yield of 84.2 %. Molecular weight of the purified xylanase was 55.4 KDa. Thus B. pumilus xylanase can be purified by precipitating with 50 % (NH4)2SO4 saturation and DEAE-Sepharose ion exchange chromatography.
DOI: http://dx.doi.org/10.4038/jnsfsr.v42i4.7736
J.Natn.Sci.Foundation Sri Lanka 2014 42 (4):365-368
© 2014 Ranganathan Kapilan, Vasanthy Arasaratnam, published by National Science Foundation of Sri Lanka
This work is licensed under the Creative Commons License.