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. 2014 Aug 6;2:60. doi: 10.3389/fchem.2014.00060

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Copyright © 2014 Rahman, Inoue and Ojima.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Purification of AkEG21 by Superdex 200 gel filtration. The P-2 fraction obtained in the TOYOPEARL CM-650M column chromatography was subjected to gel filtration through Superdex 200 10/300 GL. Fractions 14–16 were pooled as the purified AkEG21. SDS-PAGE for cellulase preparations from A. kurodai is shown in the inset. Mk, marker protein; P-2, the sample after TOYOPEARL CM-650M chromatography; Fr. 15, purified AkEG21.