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. 2017 Apr 20;10:100. doi: 10.1186/s13068-017-0783-3

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© The Author(s) 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 4 — Effect of the point mutation XlnR^A871V on the production of extracellular enzymes on wheat bran. FPase (a), pNPCase (b), CMCase (c), pNPGase (d), xylanase (e) and pNPXase activities (f), and extracellular protein concentrations (g) of supernatants from wild-type, xlnR ^A871V, and gpdA(p)::xlnR strains were analyzed. All error bars represent the standard deviations. Statistical significance of the differences between wild-type and xlnR ^A871V at 120 h was calculated. *p < 0.05, **p < 0.01, ***p < 0.001. h SDS-PAGE analysis of the supernatants of the wild-type and xlnR ^A871V strains. The protein bands 1–5 were identified by MS–MS as listed in Table 2