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. 2014 Sep 12;42(18):11393–11407. doi: 10.1093/nar/gku832

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© The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 5. — The 3′ end of bmrB is required for lincomycin-induced bmrCD transcription. A. Schematic representation of a part of plasmids pRM3-bmrB162 and pRM3-bmrB109. pRM3-bmrB162 was constructed by fusing the complete sequence of bmrB and its 5′-UTR to the gfp gene. pRM3-bmrB109 was constructed by fusing a truncated version of bmrB, consisting of this gene's first 109 nucleotides to gfp. Accordingly, pRM3-bmrB109 lacks the predicted terminator within bmrB and part of the predicted anti-terminator. Panels B and C show the GFP fluorescence of B. subtilis carrying pRM3-bmrB162 (B) or pRM3-bmrB109 (C) in response to xylose, lincomycin (0.75 μg/ml), or a combination of xylose and lincomycin added at the time points indicated by arrows. Xylose-induced GFP fluorescence, given in AU, was used as measure for the level of gfp expression.