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. 2016 Mar 29;15:57. doi: 10.1186/s12934-016-0455-1

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© Ploss et al. 2016

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 — Influence of degUhy32 and rok on P(amyQ)-M promoter activity. P(amyQ)-M promoter activities were determined by fluorescence intensity measurements using LCA for the B. subtilis 168 wild-type strain (diamond) and mutants 168degUhy32 (square) or 168∆rok (open circle) carrying plasmid pDAPamy-gfp tet with the transcriptional P(amyQ)-M-gfpmut3 fusion. Strains were grown in LB medium over a cultivation period of 400 min