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. 2017 Dec 5;7:16928. doi: 10.1038/s41598-017-17155-x

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Effect of SepF overexpression on Pbp2B, FtsW and FtsL localization. Microscopic images of (A) strain GYQ72 (amyE::Pxyl-sepF aprE::Pspac-gfp-pbpB) expressing GFP-Pbp2B, (B) strain GYQ74 (amyE::Pxyl-sepF aprE::Pspac-gfp-ftsW) expressing GFP-FtsW, and (C) Strain GYQ204 (amyE::Pxyl-sepF aprE::Pspac-gfp-ftsL) expressing GFP-FtsL, grown in the absence (−) or presence (+) of 1% xylose to induce SepF expression. Membranes were fluorescently stained with FM5-95. Scale bar is 5 µm.