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. 2018 Sep 11;8:13576. doi: 10.1038/s41598-018-31851-2

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© The Author(s) 2018

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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Fluorescence microscopy of S. oneidensis MR1 cells producing GFP and mCherry fused respiratory proteins. The genetic context of the strains, the plasmids harboured (pBAD33 derivatives) and the fluorescent chimeras are indicated in each panel. Cells were grown in a rich medium supplemented with fumarate (panels: a, c, e, f, g, i, k) or with electron acceptors inducing specific respiratory systems of S. oneidensis: TMAO (panels b and d); nitrate (panels h, j, l) and that are indicated on the edge of the panels. TMAO (−) stands for no TMAO added in the medium preventing chromosomal gene expression and thus the production of the Tor components.