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. 2021 Feb 8;20:39. doi: 10.1186/s12934-021-01529-y

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 3 — Succinate titers in the growth medium of Synechocystis strains created in this study in light and darkness. Cells were grown in pre-cultures, then concentrated and incubated for four days in 20 µE m⁻² s⁻¹ light (a) or in darkness (b), before determination of succinate titers. BG11 and BG11₀ corresponds to media with nitrate or without any nitrogen source, respectively. 5 µM of NiCl₂ was added for induction of gene expression. Error bars represent the mean ± SD