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. 2022 Jan 10;21:8. doi: 10.1186/s12934-021-01735-8

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© The Author(s) 2022

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. 11 — Growth of Synechocystis engineered strains during high-density cultivation for 4 days. A schematic representation of the CellDeg HDC 6.10B system. The cultivation bath is filled with 3 M carbonate buffer and constantly creates a CO₂ rich atmosphere with diffuses through a porous hydrophobic membrane to the culture medium. Oxygen ventilation of growing cultures is provided by gas permeable membrane outlet on the lid of cultivation vessel. B growth of strains EvC, PcC, PcN; C strains EvC AtC, AtN; D strains EvC, NpC, NpN; E strains EvC, AvC, AvN; F strains EvC, TsC TsN. For each strain at least two independent cultivations experiments with biological triplicates was carried out. Error bars represent standard deviation