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. 2021 Mar 18;43(7):1323–1336. doi: 10.1007/s10529-021-03104-2

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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/.

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Fig. 6 — Deletion of creA in JR11.1 results in ferulic acid independent expression from the faeB promoter. a and b Strains JR11.1 and JR11.1 ΔcreA were grown on MM containing 1 % D-fructose and 10 mM acetamide at 30 °C for five days. c and d Lux assay was performed on strains JR11.1 and JR11.1 ΔcreA, using D-fructose as carbon source without (c) or with the addition of ferulic acid (FA) (d). Growth and luciferase activity were measured every 15 min for 24 h at 30 °C