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. 2021 Aug 25;4:1007. doi: 10.1038/s42003-021-02541-z

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© The Author(s) 2021

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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Fig. 6 — a The repression of citZ by citZ-t2 and gltA by gltA-t1 during the strain cultivation. b Changes in the transcriptional levels of citZ and gltA in DF50ΔEPSΔcas3 simultaneously expressing citZ-t2 and gltA-t1. c The cell growth of DF50ΔEPSΔcas3 with citrate synthase genes repressed. d Glucose consumption of DF50ΔEPSΔcas3 with citrate synthase genes repressed. CS represents DF50ΔEPSΔcas3 expressing both citZ-t2 and gltA-t1. Data shown for three biological replicates. Error bars indicate SDs, n = 3.