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. 2024 Nov 29;24:509. doi: 10.1186/s12866-024-03671-0

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

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Fig. 5 — CzcR-mediated induction of H₂O₂tolerance and catalase activity during Zn excess. A Survival rate of the WT and ΔczcR strains when they were treated with 1.5 mM, 2.5 mM, and 3.5 mM H₂O₂ with the pre-treatment of Zn or not. B Growth curves of the WT and ΔczcR strains when they were cultured in the presence of 0.5 mM H₂O₂ with the pre-treatment of Zn or not. C Survival rate of the WT, ΔczcR, and ΔczcR(czcR) strains when they were cultured in the presence of 3.5 mM H₂O₂ with the pre-treatment of Zn or not. D Catalase activity was measured in the WT, ΔczcR, and ΔczcR(czcR) strains when they were cultured with or without Zn treatment. Statistical significance was calculated based on two-way ANOVA (n.s., not significant; *, P < 0.05; **, P < 0.01; ***, P < 0.001)