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. 2022 Sep 6;8:71. doi: 10.1038/s41522-022-00333-9

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© The Author(s) 2022

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. 2 — Seven high-quality MAGs (completeness >90% and contamination <10%) of SRMs were included in the analysis. For comparison, the complete genomes of one aerobic acidobacterial species (i.e., Terracidiphilus gabretensis S55, non-SRM), Desulfovibrio vulgaris Hildenborough (an oxygen-tolerant cultured model SRM), and Desulfococcus multivorans DSM 2059 (an oxygen-sensitive cultured model SRM) were chosen. The names of acidobacterial genomes are in blue. The 10 most abundant glycoside hydrolase families across the genomes are shown. Those hydrogenase subgroups that are known to be involved in sulfate reduction or to be oxygen tolerant are listed. MCP methyl-accepting chemotaxis protein, BCP bacterioferritin comigratory protein, Cbo cytochrome bd oxygen reductase, Cco cytochrome c oxidase, CcPx cytochrome c peroxidase, SOD superoxide dismutase, CysK cysteine synthase, GPX glutathione peroxidase, NPX NADH peroxidase, ROO rubredoxin-oxygen oxidoreductase, SOR superoxide reductase, TPX thioredoxin peroxidase. Additional details are presented in Supplementary Tables 3–8.