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. 2021 Apr 29;12:2466. doi: 10.1038/s41467-021-22765-1

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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. 7 — Arrows indicate metaproteome gene expression data, with green representing unamended and purple indicating CT-amended pathways. Metabolite dynamics are shown in boxed graphs, with lines indicating average signal for live CT (n = 3 individual biological replicates, solid purple), and unamended control (n = 3 individual biological replicates, green) microcosms with shaded areas including the 95% confidence interval and individual data points plotted, and autoclaved CT soil (dotted light purple). The methodology used to detect the metabolite is highlighted by box color (noted in the graphical legend), with FTICR-MS (orange) data given as percent of identified peaks, NMR (black) as umol, and LC–MS (gray) as log2(peak areas). Nitrogen metabolism (blue box) is discussed in Supplementary Note 4.