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. 2021 Jan 22;9:23. doi: 10.1186/s40168-020-00975-x

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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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 4 — CAZyme fingerprinting of YM metabolism by Bt^Bov isolates. a GH enzyme families encoded within the genomes of MD40_HG and MD33_MG that differ in total number of sequences. BtVPI-5482 sequences are provided as a reference for each GH family. b Phylogenetic trees of characterized GH92s and GH76s, and Bt^Bov sequences generated with SACCHARIS [37]. Circles represent Bt^Bov sequences and white circles highlight sequences from PULs with mannan activity: 1, 2, or 3 = MAN-PULs 1, 2, or 3, respectively; H = HMNG-PUL; 55 = BtMD40 PUL55. Activities assigned to characterized enzymes within each clade for GH92 and GH76 are depicted using the provided legend. Outer ring represents characterized specificities. Numbers in parenthesis indicate the total number of enzymes within each strain