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. 2019 Feb 27;12:42. doi: 10.1186/s13068-019-1384-0

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© The Author(s) 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.

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Fig. 3 — Analysis of HiPMO1 reaction products using MALDI-TOF–MS. a Various non-oxidized and oxidized oligosaccharides: non-oxidized oligosaccharides (m/z + 0), C4-oxidized oligosaccharides (C4-ketoaldoses) or C6-oxidized oligosaccharides (C6-hexodialdoses) (m/z − 2), C1-oxidized oligosaccharides (aldonic acids) (m/z + 16), C1-/C4-oxidized oligosaccharides (m/z + 14) or C6-oxidized glucuronic acid-containing oligosaccharides (m/z + 14), C1-/C6-oxidized glucuronic acid-containing oligosaccharide lactones or C4-/C6-oxidized glucuronic acid-containing oligosaccharides (m/z + 12), C1-/C6-/C4-oxidized glucuronic acid-containing oligosaccharides or C6-/C6-oxidized glucuronic acid-containing oligosaccharides (m/z + 28). b Potential structures of various oxidized and non-oxidized DP3 oligosaccharides. Only 1 of 3 potential C6-oxidized positions was marked