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. 2013 Oct 12;6:148. doi: 10.1186/1754-6834-6-148

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Copyright © 2013 Vuong et al.; licensee BioMed Central Ltd.

This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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NMR spectra of cellobiose (A) and xylobiose (B) oxidation. (A): From top to bottom are the spectra of cellobiose, cellobiose that was oxidized by GOOX-VN, and cellobiose oxidized by Y300A; CB red. alpha and CB red. beta: H1 signals due to reducing α-glucose and reducing β-glucose units of cellobiose, correspondingly; CBA-H2 and CBA-H3: H2 and H3 signals of the cellobionate molecule. (B): From top to bottom are the spectra of untreated xylobiose and GOOX-VN oxidized xylobiose; XB red. alpha and XB red. beta: H1 signals due to reducing α-xylose and reducing β-xylose units of xylobiose, correspondingly; XBA: Overlapped signals of the xylobionate molecule (H2 and H3 signals were not well separated from other signals). 10 mM cellobiose and 10 mM xylobiose were used in oxidation reactions.