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. 2017 Aug 14;8:1399. doi: 10.3389/fpls.2017.01399

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Copyright © 2017 Zarei, Brikis, Bajwa, Chiu, Simpson, DeEll, Bozzo and Shelp.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Dependence of recombinant apple and rice GLYR activities on pH. The left and right panels, represent apple (A,B) and rice (C,D) GLYRs, respectively, whereas the upper and lower panels represent GLYR1s (A,C) and GLYR2s (B,D), respectively. The data, expressed as specific activity (μmol min^-1 mg^-1 protein), were determined using 50 μM glyoxylate and NADPH in thee buffers (50 mM each): 2-morpholino-ethanesulfonic acid, 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid and N-tris(hydroxymethyl)methyl-4-aminobutanesulfonic acid either separately (A,B) or together (C,D). Each datum represents the mean (±SD) of three technical measurements of a typical enzyme preparation.