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. 2017 Jul 20;8:1239. doi: 10.3389/fpls.2017.01239

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Copyright © 2017 Miller, O’Cualain, Selley, Knight, Karim, Hubbard and Johnson.

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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The response of the Benson-Calvin cycle to HL acclimation in WT and gpt2. Quantified proteins are diagrammatically represented in this figure, with each column representing a treatment according to the legend in the top right of the figure. Significantly different results are denoted by different letters within each column (ANOVA, p < 0.05). When more than one protein isoform was quantified, all are shown. Abbreviations: RbcL, Ribulose bisphosphate carboxylase large subunit; RbcS, Ribulose bisphosphate carboxylase small subunit; PGK1, phosphoglycerate kinase 1; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; TPI, triose phosphate isomerase; FBA, fructose-bisphosphate aldolase; FBPase, Fructose 1,6-bisphosphatase; TKL, transketolase; SBPase, sedoheptulose-1,7-bisphosphatase; RPE, ribulose 5-phosphate epimerase; RPI, ribose 5-phosphate isomerase; PRK, phosphoribulokinase. In the case of TPI, too few unique peptides were quantified to allow individual isoform discrimination, so shared peptides between TPI1 and TPI2 were used to quantify total TPI.