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. 2015 Oct 15;6:826. doi: 10.3389/fpls.2015.00826

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Copyright © 2015 Koehler, Rohloff, Wilson, Kopka, Erban, Winge, Bones, Davik, Alsheikh and Randall.

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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Cold responses of twenty-one identified proteins. Spot intensities were normalized to the highest expressor (i.e., the highest level of each protein was considered to be 1.0) and represent the average values of 3 gels (three replicate experiments) with error bars indicating standard deviations. Proteins were categorized into (A) non-chloroplastic, (B) chloroplastic metabolism, and (C) photosynthesis-related chloroplast proteins. Proteins identified and corresponding spot numbers were Gly Cleavage enzyme (SSP 0005), chl a/b, II (SSP 0110), RuBisCo Activase (SSP 0403), 26S protease regulatory subunit (SSP 1114), ATP synthase, alpha (SSP 1606), ATP synthase, delta (SSP 2004), Glyoxalase I (SSP 2208), Glutamine synthase (SSP 2405), eIF4A-2 (SSP 2507), Cyt b6-f, FeS (SSP 3007), Chl a/b p26 (SSP 3109), fumaryl acetase-like (SSP 3502), Hsp93/CLPC (SSP 3801), cyt b6-f FeS (SSP 4004), Flavanone 3 hydroxylase (SSP 4403), ATP-Zn peptidase, (SSP 4817), unknown, stress related (SSP 6711), alcohol dehydrogenase (SSP 7408), Auxin-binding (SSP 8004), RuBisCo, SS (SSP 8005).