CORRECTION article

Front. Plant Sci., 26 March 2019

Sec. Plant Physiology

Volume 10 - 2019 | https://doi.org/10.3389/fpls.2019.00325

Corrigendum: Knock-Down of the Phosphoserine Phosphatase Gene Effects Rather N- Than S-Metabolism in Arabidopsis thaliana

  • 1. Chair of Tree Physiology, Institute of Forest Sciences, Faculty of Environment and Natural Resources, University of Freiburg, Freiburg, Germany

  • 2. Institute of Plant Biochemistry, Cluster of Excellence on Plant Sciences, Heinrich Heine University, Düsseldorf, Germany

  • 3. Botanical Institute, Cluster of Excellence on Plant Sciences, University of Cologne, Cologne, Germany

  • 4. College of Science, King Saud University, Riyadh, Saudi Arabia

In the original article, there was a mistake in Figure 6 as published. On the y-axis “nmol g−1 FW” was used instead of “μmol g−1 FW” for the total NPT content measurement. The corrected Figure 6 appears below.

Figure 6

A correction has been made to the Materials and Methods, subsection Quantification of Total Non-Protein Thiols:

“For the determination of total non-protein thiols (NPT), a modified method of Queval and Noctor (2007) was applied. Total thiols in leaf extract were assayed as 5,5′-dithio-bis-[2-nitrobenzoic acid]-reactive thiols (DTNB-reactive thiols) by spectrophotometry (Beckman UV- DU650, Beckman Coulter, United States) using glutathione (GSH) as a standard. Approximately 100 mg frozen leaf powder was extracted in 1 ml 0.2N HCl. Aliquots of 0.5 ml supernatant were transferred into fresh micro tubes (Sarstedt AG & Co., Nümbrecht, Germany) and neutralized with 0.4 ml 0.2 M NaOH in the presence of 50 μl 0.2 M NaH2PO4 (pH 5.6). For thiol quantification by spectrophotometry, each semi-micro cuvette (Sarstedt AG & Co., Nümbrecht, Germany) contained 500 μl phosphate-EDTA buffer (0.2 M NaH2PO4, pH 7.5; 10 mM EDTA), 50 μl of 12 mM DTNB and 450 μl neutralized sample extract (total volume 1 ml). For standards, the extract was replaced by 450 ml of 0, 10, 20, 30, 40, 50 μmol GSH. The absorbance was measured at a wavelength of 412 nm 3 min after addition of extract or standard.”

The authors apologize for these errors and state that they do not change the scientific conclusions of the article in any way. The original article has been updated.

References

  • 1

    QuevalG.NoctorG. (2007). A plate reader method for the measurement of NAD, NADP, glutathione, and ascorbate in tissue extracts: application to redox profiling during Arabidopsis rosette development. Anal. Biochem.363, 5869. 10.1016/j.ab.2007.01.005

Summary

Keywords

amino acids, Cd treatment, cysteine, glutathione, glycine, phosphorylated pathway, serine

Citation

Samuilov S, Rademacher N, Brilhaus D, Flachbart S, Arab L, Kopriva S, Weber APM, Mettler-Altmann T and Rennenberg H (2019) Corrigendum: Knock-Down of the Phosphoserine Phosphatase Gene Effects Rather N- Than S-Metabolism in Arabidopsis thaliana. Front. Plant Sci. 10:325. doi: 10.3389/fpls.2019.00325

Received

20 February 2019

Accepted

28 February 2019

Published

26 March 2019

Volume

10 - 2019

Edited and reviewed by

Jean-Philippe Reichheld, Centre National de la Recherche Scientifique (CNRS), France

Updates

Copyright

*Correspondence: Sladjana Samuilov

This article was submitted to Plant Physiology, a section of the journal Frontiers in Plant Science

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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