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      High V‐PPase activity is beneficial under high salt loads, but detrimental without salinity

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          Summary

          • The membrane‐bound proton‐pumping pyrophosphatase (V‐PPase), together with the V‐type H +‐ATPase, generates the proton motive force that drives vacuolar membrane solute transport. Transgenic plants constitutively overexpressing V‐PPases were shown to have improved salinity tolerance, but the relative impact of increasing PP i hydrolysis and proton‐pumping functions has yet to be dissected.

          • For a better understanding of the molecular processes underlying V‐PPase‐dependent salt tolerance, we transiently overexpressed the pyrophosphate‐driven proton pump (NbVHP) in Nicotiana benthamiana leaves and studied its functional properties in relation to salt treatment by primarily using patch‐clamp, impalement electrodes and pH imaging.

          • NbVHP overexpression led to higher vacuolar proton currents and vacuolar acidification. After 3 d in salt‐untreated conditions, V‐PPase‐overexpressing leaves showed a drop in photosynthetic capacity, plasma membrane depolarization and eventual leaf necrosis. Salt, however, rescued NbVHP‐hyperactive cells from cell death. Furthermore, a salt‐induced rise in V‐PPase but not of V‐ATPase pump currents was detected in nontransformed plants.

          • The results indicate that under normal growth conditions, plants need to regulate the V‐PPase pump activity to avoid hyperactivity and its negative feedback on cell viability. Nonetheless, V‐PPase proton pump function becomes increasingly important under salt stress for generating the pH gradient necessary for vacuolar proton‐coupled Na + sequestration.

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          Salt tolerance conferred by overexpression of a vacuolar Na+/H+ antiport in Arabidopsis.

          Agricultural productivity is severely affected by soil salinity. One possible mechanism by which plants could survive salt stress is to compartmentalize sodium ions away from the cytosol. Overexpression of a vacuolar Na+/H+ antiport from Arabidopsis thaliana in Arabidopsis plants promotes sustained growth and development in soil watered with up to 200 millimolar sodium chloride. This salinity tolerance was correlated with higher-than-normal levels of AtNHX1 transcripts, protein, and vacuolar Na+/H+ (sodium/proton) antiport activity. These results demonstrate the feasibility of engineering salt tolerance in plants.
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            Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments

            The largely unused uracil-excision molecular cloning technique has excellent features in most aspects compared to other modern cloning techniques. Its application has, however, been hampered by incompatibility with proof-reading DNA polymerases. We have advanced the technique by identifying PfuCx as a compatible proof-reading DNA polymerase and by developing an improved vector design strategy. The original features of the technique, namely simplicity, speed, high efficiency and low cost are thus combined with high fidelity as well as a transparent, simple and flexible vector design. A comprehensive set of vectors has been constructed covering a wide range of different applications and their functionality has been confirmed.
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              Duplication of CaMV 35S Promoter Sequences Creates a Strong Enhancer for Plant Genes.

              A variant of the cauliflower mosaic virus 35S promoter with transcriptional activity approximately tenfold higher than that of the natural promoter was constructed by tandem duplication of 250 base pairs of upstream sequences. The duplicated region also acted as a strong enhancer of heterologous promoters, increasing the activity of an adjacent and divergently transcribed transferred DNA gene several hundredfold, and to a lesser extent, that of another transferred DNA gene from a remote downstream position. This optimized enhancer element should be very useful for obtaining high levels of expression of foreign genes in transgenic plants.
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                Author and article information

                Contributors
                marten@botanik.uni-wuerzburg.de
                Journal
                New Phytol
                New Phytol
                10.1111/(ISSN)1469-8137
                NPH
                The New Phytologist
                John Wiley and Sons Inc. (Hoboken )
                0028-646X
                1469-8137
                25 June 2018
                September 2018
                : 219
                : 4 ( doiID: 10.1111/nph.2018.219.issue-4 )
                : 1421-1432
                Affiliations
                [ 1 ] Institute for Molecular Plant Physiology and Biophysics University of Würzburg Julius von‐Sachs Platz 2 Würzburg D‐97082 Germany
                [ 2 ] Institute of Bioinformatics Center for Computational and Theoretical, Biology University of Würzburg Am Hubland Würzburg D‐97218 Germany
                [ 3 ] Centre for Organismal Studies Developmental Biology of Plants Ruprecht‐Karls‐University of Heidelberg Im Neuenheimer Feld 230 Heidelberg 69120 Germany
                [ 4 ] Plant Physiology University Kaiserslautern Postfach 3049 Kaiserslautern D‐67653 Germany
                [ 5 ] Department of Biology Tokyo Gakugei University Nukui Kitamachi 4‐1‐1 Koganei‐shi Tokyo 184‐8501 Japan
                [ 6 ] Tasmanian Institute of Agriculture University of Tasmania Hobart TAS 7001 Australia
                Author notes
                [*] [* ] Author for correspondence:

                Irene Marten

                Tel: +49 931 31‐86118

                Email: marten@ 123456botanik.uni-wuerzburg.de

                Article
                NPH15280 2018-26694
                10.1111/nph.15280
                6099232
                29938800
                3bf92efa-635e-4473-bd2f-7eee8e38e6f4
                © 2018 The Authors. New Phytologist © 2018 New Phytologist Trust

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 March 2018
                : 15 May 2018
                Page count
                Figures: 5, Tables: 0, Pages: 12, Words: 9910
                Funding
                Funded by: Deutsche Forschungsgemeinschaft
                Award ID: FOR1061
                Award ID: IRTG1830
                Award ID: KO3657/2‐4
                Categories
                Full Paper
                Research
                Full Papers
                Custom metadata
                2.0
                nph15280
                September 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.4.4 mode:remove_FC converted:20.08.2018

                Plant science & Botany
                cell death,plasma membrane voltage,proton pump currents,salt,vacuolar ph,vacuolar proton‐atpase (v‐atpase),vacuolar proton‐pyrophosphatase (v‐ppase)

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