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      Primary Metabolism in Fresh Fruits During Storage

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          Abstract

          The extension of commercial life and the reduction of postharvest losses of perishable fruits is mainly based on storage at low temperatures alone or in combination with modified atmospheres (MAs) and controlled atmospheres (CAs), directed primarily at reducing their overall metabolism thus delaying ripening and senescence. Fruits react to postharvest conditions with desirable changes if appropriate protocols are applied, but otherwise can develop negative and unacceptable traits due to the onset of physiological disorders. Extended cold storage periods and/or inappropriate temperatures can result in development of chilling injuries (CIs). The etiology, incidence, and severity of such symptoms vary even within cultivars of the same species, indicating the genotype significance. Carbohydrates and amino acids have protective/regulating roles in CI development. MA/CA storage protocols involve storage under hypoxic conditions and high carbon dioxide concentrations that can maximize quality over extended storage periods but are also affected by the cultivar, exposure time, and storage temperatures. Pyruvate metabolism is highly reactive to changes in oxygen concentration and is greatly affected by the shift from aerobic to anaerobic metabolism. Ethylene-induced changes in fruits can also have deleterious effects under cold storage and MA/CA conditions, affecting susceptibility to chilling and carbon dioxide injuries. The availability of the inhibitor of ethylene perception 1-methylcyclopropene (1-MCP) has not only resulted in development of a new technology but has also been used to increase understanding of the role of ethylene in ripening of both non-climacteric and climacteric fruits. Temperature, MA/CA, and 1-MCP alter fruit physiology and biochemistry, resulting in compositional changes in carbon- and nitrogen-related metabolisms and compounds. Successful application of these storage technologies to fruits must consider their effects on the metabolism of carbohydrates, organic acids, amino acids and lipids.

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          Thermal acclimation and the dynamic response of plant respiration to temperature.

          Temperature-mediated changes in plant respiration (R) are now accepted as an important component of the biosphere's response to global climate change. Here we discuss the underlying mechanisms responsible for the dynamic response of plant respiration to short and long-term temperature changes. The Q(10) is often assumed to be 2.0 (i.e. R doubles per 10 degrees C rise in temperature); however, the Q(10) is not constant (e.g. it declines near-linearly with increasing temperature). The temperature dependence of Q(10) is linked to shifts in the control exerted by maximum enzyme activity at low temperature and substrate limitations at high temperature. In the long term, acclimation of R to temperature is common, in effect reducing the temperature sensitivity of R to changes in thermal environment, with the temperature during plant development setting the maximal thermal acclimation of R.
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            Oxygen sensing in plants is mediated by an N-end rule pathway for protein destabilization.

            The majority of eukaryotic organisms rely on molecular oxygen for respiratory energy production. When the supply of oxygen is compromised, a variety of acclimation responses are activated to reduce the detrimental effects of energy depletion. Various oxygen-sensing mechanisms have been described that are thought to trigger these responses, but they each seem to be kingdom specific and no sensing mechanism has been identified in plants until now. Here we show that one branch of the ubiquitin-dependent N-end rule pathway for protein degradation, which is active in both mammals and plants, functions as an oxygen-sensing mechanism in Arabidopsis thaliana. We identified a conserved amino-terminal amino acid sequence of the ethylene response factor (ERF)-transcription factor RAP2.12 to be dedicated to an oxygen-dependent sequence of post-translational modifications, which ultimately lead to degradation of RAP2.12 under aerobic conditions. When the oxygen concentration is low-as during flooding-RAP2.12 is released from the plasma membrane and accumulates in the nucleus to activate gene expression for hypoxia acclimation. Our discovery of an oxygen-sensing mechanism opens up new possibilities for improving flooding tolerance in crops. © 2011 Macmillan Publishers Limited. All rights reserved
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              Lipid biosynthesis.

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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/317971
                URI : https://loop.frontiersin.org/people/131120
                URI : https://loop.frontiersin.org/people/40644
                URI : https://loop.frontiersin.org/people/360254
                URI : https://loop.frontiersin.org/people/29000
                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                19 February 2020
                2020
                : 11
                : 80
                Affiliations
                [1] 1 Institute of Life Sciences, Scuola Superiore Sant'Anna , Pisa, Italy
                [2] 2 Department of Agricultural Sciences, Biotechnology & Food Science, Cyprus University of Technology , Lemesos, Cyprus
                [3] 3 School of Integrative Plant Science, College of Agriculture and Life Sciences, Cornell University , Ithaca, NY, United States
                Author notes

                Edited by: Robert Peter Walker, University of Perugia, Italy

                Reviewed by: María Serrano, Universidad Miguel Hernández de Elche, Spain; Leon A. Terry, Cranfield University, United Kingdom

                *Correspondence: Pietro Tonutti, pietro.tonutti@ 123456sssup.it

                This article was submitted to Plant Metabolism and Chemodiversity, a section of the journal Frontiers in Plant Science

                Article
                10.3389/fpls.2020.00080
                7042374
                32140162
                67b85fb2-d47c-4cce-b0aa-ac89d62cec2b
                Copyright © 2020 Brizzolara, Manganaris, Fotopoulos, Watkins and Tonutti

                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) and the copyright owner(s) 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.

                History
                : 02 November 2019
                : 21 January 2020
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 185, Pages: 16, Words: 8899
                Categories
                Plant Science
                Review

                Plant science & Botany
                low temperature,controlled atmospheres,modified atmospheres,hypoxia,ethylene,1-methylcyclopropene,fruit composition,post-harvest

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