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      Application of Trichoderma harzianum, 6-Pentyl-α-pyrone and Plant Biopolymer Formulations Modulate Plant Metabolism and Fruit Quality of Plum Tomatoes

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          Abstract

          Many Trichoderma are successfully used to improve agriculture productivity due to their capacity for biocontrol and to stimulate plant growth and tolerance to abiotic stress. This research elucidates the effect of applications with Trichoderma harzianum strain T22 (T22), or biopolymer (BP) alone or in combination (BP + T22 or BP + 6-pentyl-α-pyrone (6PP); a Trichoderma secondary metabolite) on the crop performance, nutritional and functional quality of greenhouse tomato ( Solanum lycopersicum L. cultivar Pixel). T22 elicited significant increases in total yield (+40.1%) compared to untreated tomato. The content of lycopene, an important antioxidant compound in tomatoes, significantly increased upon treatment with T22 (+ 49%), BP + T22 (+ 40%) and BP + 6PP (+ 52%) compared to the control. T22 treatments significantly increased the content of asparagine (+37%), GABA (+87%) and MEA (+102%) over the control; whereas BP alone strongly increased GABA (+105%) and MEA (+85%). The synthesis of these compounds implies that tomato plants are able to reuse the photorespiratory amino acids and ammonium for producing useful metabolites and reduce the pressure of photorespiration on plant metabolism, thus optimizing photosynthesis and growth. Finally, these metabolites exert many beneficial effects for human health, thus enhancing the premium quality of plum tomatoes.

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          Overview of Mechanisms and Uses of Trichoderma spp.

          ABSTRACT Fungi in the genus Trichoderma have been known since at least the 1920s for their ability to act as biocontrol agents against plant pathogens. Until recently, the principal mechanisms for control have been assumed to be those primarily acting upon the pathogens and included mycoparasitism, antibiosis, and competition for resources and space. Recent advances demonstrate that the effects of Trichoderma on plants, including induced systemic or localized resistance, are also very important. These fungi colonize the root epidermis and outer cortical layers and release bioactive molecules that cause walling off of the Trichoderma thallus. At the same time, the transcriptome and the proteome of plants are substantially altered. As a consequence, in addition to induction of pathways for resistance in plants, increased plant growth and nutrient uptake occur. However, at least in maize, the increased growth response is genotype specific, and some maize inbreds respond negatively to some strains. Trichoderma spp. are beginning to be used in reasonably large quantities in plant agriculture, both for disease control and yield increases. The studies of mycoparasitism also have demonstrated that these fungi produce a rich mixture of antifungal enzymes, including chitinases and beta-1,3 glucanases. These enzymes are synergistic with each other, with other antifungal enzymes, and with other materials. The genes encoding the enzymes appear useful for producing transgenic plants resistant to diseases and the enzymes themselves are beneficial for biological control and other processes.
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            Trichoderma–plant–pathogen interactions

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              Trichoderma-based Products and their Widespread Use in Agriculture

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                Author and article information

                Journal
                Plants (Basel)
                Plants (Basel)
                plants
                Plants
                MDPI
                2223-7747
                19 June 2020
                June 2020
                : 9
                : 6
                : 771
                Affiliations
                [1 ]Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, University of Campania “Luigi Vanvitelli”, Via Vivaldi 43, 81100 Caserta, Italy; petronia.carillo@ 123456unicampania.it (P.C.); giovannamarta.fusco@ 123456unicampania.it (G.M.F.)
                [2 ]Department of Pharmacy, University of Naples Federico II, 80131 Naples, Italy
                [3 ]Task Force on Microbiome Studies, University of Naples Federico II, 80055 Portici, Italy
                [4 ]National Research Council, Institute for Sustainable Plant Protection, 80055 Portici, Italy; frvinale@ 123456unina.it
                [5 ]Department of Agricultural Sciences, University of Naples Federico II, 80055 Portici, Italy; ernesto.comite@ 123456unina.it (E.C.); Nakhel_Christophe@ 123456hotmail.com (C.E.-N.); youssef.rouphael@ 123456unina.it (Y.R.); stefania.lanzuise@ 123456unina.it (S.L.)
                [6 ]National Research Council, Institute for Composite Polymers and Biomaterials, 80125 Napoli, Italy; assunta.borzacchiello@ 123456cnr.it
                [7 ]Department of Veterinary Medicine and Animal Productions, University of Naples Federico II, 80137 Naples, Italy
                Author notes
                [* ]Correspondence: woo@ 123456unina.it
                Author information
                https://orcid.org/0000-0003-3723-0398
                https://orcid.org/0000-0001-8611-6140
                https://orcid.org/0000-0002-1200-2834
                https://orcid.org/0000-0002-1002-8651
                https://orcid.org/0000-0002-5090-8127
                Article
                plants-09-00771
                10.3390/plants9060771
                7356659
                32575500
                4c655f79-8819-4560-a321-042efa14b99c
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 23 May 2020
                : 17 June 2020
                Categories
                Article

                microbial biostimulant,non-microbial biostimulant,carboxymethyl cellulose,pluronic f-127,amino acids,lycopene,gaba,solanum lycopersicum l.

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