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      Plant growth-promoting rhizobacteria and root system functioning

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          Abstract

          The rhizosphere supports the development and activity of a huge and diversified microbial community, including microorganisms capable to promote plant growth. Among the latter, plant growth-promoting rhizobacteria (PGPR) colonize roots of monocots and dicots, and enhance plant growth by direct and indirect mechanisms. Modification of root system architecture by PGPR implicates the production of phytohormones and other signals that lead, mostly, to enhanced lateral root branching and development of root hairs. PGPR also modify root functioning, improve plant nutrition and influence the physiology of the whole plant. Recent results provided first clues as to how PGPR signals could trigger these plant responses. Whether local and/or systemic, the plant molecular pathways involved remain often unknown. From an ecological point of view, it emerged that PGPR form coherent functional groups, whose rhizosphere ecology is influenced by a myriad of abiotic and biotic factors in natural and agricultural soils, and these factors can in turn modulate PGPR effects on roots. In this paper, we address novel knowledge and gaps on PGPR modes of action and signals, and highlight recent progress on the links between plant morphological and physiological effects induced by PGPR. We also show the importance of taking into account the size, diversity, and gene expression patterns of PGPR assemblages in the rhizosphere to better understand their impact on plant growth and functioning. Integrating mechanistic and ecological knowledge on PGPR populations in soil will be a prerequisite to develop novel management strategies for sustainable agriculture.

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          Most cited references195

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          Genome-wide insertional mutagenesis of Arabidopsis thaliana.

          J Alonso (2003)
          Over 225,000 independent Agrobacterium transferred DNA (T-DNA) insertion events in the genome of the reference plant Arabidopsis thaliana have been created that represent near saturation of the gene space. The precise locations were determined for more than 88,000 T-DNA insertions, which resulted in the identification of mutations in more than 21,700 of the approximately 29,454 predicted Arabidopsis genes. Genome-wide analysis of the distribution of integration events revealed the existence of a large integration site bias at both the chromosome and gene levels. Insertion mutations were identified in genes that are regulated in response to the plant hormone ethylene.
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            Indole-3-acetic acid in microbial and microorganism-plant signaling.

            Diverse bacterial species possess the ability to produce the auxin phytohormone indole-3-acetic acid (IAA). Different biosynthesis pathways have been identified and redundancy for IAA biosynthesis is widespread among plant-associated bacteria. Interactions between IAA-producing bacteria and plants lead to diverse outcomes on the plant side, varying from pathogenesis to phyto-stimulation. Reviewing the role of bacterial IAA in different microorganism-plant interactions highlights the fact that bacteria use this phytohormone to interact with plants as part of their colonization strategy, including phyto-stimulation and circumvention of basal plant defense mechanisms. Moreover, several recent reports indicate that IAA can also be a signaling molecule in bacteria and therefore can have a direct effect on bacterial physiology. This review discusses past and recent data, and emerging views on IAA, a well-known phytohormone, as a microbial metabolic and signaling molecule.
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              Ethylene Biosynthesis and its Regulation in Higher Plants

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                Author and article information

                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                17 September 2013
                2013
                : 4
                : 356
                Affiliations
                [1] 1Université de Lyon Lyon, France
                [2] 2Université Claude Bernard Lyon 1 Villeurbanne, France
                [3] 3Centre National de la Recherche Scientifique, UMR 5557, Ecologie Microbienne, Université Lyon 1 Villeurbanne, France
                [4] 4Laboratoire des Symbioses Tropicales et Méditerranéennes, UMR 113, Université Montpellier 2/Institut de Recherche Pour le Développement/Centre de Coopération Internationale en Recherche Agronomique pour le Développement/SupAgro/Institut National de la Recherche Agronomique Montpellier, France
                [5] 5Institut National de la Recherche Agronomique, UMR 1347, Agroécologie, Interactions Plantes-Microorganismes Dijon, France
                Author notes

                Edited by: Boris Rewald, University of Natural Resources and Life Sciences, Austria

                Reviewed by: Francesco De Bello, Institute of Botany, Czech Academy of Sciences, Czech Republic; Faina Kamilova, Koppert Biological System, Netherlands

                *Correspondence: Claire Prigent-Combaret, Centre National de la Recherche Scientifique, UMR 5557, Ecologie Microbienne, Université Lyon 1, 43 Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cedex, France e-mail: claire.prigent-combaret@ 123456univ-lyon1.fr

                This article was submitted to Functional Plant Ecology, a section of the journal Frontiers in Plant Science.

                Article
                10.3389/fpls.2013.00356
                3775148
                24062756
                b2f6679b-d745-4b8d-8834-806d1384cd0e
                Copyright © Vacheron, Desbrosses, Bouffaud, Touraine, Moënne-Loccoz, Muller, Legendre, Wisniewski-Dyé and Prigent-Combaret.

                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.

                History
                : 29 May 2013
                : 23 August 2013
                Page count
                Figures: 3, Tables: 0, Equations: 2, References: 247, Pages: 19, Words: 0
                Categories
                Plant Science
                Review Article

                Plant science & Botany
                plant-pgpr cooperation,rhizo-microbiome,rhizosphere,phytohormone,plant nutrition,isr,functional group

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