| Literature DB >> 27663407 |
Ángela María Sánchez-López1,2,3,4, Abdellatif Bahaji1,2,3,4, Nuria De Diego1,2,3,4, Marouane Baslam1,2,3,4, Jun Li1,2,3,4, Francisco José Muñoz1,2,3,4, Goizeder Almagro1,2,3,4, Pablo García-Gómez1,2,3,4, Kinia Ameztoy1,2,3,4, Adriana Ricarte-Bermejo1,2,3,4, Ondřej Novák1,2,3,4, Jan F Humplík1,2,3,4, Lukáš Spíchal1,2,3,4, Karel Doležal1,2,3,4, Sergio Ciordia1,2,3,4, María Carmen Mena1,2,3,4, Rosana Navajas1,2,3,4, Edurne Baroja-Fernández1,2,3,4, Javier Pozueta-Romero5,6,7,8.
Abstract
Volatile compounds (VCs) emitted by phylogenetically diverse microorganisms (including plant pathogens and microbes that do not normally interact mutualistically with plants) promote photosynthesis, growth, and the accumulation of high levels of starch in leaves through cytokinin (CK)-regulated processes. In Arabidopsis (Arabidopsis thaliana) plants not exposed to VCs, plastidic phosphoglucose isomerase (pPGI) acts as an important determinant of photosynthesis and growth, likely as a consequence of its involvement in the synthesis of plastidic CKs in roots. Moreover, this enzyme plays an important role in connecting the Calvin-Benson cycle with the starch biosynthetic pathway in leaves. To elucidate the mechanisms involved in the responses of plants to microbial VCs and to investigate the extent of pPGI involvement, we characterized pPGI-null pgi1-2 Arabidopsis plants cultured in the presence or absence of VCs emitted by Alternaria alternata We found that volatile emissions from this fungal phytopathogen promote growth, photosynthesis, and the accumulation of plastidic CKs in pgi1-2 leaves. Notably, the mesophyll cells of pgi1-2 leaves accumulated exceptionally high levels of starch following VC exposure. Proteomic analyses revealed that VCs promote global changes in the expression of proteins involved in photosynthesis, starch metabolism, and growth that can account for the observed responses in pgi1-2 plants. The overall data show that Arabidopsis plants can respond to VCs emitted by phytopathogenic microorganisms by triggering pPGI-independent mechanisms.Entities:
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Year: 2016 PMID: 27663407 PMCID: PMC5100789 DOI: 10.1104/pp.16.00945
Source DB: PubMed Journal: Plant Physiol ISSN: 0032-0889 Impact factor: 8.340