Fredy Carrera

Dr. Fredy Carrera

Universidad de las Fuerzas Armadas ESPE, Sangolquí, Ecuador.
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Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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22 April 2021 in Agronomy
Verified
Journal Article
Open access
PDF file
Fredy CarreraFredy Carrera
Fredy Carrera
CNCarlos Noceda
Carlos Noceda
MMMaría G. Maridueña-Zavala
María G. Maridueña-Zavala
JCJuan Cevallos-Cevallos
Juan Cevallos-Cevallos
Metabolomics is a technology that generates large amounts of data and contributes to obtaining wide and integral explanations of the biochemical state of a living organism. Plants are continuously affected by abiotic stresses such as water scarcity, high temperatures and high salinity, and metabolomics has the potential for elucidating the response-to-stress mechanisms and develop resistance strategies in affected cultivars. This review describes the characteristics of each of the stages of metabolomic studies in plants and the role of metabolomics in the characterization of the response of various plant species to abiotic stresses.

26 February 2021 in Horticulturae
Verified
Journal Article
Open access
PDF file
Fredy CarreraFredy Carrera
Fredy Carrera
CNCarlos Noceda
Carlos Noceda
MMMaría G. Maridueña-Zavala
María G. Maridueña-Zavala
JGJosé A. García
José A. García
OROmar Ruiz-Barzola
Omar Ruiz-Barzola
JCJuan Cevallos-Cevallos
Juan Cevallos-Cevallos
Micropropagation techniques allow the mass production of banana plants but can cause somaclonal variations such as dwarfism. Changes in the metabolite profile during micropropagation of normal (NP) and dwarf (DP) banana plants have not been described. Both, NPs and DPs of banana Musa AAA cv. Williams were micropropagated and the metabolite profile of vitroplants was assessed at the proliferation (PP), rooting (RP) and the second greenhouse-acclimatization (APII) phases of tissue culture. Metabolites from 10 DPs and 10 NPs meristems from each micropropagation phase were extracted and identified by gas chromatography coupled with mass spectrometry (GC-MS). Principal component analysis (PCA) and test of statistical significance were applied to detect differentially accumulated metabolites. The PCA showed a clear grouping of DPs separated from NPs in RP and APII. Among the differentially accumulated metabolites, various precursors of apoplast components including arabinose and galactose or deoxygalactose in both PP and RP, as well as mannose and fucose in APII were under-accumulated in DPs. Results suggest affected apoplast composition during micropropagation of DPs.