Establishment of a Protocol for the Characterization of Secreted Biomolecules in Somatic Embryogenic Cultures of <i>Olea europaea</i> L.

Somatic embryogenesis (SE) involves the formation of embryo-like structures from somatic cells without fertilization and is widely used for clonal propagation and genetic transformation. However, in olive (<i>Olea europaea</i> sp. <i>europaea</i>), SE remains challenging due...

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Main Authors: Rita Pires, Lénia Rodrigues, Fátima Milhano Santos, Iola F. Duarte, Sergio Ciordia, Augusto Peixe, Hélia Cardoso
Format: Article
Language:English
Published: MDPI AG 2025-03-01
Series:Horticulturae
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Online Access:https://www.mdpi.com/2311-7524/11/3/331
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author Rita Pires
Lénia Rodrigues
Fátima Milhano Santos
Iola F. Duarte
Sergio Ciordia
Augusto Peixe
Hélia Cardoso
author_facet Rita Pires
Lénia Rodrigues
Fátima Milhano Santos
Iola F. Duarte
Sergio Ciordia
Augusto Peixe
Hélia Cardoso
author_sort Rita Pires
collection DOAJ
description Somatic embryogenesis (SE) involves the formation of embryo-like structures from somatic cells without fertilization and is widely used for clonal propagation and genetic transformation. However, in olive (<i>Olea europaea</i> sp. <i>europaea</i>), SE remains challenging due to the recalcitrant behavior of adult tissues when used as initial explants. Bioactive molecules released into the culture medium (conditioned medium, CM) by embryogenic cultures have been identified as modulators of the SE response. However, their potential role in enhancing SE efficiency in olive and overcoming tissue recalcitrance remains largely unexplored. To investigate the role of these biomolecules in olive SE, a protocol was established using SE cultures of cv. ‘Galega Vulgar’. Proteins and metabolites were separated by filtration, concentrated through lyophilization, and precipitated using three methods: Acetone, TCA/Acetone, and Methanol/Chloroform. The efficiency of these methods was evaluated through total protein quantification and via SDS-PAGE electrophoresis. LC-MS/MS was employed to analyze secretome composition using the TCA/Acetone precipitation method. Additionally, metabolite profiles were analyzed using <sup>1</sup>H NMR spectroscopy. The results led to the identification of 1096 (526 protein groups) <i>Olea europaea</i> proteins, including well-known SE biomarkers such as kinases and peroxidases. NMR spectroscopy identified several metabolites secreted into the medium or resulting from the metabolic activity of secreted enzymes, confirming the applicability of the procedure. Although extracting secreted biomolecules from the culture medium presents significant challenges, the protocol established in this study successfully enabled the isolation and identification of both proteins and metabolites, revealing a valuable workflow for future in-depth analyses of secreted biomolecules in olive SE.
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spelling doaj-art-7e468a1586b14fdbaceb4b510afbe0b22025-08-20T03:43:31ZengMDPI AGHorticulturae2311-75242025-03-0111333110.3390/horticulturae11030331Establishment of a Protocol for the Characterization of Secreted Biomolecules in Somatic Embryogenic Cultures of <i>Olea europaea</i> L.Rita Pires0Lénia Rodrigues1Fátima Milhano Santos2Iola F. Duarte3Sergio Ciordia4Augusto Peixe5Hélia Cardoso6MED—Mediterranean Institute for Agriculture, Environment and Development & CHANGE—Global Change and Sustainability Institute, Instituto de Investigação e Formação Avançada, Universidade de Évora, Pólo da Mitra, Ap. 94, 7002-554 Évora, PortugalMED—Mediterranean Institute for Agriculture, Environment and Development & CHANGE—Global Change and Sustainability Institute, Instituto de Investigação e Formação Avançada, Universidade de Évora, Pólo da Mitra, Ap. 94, 7002-554 Évora, PortugalHealth Research Institute-Fundación Jiménez Díaz University Hospital, Autonomous University of Madrid (IIS-FJD, UAM), 28040 Madrid, SpainDepartment of Chemistry, LAQV-REQUIMTE & CICECO—Aveiro Institute of Materials, University of Aveiro, Campus de Santiago, 3810-193 Aveiro, PortugalFunctional Proteomics Laboratory, National Center for Biotechnology (CNB-CSIC), Darwin 3, 28049 Madrid, SpainMED—Mediterranean Institute for Agriculture, Environment and Development & CHANGE—Global Change and Sustainability Institute, Escola de Ciências e Tecnologia, Universidade de Évora, Pólo da Mitra, Ap. 94, 7002-554 Évora, PortugalMED—Mediterranean Institute for Agriculture, Environment and Development & CHANGE—Global Change and Sustainability Institute, Escola de Ciências e Tecnologia, Universidade de Évora, Pólo da Mitra, Ap. 94, 7002-554 Évora, PortugalSomatic embryogenesis (SE) involves the formation of embryo-like structures from somatic cells without fertilization and is widely used for clonal propagation and genetic transformation. However, in olive (<i>Olea europaea</i> sp. <i>europaea</i>), SE remains challenging due to the recalcitrant behavior of adult tissues when used as initial explants. Bioactive molecules released into the culture medium (conditioned medium, CM) by embryogenic cultures have been identified as modulators of the SE response. However, their potential role in enhancing SE efficiency in olive and overcoming tissue recalcitrance remains largely unexplored. To investigate the role of these biomolecules in olive SE, a protocol was established using SE cultures of cv. ‘Galega Vulgar’. Proteins and metabolites were separated by filtration, concentrated through lyophilization, and precipitated using three methods: Acetone, TCA/Acetone, and Methanol/Chloroform. The efficiency of these methods was evaluated through total protein quantification and via SDS-PAGE electrophoresis. LC-MS/MS was employed to analyze secretome composition using the TCA/Acetone precipitation method. Additionally, metabolite profiles were analyzed using <sup>1</sup>H NMR spectroscopy. The results led to the identification of 1096 (526 protein groups) <i>Olea europaea</i> proteins, including well-known SE biomarkers such as kinases and peroxidases. NMR spectroscopy identified several metabolites secreted into the medium or resulting from the metabolic activity of secreted enzymes, confirming the applicability of the procedure. Although extracting secreted biomolecules from the culture medium presents significant challenges, the protocol established in this study successfully enabled the isolation and identification of both proteins and metabolites, revealing a valuable workflow for future in-depth analyses of secreted biomolecules in olive SE.https://www.mdpi.com/2311-7524/11/3/331somatic embryogenesisoliveconditioned mediumsecretomeproteomemetabolome
spellingShingle Rita Pires
Lénia Rodrigues
Fátima Milhano Santos
Iola F. Duarte
Sergio Ciordia
Augusto Peixe
Hélia Cardoso
Establishment of a Protocol for the Characterization of Secreted Biomolecules in Somatic Embryogenic Cultures of <i>Olea europaea</i> L.
Horticulturae
somatic embryogenesis
olive
conditioned medium
secretome
proteome
metabolome
title Establishment of a Protocol for the Characterization of Secreted Biomolecules in Somatic Embryogenic Cultures of <i>Olea europaea</i> L.
title_full Establishment of a Protocol for the Characterization of Secreted Biomolecules in Somatic Embryogenic Cultures of <i>Olea europaea</i> L.
title_fullStr Establishment of a Protocol for the Characterization of Secreted Biomolecules in Somatic Embryogenic Cultures of <i>Olea europaea</i> L.
title_full_unstemmed Establishment of a Protocol for the Characterization of Secreted Biomolecules in Somatic Embryogenic Cultures of <i>Olea europaea</i> L.
title_short Establishment of a Protocol for the Characterization of Secreted Biomolecules in Somatic Embryogenic Cultures of <i>Olea europaea</i> L.
title_sort establishment of a protocol for the characterization of secreted biomolecules in somatic embryogenic cultures of i olea europaea i l
topic somatic embryogenesis
olive
conditioned medium
secretome
proteome
metabolome
url https://www.mdpi.com/2311-7524/11/3/331
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