Biolistics transformation of callus and cell suspension cultures of Capsicum annuum L. ‘Serrano’ is useful for in vitro studies of the relative contents of secondary metabolites

Capsicum annuum is a crop species of economic importance able to produce capsaicinoids, capsinoids, and pigments with nutritional and medicinal value. Methods to propagate and transform this species have been reported, but most are phenotype dependent, rely on Agrobacterium for transformation, and t...

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Veröffentlicht in:Acta Agrobotanica 2019-01, Vol.72 (4)
Hauptverfasser: Brito-Sánchez, Sara Cristina, Zaragoza-Pérez, Fredy Alan, Olivera-Flores, Teresa de Jesús, Rivero-Cruz, José Fausto, Amacosta, Jessica, Gutiérrez-Luna, Francisca Morayna, Valencia-Turcotte, Lilián Gabriela, Rodríguez-Sotres, Rogelio
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Sprache:eng
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Zusammenfassung:Capsicum annuum is a crop species of economic importance able to produce capsaicinoids, capsinoids, and pigments with nutritional and medicinal value. Methods to propagate and transform this species have been reported, but most are phenotype dependent, rely on Agrobacterium for transformation, and their success has been limited. This relates to only one commercial transgenic variety currently on trial. In the present work, we report the conditions to produce callus and cell suspension cultures of C. annuum ‘Serrano’ using commercial seeds. The culture could be induced to produce capsaicin and dihydrocapsaicin in detectable quantities and was amenable to transformation using biolistics. The expression of the Arabidopsis thaliana soluble inorganic pyrophosphatase 4 fused to a fluorescent protein was demonstrated using confocal microscopy. Evidence of the integrity of the fusion was obtained by immunoblot. The transformation induced a change in the ratio of capsaicin to dihydrocapsaicin measured using high resolution direct sample analysis-mass spectrometry (DSA-MS). The method is thus useful for the study of capsaicinoid production under controlled conditions for special purposes and metabolic studies.
ISSN:2300-357X
0065-0951
2300-357X
DOI:10.5586/aa.1792