CONTRATADOS
GIULIETTI Ana Maria
congresos y reuniones científicas
Título:
PROLINE EFFECTS ON SECONDARY METABOLIC PATHWAYS IN RUBIA TINCTORUM CELL SUSPENSIONS.
Autor/es:
CARLA QUEVEDO; ANA MARIA GIULIETTI; JULIAN RODRIGUEZ TALOU
Lugar:
Pinamar
Reunión:
Congreso; XLI Congreso de SAIB, Diciembre 2005; 2005
Resumen:
XLI Congreso de SAIB, Diciembre 2005, Pinamar. Proline effects on secondary metabolic pathways in Rubia tinctorum cell suspensions. Quevedo, Carla; Busto, Victor; Ianone, Florencia; Giulietti1, Ana M. and Rodriguez Talou, Julián.   Proline effects on secondary metabolic pathways in Rubia tinctorum cell suspensions.   Quevedo, Carla; Busto, Victor; Ianone, Florencia; Giulietti1, Ana M. and Rodriguez Talou, Julián1. 1Microbiología Industrial y Biotecnología, 2Farmacología, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires,Argentina. e-mail:jrtalou@ffyb.uba.ar   Proline biosynthesis in plants stimulates the pentose phosphate pathway which results in an increasing carbon flux through the shikimate pathway. Shikimate pathway supplies carbon structures for many secondary metabolic pathways  in plants. Chorismate, which is the end product of the shikimate pathway, becomes the branch point for the synthesis of phenylpropanoid and anthraquinones (AQs) in Rubia tinctorum secondary metabolism. We tested the effect of proline addition in plant suspension cultures of R. tinctorum in order to study the competition between the two above mentioned secondary metabolic pathways. Suspension cultures were treated with  proline at different concentrations 0.25, 5 and 25 mM. Low proline level (0.25mM) produced an increase on AQs (50%) while high levels of proline ( 5 and 25 mM) showed a significant decrease on AQs accumulation ( 35 % an 50 %) and an increase in phenolics concentration. The increase on phenolic acids content was preceded by an induction on PAL activity. Glucose-6-phosphate dehydrogenase was induced during  stationary phase of the growth curve. Suspension cultures treated with proline 5 y 25 mM showed lower levels of Peroxidase activities than the control treatment.