Abstract
A "novel" protocol is presented for easy and reliable estimation of soluble hydroxycinnamate levels in Cichorium intybus L. leaf tissue in large-scale experiments. Samples were standardized by punching 6 discs per leaf, and hydroxycinnamates were extracted by submerging the discs in 80% ethanol with 5% acetic acid for at least 48 h in the darkness at 4°C. Residual dry mass of the discs was used for a posteriori correction of compound levels. Chlorophyll was eliminated by chloroform, and the aqueous phases were transferred to microplates, dried, and dissolved in 50% methanol for HPLC analysis and storage. An HPLC program of 8 min was developed for the analysis of the extracts. Comparisons with extractions of liquid nitrogen powders indicated that the novel extraction method was reliable. No degradation of the major hydroxycinnamates - caftaric, chlorogenic, and chicoric acids - was observed, during maceration at ambient temperatures, or after storage for 1 year. © 2012 Meriem Bahri et al.
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CITATION STYLE
Bahri, M., Hance, P., Grec, S., Quillet, M. C., Trotin, F., Hilbert, J. L., & Hendriks, T. (2012). A “novel” protocol for the analysis of hydroxycinnamic acids in leaf tissue of chicory (Cichorium intybus L., Asteraceae). The Scientific World Journal, 2012. https://doi.org/10.1100/2012/142983
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