TY - JOUR
T1 - Quantification of free and total salicylic acid in plants by solid-phase extraction and isocratic high-performance anion-exchange chromatography
AU - Rozhon, Wilfried
AU - Petutschnig, Elena
AU - Wrzaczek, Michael
AU - Jonak, Claudia
N1 - Funding Information:
Acknowledgements This work was supported by the Lower Austrian State Academy and the Austrian Science Foundation. We thank Karin Zwerger, Stefan Kempa, and Andreas Verhounig for critical reading of the manuscript and Andreas Rizzi for helpful discussion. We appreciate the gift of Pseudomonas syringe DC3000 (pVSP61) from Andrew F. Bent (University of Wisconsin-Madison, USA). Thanks to Anneliese Auer for taking care of the plants.
PY - 2005/7
Y1 - 2005/7
N2 - Salicylic acid (SA) is an important signaling compound in plants and is involved in various defense responses. Here we report a new method for quantification of free and total soluble SA in Arabidopsis thaliana with 5-fluorosalicylic acid (5-FSA) as internal standard. The SA was isolated from leaf extracts by solid-phase extraction with phenyl-phase cartridges and selectively eluted as the cationic iron(III)-complex. Recoveries of SA and 5-FSA were equal and exceeded 90%. Free SA was subsequently released from the iron(III)-complex by addition of 2,2′-bipyridyl and high-performance anion-exchange chromatography was performed on an NH2 column. The SA appeared as last peak with a retention time of 15 min, baseline-separated from other substances. On-line detection was performed fluorimetrically for both SA and 5-FSA at an excitation wavelength of 300 nm and an emission wavelength of 410 nm, because both substances give similar fluorescence spectra. The detection limit for SA was 5 ng g-1 FW for a sample size of 100 mg. Thus the main advantages of the method are highly selective sample preparation, increased sensitivity, reduced analysis time compared with reversed-phase HPLC, and use of a novel internal standard detectable under the same conditions as SA. The techniques described are applicable to other plant materials.
AB - Salicylic acid (SA) is an important signaling compound in plants and is involved in various defense responses. Here we report a new method for quantification of free and total soluble SA in Arabidopsis thaliana with 5-fluorosalicylic acid (5-FSA) as internal standard. The SA was isolated from leaf extracts by solid-phase extraction with phenyl-phase cartridges and selectively eluted as the cationic iron(III)-complex. Recoveries of SA and 5-FSA were equal and exceeded 90%. Free SA was subsequently released from the iron(III)-complex by addition of 2,2′-bipyridyl and high-performance anion-exchange chromatography was performed on an NH2 column. The SA appeared as last peak with a retention time of 15 min, baseline-separated from other substances. On-line detection was performed fluorimetrically for both SA and 5-FSA at an excitation wavelength of 300 nm and an emission wavelength of 410 nm, because both substances give similar fluorescence spectra. The detection limit for SA was 5 ng g-1 FW for a sample size of 100 mg. Thus the main advantages of the method are highly selective sample preparation, increased sensitivity, reduced analysis time compared with reversed-phase HPLC, and use of a novel internal standard detectable under the same conditions as SA. The techniques described are applicable to other plant materials.
KW - 5-Fluorosalicylic acid
KW - Arabidopsis
KW - High-performance anion-exchange chromatography
KW - Salicylic acid
KW - Solid-phase extraction
UR - http://www.scopus.com/inward/record.url?scp=23244449730&partnerID=8YFLogxK
U2 - 10.1007/s00216-005-3326-x
DO - 10.1007/s00216-005-3326-x
M3 - Article
C2 - 15997378
AN - SCOPUS:23244449730
SN - 1618-2642
VL - 382
SP - 1620
EP - 1627
JO - Analytical and Bioanalytical Chemistry
JF - Analytical and Bioanalytical Chemistry
IS - 7
ER -