A method of analysis of 3-indolylacetic acid (IAA) and abscisic acid (ABA), allowing the simultaneous extraction of both regulators from plant material, has been developed. The method involves extraction with methanol, isolation of the acid fraction, diazomethane methylation, separation of the hormo
Analysis of abscisic acid by high-performance liquid chromatography
โ Scribed by Nancy L. Cargile; Rolf Borchert; James D. McChesney
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- English
- Weight
- 638 KB
- Volume
- 97
- Category
- Article
- ISSN
- 0003-2697
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โฆ Synopsis
Methodology for the ready analysis of abscisic acid (ABA) in plant tissues based upon application of high-performance liquid chromatography (hplc) has been developed. The method involves isolation of the acid fraction, preparation of the methyl esters with diazomethane, and hplc using a combination procedure of two columns: (1) reversed-phase C,,, and (2) porous silica in the absorption mode. Only isocratic elution is required so the method is readily adaptable to laboratories having limited hplc capability. Measured recoveries are 70% and the use of an internal standard allows quantification of ABA levels to I rig/g of tissue with minimum absolute detectable levels of ABA of 20 ng. The method is illustrated by analysis of ABA concentration in potato tubers at various times postcutting.
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The direct resolution of racemic jasmonic acid (JA) and abscisic acid (ABA), as the free acids, into the corresponding enantiomers by high performance liquid chromatography on a Nucleodex p-PM column is reported. The resolution factors (R,,,=1.38; R,,,,=1.65) were such that the method could be appli
A HPLC assay for ABA and bound ABA is described. The method uses conventional acid-base ether extractions for partial cleanup of the plant extracts followed by Sephadex G-25 column fractionation. The ABA is separated and detected by HPLC on a 3 m x 2.1 mm i.d. column of SCX-Zipax with a uv detector.
Three different well-characterized preparations of proteoglycan subunits were analyzed by high-performance liquid chromatography on a silica-based material bonded with an amide phase. The biochemical integrity of the proteoglycan subunits was retained during this procedure. The high sensitivity coup