1991
DOI: 10.1016/0021-9673(91)85086-u
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Dertermination of chlorophylls and carotenoids by high-performance liquid chromatography during olive lactic fermentation

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Cited by 102 publications
(59 citation statements)
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“…Violaxanthin, neoxanthin, anteraxanthin, δ-carotene and γ-carotene were supplied by Carote Nature (Lupsingen, Switzerland). Luteoxanthin and mutatoxanthin were obtained by acidification with 1 M HCl in ethanol (Khachik et al, 1986), purified by NP-and RP-TLC (Mínguez-Mosquera et al, 1991).…”
Section: Isolation Of Carotenoid Standards For Hplcmentioning
confidence: 99%
See 1 more Smart Citation
“…Violaxanthin, neoxanthin, anteraxanthin, δ-carotene and γ-carotene were supplied by Carote Nature (Lupsingen, Switzerland). Luteoxanthin and mutatoxanthin were obtained by acidification with 1 M HCl in ethanol (Khachik et al, 1986), purified by NP-and RP-TLC (Mínguez-Mosquera et al, 1991).…”
Section: Isolation Of Carotenoid Standards For Hplcmentioning
confidence: 99%
“…The separation was performed using a gradient (flow 1.25 mL·min −1 ) with the mobile phases: water/ion pair/methanol (1/1/8, v/v/v) and methanol/acetone (1/1, v/v). The ion pair was 0.05 M tetrabutylammonium and 1 M ammonium acetate in water (Mínguez-Mosquera et al, 1991). A photodiode array detector was used for detection, registering the signal between 350 nm−800 nm, although the quantification was performed between 430 nm−450 nm, depending on the maximum absorption of the carotenoids.…”
Section: Analysis Of Carotenoids By Hplcmentioning
confidence: 99%
“…The C-13 epimer of Chl a was prepared by treatment with chloroform (Watanabe et al, 1984), and 13 2 -OH-Chl a and b were obtained as described by Laitalainen et al (1990). All standards were purified by normal-phase and reverse-phase TLC (Mínguez-Mosquera et al, 1991. The separation and quantification of Chl degradation products were carried out by HPLC (HP1100 Hewlett-Packard liquid chromatograph fitted with a HP1100 automatic injector) using a stainless-steel column (25 3 0.46 cm i.d.)…”
Section: Chl and Derivative Extraction And Hplc Analysismentioning
confidence: 99%
“…packed with a 5-mm C 18 Superior ODS-2 (Teknokroma). Separation was performed using an elution gradient (2 mL min 21 ) with the mobile phases water:ion pair reagent:methanol (1:1:8, v/v/v) and methanol:acetone (1:1, v/v), as described by Mínguez-Mosquera et al (1991). Sequential detection was performed with a photodiode array detector at 650 nm for series b and 666 nm for series a compounds.…”
Section: Chl and Derivative Extraction And Hplc Analysismentioning
confidence: 99%
“…The purity of the isolated pigment was checked by HPLC. 17 Activity assay A reaction mixture containing 0.1 mmol of substrate (Chl a) dissolved in acetone (0.1 ml), 100 mM TrisHCl buffer (pH 8.5) and crude chlorophyllase extract in a ratio of 1:5:5 (total volume 1.1 ml) was prepared. The reaction was carried out using 1.5 ml microfuge tubes (Threff Lab, Degersheim, Switzerland) in a thermostatic bath at 50°C in the dark for 1 h with continuous shaking.…”
Section: Preparation Of Substrate and Standardsmentioning
confidence: 99%