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Ultra-high-performance liquid chromatography fingerprinting method for chemical screening of metabolites in cultivation broth
Authors:Zdeněk Kameník  Franz Hadacek  Markéta Marečková  Dana Ulanova  Jan Kopecký  Vladimír Chobot  Kamila Plháčková  Jana Olšovská
Institution:1. Institute of Microbiology of the Academy of Sciences of the Czech Republic, v.v.i., Vídeňská 1083, 142 20 Prague 4, Czech Republic;2. Charles University, Faculty of Science, Department of Analytical Chemistry, Albertov 8, 128 40 Prague 2, Czech Republic;3. University of Vienna, Faculty of Life Sciences, Department of Chemical Ecology and Ecosystem Research, Althanstrasse 14, 1090 Vienna, Austria;4. Crop Research Institute, Drnovská 507, 161 06 Prague 6, Czech Republic
Abstract:A fingerprinting method for chemical screening of microbial metabolites, potential antibiotics, in spent cultivation broths is described. The method is based on high-throughput ultra-high-performance liquid chromatography (UHPLC) separation with UV detection (photodiode array detector). Thirteen antibiotic standards and four cultivation broths were used for the method development. The comparison of ten liquid–liquid and solid phase extraction protocols for sample clean-up and pre-concentration revealed that Oasis HLB C18 sorbent gives the best recoveries. The Acquity BEH C18 chromatographic column was chosen for the samples separation with respect to its universality, selectivity, efficiency and robustness. The method is presented by two 3D fingerprints for every sample that was obtained under different, acidic and alkaline, UHPLC conditions. The acidic mobile phase consisted of 0.5% phosphoric acid with methanol and the alkaline mobile phase of 1 mM ammonium formate, pH 9 with acetonitrile. Each pair of 3D fingerprints includes the following physico-chemical information: polarity (retention time), presence and characterization of chromophores (UV spectra), compound concentration (detector response), and acid–base properties (influence of different pH of the aqueous parts of mobile phases on retention times). The sample extraction and method validation were assessed with relative standard deviation (RSD) of 0.5, 5.0 and 20.0% for retention times, peak areas and minor compound peak areas, respectively.
Keywords:UHPLC  High-throughput fingerprinting  Secondary metabolites  Antibiotics  Cultivation broth  Actinomycetes
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