Quantitative investigation of resolution increase of free-flow electrophoresis via simple interval sample injection and separation

• Published in: Electrophoresis Vol. 33; no. 14; pp. 2065 - 2074
• Main Authors: Shao, Jing, Fan, Liu-Yin, Cao, Cheng-Xi, Huang, Xian-Qing, Xu, Yu-Quan
• Format: Journal Article
• Language: English
• Published: Germany Blackwell Publishing Ltd 01.07.2012
• Subjects: Anti-Bacterial Agents - isolation & purification; Bandwidth; Coloring Agents - isolation & purification; Diffusion; Electrophoresis - economics; Electrophoresis - methods; Fermentation; Free-flow electrophoresis; Interval sample injection; Phenazines - isolation & purification; Phenols - isolation & purification; Pseudomonas aeruginosa - metabolism; Pyrroles - isolation & purification; Resolution; Sensitivity and Specificity
• ISSN: 0173-0835; 1522-2683; 1522-2683
• DOI: 10.1002/elps.201200169

Interval free‐flow zone electrophoresis (FFZE) has been used to suppress sample band broadening greatly hindering the development of free‐flow electrophoresis (FFE). However, there has been still no quantitative study on the resolution increase of interval FFZE. Herein, we tried to make a comparison between bandwidths in interval FFZE and continuous one. A commercial dye with methyl green and crystal violet was well chosen to show the bandwidth. The comparative experiments were conducted under the same sample loading of the model dye (viz. 3.49, 1.75, 1.17, and 0.88 mg/h), the same running time (viz. 5, 10, 15, and 20 min), and the same flux ratio between sample and background buffer (= 10.64 × 10−3). Under the given conditions, the experiments demonstrated that (i) the band broadening was evidently caused by hydrodynamic factor in continuous mode, and (ii) the interval mode could clearly eliminate the hydrodynamic broadening existing in continuous mode, greatly increasing the resolution of dye separation. Finally, the interval FFZE was successfully used for the complete separation of two‐model antibiotics (herein pyoluteorin and phenazine‐1‐carboxylic acid coexisting in fermentation broth of a new strain Pseudomonas aeruginosa M18), demonstrating the feasibility of interval FFZE mode for separation of biomolecules.