abstract
Albeit ionic-liquid-based aqueous biphasic systems (ABS) have been largely explored as liquid-liquid extractive approaches for a large array of (bio)molecules, the application of biodegradable and nontoxic salts as phase constituents of these systems has been seldom investigated. In this work 15 ionic liquids were evaluated toward their ability to form ABS in the presence of a common biodegradable organic salt: potassium citrate. The ternary phase diagrams, tie-lines, and respective tie-line lengths, were determined at 25 degrees C. The gathered data allowed the evaluation of the effects of the ionic liquid cation core, of the cation side alkyl chain length, and of the anion nature, to form two-phase systems. It is shown that the ionic liquids aptitude to undergo liquid-liquid demixing is mainly controlled by their hydrophobicity. The large differences observed between the phase diagrams behavior suggest the possibility of tailoring the aqueous phases' polarities for a specific extraction. Therefore, the partitioning of a hydrophobic amino acid produced by bacteria fermentation, L-tryptophan, was also addressed aiming at exploring the applicability of the proposed systems in the biotechnology field. Single-step extraction efficiencies of L-tryptophan for the ionic-liquid-rich phase range between 72% and 99%. (C) 2012 Elsevier B.V. All rights reserved.
keywords
2-PHASE SYSTEMS; 1-BUTYL-3-METHYLIMIDAZOLIUM BROMIDE; TRYPTOPHAN PRODUCTION; GENETIC MANIPULATION; POLYETHYLENE-GLYCOL; POTASSIUM CITRATE; PHASE-SEPARATION; AMINO-ACIDS; EXTRACTION; SODIUM
subject category
Biotechnology & Applied Microbiology; Engineering
authors
Passos, H; Ferreira, AR; Claudio, AFM; Coutinho, JAP; Freire, MG
our authors
Groups
G4 - Renewable Materials and Circular Economy
G5 - Biomimetic, Biological and Living Materials
Projects
acknowledgements
This work was financed by national funding from FCT-Fundacao para a Ciencia e a Tecnologia, through the projects PTDC/QUI-QUI/121520/2010 and the Pest-C/CTM/LA0011/2011. The authors also acknowledge FCT for the post-doctoral and doctoral grants SFRH/BPD/41781/2007, SFRH/BDE/33835/2009, and SFRH/BD/74503/2010 of M.G. Freire, A.R. Ferreira, and A.F.M. Claudio, respectively.