Evaluation of Aqueous Biphasic Electrophoresis System Based on Halide-Free Ionic Liquids for Direct Recovery of Keratinase

Aqueous biphasic electrophoresis system (ABES) incorporates electric fields into the biphasic system to separate the target biomolecules from crude feedstock. Ionic liquid (IL) is regarded as an excellent candidate as the phase-forming components for ABES because of the great electrical conductivity, which can promote the electromigration of biomolecules in ABES, and thereby enhances the separation efficiency of the target biomolecules from crude feedstock. The application of electric fields to the conventional biphasic system expedites the phase settling time of the biphasic system, which eases the subsequent scaling-up steps and reduces the overall processing time of the recovery process. Alkyl sulphate-based IL is a green and economical halide-free surfactant when compared to the other halide-containing IL. The feasibility of halide-free IL-based ABES to recover Kytococcus sedentarius TWHK01 keratinase was studied. Optimum partition coefficient (Ke = 7.53 ± 0.35) and yield (YT = 80.36% ± 0.71) were recorded with IL-ABES comprised of 15.0% (w/w) [EMIM][ESO4], 20.0% (w/w) sodium carbonate and 15% (w/w) crude feedstock. Selectivity (S) of 5.75 ± 0.27 was obtained with the IL-ABES operated at operation time of 5 min with 10 V voltage supplied. Halide-free IL is proven to be a potential phase-forming component of IL-ABES for large-scale recovery of keratinase.

THE EFFECT OF THE FORMATION OF POLYMER /SURFACTANT COMPLEXES ON SELECTED TRIBOLOGICAL PROPERTIES OF THEIR AQUEOUS SOLUTIONS

Aqueous solutions of sodium alkyl sulphate (surfactant) and polyvinylpyrrolidone (polymer) whose physicochemical properties, including complexing ability, have been widely described in the literature were proposed as a model lubricant. It has been assumed that aqueous solutions of these compounds will favourably modify lubricating properties of water under high load conditions. For this purpose, measurements were made on a four-ball apparatus (T-02 Tester) for aqueous solutions of these compounds. Two kinds of tests were carried out: at constant loads (2, 3, and 4 kN) and variable loads within the range of 0 to 7.2 kN. Unexpectedly, high decreases in motion resistance and wear as well as an increase in antiseizure properties were found in relation to water as a base. The results obtained are so promising that solutions with an optimized composition can find practical applications. The surprisingly high effectiveness of the additives used results from the formation of surfactant/polymer complexes. These adducts adsorb at the interface, and, under friction conditions, they form a lubricant film capable of carrying high loads.

Biocatalytic approaches for the quantitative production of single stereoisomers from racemates

Strategies for the chemoenzymatic transformation of a racemate into a single stereoisomeric product in quantitative yield have been developed. A range of industrially relevant α-hydroxycarboxylic acids was deracemized in a stepwise fashion via lipase-catalysed enantioselective O-acylation, followed by mandelate racemase-catalysed racemization of the remaining non-reacted substrate enantiomer. Alternatively, aliphatic α-hydroxycarboxylic acids were enzymatically isomerized using whole resting cells of Lactobacillus spp. Enantioselective hydrolysis of rac-sec-alkyl sulphate esters was accomplished using novel alkyl sulphatases of microbial origin. The stereochemical path of catalysis could be controlled by choice of the biocatalyst. Whereas Rhodococcus ruber DSM 44541 and Sulfolobus acidocaldarius DSM 639 act through inversion of configuration, stereo-complementary retaining sulphatase activity was detected in the marine planctomycete Rhodopirellula baltica DSM 10527.