cBSA-147 for the preparation of bacterial biofilms in a microchannel reactor
Author(s) -
Jeck Fei Ng,
Stephan Jaenicke,
Klaus Eisele,
Jan Dorn,
Tanja Weil
Publication year - 2010
Publication title -
biointerphases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.633
H-Index - 45
eISSN - 1934-8630
pISSN - 1559-4106
DOI - 10.1116/1.3474475
Subject(s) - microreactor , chemistry , biocatalysis , biofilm , bioreactor , microchannel , chromatography , bovine serum albumin , catalysis , chemical engineering , cationic polymerization , enantioselective synthesis , nanotechnology , bacteria , organic chemistry , materials science , ionic liquid , biology , engineering , genetics
Whole cells are attractive biocatalysts, particularly if the reaction requires cofactors or involves multiple transformations. Immobilization of the catalyst is often a prerequisite for continuous processes. The highly cationic chemically modified plasma protein bovine serum albumin (cBSA-147) has been applied for the electrostatically mediated immobilization of the planktonic bacterium E. coli BL21 star (DE3), and the resulting biofilms were superior to those formed on poly-L-lysine coated surfaces. The biocatalyst was immobilized in a capillary column (inside diameter of 530 μm and L=30 m) and evaluated in the enantioselective reduction of ethyl acetoacetate to R-(-)ethyl hydroxybutyrate. In continuous operation in the microreactor format, the productivity of the cells was about 30% higher than that determined in a bench-scale fermentation system. This increase is attributed to the improved mass transfer over short geometrical dimensions. The similarity in the results indicates that studies on a biofilm-coated microreactor can be used for the accelerated collection of data for process optimization.
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