High-level production of Fc-fused kringle domain in Pichia pastoris

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Recently, as a new non-immunoglobulin-based protein scaffold, a human kringle domain was successfully engineered toward biologically functional agonists and antagonists. In this study, the fed-batch cultivation conditions were optimized for enhanced production of an Fc-fused kringle domain (KD548-Fc) in Pichia pastoris. Fed-batch cultivations were performed in 5-l laboratory-scale bioreactors, and in order to find the optimal conditions for high-level production of KD548-Fc, several parameters including the initial carbon source (glycerol) concentration, temperature, and pH were investigated. When cells were cultivated at pH 4.0 and 25 A degrees C with 9.5 % glycerol in the initial medium, the highest production yield (635 mg/l) was achieved with high productivity (7.2 mg/l/h). Furthermore, functional KD548-Fc was successfully purified from the culture broth using a simple purification procedure with high purity and recovery yield.
Publisher
SPRINGER HEIDELBERG
Issue Date
2014-06
Language
English
Article Type
Article
Keywords

FED-BATCH FERMENTATION; PROTEIN-PRODUCTION; MOLECULAR RECOGNITION; RECOMBINANT PROTEIN; EXPRESSION SYSTEM; BINDING-PROTEINS; DEATH RECEPTORS; OPTIMIZATION; STRATEGIES; ANTIBODIES

Citation

JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, v.41, no.6, pp.989 - 996

ISSN
1367-5435
DOI
10.1007/s10295-014-1435-2
URI
http://hdl.handle.net/10203/193044
Appears in Collection
CBE-Journal Papers(저널논문)
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