| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 10843163 | Protein Expression and Purification | 2013 | 8 Pages | 
Abstract
												Expression of scFv in Brevibacillus choshinensis was tested using combinations of three different promoters and four different secretion signals. Two model scFv constructs, i.e., His-scFvFLU and His-scFvHEL, were successfully expressed with some of the combinations. Ni Sepharose column and size exclusion chromatography resulted in fairly pure preparations of these two proteins. The purified His-scFvFLU inhibited fluorescence from fluorescein, while the purified His-scFvHEL inhibited lysozyme activity. Relatively high yield of His-scFvFLU (â¼40%) and His-scFvHEL (â¼30%) was achieved with the expression and purification system described here.
											Keywords
												
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											Authors
												Hiromasa Onishi, Makoto Mizukami, Hiroshi Hanagata, Masao Tokunaga, Tsutomu Arakawa, Akira Miyauchi, 
											