Abstract
The previously cloned Bacillus subtilis lipase gene (lip) was mapped on the chromosome and used in the construction of a B. subtilis derivative totally devoid of any lip sequence. Homologous overexpression was performed in this strain by subcloning the lip open reading frame on a multicopy plasmid under the control of a strong gram-positive promoter. A 100-fold overproducing strain was obtained, which should facilitate purification of the secreted protein. Furthermore, the Δlip strain BCL1050 constitutes an ideal host for the cloning of heterologous lipase genes.
| Original language | English |
|---|---|
| Pages (from-to) | 1670-1673 |
| Number of pages | 4 |
| Journal | Applied and Environmental Microbiology |
| Volume | 60 |
| Issue number | 5 |
| DOIs |
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| State | Published - 1994 |
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