Phosphate limited inducible promoter and a
An evolvable production strain of B. subtilis exhibiting continuous or high level expression during protein evolution is described. An evolved Bacillus subtilis pstS promoter facilitates screening and production of secreted proteins.
1. A method for controlling the expression kinetics of a protein of interest, said method comprising culturing under phosphate limiting conditions, a Bacillus host cell comprising a nucleic acid comprising a Bacillus subtilis PstS promoter variant, said PstS promoter variant comprising a sequence corresponding to nucleotides −100 to +106 of PstS promoter from B. subtilis strain W168, wherein said sequence comprises at least one mutation chosen from A17T, A26G, A32G and T86C.
2. The method of claim 1 , wherein said nucleic acid is integrated into the chromosome of said host cell.
3. The method of claim 1 , wherein said host cell further comprises a nucleic acid encoding a polypeptide of interest under the transcriptional control of said PstS promoter variant.
4. The method of claim 1 , wherein said host cell expresses a heterologous sequence under nutrient limited conditions.
5. The method of claim 4 , wherein said expression is prolonged.
6. A method of producing a protein, comprising:
providing a host cell transformed with an expression vector comprising a nucleic acid comprising a Bacillus subtilis PstS promoter variant, said PstS promoter variant comprising a sequence corresponding to nucleotides −100 to +106 of PstS promoter from B. subtilis strain W168, wherein said sequence comprises at least one mutation chosen from A17T, A26G, A32G and T86C;
cultivating said transformed host cell under conditions suitable for said host cell to produce said protein; and
recovering said protein.
7. A method of screening mutants cells for protein secretion comprising:
providing a host cell transformed with an expression vector comprising a nucleic acid comprising a Bacillus subtilis PstS promoter variant, said PstS promoter variant comprising a sequence corresponding to nucleotides −100 to +106 of PstS promoter from B. subtilis strain W168, wherein said sequence comprises at least one mutation chosen from A17T, A26G, A32G and T86C;
cultivating said transformed host cell under conditions suitable for said host cell to produce said protein in the presence of a hydrolysable substrate; and
measuring the extent of hydrolysis of the substrate.