Methods for producing a polypeptide in a
View Patent ↗The present invention relates to methods for producing a polypeptide, comprising: (a) cultivating a Bacillus host cell in a medium conducive for the production of the polypeptide, wherein the Bacillus cell comprises a nucleic acid construct comprising (i) a tandem promoter in which each promoter sequence of the tandem promoter is operably linked to a single copy of a nucleic acid sequence encoding the polypeptide and alternatively also (ii) an mRNA processing/stabilizing sequence located downstream of the tandem promoter and upstream of the nucleic acid sequence encoding the polypeptide; and (b) isolating the polypeptide from the cultivation medium. The present invention also relates to methods for producing a polypeptide, comprising: (a) cultivating a Bacillus host cell in a medium conducive for the production of the polypeptide, wherein the Bacillus cell comprises a nucleic acid construct comprising (i) a “consensus” promoter having the sequence TTGACA for the “−35” region and TATAAT for the “−10” region operably linked to a single copy of a nucleic acid sequence encoding the polypeptide and (ii) an mRNA processing/stabilizing sequence located downstream of the “consensus” promoter and upstream of the nucleic acid sequence encoding the polypeptide; and (b) isolating the polypeptide from the cultivation medium.
1. A Bacillus cell comprising a nucleic acid construct which comprises (a) a “consensus” promoter of a Bacillus amyloliquefaciens alpha-amylase gene (amyQ) having the sequence TTGACA for the “−35” region and TATAAT for the “−10” region and having the nucleic acid sequence of SEQ ID NO:26 or SEQ ID NO:27 further operably linked to a single copy of a nucleic acid sequence encoding a polypeptide, and (b) a cryIIIA mRNA processing/stabilizing sequence located downstream of the “consensus” promoter and upstream of the nucleic acid sequence encoding the polypeptide, wherein the mRNA processing/stabilizing sequence increases expression of the nucleic acid sequence encoding the polypeptide.
2. The Bacillus cell of claim 1 , which contains one or more copies of the nucleic acid construct.
3. The Bacillus cell of claim 1 , which contains one copy of the nucleic acid construct.
4. The Bacillus cell of claim 1 , wherein the nucleic acid construct further comprises a selectable marker gene.
5. The Bacillus cell of claim 1 , which contains no selectable marker gene.
6. The Bacillus cell of claim 1 , wherein the nucleic acid sequence encodes a polypeptide heterologous to the Bacillus cell.
7. The Bacillus cell of claim 1 , wherein the polypeptide is a hormone, enzyme, receptor, antibody, or reporter.
8. The Bacillus cell of claim 7 , wherein the enzyme is an oxidoreductase, transferase, hydrolase, lyase, isomerase, or ligase.
9. The Bacillus cell of claim 7 , wherein the enzyme is an aminopeptidase, amylase, carbohydrase, carboxypeptidase, catalase, cellulase, chitinase, cutinase, cyclodextrin glycosyltransferase, deoxyribonuclease, esterase, alpha-galactosidase, beta-galactosidase, glucoamylase, alpha-glucosidase, beta-glucosidase, invertase, laccase, lipase, mannosidase, mutanase, oxidase, a pectinolytic enzyme, peroxidase, phytase, polyphenoloxidase, proteolytic enzyme, ribonuclease, transglutaminase, or xylanase.
10. The Bacillus cell of claim 1 , wherein the nucleic acid sequence is contained in the chromosome of the Bacillus cell.
11. The Bacillus cell of claim 1 , wherein the nucleic acid sequence is contained on an extrachromosomal element.
12. The Bacillus cell of claim 1 , which is a Bacillus alkalophilus, Bacillus amyloliquefaciens, Bacillus brevis, Bacillus circulans, Bacillus clausli, Bacillus coagulans, Bacillus firmus, Bacillus lautus, Bacillus lentus, Bacillus licheniformis, Bacillus megaterium, Bacillus pumilus, Bacillus stearothermophilus, Bacillus subtilis , or Bacillus thuringiensis cell.
13. The Bacillus cell of claim 1 , which is a Bacillus subtilis cell.