Production of weakly active or inactive mutants of alkaline phosphatase and their expression in yeast
View Patent ↗The invention concerns a method for the recombinant production or expression of eukaryotic alkaline phosphatase mutants in yeast cells wherein the specifically introduced mutations result in a reduction of the specific AP activity by at least a factor 1:100. The invention also concerns a method for inserting corresponding nucleic acid sequences into a vector for expression in methylotrophic yeast strains and it concerns corresponding vectors and host strains.
1. A recombinant DNA coding for a mutant of eukaryotic alkaline phosphatase, wherein said DNA comprises the nucleic acid sequence of SEQ ID NO: 8.
2. A vector comprising a nucleic acid encoding an alkaline phosphatase, wherein said nucleic acid comprises SEQ ID NO: 8.
3. A vector of claim 2 , wherein said vector is selected from the group of vectors consisting of pPICZαA, B, C; pPICZ, pPICZ-E, pPICZα-E; pPIC6, pPIC6αA, B, C; pGAPZ, pGAPZαA, B, C; pPIC9; pPIC9K, pPIC3.5, pPIC3.5K, pAO815, pMET, pMETαA, B, C; pYES-DEST52, pYES2.1/V5-His-TOPO, pYC2-E, pYES2.1-E; YES-vectors, pTEF1/Zeo, pTEF1/Bsd, pNMT-TOPO.
4. A host cell transformed with the vector of claim 2 or 3 .
5. The host cell of claim 4 , wherein the cell is Pichia pastoris.
6. A method for producing a eukaryotic alkaline phosphatase in yeast cells comprising the steps:
a) preparing a first vector construct and a second vector construct wherein the first and second vector constructs each comprise a recombinant DNA encoding the polypeptide of SEQ ID NO: 4, wherein the first vector construct comprises a resistance gene to a first selection marker and the second vector construct comprises a resistance gene to a second selection marker,
b) transforming said yeast cells with the first and second vector constructs, wherein said transforming comprises:
i. selecting transformants which have integrated DNA from the first vector construct into a genome of the yeast cells by selected growth of the yeast cells on nutrient medium containing a low concentration of a first selection marker,
ii. increasing copy number of the integrated DNA from the first vector construct by multiple transfections of the yeast cells and further selected growth of the yeast cells on nutrient medium containing increased concentrations of a first selection marker,
iii. selecting transformants which have integrated DNA from the second vector construct into the genome of the host cell by selected growth of the yeast cells on nutrient medium containing a low concentration of a second selection marker,
iv. increasing copy number of the integrated DNA from the second vector construct by multiple transfections of the yeast cells and further selected growth of the yeast cells on nutrient medium containing increased concentrations of a second selection marker,
c) expressing the alkaline phosphatase and
d) purifying the alkaline phosphatase.
7. The method of claim 6 , wherein methylotrophic yeast cells are used.
8. The method of claim 7 , wherein Pichia pastoris is used as the yeast cell.
9. The method of claim 6 , wherein the first and second vectors are independently selected from the group of vectors consisting of pPICZαA, B, C; pPICZ, pPICZ-E, pPICZα-E; pPIC6, pPIC6αA, B, C; pGAPZ, pGAPZαA, B, C; pPIC9; pPIC9K, pPIC3.5, pPIC3.5K, pAO815.
10. An isolated polynucleotide encoding the polypeptide of SEQ ID NO: 4.
11. A vector comprising the polynucleotide of claim 10 .
12. The vector of claim 11 wherein the vector is selected from the group consisting of pPICZαA, B, C; pPICZ, pPICZ-E, pPICZα-E; pPIC6, pPICαA, B, C; pGAPZαA, B, C; pPIC9; pPIC9K, pPIC3.5, pPIC3.5K, pAO815, pMET, pMETαA, B, C; pYES-DEST52, pYES2.1/V5-His-TOPO, pYC2-E, pYES2.1-E; YES-vectors, pTEF1/Zeo, pTEF1/Bsd, and pNMT-TOPO.
13. A host cell transformed with the vector of claim 11 or 12 .
14. The host cell of claim 13 wherein the cell is Pichia pastoris.