Method of eliminating dependence of methanol induced promoter on single methanol carbon source
Provided is a method of eliminating the dependence of methanol induced promoter on a single methanol carbon source for expressing foreign polypeptide. The method comprises activating the expression of the promoter requiring methanol induction by increasing the expression quantity of Mit1 polypeptide in cells of methylotrophic yeast, so that the promoter originally depending on methanol induction no longer depends on single methanol and can also express foreign polypeptide.
1. A method for eliminating the dependence on methanol as the single carbon source of a methanol inducible promoter for driving the expression of an exogenous polypeptide encoding gene, comprising:
(1) providing a methylotrophic yeast, said methylotrophic yeast comprises:
expression cassette 1, which expresses an exogenous Mit1 polypeptide; and
expression cassette 2, which comprises a methanol inducible promoter and an exogenous polypeptide encoding gene which is operably linked to the promoter;
(2) culturing the methylotrophic yeast in (1) under the conditions wherein there is no methanol or methanol is not the only carbon source,
wherein the condition of when methanol is not the only carbon source is a condition wherein the carbon source comprises glycerol and methanol or a condition containing glucose and methanol;
wherein the Mit1 polypeptide is
a polypeptide with an amino acid sequence as set forth in SEQ ID NO: 2 or a polypeptide with an amino acid sequence having more than 95% identity to the amino acid sequence as set forth in SEQ ID NO: 2 and having the ability to induce a methanol inducible promoter to express an exogenous polypeptide with carbon sources other than methanol.
2. The method according to claim 1 , wherein said methanol inducible promoter comprises: AOX1 promoter, DHAS promoter, DAS promoter, FDH promoter, FMDH promoter, MOX promoter, AOX2 promoter, ZZA1, PEX5-, PEX8-, PEX14-promoter, PMP20 promoter, PMP47 promoter, AOD1 promoter, or AOD2 promoter.
3. The method according to claim 1 , wherein the methylotrophic yeast comprises: Pichia, Hansenula, Candida , or Torulopsis.
4. The method according to claim 3 , wherein the Pichia comprises GS115 , Pichia wherein the MIG1 gene and MIG2 gene are unexpressed, Pichia wherein the NRG1 gene, MIG1 gene and MIG2 gene are unexpressed, or Pichia wherein the HXS1 gene is unexpressed.
5. The method according to claim 1 , wherein the expression cassette 1 comprises a promoter and a Mit1 polypeptide encoding gene which is operably linked to the promoter.
6. The method according to claim 5 , wherein the promoter comprises a constitutive promoter, an inducible promoter, a tissue or organ specific promoter, or a temporal and spatial specificity expression promoter.
7. The method according to claim 1 , wherein a yeast medium containing glycerol and/or glucose is used in step (2).
8. A recombinant methylotrophic yeast, said methylotrophic yeast comprises:
expression cassette 1, which expresses an exogenous Mit1 polypeptide, the Mit1 polypeptide being a polypeptide with an amino acid sequence as set forth in SEQ ID NO: 2 or a polypeptide with an amino acid sequence having more than 95% identity to the amino acid sequence as set forth in SEQ ID NO: 2 and having the ability to induce a methanol inducible promoter to express an exogenous polypeptide with carbon sources other than methanol; and
expression cassette 2, which comprises a methanol inducible promoter and an exogenous polypeptide encoding gene which is operably linked to the promoter.
9. The recombinant methylotrophic yeast according to claim 8 , wherein the methylotrophic yeast comprises: Pichia, Hansenula, Candida , or Torulopsis.
10. The recombinant methylotrophic yeast according to claim 9 , wherein the Pichia comprises GS115 , Pichia wherein the MIG1 gene and MIG2 gene are unexpressed, Pichia wherein the NRG1 gene, MIG1 gene and MIG2 gene are unexpressed, or Pichia wherein the HXS1 gene is unexpressed.
11. The recombinant methylotrophic yeast according to claim 10 , wherein the MIG1 gene has a nucleotide sequence as set forth in SEQ ID NO: 9;
the MIG2 gene with a nucleotide sequence as set forth in SEQ ID NO: 10;
the HXS1 gene with a nucleotide sequence as set forth in SEQ ID NO: 3; or
the NRG1 gene with a nucleotide sequence as set forth in SEQ ID NO:8.