Methods for producing polypeptidies in protease-deficient mutants of trichoderma
The present invention relates to mutants of a parent Trichoderma strain, comprising a polynucleotide encoding a polypeptide and one or more (several) genes selected from the group consisting of a first subtilisin-like serine protease gene, a first aspartic protease gene, a trypsin-like serine protease gene, a second subtilisin-like serine protease gene, and a second aspartic protease gene, wherein the one or more (several) genes are modified rendering the mutant strain deficient in the production of one or more (several) enzymes selected from the group consisting of a first subtilisin-like serine protease, a first aspartic protease, a trypsin-like serine protease, a second subtilisin-like serine protease, and a second aspartic protease, respectively, compared to the parent Trichoderma strain when cultivated under identical conditions. The present invention also relates to methods of producing a polypeptide in such mutants and methods for producing such mutants.
1. An isolated mutant strain, of a parent Trichoderma strain comprising a polynucleotide encoding a polypeptide and a first subtilisin-like serine protease gene, a first aspartic protease gene, a trypsin-like serine protease gene, a second subtilisin-like serine protease gene, and a second aspartic protease gene,
wherein the first subtilisin-like serine protease gene, the first aspartic protease gene, the trypsin-like serine protease gene, the second subtilisin-like serine protease gene, and the second aspartic protease gene are modified rendering the mutant strain at least 95% deficient in the production of each of the first subtilisin-like serine protease, the first aspartic protease, the trypsin-like serine protease, the second subtilisin-like serine protease, and the second aspartic protease, respectively, compared to the parent Trichoderma strain when cultivated under identical conditions;
wherein the first subtilisin-like serine protease is selected from the group consisting of:
(a) a polypeptide comprising an amino acid sequence having at least 95% sequence identity to SEQ ID NO: 2 or amino acids 20 to 882 of SEQ ID NO: 2; and
(b) a polypeptide encoded by a polynucleotide comprising a nucleotide sequence having at least 95% sequence identity to SEQ ID NO: 1 or nucleotides 58 to 2774 of SEQ ID NO: 1, or the cDNA thereof;
wherein the first aspartic protease is selected from the group consisting of:
(a) a polypeptide comprising an amino acid sequence having at least 95% sequence identity to SEQ ID NO: 4 or amino acids 21 to 407 of SEQ ID NO: 4; and
(b) a polypeptide encoded by a polynucleotide comprising a nucleotide sequence having at least 95% sequence identity to SEQ ID NO: 3 nucleotides 61 to 1299 of SEQ ID NO: 3, or the cDNA thereof;
wherein the trypsin-like serine protease is selected from the group consisting of:
(a) a polypeptide comprising an amino acid sequence having at least 95% sequence identity to SEQ ID NO: 6 or amino acids 20 to 259 of SEQ ID NO: 6; and
(b) a polypeptide encoded by a polynucleotide comprising a nucleotide sequence having at least 95% sequence identity to SEQ ID NO: 5 or nucleotides 58 to 930 of SEQ ID NO: 5, or the cDNA thereof;
wherein the second subtilisin-like serine protease is selected from the group consisting of:
(a) a polypeptide comprising of an amino acid sequence having at least 95% sequence identity to SEQ ID NO: 100 or amino acids 16 to 540 of SEQ ID NO: 100; and
(b) a polypeptide encoded by a polynucleotide comprising a nucleotide sequence having at least 95% sequence identity to SEQ ID NO: 99 or nucleotides 46 to 1681 of SEQ ID NO: 99 or the cDNA thereof;
wherein the second aspartic protease is selected from the group consisting of:
(a) a polypeptide comprising an amino acid sequence having at least 95% sequence identity to SEQ ID NO: 108 or amino acids 18 to 395 of SEQ ID NO: 108; and
(b) a polypeptide encoded by a polynucleotide comprising a nucleotide sequence having at least 95% sequence identity to SEQ ID NO: 107 or nucleotides 52 to 1339 of SEQ ID NO: 107, or the cDNA thereof; and
wherein the polypeptide is native or foreign to the parent Trichoderma strain.
2. The isolated mutant of claim 1 , wherein the parent Trichoderma strain is selected from the group consisting of Trichoderma harzianum, Trichoderma koningii, Trichoderma longibrachiatum, Trichoderma reesei , and Trichoderma viride.
3. The isolated mutant of claim 1 , wherein the parent Trichoderma strain is Trichoderma reesei.
4. The isolated mutant of claim 1 , which is completely deficient in the first subtilisin-like serine protease, the first aspartic protease, the trypsin-like serine protease, the second subtilisin-like serine protease, and the second aspartic protease compared to the parent Trichoderma strain when cultivated under identical conditions.
5. The isolated mutant of claim 1 , wherein the first subtilisin-like serine protease comprises
SEQ ID NO: 2 or amino acids 20 to 882 of SEQ ID NO: 2.
6. The isolated mutant of claim 1 , wherein the first aspartic protease comprises
SEQ ID NO: 4 or amino acids 21 to 407 of SEQ ID NO: 4.
7. The isolated mutant of claim 1 , wherein the trypsin-like serine protease comprises
SEQ ID NO: 6 or amino acids 20 to 259 of SEQ ID NO: 6.
8. The isolated mutant of claim 1 , wherein the second subtilisin-like serine protease comprises
SEQ ID NO: 100 or amino acids 16 to 540 of SEQ ID NO: 100.
9. The isolated mutant of claim 1 , wherein the second aspartic protease comprises
SEQ ID NO: 108 or amino acids 18 to 395 of SEQ ID NO: 108.
10. A method of producing a polypeptide, comprising:
(a) cultivating the isolated mutant of claim 1 in a medium for the production of the polypeptide; and
(b) recovering the polypeptide from the cultivation medium.
11. The method of claim 10 , wherein the parent Trichoderma strain is selected from the group consisting of Trichoderma harzianum , Trichoderma koningii , Trichoderma Iongibrachiatum , Trichoderma reesei , and Trichoderma viride .
12. The method of claim 10 , wherein the parent Trichoderma strain is Trichoderma reesei .
13. The method of claim 10 , wherein the mutant is completely deficient in the first subtilisin-like serine protease, the first aspartic protease, the trypsin-like serine protease, the second subtilisin-like serine protease, and the second aspartic protease compared to the parent Trichoderma strain when cultivated under identical conditions.
14. The method of claim 10 , wherein the first subtilisin-like serine protease comprises SEQ ID NO: 2 or amino acids 20 to 882 of SEQ ID NO: 2.
15. The method of claim 10 , wherein the first aspartic protease comprises SEQ ID NO: 4 or amino acids 21 to 407 of SEQ ID NO: 4.
16. The method of claim 10 , wherein the trypsin-like serine protease comprises SEQ ID NO: 6 or amino acids 20 to 259 of SEQ ID NO: 6.
17. The method of claim 10 , wherein the second subtilisin-like serine protease comprises SEQ ID NO: 100 or amino acids 16 to 540 of SEQ ID NO: 100.
18. The method of claim 10 , wherein the second aspartic protease comprises SEQ ID NO: 108 or amino acids 18 to 395 of SEQ ID NO: 108.
19. A method for obtaining the mutant of claim 1 , comprising:
(a) modifying the first subtilisin-like serine protease gene, the first aspartic protease gene, the trypsin-like serine protease gene, the second subtilisin-like serine protease gene, and the second aspartic protease gene in the parent Trichoderma strain; and
(b) identifying a mutant strain from step (a) wherein the first subtilisin-like serine protease gene, the first aspartic protease gene, and the trypsin-like serine protease gene are modified rendering the mutant strain deficient in the production of the first subtilisin-like serine protease, the first aspartic protease, a trypsin-like serine protease, the second subtilisin-like serine protease, and the second aspartic protease, respectively, compared to the parent Trichoderma strain when cultivated under identical conditions.
20. The method of claim 19 , wherein the parent Trichoderma strain is selected from the group consisting of Trichoderma harzianum , Trichoderma koningii , Trichoderma Iongibrachiatum , Trichoderma reesei , and Trichoderma viride .
21. The method of claim 19 , wherein the parent Trichoderma strain is Trichoderma reesei .
22. The method of claim 19 , wherein the mutant is completely deficient in the first subtilisin-like serine protease, the first aspartic protease, the trypsin-like serine protease, the second subtilisin-like serine protease, and the second aspartic protease compared to the parent Trichoderma strain when cultivated under identical conditions.
23. The method of claim 19 , wherein the first subtilisin-like serine protease comprises SEQ ID NO: 2 or amino acids 20 to 882 of SEQ ID NO: 2; the first aspartic protease comprises SEQ ID NO: 4 or amino acids 21 to 407 of SEQ ID NO: 4; the trypsin-like serine protease comprises SEQ ID NO: 6 or amino acids 20 to 259 of SEQ ID NO: 6; the second subtilisin-like serine protease comprises SEQ ID NO: 100 or amino acids 16 to 540 of SEQ ID NO: 100; and the second aspartic protease comprises SEQ ID NO: 108 or amino acids 18 to 395 of SEQ ID NO: 108.