IP Library › Granted Patent US 9,567,596
Granted Patent B2
US 9,567,596 · App. 14/370,255 · Granted Feb 14, 2017

Protease deficient filamentous fungal cells and methods of use thereof

Inventors: Christopher Landowski (Helsinki, FI); Anne Huuskonen (Helsinki, FI); Juhani Saarinen (Helsinki, FI); Ann Westerholm-Parvinen (Kirkkonummi, FI); Anne Kanerva (Helsinki, FI); Jari Natunen (Vantaa, FI); Anna-Liisa Hanninen (Helsinki, FI); Noora Salovuori (Helsinki, FI); Merja Penttila (Helsinki, FI); Markku Saloheimo (Helsinki, FI)
Assignee: Glykos Finland OY
C12N15/80C07K14/56C07K14/61C07K14/65C12N9/58C12P21/005C12P21/02Y02P20/52
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,567,596
App. No.
14/370,255
Granted
Feb 14, 2017
Kind
B2
Abstract

The present disclosure relates to compositions and methods useful for the production of heterologous proteins in filamentous fungal cells.

Claims (34)

1. A Trichoderma cell comprising at least three endogenous proteases having reduced or eliminated activity wherein nucleic acids encoding the proteases are modified to reduce or eliminate expression of the proteases and further comprising a recombinant polynucleotide encoding a heterologous polypeptide, wherein the heterologous polypeptide is produced at a level of at least twofold higher than the production level of the polypeptide in a corresponding parental Trichoderma cell, and wherein the Trichoderma cell has reduced or eliminated activity in at least

(i) a gap1 protease of SEQ ID NO: 118, SEQ ID NO: 119, SEQ ID NO: 120, or homologues thereof having at least 90% sequence identity thereto,

(ii) a gap2 protease of SEQ ID NO: 129, SEQ ID NO:130, SEQ ID NO:131, or homologues thereof having at least 90% sequence identity thereto, and

(iii) a pep3 protease of SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, or SEQ ID NO: 21, or homologues thereof having at least 90% sequence identity thereto.

2. The Trichoderma cell of claim 1 , wherein at least one of the nucleic acids is a gene comprising a mutation within the coding sequence of the gene that reduces or eliminates the protease activity.

3. The Trichoderma cell of claim 1 , wherein the Trichoderma cell is further modified to reduce or eliminate expression of the protease activity of at least one other Trichoderma protease selected from the group consisting of

a pep1 protease of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, or homologues thereof having at least 90% sequence identity thereto,

a pep2 protease of SEQ ID NO: 182, SEQ ID NO: 183, SEQ ID NO: 184, or homologues thereof having at least 90% sequence identity thereto,

a pep4 protease of SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, or homologues thereof having at least 90% sequence identity thereto,

a pep5 protease of SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, or homologues thereof having at least 90% sequence identity thereto,

a pep8 protease of SEQ ID NO: 507, SEQ ID NO: 508, SEQ ID NO: 509 or homologues thereof having at least 90% sequence identity thereto,

a pep11 protease of SEQ ID NO: 522, SEQ ID NO: 523, SEQ ID NO: 524, or homologues thereof having at least 90% sequence identity thereto,

a pep12 protease of SEQ ID NO: 530, SEQ ID NO: 531, SEQ ID NO: 532, or homologues thereof having at least 90% sequence identity thereto,

a tsp1 (protease of SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, or homologues thereof having at least 90% sequence identity thereto,

a slp1 protease of SEQ ID NO: 82, SEQ ID NO: 83, SEQ ID NO: 84, SEQ ID NO: 85, SEQ ID NO:86, or homologues thereof having at least 90% sequence identity thereto,

a slp2 protease of SEQ ID NO: 98, SEQ ID NO: 99, SEQ ID NO:100, SEQ ID NO: 101, or homologues thereof having at least 90% sequence identity thereto,

a slp3 protease of SEQ ID NO: 166, SEQ ID NO: 167, SEQ ID NO:168, SEQ ID NO: 169, or homologues thereof having at least 90% sequence identity thereto, and

a slp7 protease of SEQ ID NO: 231, SEQ ID NO:232, SEQ ID NO:233, or homologues thereof having at least 90% 4 sequence identity thereto.

4. The Trichoderma cell of claim 1 , wherein the heterologous polypeptide is a mammalian polypeptide that is either a naturally non-glycosylated polypeptide or a naturally glycosylated polypeptide.

5. The Trichoderma cell of claim 4 , wherein the mammalian polypeptide is a glycosylated mammalian polypeptide.

6. The Trichoderma cell of claim 4 , wherein the mammalian polypeptide is selected from the group consisting of an antibody, an antigen-binding fragment of an antibody, a growth factor, an interferon, a cytokine, and an interleukin.

7. The Trichoderma cell of claim 1 , wherein the Trichoderma cell further comprises a modification to reduce or eliminate the activity of an ALG3 gene encoding dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase.

8. The Trichoderma cell of claim 7 , wherein the gene encoding ALG3 is deleted from the Trichoderma cell.

9. The Trichoderma cell of claim 1 , wherein the Trichoderma cell further comprises a polynucleotide encoding an α-1,2-mannosidase.

10. The Trichoderma cell of claim 1 , further comprising a polynucleotide encoding an N-acetylglucosaminyltransferase I catalytic domain.

11. The Trichoderma cell of claim 10 , further comprising a polynucleotide encoding an N-acetylglucosaminyltransferase II catalytic domain.

12. The Trichoderma cell of claim 1 , further comprising a polynucleotide encoding a mannosidase II and/or a galactosyl transferase.

13. A method of improving the extracellular stability of a polypeptide, comprising

a) providing the Trichoderma cell of claim 1 , and

b) culturing the Trichoderma cell such that the heterologous polypeptide is expressed, wherein the heterologous polypeptide exhibits increased extracellular stability compared to the heterologous polypeptide when produced in a corresponding parental Trichoderma cell.

14. A method of making a heterologous polypeptide, comprising

a) providing the Trichoderma cell of claim 1 ,

b) culturing the Trichoderma cell such that the heterologous polypeptide is expressed, and

c) purifying the heterologous polypeptide.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2021
From: NOVARTIS AG; GLYKOS FINLAND OY
To: GLYKOS FINLAND OY
Reel/Frame 056061/0610 →
Continuity (2)
Provisional Application 61583559 · Jan 5, 2012
Related Publication 20140370546A1 · Dec 18, 2014