IP Library Granted Patent US 7,332,341
Granted Patent B2
US 7,332,341 · App. 11/095,491 · Granted Feb 19, 2008

Methods for producing heterologous polypeptides in trichothecene-deficient filamentous fungal mutant cells

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Quick Facts
Patent No.
US 7,332,341
App. No.
11/095,491
Granted
Feb 19, 2008
Kind
B2
Abstract

The present invention relates to mutants cells comprising a marker-free modification of a gene, and methods for obtaining and using such mutant cells.

Claims (12)

1. A method for obtaining a mutant Fusarium venenatum cell, comprising:

(a) introducing into an endogenous gene of the genome of a parent Fusarium venenatum cell, a nucleic acid construct comprising a nucleic acid sequence of the endogenous gene inactivated with a nitrate reductase gene to produce a mutant Fusarium venenatum cell comprising an endogenous gene incapable of expressing the endogenous gene product wherein the endogenous gene is one or more genes selected from the group consisting of a tri3 gene, a tri4 gene, a tri6 gene, a trill gene, a tri12 gene, and a tril01 gene;

(b) selecting the resulting mutant Fusarium venenatum cell from step (a) for the presence of the nitrate reductase gene and loss of production of the gene product;

(c) introducing into the mutant Fusarium venenatum cell from step (b) a second nucleic acid construct comprising a second inactivated nucleic acid sequence of the endogenous gene comprising 5′ and 3′ regions of the inactivated nucleic acid sequence of the endogenous gene, but lacking the nitrate reductase gene, wherein the second nucleic acid construct incorporates into the genome of the mutant Fusarium venenatum cell replacing the inactivated nucleic acid sequence and is incapable of expressing the endogenous gene product; and

(d) selecting a mutant Fusarium venenatum cell from step (c) in the absence of the nitrate reductase gene.

2. The method of claim 1 , further comprising introducing into the parent Fusarium venenatum cell a nucleic acid construct comprising a tri5 gene inactivated with the nitrate reductase gene.

3. The method of claim 1 , wherein the endogenous nucleic acid sequence is a tri3 gene.

4. The method of claim 1 , wherein the endogenous nucleic acid sequence is a tri4 gene.

5. The method of claim 1 , wherein the endogenous nucleic acid sequence is a tri6 gene.

6. The method of claim 1 , wherein the endogenous nucleic acid sequence is a tri11 gene.

7. The method of claim 1 , wherein the endogenous nucleic acid sequence is a tri12 gene.

8. The method of claim 1 , wherein the endogenous nucleic acid sequence is a tri101 gene.

Assignments (1)
CHANGE OF NAME Recorded Sep 1, 2005
From: NOVOZYMES, INC.
To: NOVOZYMES, INC.
Reel/Frame 016937/0522 →