Method for the expression of biosynthetic genes in plant seeds using multiple expression constructs

• US 20040049805A1
• Filed: 07/07/2003
• Published: 03/11/2004
• Est. Priority Date: 01/19/2001
• Status: Abandoned Application

• Current Assignee: BASF Plant Science GmbH (BASF SE)
• Original Assignee: BASF Plant Science GmbH (BASF SE)
• Inventors: Drexler, Hjordis, Scheffler, Jodi, Bischoff, Friedrich, Lerchl, Jens, Duwenig, Elke, Heinz, Ernst
• Application Number:
  US10/250,821
• Publication Number:
  US 20040049805A1
• Time in Patent Office: Days
• US Class Current: 800/281
• CPC Class Codes: C12N 15/8247 involving modified lipid metabolism, e.g. seed oil composition
• CPC Class Codes: C12N 9/0083 Miscellaneous (1.14.99)
• CPC Class Codes: C12N 9/1029 transferring groups other than amino-acyl groups (2.3.1)

Abstract

The present invention relates to expression cassettes, to their combination and vectors comprising the expression cassettes comprising plant promoters with an expression specificity for plant seeds, in particular linseed, and to the use of these expression cassettes or vectors for the recombinant expression of heterologous genes in plants. The invention furthermore relates to transgenic plants which have been transformed with these expression cassettes or vectors, to cultures, parts or transgenic propagation material derived therefrom, and to their use as food, feed or seed, pharmaceuticals, fine chemicals or as industrial feedstock.

Claims

1. An expression cassette with a structure selected from the group consisting of:

a) L1-promoter-structural gene-L2,

b) L1-promoter-structural gene-L2-L1-promoter-structural gene-L2,

c) L1-promoter-structural gene-L2-L1-promoter-structural gene-L2-L1-promoter-structural gene-L2,

where L1, L2, promoter and structural gene have the following meanings;

L1=SEQ ID NO;

32 or a sequence comprising equivalent restriction cleavage sites,

L2=independently of one another SEQ ID NO;

33, 34 or 35 or sequences comprising equivalent restriction cleavage sites,

promoter=plant promoter

structural gene=a nucleic acid sequence which can be expressed in plants.

2. An expression cassette as claimed in claim 1, wherein the structural gene is a biosynthesis gene.

3. An expression cassette as claimed in claim 1 or 2, wherein the structural gene is a biosynthesis gene of the lipid or fatty acid metabolism.

4. An expression cassette as claimed in any of claims 1 to 3, wherein the structural gene is a plant gene.

5. An expression cassette as claimed in any of claims 1 to 4, wherein the gene is a nucleic acid sequence encoding proteins selected from the group consisting of:

acyl-CoA dehydrogenase(s), acyl-ACP[=acyl carrier protein] desaturase(s), acyl-ACP thioesterase(s), fatty acid acyl transferase(s), fatty acid synthase(s), fatty acid hydroxylase(s), acetyl-coenzyme A carboxylase(s), acyl-coenzyme A oxidase(s), fatty acid desaturase(s), fatty acid acetylenases, lipoxygenases, triacylglycerol lipases, allenoxide synthases, hydroperoxide lyases or fatty acid elongase(s).

6. An expression cassette as claimed in any of claims 1 to 5, wherein the gene is a nucleic acid sequence selected from the group consisting of:

a) a nucleic acid sequence with the sequence shown in SEQ ID NO;

1, SEQ ID NO;

3, SEQ ID NO;

5 or SEQ ID NO;

11,

b) nucleic acid sequences which, owing to the degeneracy of the genetic code, are obtained by backtranslating the amino acid sequences shown in SEQ ID NO;

2, SEQ ID NO;

4, SEQ ID NO;

6 or SEQ ID NO;

12,

c) derivatives of the nucleic acid sequence shown in SEQ ID NO;

1, SEQ ID NO;

3, SEQ ID NO;

5 or SEQ ID NO;

11, which encode polypeptides with the amino acid sequences shown in SEQ ID NO;

2, SEQ ID NO;

4, SEQ ID NO;

6 or SEQ ID NO;

12 and have at least 50% homology at the amino acid level, without essentially reducing the enzymatic action of the polypeptides.

7. The use of expression cassettes as claimed in any of claims 1 to 8 in a method for the production of fatty acid esters with an increased content of polyunsaturated fatty acids having at least two double bonds, which comprises introducing the expression cassette into an organism producing fatty acid esters, growing the organism and isolating the fatty acid esters present in the organism.

8. A method as claimed in claim 7, wherein the fatty acid esters produced by the method comprise polyunsaturated C₁₈-, C₂₀- or C₂₂-fatty acid molecules with at least two double bonds in the fatty acid ester.

9. A method as claimed in claim 7 or 8, wherein the C₁₈-, C₂₀- or C₂₂-fatty acid molecules are isolated from the organism in the form of an oil or lipid.

10. A method as claimed in any of claims 7 to 9, wherein the organism is a transgenic plant.

11. A method as claimed in any of claims 7 to 10, wherein the fatty acid esters contain C₁₈-, C₂₀- or C₂₂-fatty acids with three, four or five double bonds in the fatty acid ester.

12. A method as claimed in any of claims 7 to 11, wherein the polyunsaturated fatty acids present in the fatty acid esters are liberated.

13. A vector comprising an expression cassette as claimed in any of claims 1 to 6.

14. An organism comprising at least one expression cassette as claimed in any of claims 1 to 6 or at least one vector as claimed in claim 13.

15. An organism as claimed in claim 14, which is a plant.

16. A transgenic plant comprising a functional or nonfunctional nucleic acid sequence in an expression cassette as claimed in any of claims 1 to 6.

17. The use of an expression cassette as claimed in any of claims 1 to 6 for generating transgenic plants.