Xylose isomerases that confer efficient xylose fermentation capability to yeast

Patent metadata

Field	Value
Publication number	US-11692187-B2
Application number	US-201716472514-A
Country	US
Kind code	B2
Filing date	Dec 21, 2017
Priority date	Dec 21, 2016
Publication date	Jul 4, 2023
Grant date	Jul 4, 2023

Abstract

The present invention relates to novel nucleic acid sequences encoding bacterial xylose isomerases that upon transformation of a eukaryotic microbial host cell, such as yeast, to confer to the host cell the ability of isomerising xylose to xylulose. The nucleic acid sequences encode xylose isomerases that originate from bacteria such as Eubacterium sp., Clostridium cellulosi and others. The invention further relates to fermentation processes wherein the transformed host cells ferment a xylose-containing medium to produce ethanol or other fermentation products.

First claim

The invention claimed is:

1. A genetically engineered fungal cell that is able to grow on xylose as a sole carbon source, wherein the fungal cell comprises a polynucleotide encoding a xylose isomerase having at least 95% sequence identity with SEQ ID NO: 7.

2. The fungal cell according to claim 1 , wherein the fungal cell is a yeast or a filamentous fungus of a genus selected from the group consisting of Saccharomyces, Kluyveromyces, Candida, Pichia, Schizosaccharomyces, Hansenula, Kloeckera, Schwanniomyces, Yarrowia, Kazachstania Naumovia, Aspergillus, Trichoderma, Humicola, Acremonium, Fusarium , and Penicillium.

3. The fungal cell according to claim 2 , wherein the fungal cell is a yeast that is capable of performing anaerobic alcoholic fermentation.

4. The fungal cell according to claim 3 , wherein the yeast belongs to a Saccharomyces species selected from the group consisting of S. cerevisiae, S. bayanus, S. bulderi, S. cervazzii, S. cariocanus, S. castellii, S. dairenensis, S. exiguus, S. kluyveri, S. kudriazevii, S. mikatae, S. paradoxus, S. pastorianus, S. turicensis and S. unisporus.

5. The fungal cell according to claim 1 , wherein the polynucleotide encoding the xylose isomerase is operably linked to a promoter that is insensitive to catabolite repression and that does not require xylose for induction.

6. The fungal cell according to claim 1 , wherein the fungal cell is further genetically modified to comprise a polynucleotide encoding a xylulose kinase.

7. The fungal cell according to claim 1 , wherein the fungal cell further comprises at least one genetic modification that results in a characteristic selected from the group consisting of:
a) increased tolerance to ethanol;
b) increased tolerance to acetic acid;
c) reduced production of glycerol;
d) increased xylose to ethanol fermentation rate; and,
e) increased thermotolerance.

8. The fungal cell according to claim 1 , wherein the polynucleotide encoding the polypeptide with xylose isomerase activity is integrated into the genome of the fungal cell.

9. The fungal cell according to claim 1 , wherein the fungal cell is suitable for large scale industrial fermentation.

10. The fungal cell according to claim 1 , wherein the fungal cell is a diploid, aneuploid, or polyploid cell.

11. The fungal cell according to claim 1 , wherein the fungal cell has the ability to produce at least one fermentation product selected from the group consisting of ethanol, lactic acid, 3-hydroxy-propionic acid, acrylic acid, acetic acid, succinic acid, citric acid, amino acids, 1,3-propane-diol, ethylene, glycerol, butyric acid, caproate, butanol, glyoxylate, muconic acid, fatty alcohols, fatty acids, β-lactam antibiotics, and cephalosporins.

12. The fungal cell of claim 6 , wherein the xylulose kinase is XKS1.

Assignees

• Vib Vzw
• Univ Leuven Kath
• Globalyeast N V

Inventors

• Thevelein Johan
• Demeke Mekonnen
• Foulquié Moreno Maria Remedios
• De Graeve Stijn
• Valdomiro Charles Belo Edgard

Classifications

• C12N9/92 Primary

  Glucose isomerase {(5.3.1.5; 5.3.1.9; 5.3.1.18)} · CPC title

• C12P7/18

  polyhydric · CPC title

• C12N15/905

  in yeast · CPC title

• C12N15/87

  Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation · CPC title

• C12P13/04

  Alpha- or beta- amino acids {(other amino acids C12P13/005)} · CPC title