Xylose utilization in recombinant zymomonas
View Patent ↗Xylose-utilizing Zymomonas strains studied were found to accumulate ribulose when grown in xylose-containing media. Engineering these strains to increase ribose-5-phosphate isomerase activity led to reduced ribulose accumulation, improved growth, improved xylose utilization, and increased ethanol production.
1. A recombinant bacterial host cell comprising:
a) a xylose metabolic pathway comprising at least one gene encoding a polypeptide having xylose isomerase activity;
b) at least one gene encoding a polypeptide having ribose-5-phosphate isomerase activity selected from the group consisting of ribose-5-phosphate isomerase A and ribose-5-phosphate isomerase B; and
c) at least one genetic modification which increases ribose-5-phosphate isomerase activity in the host cell as compared with ribose-5-phosphate isomerase activity in the host cell lacking said genetic modification;
wherein the bacterial host cell utilizes xylose to produce ethanol; and
wherein the bacterial host cell is selected from the group consisting of Zymomonas and Zymobacter.
2. The recombinant host cell of claim 1 wherein the at least one genetic modification of step (c) is over-expression of an endogenous gene encoding a polypeptide having ribose-5-phosphate isomerase activity.
3. The recombinant host cell of claim 1 wherein the at least one genetic modification of step (c) is expression of at least one non-endogenous gene encoding a polypeptide having ribose-5-phosphate isomerase activity.
4. The recombinant microorganism of claim 1 wherein the polypeptide having ribose-5-phosphate isomerase activity has the EC classification EC 5.3.1.6.
5. The recombinant host cell of claim 1 wherein the ribose-5-phosphate isomerase A polypeptide:
i) gives an E-value score of 0.1 or less when queried using a Profile Hidden Markov Model prepared using SEQ ID NOs:, 86, 96, and 97; the query being carried out using the hmmsearch algorithm wherein the Z parameter is set to 1 billion, and
ii) has aspartic acid and glutamic acid at positions corresponding to 107 and 129, respectively, in the Saccharomyces cerevisiae RPI-A protein of SEQ ID NO:97.
6. The recombinant host cell of claim 1 wherein the ribose-5-phosphate isomerase A has an amino acid sequence having at least 90% identity to an amino acid sequence selected from the group consisting of SEQ ID NOs:86, 96 and 97 based on the Clustal W method of alignment using the default parameters of GAP PENALTY=10, GAP LENGTH PENALTY=0.1, and Gonnet 250 series of protein weight matrix.
7. The recombinant host cell of claim 6 wherein the ribose-5-phosphate isomerase A has an amino acid sequence having at least 90% identity to an amino acid sequence selected from the group consisting of SEQ ID NOs: 86, 96, and 97 based on the Clustal W method of alignment using the default parameters of GAP PENALTY=10, GAP LENGTH PENALTY=0.1, and Gonnet 250 series of protein weight matrix.
8. The recombinant host cell of claim 1 wherein said microorganism further comprises at least one genetic modification which increases xylose isomerase activity as compared to xylose isomerase activity in the microorganism lacking said genetic modification.
9. The recombinant host cell of claim 1 wherein the gene encoding a polypeptide having xylose isomerase activity is over-expressed.
10. The recombinant microorganism of claim 1 wherein the gene encoding a polypeptide having xylose isomerase activity is expressed in multicopy.
11. A process for producing ethanol comprising:
a) providing a recombinant bacterial host cell of claim 1 ; and
b) culturing the bacterial host cell of (a) in a medium comprising xylose whereby xylose is converted to ethanol.
12. The process of claim 11 wherein the medium comprises either a mixture of sugars including xylose or xylose as a sole sugar.