Transgenic microbial polyhydroxyalkanoate producers
View Patent ↗Transgenic microbial strains are provided which contain the genes required for PHA formation integrated on the chromosome. The strains are advantageous in PHA production processes, because (1) no plasmids need to be maintained, generally obviating the required use of antibiotics or other stabilizing pressures, and (2) no plasmid loss occurs, thereby stabilizing the number of gene copies per cell throughout the fermentation process, resulting in homogeneous PHA product formation throughout the production process. Genes are integrated using standard techniques, preferably transposon mutagenesis. In a preferred embodiment wherein mutiple genes are incorporated, these are incorporated as an operon. Sequences are used to stabilize mRNA, to induce expression as a function of culture conditions (such as phosphate concentration), temperature, and stress, and to aid in selection, through the incorporation of selection markers such as markers conferring antibiotic resistance.
1. A genetically engineered microorganism producing polyhydroxyalkanoate, the improvement comprising having at least one heterologous bacterial gene encoding enzyme involved in the synthesis of polyhydroxalkanoates selected from the group consisting of thiolase, reductase, PHB synthase, PHA synthase, acyl-CoA transferase, and enoyl-CoA hydratase integrated into the chromosome, which stably expresses the enzyme and thereby has enhanced production of polyhydroxyalkanoate.
2. The microorganism of claim 1 selected from the group consisting of E. coil, Azotobacter, Pseudomonas putida, and Ralstonia eutropha(Alcaligenes eutrophus ).
3. The microorganism of claim 1 wherein the heterologous bacterial gene is inserted using transposon delivery.
4. The microorganism of claim 1 comprising multiple integrated bacterial genes expresing enzymes involved in synthesis of polyhydroxyalkcanoate wherein the integrated genes are operably linked as an operon.
5. The microorganism of claim 1 wherein the integrated bacterial gene is operably linked under the control of a promoter.
6. The microorganism of claim 1 wherein the integrated bacterial gene is operably linked with upstream activating sequences.
7. The microorganism of claim 1 wherein the integrated bacterial gene is operably linked with mRNA stabilizing sequences.
8. The microorganism of claim 5 wherein the promoter includes a consensus E. coil pho box and −35 promoter region that is regulated by the phosphate concentration in the medium.
9. The microorganism of claim 5 wherein the promoter is selected from the group consisting of a promoter that induces expression under general stress conditions such as nutrient limitation, pH or heat shock, and administration of toxic chemicals.
10. The microorganism of claim 1 wherein the integrated bacterial gene is operably linked with a selection marker.
11. The microorganism of claim 1 wherein the integrated bacterial gene is isolated or derived from a microorganism selected from the group consisting of A. eutrophus, Aeromonas caviae, Zoogleoa ramigera, Nocardia, Rhodococcus, Pseudomonas Sp. 6-3, Pseudomonas acidophila, Pseudomonas oleovarans, Chromobacterium violaeuum, and Alcaligenes latus.
12. The microorganism of claim 1 wherein the integrated bacterial gene encodes an enzyme selected from the group consisting of PHB polymerase from R. eutropha (C1), PHA polymerase from P. oleovorans (C3), PHB polymerase from A. caviae (C12), ACP::CoA transacylase from P. putida (G3), (R)-specific enouyl-CoA hydratase from A. caviae (J12), a broad substrate specific 3-ketoacyl-CoA thilase from R. eutropha (A1-II), and phasins from R. eutropha (P1-I and P1-II).
13. The microorganism of claim 1 wherein the bacterial gene is integrated as a single copy on the chromosome of the microorganism.
14. A method for screening for a bacterial gene involved in synthesis of polyhydroxyalkanoates that enhances production comprising
mutating a genetically engineered microorganism having at least one bacterial gene encoding an enzyme involved in synthesis of polyhydroxyalkanoates selected from group consisting of thiolase, reductase, PHB synthase, PHA synthase, acyl-CoA transferase enoyl-CoA hydratase, wherein the gene is integrated into the chromosome, which stably expresses the enzyme so that the microorganism produces polyhydroxyalkanoate, and screening for enhanced production of polyhydroxyalkanoates relative to production of polyhydroxyalkanoate by the microorganism expressing the enzyme from a gene which is not integrated, by measuring the increase in the percent by weight of the polhydyroxyalkanoate.
15. The method of claim 14 wherein the integrated bacterial gene is isolated or derived from a microorganism selected from the group consisting of A. eutrophus, Aeromonas caviae, Zoogloea ramigera, Nocardia, Rhodococcus, Pseudomonas Sp. 61-3, Pseudomonas acidophila, Pseudomonas oleovarans, Chromobacterium violaceum, and Alcaligenes latus .
16. A method for producing polyhydroxyalkanoates comprising culturing genetically engineered microorganisms capable of producing polyhydroxyalkanoates having at least one bacterial gene encoding an enzyme involved in synthesis of polyhydroxyalkanoates selected from the group consisting of thiolase, reductas, PHB synthase, PHA synthase, acyl-CoA transferase, enoyl-CoA hydratase, integrated into the chromosome, with appropriate substrate under conditions wherein the microorganisms produce polyhydroxyalkanoate.
17. The method of claim 16 wherein the microorganisms comprise multiple integrated bacterial genes involved in synthesis of polyhydroxyalkanoate wherein the integrated genes are operably linked as an operon.
18. The method of claim 16 wherein the microorganisms comprise bacterial genes selected from the group consisting of genes integrated operably linked under the control of a promoter, genes integrated and operably linked with upstream activating sequences, genes integrated and operably linked with mRNA stabilizing sequences, genes operably linked with a promoter including a consensus E. coli pho box and −35 promoter region that is regulated by the phosphate concentration in the medium, and genes integrated and operably linked with a selection marker.