Car enzymes and improved production of fatty alcohols
The disclosure relates to variant carboxylic acid reductase (CAR) enzymes for the improved production of fatty alcohols in recombinant host cells.
1. A variant carboxylic acid reductase (CAR) polypeptide comprising an amino acid sequence having at least about 85% sequence identity to SEQ ID NO: 7, wherein the variant CAR polypeptide is genetically engineered to have at least one mutation at an amino acid position selected from the group consisting of amino acid positions 3, 18, 20, 22, 80, 87, 191, 288, 473, 535, 750, 827, 870, 873, 926, 927, 930, and 1128.
2. The variant CAR polypeptide of claim 1 , wherein expression of the variant CAR polypeptide in a recombinant host cell results in a higher titer of fatty alcohol compositions compared to a recombinant host cell expressing a corresponding wild type polypeptide.
3. The variant CAR polypeptide of claim 1 , wherein the CAR polypeptide is a CarB polypeptide.
4. The variant CAR polypeptide of claim 1 , wherein the variant CAR polypeptide comprises a mutation selected from the group consisting of S3R, D18R, D18L, D18T, D18P, E20V, E20S, E20R, S22R, S22N, S22G, L80R, R87G, R87E, V191S, F288R, F288S, F288G, Q473L, Q473W, Q473Y, Q473I, Q473H, A535S, D750A, R827C, R827A, 1870L, R873S, V926A, V926E, S927K, S927G, M930K, M930R and L1128W.
5. The variant CAR polypeptide of claim 4 , wherein the variant CAR polypeptide comprises mutation A535S.
6. The variant CAR polypeptide of claim 4 , wherein the variant polypeptide comprises a combination of mutations selected from the group consisting of:
E20R, F288G, Q473I, A535S;
E20R, F288G, Q473H, A535S, R827A, S927G;
E20R, S22R, F288G, Q473H, A535S, R827A, S927G;
S3R, E20R, S22R, F288G, Q473H, A535S, R873S, S927G, M930R, L1128W;
E20R, S22R, F288G, Q473H, A535S, R873S, S927G, M930R, L1128W;
D18R, E20R, S22R, F288G, Q473I, A535S, S927G, M930K, L1128W;
E20R, S22R, F288G, Q473I, A535S, R827C, V926E, S927K, M930R;
D18R, E20R, 288G, Q473I, A535S, R827C, V926E, M930K, L1128W;
E20R, S22R, F288G, Q473H, A535S, R827C, V926A, S927K, M930R;
E20R, S22R, F288G, Q473H, A535S, R827C;
E20R, S22R, F288G, Q473I, A535S, R827C, M930R;
E20R, S22R, F288G, Q473I, A535S, I870L, S927G, M930R;
E20R, S22R, F288G, Q473I, A535S, I870L, S927G;
D18R, E20R, S22R, F288G, Q473I, A535S, R827C, I870L, V926A, S927G;
E20R, S22R, F288G, Q473H, A535S, R827C, I870L, L1128W;
D18R, E20R, S22R, F288G, Q473H, A535S, R827C, I870L, S927G, L1128W;
E20R, S22R, F288G, Q473I, A535S, R827C, I870L, S927G, L1128W;
E20R, S22R, F288G, Q473I, A535S, R827C, I870L, S927G, M930K, L1128W;
E20R, S22R, F288G, Q473H, A535S, I870L, S927G, M930K;
E20R, F288G, Q473I, A535S, I870L, M930K;
E20R, S22R, F288G, Q473H, A535S, S927G, M930K, L1128W;
D18R, E20R, S22R, F288G, Q473I, A535S, S927G, L1128W;
E20R, S22R, F288G, Q473I, A535S, R827C, I870L, S927G;
D18R, E20R, S22R, F288G, Q473I, A535S, R827C, I870L, S927G, L1128W;
D18R, E20R, S22R, F288G, Q473I, A535S, S927G, M930R, L1128W;
E20R, S22R, F288G, Q473H, A535S, V926E, S927G, M930R; and
E20R, S22R, F288G, Q473H, A535S, R827C, I870L, V926A, L1128W.
7. A recombinant host cell comprising an exogenous polynucleotide sequence encoding a variant carboxylic acid reductase (CAR) polypeptide having at least 85% sequence identity to SEQ ID NO: 7 and having at least one mutation at an amino acid position selected from the group consisting of position 3, 18, 20, 22, 80, 87, 191, 288, 473, 535, 750, 827, 870, 873, 926, 927, 930, and 1128, wherein the recombinant host cell produces a fatty alcohol composition at a higher titer or yield than a host cell expressing a corresponding wild type CAR polypeptide when cultured in a medium containing a carbon source under conditions effective to express the variant CAR polypeptide.
8. The recombinant host cell of claim 7 , wherein the SEQ ID NO: 7 is the corresponding wild type CAR polypeptide.
9. The recombinant host cell of claim 7 , further comprising a polynucleotide encoding a) a thioesterase polypeptide; b) a FabB polypeptide and a FadR polypeptide; or c) fatty aldehyde reductase (AlrA) polypeptide.
10. The recombinant host cell of claim 7 , wherein the host cell is selected from the group consisting of a plant cell, an insect cell, a fungal cell, an algal cell, and a bacterial cell.
11. The recombinant host cell of claim 10 , wherein the host cell is a bacterial cell.
12. The recombinant host cell of claim 11 , wherein the bacterial cell is an E. coli cell.
13. A method of making a fatty alcohol composition comprising culturing a recombinant host cell comprising an exogenous polynucleotide sequence encoding a variant carboxylic acid reductase (CAR) polypeptide having at least 85% sequence identity to SEQ ID NO: 7 and having at least one mutation at an amino acid position selected from the group consisting of amino acid positions 3, 18, 20, 22, 80, 87, 191, 288, 473, 535, 750, 827, 870, 873, 926, 927, 930, and 1128, in a culture medium comprising a carbon source under conditions suitable to produce the fatty alcohol composition, wherein the fatty alcohol composition is released from the host cell into the culture medium.
14. The method of claim 13 , wherein the variant CAR polypeptide comprises a mutation selected from the group consisting of S3R, D18R, D18L, D18T, D18P, E20V, E20S, E20R, S22R, S22N, S22G, L80R, R87G, R87E, V191S, F288R, F288S, F288G, Q473L, Q473W, Q473Y, Q473I, Q473H, A535S, D750A, R827C, R827A, I870L, R873S, V926A, V926E, S927K, S927G, M930K, M930R, and L1128W.
15. The method of claim 14 , wherein the variant CAR polypeptide comprises mutation A535S.
16. The method of claim 14 , wherein the variant CAR polypeptide comprises a combination of mutations selected from the group consisting of:
E20R, F288G, Q473I, A535S;
E20R, F288G, Q473H, A535S, R827A, S927G;
E20R, S22R, F288G, Q473H, A535S, R827A, S927G;
S3R, E20R, S22R, F288G, Q473H, A535S, R873S, S927G, M930R, L1128W;
E20R, S22R, F288G, Q473H, A535S, R873S, S927G, M930R, L1128W;
D18R, E20R, S22R, F288G, Q473I, A535S, S927G, M930K, L1128W;
E20R, S22R, F288G, Q473I, A535S, R827C, V926E, S927K, M930R;
D18R, E20R, 288G, Q473I, A535S, R827C, V926E, M930K, L1128W;
E20R, S22R, F288G, Q473H, A535S, R827C, V926A, S927K, M930R;
E20R, S22R, F288G, Q473H, A535S, R827C;
E20R, S22R, F288G, Q473I, A535S, R827C, M930R;
E20R, S22R, F288G, Q473I, A535S, I870L, S927G, M930R;
E20R, S22R, F288G, Q473I, A535S, I870L, S927G;
D18R, E20R, S22R, F288G, Q473I, A535S, R827C, I870L, V926A, S927G;
E20R, S22R, F288G, Q473H, A535S, R827C, I870L, L1128W;
D18R, E20R, S22R, F288G, Q473H, A535S, R827C, I870L, S927G, L1128W;
E20R, S22R, F288G, Q473I, A535S, R827C, I870L, S927G, L1128W;
E20R, S22R, F288G, Q473I, A535S, R827C, I870L, S927G, M930K, L1128W;
E20R, S22R, F288G, Q473H, A535S, I870L, S927G, M930K;
E20R, F288G, Q473I, A535S, I870L, M930K;
E20R, S22R, F288G, Q473H, A535S, S927G, M930K, L1128W;
D18R, E20R, S22R, F288G, Q473I, A535S, S927G, L1128W;
E20R, S22R, F288G, Q473I, A535S, R827C, I870L, S927G;
D18R, E20R, S22R, F288G, Q473I, A535S, R827C, I870L, S927G, L1128W;
D18R, E20R, S22R, F288G, Q473I, A535S, S927G, M930R, L1128W;
E20R, S22R, F288G, Q473H, A535S, V926E, S927G, M930R; and
E20R, S22R, F288G, Q473H, A535S, R827C, I870L, V926A, L1128W.
17. The method of claim 13 , wherein the host cell further comprises a polynucleotide encoding a) a thioesterase polypeptide; b) a FabB polypeptide and a FadR polypeptide; or c) fatty aldehyde reductase (AlrA) polypeptide.
18. The method of claim 13 , wherein the host cell is selected from the group consisting of a plant cell, an insect cell, a fungal cell, an algal cell, and a bacterial cell.
19. The method of claim 18 , wherein the host cell is a bacterial cell.
20. The method of claim 19 , wherein the bacterial cell is an E. coli cell.