Thioesterase variants having improved activity for the production of medium-chain fatty acid derivatives
The disclosure relates to engineered plant acyl-ACP thioesterases having improved activity for the production of medium-chain fatty acid derivatives including e.g., eight carbon and ten carbon fatty acids and fatty acid derivatives. The disclosure further relates to recombinant host cells comprising the engineered plant acyl-ACP thioesterases having improved activity for the production of medium-chain fatty acid derivatives. The disclosure also relates to methods of decreasing toxicity and improving production of medium-chain fatty acids and derivatives.
1. A method for producing a medium-chain fatty acid derivative at commercial titers, the method comprising: culturing a recombinant host cell that comprises an engineered thioesterase variant in the presence of a carbon source under conditions suitable for the production of the medium-chain fatty acid derivative,
wherein the engineered thioesterase variant has an amino acid sequence that has at least 90% sequence identity to SEQ ID NO:1 and at least one substitution mutation at an amino acid position selected from the group consisting of: 3, 4, 6, 14, 15, 17, 22, 37, 44, 45, 50, 54, 56, 64, 67, 73, 76, 91, 99, 102, 110, 111, 114, 129, 132, 137, 158, 162, 165, 176, 178, 185, 186, 196, 197, 198, 203, 213, 217, 225, 227, 236, 244, 254, 256, 258, 278, 282, 292, 297, 298, 299, 300, 301, 302, 316, 321, and 322,
wherein the recombinant host cell comprises one or more heterologous genes that encode a biochemical pathway that converts a first fatty acid derivative to a second fatty acid derivative, and wherein the second fatty acid derivative has a higher minimum inhibitory concentration (MIC) than the first fatty acid derivative, and wherein the presence of the second fatty acid derivative increases the MIC of the first fatty acid derivative.
2. The method of claim 1 , wherein:
(i) the first fatty acid derivative is a medium-chain fatty acid and the second fatty acid derivative is a medium-chain fatty acid alkyl ester, and wherein the biochemical pathway comprises an ester synthase and fatty acyl-CoA synthetase,
or
(ii) the first fatty acid derivative is a medium-chain fatty acid and the second fatty acid derivative is a medium-chain fatty acid alkyl ester selected from a medium-chain fatty acid methyl ester or a medium-chain fatty acid ethyl ester,
or
(iii) the first fatty acid derivative is a medium-chain fatty alcohol and the second fatty acid derivative is a medium-chain fatty alcohol acetate, and wherein the biochemical pathway comprises a carboxylic acid reductase and an alcohol-O-acetyl transferase,
or
(iv) the engineered thioesterase variant has at least one substitution mutation that is a member selected from the group consisting of: (a) a lysine at amino acid position 3; (b) a methionine at amino acid position 4; (c) an arginine at amino acid position 6; (d) a glycine or an arginine at amino acid position 14; (e) a leucine or a tryptophan at amino acid position 15; (f) an alanine or a cysteine at amino acid position 17; (g) an arginine at amino acid position 22; (h) a proline at amino acid position 37; (i) a glycine or isoleucine at amino acid position 44; (j) a serine at position 45; (k) a tryptophan at amino acid position 50; (l) an arginine at amino acid position 54; (m) a lysine or a cysteine at amino acid position 56; (n) an arginine or a proline at amino acid position 64; (o) a leucine at amino acid position 67; (p) a valine at position 73; (q) a methionine at amino acid position 91; (r) an isoleucine at amino acid position 102; (s) a leucine at amino acid position 1-10; (t) a threonine at position 111; (u) a lysine at position 1-14; (v) a valine at amino acid position 129; (w) a tryptophan at amino acid position 132; (x) a cysteine at amino acid position 137; (y) a glutamine at amino acid position 158; (z) a glutamic acid at amino acid position 162; (aa) a valine at amino acid position 176; (bb) a proline at amino acid position 178; (cc) an alanine at amino acid position 185; (dd) a glycine at amino acid position 186; (ee) a valine at amino acid position 196; (ff) an asparagine at amino acid position 197; (gg) a tryptophan at amino acid position 198; (hh) an arginine at amino acid position 203; (ii) a histidine or an arginine at amino acid position 213; (jj) an arginine at amino acid position 217; (kk) a leucine at amino acid position 225; (ll) a glycine at amino acid position 227; (mm) a threonine at amino acid position 236; (nn) a methionine or an arginine at amino acid position 244; (oo) a glycine at amino acid position 254; (pp) a cysteine or an arginine at amino acid position 256; (qq) a threonine or a valine at amino acid position 258; (rr) a lysine or a valine at amino acid position 278; (ss) a serine or a valine at amino acid position 282; (tt) a phenylalanine at amino acid position 292; (uu) a threonine or an aspartic acid or a valine at amino acid position 297; (vv) a valine or a cysteine at amino acid position 298; (ww) a leucine at amino acid position 299; (xx) a lysine or a tryptophan or a leucine at amino acid position 300; (yy) a cysteine at amino acid position 301; (zz) a threonine at amino acid position 302; (aaa) an arginine at amino acid position 316; (bbb) an arginine at amino acid position 321; and (ccc) a lysine at amino acid position 322,
or
(v) the engineered thioesterase variant is a member selected from the group consisting of: SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO: 12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID NO:19, SEQ ID NO:20, SEQ ID NO:21, SEQ ID NO:22, SEQ ID NO:23, SEQ ID NO:24, SEQ ID NO:25, SEQ ID NO:26, SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO:29, SEQ ID NO:30, SEQ ID NO:31, SEQ ID NO:32, SEQ ID NO:33, SEQ ID NO:34, SEQ ID NO:35, SEQ ID NO:36, SEQ ID NO:37, SEQ ID NO:38, SEQ ID NO:39, SEQ ID NO:40, SEQ ID NO:41, SEQ ID NO:42, SEQ ID NO:43, SEQ ID NO:44, SEQ ID NO:45, SEQ ID NO:46, SEQ ID NO:47, SEQ ID NO:48, SEQ ID NO:49, SEQ ID NO:50, SEQ ID NO:51, SEQ ID NO:52, SEQ ID NO:53, SEQ ID NO:54, SEQ ID NO:55, SEQ ID NO:56, SEQ ID NO:57, SEQ ID NO:58 and SEQ ID NO:59,
or
(vi) the engineered thioesterase variant has an increased positive surface charge by comparison to SEQ ID NO:1,
or
(vii) the engineered thioesterase variant has an increased positive surface charge by comparison to SEQ ID NO:4,
or
(viii) the engineered thioesterase variant is a member selected from the group consisting of: SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID NO: 19, SEQ ID NO:20, SEQ ID NO:21, SEQ ID NO:22, SEQ ID NO:23, SEQ ID NO:24, SEQ ID NO:25, SEQ ID NO:26, SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO:29, SEQ ID NO:30, SEQ ID NO:32, SEQ ID NO:33, SEQ ID NO:34, SEQ ID NO:35, SEQ ID NO:36, SEQ ID NO:37, SEQ ID NO:38, SEQ ID NO:39, SEQ ID NO:40, SEQ ID NO:41, SEQ ID NO:42, SEQ ID NO:43, SEQ ID NO:44, SEQ ID NO:45, and SEQ ID NO:46,
or
(ix) the engineered thioesterase variant has an increased positive surface charge by comparison to SEQ ID NO:15,
or
(x) the engineered thioesterase variant is a member selected from the group consisting of: SEQ ID NO:47, SEQ ID NO:48, SEQ ID NO:49, SEQ ID NO:50 and SEQ ID NO:51,
or
(xi) the engineered thioesterase variant has improved solubility,
or
(xii) the engineered thioesterase variant has improved solubility by comparison to SEQ ID NO:49,
or
(xiii) the engineered thioesterase variant has a truncation mutation between amino acids 2 and 40 of SEQ ID NO:49,
or
(xiv) the engineered thioesterase variant is a member selected from the group consisting of: SEQ ID NO:52, SEQ ID NO:53, SEQ ID NO:54, SEQ ID NO:55, SEQ ID NO:56, SEQ ID NO:57, SEQ ID NO:58 and SEQ ID NO:59.
3. The method of claim 1 , wherein the commercial titer is 10 g/L or more.
4. The method of claim 1 , wherein the recombinant host cell is from a genus selected from the group consisting of Escherichia, Bacillus, Lactobacillus, Zymomonas, Rhodococcus, Pseudomonas, Aspergillus, Trichoderma, Neurospora, Fusarium, Humicola, Rhizomucor, Kluyveromyces, Pichia, Mucor, Myceliophtora, Marinobacter, Penicillium, Phanerochaete, Pleurotus, Trametes, Chrysosporium, Saccharomyces, Stenotrophomonas, Schizosaccharomyces, Yarrowia , and Streptomyces.
5. The method of claim 1 , wherein the recombinant host cell is from a genus selected from the group consisting of Synechococcus and Synechocysistis.
6. The method of claim 1 further comprising recovering the medium chain fatty acid derivative from a culture or isolating the medium chain fatty acid derivative from the recombinant host cell.
7. The method of claim 1 , wherein the biochemical pathway comprises an ester synthase and a fatty acyl-CoA synthetase and the recombinant host cell produces a medium chain fatty acid ester.
8. The method of claim 7 , wherein the medium chain fatty acid ester is a medium chain fatty acid methyl ester and/or a medium chain fatty acid ethyl ester.