BIOCATALYSTS AND METHODS FOR HYDROXYLATION OF CHEMICAL COMPOUNDS
The present disclosure provides engineered proline hydroxylase polypeptides for the production of hydroxylated compounds, polynucleotides encoding the engineered proline hydroxylases, host cells capable of expressing the engineered proline hydroxylases, and methods of using the engineered proline hydroxylases to prepare compounds useful in the production of active pharmaceutical agents.
1 . An engineered polypeptide having proline hydroxylase activity, comprising an amino acid sequence having at least 80% sequence identity to SEQ ID NO:2 and one or more residue differences as compared to the sequence of SEQ ID NO:2 at residue positions selected from: X66, X92, X140, X24;
X88, and X57.
2 . The engineered polypeptide of claim 1 in which the residue differences at residue positions X66, X92, X140, X24; X88, and X57 are selected from X66Q, X92V, X140L, X24S, X24R, X88R, X57A, and X57T.
3 . The engineered polypeptide of claim 1 , in which the amino acid sequence comprises at least a combination of features selected from:
(a) X66Q;
(b) X92V;
(c) X66Q, X103L, and X166Q;
(d) X66Q, X92V, X103L, and X166Q;
(e) X66Q, X92V, X103L, X113E, X115S, and X166Q;
(f) X92V, X103L, and X166Q;
(g) X25R, X66Q, X92V, X103L, X115E, and X166Q;
(h) X3S, X25R, X66Q, X92V, X103L, X115E, and X166Q;
(i) X3S, X25R, X66Q, X92V, X103L, X115E, and X166Q;
(j) X25R, X66Q, X92V and X115E; and
(k) X25R, X66Q, X92V, X103L, X115E, and X166Q.
4 . The engineered polypeptide of claim 1 , which further comprises one or more residue differences as compared to the sequence of SEQ ID NO: 2 at residue positions selected from: X2, X4, X5, X9, X13, X17, X25, X26, X29, X30, X36, X42, X52, X58, X59, X62, X86, X95, X98, X112, X113, X114, X115, X116, X121, X131, X150, X151, X186, X188, X205, X225, X230, X270, and X271.
5 . The engineered polypeptide of claim 4 in which the residue differences at residue positions X2, X4, X5, X9, X13, X17, X25, X26, X29, X30, X36, X42, X52, X58, X59, X62, X86, X95, X98, X112, X113, X114, X115, X116, X121, X131, X150, X151, X186, X188, X205, X225, X230, X270, and X271 are selected from X2K, X2T, X4Q, X4L, X4E, X4S, X5I, X5L, X5M, X9I, X13T, X17V, X25R, X26T, X26R, X26W, X29A, X30V, X30P, X36T, X42E, X52P, X58A, X59G, X62Q, X86S, X95M, X98F, X98T, X112T, X112V, X113E, X114N, X115E, X115H, X115D, X115G, X115S, X115A, X116L, X121F, X131Y, X131F, X150S, X151A, X151H, X151S, X186G, X188G, X205V, X225L, X225Y, X225W, X230V, X270E, X271K, and X271R.
6 . The engineered polypeptide of claim 1 , which converts substrate compound (2), (2S)-piperidine-2-carboxylic acid,
to product compound (1), (2S,5S)-5-hydroxypiperidine-2-carboxylic acid,
under suitable reaction conditions.
7 . The engineered polypeptide of claim 6 in which the polypeptide converts substrate compound (2) to product compound (1) with at least 2 fold the activity of SEQ ID NO:2, wherein the amino acid sequence comprises one or more residue differences selected from the group consisting of:
X66Q, X92V, X140L, X24S, X24R, X88R, X57A, and X57T.
8 . The engineered polypeptide of claim 1 , which converts substrate compound (2) to product compound (1) in excess of product compound (1a), (2S,3R)-3-hydroxypiperidine-2-carboxylic acid,
wherein the amino acid sequence comprises one or more residue differences selected from the group consisting of: X66Q, X92V, X140L, X24S, X24R, X88R, X57A, and X57T.
9 . The engineered polypeptide of claim 1 , which forms product compound (1),
in diastereomeric excess of product compound (1R), (2S,5R)-5-hydroxypiperidine-2-carboxylic acid,
10 . The engineered polypeptide of claim 1 having proline hydroxylase activity in which the amino acid sequence comprises a sequence selected from the group consisting of SEQ ID NO: 34, 38, 44, 92, 114, 118, 120, 122, 124, 126, 128, 130, 132, 134, 138, 140, 142, 144, 146, 148, 150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, and 228.
11 . A polynucleotide encoding the engineered polypeptide of claim 1 , the polynucleotide optionally comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO: 33, 37, 43, 91, 113, 117, 119, 121, 123, 125, 127, 129, 131, 133, 137, 139, 141, 143, 145, 147, 149, 151, 153, 155, 157, 159, 161, 163, 165, 167, 169, 171, 173, 175, 177, 179, 181, 183, 185, 187, 189, 191, 193, 195, 197, 199, 201, 203, 205, 207, 209, 211, 213, 215, 217, 219, 221, 223, 225, and 227.
12 . A polynucleotide encoding the polypeptide of SEQ ID NO: 2, comprising a nucleic acid sequence optimized for expression in E. coli, optionally comprising a sequence having at least 80% or more identity to a nucleic acid sequence selected from SEQ ID NO: 1, 3, and 5.
13 . An expression vector comprising the polynucleotide of claim 11 , further comprising a control sequence.
14 . A host cell comprising the polynucleotide of claim 11 , wherein the host cell is Escherichia coli.
15 . A method of preparing an engineered polypeptide, comprising culturing the host cell of claim 14 under conditions suitable for expression of the polypeptide, the method further comprises a step of isolating the engineered polypeptide.