Biocatalysts and methods for hydroxylation of chemical compounds
View Patent ↗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 that is at least 95% identical to the amino acid sequence set forth in SEQ ID NO:2 and having a residue difference at position X103.
2. The engineered polypeptide of claim 1 , further comprising residue differences at residue positions X2; X4; X5; X9; X13; X25; X26; X29; X30; X36; X42; X52, X57; X58; X59; X66; X92; X95; X112; X115; X116; X121; X131; X150; X151; X225; X230; and X271 are selected from X2K; X2T; X4Q; X4L; X4E; X4S; X5I; X5L; X5M; X9I; X13T; X25R; X26T; X29A; X30V; X30P; X36T; X42E; X52P; X57T; X57A; X58A; X59G; X66Q; X86S; X92V; X95M; X112T; X112V; X113E, X115E; X115H; X115D; X115G; X115S; X115A; X116L; X121F; X131Y; X131F; X150S; X151S; X225L; X225Y; X225W; X230V; X270E; X271K; and X271R.
3. The engineered polypeptide of claim 1 , wherein the amino acid sequence comprises at least a combination of features selected from:
(a) X166Q;
(b) X52P and X255Y;
(c) X4E/L/S and X115A;
(d) X25R and X58A;
(e) X29A and X166T/Q/L;
(f) X115H/D/G and X121F;
(g) X3S, and X166Q;
(h) X131Y/F and X166T/Q/L;
(i) X26T and X166T/Q/L;
(j) X25R, X66Q, X92V and X115E;
(k) X25R, X66Q, X92V, X115E, and X166Q; and
(l) X3S, X25R, X66Q, X92V, X115E, and X166Q.
4. The engineered polypeptide of claim 1 , wherein the polypeptide further comprises one or more residue differences as compared to the sequence of SEQ ID NO: 2 at residue positions selected from: X17, X24, X26, X62, X88, X98, X114, X140, X151, X186, X188, and X205.
5. The engineered polypeptide of claim 4 , wherein the residue differences at residue positions X17, X24, X26, X62, X88, X98, X114, X140, X151, X186, X188, and X205 are selected from X17V, X24R, X24S, X26R, X26W, X62Q, X88R, X98F, X98T, X114N, X140L, X151A, X151H, X186G, X188G, and X205V.
6. The engineered polypeptide of claim 1 , wherein the polypeptide 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 , wherein the polypeptide converts substrate compound (2), (2S)-piperidine-2-carboxylic acid,
to product compound (1), (2S,5S)-5-hydroxypiperidine-2-carboxylic acid,
with at least 2 fold the activity of SEQ ID NO:2, and wherein the amino acid sequence comprises one or more residue differences selected from the group consisting of: X4Q; X4L; X5I; X5L; X24S; X25R; X30P; X66Q; X86S; X92V; X113E; X115E; X150S; X166Q; X151S; X225L; and X270E.
8. The engineered polypeptide of claim 1 , wherein the polypeptide converts substrate compound (2), (2S)-piperidine-2-carboxylic acid,
to product compound (1), (2S,5S)-5-hydroxypiperidine-2-carboxylic acid,
in excess of product compound (1a), (2S,3R)-3-hydroxypiperidine-2-carboxylic acid,
and wherein the amino acid sequence comprises one or more residue differences selected from the group consisting of: X115E; X131Y and X166Q.
9. The engineered polypeptide of claim 1 , wherein the polypeptide which forms product compound (1),
in diastereomeric excess of product compound (1R), (2S,5R)-5-hydroxypiperidine-2-carboxylic acid,