Biocatalysts and methods for the synthesis of substituted lactams
The present disclosure relates to transaminase polypeptides capable of aminating a dicarbonyl substrate, and polynucleotides, vectors, host cells, and methods of making and using the transaminase polypeptides.
1. An engineered transaminase polypeptide comprising an amino acid sequence having at least 80% sequence identity to reference sequence SEQ ID NO:4 and at least an amino acid residue difference as compared to SEQ ID NO:4 at residue position X323.
2. The engineered polypeptide of claim 1 , in which X323 is C.
3. The engineered polypeptide of claim 2 , wherein the amino acid sequence further comprises one or more residue differences as compared to SEQ ID NO:4 selected from: X42G; X54P; X54R; X69A; X69G; X69T; X122M; X124F; X124L; X124N; X124R; X126A; X126T; X150S; X152C; X152G; X1521; X152L; X1525; X156A; X1565; X156T; X157L; X165N, X192A, X193G, X192H, X192K, X192N, X193Q, X192R, and X1925.
4. The engineered polypeptide of claim 2 , wherein the amino acid sequence further comprises a combination of residue differences selected from:
(a) X124W and X327L;
(b) X209M and X300G;
(c) X122F, X223V and X284A;
(d) X192A, X215H and X311T;
(e) X62N, X124F, X126A and X136L;
(f) X124W, X126A, X136L, X192A and X284A; and
(g) X124W, X126A, X136L, X152R/X152L/X1521, and X192A.
5. The engineered polypeptide of claim 1 , in which the amino acid sequence further comprises a residue difference as compared to SEQ ID NO:4 of X284A.
6. An engineered polynucleotide encoding the polypeptide of claim 1 .
7. A vector comprising the polynucleotide of claim 6 .
8. A host cell comprising the vector of claim 7 .
9. A method of converting compound 2 to compound 1,
comprising contacting compound 2 with the engineered polypeptide of claim 1 , under suitable reaction conditions to produce compound 1.
10. A method of converting compound 2 to compound 1d and compound 1a
comprising contacting compound 2 with the engineered polypeptide of claim 1 , under suitable reaction conditions to produce compound 1d and 1a, under suitable reaction conditions wherein said engineered polypeptide comprises at least 1.5 fold the activity of SEQ ID NO:4.