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 90% sequence identity to SEQ ID NO: 4, wherein the amino acid sequence comprises residue differences at position X136 and position X323 as compared to SEQ ID NO: 4.
2. The engineered transaminase polypeptide of claim 1 , 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; X152I; X152L; X152S; X156A; X156S; X156T; X157L; X165N, X192A, X193G, X192H, X 192K, X192N, X193Q, X192R, and X192S.
3. The engineered transaminase polypeptide of claim 1 , 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 and X126A;
(f) X124W, X126A, X192A and X284A; and
(g) X124W, X126A, X152R/X152I/X152I, and X192A.
4. The engineered transaminase polypeptide of claim 1 , in which the amino acid sequence further comprises at least one or more residue differences as compared to SEQ ID NO: 4 selected from: X54A; X54L; X56D; X56E; X61G; X61W; X62A; X62L; X62N; X62S; X64C; X68I; X122F, X122W; X122Y; X124K; X124M; X124S; X124W; X126C; X126I; X139E; X140K; X143V; X150L; X155I; X155L; X159G; X160L; X176C; X199L; X199V; X209F; X209M; X209Q; X209V; X223S; X223T; X223V; X227I; X282L, X282V; X284A; X284P; X284S; X284T; and X284V.
5. An engineered polynucleotide encoding the transaminase polypeptide of claim 1 .
6. A vector comprising the polynucleotide of claim 5 .
7. A host cell comprising the vector of claim 6 .