Uridine diphosphate-dependent glycosyltransferase enzyme
The invention provides methods for making steviol glycosides, including RebM and glycosylation products that are minor products in stevia leaves, and provides enzymes, encoding polynucleotides, and host cells for use in these methods. The invention provides engineered enzymes and engineered host cells for producing steviol glycosylation products, such as RebM, at high purity and/or yield. The invention further provides methods of making products containing steviol glycosides, such as RebM, including food products, beverages, oral care products, sweeteners, and flavoring products.
1 . A method for making rebaudioside M comprising: culturing a host cell in the presence of rebaudioside D, the host cell expressing a uridine diphosphate-dependent glycosyltransferase (UGT) enzyme comprising an amino acid sequence that has at least 90% sequence identity to SEQ ID NO: 3 and has a L200A or L200G substitution with respect to SEQ ID NO: 3.
2 . The method of claim 1 , wherein the UGT enzyme comprises an amino acid sequence having at least 95% sequence identity to SEQ ID NO: 3.
3 . The method of claim 1 , wherein the UGT enzyme comprises an amino acid having at least 97% sequence identity to SEQ ID NO: 3.
4 . The method of claim 1 , wherein the UGT enzyme comprises an amino acid sequence having at least 98% sequence identity to SEQ ID NO: 3.
5 . The method of claim 1 , wherein the UGT enzyme comprises an amino acid sequence having at least 99% sequence identity to SEQ ID NO: 3.
6 . The method of claim 1 , wherein the UGT enzyme further comprises T284A substitution with respect to SEQ ID NO: 3.
7 . The method of claim 1 , wherein the host cell further expresses a UT enzyme comprising an amino acid sequence having at least 90% sequence identity to an amino acid sequence selected from: SEQ ID NO: 7, SEQ ID NO: 5, SEQ ID NO: 4, SEQ ID NO: 6, and SEQ ID NO: 45.
8 . The method of claim 7 , wherein the host cell further expresses a UGT enzyme comprising an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 1, and a UGT enzyme comprising an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 2.
9 . The method of claim 1 , wherein the host cell is prokaryotic.
10 . The method of claim 9 , wherein the host cell is a bacterial cell selected from E. coli, Bacillus subtillus , or Pseudomonas putida.
11 . The method of claim 1 , wherein the host cell is Saccharomyces cerevisiae, Pichia pastoris , or Yarrowia lipolytica.
12 . The method of claim 1 , wherein the host cell further comprises one or more genetic modifications increasing the availability of UDP-glucose.
13 . The method of claim 1 , wherein the UGT enzyme further comprises one or more amino acid modifications with respect to SEQ ID NO: 3 selected from: S77A, N78A, T81A, insertion of G after amino acid 194, T284A, and L379A.
14 . A method for making rebaudioside M comprising: culturing a host cell in the presence of rebaudioside D, the host cell expressing a uridine diphosphate-dependent glycosyltransferase (UGT) enzyme comprising an amino acid sequence that has at least 90% sequence identity to SEO ID NO: 3 and has one or more amino acid modifications with respect to SEO ID NO: 3 selected from: S77A, N78A, T81A, insertion of G after amino acid 194, L200A, L200G, T284A, and L379A, wherein the UGT enzyme comprises an Ala inserted or substituted at position 2, with respect to SEQ ID NO: 3.
15 . A method for making rebaudioside M comprising: culturing a host cell in the presence of rebaudioside D, the host cell expressing a uridine diphosphate-dependent glycosyltransferase (UGT) enzyme comprising an amino acid sequence that has at least 90% sequence identity to SEO ID NO: 3 and has one or more amino acid modifications with respect to SEO ID NO: 3 selected from: S77A, N78A, T81A, insertion of G after amino acid 194, L200A, L200G, T284A, and L379A, wherein the host cell further comprises one or more genetic modifications increasing the availability of UDP-glycose, wherein the host cell is E. coli comprising one or more genetic modifications selected from ΔgalE, ΔgalT, ΔgalK, ΔgalM, ΔushA, Δagp, Δpgm, duplication of E. coli GALU, and expression of Bacillus substillus UGPA, BaSP.