Engineered glycosyltransferases with expanded substrate specificity
The present invention provides engineered glycosyltransferase enzymes and method for making and using the same possessing an expanded substrate specificity as compared to corresponding non-mutated glycosyltransferase enzymes. Such enzymes expand the variety of substrates that can be used in enzymatic glycosylation methods, including enzymatic glycorandomization, thereby providing increased diversity in chemical products.
1. An isolated mutant oleD glycosyltransferase having the amino acid sequence set forth in SEQ ID NO:1 mutated at one or more amino acids selected from the group consisting of P67, I112, S132 and A242 wherein said isolated mutant oleD glycosyltransferase exhibits an expanded substrate specificity as compared to a corresponding non-mutated oleD glycosyltransferase.
2. The isolated mutant oleD glycosyltransferase according to claim 1 wherein the amino acid sequence set forth in SEQ ID NO:1 is mutated to contain a mutation P67T, I112T or I112K, S132F, A242V, or combinations thereof.
3. The isolated mutant oleD glycosyltransferase according to claim 1 wherein the amino acid sequence set forth in SEQ ID NO:1 is mutated to contain mutations P67T, S132F and A242V.
4. The isolated mutant oleD glycosyltransferase according to claim 1 wherein the amino acid sequence set forth in SEQ ID NO:1 is mutated to contain mutations P67T, I112T and A242V.
5. The isolated mutant oleD glycosyltransferase according to claim 1 wherein the amino acid sequence set forth in SEQ ID NO:1 is mutated to contain mutations P67T, I112K and A242V.
6. A fluorescent-based assay for identifying a mutant glycosyltransferase exhibiting expanded substrate specificity as compared to a corresponding non-mutated glycosyltransferase, comprising:
(a) providing a library of isolated mutant glycosyltransferases, wherein the mutant glycosyltransferases each have the amino acid sequence set forth in SEQ ID NO:1 mutated at one or more amino acids selected from the group consisting of P67, I112, S132 and A242;
(b) incubating each mutant glycosyltransferase with a nucleotide sugar and a fluorescent sugar acceptor; and
(c) measuring a change in fluorescence intensity of the fluorescent sugar acceptor incubated with each mutant glycosyltransferase, each mutant glycosyltransferase's ability to transfer a sugar from said nucleotide sugar to said fluorescent sugar acceptor indicated by a quenching of the fluorescence of the fluorescent sugar acceptor incubated with each mutant glycosyltransferase;
wherein a mutant glycosyltransferase exhibits an expanded substrate specificity by displaying an increase in quenched fluorescence as compared to a corresponding non-mutated glycosyltransferase.
7. The method according to claim 6 wherein the amino acid sequence set forth in SEQ ID NO:1 is mutated to contain a mutation P67T, I112T or I112K, S132F, A242V, or combinations thereof.
8. The method according to claim 6 wherein the amino acid sequence set forth in SEQ ID NO:1 is mutated to contain mutations P67T, S132F and A242V.
9. The method according to claim 6 wherein the amino acid sequence set forth in SEQ ID NO:1 is mutated to contain mutations P67T, I112T and A242V.
10. The method according to claim 6 wherein the amino acid sequence set forth in SEQ ID NO:1 is mutated to contain mutations P67T, I112K and A242V.
11. The method according to claim 6 wherein the method is carried out in vitro.
12. The method according to claim 6 wherein the nucleotide sugar is selected from the group consisting of UDP-glc, TDP-glc, UDP-xylose, UDP-6-deoxy-glc, UDP-6-thio-glc, UDP-6-azido-glc, UDP-4-deoxy-glc, UDP-4-amino-glc, UDP-4,6-dideoxy-glc, UDP-4 -amino-6-deoxy-glc, UDP-3-deoxy-glc, UDP-3-amino-glc, UDP-3-amino-6-deoxy-glc, UDP-2-amino-glc, UDP-2 -acetamido-glc and mixtures thereof.
13. The method according to claim 6 wherein more than one type of nucleotide sugar is combined with the isolated mutant oleD glycosyltransferase and the aglycon to thereby produce a diverse population of glycosylated compounds.
14. The method according to claim 6 wherein the aglycon is selected from the group consisting of oleandomycin, 4-Me-umb, 7-hydroxycoumarin-4-acetic acid, 7-hydroxycoumarin -3-carboxylic acid, novobiocic acid, kaempferol, daidzein and genistein.
15. The method according to claim 6 wherein more than one type of aglycon is combined with the isolated mutant oleD glycosyltransferase and the nucleotide sugar to thereby produce a diverse population of glycosylated compounds.
16. The method according to claim 6 wherein the aglycon is a macrolide, flavonoid, isoflavone, coumarin, aminocouramin or coumarin acid.
17. The method according to claim 6 wherein the aglycon is selected from the group consisting of natural or synthetic pyran rings, furan rings, enediynes, anthracyclines, angucyclines, aureolic acids, orthosomycins, macrolides, aminoglycosides, non-ribosomal peptides, polyenes, steroids, lipids, indolocarbazoles, bleomycins, amicetins, benzoisochromanequinones, flavonoids, isoflavones, coumarins, aminocoumarins, coumarin acids, polyketides, pluramycins, aminoglycosides, oligosaccharides, nucleosides, peptides and proteins.
18. The method according to claim 6 further comprising the step of preparing the nucleotide sugar by combining an NTP and a sugar phosphate in the presence of a nucleotidyltransferase.
19. The method according to claim 6 wherein the method is carried out in a single reaction vessel.
20. The method according to claim 6 wherein the nucleotidyltransferase is LT2 rmlA-encoded alpha-D-glucopyranosyl phosphate thymidylyltransferase (E p ).
21. The method according to claim 18 wherein the nucleotidyltransferase is LT2 rmlA-encoded alpha-D-glucopyranosyl phosphate thymidylyltransferase (E p ) containing mutations L89T, T201A, Y224H, or combinations thereof.