Mogrol glycosyltransferase and gene encoding same
US-2017335362-A1 · Nov 23, 2017 · US
US10407706B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10407706-B2 |
| Application number | US-201515519326-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 16, 2015 |
| Priority date | Oct 17, 2014 |
| Publication date | Sep 10, 2019 |
| Grant date | Sep 10, 2019 |
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To provide a mogrol glycosyltransferase and a method for producing a mogrol glycoside using the enzyme. The present invention provides a mogrol glycosyltransferase and a method for producing a mogrol glycoside using the enzyme, and a transformant into which a mogrol glycosyltransferase gene is introduced and a method for preparing the transformant.
Opening claim text (preview).
The invention claimed is: 1. A method for producing a mogrol glycoside comprising reacting a protein selected from the group consisting of the following (a) to (c), a UDP-sugar, and the compound represented by formula (I) to obtain a mogrol glycoside; and purifying the mogrol glycoside: (a) a protein consisting of the amino acid sequence of SEQ ID NO: 2; (b) a protein consisting of an amino acid sequence in which 1 to 45 amino acids are deleted, substituted, inserted, and/or added in the amino acid sequence of SEQ ID NO: 2 and having an activity of adding a sugar molecule to an R 1 group at position 24 of a compound represented by the following formula (I); and (c) a protein having an amino acid sequence having 90% or more sequence identity with the amino acid sequence of SEQ ID NO: 2 and having the activity of adding a sugar molecule to an R 1 group at position 24 of the compound represented by formula (I), where R and R 1 each independently represent H, a monosaccharide, or a disaccharide. 2. The method according to claim 1 , wherein the UDP-sugar is a UDP-hexose. 3. The method according to claim 1 , wherein the UDP-sugar is selected from the group consisting of UDP-glucose, UDP-mannose, and UDP-galactose. 4. The method according to claim 1 , wherein the R and R 1 is each independently H or a sugar residue of a glucose monomer or a glucose dimer. 5. The method according to claim 1 , wherein the compound represented by formula (I) is mogrol or a mogrol glycoside. 6. The method according to claim 1 , which yields mogroside IA, mogroside Ib, mogroside IE, mogroside IIA, mogroside II 1 , mogroside IIE, mogroside III, mogroside IIIA 1 , mogroside IIIA 2 , mogroside IIIE, mogroside IV, mogroside IVA, mogroside V, siamenoside I, 11-oxomogroside V, mogrol pentaglycoside, or a combination thereof. 7. The method according to claim 2 , which yields mogroside IA, mogroside Ib, mogroside IE, mogroside IIA, mogroside IIA 1 , mogroside IIE, mogroside III, mogroside IIIA 1 , mogroside IIIA 2 , mogroside IIIE, mogroside IV, mogroside IVA, mogroside V, siamenoside I, 11-oxomogroside V, mogrol pentaglycoside, or a combination thereof. 8. The method according to claim 3 , which yields mogroside IA, mogroside Ib, mogroside IE, mogroside IIA, mogroside IIA 1 , mogroside IIE, mogroside III, mogroside IIIA 1 , mogroside IIIA 2 , mogroside IIIE, mogroside IV, mogroside IVA, mogroside V, siamenoside I, 11-oxomogroside V, mogrol pentaglycoside, or a combination thereof. 9. The method according to claim 4 , which yields mogroside IA, mogroside Ib, mogroside IE, mogroside IIA, mogroside IIA 1, mogroside IIE, mogroside III, mogroside IIIA 1 , mogroside IIIA 2 , mogroside IIIE, mogroside IV, mogroside IVA, mogroside V, siamenoside I, 11-oxomogroside V, mogrol pentaglycoside, or a combination thereof. 10. The method according to claim 5 , which yields mogroside IA, mogroside Ib, mogroside IE, mogroside IIA, mogroside IIA 1 , mogroside IIE, mogroside III, mogroside IIIA 1 , mogroside IIIA 2 , mogroside IIIE, mogroside IV, mogroside IVA, mogroside V, siamenoside I, 11-oxomogroside V, mogrol pentaglycoside, or a combination thereof.
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