Difunctional C-glycoside glycosyltransferase and application thereof
A technology of glycosyltransferase and carbon glycosides, which is applied in the field of synthetic biology and can solve problems that have not yet been solved
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Embodiment 1
[0121] Embodiment 1, novel uridine diphosphate (UDP)-glycosyltransferase
[0122] 1. Cloning of carboside glycosyltransferase gene and construction of expression plasmid
[0123] Take mature leaves or seedlings of gramineous plants (moso bamboo, japonica rice, indica rice, sorghum, millet, Brachypodium distachyon, corn), clean the surface stains with clean water, gently wipe the water stains on the surface of dry leaves with absorbent paper, and weigh them for later use. Genomic DNA was extracted according to the instructions provided by the TIANGEN Plant Genome Extraction Kit.
[0124] The amino acid sequence of the described carboside glycosyltransferase is as follows:
[0125] >PhCGT3 (SEQ ID NO: 1)
[0126] MAPPATLRSGEPDRDTPHVIFIPSAGMGHLYPFFRFIAALSSYGVDISVVTILPTVSAAEADHFAGLFAAFPSIRRIDFHLLPLDTNEFPGADPFFLRWEELRRSAHLLGPLIASATPRVSTIVSDVTLASHVIPIAKELHIPCHVLFISCATMLSLNAYFPVYLDTKAGMDGIGDVDIPGVCRIPKSSLPQALLDLNKLFTKQFIENGREITKADGILVNTFDALEPKALATLRDGTVVTRFPPVFAIGPLTSHSPAAGERVDAGFP...
Embodiment 2
[0168] Embodiment 2, the synthesis of flavonoid carbon glycoside compound schaftoside etc.
[0169] In this example, PhCGT1 and OsiCGT4 were used to synthesize schaftoside and its isomers in Escherichia coli.
[0170] Predicted biosynthetic pathways of schaftosides and their isomers such as Figure 10 shown. Arrows TAL (or PAL), 4CL, CHS, CHI represent the main enzymes responsible for naringenin biosynthesis. Arrow F2H is flavanone 2-hydroxylase (F2H), which constitutes the backbone of 2-hydroxyflavanone. C-Glycosyltransferase (CGT) is indicated by the arrow CGT. After the formation of a C-glycosylated intermediate, the dehydration reaction occurs spontaneously in an acidic solvent (arrow H + ).
[0171] 1. Plasmid construction
[0172] (1) Construction of the expression cassette for the synthetic precursor gene of the flavanone naringenin
[0173] The artificially synthesized and codon-optimized precursor synthetic gene sequence was constructed on the pET28a vector to ...
Embodiment 3
[0201] Embodiment 3, the synthesis of flavonoid carbon glycosides apigenin-C-arabinoside etc.
[0202] In this example, OsiCGT6 was used to synthesize apigenin-6-C-arabinoside, apigenin-8-C-arabinoside and apigenin-6,8-C-diarabinoside in Escherichia coli.
[0203] The synthetic pathway of apigenin-6-C-arabinoside, apigenin-8-C-arabinoside and apigenin-6,8-C-bisarabinoside is as follows: Figure 15 shown. Arrows PAL (or TAL), 4CL, CHS, CHI represent the main enzymes responsible for naringenin biosynthesis. Arrow F2H is flavanone 2-hydroxylase (F2H), which constitutes the backbone of 2-hydroxyflavanone. C-Glycosyltransferase (CGT) is indicated by the arrow CGT. After the formation of a C-glycosylated intermediate, the dehydration reaction occurs spontaneously in an acidic solvent (arrow H + ).
[0204] 1. Plasmid construction
[0205] (1) The construction of the expression cassette for the synthetic precursor gene of the flavanone naringenin is the same as in Example 2.
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