Sequential glucosylation determined by NMR in the biosynthesis of mulberroside D, a cis-oxyresveratrol diglucoside, in Morus alba L. cell cultures

Cellular and Molecular Life Sciences

Volumn 53, Issue 3, 1997, Pages 237-241

  Hano, Y ^a   Goi, K ^a   Nomura, T ^a   Ueda, S ^b  

^a TOHO UNIVERSITY   (Japan)

^b KYOTO UNIVERSITY   (Japan)

Author keywords

Biosynthesis; Cinnamoylpolyketide; Glucoside; Glucosylation; Morus alba cell cultures; Oxyresveratrol

Indexed keywords

CARBON 13; CHALCONE DERIVATIVE; GLUCOSE; GLUCOSIDE;

ARTICLE; CARBOHYDRATE SYNTHESIS; GLYCOSYLATION; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PLANT; PLANT CELL;

MORUS ALBA;

EID: 0030758823     PISSN: 1420682X     EISSN: None     Source Type: Journal    
DOI: 10.1007/PL00000597     Document Type: Article

References (10)

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2. Hano Y., Nomura T. and Ueda S. (1994) A direct NMR evidence for the equivalent participation of L-phenylalanine and L-tyrosine in the biosynthesis of the intermolecular Diels-Alder type adducts of prenylchalcone and prenylated 2-arylbenzofuran in Morus alba cell cultures. Can. J. Chem. 72: 12-14
3. Hano Y., Nomura T. and Ueda S. (1994) Parallel contribution of L-phenylalanine and L-tyrosine to the biosynthesis of prenylchalcones in Morus alba cell cultures. Naturwissenschaften 81: 507-509
4. Ikuta (nèe Matsumoto) J., Fukai T., Nomura T. and Ueda S. (1986) Constituents of Morus alba L. cell cultures (1). Structures of four new natural Diels-Alder type adducts, kuwanon J. Q, R, and V. Chem. Pharm. Bull. 34: 2471-2478
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8. Hirakura K., Fujimoto Y., Fukai T. and Nomura T. (1986) Two phenolic glycosides from the root bark of the cultivated mulberry tree (Morus lhou). J. Nat. Prod. 49: 218-224
9. Basnet P., Kadota S., Terashima S., Shimizu M. and Namba T. (1993) Two new 2-arylbenzofuran derivatives from hypoglycemic activity-bearing fractions of Morus insignis. Chem. Pharm. Bull. 41: 1238-1243
10. Hano Y., Nomura T. and Ueda S. (1989) Biosynthesis of chalcomoracin and kuwanon J, the Diels-Alder type adducts, in Morus alba cell cultures. Chem. Pharm. Bull. 37: 554-556