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Formation of optically active neolignans from achiral coniferyl alcohol by cell-free extracts of Eucommia ulmoides

References

  1. 1.

    Davin LB, Bedgar DL, Katayama T, Lewis NG (1992) On the stereo selective synthesis of (+)-pinoresinol in Forsythia suspensa from its achiral precursor, coniferyl alcohol. Phytochemistry 31:3869–3874

  2. 2.

    Paré PW, Wang H-B, Davin LB, Lewis NG (1994) (+)-Pinoresinol synthase: a stereoselective oxidase catalysing 8,8′-lignan formation in Forsythia intermedia. Tetrahedron Lett 35:4731–4734

  3. 3.

    Davin LB, Wang H-B, Crowell AL, Bedgar DL, Martin DM, Sarkanen S, Lewis NG (1997) Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center. Science 275:362–366

  4. 4.

    Deyama T, Ikawa T, Kitagawa S, Nishibe S (1987) The constituents of Eucommia ulmoides Oliv. V. Isolation of dihydroxydehydrodiconiferyl alcohol isomers and phenolic compounds. Chem Pharm Bull (Tokyo) 35:1785–1789

  5. 5.

    Deyama T, Ikawa T, Kitagawa S, Nishibe S (1987) The constituents of Eucommia ulmoides Oliv. VI. Isolation of a new sesquilignan and neolignan glycosides. Chem Pharm Bull (Tokyo) 35:1803–1807

  6. 6.

    Katayama T, Davin LB, Lewis NG (1992) An extraordinary accumulation of (−)-pinoresinol in cell-free extracts of Forsythia intermedia: evidence for enantiospecific reduction of (+)pinoresinol. Phytochemistry 31:3875–3881

  7. 7.

    Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Chem 72:248–252

  8. 8.

    Katayama T, Masaoka T, Yamada H (1997) Biosynthesis and stereochemistry of lignans in Zanthoxylum ailanthoides. I. (+)-Lariciresinol formation by enzymatic reduction of (±)pinoresinols. Mokuzai Gakkaishi 43:580–588

  9. 9.

    Hirai N, Okamoto M, Udagawa H, Yamamuro M, Kato M, Koshimizu K (1994) Absolute configuration of dehydrodiconiferyl alcohol. Biosci Biotech Biochem 58:1679–1684

  10. 10.

    Orr JD, Lynn DG (1992) Biosynthesis of dehydrodiconiferyl alcohol glucosides: implications for the control of tobacco cell growth. Plant Physiol 98:343–352

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Correspondence to Takeshi Katayama.

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Katayama, T., Kado, Y. Formation of optically active neolignans from achiral coniferyl alcohol by cell-free extracts of Eucommia ulmoides . J Wood Sci 44, 244–246 (1998). https://doi.org/10.1007/BF00521971

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Key words

  • Biosynthesis
  • Neolignan
  • Lignan
  • Guaiacylglycerol-β-coniferyl ether
  • Eucommia ulmoides