Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Biosynthesis of Arbutin from Some Phenylpropanoid Compounds in Pyrus communis

Abstract

HIGHER plants are capable of synthesizing aromatic compounds from shikimic acid, possibly through a pathway similar to that described by Davis et al. 1. Certain benzene rings, however, are formed from acetate in accordance with the hypothesis of Birch and Donovan2. Thus the B ring of quercitin is synthesized from shikimic acid3 whereas the A ring is an acetate-formed ring4.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Davis, B. D., Symposium on Amino-Acid Metabolism, edit. by McElroy, W. D., and Glass, B. H., 799 (Johns Hopkins Press, Baltimore, Md., 1955).

    Google Scholar 

  2. Birch, A. J., and Donovan, F. W., Austral. J. Chem., 6, 360 (1953).

    Article  CAS  Google Scholar 

  3. Underhill, E. W., Watkin, J. E., and Neish, A. C., Canad. J. Biochem. Physiol., 35, 219 (1957).

    Article  CAS  Google Scholar 

  4. Watkin, J. E., Underhill, E. W., and Neish, A. C., Canad. J. Biochem Physiol., 35, 229 (1957).

    Article  CAS  Google Scholar 

  5. Friedrich, H., Pharmazie, 13, 153 (1958).

    CAS  PubMed  Google Scholar 

  6. Gloor, U., and Wiss, O., Experientia, 14, 410 (1958).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

GRISDALE, S., TOWERS, G. Biosynthesis of Arbutin from Some Phenylpropanoid Compounds in Pyrus communis . Nature 188, 1130–1131 (1960). https://doi.org/10.1038/1881130b0

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1038/1881130b0

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing