Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 7 January 1966:
Vol. 151. no. 3706, pp. 79 - 80
DOI: 10.1126/science.151.3706.79
Prev | Table of Contents | Next

Articles

Cyclopentanoid Terpene Biosynthesis in a Phasmid Insect and in Catmint

Jerrold Meinwald 1, George M. Happ 1, John Labows 1, and Thomas Eisner 1

1 Department of Chemistry and Division of Biology, Cornell University, Ithaca, New York

The stick insect, Anisomorpha buprestoides, and the catmint, Nepeta cataria, produce closely related cyclopentanoid terpenes, anisomorphal and nepetalactone. Tracer experiments with isotopes indicate that anisomorphal is synthesized by the walking stick from normal terpene precursors (acetate or mevalonate). In the catmint plant, isolated leaf disks synthesized nepetalactone, utilizing the same precursors.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Allelochemics: Chemical Interactions between Species.
R. H. Whittaker and P. P. Feeny (1971)
Science 171, 757-770
   PDF »
Defensive Secretions of Arthropods.
T. Eisner and J. Meinwald (1966)
Science 153, 1341-1350
   PDF »


To Advertise     Find Products

Science. ISSN 0036-8075 (print), 1095-9203 (online)