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Octadecanoid Precursors of Jasmonic Acid Activate the Synthesis of Wound-Inducible Proteinase Inhibitors.

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Farmer, E. E., Ryan, C. A.·1992·The Plant Cell

Abstract

Jasmonic acid and methyl jasmonate have been shown previously to be powerful inducers of proteinase inhibitors in tomato, tobacco, and alfalfa leaves. We show here that when proposed octadecanoid precursors of jasmonic acid, i.e., linolenic acid, 13(S)-hydroperoxylinolenic acid, and phytodienoic acid, were applied to the surfaces of tomato leaves, these compounds also served as powerful inducers of proteinase inhibitor I and II synthesis, a simulation of a wound response. By contrast, compounds closely related to the precursors but which are not intermediates in the jasmonic acid biosynthetic pathway did not induce proteinase inhibitor synthesis. These results suggest that the octadecanoid intermediates may participate in a lipid-based signaling system that activates proteinase inhibitor synthesis in response to insect and pathogen attack.

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Metadata

Authors
Farmer, E. E., & Ryan, C. A.
Venue
The Plant Cell
Published
1992-02-01
Volume
4
Issue
2
Pages
129-134
ISSN
  • 1040-4651 (ISSN-L)
  • 1532-298X
OpenAlex
W2132886964
Cited by
1,096
References
0
FWCI
130.62
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Octadecanoid Precursors of Jasmonic Acid Activate the Synthesis of Wound-Inducible Proteinase Inhibitors. https://app.cochat.ai/papers/10.1105/tpc.4.2.129
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Farmer, E. E., & Ryan, C. A. (1992). Octadecanoid Precursors of Jasmonic Acid Activate the Synthesis of Wound-Inducible Proteinase Inhibitors. The Plant Cell. https://doi.org/10.1105/tpc.4.2.129

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