<?xml version="1.0" encoding="utf-8" standalone="yes"?>
<rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom">
  <channel>
    <title>Plant-Defense on emsenn.net</title>
    <link>https://emsenn.net/tags/plant-defense/</link>
    <description>Recent content in Plant-Defense on emsenn.net</description>
    <generator>Hugo</generator>
    <language>en</language>
    <lastBuildDate>Thu, 02 Apr 2026 00:00:00 +0000</lastBuildDate>
    <atom:link href="https://emsenn.net/tags/plant-defense/index.xml" rel="self" type="application/rss+xml" />
    <item>
      <title>Phytoalexin</title>
      <link>https://emsenn.net/library/domains/science/domains/medicine/domains/pharmacology/terms/phytoalexin/</link>
      <pubDate>Thu, 02 Apr 2026 00:00:00 +0000</pubDate>
      <guid>https://emsenn.net/library/domains/science/domains/medicine/domains/pharmacology/terms/phytoalexin/</guid>
      <description>&lt;p&gt;A phytoalexin is a defensive compound that a plant synthesizes &lt;em&gt;de novo&lt;/em&gt; in response to stress — pathogen infection, ultraviolet radiation, physical damage, or herbivore attack. Unlike constitutive defenses (compounds always present), phytoalexins are induced: the plant produces them only when threatened. The term was coined by Müller and Börger in 1940 from Greek &lt;em&gt;phyton&lt;/em&gt; (plant) + &lt;em&gt;alexein&lt;/em&gt; (to ward off).&lt;/p&gt;&#xA;&lt;p&gt;Phytoalexins are typically low-molecular-weight antimicrobial compounds that accumulate at the site of infection, creating a localized chemical barrier against the invading pathogen. They belong to diverse chemical classes depending on the plant family: &lt;a href=&#34;stilbenoid.md&#34; class=&#34;link-internal&#34;&gt;stilbenoids&lt;/a&gt; in Vitaceae (grapes) and &lt;a href=&#34;../../../../biology/domains/botany/terms/polygonaceae.md&#34; class=&#34;link-internal&#34;&gt;Polygonaceae&lt;/a&gt; (knotweeds), isoflavonoids in Fabaceae (legumes), sesquiterpenes in Solanaceae (nightshades), indole derivatives in Brassicaceae (mustards).&lt;/p&gt;</description>
    </item>
    <item>
      <title>Plant Signaling: Molecular Mechanisms</title>
      <link>https://emsenn.net/library/domains/science/domains/biology/domains/botany/terms/plant-signaling-molecular/</link>
      <pubDate>Sat, 28 Mar 2026 00:00:00 +0000</pubDate>
      <guid>https://emsenn.net/library/domains/science/domains/biology/domains/botany/terms/plant-signaling-molecular/</guid>
      <description>&lt;p&gt;This file covers the biochemistry and molecular biology of plant signaling systems. For the ecological and relational framing, see &lt;a href=&#34;./plant-signaling.md&#34; class=&#34;link-internal&#34;&gt;plant-signaling.md&lt;/a&gt;.&lt;/p&gt;&#xA;&lt;hr&gt;&#xA;&lt;h2 id=&#34;1-phytohormone-signaling&#34;&gt;&lt;a href=&#34;#1-phytohormone-signaling&#34; class=&#34;heading-anchor&#34; aria-label=&#34;Link to this section&#34;&gt;¶&lt;/a&gt;1. Phytohormone Signaling&#xA;&lt;/h2&gt;&#xA;&lt;p&gt;Plants use at least nine major classes of hormone. Each is synthesized through specific enzymatic pathways, perceived by identified receptor proteins, and transduced through defined signaling cascades.&lt;/p&gt;&#xA;&lt;h3 id=&#34;11-auxin-indole-3-acetic-acid-iaa&#34;&gt;&lt;a href=&#34;#11-auxin-indole-3-acetic-acid-iaa&#34; class=&#34;heading-anchor&#34; aria-label=&#34;Link to this section&#34;&gt;¶&lt;/a&gt;1.1 Auxin (Indole-3-Acetic Acid, IAA)&#xA;&lt;/h3&gt;&#xA;&lt;p&gt;&lt;strong&gt;Function.&lt;/strong&gt; Cell elongation, apical dominance, tropisms (photo- and gravitropism), vascular differentiation, lateral root initiation, embryo patterning.&lt;/p&gt;</description>
    </item>
  </channel>
</rss>
