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Inhibition of the Conversion of 1-Aminocyclopropane-1-carboxylic Acid to Ethylene by Structural Analogs, Inhibitors of Electron Transfer, Uncouplers of Oxidative Phosphorylation, and Free Radical Scavengers

Cyclopropane carboxylic acid (CCA) at 1 to 5 millimolar, unlike related cyclopropane ring analogs of 1-aminocyclopropane-1-carboxylic acid (ACC) which were virtually ineffective, inhibited C(2)H(4) production, and this inhibition was nullified by ACC. Inhibition by CCA is not competitive with ACC si...

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Vydáno v:Plant Physiol
Hlavní autoři: Apelbaum, Akiva, Wang, Shiow Y., Burgoon, Alan C., Baker, James E., Lieberman, Morris
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 1981
Témata:
On-line přístup:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC425624/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/16661637/
https://ncbi.nlm.nih.govhttps://doi.org/10.1104/pp.67.1.74
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