Use of plant cell cultures to study graminicide effects on lipid metabolism

Phytochemistry. 2003 Jul;63(5):533-41. doi: 10.1016/s0031-9422(03)00180-8.

Abstract

Graminicides belonging to the cyclohexanedione and aryloxyphenoxypropionate classes are well established to act by disrupting acyl lipid biosynthesis via specific inhibition of acetyl-CoA carboxylase. Species of grass inherently resistant to such herbicides, or biotypes of grassy weed species which display acquired resistance to recommended rates of graminicide application, are known to possess an altered plastidic multifunctional acetyl-CoA carboxylase showing reduced sensitivity to these herbicides in vitro. Studies reported here demonstrate that cell suspension cultures of maize, a graminicide-sensitive species and Poa annua, a graminicide-insensitive species, display a similar differential sensitivity of acyl lipid biosynthesis as tissue from corresponding intact plants. Acyl lipid biosynthesis in P. annua can be inhibited if sufficiently high concentrations of graminicide are used. The major plastidic form and the minor cytosolic forms of acetyl-CoA carboxylase were successfully purified from maize cell suspensions, were compared to those from leaf tissue and were shown to be differentially inhibited by graminicides in a similar manner to their counterparts from leaf tissue. These studies demonstrate that cell suspensions are useful for studying the mode of action of graminicides, especially in view of the limited amount of material obtainable from many grassy species which are very fine-growing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetyl-CoA Carboxylase / antagonists & inhibitors
  • Acetyl-CoA Carboxylase / metabolism
  • Cell Culture Techniques
  • Cyclohexanones / pharmacology*
  • Lipid Metabolism*
  • Plant Leaves / drug effects
  • Plant Leaves / enzymology
  • Plant Leaves / metabolism
  • Poa / cytology
  • Poa / drug effects*
  • Poa / enzymology
  • Poa / metabolism*
  • Propionates / pharmacology*
  • Quinoxalines / pharmacology*
  • Species Specificity
  • Zea mays / cytology
  • Zea mays / drug effects*
  • Zea mays / enzymology
  • Zea mays / metabolism*

Substances

  • Cyclohexanones
  • Propionates
  • Quinoxalines
  • sethoxydim
  • quizalofop
  • quizalofop-ethyl
  • Acetyl-CoA Carboxylase