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. 1994 Dec;106(4):1541–1546. doi: 10.1104/pp.106.4.1541

Immediate Activation of Respiration in Petroselinum crispum L. in Response to the Phytophthora megasperma f. sp. Glycinea Elicitor.

E G Norman 1, A B Walton 1, D H Turpin 1
PMCID: PMC159696  PMID: 12232429

Abstract

Treatment of parsley (Petroselinum crispum L.) cell cultures with the Phytophthora megasperma elicitor isolated from the fungus Phytophthora megasperma f. sp. Glycinea caused an immediate increase in the rate of respiratory CO2 evolution in the dark. The respiratory response was biphasic, showing a rapid enhancement in the first 20 min and then a slower increase until a steady rate was attained 60 min posttreatment. The enhanced rate of CO2 evolution corresponded to the activation of phosphofructokinase and glucose-6-phosphate dehydrogenase, key enzymes in the regulation of carbohydrate flow to glycolysis and the oxidative pentose phosphate (OPP) pathway, respectively. The increased rate of CO2 evolution and the activation of phosphofructokinase and glucose-6-phosphate dehydrogenase were maintained for the duration of the experiments, indicating long-term stimulation of respiration through both glycolysis and the OPP pathway. A 23% decrease in the C6:C1 ratio of 14CO2 evolution from labeled glucose 60 min after the addition of Phytophthora megasperma elicitor is consistent with an increased contribution of the OPP pathway to cellular respiration. Long-term activation of the OPP pathway following elicitation could serve to maintain the pools of substrates necessary during activation of the shikimic acid pathway, leading to the production of defensive compounds.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Apostol I., Heinstein P. F., Low P. S. Rapid Stimulation of an Oxidative Burst during Elicitation of Cultured Plant Cells : Role in Defense and Signal Transduction. Plant Physiol. 1989 May;90(1):109–116. doi: 10.1104/pp.90.1.109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ayers A. R., Ebel J., Valent B., Albersheim P. Host-Pathogen Interactions: X. Fractionation and Biological Activity of an Elicitor Isolated from the Mycelial Walls of Phytophthora megasperma var. sojae. Plant Physiol. 1976 May;57(5):760–765. doi: 10.1104/pp.57.5.760. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  4. Dietrich A., Mayer J. E., Hahlbrock K. Fungal elicitor triggers rapid, transient, and specific protein phosphorylation in parsley cell suspension cultures. J Biol Chem. 1990 Apr 15;265(11):6360–6368. [PubMed] [Google Scholar]
  5. Kelly G. J., Turner J. F. The regulation of pea-seed phosphofructokinase by phosphoenolpyruvate. Biochem J. 1969 Nov;115(3):481–487. doi: 10.1042/bj1150481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Kneusel R. E., Matern U., Nicolay K. Formation of trans-caffeoyl-CoA from trans-4-coumaroyl-CoA by Zn2+-dependent enzymes in cultured plant cells and its activation by an elicitor-induced pH shift. Arch Biochem Biophys. 1989 Mar;269(2):455–462. doi: 10.1016/0003-9861(89)90129-x. [DOI] [PubMed] [Google Scholar]
  7. Kuhn D. N., Chappell J., Boudet A., Hahlbrock K. Induction of phenylalanine ammonia-lyase and 4-coumarate:CoA ligase mRNAs in cultured plant cells by UV light or fungal elicitor. Proc Natl Acad Sci U S A. 1984 Feb;81(4):1102–1106. doi: 10.1073/pnas.81.4.1102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ragg H., Kuhn D. N., Hahlbrock K. Coordinated regulation of 4-coumarate:CoA ligase and phenylalanine ammonia-lyase mRNAs in cultured plant cells. J Biol Chem. 1981 Oct 10;256(19):10061–10065. [PubMed] [Google Scholar]
  9. Wirtz W., Stitt M., Heldt H. W. Enzymic determination of metabolites in the subcellular compartments of spinach protoplasts. Plant Physiol. 1980 Jul;66(1):187–193. doi: 10.1104/pp.66.1.187. [DOI] [PMC free article] [PubMed] [Google Scholar]

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