Plant activation of m‐phenylenediamine by tobacco, cotton, and carrot cell suspension cultures

Monica A. Lhotka, Michael J. Plewa, James M. Gentile

Research output: Contribution to journalArticle

Abstract

Tobacco, cotton, and carrot plant cell suspension cultures activated the promutagen m‐phenylenediamine into a mutagen as detected by Salmonella typhimurium strain TA98 with the use of the plant cell/microbe coincubation assay. For each cell line, mid‐log phase plant cells at a density of 100–150 mg/ml were coincubated for 1 hr with concentrations of m‐phenylenediamine that ranged from 0.1 to 10 μmol per reaction tube in the preincubation test of the plant cell/microbe coincubation assay. Further experiments were conducted to optimize the activation response for each plant cell line. The density of plant cells in the reaction mixture, the time of coincubation of the reaction mixture, and the stage of the growth curve at which the plant cells were harvested for use in the reaction mixture all affected the response. Experiments that used the conditions determined as optimum for each plant cell line were then conducted. With each cell line, the optimized conditions enhanced the activation response that had been observed with the preliminary conditions. A ranking order based on the concentration‐response curves indicated a relationship of tobacco cells >> carrot cells > cotton cells. Tobacco cells were able to activate m‐phenylenediamine into a mutagen at concentrations of less than 10 nmol per plate when using TA98 as the genetic indicator organism. Finally, experiments to determine the type of genetic lesion induced by plant‐activated m‐phenylenediamine were conducted. By using five of the Ames strains, m‐phenylenediamine was shown to be active in inducing revertants in strains TA1538 and TA98 following activation by tobacco cells under the optimized conditions. We conclude that m‐phenylenediamine is activated by plant cells into a mutagen that primarily induces frameshift mutations.

Original languageEnglish (US)
Pages (from-to)79-88
Number of pages10
JournalEnvironmental and Molecular Mutagenesis
Volume10
Issue number1
DOIs
StatePublished - 1987

Fingerprint

Daucus carota
Plant Cells
Tobacco
Suspensions
Cell Culture Techniques
Mutagens
Cell Line
Gossypium
Frameshift Mutation
Salmonella typhimurium

Keywords

  • plant cell/microbe coincubation assay

ASJC Scopus subject areas

  • Epidemiology
  • Genetics(clinical)
  • Health, Toxicology and Mutagenesis

Cite this

Plant activation of m‐phenylenediamine by tobacco, cotton, and carrot cell suspension cultures. / Lhotka, Monica A.; Plewa, Michael J.; Gentile, James M.

In: Environmental and Molecular Mutagenesis, Vol. 10, No. 1, 1987, p. 79-88.

Research output: Contribution to journalArticle

Lhotka, Monica A. ; Plewa, Michael J. ; Gentile, James M. / Plant activation of m‐phenylenediamine by tobacco, cotton, and carrot cell suspension cultures. In: Environmental and Molecular Mutagenesis. 1987 ; Vol. 10, No. 1. pp. 79-88.
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