Lipoxygenase isoforms in elicitor-treated parsley cell suspension cultures

2000 ◽  
Vol 28 (6) ◽  
pp. 827-829 ◽  
Author(s):  
C. Noehringer ◽  
D. Scheel ◽  
E. Blée
Keyword(s):  
Jasmonic Acid ◽  
Cell Suspension ◽  
Cell Cultures ◽  
De Novo ◽  
Cell Suspension Cultures ◽  
Suspension Cultures ◽  
Defence Response ◽  
Fungal Elicitor ◽  
De Novo Synthesis

Treatment of parsley cell cultures with a fungal elicitor triggered the induction of a lipoxygenase isoform which may be involved in the de novo synthesis of defence-response inducers, such as jasmonic acid or 12-oxo-phytodienoic acid.

scholarly journals Oxidative burst and cell death induced by b-quercinin and zoospores of Phytophthora quercina in tobacco cell cultures

2017 ◽  
Vol 38 (SI 2 - 6th Conf EFPP 2002) ◽  
pp. 446-448 ◽  
Author(s):  
J. Koehl ◽  
E.F. Elstner ◽  
W. Oßwald ◽  
I. Heiser
Keyword(s):  
Cell Death ◽  
Cell Suspension ◽  
Cell Cultures ◽  
Oxidative Burst ◽  
Mode Of Action ◽  
Cell Suspension Cultures ◽  
Suspension Cultures ◽  
Tobacco Cell ◽  
Tobacco Cell Suspension

Mode of action of β-quercinin, a novel elicitin on tobacco cell suspension cultures (cvs. Bel B and Bel W3) was investigated by measuring the oxidative burst and cell death in these cell cultures. β-quercinin induced an oxidative burst comparable to that excited by zoospores from P. quercina. Adding superoxidedismutase, catalase and diphenyleneiodonium to elicited cell cultures, it could be demonstrated, that the induction of cell death in tobacco cell cultures is not correlated to the oxidative burst.

Effects of Plant Bioregulators on the Production of Iridoid Derived Terpenoids in Valeriana wallichii and Fedia cornucopiae Cell Suspension Cultures

1987 ◽  
Vol 42 (1-2) ◽  
pp. 33-40 ◽  
Author(s):  
Wolfram Förster ◽  
Hans Becker
Keyword(s):  
Cell Suspension ◽  
Cell Cultures ◽  
Exponential Growth ◽  
Cell Suspension Cultures ◽  
Growth Cycle ◽  
Suspension Cultures ◽  
Tissue Cultures ◽  
Cell Systems ◽  
Optimal Activity ◽  
Plant Tissue Cultures

Abstract Four plant bioregulators were tested for their effects on production of valepotriates in Valeriana wallichii and Fedia cornucopiae cell suspension cultures. Concentrations of more than 10 ppm reduced valepotriate yield. At lower concentrations production was increased. For optimal activity, bioregulators had to be applied during early exponential growth, up to day 8 of the growth cycle. At equimolar concentrations dim ethylm orpholinium bromide (4 ppm) and dimethylpiperidinium chloride (3 ppm) significantly im proved total valepotriates in V. wallichii (up to 23%) and in F cornucupiae (up to 50% ) 2-(3,4-dichlorophenoxy ) - triethylamine (6 ppm ) and 2-(3,5-diisopropylphenoxy)-triethylam ine (6.4 ppm) increased valepotriate production in both cell cultures up to 40%. With dimethylpiperidinium chloride and dimethylmorpholinium bromide the ratio of m onoene to diene valepotriates in both cell systems was significantly shifted to the m onoene com pounds. A general use of these bioregulators to increase production of terpenoid secondary m etabolites in plant tissue cultures is indicated.

scholarly journals Glutaric Acid as a Catabolite of Nicotinic Acid in Parsley Cell Suspension Cultures

1988 ◽  
Vol 43 (11-12) ◽  
pp. 843-849 ◽  
Author(s):  
Dieter Komoßa ◽  
Wolfgang Barz
Keyword(s):  
Nicotinic Acid ◽  
Cell Suspension ◽  
Cell Cultures ◽  
Degradation Product ◽  
Glutaric Acid ◽  
Cell Suspension Cultures ◽  
Suspension Cultures ◽  
Carbon Skeleton ◽  
Intermediate Products ◽  
H Nmr

Abstract A degradation product of nicotinic acid representing the pyridine carbon skeleton was isolated and purified from parsley cell suspension cultures after incubation with [6-14C]nicotinic acid for 70 h. The catabolite was identified as glutaric acid by means of spectroscopic (GC-MS and 1H NMR) and chromatographic (TLC, HPLC) techniques. Glutaric acid when applied to parsley cell cultures was readily degraded to CO2 but intermediate products could not be identified.

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