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   <subfield code="a">Copper-induced changes in the growth, oxidative metabolism, and saponin production in suspension culture roots of Panax ginseng in bioreactors</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Mohammad Ali, Eun-Joo Hahn, Kee-Yoeup Paek]</subfield>
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   <subfield code="a">Roots of Panax ginseng exposed to various concentrations of Cu (0.0, 5, 10.0, 25.0, and 50.0μM) accumulated high amounts of Cu in a concentration-dependent and duration-dependent manner. Roots treated with 50μM Cu resulted in 52% and 89% growth inhibition after 20 and 40 days, respectively. Saponin synthesis was stimulated at a Cu concentration between 5 and 25μM but decreased at 50μM Cu. Malondialdehyde content (MDA), lipoxygenase activity (LOX), superoxide ion (O2 •−) accumulation, and H2O2 content at 5 and 10μM Cu-treated roots were not increased but strongly increased at 50μM Cu resulting in the oxidation of ascorbate (ASC) and glutathione (GSH) to dehydroascorbate (DHA) and glutathione disulfide (GSSG), respectively indicating a clear oxidative stress. Seven well-resolved bands of superoxide dismutase (SOD) were detected in the gel and an increase in SOD activity seemed to be mainly due to the induction of Fe-SOD 3. Five to 10μM Cu slightly induced activity of ascorbate peroxidase (APX) and dehydroascorbate reductase (DHAR), guaiacol peroxidase (G-POD) but inhibited monodehydroascorbate reductase (MDHAR) and glutathione reductase (GR) enzyme activities. No changes in catalase (CAT) activity and in activity gel were found up to 25μM Cu, but both G-POD and CAT activities were inhibited at 50μM Cu. Glutathione metabolism enzymes such as γ-glutamylcysteine synthetase (γ-GCS), glutathione-S-transferase (GST), and glutathione peroxidase activities (GPx) were activated at 5 and 10μM Cu but were strongly inhibited at 50μM Cu due to the Cu accumulation in root tissues. The strong depletion of GSH at 50μM Cu was associated to the strong induction of γ-glutamyltranspeptidase (γ-GGT) activity. These results indicate that plant could grow under Cu stress (5-25μM) by modulating the antioxidant defense mechanism for combating Cu induced oxidative stress.</subfield>
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   <subfield code="u">National Food Research Institute, Cell Function Laboratory, Ibaraki-305-8642, Tsukuba, Japan</subfield>
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   <subfield code="t">Plant Cell Reports</subfield>
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