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   <subfield code="a">Influence of GA3, sucrose and solid medium/bioreactor culture on in vitro flowering of Spathiphyllum and association of glutathione metabolism</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Yaser Dewir, Debasis Chakrabarty, Mohammed Ali, Nisha Singh, Eun-Joo Hahn, Kee-Yoeup Paek]</subfield>
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   <subfield code="a">Hormonal control of flower induction and inflorescence development in vitro was investigated in Spathiphyllum. The effects of gibberellic acid (GA3) and sucrose on inflorescence development were studied in plantlets regenerated in tissue culture. GA3 was mandatory for the shift from the vegetative to the reproductive stage. The effect of sucrose concentration on inflorescence bud development was studied in plantlets cultured in MS medium supplemented with 10mgl−1 GA3. Sucrose concentration at 3 or 6% induced inflorescence development in, respectively, 83-85% of the plantlets. The effect of GA3 and sucrose on inflorescence differentiation and development were also recorded in liquid culture using air-lift bioreactor. The best response was found in the same medium which was standardized as an optimum for solid culture, but the results were better than solid culture. In order to study the relationship between glutathione (GSH) and flowering, we also measured the oxidized and reduced GSH content in leaves throughout the culture period on 2 weeks interval. The GSH accumulation was more after 4 weeks until 6 weeks in GA3 treated plantlets. Similarly, glutathione reductase which is involved in the recycling of reduced GSH providing a constant intracellular level of GSH, was also higher in GA3 treated plantlets. The transient increase in GSH contents also correlated with the changes in measured γ-glutamylcysteine synthetase (γ-ECS) activity over the same period. The antioxidant enzyme activity in GA3 treated plantlets also suggests that the plants suffered increased oxidative stress during the period of GA3 treatment which subsequently increases GSH synthesis through activation of γ-ECS and this promotes flowering by increasing endogenous GSH.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2007</subfield>
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   <subfield code="a">Bioreactor culture</subfield>
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   <subfield code="a">APX : Ascorbate peroxidase</subfield>
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   <subfield code="a">BTBB : Balloon type bubble bioreactor</subfield>
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   <subfield code="a">CAT : Catalase</subfield>
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   <subfield code="a">DHAR : Dehydroascorbate reductase</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">DTNB : 5,5′-Dithiobis-2-nitrobenzoic acid</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">GA : Gibberellin</subfield>
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   <subfield code="a">GA3 : Gibberellic acid</subfield>
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   <subfield code="a">G-POD : Guaiacol peroxidase</subfield>
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   <subfield code="a">MDHAR : Monodehydroascorbate reductase</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">MS : Murashige and Skoog's medium</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PPF : Photosynthetic photon flux</subfield>
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   <subfield code="a">SAM : Shoot apical meristem</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">γ-ECS : γ-Glutamylcysteine synthetase</subfield>
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