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   <subfield code="a">Effect of enzyme concentrations on protoplast isolation and protoplast culture of Spathiphyllum and Anthurium</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Barbara Duquenne, Tom Eeckhaut, Stefaan Werbrouck, Johan Van Huylenbroeck]</subfield>
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   <subfield code="a">Vital protoplasts from Spathiphyllum wallisii ‘Alain' and Anthurium scherzerianum ‘238' were isolated from both somatic embryos and leaves. The highest yields were obtained when 1.5% cellulase, 0.5% macerase and 0.5% driselase were used for Spathiphyllum wallisii leaves and 0.5% cellulase, 0.3% macerase and 0.5% driselase for Anthurium scherzerianum embryos. About 1×106 protoplasts g−1 and 1×105 protoplasts g−1 could be isolated from leaves and embryos, respectively. For protoplast fusion Spathiphyllum wallisii ‘Alain' and Anthurium scherzerianum ‘238' were mixed in a 1:1 ratio in a fusion solution containing 1mM CaCl2·2H2O, 1mM MES and 0.5M mannitol. Fusion was performed by protoplast alignment under 500Vcm−1 alternating current for 60s and subsequent generation of two pulses of 4500Vcm−1 direct current during 50μs. Development until colony stage was achieved using agarose beads for protoplast culture.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2007</subfield>
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   <subfield code="a">Araceae</subfield>
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   <subfield code="a">Cellulase</subfield>
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   <subfield code="a">Driselase</subfield>
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   <subfield code="a">Agarose beads</subfield>
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   <subfield code="a">AC : Alternating current</subfield>
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   <subfield code="a">FDA : Fluorescein diacetate</subfield>
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   <subfield code="a">FW : Fresh weight</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">KM : Kao and Michayluk</subfield>
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   <subfield code="a">MES : Morpholino-ethane sulfonic acid</subfield>
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   <subfield code="a">PP : Protoplasts</subfield>
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