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   <subfield code="a">10.1007/s11240-007-9223-6</subfield>
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   <subfield code="a">Plant regeneration from embryogenic suspension-derived protoplasts of ginger ( Zingiber officinale Rosc.)</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Yinghua Guo, Jinhe Bai, Zhenxian Zhang]</subfield>
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   <subfield code="a">A procedure is described to regenerate plants from embryogenic suspension-derived protoplasts of ginger (Zingiber officinale Rosc.). Somatic embryogenic calli were induced from ginger shoot tips on solid MS medium with half the concentration of NH4NO3 and supplemented with 1.0mgl−1 2,4-Dichloroacetic acid (2, 4-D) and 0.2mgl−1Kin. Rapid-growing and well-dispersed suspension cultures were established by subculturing the embryogenic calli in the same liquid medium. Protoplasts were isolated from embryogenic suspensions with an enzyme solution composed of 4.0mgl−1 cellulase, 1.0mg l−1 macerozyme, 0.1mgl−1 pectolyase, 11% mannitol, 0.5% CaCl2 and 0.1% 2-(N-morpholino) ethane sulphonic acid (MES) for 12-14h at 27°C with a yield of 6.27×106 protoplastsg−1 fresh weight. The protoplasts were cultured initially in liquid MS medium with 1.0mgl−1 2, 4-D and 0.2mgl−1Kin. Then the protoplast-derived calli (1.5cm2) were transferred to a basal MS medium containing 0.2mgl−1 2, 4-D, 5.0mgl−1 benzyladenine (BA), 3% sucrose and 0.7% agar. The white somatic embryos were transferred to MS medium lacking growth regulators for shoot development. Shoots developed into complete plantlets on a solid MS medium supplemented with 2.0mgl−1 BA and 0.6mgl−1 α-Naphthaleneacetic acid (NAA). In addition, the effects of AgNO3, activated charcoal (AC) and ascorbic acid (AA) on browning of protoplast-derived calli are discussed.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2007</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Ginger</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Protoplast</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Embryogenic suspensions</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Plant regeneration</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">2,4-D : 2,4-Dichlorophenoxyacetic acid</subfield>
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   <subfield code="a">AC : Activated charcoal</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">AA : Ascorbic acid</subfield>
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   <subfield code="a">BA : Benzyladenine</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">CH : Casein hydrolysate</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">DTT : Citric acid and 1,4-dithio-dl-threitol</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">FDA : Fluorescein diacetate</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Kin : 6-Furfurylaminopurine</subfield>
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   <subfield code="a">MES : 2-(N-morpholino) ethane sulphonic acid</subfield>
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   <subfield code="a">MS : Murashige and Skoog medium (Murashige and Skoog 1962)</subfield>
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   <subfield code="a">NAA : α-Naphthaleneacetic acid</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PVP : Polyvinylpyrrolidone</subfield>
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   <subfield code="t">Plant Cell, Tissue and Organ Culture</subfield>
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   <subfield code="g">89/2-3(2007-05-01), 151-157</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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