• Proceedings of the Korean Society of Applied Entomolohy Conference
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• 2001.11a
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• pp.140-141
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• 2001

• Journal of Plant Biotechnology
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• v.34 no.4
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• pp.355-361
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• 2007

Cotyledons of perilla6 were cultured on MS medium containing 0.5 mg/l NAA and 0.5 mg/l BA for 7 weeks. The activity of perilla peroxidase was observed to increase following culture stages as assessed by peroxidase assay. A peroxidase (POD) was purified from perilla tissue cultured on MS medium for 7 weeks. The peroxidase was purified using ion exchange and gel nitration chromatography. The perilla peroxidase had a molecular mass of 30 kDa by SDS-PAGE. We showed that the N-terminal amino acid sequence of this protein shared 67% identity with the tea peroxidase. As indicated by SDS-PAGE, the banding pattern of the 30 kDa polypeptide present in total soluble protein from perilla tissue was increased following culture stages. Immunoblot analysis indicated that perilla peroxidase protein appeared after 3 weeks of perilla tissue culture, and continued to increase with extended duration of tissue culture for at least 7 weeks.

• Proceedings of the Plant Resources Society of Korea Conference
• /
• 2005.11a
• /
• pp.169-169
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• 2005

• Proceedings of the PSK Conference
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• 2001.10a
• /
• pp.148.1-148.1
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• 2001

• Proceedings of the Korean Society of Life Science Conference
• /
• 2006.09a
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• pp.45.2-45.2
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• 2006

• Proceedings of the Korean Society of Life Science Conference
• /
• 2006.09a
• /
• pp.45.1-45.1
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• 2006

• Proceedings of the Korean Society of Life Science Conference
• /
• 2006.09a
• /
• pp.46.1-46.1
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• 2006

• Proceedings of the Korean Society of Life Science Conference
• /
• 2003.05a
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• pp.81-81
• /
• 2003

• Proceedings of the Korean Society of Applied Entomolohy Conference
• /
• 2002.11a
• /
• pp.136-136
• /
• 2002

• Proceedings of the Korean Society of Life Science Conference
• /
• 2001.09a
• /
• pp.82-82
• /
• 2001