2004•Journal of Peanut ScienceRequires access

Young Leaf Tissue Cultures and Efficient Plant Regeneration in Peanut

LI Mei-qin

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Abstract

Somatic embryogenesis and plant regeneration in young leaf tissue cultures of peanut (Arachis hypogaea L.) cultivar BaiShaGuo were studied. The young leaves were cut into 1 mm×1 mm, and cultured on MS medium supplemented with 1~3 mg/L 2,4-D and 1~5 mg/L BAP. High frequency (89% to 96%) embryogenic clusters derived from leaf explant were obtained on all media used. When the embryogenic clusters were being transferred onto MS medium supplemented with 10 mg/L BAP, or supplemented with 3 mg/LBAP and 1 mg/L ABA, 57% to 100% of calli with embryogenic cluster formed somatic embryos. The emberyos germinated and developed into shoots after being transferred onto MS medium supplemented with BAP (3, 4, 10 mg/L) and ABA (0, 1 mg/L). The highest frenquency of shoot regeneration was up to 96%.

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Somatic embryogenesis and plant regeneration in young leaf tissue cultures of peanut (Arachis hypogaea L.) cultivar BaiShaGuo were studied. The young leaves were cut into 1 mm×1 mm, and cultured on MS medium supplemented with 1~3 mg/L 2,4-D and 1~5 mg/L BAP. High frequency (89% to 96%) embryogenic clusters derived from leaf explant were obtained on all media used. When the embryogenic clusters were being transferred onto MS medium supplemented with 10 mg/L BAP, or supplemented with 3 mg/LBAP and 1 mg/L ABA, 57% to 100% of calli with embryogenic cluster formed somatic embryos. The emberyos germinated and developed into shoots after being transferred onto MS medium supplemented with BAP (3, 4, 10 mg/L) and ABA (0, 1 mg/L). The highest frenquency of shoot regeneration was up to 96%.

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Available abstract

Somatic embryogenesis and plant regeneration in young leaf tissue cultures of peanut (Arachis hypogaea L.) cultivar BaiShaGuo were studied. The young leaves were cut into 1 mm×1 mm, and cultured on MS medium supplemented with 1~3 mg/L 2,4-D and 1~5 mg/L BAP. High frequency (89% to 96%) embryogenic clusters derived from leaf explant were obtained on all media used. When the embryogenic clusters were being transferred onto MS medium supplemented with 10 mg/L BAP, or supplemented with 3 mg/LBAP and 1 mg/L ABA, 57% to 100% of calli with embryogenic cluster formed somatic embryos. The emberyos germinated and developed into shoots after being transferred onto MS medium supplemented with BAP (3, 4, 10 mg/L) and ABA (0, 1 mg/L). The highest frenquency of shoot regeneration was up to 96%.

Key concepts: Arachis hypogaea, Somatic embryogenesis, Explant culture, Shoot, Biology, Murashige and Skoog medium, Germination, Tissue culture

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