Abstract

Codonopsis javania (Blume) Hook.f. et Thomson a traditional medicine plant and now an endangered species in Vietnam is grown for roots. The research was carried out to establish the plant propagation for the purpose of concerving and exploting this endangered medicinal herbs. In vitro shoot tip explants (1 – 1.5 cm) were induced to form callus on MS medium containing NAA (0.5 – 2 mg /L) with TDZ 0.1 mg/L. After four weeks of culture, in the MS medium combine with NAA 1 mg/L and TDZ 0.1 mg/L the explant induced compact callus (green, solid) wsa achieved 85.33%. The callus induction to form shoots on medium MS containing BA (0.5 – 2.0 mg/L) with NAA 0.2 mg/L. After 4 weeks of culture, shoot formation was higher in the MS medium containing BA 1.0 mg /L and NAA 0.2 mg/L and achieved of 82.67 % with 9.92 shoots/explant. The best shoot proliferation (2 – 3 cm) was excised and transferred to a medium shoot multiplication with the same composition as the shoot induction medium in which NAA 0.2 mg/L was replaced by NAA 0.5 mg/L. When compared the shoot multiplication between the two mediums at the same BA concentration (2 mg/L), all shoots increased and reached 5.87 times after 60 days cultured. On rooting MS medium with IBA 1 mg/L, 88.67 % in vitro rooting was observed with the average root yield of 4.33 roots/shoot and the length of 8.27 cm. Root length and their yield quality were highly improved when using of coconut fiber (30 %) and earthworms compost (70 %) (v/v) in the transfer medium after acclimatisation stages.

Highlights

  • Sau 30 ngày các chồi đã hình thành rõ rệt trên tất cả các môi trường với tỷ lệ mẫu tạo chồi và số lượng chồi/mẫu có sự khác biệt đáng kể giữa các công thức (Bảng 2), tỷ lệ tái sinh chồi tăng từ 13,33 – 82,67 % khi kết hợp BA ở nồng độ từ 0,5 – 2 mg/L với naphthaleneacetic acid (NAA) 0,2 mg/L

  • In vitro shoot tip explants (1 – 1.5 cm) were induced to form callus on MS medium containing naphthaleneacetic acid (NAA) (0.5 – 2 mg /L) with TDZ 0.1 mg/L

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Summary

Vật liệu

Hạt Đảng sâm được thu thập tại vùng núi của xã Trà Nam, huyện Nam Trà My, tỉnh Quảng Nam. Hạt được ngâm với nước cất vô trùng ở 500C, trong 2 giờ, sau đó gieo trên môi trường khoáng MS (Murashige và Skoog, 1962) [8]

Tạo rễ in vitro
Điều kiện nuôi cấy
Đặc điểm của sẹo
Nhân nhanh chồi Đảng sâm
Chất ĐHST Hệ số nhân chồi
Tái sinh cây Đảng sâm từ chồi in vitro
Thích nghi cây ngoài vườn ươm
Xơ dừa

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