In-vitro conservation method for liparis nervosa
A technology of in vitro preservation and see blood green, which is applied in the field of in vitro preservation of plants see blood green, to achieve the effect of alleviating over-harvesting
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Embodiment 1
[0017] 1. Materials: See Liparisnervosa (Thunb. ex A. Murray) Lindl.).
[0018] 2. Material category: see Xueqing seeds.
[0019]3. Culture conditions: (1) Seed germination medium: Basic medium is 1 / 2MS (macronutrients in MS are halved, and the rest are the same as MS); (2) Bud proliferation medium: MS+B5 vitamins+IAA0. 5mg / L+KT0.5mg / L+inositol 100mg / L; (3) in vitro preservation medium: 1 / 2MS+PPP 333 2.0mg / L+NAA0.5mg / L. Above medium (1) and (2) add 20g / L sucrose, (3) add 40g / L sucrose, activated carbon 1-2g / L. All media were solidified by adding agar 5.8g / L, pH5.8, culture temperature was 25±2℃, light intensity was 10-20μmol / (m 2 s), light 12h / d. The culture bottles used are all white transparent glass bottles, with a diameter of 7.5cm x height of 9.0cm, and a volume of about 300ml; the medium used in (1) and (2) is about 40ml, and the medium used in (3) for in vitro preservation is about 75ml .
[0020] 4. Growth and differentiation
[0021] 4.1 Obtaining of explants: ...
Embodiment 2
[0026] 1. Materials: See Liparisnervosa (Thunb. ex A. Murray) Lindl.).
[0027] 2. Material category: see Xueqing seeds.
[0028] 3. Culture conditions: (1) Seed germination medium: Basic medium is 1 / 2MS (macronutrients in MS are halved, and the rest are the same as MS); (2) Bud proliferation medium: MS+B5 vitamins+IAA0. 5mg / L+KT0.5mg / L+inositol 100mg / L; (3) in vitro preservation medium: 1 / 2MS+PPP 333 2.0mg / L+NAA0.5mg / L. Above medium (1) and (2) add 20g / L sucrose, (3) add 40g / L sucrose, activated carbon 1.5g / L. All media were solidified by adding 5.8g / L of agar, pH5.8, the culture temperature was 25±2℃, and the light intensity was 15μmol / (m 2 s), light 12h / d. The culture bottles used are all white transparent glass bottles, with a diameter of 7.5cm x height of 9.0cm, and a volume of about 300ml; the medium used in (1) and (2) is about 40ml, and the medium used in (3) for in vitro preservation is about 75ml .
[0029] 4. Growth and differentiation
[0030] 4.1 Obtaining ...
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