Rapid propagation method for tissue cultivation of dendrobium candidum stem

A technology for Dendrobium officinale and stem segments, which is applied to the field of rapid tissue culture propagation of Dendrobium officinale stem segments, can solve the problems of long reproductive cycle, low multiplying multiples, limited maternal traits, etc., and achieves good economic and social benefits and stable genetic traits. , the effect of maintaining the characteristics of the mother

A technology for Dendrobium officinale and stem segments, which is applied to the field of rapid tissue culture propagation of Dendrobium officinale stem segments, can solve the problems of long reproductive cycle, low multiplying multiples, limited maternal traits, etc., and achieves good economic and social benefits and stable genetic traits. , the effect of maintaining the characteristics of the mother

CN103053425BInactive Publication Date: 2014-11-12杨宝明

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0019] Select the stems of a single plant with strong growth, vigorous growth, good character, good rod shape and strong disease resistance as explants, wash the whole section of fresh strips and air-dry to remove 40% of the water in the fresh strips; Under sterile conditions, soak the explants in 75% alcohol for 30 seconds, then sterilize them with mercuric chloride solution with a concentration of 0.1% by weight for 15 minutes, and then rinse them with sterile water for 6 times, then take sterile filter paper to absorb the explants After burning the water on the surface of the implant, cut it into a stem segment with one node; cut off both ends of the stem segment, and inoculate it into the following induction medium: 1 / 2MS+0.5mg / L6- BA+0.2mg / L NAA+potato juice 10g / L+banana juice 10g / L+agar 5g / L+sucrose 20g / L+activated carbon 0.5g / L, the pH value is 5.4; the culture temperature for induction culture is 22℃, and the light intensity is 1600Lux, the light time is 8 hours / day, a...

Embodiment 2

[0021] Select a single plant stem with strong growth, vigorous growth, good character, good rod shape and strong disease resistance as explants, wash the whole section of fresh strips and air-dry to remove 35% of the water in the fresh strips; Under sterile conditions, soak the explants in 75% alcohol for 30 seconds, then sterilize them with mercuric chloride solution with a concentration of 0.1% by weight for 15 minutes, and then rinse them with sterile water for 6 times, then take sterile filter paper to absorb the explants After burning on the flame of an alcohol lamp, cut into a stem segment with one node; cut off both ends of the stem segment, and inoculate into the following induction medium: 1 / 2MS+1.0mg / L6-BA +0.5mg / L NAA+potato juice 10g / L+banana juice 10g / L+agar 5g / L+sucrose 20g / L+activated carbon 0.5g / L, the pH value is 5.6; the culture temperature for induction culture is 28℃, and the light intensity is 2000Lux , the light time is 8 hours / day, and the culture time i...

Embodiment 3

[0023]Select the stems of a single plant with strong growth, vigorous growth, good character, good rod shape and strong disease resistance as explants, wash the whole section of fresh strips and air-dry to remove 45% of the water in the fresh strips; Under sterile conditions, soak the explants in 75% alcohol for 30 seconds, then sterilize them with mercuric chloride solution with a concentration of 0.1% by weight for 15 minutes, and then rinse them with sterile water for 6 times, then take sterile filter paper to absorb the explants After burning on the flame of an alcohol lamp, cut into a stem segment with one node; cut off both ends of the stem segment, and inoculate into the following induction medium: 1 / 2MS+0.8mg / L6-BA +0.2mg / L NAA+potato juice 10g / L+banana juice 10g / L+agar 5g / L+sucrose 20g / L+activated carbon 0.5g / L, the pH value is 5.2; the culture temperature during induction culture is 25℃, and the light intensity is 1800Lux , the light time is 8 hours / day, and the cult...

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Abstract

The invention relates to a rapid propagation method for tissue cultivation of a dendrobium candidum stem, belonging to the technical field of artificial cultivation of dendrobe. The method comprises the following steps of preparing an explant, inducing axillary bud and protocorm, conducting propagation cultivation, and rooting and seeding cultivation. The rapid propagation method has the beneficial effects that the technical problems of insufficient explant sterilization, high pollution rate, incapability of conducting axenic cultivation, slow protocorm differentiation, less differentiation, long propagation period, high production cost and the like can be well solved. Compared with the prior art, the rapid propagation method has the advantages that rapid propagation can be achieved; and the propagation period can be reduced by over 60 days. In addition, according to the rapid propagation method, seeding genetic traits are stable, the variation is small, the variety is pure, and the parent characteristics and features can be well kept. Thus, excellent seeding guarantee is provided for development of plant industry of dendrobium candidum, and the rapid propagation method has good economic benefit and social benefit.

Description

technical field [0001] The invention belongs to the technical field of dendrobium candidum artificial cultivation, and in particular relates to a method for tissue culture and rapid propagation of stem segments of dendrobium candidum. Background technique [0002] In the production of Dendrobium officinale seedlings, the fruit (seed) is generally used as explants for rapid propagation. However, the seedlings bred by this method have limited traits of the mother body, large differences in traits, miscellaneous varieties, large variations, easy degradation, difficult quality assurance, and difficult maintenance of excellent seed properties. And when using stem tip or stem segment as propagation material, when carrying out tissue culture asexual rapid propagation, although can obtain the seedling with strong target selection, consistent character, consistent quality, high purity, but there is explant base number is small, difficult to sterilize , slow differentiation of protoc...

Claims

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Application Information

Patent Timeline
12 Nov 2014
Publication
CN103053425B
IPC
A01H4/00
Inventors
杨宝明; 李永平