Dendrobium candidum endophyte with growth promotion function and use thereof
A technology of Dendrobium officinale and uses is applied in the field of endophytic bacteria of natural medicinal plants, which can solve the problems of less research on endophytic bacteria and no research report on tissue culture of Dendrobium officinale, and achieve the effect of shortening production time.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0029] Embodiment 1, the isolation culture method of Sphingomonas CCTCC NO: M 2010041, carries out the following steps successively:
[0030] 1. Collect the root samples of wild healthy Dendrobium officinale plants in Tonglu, Zhejiang, wash them thoroughly with tap water, and treat them with 25KHz ultrasonic waves for 5 minutes;
[0031] 2. Under aseptic conditions, wash the test material obtained in step 1 twice with sterile water, and then use 75% alcohol and saturated bleach solution to disinfect the surface of the test material successively, so as to kill the test material. microorganisms on the surface of materials;
[0032] 3. In a sterile environment, rinse the test material obtained in step 2 with sterile water for 3 times, take 100 μl of the sterile water rinse produced in the last rinse, and inoculate it in the basal NA medium, at 30°C After culturing for 24 hours, observe whether there are colonies. Based on this, verify whether this disinfection method completely...
Embodiment 2
[0040] Embodiment 2, the cultivation seed production method of Sphingomonas CCTCC NO:M 2010041, carries out the following steps successively:
[0041] 1. Transfer the Sphingomonas CCTCC NO: M 2010041 to the slant of the basic NA medium, and cultivate it at 30°C for 2 days; get the slant seeds;
[0042] The slant formula of the basic NA medium is: peptone 10g, beef extract 3g, NaCl 5g, agar 18g and H 2 O1000ml, pH=7.4~7.6.
[0043] 2. Use an inoculation loop to pick 0.5g of the slant strain obtained in step 1, inoculate it into a 250ml Erlenmeyer flask containing 100ml of LB liquid medium, and culture it at 28°C for 30h at a speed of 200r / m to obtain Sphingomonas CCTCC NO: M2010041 fermentation stock solution;
[0044] The formula of LB liquid medium is: peptone 10g, yeast extract 10g, NaCl 5g and H 2 O1000ml, pH=7.4~7.6.
Embodiment 3
[0045] Embodiment 3, sphingomonas CCTCC NO: M 2010041 promotes the growth of Dendrobium candidum tissue culture seedling growth experiment:
[0046] The following experiments all use the tissue-cultured seedlings of Dendrobium candidum that have been cultivated in the improved tissue culture medium of Dendrobium candidum as the experimental objects.
[0047] The formula of the improved Dendrobium candidum tissue culture medium is: adopt 1 / 2MS as basic medium, add banana juice 10% / L, agar 7g / L, sucrose 20g / L, adjust pH value to 5.8 with 1mol / L NaOH . That is: add 0.1L banana juice, 7g agar and 20g sucrose to every L of 1 / 2MS, and adjust the pH value to 5.8.
[0048] Experiment 1. Sphingomonas CCTCC NO: M 2010041 fermentation stock solution on growth promotion of Dendrobium officinale tissue culture seedlings 1:
[0049] Utilize the Sphingomonas CCTCC NO:M 2010041 fermented stock solution obtained in the above-mentioned Example 2, dilute the fermented stock solution with steri...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com