Preventing and treating method for albinism of kelp
A treatment method, a technology for albinism, applied in horticultural methods, botanical equipment and methods, seaweed cultivation, etc., can solve problems such as affecting the supply of healthy kelp seedlings, breeding and production, and poor results.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0017] Example 1: The effect of light on the growth of the pathogenic bacterium Pseudoalteromonas X-8
[0018] The applicant first conducted experiments on Pseudoalteromonas X-8, the causative bacterium of kelp albinism.
[0019] Among them, the pathogenic bacterium Pseudoalteromonas X-8 was selected from albino kelp seedlings in a kelp nursery in Rongcheng, Shandong in December 2017. The counterstaining experiment proved that this strain can cause healthy kelp seedlings to produce albinism.
[0020] Cultivate in Zobell 2216E medium, when X-8 reaches the exponential phase, use UV-6000 UV-Vis spectrophotometer (METASH) to measure the absorbance of bacterial growth at OD 600 (optical density at 600 nm). Purchase white light, blue light (400-450nm) and red light (620-760nm) two monochromatic LED light sources at Ningbo Jiangnan Instrument Factory. Set the light intensity of white light, blue light and red light to 40μmol·m -2 ·S -1 , 60μmol·m -2 ·S -1 ,, 160μmol·m -2 ·S -1 . Culture c...
Embodiment 2
[0021] Example 2: Cluster motility analysis
[0022] Under dark conditions, Pseudoalteromonas X-8 was cultured to the logarithmic growth phase at 25°C. Subsequently, the bacterial solution was centrifuged at 6000 g for 10 minutes at room temperature to obtain a cell pellet homogenate. Use an inoculating loop to inoculate the bacterial pellet onto the bacterial solid medium. Cultivate for 24 hours under blue, red, white and dark conditions at a temperature of 10±1°C. Three replicates are designed for each group of experiments. The light intensity is 80μmol·m -2 ·S -1 . It was found that at 80μmol·m -2 ·S -1 Under the conditions, white light and blue light inhibited the movement of Pseudoalteromonas X-8, while red light and darkness promoted the movement of Pseudoalteromonas X-8.
Embodiment 3
[0023] Example 3: Pathogenic bacteria-kelp counterstaining experiment
[0024] Take out the stored bacterial solution from the refrigerator at -20℃, pipette 1mL in 100mL Zobell 2216E liquid medium and culture in a shaking incubator. After 24 hours, pipette 1mL into 100mL Zobell 2216E liquid medium and continue culturing. After 12h, pipette 2mL overnight culture solution. Continue to culture in 200mL Zobell 2216E liquid medium, culture condition is 25℃, rotation speed is 120r / min. After 4h, draw the bacteria liquid to measure the concentration of the bacteria liquid; at this time, the growth of the bacteria liquid is in the logarithmic growth phase.
[0025] Select healthy and healthy kelp seedlings, place them in a petri dish filled with sterile seawater, and then cut the sporophytes into small pieces (1.0cm x 1.0cm) with a sterile blade. Put the kelp tissue block into the culture plate, and add 1mL Pseudoalteromonas X-8 bacterial solution (concentration 10 8 cfu / mL), cultured und...
PUM

Abstract
Description
Claims
Application Information

- R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com