Radiation Tolerant Desert Rhodobacter and Its Application
A technology of red bacteria and radiation resistance, applied in the field of microorganisms, can solve the problems of rarely reported strains with radiation resistance and radiation resistance, and achieve the effect of promoting environmental protection
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0052] The isolation and cultivation of embodiment 1 radiation resistant desert rhodobacter
[0053] Sandy soil was collected from the rhizosphere soil of red willow on the edge of the Taklimakan Desert in Xinjiang. Weigh 1.0 g of the soil sample, put it into a triangular flask containing 99 mL of sterile water, and place it on a shaker for 20 minutes to disperse the soil evenly to form a soil suspension (10 -2 ). Use a 100 μL pipette gun to draw 100 μL of soil suspension, inject it into a centrifuge tube filled with 900 μL sterile water, blow and suck 3 times, shake evenly (10 -3 ). Then use the same method to configure a dilution of 10 -4 , 10 -5 soil bacterial suspension. Take 200 μL of a suitable concentration of bacterial suspension and spread it on an LB agar medium plate, turn the plate over and place it in an incubator at 30°C for 3 days, and then obtain the radiation-tolerant Rhodobacter desert in the present invention.
Embodiment 2
[0056] Embodiment 2 The ultraviolet tolerance test of radiation-resistant desert rhodobacter
[0057] 1. Test method
[0058]Inoculate the radiation-resistant Rhodobacter desert bacterium strain of the present invention in LB liquid medium, culture it on a shaker until the logarithmic phase of growth, collect the bacteria by centrifuging at 5000 rpm for 10 minutes at 4°C; resuspend the bacteria in an equal volume of 0.1M phosphoric acid Potassium Buffer(pH7.0)(K 2 HPO 4 27.816g, KH 2 PO 4 10.608g, dissolved in 1L distilled water, sterilized at 121°C for 20min), then centrifuged at 5000rpm at 4°C for 10min to collect the bacteria, and resuspended the bacteria again in an equal volume of 0.1M potassium phosphate buffer (pH7.0).
[0059] Place the bacterial solution in a Petri dish and stir it with a sterilized iron wire to make the bacterial cells uniform. Place the petri dishes at 0~3600J / m 2 Under different doses of ultraviolet irradiation; take the irradiated bacterial ...
Embodiment 3
[0066] Example 3 Extraction of Radiation-resistant Rhodobacter desert Rhodobacter strain 16SrDNA
[0067] The present invention also provides genome extraction, 16SrDNA amplification and sequencing methods of radiation-resistant desert rhodobacteria (R.shamoensisW402), specifically according to the following operations:
[0068] 1. Genome extraction method
[0069] Genome use of radiation-resistant desert rhodobacter according to the present invention The company's bacterial genomic DNA extraction kit (centrifugal column) for extraction, see its instructions for details.
[0070] 2. PCR amplification method
[0071] The general primer sequence used for the PCR amplification of the 16SrDNA of the radiation-tolerant Rhodobacter desert bacterium according to the present invention refers to the article of WilliamG. Weisburg (1991), and the primer is synthesized by Beijing Qingke Biotechnology Company. The kits used for the amplification were purchased from Treasure Bioengineer...
PUM
| Property | Measurement | Unit |
|---|---|---|
| Dilution degree | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 