Xylaria fungus strain E68 and application thereof
A technology of the genus Anthracera and fungi, which is applied in the fields of fungi, water/sludge/sewage treatment, biochemical equipment and methods, etc., can solve the problems of pregnant women who are prone to miscarriage, the content exceeds the safe value, and destroys the natural environment, and achieves Important industrial application value, good market prospect, easy industrialization effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0020] Example 1 : Isolation, screening and identification of Xylaria sp. E68
[0021] 1.1 Experimental materials
[0022] Inorganic salt medium: 1 g of ammonium nitrate, 1.5 g of dipotassium hydrogen phosphate, 0.5 g of potassium dihydrogen phosphate, 0.1 g of crystalline magnesium sulfate, 45.72 mg of ferrous sulfate (7 water), 1 L of water, 40 g of agar.
[0023] LB medium: 10g tryptone, 5g yeast powder, 10g sodium chloride, 1L water, 40g agar.
[0024] PDA medium: 200g potatoes, 20g glucose, 500-600mL water, boiled for about half an hour, passed through gauze, dilute to 1 liter, add 40g agar.
[0025] The degradation solution is a mixture of inorganic salt medium and dimethyltetrachloride.
[0026] 1.2 Separation and identification methods
[0027] Xylaria sp. E68 of the present invention is obtained from Mingyang, Guangxi sampling, isolation and screening, and is preserved by the Guangdong Microbial Culture Collection Center, and its preservation number is GDMCC No.6...
Embodiment 2
[0041] Example 2 : Study on the Effect of Xylaria sp. E68 on the Degradation of Dimethyltetrachloride
[0042] 2.1 Cultivation of degrading bacteria
[0043] Prepare PDB medium, sterilize it, and put it in sterilized 30mL vials with caps, 10mL per bottle, scrape the purified fungal hyphae in PDA medium with an inoculation loop, and insert them into PDA medium vials respectively, To obtain expanded cultured cells, the culture condition is to cultivate at 28°C for 3-4 days and wait for use.
[0044] 2.2 Screening of degrading bacteria
[0045] Prepare the degradation test medium of degrading bacteria, and distribute it in sterile 30mL vials with caps, 10mL per bottle. Add 0.55g / L (by dry weight) to expand the cultured cells and mix with the subpackaged degrading bacteria degradation test medium. Before mixing, wash with the degradation bacteria degradation test medium for 3 times and then mix with the degradation test medium , three parallel treatments and a blank control w...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


