Screening method and use of trichoderma asperellum
A screening method, Trichoderma technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, fungi, etc., can solve problems such as limited laboratory research stages, and achieve the effect of ensuring normal growth
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Embodiment 1
[0034] Example 1 Isolation and screening of Trichoderma aculeatus
[0035] Collect arsenic-contaminated soil samples from arsenic-contaminated areas, isolate fungi from the soil samples in the laboratory, culture them on solid PGP medium (potato-glucose-peptone medium) containing a certain concentration of arsenic, and observe their growth in Colony growth under different arsenic concentrations to screen out robust and arsenic-resistant Trichoderma aculeatus.
[0036] Specifically include steps:
[0037]The above-mentioned arsenic-contaminated soil sample comes from the slag accumulation place near the realgar mine in Shimen area, Hunan Province. The soil sample was serially diluted and spread on the Martin medium with an arsenic content of 400-600 mg / L to isolate the fungus. The Martin medium Ingredients include: Dextrose, Peptone, KH 2 PO 4 , MgSO 4 ·7H 2 O, agar and water, its weight ratio is 20:10:2:1:80:4000.
[0038] After the isolated fungus has been purified and ...
Embodiment 2
[0039] Example 2 Experiment on the growth of Trichoderma aculeatus in different solutions containing arsenic
[0040] Prepare PGP medium with arsenic content of 0, 10, 30, 50, 80, 100, 200mg / L respectively, and after sterilizing at 120-122°C for 14-16 minutes, 8-10mm Echinococcus sp. Trichoderma bacteria blocks were added to the above treatments, and cultured on a shaker at a temperature of 23-27°C and a rotational speed of 138-142rmp; after 5 days of cultivation, the culture solution was centrifuged at 3800-4200rmp for 8-12 minutes, and the suspension Count the number of spores in the solution; then wash the bacteria repeatedly with ultrapure water 4 times, wash off the residual culture medium, dry the bacteria at 48-52°C to constant weight, and then weigh the bacteria Mass weight, the biomass of Trichoderma aculeatus.
[0041] Such as figure 1 Shown is the biomass of Trichoderma aculeatus at the above-mentioned different levels of arsenic concentration (ie, arsenic content...
Embodiment 3
[0042] Example 3 Determination experiment of Trichoderma aculeatus on bioaccumulation and volatilization of arsenic
[0043] Prepare a PGP medium with a total arsenic content of 50mg / L, sterilize it at 120-125°C for 14-17 minutes, and insert 0.1ml of Trichoderma aculeatus with a content of 10 4 For cfu / ml bacterial suspension, the culture temperature is 24-27°C, and the speed is 138-142rmp. After 5 days of cultivation, centrifuge at a speed of 3800-4200rmp for 8-12 minutes, and wash the bacteria repeatedly with ultrapure water 4 times. , wash off the residual culture medium, dry the fungus at 48-52°C to constant weight, then weigh the fungus, and use 11-13ml of HNO with a volume ratio of 4-6:1 3 , HClO 4 The mixed solution was digested at 158-162°C for 10 hours, and the total arsenic content in the bacteria was measured by atomic fluorescence; The total arsenic content in the serum was also determined by atomic fluorescence.
[0044] The total arsenic content in the fungus ...
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