A kind of rapid cultivation method of fungi and fungi-cyanobacteria compound lichen crust
A cultivation method and technology of cyanobacteria, applied in the field of environmental biology, can solve the problems of high maintenance costs, moss materials not suitable for large-scale production, and desertification soil restoration, etc., achieve short cultivation period, increase carbon and nitrogen content and soil enzyme activity , Improve the effect of physical and chemical properties
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Embodiment 1
[0033] Example 1 Screening of high-yielding exopolysaccharide strains and identification of fermentation products
[0034] Collect the complete lichen crusts that grow naturally in arid areas, weigh 10g, put them in a 250mL Erlenmeyer flask filled with 90mL sterile water, vibrate at 30°C for 20min at 150r / min, and let stand for 10min to obtain a soil suspension. Dilute the bacterial suspension to 10 –6 After that, take 10 of them -4 , 10 -5 , 10 -6 200 μL of the solution under 3 dilution gradients, spread on the PDA medium, and culture it upside down in a constant temperature incubator at 30°C for 48 hours, select different types of typical single colonies, and after repeated purification on the plate, store them in the PDA slant medium at 4°C stand-by.
[0035] Add 100mL sterilized liquid PDA medium (containing sterile glass beads) to a 250mL Erlenmeyer flask, inoculate each bacterial strain stored on the PDA slant medium into the PDA medium, and shake at 150rpm for 3 da...
Embodiment 2
[0044] The soil fertility comparison of embodiment 2 fungus-cyanobacteria compound crust and single algal crust
[0045] Inoculate the outer bottle mold Zh2 into the PDA medium, shake and culture at 150rpm for 3 days, and wait until it reaches the logarithmic growth phase, and set aside; Depository Center (FACHB-886). The algae is isolated from the biological soil crust in Shapotou, Ningxia. It is an excellent algae used for sand fixation in the Kubuqi Desert. The algae is inoculated in sterile BG 110 culture medium, placed in a light incubator with a light intensity of 50 μE / (m 2 s), 25±1°C, continuous light, and aeration to the logarithmic phase.
[0046] Cultivate the exophyll mold Zh2 and Algae spp. to the logarithmic phase, determine the biomass by blood counting and colorimetry, mix after dilution, so that the mixed culture contains 5-10 μg (chlorophyll a) / mL cyanobacteria and 10 6 ~10 8 CFU / mL outer bottle mold Zh2. With 1±0.3μg (chlorophyll a) / cm 2 The amount of ...
Embodiment 3
[0050] Example 3 Comparison of the growth curves of fungi-cyanobacteria composite crusts and single cyanobacteria crusts under different drought stresses
[0051] Different soil moisture content groups (0, 5%, 10%, 15% and 20%) are set, and the fungus-cyanobacteria mixture and single cyanobacteria are respectively inoculated on the quicksand surface, and the inoculation method is the same as that of embodiment 3. Continuous light and constant temperature cultivation, during which water should be replenished according to the soil water content at 9:00 every day. Every 5 days during the culture period, take the crust per unit area into a 10mL centrifuge tube, add 5mL of 95% ethanol, vortex and mix evenly, then place in a refrigerator at 4°C for extraction for 24h, shake at least 3 times during the period, and centrifuge at 8000g for 10min after the extraction. The absorbance was measured at 665nm and 649nm, and the content of chlorophyll a was calculated. The change curve of cr...
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