Method for accelerating growth of muscodor fengyangensis and adopted pretreated active carbon granules
A technology of activated carbon granules and Fengyang gas-producing mold, applied in the field of microbial fermentation, can solve problems such as slow growth of gas-producing mold
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Embodiment 1
[0041] Embodiment 1, preservation and activation culture of bacterial strain (belong to routine technology)
[0042] 1. Normal temperature or low temperature storage of strains
[0043]On the ultra-clean workbench, add no more than 1.5ml of melted PDA medium to a 2ml sterile cryopreservation tube, cover it, and place it at an angle. After solidification, inoculate the preserved strains to the slant medium. After a few days, the mycelium successfully colonizes the slant, and fresh mycelium can be seen growing. Add the paraffin that has been sterilized three times to submerge the mycelium, and cover it. Store at room temperature or in a refrigerator at 10°C. When in use, use a sterile toothpick to pick out the bacterial tissue and inoculate it on a flat PDA medium for activation.
[0044] 2. Cryopreservation of strains
[0045] On the ultra-clean workbench, dig out 4-5 pieces of bacteria from the colony on the PDA, put them in a 2ml sterile cryopreservation tube, add high-pre...
Embodiment 2
[0048] Embodiment 2, the pretreatment of gac
[0049] In order to ensure the high adsorption activity of activated carbon, the activated carbon is pretreated as follows, and the following steps are carried out in sequence:
[0050] 1), heating washing:
[0051] Weigh 100g of Hushi brand granular activated carbon that has just been opened, put it in a 1000ml large beaker, add 500ml of deionized water, boil in an electric heating pot for 30min, discard the waste liquid, and repeat 4 times (i.e., carry out 5 times in total); Activated carbon granules after initial wash;
[0052] 2), ultrasonic cleaning:
[0053] Use clean gloves to squeeze the activated carbon particles after the initial washing, drain the water, transfer it to a 1000ml large beaker, add 800ml deionized water, place it in a 53KHZ ultrasonic cleaner for 30min, discard the waste liquid, and obtain the second washing Activated carbon particles;
[0054] 3) Repeatedly wash the activated carbon particles after the...
Embodiment 3
[0058] Inoculate the Mycobacterium aerogenes ZJLQ024 strain on a flat plate PDA medium from the cryopreservation tube for storing the strain, and use it when the diameter of the colony reaches 6-7 cm. Pour the melted PDA medium into one compartment of a sterile three-compartment petri dish, and wait for the medium to cool and solidify for later use. Take the cultured Mold aerogenes ZJLQ024 colony, use a 5mm hole puncher to punch a hole at the edge of the colony to obtain a 5mm diameter bacterial cake, inoculate the bacterial cake in this grid of the plate culture medium that contains the PDA medium, and another Add 1.0 g of activated carbon after autoclaving (obtained in Example 2) to the grid, and seal the culture dish with double-layer Parafilm sealing film. No active carbon was added, and only M. aerogenes ZJLQ024 was added as the control group (that is, the culture medium of M. aerogenes ZJLQ024 without adding activated carbon was used as the control group), and cultured i...
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