|Culture medium||CDA: 3g of sodium nitrate, 1g of dipotassium hydrogen phosphate, 0.5g of magnesium sulfate, 0.5g of potassium chloride, 0.01g of ferrous sulfate, 30g of sucrose, 15g of agar, 1.0L of distilled water and 6.2±0.2 of pH. Sterilization at 121 ℃ for 15min.|
|Subculture procedure||(1) Prepare a test tube containing 5~10mL of liquid medium and 2 plates; (2) Open it in the safety cabinet, heat the tip of ampoule in a flame, quickly drop sterile water to creak it, then break it with forceps; (3) draw 0.5mL of liquid culture medium into a freeze dried ampoule, fully rehydrate and transfer the solution to the liquid test tube, mix evenly; (4) inoculate a plate with 0.2mL of suspension liquid, repeat the step to obtain two plates; ⑤ Put all the liquid test tubes and plates under the above culture conditions for cultivation, and the strains can be used when they grow.|
|Growth conditions||28 ℃;5-7 days; Aerobic;|
|Storage conditions||2-8 ℃|
|morphology||Filamentous fungi, the colony is obvious on the comprehensive PDA medium, the hyphae are white, dense and low, the hyphae are vigorous and spread, and black spores are produced.|
|application||Anti-mildew and antibacterial. "Environmental Tests for Electronic and Electrical Products Part 2: Experimental Methods Test J and Guidelines: Long Mould" (GB/T 2423.16-2008) specifies the use of strains, GJB 150.10 "Environmental Test Methods for Military Equipment Mould Test"|
|Sharing mode||Public welfare sharing|
Storage conditions: 2~8 ℃
Product format： freeze dried, 200ul
Validity period: 6 years
Biosafety level: 1, handle in ultra-clear table or safety cabinet
Receiving notice: if any abnormality is found on the day of receipt, please contact the customer service within 24 hours. If it is overdue, it is deemed that the bacteria are well. The freeze dried culture shall be used up once and shall not be retained. The bacterial viability will resume after 1-2 generation of recovery and can be used normally. Handling instructions of agar slant and suspension liquid is enclosed. Please operate in strict accordance with this instruction, otherwise the replacement of bacteria are not be available in case of aberrant growth and loss of viability.
Growth conditions: 28℃, aerobic, comprehensive PDA, 5-7 days, comprehensive PDA: potato cooking liquid 1.0L, glucose 20.0g, KH2PO4 3.0g, MgSO4·7H2O 1.5g, vitamin B1 trace, agar 20.0g, pH 6.0±0.2. Sterilize at 121°C for 15min. Potato cooking liquid: Weigh 200g of peeled potato pieces, boil in boiling water for 30min, collect the filtrate and dilute to 1.0L.
(1)Prepare 1-2 of above mentioned plates;
(2)Open it in the biosafety cabinet, sterilize of the ampoule, heat the tip in a flame, quickly drop sterile water to creak it, then break it with forceps;
(3) Draw 0.5ml of sterile water into the freeze dried ampoule, make it fully dissolved, and distribute the solution to the plates well in 200ul/plate;
(4) Put the plates under the above culture conditions for cultivation for 5-7days.
Recovery record: According to the recovery instructions, the results of the recovery are reported as follows:
|viability||good viability, in 5-7 days, plate colony is obvious|
Small filamentous fungi, with obvious colonies on comprehensive PDA medium, and yellow initial hyphae,
dense exuberant, post-producing black spores full of plates
|Conclusion:||good viability, no abnormal colony morphology, qualified|