Brazilian Aspergillus|352057 |BNCC

BeNa Culture Collection

Brazilian Aspergillus-BNCC
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  • Aspergillus brasiliensis Varga et al.-BNCC

Aspergillus brasiliensis Varga et al.

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  • number:352057
  • Form:
    Filamentous fungi have distinct colonies on a comprehensive PDA medium, with white, dense/flat hyphae that vigorously spread and grow, producing a large number of black spores
Standard strain Quantitative strain DNA extraction
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Essential Information Certificate Related Products
Aspergillus brasiliensis Varga et al.
Subculture procedure ① Prepare one test tube containing 5-10 mL of liquid culture medium and two plates; ② Open the safety cabinet, burn the top with an alcohol lamp, quickly drip sterile water to break it, and then use tweezers to crush it; ③ Transfer 0.5mL of liquid culture medium into a freeze-drying tube, dissolve it thoroughly, and then transfer it back into the liquid test tube, mixing well; ④ Transfer 0.2mL of bacterial suspension into a Agar plate, apply evenly, and repeat twice to obtain two plates; ⑤ Place all liquid test tubes and plates under the above cultivation conditions, and the bacterial strains can be used once they grow.
Growth conditions 28 ℃, 5-7 days; aerobic
Storage conditions 2-8 ℃
Safety level 1
morphology Filamentous fungi have distinct colonies on a comprehensive PDA medium, with white, dense/flat hyphae that vigorously spread and grow, producing a large number of black spores
Sharing mode Public welfare sharing

Aspergillus brasiliensis

Storage conditions : 2~8 ℃

No. 352057

Product format: freeze dried, 200ul

Validity : 6 years

Biosafety level : 1 , handle in ultra-clean 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, 5-7 days, comprehensive PDA agar medium: potato boil 1.0L, glucose 20.0g,KH2PO4 3.0g,MgSO4·7H2O 1.5g, vitamin B1 trace, agar 20.0g,pH 6.0±0.2. Sterilization at 121 ℃ for 15min. Potato boiling solution: weigh 200g of peeled potato pieces, boil in boiling water for 30min, and collect filtrate to a constant volume of 1.0L.

Recovery steps:
(1) Prepare a test tube containing 5-10mL of liquid culture medium and 2 plates; 
(2) Open the ampoule in the biosafety 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.
Recovery record:  According to the recovery instructions, the results of the recovery are reported as follows:

Item test results
viability: good viability, in 3 days, floc growth at the top of the culture solution, 5 days strain layer become obvious,  colony is typical
colony morphology: (above)

filamentous fungi have obvious colonies on comprehensive PDA culture medium,

hyphae are white, dense/low, hyphae are flourishing and grow, producing a large number of black spores

Conclusion: good viability, no abnormal colony morphology, qualified

 

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