Onion Aspergillus|357831 |BNCC

BeNa Culture Collection

Onion Aspergillus-BNCC
  • BNCC
  • Aspergillus alliaceus-BNCC

Aspergillus alliaceus

  • Price: Contact
  • number:357831
  • Form:
    Small filamentous fungi, with obvious colonies on comprehensive PDA medium, white and wrinkled colonies on agar plates, spreading and growing towards the edges
Standard strain Quantitative strain DNA extraction
Package:
Essential Information Certificate Related Products
Aspergillus alliaceus
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 ° C; 3-5 days; aerobic;
Storage conditions 2-8 ℃
Safety level 1
morphology Small filamentous fungi, with obvious colonies on comprehensive PDA medium, white and wrinkled colonies on agar plates, spreading and growing towards the edges
Sharing mode Public welfare sharing

Aspergillus alliaceus

Storage conditions : 2~8 ℃

No. : 357831

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°C, aerobic, integrated PDA, 3-5 days. Comprehensive PDA: Potato cooking liquid 1.0L, glucose 20.0g, KH2PO4 3.0g, MgSO4 7H2O 1.5g, trace amount of vitamin B1, agar 20.0g, pH 6.0±0.2. Sterilize at 121℃ 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.

Recovery steps:

(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 3-5 days.

Recovery record:  According to the recovery instructions, the results of the recovery are reported as follows:

Item test results
viability good viability,in 4 days plate colony is obvious
colony morphology small filamentous fungi have obvious colonies on the integrated PDA medium, with white plate colonies, folds, spreading and growing to the edge, and yellow on the back of the medium
conclusion good viability, no abnormal colony morphology, qualified

 

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