BeNa Culture Collection
info@bncc.com
| Subculture procedure | ① Prepare 1 test tube containing 5-10 mL of liquid culture medium and 2 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 | Spread and grow, producing black spores with a black front, purity: pure |
| Sharing mode | Public welfare sharing |
Aspergillus niger van Tieghem
Storage conditions: 2~8 ℃
No.: 336166
Product format: freeze dried, 200ul
Validity period: 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 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 lose of viability.
Growth conditions:28 ℃, aerobic, 2-4 days, comprehensive PDA: 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 liquid: weigh 200g of peeled potato pieces, boil in boiling water for 30min, and collect the filtrate to a constant volume of 1.0L.
Recovery steps:
(1)Prepare 1-2 of above mentioned agar plates
(2)Sterilizing the ampoule, open it in 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 the freeze dried ampoule,make the strain pellet fully dissolved and inoculate a plate with the solution, then distribute it well in 200ml/plate;
(4)Put the agar plates under the above culture conditions for cultivation 5-7days
Recovery record: According to the recovery instructions, the results of the recovery are reported as follows:

| item | test result |
| viability | good viability, in 2-4 days strain layer is obvious and colony is typical |
| colony morphology: (above) | filamentous fungi have obvious colonies on comprehensive PDA medium, white hyphae, dense/low-flat hyphae, vigorous spread and brown spores. |
| conclusion | good viability, no abnormal colony morphology, qualified |
Aspergillus niger van Tieghem(Aspergillus niger van Tieghem)
251995
Aspergillus niger van Tieghem(Aspergillus niger van Tieghem)
336588
Aspergillus niger van Tieghem(Aspergillus niger van Tieghem)
336166
Aspergillus niger van Tieghem(Aspergillus niger van Tieghem)
336179
Aspergillus niger van Tieghem(Aspergillus niger van Tieghem)
336180
Aspergillus niger van Tieghem(Aspergillus niger van Tieghem)
336165