BeNa Culture Collection
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| Subculture procedure | ① Prepare 2 of the above plates; ② After disinfecting the surface of the ampoule tube, open it in a safety cabinet, burn the top with an alcohol lamp, quickly drip sterile water to break it, and then use tweezers to crush it; ③ Take 0.5mL of sterile water and transfer it into a freeze-drying tube. After fully dissolving the bacterial powder, transfer it into 2 plates at a rate of 200 μ L per Agar plate and apply evenly; ④ Place the petri dish under the above cultivation conditions for cultivation, and once the bacterial strain grows, it can be used. |
| Growth conditions | 45 ℃; 24-48 hours; aerobic |
| Storage conditions | 2-8 ℃ |
| Safety level | 1 |
| morphology | The colony has a diameter of 1-2mm, irregular shape, irregular edges, opacity, gray white front, flat shape, rough surface, wrinkled surface, dry texture, difficult to pick, G+(blue purple), Bacillus, purity: pure |
| Sharing mode | Public welfare sharing |
Saccharomonospora viridis
Storage conditions : 2~8 ℃
No. : 153031
Product format :freeze dried, 200ul
Validity : 6 years
Biosafety level : 1, safety cabinet operation
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 plate 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: 45 ℃, aerobic, Streptomyces medium No. 2, 24-48h. Streptomyces medium No. 2: yeast powder 4.0g, malt powder 10.0g, glucose 4.0g, agar 20.0g,pH 7.2±0.2. Sterilization at 121 ℃ for 15min.
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 48hours strain layer become obvious;colony is typical on the streaked plate |
| colony morphology: (above) |
Size: 1-2mm Shape: Round Edge: Untidy Transparency: Opaque Color: Off-white Bulge: Middle bulge Surface: Rough Texture: Dry and hard to lift |
| Conclusion: | good viability, no abnormal colony morphology, qualified |