BeNa Culture Collection
info@bncc.com
| Subculture procedure | ① Prepare 1-2 plates as specified above.② Open the vial in a biosafety cabinet, briefly flame the top with an alcohol lamp, and immediately add sterile water to break the seal. Then crush the vial using sterile forceps.③ Aspirate 0.5 mL of sterile water into the freeze-dried vial, fully dissolve the bacterial powder, then transfer approximately 200 µL of the suspension onto each of the two plates and spread evenly.④ Incubate the plates under the specified culture conditions. The strain can be used once growth appears. |
| Growth conditions | 30 ℃; 18-24h; aerobic |
| Storage conditions | 2-8 ℃ |
| Safety level | 1 |
| morphology | Size: 2-4 mm,Shape: Circular,Margin: Regular,Transparency: Opaque,Color: Golden yellow,Elevation: Raised center,Surface: Smooth and glossy,Texture: Moist and viscous |
| Sharing mode | Public welfare sharing |
Sphingomonas sanxanigenens
Storage conditions: 2~8 ℃
No.: 188194
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:30°C, aerobic, nutrient agar medium, 18-24h. Nutritional agar medium: beef paste 3.0g, peptone 10.0g,NaCl 5.0g, agar 20.0g (not included in liquid medium), distilled water 1.0L,pH7.0. Sterilization at 121 ℃ for 15min.
Recovery steps:
(1) Prepare a test tube containing 5-10mL of liquid culture medium and 2 plates;
(2) Open it 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 result |
| viability | good viability,in 24 hours liquid medium become turbid, obvious strain layer occurs on the plate,colony is typical on marked plate. |
| colony morphology: (above) | size: 2-4mm shape: round edge: neat transparency: opaque color: golden yellow uplift: middle convex surface: smooth and bright texture: moist and viscous |
| Conclusion | good viability, no abnormal colony morphology, qualified |