BeNa Culture Collection
info@bncc.com
| Subculture procedure | ① Prepare 1 tube containing 5-10mL liquid medium and 2 plates; ② Open in a safety cabinet, cauterize the top with a酒精灯, then quickly add sterile water to rupture it; break it into pieces with forceps; ③ Pipette 0.5mL liquid medium into the freeze-dried vial, dissolve completely, then return to the liquid test tube and mix thoroughly; ④ Pipette 0.2mL bacterial suspension onto a Agar plate, spread evenly; repeat twice to obtain two plates; ⑤ Incubate all liquid tubes and plates under the specified conditions. The strain is ready for use once growth appears. |
| Growth conditions | 37°C, 24-48h, anaerobic |
| Storage conditions | 2-8°C |
| Safety level | 1 |
| morphology | Colony diameter: 0.5–2 mm; circular with irregular margins; opaque; white upper surface; centrally convex; smooth surface; glossy appearance; moist texture; viscous consistency; G+ (blue-violet); bacillus; purity: pure |
| Sharing mode | Public welfare sharing |
Bifidobacterium longum subsp.
Storage conditions: 2~8 ℃
No. 134296
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.
Growthe conditions: 37℃, anaerobic, 24-48h, ①Columbia blood plate (ready-to-use) ②MRS medium: peptone 10.0g, beef extract 10.0g, yeast powder 4.0g, glucose 20.0g, magnesium sulfate 0.2g, sodium acetate 5.0g , 2.0 g of triammonium citrate, 2.0 g of dipotassium hydrogen phosphate, 0.04 g of manganese sulfate, 1.0 g of Tween 80, 20.0 g of agar (not included in liquid medium), and 1.0 L of distilled water. pH 5.7±0.2. Sterilize at 121℃ for 15min.
Recovery steps:
(1) Prepare sterile test tube of 5-10ml liquid medium and 2 plates; Silica gel plug is used for liquid test tube of liquid medium to ensure ventilation and facilitate deoxygenation. Please put the liquid medium and plate in an anaerobic environment for 24h before usage.
(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 liquid culture medium into a freeze dried ampoule, fully rehydrate and transfer the solution to the liquid test tube, mix evenly;
(4) Put the plates under the above culture conditions for cultivation for 24-48 hours.
Recovery record: According to the recovery instructions, the results of the recovery are reported as follows:

| item | test results |
| viability: | good viability,in 48h strain layer become obvious, colony is typical on the streaked plate. |
| colony morphology: (above) |
size: 1-2mm ; Shape: round ; Edge: neat ; Transparency: opaque color: white ; Protuberance: middle bulge ; Surface: bright and smooth ; Texture: moist |
| Conclusion: | good viability, no abnormal colony morphology, qualified |