Saccharomyces cerevisiae|280126 |BNCC

BeNa Culture Collection

Saccharomyces cerevisiae-BNCC
Saccharomyces cerevisiae-BNCC
Saccharomyces cerevisiae-BNCC
  • BNCC
  • Komagataeibacter sucrofermentans-BNCC
  • Komagataeibacter sucrofermentans-BNCC
  • Komagataeibacter sucrofermentans-BNCC

Komagataeibacter sucrofermentans

Literatures(7)
  • Price: Contact
  • number:280126
  • Form:
    The colony diameter is 0.5-1mm, circular, with neat edges, opaque, yellow on the front, light color, raised in the middle, smooth surface, moist texture, easy to pick
Standard strain Quantitative strain DNA extraction
Package:
Essential Information References Certificate Related Products
Komagataeibacter sucrofermentans
Subculture procedure ① Dissolve the frozen tube in a 30 ℃ water bath and shake quickly to dissolve; ② Wipe the outer wall of the Frozen vial with an alcohol swab for disinfection, and then transfer it to a safe cabinet for operation; ③ Unscrew the cap of the tube, aspirate all the dissolved solution, and transfer it into 1-2 agar plates (approximately 200 μ L per Agar plate); ④ After uniform coating, transfer to the above cultivation conditions for cultivation.
Growth conditions 28 ℃; 4-5 days; aerobic
Storage conditions -80 ℃
Safety level 1
morphology The colony diameter is 0.5-1mm, circular, with neat edges, opaque, yellow on the front, light color, raised in the middle, smooth surface, moist texture, easy to pick
Sharing mode Public welfare sharing

Gluconacetobacter xylinus

Storage conditions: 2~8 ℃

No.: 280126

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 ℃, aerobic, acetic acid bacteria medium (YGC),4-10d. Acetic acid bacteria medium (YGC): yeast extract 5.0g, glucose 50.0g, agar 15.0g,CaCO3 12.5g, distilled water 1.0L. pH 6.6 - 7.0. 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 4d liquid medium become turbid, obvious strain layer occurs on the plate,colony is typical on marked plate.

colony morphology:

(above)

Size: 1-2mm Shape: Round Edge: Neat Transparency: Opaque

color: yellow uplift: middle convex surface: bright and smooth texture: moist and viscous

Conclusion good viability, no abnormal colony morphology, qualified
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