Fly ash sphingomonas|337151 |BNCC

BeNa Culture Collection

Fly ash sphingomonas-BNCC
Fly ash sphingomonas-BNCC
  • BNCC
  • Sphingobium fuliginis-BNCC
  • Sphingobium fuliginis-BNCC

Sphingobium fuliginis

  • Price: Contact
  • number:337151
  • Form:
    The colony diameter is 1-2mm, circular, with neat edges, opaque, golden yellow on the front and back, raised in the middle, smooth and bright on the surface, moist texture, easy to pick up, G - (red), Bacillus, purity: pure
Standard strain Quantitative strain DNA extraction
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Essential Information Certificate Related Products
Sphingobium fuliginis
Subculture procedure ① Prepare 1-2 of the above 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 Take 0.5mL of sterile water and transfer it into a freeze-drying tube. After fully dissolving the bacterial powder, transfer it into a Agar plate at a rate of 200 μ L per piece 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 30 ℃; 18-24h; aerobic
Storage conditions 2-8 ℃
Safety level 1
morphology The colony diameter is 1-2mm, circular, with neat edges, opaque, golden yellow on the front and back, raised in the middle, smooth and bright on the surface, moist texture, easy to pick up, G - (red), Bacillus, purity: pure
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1.Description

1. Name: Sphingomonas paucimobilis

2. BNCC No.: 337151

3. Biosafety level:4

2.Storage conditions

Storage of freezed dried ampoule and agar slant at 2°C to 8°C

3. Growth Conditions

1. Nutritious gravy agar: peptone 5.0g, beef extract 3.0g,NaCl 5.0g, agar 15.0g, distilled water 1.0L,pH7.0. [Note] Add 5mg MnSO4·H2O when culturing Bacillus,which is beneficial to spore production. 121 ℃,15min. 121 ℃,15min.

2.Atmosphere:aerobic

3, Temperature: 37 ℃,24h

4.Notes:

1.Normal culturing time, 1-2days for bacterial, 3 days for yeast, 5-7days for mould, 7-10days for fungal.

2.Agar slant shall be inoculated asap, and long-term storage is not recommended.

3.Please recover the strains in strict accordance with this instruction, otherwise the replacement of the strain are not be available in case of viability loss caused by different media or growth conditions.

4.Users should ensure the safe storage and operation of the strain.Waste generated from the handling process should be discarded after high-pressure sterilization.

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