Pseudomonas genus|192937 |BNCC

BeNa Culture Collection

Pseudomonas genus-BNCC
  • BNCC
  • Pseudomonas sp.-BNCC

Pseudomonas sp.

  • Price: Contact
  • number:192937
  • Form:
    The colony diameter is 0.5-1mm, circular, with neat edges, opaque, yellow on the front, light in color, raised in the middle, smooth on the surface, easy to pick up, G - (red), Bacillus, purity: pure
Standard strain Quantitative strain DNA extraction
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Essential Information Certificate Related Products
Pseudomonas sp.
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 30 ℃; 18-24h; aerobic
Storage conditions 2-8 ℃
Safety level 1
morphology The colony diameter is 0.5-1mm, circular, with neat edges, opaque, yellow on the front, light in color, raised in the middle, smooth on the surface, easy to pick up, G - (red), Bacillus, purity: pure
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1.Description

1. Name:Pseudomonas fluorescens biotype F

2. BNCC No.:192937

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, LB medium: yeast extract 5.0g peptone 10.0g NaCl 10.0g agar 15.0g distilled water 1.0 L pH 7.0.

2. Atmosphere:aerobic

3. Temperature:  26-30 ℃

4.Notes: 

1.Normal culturing time, 24-48hours for bacterial, 72 hours for yeast, 5-7days for mould, 7-10days for fungal.

2.Agar slant shall be inoculated asap, and do not keep the storage for more than 3 months.

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.Waste generated from the handling process should be discarded after high-pressure sterilization
 

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