Pseudomonas genus|193134 |BNCC

BeNa Culture Collection

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

Pseudomonas sp.

  • Price: Contact
  • number:193134
  • Form:
    The colony diameter is 1-2mm, circular, with neat edges, opaque, milky white on the front, raised in the middle, smooth on the surface, moist texture, easy to pick up, G - (red), rod-shaped
Standard strain Quantitative strain DNA extraction
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Essential Information Certificate Related Products
Pseudomonas sp.
Subculture procedure ① Prepare 1-2 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 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 37 ℃; 18-24h; aerobic
Storage conditions 2-8 ℃
Safety level 1
morphology The colony diameter is 1-2mm, circular, with neat edges, opaque, milky white on the front, raised in the middle, smooth on the surface, moist texture, easy to pick up, G - (red), rod-shaped
Sharing mode Public welfare sharing

1.Description 

1. Name:Pseudoxanthomonas sp.

2. BNCC No.:193134

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.

2. Atmosphere:aerobic

3. Temperature:   37 ℃,24h

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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