Saccharomyces cerevisiae|189121 |BNCC

BeNa Culture Collection

Saccharomyces cerevisiae-BNCC
  • BNCC
  • Yarrowia lipolytica-BNCC

Yarrowia lipolytica

  • Price: Contact
  • number:189121
  • Form:
    The colony diameter is 1-2mm, circular, with irregular edges, opaque, milky white on the front, raised in the middle, G+(blue purple), cocci, purity: pure
Standard strain Quantitative strain DNA extraction
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Essential Information Certificate Related Products
Yarrowia lipolytica
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 ℃; 24-48 hours; aerobic
Storage conditions 2-8 ℃
Safety level 1
morphology The colony diameter is 1-2mm, circular, with irregular edges, opaque, milky white on the front, raised in the middle, G+(blue purple), cocci, purity: pure
Sharing mode Public welfare sharing

1. Description 

1. Name: Candida lipolytica

2. BNCC No.:  189121

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, YM medium: yeast extract, 3.0g malt extract, 3.0g glucose, 10.0g protein block, 5.0g agar, 20.0g distilled water 1000 ml ,pH 6.2 +/- 0.2.

2. Atmosphere: aerobic

3. Temperature:  28 ℃

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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