Penicillium chrysotoxum|336235 |BNCC

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Penicillium chrysotoxum-BNCC
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  • Penicillium citreonigrum-BNCC

Penicillium citreonigrum

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  • Price: Contact
  • number:336235
  • Form:
    Spread and grow, producing green colored spores with irregular and opaque edges. The hyphae are white to light yellow in the early stage, and then produce green spores
Standard strain Quantitative strain DNA extraction
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Penicillium citreonigrum
Subculture procedure ① Prepare 2 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 pour it into the freeze-drying tube. After fully dissolving, mix well; ④ Transfer 0.2mL of bacterial suspension into a Agar plate, apply evenly, and repeat twice to obtain two plates; ⑤ Place all the plates under the above cultivation conditions, and once the strains grow, they can be used.
Growth conditions 28 ℃; 5-7 days; aerobic
Storage conditions 2-8 ℃
Safety level 1
morphology Spread and grow, producing green colored spores with irregular and opaque edges. The hyphae are white to light yellow in the early stage, and then produce green spores
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1.Description 

1. Name:Penicillium citreo-virideBiourge

2. No.: 336235

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. Comprehensive PDA: potato boiled juice 1000mL, potassium dihydrogen phosphate 3g, magnesium sulfate 1.5g, glucose 20g, vitamin B1 10mg, agar 20g,pH natural. Potato boiling solution: 200g of potato, peeled, cut into pieces, boiled in distilled water for 30min, constant volume of filtrate to 1000mL for later use. 121 ℃,15min.

2. Atmosphere:aerobic

3.Temperature: : 25-26 ℃

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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