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BeNa Culture Collection

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  • Grifola frondosa(Fr.)S.F.Gray-BNCC
  • Grifola frondosa(Fr.)S.F.Gray-BNCC
  • Grifola frondosa(Fr.)S.F.Gray-BNCC

Grifola frondosa(Fr.)S.F.Gray

  • Price: Contact
  • number:336082
  • Form:
    Small filamentous fungi have obvious colonies on comprehensive PDA medium, white mycelium, dense and vigorous, and spread and grow in concentric circles towards the edge of the Agar plate
Standard strain Quantitative strain DNA extraction
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Essential Information Certificate Related Products
Grifola frondosa(Fr.)S.F.Gray
Subculture procedure ① Dissolve the cryovial in a water bath (mold at 30 ℃) and shake rapidly to dissolve; ② Wipe the outer wall of the cryovial with an alcohol swab for disinfection, and then transfer it to a safe cabinet for operation; ③ Unscrew the tube cap, aspirate all the dissolved solution, and transfer it into 1-2 agar plates; ④ After uniform coating, transfer to the above cultivation conditions for cultivation.
Growth conditions 28 ℃; 7-10 days; aerobic
Storage conditions -80 ℃
Safety level 1
morphology Small filamentous fungi have obvious colonies on comprehensive PDA medium, white mycelium, dense and vigorous, and spread and grow in concentric circles towards the edge of the Agar plate
Sharing mode Public welfare sharing

Grifola frondosa (fr.) s. f. gray

Storage conditions: 2~8 ℃

No.: 336082

Product format: agar slant in 14mm test tube 

Validity period:  growing culture  within 30 days

Biosafety level: 1 , handle in ultra-clean table or safety cabinet

Receiving notice: if any abnormality is found on the day of receipt, please contact the customer service within 24 hours. If it is overdue, it is deemed that the bacteria are well. The freeze dried culture shall be used up once and shall not be retained. The bacterial viability will resume after 1-2 generation of recovery and can be used normally. Handling instructions agar slant and suspension liquid is enclosed. Please operate in strict accordance with this instruction, otherwise the replacement of bacteria are not be available in case of aberrant growth and lose of viability.

Growth conditions:25-28 ℃, aerobic, integrated PDA,7-10 days. Comprehensive PDA: potato boiling solution 1.0L, glucose 20.0g,KH2PO4 3.0g,MgSO4·7H2O 1.5g, vitamin B1 trace, agar 20.0g,pH 6.0±0.2. Sterilization at 121 ℃ for 15min. Potato boiling liquid: weigh 200g of peeled potato pieces, boil in boiling water for 30min, and collect the filtrate to a constant volume of 1.0L.

Recovery steps:
(1)Prepare 1-2 pieces of PDA plates; 
(2)Sterilize the surface of test tube for the agar slant, open it in the biosafety cabinet; 
(3)Cut into the pieces with aseptic inoculation hoe and inoculation shovel (see attached page). the size of square pieces is 0.5 × 0.5cm2; 
(4)Lay flat the small pieces to the center of the agar plate;
(5)Put the plates under the above culture conditions, and the strains can be used when they grow.
Recovery record:  According to the recovery instructions, the results of the recovery are reported as follows:

  

item test result
viability good viability, in 7-10 days strain layer is obvious
colony morphology small filamentous fungi have obvious colonies, white hyphae, dense and vigorous on the integrated PDA medium, spreading to concentric circles on the edge of the plate and not producing spores.
conclusion good viability, no abnormal colony morphology, qualified
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