Red mushroom|111197 |BNCC

BeNa Culture Collection

Red mushroom-BNCC
Red mushroom-BNCC
Red mushroom-BNCC
  • BNCC
  • Pleurotus djamor (Rumph. ex Fr.) Boedijn-BNCC
  • Pleurotus djamor (Rumph. ex Fr.) Boedijn-BNCC
  • Pleurotus djamor (Rumph. ex Fr.) Boedijn-BNCC

Pleurotus djamor (Rumph. ex Fr.) Boedijn

  • Price: Contact
  • number:111197
  • Form:
    Small filamentous fungi, with obvious colonies on PDA medium, white color, dense and vigorous hyphae, spreading and growing towards concentric circles on the edge of the plate, without producing spores
Standard strain Quantitative strain DNA extraction
Package:
Essential Information Certificate Related Products
Pleurotus djamor (Rumph. ex Fr.) Boedijn
Subculture procedure ① Dissolve the frozen tube in a water bath (mold at 30 ℃) and shake quickly 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 ℃; 5-7 days; Aerobic
Storage conditions -80 ℃
Safety level 1
morphology Small filamentous fungi, with obvious colonies on PDA medium, white color, dense and vigorous hyphae, spreading and growing towards concentric circles on the edge of the plate, without producing spores
Sharing mode Public welfare sharing

Pleurotus djamor

Storage conditions: 2~8 ℃

No. : 111197

Product format: agar slant in 14mm test tube

Validity period: growing culture, in 30 days

Biosafety  level : 1, handle in ultra-clear 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 of 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 loss of viability.

Growth conditions : 28°C, aerobic, integrated PDA, 5-7 days. Comprehensive PDA: Potato cooking liquid 1.0L, glucose 20.0g, KH2PO4 3.0g, MgSO4 7H2O 1.5g, vitamin B1 trace, agar 20.0g, pH 6.0±0.2. Sterilize at 121℃ for 15min. Potato cooking liquid: Weigh 200g of peeled potato pieces, boil in boiling water for 30min, collect the filtrate and dilute to 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 results
viability: good viability, in 5-7 days plate colony is obvious
colony morphology: small filamentous fungi, the colony is obvious on the integrated PDA medium, white, dense and vigorous hyphae, 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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