BeNa Culture Collection
info@bncc.com
| Subculture procedure | ① Dissolve the Frozen vial in a water bath (fungi at 30 ℃) and shake rapidly to dissolve; ② Wipe the outer wall of the Frozen vial 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 ℃; 3-5 days; aerobic |
| Storage conditions | -80 ℃ |
| Safety level | 1 |
| morphology | Filamentous, spreading growth, white on the front, yellow on the back, light in color |
| Sharing mode | Public welfare sharing |
Hypsizygus marmoreus
Storage conditions: 2~8 ℃
No. 361130
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 ℃, aerobic, PDA,3-5 days. PDA: potato boiling solution 1.0L, glucose 20.0g, agar 15.0g (not included in liquid medium), natural pH. Sterilization at 121 ℃ for 15min. Potato boiling solution: weigh 200g of peeled potato pieces, boil in boiling water for 30min, and collect filtrate to a constant volume of 1.0L.
Recovery steps:
(1)Prepare 1-2 of above mentioned plates;
(2)Open it in the biosafety cabinet, sterilize of the ampoule, heat the tip in a flame, quickly drop sterile water to creak it, then break it with forceps;
(3)Draw 0.5ml of sterile water into the freeze dried ampoule, make it fully dissolved, and distribute the solution to the plates well in 200ul/plate;
(4)The plate is cultured under the above-mentioned 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 4 days plate colony is obvious |
| colony morphology: |
Small filamentous fungi, with obvious colonies on PDA medium, and white hyphae, dense and vigorous, the bacterial layer is low and flat, and the back of the medium is light yellow |
| Conclusion: | good viability, no abnormal colony morphology, qualified |