Penicillium citrinum|BNCC146100 |BNCC

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Penicillium citrinum

Culture medium	CDA: 3g of sodium nitrate, 1g of dipotassium hydrogen phosphate, 0.5g of magnesium sulfate, 0.5g of potassium chloride, 0.01g of ferrous sulfate, 30g of sucrose, 15g of agar, 1.0L of distilled water and 6.2±0.2 of pH. Sterilization at 121 ℃ for 15min.
Subculture procedure	(1) Prepare a test tube containing 5~10mL of liquid medium and 2 plates; (2) Open it in the safety cabinet, heat the tip of ampoule in a flame, quickly drop sterile water to creak it, then break it with forceps; (3) draw 0.5mL of liquid culture medium into a freeze dried ampoule, fully rehydrate and transfer the solution to the liquid test tube, mix evenly; (4) inoculate a plate with 0.2mL of suspension liquid, repeat the step to obtain two plates; ⑤ Put all the liquid test tubes and plates under the above culture conditions for cultivation, and the strains can be used when they grow.
Growth conditions	28 ℃;5-7 days; Aerobic;
Storage conditions	2-8 ℃
morphology	Small filamentous fungus, with prominent colonies on Czapek's agar medium, with white initial hyphae, dense and vigorous, overgrown with plates, dorsal The face is yellow.
application	Phosphate-producing dilipase
Sharing mode	Public welfare sharing

Penicillium citrinum

Storage conditions: 2~8 ℃

No. 146100

Product format： freeze dried, 200ul

Validity period: 6 years

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, Czapek's agar, 5-7 days, Czapek's agar: sucrose 30.0 g, NaNO3 3.0 g, MgSO4 7H2O 0.5 g, KCl 0.5 g, FeSO4 4H2O 0.01 g, K2HPO4 1.0 g, agar 15.0 g, distilled water 1.0 L, pH 6.0-6.5

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)Put the plates under the above culture conditions for cultivation

Recovery record: According to the recovery instructions, the results of the recovery are reported as follows:

Item	test results
viability	good viability,in 5 days plate colony is obvious
colony morphology:	small filamentous fungus, with obvious colonies on Czapek ' sagar medium, with white initial hyphae, Dense and exuberant, full of plates, yellow on the back
Conclusion:	good viability, no abnormal colony morphology, qualified

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