Zygosaccharomyces rouxii(Saito)Lodd|BNCC353374 |BNCC

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Zygosaccharomyces rouxii(Saito)Lodd

Culture medium	Glucose agar (SDA): 40g glucose, 10g peptone (casein trypsin digest, gastric enzyme digest of animal tissue), 15g agar (without liquid medium), 1.0L distilled water, pH 5.6±0.2. 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 biosafety cabinet, heat the tip of ampoule in the flame, quickly drop sterile water to creak it, and 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	30 ℃;6 days; Aerobic;
Storage conditions	2-8 ℃
morphology	Size: 2-4mm Shape: Round Edge: Neat Transparency: Opaque Color: Milk White Protuberance: Middle Protuberance Surface: Bright and Smooth Texture: Wet and Easy to Stir
application	High osmotic pressure resistance, soy sauce.
Sharing mode	Public welfare sharing

Zygosaccharomycesrouxii

Storage conditions : 2~8 ℃

No. : 353374

Product format: freeze dried, 200ul

Validity period: 6 years

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 :30°C, aerobic, nutrient agar medium, 6d. SDA: glucose 20g, peptone (casein trypsin digest, gastric enzyme digest of animal tissue) 10g, agar 15g (without liquid medium), distilled water 1.0L,pH 5.6±0.2. Sterilization at 121 ℃ for 15min.

Recovery steps:
(1)Prepare a test tube containing 5-10mL of liquid culture medium and 2 plates;
(2)Open the biosafety 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.

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

item	test result
viability	good viability, in 6 days liquid medium become turbid, obvious strain layer occurs on the plate; colony is typical on marked plate
colony morphology: (above)	size: 2-4mm shape: round edge: neat transparency: opaque color: milky white uplift: middle raised surface: bright and smooth texture: moist and easy to lift
conclusion	good viability, no abnormal colony morphology, qualified

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