Streptomyces mobaraensis|BNCC153558 |BNCC

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Streptomyces mobaraensis

Culture medium	Streptomyces medium No. 2 (ISP-2): yeast powder 4.0g, malt powder 10.0g, glucose 4.0g, agar 20.0g,pH 7.2±0.2. Sterilization at 121 ℃ for 15min.
Subculture procedure	(1) Prepare 1-2 pieces of the plate; (2) sterilize the surface of the plate and open it in biosafety cabinet; (3) Absorb 1-3ml of sterile water into the plate, scrape the bacterial lawn back and forth on the surface of the plate with a sterile spreader to make a bacterial suspension; (4) suck the bacteria suspension with a pasteur pipette, dispense it into a fresh plate evenly. (5) put the plates under the growth conditions.
Growth conditions	28 ℃,3-5 days, aerobic
Storage conditions	2-8 ℃
morphology	Size: 4-8mm Shape: Round Edge: Neat Transparency: Opaque Color: white bulge: middle bulge surface: rough texture: dry
Separation substrate	faecal sample from healthy Japanese male
application	Type strain; Generate bleomycin, detoxin, piericidins a, B.
Sharing mode	Public welfare sharing

Streptomyces moglabra

Storage conditions : 2~8 ℃

No. : 153558

Product format :freeze dried, 200ul

Validity : 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 of agar plate 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, Streptomyces medium No. 2, 3-5 days. Streptomyces medium No. 2: yeast powder 4.0g, malt powder 10.0g, glucose 4.0g, agar 20.0g,pH 7.2±0.2. Sterilization at 121 ℃ for 15min.

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.

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

Item	test results
viability:	good viability, in 3days strain layer become obvious;colony is typical on the streaked plate
colony morphology: (above)	Size: 4-8mm Shape: Round Edge: Neat Transparency: Opaque Color: White Rise: Middle Raised Surface: Rough Texture: Dry
Conclusion:	good viability, no abnormal colony morphology, qualified

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