Prevotella aeruginosa|359116 |BNCC

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Prevotella histicola Downes et al. 2008

Culture medium	BNCC352241
Description	Columbia blood agar plate
Composition	Special Peptone:23.0g, Soluble Starch:1.0g, NaCl:5.0g, Agar:10.0g, Defibrinated Sheep Blood:5%(added at 50℃), pH:7.3±0.2(25℃)
Growth conditions	37 ℃; 48-72h; anaerobic;
Subculture procedure	①Draw a line on the Agar plate and prepare 2 plates (equilibrate in anaerobic environment for 24 hours) with typical bacterial colonies; ② After disinfecting the surface of the ampoule tube, open it in a safety cabinet, burn the top with an alcohol lamp, quickly drip sterile water to break it, and then use tweezers to crush it; ③ Take 0.5mL of sterile water (placed in an anaerobic environment for 24 hours) and transfer it into a freeze-drying tube. After fully dissolving the bacterial powder, transfer it into 2 plates at a rate of 200 μ L per Agar plate and apply evenly; ④ Place the petri dish under the above cultivation conditions for cultivation, and once the bacterial strain grows, it can be used.
Storage conditions	2-8 ℃
Safety level	1
morphology	Colony diameter: 1-2 mm, circular, with well-defined margins. Superficial appearance: grayish-white, convex in the center, smooth surface, glossy, moist texture, easily lifted. Gram-negative (red), bacillus. Purity: Pure.
Sharing mode	Public welfare sharing