Fusobacterium nuclei subspecies|BNCC337404 |BNCC

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Fusobacterium nuclei subspecies

Culture medium	Liquid thioglycolate medium (FT): 15.0g of caseptone (trypsin hydrolysis), 5.0g of yeast extract, 5.0g of glucose, 0.5g of sodium thioglycolate, 0.5g of L-cystine, 2.5g of sodium chloride, 0.001g of azure, 0.75g of agar, 1.0L of distilled water and 7.1±0.2 of pH value. Sterilization at 121 ℃ for 15min.
Subculture procedure	(1) Prepare a φ18mm test tube of 10ml liquid medium ( put in an anaerobic environment for 24h before handling); (2) sterilizing the ampoule, open it in 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 the freeze dried ampoule, fully rehydrate and transfer the solution to the liquid test tube, mix evenly; (4) Place the liquid test tube under the above-mentioned specified "culture conditions" for cultivation, and the bacterial liquid is turbid or there is a large amount of bacterial growth at the bottom.
Growth conditions	37 ℃;48-72h; Anaerobic
Storage conditions	2-8 ℃
morphology	Fusobacterium nuclei subspecies, a gram-negative bacterium, has a slender shape, and the ends are as thin as a shuttle. The liquid culture medium of thioglycolate is turbid. It is recommended to use liquid culture.
Sharing mode	Public welfare sharing

1.Description

1. Name: Fusobacterium nucleatum subsp nucleatum

2.BNCC No.:337404

3.Biosafety level: 3

2.Storage conditions:

Storage of freezed dried ampoule and agar slant at 2°C to 8°C

3.Growth Conditions

1. Culture medium: Columbia blood plate (finished product)

2.Atmosphere: anaerobic

3.Temperature: 37 ℃

4.Notes:

1.Normal culturing time, 1-2days for bacterial, 3 days for yeast, 5-7days for mould, 7-10days for fungal.

2.Agar slant shall be inoculated asap, and long-term storage is not recommended.

3.Please recover the strains in strict accordance with this instruction, otherwise the replacement of the strain are not be available in case of viability loss caused by different media or growth conditions.

4.Users should ensure the safe storage and operation of the strain.Waste generated from the handling process should be discarded after high-pressure sterilization.

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