BeNa Culture Collection
info@bncc.com
| Subculture procedure | ① Prepare 1-2 of the above plates; ② Open the 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 and transfer it into a freeze-drying tube. After fully dissolving the bacterial powder, transfer it into a Agar plate at a rate of 200 μ L per piece 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. |
| Growth conditions | 30 ° C; 3-4 days; aerobic |
| Storage conditions | 2-8 ℃ |
| Safety level | 2 |
| morphology | The colony diameter is 0.5-1mm, circular, with irregular edges, opaque, golden yellow on the front, light color, raised in the middle, rough surface, dry texture, easy to pick up, G+(blue purple), Bacillus subtilis |
| Sharing mode | Public welfare sharing |
Mycobacterium marinum
Strain number: 360708
Batch number: 220531
Biosafety level: 2, handle in safety cabinet
Provide form: Freeze-dried beveled bacterial liquid plate
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. The freeze-dried powder is stored at 2~8℃, and the validity period is 6 years; the slant surface is stored at 2~8℃, and the validity period is 1~3 months; the plate and bacterial liquid are stored at 4℃, and the validity period is 7 days. 2 years. Please strictly follow these instructions for activation and preservation, otherwise, the reissue service will not be provided due to abnormal bacteria, inactivation, etc.
Medium: 7H10 agar medium (English name: 7H10): ammonium sulfate 0.5g, potassium dihydrogen phosphate 1.5g, disodium hydrogen phosphate 1.5g, sodium citrate 0.4g, magnesium sulfate 0.025g, calcium chloride 0.5mg, zinc sulfate 0.001 g, copper sulfate 0.001g, sodium L-glutamate 0.5g, ferric ammonium citrate 0.04g, pyridoxine hydrochloride 0.001g, biotin 0.5mg, malachite green 0.25mg, agar 15.0g, and draw 5ml of glycerol, Add 900ml of distilled water, heat and stir to dissolve, boil for 1 minute, pH 6.4-6.8. Autoclave at 121°C for 10 minutes. When cooled to 50-55°C, add 100ml of filter-sterilized OADC additive, mix well, and pour into a plate or test tube.
Growth conditions: 30°C;3-4 days; aerobic
Recovery steps:
(1)Prepare a test tube containing 5-10mL of liquid culture medium and 2 plates;
(2)Open the ampoule in 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.
Viability: good viability, 3-5 days, with obvious bacterial layer on the plate; colony is typical on the streaked plate
Morphological characteristics: Colony diameter is 1-2mm, irregular shape, irregular edge, opaque, front gray-white, reverse gray-white, flat shape, rough surface, dry texture, easy to provoke, acid-fast staining positive (red), bacilli, purity: pure
Quality inspection map:


Conclusion:good viability, no abnormal colony morphology, qualified