BeNa Culture Collection
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| Subculture procedure | ① Prepare one test tube containing 5-10 mL of liquid culture medium and two 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 Transfer 0.5mL of liquid culture medium into a freeze-drying tube, dissolve it thoroughly, and then transfer it back into the liquid test tube, mixing well; ④ Transfer 0.2mL of bacterial suspension into a Agar plate, apply evenly, and repeat twice to obtain two plates; ⑤ Place all liquid test tubes and plates under the above cultivation conditions, and the bacterial strains can be used once they grow. |
| Growth conditions | 26 ℃; 18-24h; aerobic; |
| Storage conditions | 2-8 ℃ |
| Safety level | 1 |
| morphology | Size: Small Color: Orange-red Shape: Circular Margin: Entire Moisture: Moist Smoothness: Smooth Opacity: Opaque Elevation: Raised |
| Sharing mode | Public welfare sharing |
Serratia marcescens
Storage conditions: 2~8 ℃
No. 185953
Product format: freeze dried, 200ul
Validity period: Freeze-dried tube for 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.
Activation/passage:26 ℃, aerobic, nutritious gravy medium. Nutritional agar medium: beef paste 3.0g, peptone 10.0g,NaCl 5.0g, agar 20.0g (without liquid medium), distilled water 1.0L,pH7.0. 121 ℃,15min.
Recovery steps:
(1)Prepare a test tube containing liquid culture medium or 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 medium into the freeze dried ampoule,make the strain pellet fully dissolved. transfer the liquid suspension to the liquid media, and culture in plate shaker at 26℃ for 18-24 hours (140r/min); or directly dispense 200ul of the liquid suspension into a NA agar plate evenly, then put the plates in incubator at 26℃ for 24-48 hours.
Recovery record: According to the recovery instructions, the results of the recovery are reported as follows:

| item | test result |
| viability | good viability, in 20h liquid medium become turbid, obvious strain layer occurs on the plate; colony is typical on marked plate |
| colony morphology |
Size: Small Color: Orange Red Shape: Round Edge: Neat Wet and dry: moist smooth: smooth transparency: opaque uplift: uplift |
| Conclusion | good viability, and colony morphology is not abnormal, completely consistent with the above figure, qualified |