Diplophrys parva Anderson and Cavalier-Smith (ATCC® 50360)

Strain Designations: GF  /  Depositor: SA Schaffer  /  Biosafety Level: 1

Permits and Restrictions

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Deposited As Diplophrys sp.
Strain Designations GF
Biosafety Level 1
Isolation Intestinal tract, goldfish, Carassius auratus, Baltimore, MD, 1992
Product Format frozen
Storage Conditions Frozen: -70°C or colder
Freeze-Dried: 2°C to 8°C
Live Culture: See Protocols Section
Type Strain yes
Medium Medium 802: Sonneborn's Paramecium medium
Growth Conditions
Temperature: 25°C
Culture System: Xenic, grown with Enterobacter aerogenes (ATCC® 13048™) and mixed bacteria
Cryopreservation Reagents
Cryoprotective Solution
DMSO, 1.5 mL
Fresh growth medium w/o bacteria, 8.5 mL


Harvest and Preservation
  1. Mix the components in the order listed. When the medium is added to the DMSO the solution will warm up due to chemical heat.
  2. Harvest cells from a culture that is at or near peak density by filtration and centrifugation at 800 x g for 5 min.
  3. Adjust the concentration of cells to at least 2 x 106/mL in fresh medium.
  4. Mix the cell preparation and the cryoprotective solution in equal portions.
  5. Dispense in 0.5 mL aliquots into 1.0 - 2.0 mL sterile plastic screw-capped cryules (special plastic vials for cryopreservation).
  6. Place vials in a controlled rate freezing unit. From room temperature cool at -1°C/min to -40°C. If freezing unit can compensate for the heat of fusion, maintain rate at -1 C/min through heat of fusion. At -40°C plunge ampules into liquid nitrogen. Alternatively, place the vials in a Nalgene 1°C freezing apparatus.  Place the apparatus at -80°C for 1.5 to 2 hours and then plunge ampules into liquid nitrogen.  (The cooling rate in this apparatus is approximately -1°C/min.)  
  7. Ampules are stored in either the vapor or liquid phase of a nitrogen refrigerator.
  8. To establish a culture from the frozen state place the vial in a 35°C water bath.  Immerse the vial to a level just above the surface of the frozen material. Do not agitate the vial.   Immediately after thawing, do not leave in water bath, aseptically remove the contents of the ampule and inoculate into a T-25 tissue culture flask containing 10 mL ATCC media 802 and 2348, combined in equal parts and bacterized with Klebsiella pneumoniae subsp. pneumoniae (ATCC® 700831™) or Enterobacter aerogenes (ATCC® 13048™).
  9. Incubate at 25°C with the cap screwed on tightly.
  10. Once the culture is established, vigorously agitate the flask and aseptically transfer 0.5 mL to 10.0 mL of bacterized medium.
  11. Follow the protocol for maintenance of culture.
Name of Depositor SA Schaffer
Year of Origin 1992
References

Anderson OR, et al. Ultrastructure of Diplophrys parva, a new small freshwater species, and a revised analysis of Labyrinthulea (Heterokonta). Acta Protozool. 51: 291-304, 2012.

Notice: Necessary PermitsPermits

These permits may be required for shipping this product:

  • Customers located in the state of Hawaii will need to contact the Hawaii Department of Agriculture to determine if an Import Permit is required. A copy of the permit or documentation that a permit is not required must be sent to ATCC in advance of shipment.
Basic Documentation