Botrytis cinerea (tomato early blight pathogen)|337910 |BNCC

BeNa Culture Collection

Botrytis cinerea (tomato early blight pathogen)-BNCC
Botrytis cinerea (tomato early blight pathogen)-BNCC
Botrytis cinerea (tomato early blight pathogen)-BNCC
  • BNCC
  • Alternaria solani-BNCC
  • Alternaria solani-BNCC
  • Alternaria solani-BNCC

Alternaria solani

Literatures(13)
  • Price: Contact
  • number:337910
  • Form:
    The initial hyphae are white, but later turn grayish black. The colony is fuzzy and thick, with a black center on the back and yellow edges
Standard strain Quantitative strain DNA extraction
Package:
Essential Information References Certificate Related Products
Alternaria solani
Subculture procedure ① Dissolve the frozen tube in a water bath (fungi at 30 ℃) and shake quickly to dissolve; ② Wipe the outer wall of the Frozen vial with an alcohol swab for disinfection, and then transfer it to a safe cabinet for operation; ③ Unscrew the tube cap, aspirate all the dissolved solution, and transfer it into 1-2 agar plates (each Agar plate contains approximately 200 μ L, and for anaerobic bacteria cultivation, the culture medium needs to be placed in an anaerobic environment for 24 hours to remove oxygen); ④ After uniform coating, transfer to the above cultivation conditions for cultivation.
Growth conditions 28 ℃; 5-7 days; aerobic
Storage conditions Liquid nitrogen
Safety level 1
morphology The initial hyphae are white, but later turn grayish black. The colony is fuzzy and thick, with a black center on the back and yellow edges
Sharing mode Public welfare sharing

Alternaria solani

Storage conditions: 2~8 ℃

No.: 337910

Product format: agar slant in 14mm test tube 

Validity period: 30 days

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 of 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 loss of viability.

Growth conditions :25-28 ℃, aerobic, integrated PDA. Comprehensive PDA:20% potato juice 1L, glucose 20g ,KH2PO4 3g, MgSO4.7H2O 1.5g, thiamine trace, agar 15g,pH natural.

Recovery steps:
(1)    Prepare 1-2 pieces of PDA plates; 
(2)    Sterilize the surface of test tube for the agar slant, open it in the biosafety cabinet; 
(3)     Cut into the pieces with aseptic inoculation hoe and inoculation shovel (see attached page). the size of square pieces is 0.5 × 0.5cm2
(4)     Lay flat the small pieces to the center of the agar plate;
(5)    Put the plates under the above culture conditions, 5-7 days.Or contact our technicians for the inoculation of agar slant - filamentous fungi.

Recovery record:  According to the recovery instructions, the results of the recovery are reported as follows:
 

    

item test result
viability good viability, in 5 days strain layer is obvious
colony morphology small filamentous fungi, colonies are obviously visible on integrated PDA culture medium, hyphae are gray-white to black, hyphae are dense and thick, grow rapidly, and the back is black.
conclusion good viability, no abnormal colony morphology, completely consistent with the above figure, qualified

 

Download certificate
Please set your password: