Active extract of facultative anaerobic sea Pseudomonas stuszeri as well as production method and use thereof
A Pseudomonas stutzeri, facultative anaerobic technology, applied in the field of active extracts of facultative anaerobic marine denitrifying bacterial cultures
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Embodiment 1
[0048] Embodiment 1. liquid culture medium is:
[0049] Sodium acetate 20.0g;
[0050] KNO 3 2.0g;
[0051] K 2 HPO 4 0.5g;
[0052] MgSO 4 0.2g;
[0053] NaCl 25.0g;
[0054] MgSO 4 ·7H 2 O 3.0g;
[0055] CaCl 2 2H 2 O 0.05g;
[0056] Distilled water 1000ml;
[0057] Adjust the pH to 7.2±0.2 with sodium hydroxide at a concentration of 0.1 mol / L.
[0058] A. Seed culture: Fill the liquid medium into the serum bottle, leave a gap of 2cm in the bottle, tighten the cap of the serum bottle slightly to facilitate ventilation, and sterilize in a high-pressure sterilizer at 121°C and 0.105Mpa for 20min; after cooling Inoculate the marine strain DN7, fill it up with sterile medium, and tighten the bottle cap tightly; place the serum bottle in a constant temperature incubator for cultivation at 35-37°C. The culture time is 10-15 days;
[0059] B. Expanded cultivation: inoculate with 5-10% seed culture solution...
Embodiment 2
[0062] Embodiment 2. liquid culture medium is:
[0063] Sodium Potassium Tartrate 20.0g
[0064] KNO 3 2.0g
[0065] K 2 HPO 4 0.5g
[0066] MgSO 4 0.2g
[0067] Artificial sea water (or old sea water) 1000ml
[0068] Use sodium hydroxide with a concentration of 0.3mol / L to adjust the pH to 7.2-7.5.
[0069] Artificial Seawater Formula:
[0070] NaCl 25.0g
[0071] Na 2 SO 4 4.0g
[0072] KCl0.7g
[0073] NaHCO 3 0.20g
[0074] KBr 0.10g
[0075] h 3 BO 3 0.03g
[0076] NaF0.003g
[0077] 1.0mol / L MgCl 2 Solution 53mL
[0078] 1.0mol / l CaCl 2 Solution 10mL
[0079] 0.1mol / L SrO 2 Solution 0.90ml
[0080] Distilled water 1000ml
[0081] Use sodium hydroxide with a concentration of 0.2mol / L to adjust the pH to 7.2-7.5.
[0082] A. Seed culture: Fill the liquid medium into the serum bottle, leave a gap of 2cm in the bottle, tighte...
Embodiment 3
[0086] Example 3. Active component activity assay results
[0087] Using the agar dilution method (National Committee for Clinical Laboratory Standards. 2000. Approved standard: M2 ~ A7, 7th ed. NCCLS, Wayne, Pa.) to determine the MIC value of Pseudomonas aeruginosa and Bacillus subtilis, confirm the culture medium The ethyl acetate extract phase has antibacterial activity: the MIC values of the prepared active components against Pseudomonas aeruginosa were 0.64 μg / mL, and the MIC values against Bacillus subtilis were 1.28 μg / mL.
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