Rhodococcus rhodochrous bacterial strain XHRR1 for purifying ammonia in aquatic water and application thereof
A technology of Rhodococcus rhodococcus and breeding water, which is applied in the direction of bacteria, water pollutants, chemical instruments and methods, etc., can solve the problems of ignoring the specific actual needs of breeding organisms and production safety, high efficiency and sustainable development, and achieve good results Environmental adaptability, reduced water body replacement, good application effect
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Embodiment 1
[0024] Example 1 Screening and cultivation of Rhodococcus rhodococcus XHRR1 for purifying ammonia in aquaculture water
[0025] 1. Material preparation
[0026] 1.1. Bacterial source
[0027] Water samples from 50 to 75 days of intensive prawn culture ponds were collected, and photosynthetic bacteria medium plates were used for isolation and culture.
[0028] 1.2. Medium
[0029] (1) Photosynthetic bacteria liquid medium: CH 3 COONa: 1g, yeast extract: 1g, MgSO 4 ·7H 2 O: 0.4g, NaCl: 0.1g, CaCl 2 2H 2 O: 0.05g, NaHCO 3 : 0.3g, KH 2 PO 4 : 1g, trace element solution 1mL, the above drugs were dissolved in distilled water, and fixed to 1000mL, pH7.0.
[0030] Trace element solution: EDTA: 2.5g, ZnSO 4 ·7H 2 O: 10.95g, MnSO 4 ·H 2 O: 1.54g, CuS0 4 ·5H 2 O: 0.39g, CoCl 2 ·6H 2 O: 0.2g, FeSO 4 ·7H 2 O: 7g, the above drugs were dissolved in distilled water, and fixed to 1000ml, pH7.0.
[0031] (2) Photosynthetic bacteria solid plate culture medium: add agar powde...
Embodiment 2
[0035] Example 2 Identification of Rhodococcus rhodococcus XHRR1 for purifying ammonia in aquaculture water
[0036] The present invention identifies the 16S rDNA molecule of Rhodococcus rhodococcus rose XHRR1 for purifying ammonia in cultured water, and determines the species of the strain from the molecular level, combined with the analysis of the morphological characteristics of the bacteria and the physiological and biochemical characteristics. 16S rDNA sequence analysis mainly follows the following steps:
[0037] 1. Extraction of bacterial genomic DNA:
[0038] (1) Use a sterile toothpick to pick a single colony and inoculate it in the expansion medium for cultivation;
[0039] (2) Take 1.5 mL of bacterial culture solution, centrifuge at 10,000 rpm (11,500 g) for 1 minute, and suck up the supernatant as much as possible;
[0040] (3) Add 200 μL buffer GA to the cell pellet, shake until the cell is completely suspended, add 180 μL lysozyme with a final concentration of ...
Embodiment 3
[0065]Example 3 Small-scale application of Rhodococcus rhodococcus XHRR1 for purifying ammonia in aquaculture water
[0066] 1. Growth of the strain
[0067] The strain Rhodococcus rhodococcus XHRR1 that embodiment 1 obtains is pressed 10 6 CFU / mL was inoculated into sterilized culture pond water, and the bacterial concentration was stable at 10 during 2 to 5 days. 8 CFU / mL quantity level, the growth curve of strain XHRR1 is as follows figure 1 shown in .
[0068] 2. The removal effect of the strain on ammonia in different salinity aquaculture water
[0069] The sterilized aquaculture pond water (water body salinity is 25) is used as the basis for testing the water body, with NH 4 Cl adjusts the concentration of ammonia in the water body to about 24mg / L, and adjusts the salinity of the water body to 5, 15, 25, 35, 45 with distilled water and sea salt. The strain Rhodococcus rhodococcus XHRR1 that embodiment 1 obtains is pressed 10 6 CFU / mL was inoculated into the experim...
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