Photosynthetic bacteria SC01 as well as fast cultivation method and application thereof
A technology of photosynthetic bacteria and cultivation methods, which is applied in the directions of bacteria, applications, and microorganism-based methods to achieve the effect of promoting long-term stability and sustainable development, being beneficial to the health of cultured organisms, and having obvious use effects.
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Embodiment 1
[0025] The screening of embodiment 1 photosynthetic bacteria
[0026] 1) Sampling and treatment: Take 8g of seawater from the bottom of the drainage ditch of the turbot nursery factory, pond wall attachments, pond bottom sludge, bottom seawater, attachments, pond walls and bottom sludge of the nursery and culture ponds, Add 100ml of sterilized seawater, place it in a 300ml sterile Erlenmeyer flask, shake it fully for 15 minutes, remove large particles such as weeds and rocks, and prepare a sample suspension.
[0027] 2) Enrichment culture: Take 5mL of the sample suspension and add 50mL of sterile enrichment medium (KH 2 PO 4 0.5g / L, yeast extract 1.5g / L, tryptone 0.05g, CaCl0.05g, NaAc1.0g / L, NH 4 Cl0.2g / L, MnSO 4 0.05g, MgSO 4 0.025g, FeSO 4 0.002g, pH value 7.2, dilute to 1000mL with distilled water), add 10ml paraffin oil, and seal with parafilm. 28 ℃, 2000lux light culture. Observe the color change of the culture medium every 48h. This enrichment culture process la...
Embodiment 2
[0029] The cultivation of embodiment 2 photosynthetic bacteria SC01
[0030] The photosynthetic bacteria obtained in the above examples were rapidly cultured, and 50ul-80°C frozen SC01 was inoculated into 10ml rapid medium (K 2 HPO 4 0.25g / L, KH 2 PO 4 0.25g / L, yeast extract 3.0g / L, NaAc2.0g / L, NH 4 Cl1.0g / L, pH 6.8, dilute to 1000mL with old sea water (remove the sediment after standing for 14 days). ), 28°C, 300rpm, cultured under natural light for 120h to OD 600 to 1.0, use this as the seed solution, inoculate the seed solution in the fast medium according to the inoculum amount of 5% (volume ratio), culture at 28°C, 150rpm, and under natural light for 120h. Take out the culture medium at intervals of 2 hours to measure OD 600 . Plot the growth curve of SC01 ( figure 1 ).
[0031] Use the plate count method to calculate the colony-forming unit (CFU, colony-forming unit) per unit volume: to be SC01 bacterial solution OD 600 to 1.0, take 1m with sterile sea water a...
Embodiment 3
[0032] The influence of embodiment 3SC01 on residual bait rate
[0033] Take OD 600 5ml of SC01 culture solution to 1.0 was added to the holding pond of 50L seawater, and 10 healthy turbot with a total body length of 6-8cm were put into each breeding pond. Under normal indoor light, the aeration rate of the breeding pond is 6.5L per minute, and the amount of conventional compound granular bait for farming (the granular bait usually does not disintegrate in seawater for 2 hours) is based on 300 grains (about 10g) of granular bait per pond per day. Add 3 times. 2 hours after each feeding, the residual bait in the culture ponds was fished out, the quantity of the residual bait in each culture pond was counted, and the residual bait rate was calculated. At the same time, taking the temporary culture pond without adding SC01 culture medium as a control, it was observed that in the culture ponds added with photosynthetic bacteria SC01, turbot had a strong desire to eat and compete...
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