A Capsulated Rhodobacter and Its Application
A technology of capsular rhodobacteria and water bodies, applied in bacteria, biological water/sewage treatment, microorganisms, etc., can solve the problem of less photosynthetic bacteria of benzene series and formaldehyde, and achieve a wide range of effects
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Embodiment 1
[0035] Example 1: Isolation, purification and identification of Rhodobacter capsularis DC-1
[0036] 1. After removing impurities from the sewage collected from the entrance of Dianchi Wetland Park in Kunming, pour it into 500mL enrichment culture solution (formula NaCl 2.5 g, MgSO 4 ·7H 2 O 0.05 g, NH4Cl 1.0 g, NaHCO 3 2.5 g, KH 2 PO 4 2.75 g, CH 3 COONa 6 g, yeast powder 2 g, distilled water 1000 mL, pH value 7.0) in a mineral water bottle, mix well, seal; finally place at 28 ℃, 60W incandescent light culture for 7-8 days; Red or blood red, suck out 50mL of red liquid, pour it into a mineral water bottle filled with fresh enriched culture medium, and enrich and cultivate continuously for 3 times; use RCVBN culture medium (the formula is CH 3 COONa 5.0g, CH 3 CH 2 COONa 3.0g, NaCl 2.5g, MgSO 4 ·7H 2 O 1.5g, (NH 4 ) 2 SO 4 0.5g, KH 2 PO 4 1.5g, K 2 HPO 4 0.6g, CaCl 2 0.05g, MnSO 4 5mg, FeSO 4 5mg, yeast extract 0.5g, peptone 20mg, glutamic acid 0.5mg...
Embodiment 2
[0055] Embodiment 2: the optimization of photosynthetic bacteria culture condition
[0056] 1. Determination of temperature Add 20% seed liquid into a 25mL anaerobic tube, and use liquid medium (the formula is CH 3 CH 2 COONa 5g / L, (NH 4 ) 2 SO 4 2.0g / L, MgSO 4 •7H 2 O 0.2g / L, NaH 2 PO 4 •H 2 O 0.5g / L, K 2 HPO 4 0.66 g / L, CaCl 2 • 2H 2 O 0.1 g / L. ) was filled with anaerobic tubes, and under the condition of pH 7, the culture temperature was set to 20, 25, 30, and 35°C respectively; the light culture was 7 days, and the experiment was repeated 3 times, and the bacterial culture solution was measured every 24 hours The OD value at 375nm was used to determine the optimal culture temperature. Figure 6 is the effect of temperature on the growth of strain DC-1, by Figure 6 It can be seen that the optimal culture temperature of strain DC-1 is 30°C.
[0057] 2. Determination of pH Add 20% seed liquid into a 25mL anaerobic tube, and use a liquid medium (the formula i...
Embodiment 3
[0061] Embodiment 3: the ability of bacterial strain DC-1 to purify benzene series
[0062] The liquid culture of the strain DC-1 with a concentration of 20% was inoculated in the liquid medium containing 2mM, 4mM, and 6mM benzene respectively, and cultured at 30°C under the light of 60W incandescent lamp for 0, 1, 2, 3, 4, 5, 6 , 7, and 8 days, the experiment was set for 3 repetitions, and the cell concentration and residual liquid benzene concentration of strain DC-1 were measured at each time point; the specific steps for the determination of benzene content were as follows:
[0063] 1. Preparation of formaldehyde-sulfuric acid solution: add 0.10 mL of 10% formaldehyde solution to 100 mL of high-grade concentrated sulfuric acid, mix, store in ice cold (prepared when used);
[0064] (In the presence of sulfuric acid, benzene series reacts with formaldehyde to form a yellow-brown diphenylmethane polymer. The maximum absorption wavelength of this colored compound is 465 nm. Us...
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