Method for improving tolerance and increasing degradation rate of chlorella on phenol
A chlorella, degradation rate technology, applied in the methods of using microorganisms, microorganism-based methods, biochemical equipment and methods, etc., can solve the problems of poor initial inoculation density phenol tolerance and low degradation rate, etc. Poor receptivity, low degradation rate, and shortened time
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Embodiment 1
[0043] This embodiment takes Chlorella sp. with an initial non-degradable concentration of 500 mg / L phenol as an example to illustrate the feasibility of the technical solution.
[0044] The basal medium of Chlorella is the above-mentioned TAP liquid medium, culture conditions: initial pH=6.0, temperature 29±0.8°C, light intensity 117.67±6.89 μmol / m 2 / s, continuous light, 150rpm shaker shaking culture, the phenol concentration in the culture solution is 500mg / L.
[0045] In the first generation, Chlorella was inoculated in 100mL TAP medium (250mL Erlenmeyer flask) with an initial inoculation density of 0.6g / L containing phenol concentration of 500mg / L, and its dry weight and liquid medium were measured after 3 days of cultivation. The remaining phenol concentration.
[0046] Then, the chlorella of the first generation after being cultivated for 3 days was diluted and continued to be inoculated with an initial inoculation density of 0.6g / L in 100mL TAP liquid medium (the medi...
Embodiment 2
[0062] The basal medium of Chlorella is the above-mentioned TAP liquid medium, culture conditions: initial pH=6.0, temperature is 25°C, light intensity is 100 μmol / m 2 / s, continuous light, 100rpm shaker shaking culture, the phenol concentration in the culture solution is 450mg / L.
[0063] In the first generation, Chlorella was inoculated in 100mL TAP medium (250mL Erlenmeyer shake flask) containing 450mg / L phenol concentration at an initial inoculation density of 0.8g / L, and its dry weight and liquid medium were measured after 2 days of cultivation. The remaining phenol concentration.
[0064]Then, the chlorella of the first generation after being cultivated for 2 days was diluted and continued to be inoculated with an initial inoculation density of 0.8g / L in 100mL TAP liquid medium containing phenol concentration of 450mg / L (the medium was newly prepared) and cultivated for 2 days to measure its Dry weight and remaining phenol concentration in culture medium. Repeat above-...
Embodiment 3
[0066] The basal medium of Chlorella is the above-mentioned TAP liquid medium, culture conditions: initial pH=7.0, temperature is 35°C, light intensity is 200 μmol / m 2 / s, continuous light, 200rpm shaker shaking culture, the phenol concentration in the culture solution is 700mg / L.
[0067] In the first generation, Chlorella was inoculated in 100mL TAP medium (250mL Erlenmeyer shake flask) with an initial inoculation density of 1.0g / L containing phenol concentration of 700mg / L, and its dry weight and liquid medium were measured after 5 days of cultivation. The remaining phenol concentration.
[0068] Then, the chlorella of the first generation after being cultivated for 5 days was diluted and continued to be inoculated with an initial inoculation density of 1.0g / L in 100mL TAP liquid medium containing phenol concentration of 700mg / L (the medium was newly prepared) and cultivated for 5 days to measure its Dry weight and remaining phenol concentration in culture medium. Repeat ...
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