Rhodotorula mucilaginosa with novel metabolic characteristic and application of the same in biodegradation
A technology of red yeast and metabolic characteristics, applied in the field of bioengineering, can solve the problems of non-degradability and high salinity, and achieve the effect of enhancing processing capacity and broad application potential
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Embodiment 1
[0035] Rhodotorula gum provided by the invention, its screening steps are as follows:
[0036]Samples of aerobic activated sludge were collected from the aeration tank of Dalian Dyestuff Factory, and used as a source of bacteria for domestication and cultivation. Add 0.2% sodium pyrophosphate to 50ml of activated sludge as a deflocculant, vibrate on a shaker for 5-10min to break up the activated sludge flocs, take 5ml of activated sludge, add 95ml of inorganic salt medium to shake In the bottle, add nitrobenzene as the only carbon, nitrogen, and energy source, wherein the concentration of nitrobenzene is 200 mg / L, and carry out shaker cultivation at a temperature of 30° C. and a rotation speed of 180 r / min. Inorganic salt medium composition: Na 2 HPO 4 12H 2 O, 7g / L; KH 2 PO 4 , 1g / L; CaCl 2 2H 2 O, 10mg / L; FeCl 3 , 2mg / L; MgSO 4 ·7H 2 O, 20mg / L. When the bacterial liquid becomes turbid and nitrobenzene cannot be detected, the next transfer is carried out; after con...
Embodiment 2
[0059] Among the present invention, the application of Rhodotorula gum p-nitrobenzene aerobic degradation research, its steps are as follows:
[0060] [1] Add 100ml of inorganic salt medium to a 250ml Erlenmeyer flask, then add 450mg / L of nitrobenzene as the only carbon, nitrogen, and energy source, and sterilize at 121°C;
[0061] [2] Add the liquid culture of Rhodotorula gluei cells prepared in Example 1 into the medium of [1] above, 30°C, 180r / min, aerobic culture, figure 1 The growth and nitrobenzene degradation of Rhodotorula gum.
Embodiment 3
[0063] In the present invention, the application of Rhodotorula gluei to research on the aerobic degradation of picolinic acid, the steps are as follows:
[0064] [1] Add 100ml of inorganic salt medium to a 250ml Erlenmeyer flask, add 3500mg / L picolinic acid as the only carbon, nitrogen, and energy source, and sterilize at 121°C;
[0065] [2] Add the liquid culture of Rhodotorula gluei cells prepared in Example 1 into the medium of [1] above, 30°C, 180r / min, aerobic culture, figure 2 The growth and picolinic acid degradation of Rhodotorula glucosa.
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