A Strain of Trichosporium and Its Application in Ammonia Nitrogen Degradation in Water
A technology of trichosporon and ammonia nitrogen, which is applied in the field of microorganisms to achieve the effect of low cost, simple equipment and low technical difficulty
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Embodiment 1
[0028]Isolation and Identification of Trichosporon Monteense W02:
[0029]Water samples were collected from the US Iowa State University Food Plastics, and water samples were turbid in the oxygen enrichment culture of 30 ° C in a glucose (YPD) liquid medium containing 50 μg / ml ampicillin. After proper dilution Painting the flat plate, according to the form of the colony, a typical yeast single colony, by mirror-check, the ammonia nitrogen degradation ability is measured, and the strain monochrome falls, and inoculates the constant temperature of 30 ° C in YPD liquid medium. 48h. The total DNA of strain W02 is a template, and the ITS sequence of the strain is amplified under the guided PCR of primer ITS1 (TCCGTGTGAACCTGGG) and ITS4 (TcctcgctTttgatgc), and the PCR reaction system is 50 μl, MIX25 μL, ITS1 1 μL, ITS41 μL, DDH2O2 1 μL, 2 μl of the template, a PCR reaction condition 95 ° C 30s, 50 ° C 30s, 72 ° C 60s, and the number of cycles was 31 times. After the end of the reaction, 1%...
Embodiment 2
[0032]Liquid fermentation culture of the Trichosporon Montevideense W02:
[0033]The W02 strain was seeded in a 2% inoculation amount (V / V) in YPD liquid medium (protein 20g, yeast extract 10g, glucose 20g, water 1000 mL, sterilization of 20 min, 500 ml of triangular bottle). 150 rpm temperature culture at 30 ° C, sampling once every 2h, 100 times dilution with sterile water, and detected a blank control at an unfiltered medium, detecting the absorbed value at the wavelength of OD600NM, with the culture time as the horizontal coordinate, the OD value is vertical The coordinates are mapped to the growth curve of yeast. The strain grows rapidly in YPD medium, and the culture is about 12 h and the maximum biomass (image 3 ).
Embodiment 3
[0035]Effects of different carbon sources on ammonia nitrogen degradation:
[0036]The spore yeast W02 was cultured in a 2% inoculation amount (V / V) to 50 ml of YPD liquid medium at 30 ° C for 24 h, centrifugal removal medium for 50 ml of sterile water resuscitation, and the number of live bacteria after resuspend is 5 100 million / ml.
[0037]The 1.0 ml of hemacrobacterial fluid is drawn to 100 ml of 45 mg / L ammonia nitrogen-sterilized artificial sewage (0.5 g of hydrogen phosphate, 0.5 g of magnesium sulfate, potassium chloride 0.01g, iron sulfate 0.01 g, water 1000ml, Add Ammonium chloride to final concentration 45 mg / L), add end concentration 2 g / l glucose, sucrose, ethanol, sodium acetate, sodium citrate as carbon sources, and no carbon source as a control group, 3 repetitions, 25 ° C The ammonia nitrogen concentration was measured after 150 rpm culture for 24 h. It can be seen from Table 1, glucose and sucrose are good carbon sources for ammonia nitrogen degradation of stra...
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