Pantoea and bacterium manganese mixture and application of bacterium manganese mixture in degradation of malachite green
A malachite green and mixture technology, applied in the field of environmental microorganisms, can solve the problems of high treatment cost, secondary pollution, and low efficiency, and achieve the effects of broad application prospects, good ecological restoration, and low use cost
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Embodiment 1
[0048] Separation and Identification of Pan Pantoea Eucrina SS01
[0049] 1. Screening of PANTOEA Eucrina SS01 in Pantococcus strains
[0050] The flush PANTOEA Eucrina SS01 of the present invention is separated from salt ground leaves, and the separation method is:
[0051] 1) The collected salt alkali plant sample is selected from the upper part of the upper part of the top part, and then washed with water, dry and weigh the record.
[0052] 2) In the sterile operating table, it is placed in Tween 80 for 5 minutes, flushing 3 times with sterile water, and then soaking in Tween 80 for 3 minutes, flushing 3 times with sterile water, the above steps are repeated 3 to 5 times. Then 0.1% HGCl 2 Soak for 1 minute, 75% ethanol soaked for 3 minutes, and finally rinsed with sterile water. At the end, the water is coated with a plate and detects whether disinfection is thorough.
[0053] 3) Transfer the ulcerous experimental sample with aseptic twisted to the mortar of the sterilized bact...
Embodiment 2
[0063] Manganese mixture was prepared:
[0064] (1) Culture of strain SS01 scrubbing and seized the single colonies in the LB liquid medium, and the rotation of the rotation of 150 to 200 rpm was overnight in a shaker of 150 to 200 rpm to obtain a large amount of bacteria. Liquid; (2) Weigh MNCL 2 A total of 125.84 g is dissolved in 500 ml of deionized water, stirred at room temperature, and the final concentration of 2 m is obtained. 2 And filtering the sterilization; (3) Inoculation of 1% step (1) in the K culture medium, placed in 30 ° C, 120 rpm constant temperature clocked bed, per hour to measure OD 600 Value, wait for OD 600 When the value is 0.8, the 2m MnCl in step (2) is added to the shake flask. 2 The final concentration was 20 mM, and 3 days were continued, and the germ manganese mixture was further cultured; (4) centribus mixture obtained in step (3) was centrifuged at 4000 rpm for 15 min, discarded, washed twice with sterile deionized water. , Centrifugation was agai...
Embodiment 3
[0066] Example 1 The fung manganese mixture obtained by the fungus mixture was referred to as the balance, 10 mg per grant, 200 mg / L, 300 mg / L, 500 mg / L, 1000mg / L of the peacock green solution resuspended, placed at 30 ° C In the shaker of 120 rpm, it was shocked in 24 hours. After 24 hours, the peacock green residual content was measured, and three parallel experiments were set each experiment, each measurement three times, and the average value was taken. The whole process remains sterile. The degradation sample was centrifuged at 12000 rpm for 5 min, and the absorbed value was determined at 620 nm using an ultraviolet visible light spectrometer to calculate the degradation rate.
[0067] Calculation mode of degradation rate: The solution absorbance value is determined at 620 nm by the ultraviolet visible light spectrometer, calculating the degradation rate:
[0068] Degradation rate (%) = (a-b) / a × 100; the formula is the OD value before degradation, b is the OD value...
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