Providencia vermicola strain, enzyme preparation and application of enzyme preparation in degradation of pesticide residues
A Providencia bacteria and enzyme preparation technology, applied in the direction of enzymes, bacteria, and microorganism-based methods, can solve the problems of mixed pesticide residues that have not been seen, and achieve the effect of removing pesticide residues
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example 1
[0034] Example 1, isolation and identification of larvae Providencia bacterial strains
[0035] 1. Acquisition of strains
[0036] 1. Collection of soil samples
[0037] Collected from the sludge at the discharge outlet of the pesticide factory.
[0038] 2. Isolation and screening of bacterial strains
[0039] Take by weighing sludge 10g in 100mL inorganic salt liquid medium, the composition of inorganic salt liquid medium is as follows:
[0040] MgSO 4 ·7H 2 O 0.2g; K 2 HPO 4 0.1g; (NH 4 ) 2 SO 4 0.1g; CaSO 4 0.04g; FeSO 4 ·7H 2 O0.001g; deionized water 1L; pH 7.0. Sterilize at 121°C for 30min.
[0041] Add chlorpyrifos with a concentration of 100mg / L to the inorganic salt liquid medium to obtain a culture solution, cultivate it on a shaker at 37°C and 180r / min, and after cultivating for one week, insert it into the fresh culture solution with a 10% inoculation amount, and then The turnover is connected once, so the domestication is repeated many times. Fina...
example 2
[0044] Example 2, induction and acclimatization of the larvae Providencia bacterial strain
[0045] 1. Chlorpyrifos induction and domestication
[0046] 1. The content range of active ingredients prepared by chlorpyrifos: 300mg / L-800mg / L. Tryptone agar containing different concentrations of chlorpyrifos was prepared. Different amounts of chlorpyrifos were added into tryptone agar to make a medium containing chlorpyrifos. Concrete steps: 1) Chlorpyrifos is prepared into a 4500 mg / L pesticide standard solution. Take 13.3mL, 17.8mL, 22.2mL, 26.6mL, 31.1mL, 35.6mL of pesticide standard solutions with a concentration of 4500mg / L and add them to 200mL tryptone agar to prepare chlorpyrifos containing 300mg / L, 400mg / L, 500mg / L , 600mg / L, 700mg / L and 800mg / L tryptone agar medium. Plate production: Pour the prepared tryptone agar containing 300mg / L-800mg / L chlorpyrifos into a plate, 15mL / plate, and use it after cooling and solidifying.
[0047] The components of tryptone agar are: ...
example 3
[0061] Example 3, utilize the larvae Providencia bacteria strain FY-4 to prepare biodegradable enzyme preparation
[0062] 1. Obtaining liquid biodegradable enzyme preparations
[0063] 1. Strain expansion culture: Inoculate refrigerated strains into 100mL sterile TSB medium, cultivate at 37°C and 180rpm for 24 hours, and then they will become first-class seeds; transfer the first-class seeds to 1L with 10% inoculum volume In the TSB medium, cultured at 37°C and 180rpm for 24 hours, it is the secondary seed. The second-grade seeds were transferred to 10 L of industrial medium according to 10% inoculum amount, and cultivated at 37° C. and 180 rpm for 24 hours to obtain the third-grade seeds.
[0064] 2. Inoculate the tertiary seeds into the fermenter, and the inoculation amount is 5% of the fermentation medium. Controlled ventilation volume is 2.5m 3 / h, the temperature is 37°C, the pH is 7.2±0.4, the rotation speed is 180rpm, samples are taken at intervals, and the OD is me...
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