Novel bacterial strain for nicotine degradation-Pseudomonas ZUTSKD and uses thereof
A technology of Pseudomonas and Pseudomonas, which is applied in the field of environmental biology and can solve problems such as lethality, paralysis of the heart, danger, etc.
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Embodiment 1
[0023] Example 1: Isolation, Identification and Nicotine Degradation Properties of Pseudomonas sp. ZUTSKD
[0024] 1. Isolation of strains
[0025] (1) Collect samples
[0026] Sampling location: The sample tobacco powder was taken from the warehouse of Hangzhou Liqun Environmental Protection Paper Co., Ltd.
[0027] (2) Strain isolation
[0028] Add 10g of tobacco powder to 100mL of distilled water, shake at 200r / min for 10min, take 10mL of leaching solution, add it to 100mL of enrichment medium, and culture at 200r / min at 30°C for 7 days. Dilute the enriched medium by 10 -5 ~10 -8 , spread on BSM agar medium, and cultured at 30°C for 48h. Pick a single colony and streak it on fresh BSM agar medium until purified bacteria are obtained.
[0029] 2. Identification of strains
[0030] (1) The morphological characteristics of the nicotine-degrading bacteria ZUTSKD and its colonies
[0031] The nicotine-degrading bacteria ZUTSKD has an ellipsoidal shape, with a size of (0....
Embodiment 2
[0040] Embodiment 2: the application of Pseudomonas (Pseudomonas sp.) ZUTSKD in waste tobacco dust treatment
[0041] Soak 4 g of dried waste tobacco powder in 60 mL of sterile water (or 0.02 mol / L phosphate buffer (pH=7.0) is also acceptable), inoculate with 2 mL of bacterial suspension (dry weight 7.1 mg / mL), and add Sterile water 2mL, 200r / min, 30 ℃ culture, continuous measurement of nicotine degradation. The results are shown in Figure 6, and it was found that nicotine continued to dissolve into the water phase. Since the phosphate buffer can maintain the pH value of the solution, it is beneficial for strain ZUTSKD to degrade nicotine.
Embodiment 3
[0042] Example 3: Analysis of intermediate products of nicotine degradation by Pseudomonas sp. ZUTSKD
[0043] Inoculate 0.1mL of bacterial suspension into 100mL of BSM (nicotine 2g / L), culture at 200r / min, 30°C. At 6h and 12h, 10mL of the culture was taken respectively, and the supernatant after centrifugation (12000r / min, 10min, 4°C) was extracted twice with 1 / 2 volume of benzene, the benzene liquid was combined, and the benzene liquid was subjected to GC- MS analysis. After the culture was centrifuged (12000r / min, 10min, 4°C), the supernatant was extracted with benzene, and the benzene liquid was analyzed by GC-MS, and 3-(3,4-dihydro-2H-pyrrol-5 Accumulation of -yl)-Pyridine (I), 2,3'-Bipyridine (II), cotinine (III) and 3-Pyridinecarboxylic acid (IV).
[0044]
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