A kit for reducing nnn content in tobacco extract
A technology of extraction solution and kit, which is applied in the field of kits for reducing NNN content in tobacco extract, and can solve the problems that have not yet been reduced.
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Embodiment 1
[0044] Take 0.01g CYP2A6 enzyme reagent (1nmol / L), 1g NADPNa by weight 2 , 12g trisodium citrate, 0.6g magnesium chloride.
[0045] After the temperature of the tobacco extract dropped below 40°C, the above CYP2A6 enzyme system was added to 1.36kg of the tobacco extract, stirred evenly, and the temperature of the reaction solution was kept at 37°C for 24 hours. Wherein, the amount of the CYP2A6 enzyme system applied in the tobacco extract is 1% of the weight of the tobacco extract.
Embodiment 2
[0047] The sample obtained in Example 1 (tobacco extract sample applied with CYP2A6 enzyme system, reacted for 24h) was diluted 20 times, and the component content was determined by high performance liquid phase-triple quadrupole mass spectrometry, and the determination was repeated 5 times , and take the average value. At the same time, a sample of the tobacco extract without the CYP2A6 enzyme system was taken, and the content of the components was determined after performing the same steps. See Table 1 and Table 2 for the test results of NNN content and other components in the applied sample and the control sample. And taking the control group as a reference, calculate the reduction rate of NNN after applying the CYP2A6 enzyme system. In Table 1, the sample obtained in Example 1 is the application group, and the tobacco extract sample without CYP2A6 enzyme system is the control group.
[0048] The specific calculation formula is:
[0049] NNN reduction rate (%) = ((NNN co...
Embodiment 3
[0057] Take 0.01g CYP2A6 enzyme reagent (1nmol / L), 2g NADPNa by weight 2 , 24g trisodium citrate, 1.2g magnesium chloride.
[0058] After the temperature of the tobacco extract dropped below 40°C, the above CYP2A6 enzyme system was added to 1.36kg of the tobacco extract, stirred evenly, and the temperature of the reaction solution was kept at 37°C for 24 hours. Wherein, the amount of the CYP2A6 enzyme system applied in the tobacco extract is 2% of the weight of the tobacco extract. The content of NNN in the treated extract samples decreased significantly, and the rate of decrease was similar to that of Example 1.
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