Method for detecting enzyme value of sucrose invertase in honey
A technology of sucrose invertase and detection method, which is applied in the field of food quality and safety detection, can solve the problem that the control of titration operation conditions is very high, there is no general detection method for sucrose invertase activity, and the titration speed, titration end point observation and measurement results have relatively little influence To achieve the effect of improving the quality evaluation system, facilitating large-scale promotion and application, and promoting vigorous development
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Embodiment 1
[0073] Weigh 2g of acacia honey into a beaker, add 10mL of acetate buffer (0.1mol / L) with a pH value of 6.0 to fully dissolve, and centrifuge at 4°C. After centrifugation, the precipitate was redissolved with acetate buffer, and the clarified solution was transferred to a 10KAmiconUltra-15 centrifugal ultrafiltration tube and centrifuged at 5000×g for 30 min at 4°C to recover the concentrated solution. Add acetate buffer to the concentrate and repeat the centrifugation step. The concentrated solution obtained again, together with the precipitate reconstituted solution in the above step, was fixed to a 50 mL volumetric flask with acetate buffer solution, that is, the enzyme solution.
[0074] Take 2.0 mL of the obtained enzyme solution and place them in two test tubes, of which test tube 1 is the experimental group and test tube 2 is the control group. Add 1 mL of NaOH solution (1 mol / L) to test tube 2. Put test tube 1, test tube 2 and 5% sucrose solution together in a water ...
Embodiment 2
[0081] The Bee Research Institute of the Chinese Academy of Agricultural Sciences detected the sucrose invertase enzyme value of the linden raw honey collected from the Heilongjiang area.
[0082] Operation method:
[0083] Weigh 3g of linden raw honey and place it in a beaker, add 10mL of acetate buffer (0.1mol / L) with a pH value of 6.0 to fully dissolve, and centrifuge at 4°C. After centrifugation, the precipitate was redissolved with acetate buffer, and the clarified solution was transferred to a 10KAmiconUltra-15 centrifugal ultrafiltration tube and centrifuged at 5000×g for 30 min at 4°C to recover the concentrated solution. Add acetate buffer to the concentrate and repeat the centrifugation step. The concentrated solution obtained again, together with the precipitate reconstituted solution in the above step, was fixed to a 50 mL volumetric flask with acetate buffer solution, that is, the enzyme solution.
[0084] Take 2.0 mL of the obtained enzyme solution and place th...
Embodiment 3
[0091] According to the detection method of Example 1, the sucrose invertase enzyme values of 20 acacia honeys and 20 linden honeys on the market were measured, and the results are shown in Table 1.
[0092] Table 1 Determination of sucrose invertase enzyme value in 40 brands of honey
[0093]
[0094]The results of 20 brand commercially available acacia honey samples and 20 brand commercially available linden honey samples detected by the sucrose invertase enzyme value assay method in honey provided by the invention. Among them, the sucrose invertase enzyme values of 20 brands of commercially available acacia honey samples were between 4.53 and 42.19 mg / (g.h), with an average value of 13.50 mg / (g.h), and the sucrose invertase enzyme values of 4 brand samples were greater than 20mg / (g.h), the sucrose invertase enzyme value of 7 brand samples is below 8mg / (g.h); the sucrose invertase enzyme value of 20 brands of commercially available linden tree honey samples is betwe...
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