Method for detecting methanal content in mushroom
A technology for formaldehyde content and shiitake mushrooms, which is applied in measuring devices, instruments, scientific instruments, etc., can solve the problems of high detection value, small increase, and no consideration, and achieve the effect of inhibiting the activity of related enzymes
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Embodiment 1
[0031] Weigh 500g of fresh shiitake mushroom samples, pre-cool at 4°C for 30 minutes, put them into a homogenizer, and homogenize in an ice-water bath environment. Weigh 5g of the homogenate and add it into a stoppered Erlenmeyer flask filled with 50ml of pre-cooled water, disperse it with a disperser and place it in ice water.
[0032] Inactivate the dispersed fresh mushroom homogenate in a boiling water bath at 100°C for 5 minutes, take it out and cool it down with ice water.
[0033] The enzyme-inactivated and cooled homogenate was sonicated for 30 minutes at full power (100W) by an ultrasonic instrument, and then taken out and placed at 4°C for 12 hours.
[0034] The samples left for 12 hours were taken out and centrifuged at 6000rpm for 5min. Take 1ml of the supernatant into a stoppered colorimetric tube, add 0.5ml of 0.05% DNPH acetonitrile solution derivatizer, derivatize in a water bath at 60°C for 15min, cool in running water, pass through a membrane, and inject into...
Embodiment 2
[0044] Weigh 50g of dried shiitake mushroom samples and pulverize them to 200 mesh with a pulverizer. Weigh 5g of dried mushroom powder and add it to a stoppered conical flask filled with 50ml of pre-cooled water, and shake well.
[0045] The shaken samples were inactivated in a boiling water bath at 100°C for 5 minutes, and then taken out and cooled with ice water.
[0046] The enzyme-inactivated and cooled homogenate was sonicated for 30 minutes at full power (100W) by an ultrasonic instrument, and then taken out and placed at 4°C for 12 hours.
[0047] The samples after standing for 12 hours were taken out and centrifuged at 6000rpm for 5min. Take 1ml of the supernatant into a stoppered colorimetric tube, add 0.5ml of 0.05% DNPH acetonitrile solution derivatizer, derivatize in a water bath at 60°C for 15min, cool in running water, pass through a membrane, and inject into HPLC for separation and detection.
[0048] HPLC chromatographic conditions:
[0049] Injection volum...
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