Method for quickly measuring total number of live bacteria of luminous bacteria by using MTT method
A luminescent bacteria, rapid determination technology, applied in the determination/inspection of microorganisms, chemiluminescence/bioluminescence, biochemical equipment and methods, etc. The detection method is simple, rapid and reproducible
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Embodiment 1
[0013] Add 0.3mL MTT solution to 3mL of properly diluted fermentation broth, mix well, place at 25°C for 2h, centrifuge at 10,000r / min for 10min, discard the supernatant, add 3mL DMSO to fully dissolve the precipitate, and use UV-Vis spectroscopy The photometer scans the maximum absorption wavelength, and measures the light absorption value in the range of 400nm-800nm. Depend on figure 1 It can be seen that its maximum absorption peak is at 500nm.
Embodiment 2
[0015] Using DMSO as a reference, sterile saline, sterile blank medium, fermentation supernatant (after centrifugation at 10,000r / min, absorb the supernatant) and dead bacteria (boiling water bath for 30min) as samples to be tested, use MTT The light absorption values measured by the method are listed in Table 1. It can be seen from the table that these substances have little interference with the measurement results. It can be seen that the MTT method is related to the amount of viable bacteria, but has nothing to do with the properties of the solids and metabolites contained in the medium, which largely solves the problem of using the turbidity method due to the solids contained in the medium. Serious interference with the measurement of live bacteria by the dry weight method of the bacteria.
[0016] Table 1 Absorbance value when different substances are blank controls
[0017]
Embodiment 3
[0019] Add 0.3mL of MTT solution to 3mL of properly diluted fermentation broth, mix well, place at 25°C for 2h, centrifuge at 10,000r / min for 10min, discard the supernatant, add 3mL of DMSO to fully dissolve the precipitate, and place at 500nm Measure the absorbance. At the same time, the centrifuged bacteria were redissolved with physiological saline, and after gradient dilution, they were spread on a plate and counted colonies.
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