Method for detecting deamination capability of amino acid of spoilage bacteria in fish flesh
A detection method, amino acid technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganism measurement/inspection, etc., can solve the evaluation method of amino acid deamination ability of fish spoilage bacteria, bad flavor, reduce  The commercial value of fish meat and other issues
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Embodiment 1
[0039] Example 1 Detection of Amino Acid Deamination Ability of Specific Putrefaction Bacteria Pseudomonas helmanticensis in Refrigerated Bighead Carp Meat
[0040] Specifically include the following steps:
[0041] (1) Preparation of microbial suspension: Pick a single colony of isolated and purified Pseudomonas helmanticensis in tryptone soybean broth, culture in a shake flask in a water bath at 30°C until the total number of colonies in the broth reaches 9.0 log CFU / mL, and use sterile physiological Adjust the concentration of the bacterial suspension with saline to 8.0log CFU / mL for later use.
[0042] (2) Preparation of amino acid substrate solution: Dissolve the glycine substrate in 0.045M, pH=7.50 phosphate buffered saline (PBS), so that the glycine concentration is 5.0mM; the solution is sterilized at 121°C for 15min, and then added after cooling Oxidized nicotinamide adenine dinucleotide (NAD + ), so that NAD + The final concentration is 0.07mM, namely the substrat...
Embodiment 2
[0066] Example 2 Detection of Amino Acid Deamination Ability of Specific Putrefaction Bacteria Shewanella putrefaciens in Refrigerated Silver Carp Meat
[0067] Specifically include the following steps:
[0068] (1) Preparation of microbial suspension: Pick a single colony of isolated and purified Shewanella putrefaciens in tryptone soybean broth, culture in a shake flask in a water bath at 30°C until the total number of colonies in the broth reaches 9.0log CFU / mL, and use sterile physiological Adjust the concentration of the bacterial suspension with saline to 8.0log CFU / mL for later use.
[0069] (2) Preparation of amino acid substrate solution: Dissolve the glycine substrate in 0.045M phosphate buffered saline (PBS), pH=7.50, so that the concentration of glycine is 5.0mM; the solution is sterilized at 121°C for 15min, and then added after cooling Oxidized nicotinamide adenine dinucleotide (NAD + ), so that NAD + The final concentration is 0.07mM, namely the substrate sol...
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