Photobacterium phosphoreum growth promoter used for monitoring water body pollutants and application of photobacterium phosphoreum growth promoter
A technology of luminescent bacteria, growth promoters, applied in the fields of adding compounds to stimulate growth, microorganism-based methods, and microbial assays/tests, which can solve the problem of bacterial decline, unsuitable recovery and culture, and poor recovery culture conditions. temperature, pH, etc.
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Embodiment 1
[0039] The growth promoter of Photobacterium luminosus used for monitoring water pollutants, the specific components and concentrations are shown in Table 1:
[0040] Table 1
[0041] components Example 1 Example 2 Example 3 Example 4 Sodium chloride g / L 30 25 22 28 Ureag / L 2 3 2 4 Glucose g / L 5 7 6 8 Magnesium chloride g / L 4 3 4 3 Oxaloacetate g / L 1.5 1.1 1.3 1.6 Adenosine g / L 0.7 0.9 0.6 0.8 Yeast extract g / L 0.2 0.4 0.5 0.3 Formic acidml / L 20 15 18 19
[0042] The preparation method comprises the following steps: taking each component in sequence according to the concentration ratio, adding them into distilled water, stirring evenly, and adjusting the pH to 7.0-7.5 to obtain the product.
Embodiment 2
[0048] Application example of growth promoter of Photobacterium luminosa.
[0049] The freeze-dried powder is commercially available Lyophilized Bacillus Brightensis (ATCC11040), 1g / tube; self-made freeze-dried powder can also be used.
[0050] Preparation method of homemade freeze-dried powder:
[0051] Under sterile conditions of the lyoprotectant, the solution of Photobacterium lumina (concentration of 1×10 9cfu / ml) and lyoprotectant (parts by weight: skimmed milk powder 10%, sucrose 8%, sodium glutamate 1%, solvent is sterile water) mixed according to the volume ratio of 1:1, packed in vials Cool down to -70°C within 60 minutes, freeze for 12 hours, then place at -40°C, vacuum freeze-dry to obtain a freeze-dried powder, and finally store at -20°C.
[0052] Methods for the recovery and expansion of Photobacteria luminosus:
[0053] Take out the lyophilized powder, put it in a 38°C water bath to thaw immediately, shake it for 60s, after it is completely thawed, add it to ...
Embodiment 3
[0055] Effects of example 1-4 growth promoters on bacterial strain proliferation and luminous intensity.
[0056] Detection method: Spectrophotometer method (OD600) is used for the detection of bacteria concentration; DXY-3 intelligent biological toxicity tester is used for detection of luminous intensity of bright photobacteria.
[0057] Test procedure: Referring to Example 2, commercially available freeze-dried powder was used. Such as figure 1 As shown, the growth promoters of Examples 1-4 can realize the rapid recovery and proliferation of bright photobacteria within 6 hours, which is beneficial to save detection time, and obtain a large amount of bacteria liquid with stable luminous efficiency in a short time, expanding the detection scale , reducing business costs.
[0058] Luminous intensity comparison:
[0059] Conventional method: Take out the freeze-dried powder, immediately place it in a 38°C water bath to thaw, shake for 60s, then add an appropriate amount of 3%...
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