Aeromonas strain and application thereof
A technology for Aeromonas and strains, which is applied to Aeromonas strains and their application fields, can solve the problems of limited treatment application, weak salt or acid resistance, and poor broad-spectrum, and achieves high degradation effect and degradation. Broad spectrum effect
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Embodiment 1
[0026] Embodiment 1 Aeromonas (Aeromonas sp.) Isolation of CM-T1
[0027] Aeromonas sp. CM-T1 was isolated from soil collected from a sewage outlet of a printing and dyeing factory in Shaoxing. The specific separation method is: take 5.0g of soil and add it to a 250mL sterilized Erlenmeyer flask containing 4 glass beads, add 95mL of sterilized physiological saline, and vibrate on a shaker at 150r / min for 3h; take the above bacterial suspension, press 2% ( The amount of v / v) was added to the 150mL rich medium (KH 2 PO 4 1.8g / L, Na 2 HPO 4 12H 2 O 3.5g / L, MgSO 4 ·7H 2 O 0.29g / L, FeCl 3 ·6H 2 O 0.01g / L, NaCl 3.0g / L, peptone 10.0g / L, beef extract 3.0g / L, pH 7.0~7.2) in a serum bottle, cultured at 30°C and 150r / min for 3 days, and the Dilution to 10 -5 , 10 -6 , 10 -7 , take 0.1mL of the diluted solution and spread it on crystal violet dye solid medium (beef extract 3.0g / L, peptone 10.0g / L, NaCl 5.0g / L, crystal violet 20mg / L, agar 15g / L, pH 7.0~ In 7.2), two parallels...
Embodiment 2
[0028] Example 2 Identification of Aeromonas (Aeromonas sp.) CM-T1
[0029] (1) Morphological characteristics
[0030] Aeromonas sp. (Aeromonas sp.) CM-T1 was cultured on solid growth medium for 48 hours, the colony was yellow, the surface was protruding, moist and shiny, and the edges were neat; electron microscope scanning showed that the cells of the strain were brevibacteria, with two ends Microcircle, with a diameter of about 1.3μm, such as figure 1 , figure 2 shown.
[0031] (2) Physiological and biochemical identification
[0032] Biochemical Indicators
result
Biochemical Indicators
result
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Oxidase
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glucose fermentation
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MR
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V-P
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Nitrate reduction
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arginine dihydrolase
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Ornithine decarboxylase
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Lysine decarboxylase
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Tr...
Embodiment 3
[0047] The best growth condition optimization of embodiment 3 Aeromonas (Aeromonas sp.) CM-T1
[0048] Strain culture medium: peptone 10g / L, beef extract 3g / L, NaCl 5g / L, pH 7~7.2
[0049] (1) Optimum growth pH of the inventive bacterial strain
[0050] Adjust the initial pH of the culture medium to 3.0, 4.0, 5.0, 6.0, 7.0, 8.0, 9.0, 10.0, 11.0 with 1.0 mol / L HCl and NaOH, respectively, insert 0.5% inoculum into CM-T1, 30°C, Cultivate at 150r / min, and after 20h, use a UV-visible spectrophotometer at OD 600 The absorbance was measured, and the culture medium without inoculation was used as the blank control.
[0051] Depend on Figure 4 It can be seen that CM-T1 grows well when the pH is between 5 and 10, and the growth range of pH is wide, but the optimum growth pH is 7.0.
[0052] (2) Optimum growth temperature of the invented strain
[0053] Inoculate CM-T1 with 0.5% (v / v) inoculum in the culture medium, place them in shaker incubators at 20°C, 25°C, 30°C, 35°C, 40°C, a...
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