Development culture medium for separating and identifying pathogens in urogenital tract
A chromogenic medium and urogenital tract technology, applied in the field of chromogenic medium for detection of pathogenic bacteria, can solve the problems of cumbersome operation, unsatisfactory, inability to separate and identify Candida, and achieve the effect of extremely easy operation and shortened time
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Embodiment 1
[0022] Embodiment 1: Using the chromogenic medium of the present invention to isolate and identify pathogenic bacteria in the genitourinary tract
[0023] 1.1 Preparation of chromogenic medium plate: Weigh each component according to the formula in Table 1, add 1000ml of purified water, adjust the pH to 6.8±0.1, sterilize at 115°C for 20min, cool to about 50°C and pour onto the plate spare;
[0024] Table 1
[0025] Element
Medium 1
source
soy peptone
6.0g
Beijing Oberstar
3.0g
OXOID
Dipotassium hydrogen phosphate (K 2 HPO 4 ·3H 2 O)
2.5g
Beijing Yili
Potassium dihydrogen phosphate (KH 2 PO 4 )
1.2g
Beijing Yili
sodium pyruvate
3.0g
Beijing Yili
N-acetyl-glucosamine
0.4g
Suzhou Yake
glucose
0.80g
Beijing Yili
0.50g
Shanghai Kangjie
0.05g
Beijing Yili
Manganese sul...
Embodiment 2
[0034] Embodiment 2: Evaluation of the nutrient capacity of the chromogenic medium of the present invention
[0035] 2.1 Chromogenic medium plate preparation: Weigh each component according to the formula in Table 3, prepare two kinds of medium, add 1000ml of purified water to each, adjust pH to 6.8±0.1, autoclave at 115°C for 20min, cool to Pour plate at about 50°C for later use.
[0036] table 3
[0037] Element
Medium 2
Medium 3
source
soy peptone
5.0g
10.0g
Beijing Oberstar
2.0g
4.0g
OXOID
Dipotassium hydrogen phosphate (K 2 HPO 4 ·3H 2 O)
2.4g
2.4g
Beijing Yili
Potassium dihydrogen phosphate (KH 2 PO 4 )
1.1g
1.1g
Beijing Yili
sodium pyruvate
3.0g
5.0g
Beijing Yili
glucose
0.80g
0.80g
Beijing Yili
N-acetyl-glucosamine
0.40g
0.40g
Suzhou Yake
0.05g
——
Beijing Yili ...
Embodiment 3
[0045] Example 3: Comparative test of the use of the chromogenic medium described in the present invention and CHROMagar's localized chromogenic medium.
[0046] 3.1 The preparation of chromogenic medium plate of the present invention
[0047] Add 9.0g of soybean peptone, 4.0g of yeast extract powder, 2.4g of dipotassium hydrogen phosphate, 1.1g of potassium dihydrogenphosphate, 0.1g of 5 bromo-4 chloro-3 indole-N-acetyl-glucosamine in 1000ml of purified water, 5-bromo-6-chloro-3-indole-β-D-galactoside 0.1g, 5-bromo-6-chloro-3-indole-β-D-glucoside 0.07g, 5-bromo-4-chloro-3-indole-β -D-glucoside 0.03g, adjust the pH to 6.8±0.1, add 15g of agar powder and then autoclave, wait to cool to about 50°C and pour it into a plate for later use;
[0048] 3.2 Prepare CHROMagar localization chromogenic medium plate according to CHROMagar localization chromogenic medium preparation instructions;
[0049] 3.3 Inoculation of microbial strains
[0050] Prepare the strain to be tested into a...
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