Pseudomonas fluorescens and an application thereof
A technology of Pseudomonas fluorescens and Pseudomonas acid, applied in the field of microorganisms, can solve problems such as low fermentation level, and achieve the effects of single composition of fermentation products and cost reduction
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Embodiment 1
[0031] The acquisition of embodiment 1 bacterial classification
[0032] 1. Starting strain
[0033] Pseudomonas fluorescens ATCC 49323 (purchased from ATCC).
[0034] 2. The cultivation process of bacteria
[0035] The starting strain Pseudomonas fluorescens was inoculated on the slant medium, cultured at 30°C for 3 days, washed with sterile water, inoculated on the seed medium at 1% (v / v) inoculum, and cultured at 28°C for 20 Hours, inoculate the fermentation medium at 2% (v / v) inoculum, and culture at 28°C for 4-5 days. Different stages of seed culture can be set according to different fermentation culture scales.
[0036] 3. HPLC analysis conditions of monocytic acid A:
[0037] The fermentation broth was taken, centrifuged at 12000rpm for 10min, and the supernatant was taken for HPLC analysis.
[0038] Mobile phase: 50mmol / L sodium dihydrogen phosphate (pH6.3): acetonitrile=75:25.
[0039] Detection wavelength: 229nm
[0040] HPLC column: C18, 250*4.6mm
[0041] F...
Embodiment 2
[0053] Embodiment 2 Morphological and cultural characteristics of Pseudomonas fluorescens CGMCC No.7147
[0054] Pseudomonas fluorescens CGMCC No.7147 is a Gram-negative bacterium that does not produce spores. It is cultured in LB medium for 3 days. milky. According to "Bergey's Handbook of Systematic Bacteriology", the physiological response of the strain is shown in Table 1, indicating that the strain is Pseudomonas fluorescens.
[0055] Table 1. Physiological responses of Pseudomonas fluorescens CGMCC No.7147
[0056]
[0057]
Embodiment 3
[0058] Example 3 Identification of 16SrDNA of Pseudomonas fluorescens CGMCC No.7147 strain
[0059] Genomic DNA was extracted from Pseudomonas fluorescens CGMCC No.7147 for 16S rDNA analysis.
[0060] Designed primers, 7F5'–CAGAGTTTGATCCTGGCT-3', and
[0061] 1540R5'–AGGAGGTGATCCAGCCGCA-3';
[0062] Carry out PCR amplification, the composition of PCR reaction system is as follows:
[0063] Reagent
Volume (μl)
Template (genomic DNA20-50ng / μl)
0.5
5×Buffer (including Mg 2+ )
2.5
dNTPs (2.5mM each)
1
7F (10 μM)
0.5
1540R (10μM)
0.5
Taq enzyme
0.5
Add double steamed H 2 O to
25
[0064] The PCR conditions are shown in the table below:
[0065]
[0066] The results of agarose gel electrophoresis of the PCR products are shown in figure 2 . DNA sequencing was performed on the PCR product, and the sequence was compared with the 16S rDNA in the Genbank database. The results are...
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