Stenotrophomonasmal-tophilia vaccine and its preparing method
A Pseudomonas preparation and Pseudomonas technology, which are applied in the field of microbial engineering, can solve the problems of high morbidity and mortality, and high mortality, so as to reduce the economic burden of patients, low prices, and low drug production costs. Effect
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Embodiment 1
[0305] The name and source of the strain
[0306] Manufacture of Pseudomonas maltophilia strains Approved by the national drug regulatory authority, kept and distributed by the national drug control agency or a unit designated by the state.
[0307] Establishment of seed batches
[0308] The strains used for production should adopt the seed batch system. Prepare the working seed lot from the master seed lot. Working seed batches are used for production. Seed Batch Bacteria Verification
[0309] Morphology and Culture Assays
[0310] Inoculate the bacteria to be tested on broth agar, Martin agar or other suitable medium with pH 7.2-7.4, which should be Gram-negative bacillus. Pili, colonies are smooth, glossy edges are neat white-gray or light yellow.
[0311] biochemical reaction
[0312] Malonate citrate and DNA tests were positive, and oxidase was negative.
[0313] serum agglutination test
[0314] Cultivate the culture at 35°C for 18-20 hours, inactivate it with 1...
Embodiment 2
[0342] The name and source of the strain
[0343] The strains (Pseudomonas maltophilia) used for the manufacture of polysaccharide vaccines and the diagnostic serum used for testing should be approved by the national drug administration authority and distributed by the national drug testing agency or a country-designated unit.
[0344] The strains used for production should adopt the seed batch system. The main seed batch was lyophilized and preserved after amplification. Prepare the working seed lot from the master seed lot.
[0345] Working seed batches are used for production.
[0346] Verification of seed batches
[0347] For the identification of bacteria, broth agar base with pH7.2-7.4 or other suitable medium can be used.
[0348] Morphological and cultural characteristics
[0349] Inoculate the strains to be tested on the improved semi-comprehensive medium or other suitable medium, and culture at 35-37°C for 16-20 hours. The microscopic examination of the smear sh...
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