Pathogen specific nucleic acid fragment and application thereof
US-2024352539-A1 · Oct 24, 2024 · US
US10253347B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10253347-B2 |
| Application number | US-201615228162-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 4, 2016 |
| Priority date | Nov 19, 2015 |
| Publication date | Apr 9, 2019 |
| Grant date | Apr 9, 2019 |
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Provided is a method of screening for a microorganism having enhanced cellulose productivity.
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What is claimed is: 1. A method of screening for a microorganism having enhanced cellulose productivity, the method comprising: culturing mutated or recombinant cellulose-producing microorganisms to obtain a plurality of cultures containing the respective microorganisms and produced cellulose; culturing one or more non-genetically modified and non-mutated cellulose-producing microorganisms to provide at least one respective control group; measuring an optical density A of each respective control group and each culture of the one or more mutated or recombinant cellulose producing microorganisms, wherein the optical density A is an optical density at a first wavelength in a visible light range of about 380 nm to about 420 nm; measuring an optical density B of each respective control group and at least one mutated or recombinant cellulose producing microorganism, wherein the optical density B is an optical density at a second wavelength in the visible light range of about 750 nm to about 800 nm; obtaining a ratio of optical density A/optical density B with respect to cultures that have an optical density A being greater than that of said respective control group; and selecting a mutated or recombinant microorganism that has a ratio of optical density A/optical density B greater than that of said respective control group as a microorganism having enhanced cellulose productivity. 2. The method of claim 1 , wherein the cellulose-producing microorganisms comprise a microorganism belonging to Gluconacetobacter sp. 3. The method of claim 1 , wherein the mutated microorganism is produced by random mutagenesis. 4. The method of claim 1 , wherein the microorganisms are cultured in the wells of a microplate. 5. The method of claim 1 , wherein the optical density B is measured only with respect to cultures in which the optical density A is greater than that of the respective control group. 6. The method of claim 1 , further comprising dispersing the produced cellulose in the culture prior to measuring the optical density A or the optical density B. 7. The method of claim 1 , wherein each of the optical density A and the optical density B is a mean value of three or more measurements with a deviation of 10% or less. 8. The method of claim 1 , wherein the optical density A and the optical density B are measured by a high throughput screening system. 9. The method of claim 1 , wherein the optical density A and the optical density B are measured during culturing. 10. The method of claim 1 , further comprising: culturing the selected mutated or recombinant microorganism having a ratio of optical density A/optical density B higher than that of the control group to obtain a culture containing cellulose; and measuring a content of the cellulose in the culture. 11. A method of producing cellulose, the method comprising: selecting a mutated or recombinant microorganism according to the method of claim 1 ; culturing the mutated or recombinant microorganism to produce cellulose; and recovering the cellulose from the culture. 12. The method of claim 11 , wherein the culturing is performed in flasks.
Polysaccharides, i.e. compounds containing more than five saccharide radicals attached to each other by glycosidic bonds · CPC title
Determining presence or kind of microorganism; Use of selective media for testing antibiotics or bacteriocides; Compositions containing a chemical indicator therefor {(C12Q1/6897 takes precedence)} · CPC title
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