Manipulation of nuclear architecture
US-2018355344-A1 · Dec 13, 2018 · US
US11098331B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11098331-B2 |
| Application number | US-202017117788-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 10, 2020 |
| Priority date | Mar 13, 2020 |
| Publication date | Aug 24, 2021 |
| Grant date | Aug 24, 2021 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention discloses a method for producing lysine by utilizing adsorption and immobilized fermentation of a recombinant Corynebacterium glutamicum, wherein the recombinant Corynebacterium glutamicum is constructed by simultaneously overexpressing an adenosine triphosphate ATPase while knocking out an extracellular nuclease ExeR in a Corynebacterium glutamicum. The recombinant Corynebacterium glutamicum can effectively improve eDNA secretion of the Corynebacterium glutamicum and reduce eDNA degradation of the Corynebacterium glutamicum, so that the Corynebacterium glutamicum can be more easily adsorbed on a surface of a solid carrier for immobilized fermentation, such that a yield of continuous immobilized fermentation of the Corynebacterium glutamicum is increased by 49.67% than that of free fermentation of an original bacterium, and a fermentation cycle is shortened by 29.17%.
Opening claim text (preview).
The invention claimed is: 1. A method for producing lysine, comprising utilizing fermentation of a recombinant Corynebacterium glutamicum , wherein an extracellular nuclease ExeR of the recombinant Corynebacterium glutamicum is inactivated, and meanwhile, expression of an adenosine triphosphate ATPase is enhanced, a nucleotide sequence of the extracellular nuclease ExeR is shown in SEQ ID NO:1, and a nucleotide sequence of the adenosine triphosphate ATPase is shown in SEQ ID NO:2. 2. The method according to claim 1 , wherein the fermentation is immobilized fermentation. 3. The method according to claim 2 , wherein the recombinant Corynebacterium glutamicum is fermented in a medium containing a solid carrier to obtain a lysine fermentation broth. 4. The method according to claim 3 , wherein the solid carrier is any one or a combination of several of cotton fiber fabric, non-woven fabric, polyester fiber, polyvinyl alcohol fiber, zeolite, bacterial cellulose membrane, silk, bagasse, corn straw, activated carbon, plastic and glass. 5. The method according to claim 3 , wherein a dosage of the solid carrier in the fermentation medium is 1 to 100 g/L. 6. The method according to claim 3 , wherein concentrations of constituents in the medium are: 80 to 300 g/L glucose, 30 to 50 g/L ammonium sulfate, 0.5 to 1.5 g/L magnesium sulfate, 10 to 25 g/L molasses, 10 to 25 g/L corn steep liquor, 1 to 5 g/L potassium dihydrogen phosphate, 100 to 300 mg/L ferrous sulfate, 100 to 200 mg/L manganese sulfate, 40 to 80 mg/L nicotinamide, 5 to 15 mg/L calcium pantothenate, 5 to 15 mg/L VB1, 0.5 to 2 mg/L copper sulfate, 0.5 to 2 mg/L zinc sulfate, 0.5 to 2 mg/L biotin, and 10 to 50 g/L calcium carbonate, and water is used as a solvent. 7. The method according to claim 3 , wherein, after each batch of fermentation, the obtained fermentation broth is replaced with a new fermentation medium for cultivation until sugar is exhausted to obtain the lysine fermentation broth. 8. The method according to claim 3 , wherein the fermentation is performed at 28 to 34° C. and 200 to 250 rpm for 20 to 90 hours.
Enzymes or microbial cells immobilised on or in an inorganic carrier · CPC title
Bacteria; Culture media therefor · CPC title
Cellulose or derivatives thereof · CPC title
Preparation of mutants without inserting foreign genetic material therein; Screening processes therefor · CPC title
Adenosine triphosphatase (3.6.1.3) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.