Bacterial colicin-immunity protein protein purification system
US-2024417426-A1 · Dec 19, 2024 · US
US9376695B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9376695-B2 |
| Application number | US-23870408-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 26, 2008 |
| Priority date | Sep 27, 2007 |
| Publication date | Jun 28, 2016 |
| Grant date | Jun 28, 2016 |
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A method for producing an L-amino acid is described, for example, L-phenylalanine and L-histidine, by fermentation using a bacterium of the Enterobacteriaceae family, wherein the bacterium has been modified by attaching a DNA fragment able to be transcribed encoding the peptide represented in SEQ ID NO: 2, or a variant thereof, particularly a portion of the ssrA gene, to the 3′-end of gene encoding for the bacterial enzyme, which influences on the L-amino acid biosynthesis, such as chorismate mutase/prephenate dehydrogenase or phosphoglucose isomerase.
Opening claim text (preview).
We claim: 1. A recombinant L-amino acid producing Escherichia coli bacterium having a DNA comprising: A) a gene selected from the group consisting of tyrA, pheA, pgi, ilvE, ilvA, tdcB, sdaA, sdaB, argA, argG, proB, thrB, and combinations thereof, and B) a DNA fragment able to be transcribed and encoding the peptide of SEQ ID NO: 2, or a variant thereof consisting of a deletion, insertion, substitution, or addition of 1 amino acid as compared to SEQ ID NO: 2, wherein said DNA fragment of B) is attached to the 3′ end of said gene of A) and consequently enhances production of an L-amino acid. 2. The bacterium of claim 1 , wherein said bacterium is an L-phenylalanine producing bacterium. 3. The bacterium of claim 1 , wherein said gene is tyrA, which encodes the bifunctional enzyme chorismate mutase/prephenate dehydrogenase. 4. The bacterium of claim 1 , wherein said bacterium is an L-histidine producing bacterium. 5. The bacterium of claim 1 , wherein said gene is pgi which encodes a phosphoglucose isomerase enzyme. 6. A method for producing an L-amino acid comprising cultivating the bacterium according to claim 1 in a culture medium, and isolating the L-amino acid from the culture medium. 7. The method according to claim 6 , wherein said L-amino acid is L-phenylalanine. 8. The method according to claim 6 , wherein said L-amino acid is L-histidine. 9. The bacterium of claim 1 , wherein the variant is the peptide of SEQ ID NO: 15.
Glucose isomerase {(5.3.1.5; 5.3.1.9; 5.3.1.18)} · CPC title
Isomerases (5.) · CPC title
having a known sequence of two or more amino acids, e.g. glutathione · CPC title
Chorismate mutase (5.4.99.5) · CPC title
Glucose-6-phosphate isomerase (5.3.1.9) · CPC title
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