Cell-free bioproduction of b-cryptoxanthin and zeaxanthin
US-2024368663-A1 · Nov 7, 2024 · US
US11414650B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11414650-B2 |
| Application number | US-202017120163-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 12, 2020 |
| Priority date | Dec 11, 2018 |
| Publication date | Aug 16, 2022 |
| Grant date | Aug 16, 2022 |
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The present disclosure relates to a construction method of a Mucor circinelloides cell factory for producing dihomo-γ-linolenic acid and a fermentation technology, belonging to the field of genetic engineering. In the present disclosure, γ-linolenic acid elongase gene glelo is obtained from Mortierella alpine by cloning, the gene is ligated to an integrative plasmid pMAT1552, and transformed into a Mucor circinelloides defective strain Mu402, and the gene glelo is integrated into Mucor circinelloides genome through homologous recombination, to obtain the recombinant strain Mc-glelo, and finally, the expression of the gene glelo in Mucor circinelloides is realized. The lipid content in the recombinant strain Mc-glelo is not obviously different from that in the control strain Mc1552, however, the lipid composition changes greatly, and dihomo-γ-linolenic acid appears in the lipids of the recombinant strain Mc-glelo, and the content thereof reaches 5.7% of the total fatty acids. Under optimized fermentation conditions and in the presence of precursor fatty acid, the DGLA content reaches 7.6%. The new recombinant strain was deposited in China General Microbiological Culture Collection Center on Jun. 20, 2018, with the address of No. 3, Courtyard 1, Beichen West Road, Chaoyang District, Beijing. The accession number given to the biological material by the collection center is CGMCC No. 15887, and the suggested taxonomic denomination is Mucor circinelloides-GLELO.
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The invention claimed is: 1. A recombinant cell producing dihomo-γ-linolenic acid, wherein the recombinant cell comprises a polynucleotide encoding γ-linolenic acid elongase, the polynucleotide encoding γ-linolenic acid elongase being operably linked to a promoter capable of driving expression of the polynucleotide in the recombinant cell; wherein the polynucleotide encoding γ-linolenic acid elongase comprises: a polynucleotide sequence shown in SEQ ID NO: 1; wherein the recombinant cell is a Mucor circinelloides cell; and wherein the recombinant cell is a recombinant strain deposited on Jun. 20, 2018 in China General Microbiological Culture Collection Center with an accession number of CGMCC No. 15887. 2. The recombinant cell according to claim 1 , wherein the recombinant cell is not derived from Mortierella alpina. 3. A method for producing dihomo-γ-linolenic acid, wherein the method comprises fermenting the recombinant cell producing dihomo-γ-linolenic acid according to claim 1 . 4. The method according to claim 3 , wherein the fermentation is performed in a fermentation medium comprising γ-linolenic acid, γ-linolenic acid compounds or precursor compounds of γ-linolenic acid. 5. The method according to claim 4 , wherein the fermentation medium comprises linoleic acid and/or linoleic acid compounds. 6. The method according to claim 4 , wherein the fermentation medium comprises vegetable oil containing linoleic acid and/or linoleic acid compounds. 7. The method according to claim 6 , wherein the vegetable oil is safflower seed oil or sunflower seed oil. 8. The method according to claim 6 , wherein the vegetable oil is initially present in the fermentation medium, or is added to the fermentation medium by feeding during the fermentation. 9. The method according to claim 5 , wherein the fermentation medium comprises vegetable oil containing linoleic acid and/or linoleic acid compounds.
acting on paired donors with incorporation of molecular oxygen (1.14) · CPC title
transferring groups other than amino-acyl groups (2.3.1) · CPC title
Mucor · CPC title
for fungi · CPC title
Fungi (culture of mushrooms A01G18/00; as new plants A01H15/00); Culture media therefor · CPC title
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