Enzymes for producing non-straight-chain fatty acids
US-2015376659-A1 · Dec 31, 2015 · US
US9963722B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9963722-B2 |
| Application number | US-201514730174-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 3, 2015 |
| Priority date | Jun 3, 2014 |
| Publication date | May 8, 2018 |
| Grant date | May 8, 2018 |
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.
A bacterial strain secreting fatty acids, the strain inducing fatty acids to be extracellularly secreted by using phospholipase expressed in the periplasmic space of cell. When a method of producing fatty acids by using the bacterial strain secreting fatty acids is used, fatty acids extracellularly secreted are continuously obtained without apoptosis, leading to lower costs and higher production efficiency. Phospholipase, unlike thioesterase, which is a typical fatty-acid degrading enzyme, decomposes phospholipid to produce free fatty acids. Accordingly, by using the substrate specificity of two different phospholipases, a fatty acid having a specific composition can be selectively produced. Unlike in a typical method in which fat is obtained from cells or tissues, fatty acids secreted during cell growth are obtainable by biding to a hydrophobic material without an extraction process using an organic solvent in large quantities. Accordingly, a more economical, environmentally friendly bio-oil production process can be realized.
Opening claim text (preview).
What is claimed is: 1. A bacterial strain, which comprises a gene coding cytochrome c2 signal peptide ligated to a gene coding phospholipase, for secreting fatty acids toward the outside a cell by expressing the phospholipase in the periplasmic space of a bacterial cell, wherein the bacterial strain is DH5α(pRK-fabD+pIND4-cycApLA1) deposited under the Access number of KCTC12599BP or DH5α(pRK-fabH+pIND4-cycApLA2) deposited under the Access number of KCTC12600BP. 2. A method of producing fatty acids, the method comprising culturing the strain of claim 1 in medium. 3. The method of claim 2 , wherein the medium comprises a carbon source, wherein the carbon source is selected from the group consisting of glucose and glycerol. 4. The method of claim 2 , wherein the carbon source in medium has an amount of 0.1% (w/v) to 4.0% (w/v).
Carboxylic ester hydrolases {(3.1.1)} · CPC title
Ligases (6) · CPC title
Phospholipase A2 (3.1.1.4) · CPC title
Beta-ketoacyl-acyl-carrier-protein synthase III (2.3.1.180) · CPC title
Long-chain-fatty-acid-CoA ligase (6.2.1.3) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.