Systems and methods for measuring cell signaling protein activity
US-2024230643-A9 · Jul 11, 2024 · US
US9688976B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9688976-B2 |
| Application number | US-201615057551-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 1, 2016 |
| Priority date | Mar 4, 2015 |
| Publication date | Jun 27, 2017 |
| Grant date | Jun 27, 2017 |
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Disclosed herein are a transformed Synechococcus elongatus strain having improved capability of producing acetone and a method for producing acetone and a method for removing carbon dioxide using the same. In an aspect, the transformed Synechococcus elongatus strain of the present disclosure can produce acetone with high selectivity using carbon dioxide as a carbon source. The present disclosure is economical because the Synechococcus elongatus strain can economically produce high value-added acetone using carbon dioxide existing in the atmosphere as a carbon source without requiring an additional catalytic reaction. Also, the present disclosure is environment-friendly because carbon dioxide in the atmosphere can be removed or reduced using the microorganism.
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What is claimed is: 1. A Synechococcus elongatus strain being capable of enhanced production of acetone, wherein the strain comprises: one or more selected from a group consisting of: an acetyl-CoA transferase gene containing SEQ ID NO: 1 and an acetyl-CoA synthase gene contains SEQ ID NO: 2; an acetoacetyl-CoA transferase gene containing SEQ ID NO: 3 or SEQ ID NO: 4; and an acetoacetate decarboxylase gene containing SEQ ID NO: 5, wherein the strain produces acetone in a molar ratio of 0.8 or greater in the total product under a condition of 30° C. and 5% carbon dioxide. 2. The strain according to claim 1 , wherein the strain is one transformed with a vector comprising: one or more selected from a group consisting of an acetyl-CoA transferase gene containing SEQ ID NO: 1 and an acetyly-CoA synthase gene containing SEQ ID NO: 2; an acetoacetyl-CoA transferase gene containing SEQ ID NO: 3 or SEQ ID NO: 4; and an acetoacetate decarboxylase gene containing SEQ ID NO: 5. 3. The strain according to claim 2 , wherein the strain is Synechococcus elongatus PCC7942 transformed with the vector. 4. The strain according to claim 2 , wherein the vector further comprises: a pUC replication origin as a replication origin; neutral sites located upstream and downstream of the replication origin; a spectinomycin resistance gene as a selection marker; a repressor selected from a group consisting of a lac I repressor, a tetR repressor and an AraC repressor; a promoter selected from a group consisting of a trc promoter, a tetA promoter or a modified tetA promoter, a BAD promoter and a cbbL promoter; and a BglII site, a BamHI site, an EcoRI site and an XhoI site as restriction enzyme sites. 5. The strain according to claim 4 , wherein one or more selected from a group consisting of an acetyl-CoA transferase gene containing SEQ ID NO: 1 and an acetyl-CoA synthase gene containing SEQ ID NO: 2; an acetoacetyl-CoA transferase gene containing SEQ ID NO: 3 or SEQ ID NO: 4; and an acetoacetate decarboxylase gene containing SEQ ID NO: 5 are located between the BglII site and the BamHI site. 6. The strain according to claim 2 , wherein the vector comprises a sequence from SEQ ID NOS: 6-9. 7. The strain according to claim 1 , wherein the strain is a Synechococcus elongatus strain of accession number KCTC12758BP, KCTC12759BP, KCTC12760BP or KCTC12761BP. 8. The strain according to claim 1 , wherein the strain absorbs and fixes carbon dioxide.
Cross-Sectional Technologies · mapped topic
transferring sulfur containing groups (2.8) · CPC title
Lyases (4.) · CPC title
Acetate-CoA ligase (6.2.1.1) · CPC title
Butyrate--acetoacetate CoA-transferase (2.8.3.9) · CPC title
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