US10385327B2ActiveUtilityA1

Enhanced E. coli for the production of fatty acids and method of producing the same

Assignee: BAERGA ORTIZ ABELPriority: Jan 5, 2012Filed: Jan 5, 2012Granted: Aug 20, 2019
Est. expiryJan 5, 2032(~5.5 yrs left)· nominal 20-yr term from priority
C12N 9/88C12N 15/70
28
PatentIndex Score
0
Cited by
6
References
7
Claims

Abstract

The invention analyzed a protein sequence using the Udwary-Merski algorithm and identified a tetradomain fragment (DH1-DH2-UMA) which consists of two predicted DH-like domains and two pseudodomains N-terminal to them. This arrangement of domains and pseudodomains is fundamentally the opposite of what is typically observed in the DH cassettes of actinobacterial polyketide synthases or mammalian fatty acid synthases, both of which feature C-terminal pseudodomains. The invention modified E. coli by over expressing DH1-DH2-UMA in E. coli resulting in an increase in the overall production of all the fatty acids normally present in the E. coli fatty acid profile.

Claims

exact text as granted — not AI-modified
We claim: 
     
       1. A gene vector for modifying  Escherichia coli  ( E. coli ) comprising:
 the dehydratase tetradomain gene fragment DH1-DH2-UMA from  Photobacterium profundum  of SEQ ID:17 cloned into the plasmid vector of SEQ ID:15. 
 
     
     
       2. The gene vector of  claim 1 , wherein said dehydratase tetradomain gene fragment encodes a DH1-DH2 protein. 
     
     
       3. The gene vector of  claim 1 , wherein said gene vector modifies  E. coli  to produce about 4-5 times more free saturated and monounsaturated fatty acids than wild-type  E. coli.    
     
     
       4. The gene vector of  claim 1 , wherein said dehydratase tetradomain gene fragment is over-expressed at about room temperature. 
     
     
       5. A method for increasing the production of free saturated and monounsaturated fatty acids in  E. coli  comprising:
 cloning the dehydratase tetradomain gene fragment DH1-DH2-UMA from  Photobacterium profundum  of SEQ ID: 17 into the plasmid vector of SEQ ID:15; and 
 inserting said cloned vector into  E. coli.    
 
     
     
       6. The method of  claim 5 , wherein said dehydratase tetradomain gene fragment is over-expressed at about room temperature. 
     
     
       7. The method of  claim 5 , wherein said dehydratase tetradomain gene fragment encodes a DH1-DH2 protein.

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