US2017175147A1PendingUtilityA1

Production of volatile dienes by enzymatic dehydration of light alkenols

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Assignee: SCIENTIST OF FORTUNE SAPriority: Aug 29, 2012Filed: Feb 27, 2017Published: Jun 22, 2017
Est. expiryAug 29, 2032(~6.1 yrs left)· nominal 20-yr term from priority
C12P 5/026C12P 5/007C12Y 402/01127C12N 9/88
67
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Claims

Abstract

Described is a method for generating conjugated dienes through a biological process. More specifically, the application describes a method for producing conjugated dienes (for example butadiene, isoprene or dimethylbutadiene) from light alkenols via enzymatic dehydration, in particular by making use of an alkenol dehydratase.

Claims

exact text as granted — not AI-modified
1 . A method for producing a conjugated diene characterized in that it comprises a step of enzymatically converting a compound responding to the general formula C n H 2n O into C n H 2n-2 +H 2 0, with 3<n<7, by making use of an alkenol dehydratase. 
     
     
         2 . The method of  claim 1  wherein the compound responding to the general formula C n H 2n O, with 3<n<7, is a primary allyl alcohol (PRA) of the formula I: 
       
         
           
           
               
               
           
         
         wherein R 1  and R 2  are independently selected from H and CH 3 . 
       
     
     
         3 . The method of  claim 1  wherein the compound responding to the general formula C n H 2n O, with 3<n<7, is a secondary or tertiary allyl alcohol (STA) of the formula II: 
       
         
           
           
               
               
           
         
         wherein R 1  and R 2  are independently selected from H and CH 3 . 
       
     
     
         4 . The method of  claim 1  wherein the compound responding to the general formula C n H 2n O, with 3<n<7, is a primary homoallyl alcohol (PHA) of the formula Ill: 
       
         
           
           
               
               
           
         
         wherein R 1  and R 2  are independently selected from H and CH 3 . 
       
     
     
         5 . The method of  claim 1  which is carried out in vitro. 
     
     
         6 . The method of  claim 1  characterized in that the method is carried by making use of a microorganism producing an alkenol dehydratase. 
     
     
         7 . The method of  claim 6 , wherein the microorganism is capable of producing a compound responding to the general formula C n H 2n O, with 3<n<7. 
     
     
         8 . Use of an alkenol dehydratase or of a microorganism producing an alkenol dehydratase for converting a compound responding to the general formula C n H 2n O into C n H 2n-2 +H 2 0, with 3<n<7. 
     
     
         9 . A composition comprising an organism which produces an alkenol dehydratase and a compound responding to the general formula C n H 2n O, with 3<n<7. 
     
     
         10 . A composition comprising an alkenol dehydratase and a compound responding to the general formula C n H 2n O, with 3<n<7. 
     
     
         11 . The method of  claim 1 , wherein the alkenol dehydratase is a protein which comprises the amino acid sequence as shown in SEQ ID NO: 1 or an amino acid sequence which is at least 30% identical to the amino acid sequence shown in SEQ ID NO: 1 and which shows the enzymatic activity of converting a compound responding to the general formula C n H 2n O into C n H 2n-2 +H 2 0, with 3<n<7. 
     
     
         12 . The method of  claim 1  wherein n is 4 and the produced diene compound is butadiene. 
     
     
         13 . The method of  claim 1 , wherein n is 5 and the produced diene compound is isoprene. 
     
     
         14 . The method of  claim 1 , wherein n is 6 and the produced diene compound is dimethyl-butadiene.

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