MICROORGANISMS AND PROCESSES FOR THE PRODUCTION OF ISOPRENE
The present invention provides a novel biosynthetic pathway for the production of isoprene from 3-methyl-2-buten-1-ol or 2-methyl-3-buten-2-ol. Further embodiments provide non-naturally occurring microorganism that have been modified to produce isoprene from 3-methyl-2-buten-1-ol or 2-methyl-3-buten-2-ol and methods of producing isoprene using said microorganism.
1 . A method of producing isoprene, the method comprising the steps of:
a) optionally converting 3-methyl-2-buten-1-ol to 2-methyl-3-buten-2-ol using a 2-methyl-3-buten-2-ol isomerase enzyme; and
b) converting 2-methyl-3-buten-2-ol to isoprene using a 2-methyl-3-buten-2-ol dehydratase enzyme.
2 . The method of claim 1 , wherein the 2-methyl-3-buten-2-ol isomerase enzyme is expressed by an exogenous nucleic acid in a microbial organism.
3 . The method of claim 1 , wherein the 2-methyl-3-buten-2-ol dehydratase enzyme is expressed by an exogenous nucleic acid in a microbial organism.
4 . The method of claim 1 , wherein the 2-methyl-3-buten-2-ol dehydratase is a bi-functional enzyme further comprising 2-methyl-3-buten-2-ol isomerase activity.
5 . The method of claim 4 , wherein the 2-methyl-3-buten-2-ol dehydratase is a linalool dehydratase-isomerase.
6 . The method of claim 5 , wherein the linalool dehydratase-isomerase is derived from Castellaniella defragrans.
7 . The method of claim 5 , wherein the linalool dehydratase-isomerase is expressed by an exogenous nucleic acid in microbial organism.
8 . The method of claim 2 , wherein the microbial organism is selected from bacteria, archaea, eubacteria, yeast and fungi.
9 . The method of claim 8 , wherein the microbial organism is an Escherichia coli.
10 . The method of claim 3 , wherein the microbial organism is selected from bacteria, archaea, eubacteria, yeast and fungi.
11 . The method of claim 10 , wherein the microbial organism is an Escherichia coli.
12 . The method of claim 7 , wherein the microbial organism is an Escherichia coli.