Reduction of carbon dioxide emission during isoprene production by fermentation

Abstract

The present invention provides methods for increasing the amount of isoprene produced by cultured cells with only a minimal increase in carbon dioxide emitted, thereby resulting in process having a greater yield of isoprene relative to carbon dioxide. In addition, the present invention provides compositions that include the cultured cells or isoprene produced there from.

We claim: 
     
         1 : Cells comprising a heterologous nucleic acid that encodes an isoprene synthase polypeptide in operable combination with a promoter wherein the cells are in culture medium comprising one or more uncommon carbon sources and wherein the ratio of carbon dioxide emitted per isoprene produced in off gas from the cultured cells is less than 500. 
     
     
         2 : The cells of  claim 1 , wherein the uncommon carbon source is selected from the group consisting of, glycerol, glycerine, dihydroxyacetone, one-carbon source, oil, animal fat, animal oil, fatty acid, lipid, phospholipid, glycerolipid, monoglyceride, diglyceride, triglyceride, microbial polypeptide, plant protein polypeptide, algae, and algae components. 
     
     
         3 : The cells of  claim 2 , wherein the uncommon carbon source is selected from the group consisting of glycerol, glycerine, cell mass, protein, alcohol, and plant-derived oil. 
     
     
         4 : The cells of  claim 1 , wherein the cells further comprise one or more heterologous nucleic acids that encode for an MVA pathway enzyme or a DXP pathway enzyme. 
     
     
         5 : The cells of  claim 4 , wherein the MVA pathway enzyme is mevalonate kinase. 
     
     
         6 : The cells of  claim 5 , wherein the mevalonate kinase is selected from the group consisting of feedback-resistant mevalonate kinase, archaeal mevalonate kinase,  M. mazei  mevalonate kinase,  Lactobacillus  mevalonate kinase polypeptide,  Lactobacillus sakei  mevalonate kinase polypeptide, yeast mevalonate kinase polypeptide,  Saccharomyces cerevisiae  mevalonate kinase polypeptide,  Streptococcus  mevalonate kinase polypeptide,  Streptococcus pneumoniae  mevalonate kinase polypeptide, and  Streptomyces  mevalonate kinase polypeptide,  Streptomyces  CL190 mevalonate kinase polypeptide. 
     
     
         7 : The cells of  claim 1 , wherein at least a portion of the cells maintain the isoprene synthase nucleic acid for at least or about 5, 10, 20, 40, 50, 60, 65, or more cell divisions in a continuous culture. 
     
     
         8 : The cells of  claim 1 , wherein the isoprene synthase polypeptide is from  Pueraria  or  Populus  or a hybrid,  Populus alba×Populus tremula.    
     
     
         9 : The cells of  claim 8 , wherein the isoprene synthase polypeptide is selected from the group consisting of  Pueraria montana  or  Pueraria lobata, Populus tremuloides, Populus alba, Populus nigra , and  Populus trichocarpa.    
     
     
         10 : The cells of  claim 1 , wherein the cells are gram-positive bacterial cells, gram-negative bacterial cells, fungal cells, or filamentous fungal cells. 
     
     
         11 : The cells of  claim 10 , wherein cells are  Escherichia cells, Pantoea cells, Trichoderma  cells, or  Aspergillus  cells, or yeast cells. 
     
     
         12 : The cells of  claim 10 , wherein the cells are selected from the group consisting of  Bacillus subtilis, Streptomyces lividans, Streptomyces coelicolor, Streptomyces griseus, Escherichia coli, Pantoea citrea, Trichoderma reesei, Aspergillus oryzae, Aspergillus niger, Yarrowia lipolytica , and  Saccharomyces cerevisiae.    
     
     
         13 : A composition for producing isoprene comprising cells of  claim 1 . 
     
     
         14 : A method of producing isoprene, the method comprising:
 (a) culturing cells of  claim 1  in culture medium under conditions suitable for the production of isoprene, wherein the culture medium comprises one or more uncommon carbon sources and the cells comprise a heterologous nucleic acid that encodes an isoprene synthase polypeptide in operable combination with a promoter; and   (b) producing isoprene, wherein the ratio of carbon dioxide emitted per isoprene produced in off gas from the cultured cells is less than 500.   
     
     
         15 : The method of  claim 14 , wherein the uncommon carbon source is selected from the group consisting of glycerol, glycerine, dihydroxyacetone, one-carbon source, oil, animal fat, animal oil, fatty acid, lipid, phospholipid, glycerolipid, monoglyceride, diglyceride, triglyceride, microbial polypeptide, plant protein polypeptide, algae, and algae components. 
     
     
         16 : The method of  claim 15  wherein the uncommon carbon source is selected from the group consisting of glycerol, glycerine, cell mass, protein, alcohol, and plant-derived oil. 
     
     
         17 : The method of  claim 16 , wherein the alcohol comprises methanol. 
     
     
         18 : The method of  claim 14 , wherein the isoprene produced as a percentage of off gas from the cultured cells is greater than 0.03%. 
     
     
         19 : The method of  claim 14 , further comprising recovering the isoprene.