Methods for the Preparation of Lysine by Fermentation of Corynebacterium Glutamicum

Abstract

The present invention features methods of increasing the production of a fine chemical, e.g., lysine from a microorganism, e.g., Corynebacterium by way of deregulating an enzyme encoding gene, i.e., fructose-1,6-bisphosphatase. In a preferred embodiment, the invention provides methods of increasing the production of lysine in Corynebacterium glutamicum by way of increasing the expression of fructose-1,6-bisphosphatase activity. The invention also provides a novel process for the production of lysine by way of regulating carbon flux towards oxaloacetate (OAA). In a preferred embodiment, the invention provides methods for the production of lysine by way of utilizing fructose or sucrose as a carbon source.

1 . A method for increasing metabolic flux through the pentose phosphate pathway in a microorganism comprising culturing a microorganism comprising a gene encoding fructose-1,6-bisphosphatase which is deregulated under conditions such that metabolic flux through the pentose phosphate pathway is increased. 
     
     
         2 . The method of  claim 1 , wherein fructose or sucrose is used as a carbon source. 
     
     
         3 . The method of  claim 1 , wherein fructose is used as a carbon source. 
     
     
         4 . The method of  claim 1 , wherein the fructose-1,6-bisphosphatase gene is derived from  Corynebacterium.    
     
     
         5 . The method of  claim 1 , wherein the fructose-1,6-bisphosphatase gene is overexpressed. 
     
     
         6 . The method of  claim 1 , wherein fructose-1,6-bisphosphatase has increased activity. 
     
     
         7 . The method of  claim 1 , wherein the microorganism is a Gram positive microorganism. 
     
     
         8 . The method of  claim 1 , wherein the microorganism belongs to the genus  Corynebacterium.    
     
     
         9 . The method of  claim 8 , wherein the microorganism is  Corynebacterium glutamicum.    
     
     
         10 . The method of  claim 1 , wherein the microorganism is fermented to produce a fine chemical. 
     
     
         11 . The method of  claim 10 , wherein the fine chemical is lysine. 
     
     
         12 . The method of  claim 1 , wherein the microorganism further comprises one or more additional deregulated gene. 
     
     
         13 . The method of  claim 12 , wherein the one or more additional deregulated gene is selected from the group consisting of an ask gene, a dapA gene, an asd gene, a dapB gene, a ddh gene, a lysA gene, a lysE gene, a pycA gene, a zwf gene, a pepCL gene, a gap gene, a zwa1 gene, a tkt gene, a tad gene, a mqo gene, a tpi gene, a pgk gene, and a sigC gene. 
     
     
         14 . The method of  claim 13 , wherein the one or more additional deregulated gene is overexpressed. 
     
     
         15 . The method of  claim 12 , wherein the one or more additional deregulated gene encodes a protein selected from the group consisting of a feed-back resistant aspartokinase, a dihydrodipicolinate synthase, an aspartate semialdehyde dehydrogenase, a dihydrodipicolinate reductase, a diaminopimelate dehydrogenase, a diaminopimelate epimerase, a lysine exporter, a pyruvate carboxylase, a glucose-6-phosphate dehydrogenase, a phosphoenolpyruvate carboxylase, a glyceraldedyde-3-phosphate dehydrogenase, an RPF protein precursor, a transketolase, a transaldolase, a menaquinine oxidoreductase, a triosephosphate isomerase, a 3-phosphoglycerate kinase, and an RNA-polymerase sigma factor sigC. 
     
     
         16 . The method of  claim 15 , wherein the protein has increased activity. 
     
     
         17 . The method of  claim 12 , wherein the one or more additional deregulated gene is selected from the group consisting of a pepCK gene, a mal E gene, a glgA gene, a pgi gene, a dead gene, a menE gene, a citE gene, a mikE17 gene, a poxB gene, a zwa2 gene, and a sucC gene. 
     
     
         18 . The method of  claim 17 , wherein the one or more additional deregulated gene is attenuated, decreased or repressed. 
     
     
         19 . The method of  claim 12 , wherein the one or more additional deregulated gene encodes a protein selected from the group consisting of a phosphoenolpyruvate carboxykinase, a malic enzyme, a glycogen synthase, a glucose-6-phosphate isomerase, an ATP dependent RNA helicase, an o-succinylbenzoic acid-CoA ligase, a citrate lyase beta chain, a transcriptional regulator, a pyruvate dehydrogenase, an RPF protein precursor, and a Succinyl-CoA-Synthetase. 
     
     
         20 . The method of  claim 19 , wherein the protein has decreased activity. 
     
     
         21 . A method for producing a fine chemical comprising:
 a) culturing a microorganism in which fructose-1,6-bisphosphatase is deregulated; and   b) accumulating the fine chemical in the medium or in the cells of the microorganisms, thereby producing a fine chemical.   
     
     
         22 . A method for producing a fine chemical comprising culturing a microorganism in which at least fructose-1,6-bisphosphatase expression or activity is deregulated under conditions such that the fine chemical is produced. 
     
     
         23 . The method of  claim 22 , wherein fructose-1,6-bisphosphatase expression is increased. 
     
     
         24 . The method of  claim 22 , wherein fructose-1,6-bisphosphatase activity is increased. 
     
     
         25 . The method of  claim 22 , further comprising recovering the fine chemical. 
     
     
         26 . The method of  claim 22 , wherein one or more additional gene is deregulated. 
     
     
         27 . The method of  claim 26 , wherein the one or more additional deregulated gene is selected from the group consisting of an ask gene, a dapA gene, an asd gene, a dapB gene, a ddh gene, a lysA gene, a lysE gene, a pycA gene, a zwf gene, a pepCL gene, a gap gene, a zwa1 gene, a tkt gene, a tad gene, a mqo gene, a tpi gene, a pgk gene, and a sigC gene. 
     
     
         28 . The method of  claim 27 , wherein the one or more additional deregulated gene is overexpressed. 
     
     
         29 . The method of  claim 26 , wherein the one or more additional deregulated gene encodes a protein selected from the group consisting of a feed-back resistant aspartokinase, a dihydrodipicolinate synthase, an aspartate semialdehyde dehydrogenase, a dihydrodipicolinate reductase, a diaminopimelate dehydrogenase, a diaminopimelate epimerase, a lysine exporter, a pyruvate carboxylase, a glucose-6-phosphate dehydrogenase, a phosphoenolpyruvate carboxylase, a glyceraldedyde-3-phosphate dehydrogenase, an RPF protein precursor, a transketolase, a transaldolase, a menaquinine oxidoreductase, a triosephosphate isomerase, a 3-phosphoglycerate kinase, and an RNA-polymerase sigma factor sigC. 
     
     
         30 . The method of  claim 29 , wherein the protein has increased activity. 
     
     
         31 . The method of  claim 26 , wherein the one or more additional deregulated gene is selected from the group consisting of a pepCK gene, a mal E gene, a glgA gene, a pgi gene, a dead gene, a menE gene, a citE gene, a mikE17 gene, a poxB gene, a zwa2 gene, and a sucC gene. 
     
     
         32 . The method of  claim 31 , wherein the one or more additional deregulated gene is attenuated, decreased or repressed. 
     
     
         33 . The method of  claim 26 , wherein the one or more additional deregulated gene encodes a protein selected from the group consisting of a phosphoenolpyruvate carboxykinase, a malic enzyme, a glycogen synthase, a glucose-6-phosphate isomerase, an ATP dependent RNA helicase, an o-succinylbenzoic acid-CoA ligase, a citrate lyase beta chain, a transcriptional regulator, a pyruvate dehydrogenase, an RPF protein precursor, and a Succinyl-CoA-Synthetase. 
     
     
         34 . The method of  claim 33 , wherein the protein has decreased activity. 
     
     
         35 . The method of  claim 22 , wherein the microorganism is a Gram positive microorganism. 
     
     
         36 . The method of  claim 22 , wherein the microorganism belongs to the genus  Corynebacterium.    
     
     
         37 . The method of  claim 36 , wherein the microorganism is  Corynebacterium glutamicum.    
     
     
         38 . The method of  claim 22 , wherein the fine chemical is lysine. 
     
     
         39 . The method of  claim 38 , wherein lysine is produced at a yield of at least 100 g/L. 
     
     
         40 . The method of  claim 38 , wherein lysine is produced at a yield of at least 150 g/L. 
     
     
         41 . The method of  claim 22 , wherein fructose or sucrose is used as a carbon source. 
     
     
         42 . The method of  claim 22 , wherein fructose is used as a carbon source. 
     
     
         43 . The method of  claim 22 , wherein fructose-1,6-bisphosphatase comprises the nucleotide sequence of SEQ ID NO:1. 
     
     
         44 . The method of  claim 22 , wherein fructose-1,6-bisphosphatase encodes a polypeptide comprising the amino acid sequence of SEQ ID NO:2. 
     
     
         45 . A recombinant microorganism comprising a deregulated gene encoding fructose-1,6-bisphosphatase. 
     
     
         46 . The recombinant microorganism of  claim 45 , wherein fructose-1,6-bisphosphatase expression is increased. 
     
     
         47 . The recombinant microorganism of  claim 45 , wherein said fructose-1,6-bisphosphatase gene encodes a fructose-1,6-bisphosphatase protein having increased activity. 
     
     
         48 . The recombinant microorganism of  claim 45 , wherein the microorganism belongs to the genus  Corynebacterium.    
     
     
         49 . The recombinant microorganism of  claim 45 , wherein the microorganism is  Corynebacterium glutamicum.    
     
     
         50 . A polypeptide encoded by the nucleotide sequence of SEQ ID NO:1, wherein said polypeptide has fructose-1,6-bisphosphatase activity.