초록 ▼

A process for producing plasmid DNA E. coli cells comprises a pre-culture and fed-batch process. The culture media of the batch phase and the culture medium added during the feeding phase are chemically defined. The culture medium of the feeding phase contains a growth-limiting substrate and is adde

A process for producing plasmid DNA E. coli cells comprises a pre-culture and fed-batch process. The culture media of the batch phase and the culture medium added during the feeding phase are chemically defined. The culture medium of the feeding phase contains a growth-limiting substrate and is added, for at least a fraction of the feeding phase, at a feeding rate that follows a pre-defined exponential function, thereby controlling the specific growth rate at a pre-defined value. The process results in high yield and homogeneity of plasmid DNA.

대표청구항 ▼

1. A process for producing plasmid DNA on a manufacturing scale, said process comprised of the steps of: a) growing E. coli cells that bear a plasmid carrying a gene of interest in a pre-culture and subsequently fermenting in a main culture, wherein the E. coli cells are from E. coli K-12 strain JM1

1. A process for producing plasmid DNA on a manufacturing scale, said process comprised of the steps of: a) growing E. coli cells that bear a plasmid carrying a gene of interest in a pre-culture and subsequently fermenting in a main culture, wherein the E. coli cells are from E. coli K-12 strain JM108 or a derivative thereof;b) recovering and purifying the plasmid DNA from the main culture;wherein the main culture is subjected to a fed-batch process comprising a batch phase and a feeding phase, wherein the batch phase and the feeding phase each comprises a chemically defined culture medium comprising a growth-limiting substrate, and wherein the feeding phase commences after the batch phase and wherein the culture medium of the feeding phase is added at a feeding rate (Ft) that follows, for at least a fraction of the feeding phase, the pre-defined exponential function of Ft=μ⋆X0YX/S⋆CS⋆eμ⁢⁢t,whereinFt is the flow rate [L/h] of the feed medium;X0 is the total amount of biomass dry cell weight [g] at start of the feeding phase;YX/S is the biomass yield coefficient (g dry cell weight per g substrate);CS is the concentration of said substrate in said feed medium [g/L];μ is the specific growth rate [h−1]; andt is the time interval [h] from start of the feeding phase, andwherein said fraction of said feeding phase during which said feeding rate follows said exponential function is such that a constant specific growth rate ranging from 0.03 to 1.5 h−1 is achieved over the entire fraction of the feeding phase. 2. The process of claim 1, wherein said preculture medium is chemically defined. 3. The process of claim 1, wherein the plasmid has a ColE1-type origin of replication. 4. The process of claim 3, wherein the plasmid is a pUC plasmid. 5. The process of claim 1, wherein a specific plasmid DNA yield of about 20 to about 45 mg/g DCW is obtained. 6. The process of claim 1, wherein the feeding rate is increased by continuously adding the medium following said exponential function. 7. The process of claim 1, wherein the feeding rate is increased in a semi-continuous mode by adding the medium step-wise following said exponential function. 8. The process of claim 1, wherein the feeding rate is increased in a discontinuous mode by adding the medium pulse-wise following said exponential function. 9. The process of claim 1, wherein the exponential function of the feeding rate is based on measurements of the amount of biomass. 10. The process of claim 1, wherein the growth limiting substrate is a carbon source. 11. The process of claim 10, wherein said carbon source is glucose. 12. The process of claim 1, wherein the growth rate is about 0.03 to about 0.2 h−1. 13. The process of claim 1, wherein the medium of the batch culture at the start of fermentation is comprised of ammonium salts as the nitrogen source. 14. The process of claim 13, wherein the ammonium salt is ammonium chloride. 15. The method of claim 1, wherein the pH value of the main culture is adjusted by addition of ammonium hydroxide. 16. The process of claim 1, wherein said culture media are free of antibiotics. 17. The process of claim 16, wherein the culture media used in the pre-culture is free of antibiotics. 18. The process of claim 1, wherein said culture medium of said batch phase and said feeding phase is comprised of a) an organic carbon source selected from glucose, glycerol, fructose, lactose, sucrose, arabinose, or a mixture thereof;b) an anorganic nitrogen source selected from ammonium salts and ammonium hydroxide, wherein the nitrogen source is present as a component of the medium or added to the medium during fermentation;c) inorganic salts; andd) isoleucine. 19. The process of claim 18, wherein said culture medium further comprises one or more substances that complement an auxotrophy of the E. coli strain. 20. The process of claim 18, wherein said culture medium is a batch medium present at the start of a batch fermentation or at the start of the batch phase of a fed-batch fermentation and is comprised of: a) glucose in concentration of about 10 to about 30 g/L;b) an ammonium salt or ammonium hydroxide in a concentration such that the ammonium concentration is about 0.5 to about 2 g/L;c) inorganic ions that serve as a supply with macro and micro elements; andd) isoleucine in a concentration of about 0.1 to about 0.3 g/L. 21. The process of claim 20, wherein said culture medium further comprises one or more substances that complement an auxotrophy of the E. coli strain. 22. The process of claim 18, wherein said culture medium is a feed medium that is added during the feeding phase of a fed-batch fermentation and is comprised of: a) glucose in concentration of about 300 to about 500 g/L;b) inorganic ions that serve to supply with macro and micro elements; andc) isoleucine in a concentration of about 6 g/L. 23. The process of claim 22, wherein said culture medium further comprises one or more substances that complement an auxotrophy of the E. coli strain. 24. The process of claim 1, wherein the medium of the feeding phase comprises isoleucine and wherein said isoleucine increases the yield of plasmid DNA in said process as compared to when the medium of the feeding phase does not comprise isoleucine. 25. The process of claim 24, wherein the medium of the batch culture comprises isoleucine in a concentration of about 0.05 to about 2 g/L. 26. The process of claim 1, wherein said fraction of said feeding phase during which said feeding rate follows said exponential function is such that more than about 20% of the total dry cell weight that is obtained in the feeding phase is generated during said fraction.