Methods for organic acid production
Microbial cell lines suitable for industrial-scale production of organic acids and methods of making and isolating such cell lines, and using the cell lines for production of organic acids.
1 . A method of producing an organic acid selected from propionic acid, lactic acid, acetic acid, butyric acid, or combinations thereof, the method comprising:
providing a P. acidipropionici cell comprising one or more loss of function mutations in genes encoding DUF1116 domain-containing protein comprising the amino acid sequence of SEQ ID NO:26 and M18 family aminopeptidase comprising the amino acid sequence SEQ ID NO: 24; and
culturing the cell in a culture medium.
2 . The method of claim 1 , wherein the culture medium is maintained at a pH of from about 5.5-7.5.
3 . The method of claim 2 , wherein the culture medium is maintained at a pH of from about 6.0-7.0.
4 . The method of claim 1 , wherein said culturing is carried out at about 30° C. for about 60 to about 120 hours.
5 . The method of claim 1 , wherein the P. acidipropionici cell further comprises one or more additional mutations in a gene encoding O-antigen ligase domain-containing protein comprising the amino acid sequence of SEQ ID NO:9; adenine glycosylase comprising the amino acid sequence of SEQ ID NO:19; amino acid permease comprising the amino acid sequence of SEQ ID NO:17; class I SAM-dependent methyltransferase comprising the amino acid sequence of SEQ ID NO: 1, MFS transporter comprising the amino acid sequence of SEQ ID NO: 2, LemA family protein comprising the amino acid sequence of SEQ ID NO: 3, Flavin reductase comprising the amino acid sequence of SEQ ID NO: 4, comprising the amino acid sequence of SEQ ID NO: 5, MFS transporter comprising the amino acid sequence of SEQ ID NO: 6, glycosyl transferase family 1 comprising the amino acid sequence of SEQ ID NO: 7, protein comprising the amino acid sequence of SEQ ID NO: 8, O-antigen ligase domain-containing protein comprising the amino acid sequence of SEQ ID NO: 10, penicillin-binding protein comprising the amino acid sequence of SEQ ID NO: 11, phosphotransferase comprising the amino acid sequence of SEQ ID NO: 12, alpha/beta hydrolase comprising the amino acid sequence of SEQ ID NO:13, protein comprising the amino acid sequence of SEQ ID NO:14, gfo/Idh/MocA family oxidoreductase comprising the amino acid sequence of SEQ ID NO: 15, alpha/beta hydrolase comprising the amino acid sequence of SEQ ID NO: 16, protein comprising the amino acid sequence of SEQ ID NO: 18, protein comprising the amino acid sequence of SEQ ID NO: 20, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit comprising the amino acid sequence of SEQ ID NO:21, amino acid permease comprising the amino acid sequence of SEQ ID NO:22, protein comprising the amino acid sequence of SEQ ID NO: 23, ATPase comprising the amino acid sequence of SEQ ID NO:25, glycosyl transferase comprising the amino acid sequence of SEQ ID NO:27, acetyl-Co A carboxylase biotin carboxyl carrier protein subunit comprising the amino acid sequence of SEQ ID NO:28, and penicillin-binding protein comprising the amino acid sequence of SEQ ID NO:29.
6 . The method of claim 1 , wherein the P. acidipropionici cell comprises a loss of function mutation in each of the genes encoding the proteins DUF1116 domain-containing protein comprising the amino acid sequence of SEQ ID NO:26, M18 family aminopeptidase comprising the amino acid sequence SEQ ID NO:24, O-antigen ligase domain-containing protein comprising the amino acid sequence of SEQ ID NO:9, adenine glycosylase comprising the amino acid sequence of SEQ ID NO:19, amino acid permease comprising the amino acid sequence of SEQ ID NO:17, class I SAM-dependent methyltransferase comprising the amino acid sequence of SEQ ID NO: 1, MFS transporter comprising the amino acid sequence of SEQ ID NO: 2, LemA family protein comprising the amino acid sequence of SEQ ID NO: 3, Flavin reductase comprising the amino acid sequence of SEQ ID NO: 4, comprising the amino acid sequence of SEQ ID NO: 5, MFS transporter comprising the amino acid sequence of SEQ ID NO: 6, glycosyl transferase family 1 comprising the amino acid sequence of SEQ ID NO: 7, protein comprising the amino acid sequence of SEQ ID NO: 8, O-antigen ligase domain-containing protein comprising the amino acid sequence of SEQ ID NO: 10, penicillin-binding protein comprising the amino acid sequence of SEQ ID NO: 11, phosphotransferase comprising the amino acid sequence of SEQ ID NO: 12, alpha/beta hydrolase comprising the amino acid sequence of SEQ ID NO: 13, protein comprising the amino acid sequence of SEQ ID NO:14, gfo/Idh/MocA family oxidoreductase comprising the amino acid sequence of SEQ ID NO: 15, alpha/beta hydrolase comprising the amino acid sequence of SEQ ID NO: 16, protein comprising the amino acid sequence of SEQ ID NO: 18, protein comprising the amino acid sequence of SEQ ID NO: 20, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit comprising the amino acid sequence of SEQ ID NO:21, amino acid permease comprising the amino acid sequence of SEQ ID NO:22, protein comprising the amino acid sequence of SEQ ID NO: 23, ATPase comprising the amino acid sequence of SEQ ID NO:25, glycosyl transferase comprising the amino acid sequence of SEQ ID NO:27, acetyl-Co A carboxylase biotin carboxyl carrier protein subunit comprising the amino acid sequence of SEQ ID NO:28, and penicillin-binding protein comprising the amino acid sequence of SEQ ID NO:29.
7 . The method of claim 1 , wherein the P. acidipropionici cell is the P. acidipropionici cell deposited in the American Type Culture Collection under Accession Number ATCC PTA-125895.
8 . The method of claim 1 , wherein the organic acid is propionic acid.
9 . The method of claim 1 , wherein the amount of organic acid produced by the method after 60 hours of culturing is at least 15% higher as compared to the amount of organic acid produced under the same conditions using wild-type P. acidipropionici.