Mutant
The invention relates to a mutant strain of bacteria, which either lacks or contains mutant genes for several key metabolic enzymes, and which produces high amounts of succinic acid under anaerobic conditions.
1. A method of producing succinate comprising:
a) generating a genetically engineered Escherichia coli bacterial cell comprising a disruption of:
i) lactate dehydrogenase (ldh), ii) alcohol dehydrogenase (adh), iii) aceBAK operon repressor (iclR), and iv) both acetate kinase and phosphotransacetylase (ack-pta),
b) culturing said bacteria under anaerobic conditions in a bioreactor, wherein a glycolytic flux from oxaloacetate (OAA) is partitioned in a ratio between 10-40% citrate and between 90-60% malate, wherein said bacteria produces greater than 1.5 moles of succinate per mol of glucose.
2. The method of claim 1 , wherein said glycolytic flux is partitioned in a ratio of about 30% citrate and about 70% malate.
3. The method of claim 1 , wherein said bacteria comprise an expression construct encoding pyruvate carboxylase (pyc), wherein said pyc is from Lactobacillus lactis.
4. A method of producing succinic acid comprising:
a) generating a genetically engineered Escherichia coli bacterial cell comprising a disruption of:
i) ldh, ii) adh, iii) iclR, and iv) ack-pta,
b) culturing said bacteria under anaerobic conditions in a fed-batch reactor, wherein a glycolytic flux from oxaloacetate (OAA) is partitioned in a ratio between 10-40% citrate and between 90-60% malate, wherein said bacteria produces greater than 1.5 moles of succinic acid per mol of glucose.
5. The method of claim 4 , wherein said glycolytic flux is partitioned in a ratio of about 30% citrate and about 70% malate.
6. The method of claim 4 , wherein said bacteria comprise an expression construct encoding pyc, wherein said pyc is from Lactobacillus lactis.