Methods for the synthesis of lactic acid using crabtree-negative yeast transformed with the lactate dehydrogenase gene
View Patent ↗The invention provides methods and materials related to the production of lactic acid. Specifically, the invention provides methods for producing lactic acid using a crabtree-negative yeast, such as of the Kluyveromyces, Pichia, Candida, Trichosporon and Yamadazmya genera, which have been transformed with a lactate dehydrogenase gene.
1. A method for making lactic acid, comprising
a) providing a microorganism exhibiting a crabtree-negative phenotype selected from the group consisting of Kluyveromyces, Pichia, and Hansenula and transformed with at least one exogenous gene encoding a naturally-occurring bovine, bacterial or fungal lactate dehydrogenase;
b) culturing said crabtree-negative microorganism in a first culture medium which includes a carbon source comprising glucose and under a first set of culture conditions, including a dissolved oxygen content of at least 20 percent relative to the amount present at saturated conditions with air at atmospheric pressure, which promote cellular respiration; and
c) then culturing the crabtree-negative microorganism in a culture medium which includes a carbon source comprising glucose under a second set of culture conditions, including a dissolved oxygen content of less than 2.0 percent relative to the amount present at saturated conditions with air at atmospheric pressure, which promote the production of lactic acid.
2. The method of claim 1 , wherein in step b) the first set of culture conditions include a dissolved oxygen content of at least 50% relative to the amount present at saturated conditions with air at atmospheric pressure.
3. A method for making lactic acid, comprising
a) providing a microorganism exhibiting a crabtree-negative phenotype selected from the group consisting of Kluyveromyces, Pichia, and Hansenula and transformed with at least one exogenous gene encoding a naturally-occurring bovine, bacterial or fungal lactate dehydrogenase;
b) culturing said crabtree-negative microorganism in a first culture medium which includes a carbon source comprising glucose and under a first set of culture conditions which promote cellular respiration; and
c) then culturing the crabtree-negative microorganism in a culture medium which includes a carbon source comprising glucose under a second set of culture conditions, including an acidic pH of greater than 1.5, which promote the production of lactic acid.
4. A method for making lactic acid, comprising
a) providing a microorganism exhibiting a crabtree-negative phenotype selected from the group consisting of Kluyveromyces thermotolerans, Kluyveromyces lactis and Kluyveromyces marxianus and transformed with at least one exogenous gene encoding a naturally-occurring bovine, bacterial or fungal lactate dehydrogenase;
b) culturing said crabtree-negative microorganism in a first culture medium which includes a carbon source comprising glucose and under a first set of culture conditions which promote cellular respiration; and
c) then culturing the crabtree-negative microorganism in a culture medium which includes a carbon source comprising glucose under a second set of culture conditions which promote the production of lactic acid.
5. The method of claim 4 wherein the first set of culture conditions includes a dissolved oxygen content of greater than 20 percent relative to the amount present at saturated conditions with air at atmospheric pressure and the second set of culture conditions includes a dissolved oxygen content of less than 2.0 percent relative to the amount present at saturated conditions with air at atmospheric pressure.
6. The method of claim 5 wherein the second set of culture conditions includes an acidic pH of greater than 1.5.
7. The method of claim 6 wherein the microorganism is Kluyveromyces marxianus.
8. A method for making lactic acid, comprising
a) providing a microorganism exhibiting a crabtree-negative phenotype selected from the group consisting of Kluyveromyces, Pichia, and Hansenula and transformed with at least one exogenous gene encoding a naturally-occurring bovine, bacterial or fungal lactate dehydrogenase and having a reduced pyruvate decarboxylase activity due to a knock-out of a native pyruvate decarboxylase gene;
b) culturing said crabtree-negative microorganism in a first culture medium which includes a carbon source comprising glucose and under a first set of culture conditions which promote cellular respiration; and
c) then culturing the crabtree-negative microorganism in a culture medium which includes a carbon source comprising glucose under a second set of culture conditions which promote the production of lactic acid.
9. The method of claim 8 wherein the microorganism is selected from the group consisting of Kluyveromyces thermotolerans, Kluyveromyces lactis and Kluyveromyces marxianus.
10. The method of claim 9 wherein the first set of culture conditions includes a dissolved oxygen content of greater than 20 percent relative to the amount present at saturated conditions with air at atmospheric pressure and the second set of culture conditions includes a dissolved oxygen content of less than 2.0 percent relative to the amount present at saturated conditions with air at atmospheric pressure.
11. The method of claim 5 wherein the second set of culture conditions includes a pH of 2.5 to 6.25.