Method of culturing microorganisms using phototrophic and mixotrophic culture conditions

Patent metadata

Field	Value
Publication number	US-9758756-B2
Application number	US-201514699633-A
Country	US
Kind code	B2
Filing date	Apr 29, 2015
Priority date	Nov 9, 2012
Publication date	Sep 12, 2017
Grant date	Sep 12, 2017

Abstract

Methods of culturing microorganisms in combinations of phototrophic, mixotrophic, and heterotrophic culture conditions are disclosed. A culture of microorganisms may be transitioned between culture conditions over the life of a culture in various combinations, utilizing various conditions in a sequential manner to optimize the culture for growth or product accumulation.

First claim

What is claimed is:

1. A method of culturing microorganisms, comprising:
a. Providing a culture of microorganisms in an aqueous culture medium capable of growth on light as an energy source, carbon dioxide as a carbon source, and at least one organic carbon source as an energy and carbon source;
b. Decreasing at least one of a total fat, oleic acid, and palmitic acid as a percentage of cell dry weight in the culture of microorganisms by transitioning the culture of microorganisms from mixotrophic culture conditions to phototrophic culture conditions, wherein:
i. Phototrophic culture conditions comprise a supply of light, a supply of carbon dioxide, and the absence of a supply of an organic carbon source; and
ii. Mixotrophic culture conditions comprise a supply of light, and a supply of at least one organic carbon source;

c. Wherein the transition from mixotrophic culture conditions to phototrophic culture conditions occurs when at least one threshold condition of the culture is met, the at least one threshold condition comprising:
i. A detected level of dissolved oxygen;
ii. A detected level of contaminating organisms; and
iii. A detected level of cell culture density.

2. The method of claim 1 , wherein the culture of microorganisms comprises at least one selected from the group consisting of microalgae and cyanobacteria.

3. The method of claim 2 , wherein the microalgae comprises Chlorella.

4. The method of claim 1 , wherein the at least one organic carbon source is selected from the group consisting of acetate, acetic acid, ammonium linoleate, arabinose, arginine, aspartic acid, butyric acid, cellulose, citric acid, ethanol, fructose, fatty acids, galactose, glucose, glycerol, glycine, lactic acid, lactose, maleic acid, maltose, mannose, methanol, molasses, peptone, plant based hydrolyzate, proline, propionic acid, ribose, sacchrose, partial or complete hydrolysates of starch, sucrose, tartaric, TCA-cycle organic acids, thin stillage, urea, industrial waste solutions, and yeast extracts.

5. The method of claim 1 , wherein the transition between culture conditions is automated by a computer and programmable logic controller receiving input from at least one sensor detecting the at least one threshold condition to control at least one of the supply of light, supply of carbon dioxide, and supply of the at least one organic carbon source.

6. The method of claim 1 , wherein the culture of microorganisms transitions from mixotrophic to phototrophic culture conditions when the detected dissolved oxygen level is below a threshold level.

7. The method of claim 1 , wherein the culture of microorganisms transitions from mixotrophic to phototrophic culture conditions when the detected level of contaminating organisms is above a threshold level.

8. The method of claim 1 , wherein the culture of microorganisms transitions from mixotrophic to phototrophic conditions when the detected level of cell culture density is above a threshold value.

9. The method of claim 1 , wherein the decrease of total fat as percentage of dry weight in the culture of microorganisms by transitioning from mixotrophic culture conditions to phototrophic culture conditions is up to 62%.

10. The method of claim 1 , wherein the decrease of oleic acid as percentage of dry weight in the culture of microorganisms by transitioning from mixotrophic culture conditions to phototrophic culture conditions is up to 86%.

11. The method of claim 1 , wherein the decrease of palmitic acid as percentage of dry weight in the culture of microorganisms by transitioning from mixotrophic culture conditions to phototrophic culture conditions is up to 58%.

12. The method of claim 1 , wherein the transition from mixotrophic culture conditions to phototrophic culture conditions further results in a suppression of the contaminating organisms below a level of 25% of total cells in the culture.

13. The method of claim 6 , wherein the threshold level of dissolved oxygen is in the range of 0.1 to 30 mg O 2 /L.

14. The method of claim 13 , wherein the threshold level of dissolved oxygen is in the range of 0.1 to 6 mg O 2 /L.

15. The method of claim 13 , wherein the threshold level of dissolved oxygen is in the range of 10 to 30 mg O 2 /L.

Assignees

• Heliae Dev Llc

Inventors

• Ganuza Taberna Eneko
• Licamele Jason D
• Tonkovich Anna Lee
• Bellefeuille Michael V
• Wyatt Cameron

Classifications

• C12Q3/00

  Condition responsive control processes (apparatus therefor C12M1/36; controlling or regulating in general G05) · CPC title

• C12N1/12 Primary

  Unicellular algae; Culture media therefor (as new plants A01H13/00) · CPC title

• C12N1/34

  Processes using foam culture · CPC title