Methods of applying acetate toxicity and inducing acetate uptake in microalgae cultures

Patent metadata

Field	Value
Publication number	US-2021284952-A1
Application number	US-201716336632-A
Country	US
Kind code	A1
Filing date	Sep 26, 2017
Priority date	Sep 30, 2016
Publication date	Sep 16, 2021
Grant date	—

Abstract

Methods of culturing microalgae in acetate toxicity conditions to induce the uptake of acetate, control contamination, increase the metabolic rate, increase the respiration rate, increase the accumulation of lipids, and decreasing the accumulation of protein are disclosed. Embodiments include methods of controlling the internal microalgae cell acetate concentration by manipulating the culture pH and residual acetate concentration.

First claim

1 . A method comprising:
a. Providing a culture comprising a population of microalgae cells, the microalgae cells having an acetate toxicity threshold level; b. Supplying the culture with at least one of acetate and acetic acid; and c. Controlling the pH of the culture medium and residual acetate concentration in the culture medium to maintain an average internal microalgae cell acetate concentration below the acetate toxicity threshold level so as to (a) detectably inhibit the growth of bacteria in the culture, (b) detectably increase the production of one or more secondary metabolites in the culture, (c) detectably increasing the growth rate of the microalgae cell population, (d) detectably decrease the production of one or more macronutrients, (e) detectably increase the average cellular respiration rate of the microalgae, (f) detectably increasing the metabolic rate of the microalgae, (g) detectably increasing acetate uptake of the microalgae, (h) detectably increasing the productive life of the culture, or a combination of any or all of (a)-(h).

2 . The method of claim 1 , wherein the step (c) further comprises adding acetic acid to the culture.

3 . The method of claim 1 , wherein the step (c) further comprises addition of a second acid that is different from acetic acid.

4 . The method of claim 3 , wherein the second acid comprises at least one acid selected from the group consisting of hydrochloric acid, phosphoric acid, and sulfuric acid.

5 . The method of claim 1 , wherein the microalgae uses the supply comprising at least one of acetate and acetic acid as an organic carbon source.

6 . The method of claim 1 , further supplying the microalgae culture with at least one organic carbon source selected from the group consisting of 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, agricultural by-products, industrial process by-products, municipal waste streams, yeast extract, and xylose.

7 . The method of claim 1 , wherein the microalgae comprises Chlorella.

8 . The method of claim 1 , wherein the average internal microalgae cell acetate concentration is maintained at up to 11 g/L.

9 . The method of claim 1 , wherein the microalgae comprises Aurantiochytrium.

10 . The method of claim 1 , wherein the average internal microalgae cell acetate concentration of at least one species of microalgae in the culture is maintained at up to 150 g/L.

11 . The method of claim 1 , wherein the culture further comprises bacteria and the at least one benefit to the microalgae culture comprises inhibiting the growth of bacteria.

12 . The method of claim 1 , wherein the method comprises increasing the production of one or more secondary metabolites in the culture, where at least some of the secondary metabolites comprise lipids.

13 . The method of claim 1 , wherein the method comprises maintaining the culture in nitrogen sufficient conditions.

14 . The method of claim 1 , wherein the method comprises maintaining the culture in nitrogen deficient conditions.

15 . The method of claim 1 , wherein the method results in the decrease of a macronutrient in the microalgae that is selected from the group consisting of protein, carbohydrate, and a combination thereof.

16 . The method of claim 1 , wherein the culture comprises one or more by-product streams from industrial, municipal, or agricultural sources.

17 . The method of claim 1 , wherein the culture comprises one or more contaminating organisms and practice of the method results in increase in the productive culture life of the microalgae in the presence of contaminating organisms.

18 . The method of claim 1 , further comprising adding monosodium glutamate to the culture as a nitrogen source.

19 . The method of claim 1 , further comprising at least one of ammonia and ammonium as a nitrogen source to the culture.

20 . A method of culturing microalgae in acetate toxicity conditions comprising:
a. Providing a culture comprising a population of microalgae cells; b. Determining an acetate toxicity threshold level for the microalgae cells; c. Supplying the culture with at least one of acetate and acetic acid; and d. Controlling the pH of the culture medium and residual acetate concentration in the culture medium to maintain an average internal microalgae cell acetate concentration below the acetate toxicity threshold level so as to (a) detectably inhibit the growth of bacteria in the culture, (b) detectably increase the production of one or more secondary metabolites in the culture, (c) detectably increasing the growth rate of the microalgae cell population, (d) detectably decrease the production of one or more macronutrients, (e) detectably increase the average cellular respiration rate of the microalgae, (f) detectably increasing the metabolic rate of the microalgae, (g) detectably increasing acetate uptake of the microalgae, (h) detectably increasing the productive life of the culture, or a combination of any or all of (a)-(h).

21 . The method of claim 20 , wherein the microalgae comprises Chlorella.

22 . The method of claim 21 , wherein the acetate toxicity threshold level of Chlorella at a pH of 7 is in the range of 6-11 g/L and the average internal microalgae cell acetate concentration is maintained below the acetate toxicity threshold level of Chlorella.

23 . The method of claim 20 , wherein the microalgae comprises Aurantiochytrium.

24 . The method of claim 23 , wherein the acetate toxicity threshold level of Aurantiochytrium at a pH of about 7 is in the range of 50-150 g/L and the average internal microalgae cell acetate concentration culture is maintained below the acetate toxicity threshold level of Aurantiochytrium.

Assignees

• Heliae Dev Llc

Inventors

• Ganuza Taberna Eneko
• Amezquita Ernult Magdalena
• Cizek Luke
• Sellers Charles
• Paolilli Bautista Kara
• Hansen Jon

Classifications

• C12N2501/999

  Small molecules not provided for elsewhere · CPC title

• C12N2500/30

  Organic components · CPC title

• C12N2500/76

  from plants · CPC title

• C12N2500/36

  Lipids · CPC title

• C12N2500/05

  Inorganic components · CPC title