C1 substrate-fed fermentation systems and methods for producing C4 compounds

Patent metadata

Field	Value
Publication number	US-10889793-B2
Application number	US-201715639120-A
Country	US
Kind code	B2
Filing date	Jun 30, 2017
Priority date	Oct 8, 2012
Publication date	Jan 12, 2021
Grant date	Jan 12, 2021

Abstract

A fermenter can have at least one hollow fluid conduit disposed at least partially within a vessel. An external circumference of the hollow fluid conduit and an interior circumference of the vessel can define a downward flow path through which a multi-phase mixture including a liquid media and compressed gas substrate bubbles flows. An interior circumference of the hollow fluid conduit can defined an upward flow path which is in fluid communication with the downward flow path. The multi-phase liquid can flow through the upward flow path and exit the fermenter. Cooling may be provided in the hollow fluid conduit or the vessel. One or more backpressor generators can be used to maintain a backpressure on the fermenter. One or more fluid movers can be used to variously create an induced and/or forced flow in the downward and upward flow paths.

First claim

What is claimed is:

1. A method for producing C 4 compounds, the method comprising culturing a methanotroph comprising a heterologous polynucleotide on a C 1 substrate comprising methane in a controlled culturing unit under conditions sufficient for the methanotroph comprising the heterologous polynucleotide to produce one or more of the products crotonic acid or salts thereof, n-butanol, isobutanol, 1,3-butanediol, 1,4-butanediol, and 2,3-butanediol, wherein the methanotroph is a Methylococcus capsulatus Bath, Methylomonas sp. 16a, Methylosinus trichosporium OB3b, Methylosinus sporium, Methylocystis parvus, Methylomonas methanica, Methylomonas albus, Methylobacter capsulatus, Methylobacterium organophilum, Methylomonas sp. AJ-3670, Methylomicrobium alcahphilum, Methylocella silvestris, Methylacidiphilum infernorum, Methylibium petroleiphilum , or a high growth variants thereof, wherein the culturing in the controlled culturing unit includes:
dispersing the C 1 substrate comprising methane in a liquid media including at least water and one or more nutrients to form a multi-phase mixture comprising C 1 substrate bubbles dispersed in the liquid media;
flowing at a first velocity and a first pressure the multi-phase mixture in one or more downward flow paths before flowing the multi-phase mixture in a number of upward flow paths each defined by a closed fluid channel, the one or more downward flow paths formed between an exterior perimeter of a number of hollow fluid conduits and an interior perimeter of a vessel at least partially surrounding the number of hollow fluid conduits, the vessel including a top and the number of hollow fluid conduits extending from the top of the vessel;
increasing the pressure of the multi-phase mixture from the first pressure to a second pressure to produce compressed C 1 substrate bubbles in the multi-phase mixture while contacting the multi-phase mixture with the methanotrophs present in the one or more downward flow paths to provide a first biomass;
flowing at a second velocity the multi-phase mixture in the number of upward flow paths, each of the respective number of upward flow paths formed by an interior perimeter of each of the number of hollow fluid conduits and maintaining the pressure at or above a third pressure to maintain compressed C 1 substrate bubbles in the multi-phase mixture while contacting the multi-phase mixture with the methanotrophs present in the number of upward flow paths to provide a second biomass; and
discharging the multi-phase mixture, flowing in the number of upward flow paths, from the vessel to outside the vessel through a top of the vessel without the multi-phase mixture from the upward flow path being recirculated within the vessel to the downward flow path.

2. The method of claim 1 , wherein the methanotroph is an obligate methanotroph.

3. The method of claim 1 , wherein the methanotroph is Methylococcus capsulatus Bath, Methylosinus trichosporium OB3b, or Methylomonas sp. 16a.

4. The method of claim 1 , wherein the methanotrophs are cultured aerobically.

5. The method of claim 1 , further comprising maintaining a first temperature in the downward flow path using a thermal transfer system thermally coupled to the downward flow path, thermally coupled to the upward flow path, or both.

6. The method of claim 1 , wherein the first velocity exceeds the rise rate of any C 1 substrate bubbles present in the multi-phase fluid present in the downward flow path.

7. The method of claim 1 , wherein the C 1 substrate includes at least one of hydrogen or a hydrogen containing compound, at least one of oxygen or an oxygen containing compound.

8. The method of claim 1 , wherein the C 1 substrate comprising methane further comprises oxygen.

9. The method of claim 8 , wherein the methane feed rate is at least about 5 grams of methane per liter of liquid media (g/l).

10. The method of claim 8 , wherein the oxygen feed rate is at least about 5 grams of oxygen per liter of liquid media (g/l).

11. The method of claim 8 , wherein the C 1 substrate is at a pressure of about 25 psi or about 50 psi or more above the pressure of the liquid media prior to dispersion in the liquid media.

12. The method of claim 1 , wherein dispersing the C 1 substrate in the liquid media including at least water and one or more nutrients to form a multi-phase mixture comprising C 1 substrate bubbles dispersed in the liquid media, further comprises controlling the flow of the C 1 substrate to maintain a dissolved oxygen concentration of less than about 10 ppm in the multi-phase mixture in the one or more downward flow paths, in the one or more upward flow paths, or both.

13. The method of claim 1 , wherein dispersing the C 1 substrate in the liquid media including at least water and one or more nutrients to form a multi-phase mixture comprising gas bubbles dispersed in the liquid media, further comprises controlling the flow of the C 1 substrate to maintain a dissolved methane concentration of less than about 5 ppm in the multi-phase mixture in the one or more downward flow paths, in the one or more upward flow paths, or both.

14. The method of claim 1 , further comprising separating the multi-phase mixture removed from the one or more upward flow paths into a plurality of phases including at least a separated gas phase and a separated liquid phase.

15. The method of claim 14 , further comprising reducing the pressure of the multi-phase mixture removed from the one or more upward flow paths to a fourth pressure prior to separating the multi-phase mixture.

16. The method of claim 15 , further comprising generating electricity by at least partially reducing the pressure of the multi-phase mixture to a fourth pressure using one or more energy capture systems.

17. The method of claim 15 , wherein the separated liquid phase includes a biomass comprising at least one of n-butanol, 1,3-butanediol, or 1,4-butanediol.

18. The method of claim 1 , wherein the first velocity comprises a superficial fluid velocity of greater than about 0.1 feet per second (f/s), the second velocity comprises a bulk fluid velocity of less than about 10 feet per second (f/s), or both.

19. The method of claim 1 , wherein
the vessel is a vertically arranged vessel including at least one fluid inlet connection fluidly coupled to at least a portion of the number of downward flow paths;
wherein each of the number of hollow fluid conduits providing a respective number of upward flow paths is fluidly coupled to at least one connection to remove the multiphase mixture from the vessel;
at least one gas distributor disposed adjacent at least one outlet of the number of hollow fluid conduits and in at least a portion of the number of downward flow paths; and
a number of structures disposed within at least a portion of at least one of: the number of downward flow paths or the number of upward flow paths, each of the number of structures to promote biological growth thereupon.

20. The method of claim 19 , further comprising at least one first thermal transfer surface disposed at least partially in a portion of the number of downward flow paths.

21. The method of claim 19 , further comprising one or more second thermal transfer surfaces disposed at least partially in at least a portion of the number of upward flow paths.

22. The method of claim 19 , wherein the at least one gas distributor comprise one or more C 1 substrate distrubutors fluidly coupled to at least one first C

Assignees

• Calysta Inc

Inventors

• Silverman Joshua A
• Resnick Sol M
• Regitsky Drew D

Classifications

• C12M23/34 Primary

  Internal compartments or partitions · CPC title

• C12M23/06

  Tubular (C12M23/08, C12M23/16 take precedence) · CPC title

• C12M1/08

  with draft tube · CPC title

• C12M1/04

  with gas introduction means · CPC title

• C12M1/02 Primary

  with agitation means; with heat exchange means · CPC title