Patent · US10280393B2 · B2 · US
High pressure bioreactor
- (11) Publication number
- US10280393B2
- (21) Application number
- 15/121,732
- (22) Filing date
- 2015-02-27
- (30) Priority date
- 2014-02-28
- (43) Publication date
- 2019-05-07
- (45) Date of grant
- 2019-05-07
- (51) IPC
- C12M 1/00; C12M 1/02; C12M 1/26; C12M 1/34
- (52) CPC
- C12M Apparatus for enzymology or microbiology; {apparatus for culturing microorganisms for producing biomass, for growing cells or for obtaining fermentation or metabolic products, i.e. bioreactors or fermenters}: 41/40, 27/00, 29/00, 33/00
- (73) Assignee
- Carnegie Institution of Washington
- (72) Inventors
- Dionysis Ioannis Foustoukos
- (54) Title
- High pressure bioreactor
- (57) Abstract
The present invention relates generally to an integrated system, apparatus and method that allows for the continuous culturing of microorganisms under high pressure conditions and at a wide range of temperatures. More specifically, the system is configured to be gas tight and operate under aerobic or anaerobic conditions. The system is also configured to permit periodic sampling of the incubated organisms under such conditions with minimal physical/chemical disturbance inside the reactor and minimal impacts of shear forces on the collected biomass.
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Claims (16)
- A high pressure bioreactor for the continuous culturing of microorganisms under high pressure, the bioreactor comprising: a.) a reactor vessel capable of operating under a pressure between about 5 MPa and about 150 MPa; b.) a back-pressure pressure regulator to measure and regulate the pressure of the reactor vessel; and c.) a sampler that will not affect the hydrostatic pressure of the microorganisms in the bioreactor while the reactor contents are sampled, wherein the bioreactor is gas-tight, the back-pressure regulator is connected to the reactor vessel through connecting tubing, the sampler comprises at least three valves arranged in series with connecting tubing, and one of the at least three valves arranged in series is located between the reactor vessel and the back-pressure regulator.
- The bioreactor of claim 1 further comprising a pump and valve adapted to add media and cells to the reactor vessel in situ under pressure conditions between about 5 MPa and 150 MPa.
- The bioreactor of claim 1 further comprising an agitator to homogenize the contents of the reactor vessel.
- The bioreactor of claim 1 which can operate under aerobic or anaerobic conditions.
- The bioreactor of claim 1 that can function as a chemostat, retentostat or batch reactor.
- The bioreactor of claim 1 wherein the valves and connecting tubing are prefilled with deionized water.
- The bioreactor of claim 1 wherein the reactor vessel is cylindrical.
- The bioreactor of claim 1, wherein the valves are micrometering valves.
- A method to allow for the continuous culturing of microorganisms under high pressure, the method comprising: a.) providing the bioreactor according to claim 1; b.) pre-enriching media solution with dissolved gases in a reservoir; c.) filling the bioreactor with growth media at high pressure and at the optimal temperature for growth; d.) inoculating the bioreactor with culture; e.) operating the bioreactor in the batch mode while the microbial community grows in density to a desired value; f.) operating the bioreactor in a continuous mode by adding a continuous flow of media; g.) increasing the pressure up to at least about 40 MPa; and h.) monitoring the growth by sampling the reactor without affecting the hydrostatic pressure of the microbial community in bioreactor.
- The method of claim 9 wherein the reactor is sampled using the at least three valves arranged in series.
- The method of claim 9 wherein the reservoir can withstand at least 60 psi of headspace partial pressure.
- The method of claim 9 wherein the dissolved gases comprise one or more of H 2, N 2, CO 2 and O 2.
- The method of claim 9 wherein the media solution is pre-heated prior to entering the bioreactor.
- The method of claim 9 wherein the bioreactor is operated under aerobic or anaerobic conditions.
- The method of claim 9 wherein sampling does not cause cell lysis of the recovered high-pressure cultures.
- The method of claim 9 wherein the pressure in the bioreactor is about 150 MPa.
Description
This invention was made with Government support under NSF-OCE Grant Nos. 1038114, 0752221, 1136608, and 1155246. The U.S. Government has certain rights in the invention.
The present invention relates generally to an integrated system, apparatus and method that allows for the continuous culturing of microorganisms under high pressure and a wide range of temperature conditions. More specifically, the system is configured to be gas-tight and allow for the employment of media enriched in dissolved gases, under aerobic or anaerobic conditions. The system is also configured to permit periodic sampling of the incubated organisms under such conditions with minimal physical/chemical disturbance inside the reactor.
Microbial culturing experiments at high pressures have implications in food science, virus-related research and studies involved in the development of energy resources. Because oxygen solubility is increased at high pressure, the occurrence of large dissolved oxygen tension induces biological oxidative stresses that can affect the function of biological membranes, the physical/-chemical properties of enzymes and regulate virulence and toxin production in pathogens (Follonier et al., Pressure to kill or pressure to boost: a review on the various effects and applications of hydrostatic pressure in bacterial biotechnology, Appl. Microbiol. Biotechnol., 93: 1805-1815, 2012, and references cited therein). Therefore, the food industry has been developing protocols to inactivate microorganisms by applying pressure stresses without the use of temperature treatment that alters food properties (Id.).
Citations (10)
- US4001090A
- US4169010A
- US5571720A
- US5342580A
- WO1993003135A1
- US20020172629A1
- US20070042490A1
- US20090126260A1
- WO2012080421A1
- WO2013004670A1
Record as JSON
{
"publication_number": "US10280393B2",
"country": "US",
"kind": "B2",
"title": "High pressure bioreactor",
"abstract": "The present invention relates generally to an integrated system, apparatus and method that allows for the continuous culturing of microorganisms under high pressure conditions and at a wide range of temperatures. More specifically, the system is configured to be gas tight and operate under aerobic or anaerobic conditions. The system is also configured to permit periodic sampling of the incubated organisms under such conditions with minimal physical/chemical disturbance inside the reactor and minimal impacts of shear forces on the collected biomass.",
"claims": [
"1. A high pressure bioreactor for the continuous culturing of microorganisms under high pressure, the bioreactor comprising: a.) a reactor vessel capable of operating under a pressure between about 5 MPa and about 150 MPa; b.) a back-pressure pressure regulator to measure and regulate the pressure of the reactor vessel; and c.) a sampler that will not affect the hydrostatic pressure of the microorganisms in the bioreactor while the reactor contents are sampled, wherein the bioreactor is gas-tight, the back-pressure regulator is connected to the reactor vessel through connecting tubing, the sampler comprises at least three valves arranged in series with connecting tubing, and one of the at least three valves arranged in series is located between the reactor vessel and the back-pressure regulator.",
"2. The bioreactor of claim 1 further comprising a pump and valve adapted to add media and cells to the reactor vessel in situ under pressure conditions between about 5 MPa and 150 MPa.",
"3. The bioreactor of claim 1 further comprising an agitator to homogenize the contents of the reactor vessel.",
"4. The bioreactor of claim 1 which can operate under aerobic or anaerobic conditions.",
"5. The bioreactor of claim 1 that can function as a chemostat, retentostat or batch reactor.",
"6. The bioreactor of claim 1 wherein the valves and connecting tubing are prefilled with deionized water.",
"7. The bioreactor of claim 1 wherein the reactor vessel is cylindrical.",
"8. The bioreactor of claim 1, wherein the valves are micrometering valves.",
"9. A method to allow for the continuous culturing of microorganisms under high pressure, the method comprising: a.) providing the bioreactor according to claim 1; b.) pre-enriching media solution with dissolved gases in a reservoir; c.) filling the bioreactor with growth media at high pressure and at the optimal temperature for growth; d.) inoculating the bioreactor with culture; e.) operating the bioreactor in the batch mode while the microbial community grows in density to a desired value; f.) operating the bioreactor in a continuous mode by adding a continuous flow of media; g.) increasing the pressure up to at least about 40 MPa; and h.) monitoring the growth by sampling the reactor without affecting the hydrostatic pressure of the microbial community in bioreactor.",
"10. The method of claim 9 wherein the reactor is sampled using the at least three valves arranged in series.",
"11. The method of claim 9 wherein the reservoir can withstand at least 60 psi of headspace partial pressure.",
"12. The method of claim 9 wherein the dissolved gases comprise one or more of H 2, N 2, CO 2 and O 2.",
"13. The method of claim 9 wherein the media solution is pre-heated prior to entering the bioreactor.",
"14. The method of claim 9 wherein the bioreactor is operated under aerobic or anaerobic conditions.",
"15. The method of claim 9 wherein sampling does not cause cell lysis of the recovered high-pressure cultures.",
"16. The method of claim 9 wherein the pressure in the bioreactor is about 150 MPa."
],
"description_excerpt": "This invention was made with Government support under NSF-OCE Grant Nos. 1038114, 0752221, 1136608, and 1155246. The U.S. Government has certain rights in the invention.\n\nThe present invention relates generally to an integrated system, apparatus and method that allows for the continuous culturing of microorganisms under high pressure and a wide range of temperature conditions. More specifically, the system is configured to be gas-tight and allow for the employment of media enriched in dissolved gases, under aerobic or anaerobic conditions. The system is also configured to permit periodic sampling of the incubated organisms under such conditions with minimal physical/chemical disturbance inside the reactor.\n\nMicrobial culturing experiments at high pressures have implications in food science, virus-related research and studies involved in the development of energy resources. Because oxygen solubility is increased at high pressure, the occurrence of large dissolved oxygen tension induces biological oxidative stresses that can affect the function of biological membranes, the physical/-chemical properties of enzymes and regulate virulence and toxin production in pathogens (Follonier et al., Pressure to kill or pressure to boost: a review on the various effects and applications of hydrostatic pressure in bacterial biotechnology, Appl. Microbiol. Biotechnol., 93: 1805-1815, 2012, and references cited therein). Therefore, the food industry has been developing protocols to inactivate microorganisms by applying pressure stresses without the use of temperature treatment that alters food properties (Id.).",
"cpc": [
"C12M 41/40",
"C12M 27/00",
"C12M 29/00",
"C12M 33/00"
],
"ipc": [
"C12M 1/00",
"C12M 1/02",
"C12M 1/26",
"C12M 1/34"
],
"assignees": [
"Carnegie Institution of Washington"
],
"inventors": [
"Dionysis Ioannis Foustoukos"
],
"filing_date": "2015-02-27",
"publication_date": "2019-05-07",
"grant_date": "2019-05-07",
"priority_date": "2014-02-28",
"application_number": "US-201515121732-A",
"family_id": "54009790",
"cited_by_count": 2,
"citations": [
"US4001090A",
"US4169010A",
"US5571720A",
"US5342580A",
"WO1993003135A1",
"US20020172629A1",
"US20070042490A1",
"US20090126260A1",
"WO2012080421A1",
"WO2013004670A1"
]
}
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