IP Library Granted Patent US 9,034,618
Granted Patent B2
US 9,034,618 · App. 12/381,193 · Granted May 19, 2015

Method for sustaining microorganism culture in syngas fermentation process in decreased concentration or absence of various substrates

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Quick Facts
Patent No.
US 9,034,618
App. No.
12/381,193
Granted
May 19, 2015
Kind
B2
Abstract

The present invention relates to methods for sustaining microorganism culture in a syngas fermentation reactor in decreased concentration or absence of various substrates comprising: adding carbon dioxide and optionally alcohol; maintaining free acetic acid concentrations; and performing the above mentioned steps within specified time.

Claims (16)

1. A method for sustaining alcohol producing microorganism culture containing at least one acetogenic bacteria wherein said microorganism culture comprising one or more strains selected from Clostridium, Moorella, Carboxydothermus and their genetic modifications in a syngas fermentation reactor at an operating temperature in decreased concentration or absence of syngas comprising: adding carbon dioxide and optionally adding alcohol; maintaining free acetic acid concentration to less than 5 g/L free acetic acid; consuming alcohol in existing solution of said fermentation reactor; performing the above mentioned steps within 30 minutes of said decreased concentration or absence of syngas; comprising a ratio of less than 0.77 consumed alcohol to initial alcohol; and subsequently recovering the microorganism culture to produce alcohol; wherein said alcohol comprises one or more of ethanol and butanol.

2. The method of claim 1 wherein said sustaining microorganism culture comprises duration of about 0-30 hours.

3. The method of claim 1 , wherein pH of the microorganism culture is maintained in the range of about 3.5-5.6.

4. The method of claim 1 , wherein a bicarbonate solution is added to control pH of the microorganism culture.

5. The method of claim 1 , wherein optionally removing said carbon dioxide from the said reactor.

6. The method of claim 1 , optionally adding nutrients to said reactor.

7. The method of claim 1 , wherein alcohol comprises one or more of ethanol and butanol.

8. The method of claim 1 , optionally changing temperature from said operating temperature to between 0-25 degrees C. if temperature is not between 0-25 degrees C.

9. The method of claim 1 , optionally adding water to said reactor.

10. The method of claim 1 , optionally adding water to said reactor comprising: fresh water, make-up water, recycle water, distilled water, deionized water or their combinations.

11. The method of claim 1 wherein said microorganism culture is returned to pre suspension conditions comprising addition of syngas.

12. The method of claim 1 wherein optionally removing permeate.

13. The method of claim 1 wherein optionally purging said reactor with inert gas.

14. The method of claim 1 wherein optionally maintaining low agitation to keep solids in suspension.

15. A method for preventing rapid loss of alcohol producing microorganism culture containing at least one acetogenic bacteria wherein said microorganism culture comprising one or more strains selected from Clostridium, Moorella, Carboxydothermus and their genetic modifications in a syngas fermentation reactor in decreased concentration or absence of syngas comprising: decreasing temperature from operating temperature to between 0-25 degrees C. if said operating temperature is not between 0-25 degrees C.; maintaining free acetic acid concentration to less than 5 g/L free acetic acid; consuming alcohol in existing solution of said fermentation reactor; performing the above mentioned steps within 30 minutes of said decreased concentration or absence of syngas; comprising a ratio of less than 0.77 consumed alcohol to initial alcohol; and subsequently recovering the microorganism culture to produce alcohol; wherein said alcohol comprises one or more of ethanol and butanol.

16. A method for sustaining alcohol producing microorganism culture containing at least one acetogenic bacteria wherein said microorganism culture comprising one or more strains selected from Clostridium, Moorella, Carboxydothermus and their genetic modifications in a syngas fermentation reactor due to decreased concentration or absence of syngas in feed gas supply comprising: decreasing temperature from operating temperature to between 0-25 degrees C. if said operating temperature is not between 0-25 degrees C.; maintaining free acetic acid concentration to less than 5 g/L free acetic acid; consuming alcohol in existing solution of said fermentation reactor; performing the above mentioned steps within 30 minutes of said decreased concentration or absence of syngas; comprising a ratio of less than 0.77 consumed alcohol to initial alcohol; and subsequently recovering the microorganism culture to produce alcohol; wherein said alcohol comprises one or more of ethanol and butanol.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2020
From: JUPENG BIO SA
To: JUPENG BIO (HK) LIMITED
Reel/Frame 053455/0132 →
CHANGE OF NAME Recorded Oct 21, 2019
From: INEOS BIO SA
To: JUPENG BIO SA
Reel/Frame 050780/0741 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2014
From: INEOS USA LLC
To: INEOS BIO SA
Reel/Frame 032351/0687 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 21, 2009
From: ADAMS, STEPHEN S.; SCOTT, SYRONA; KO, CHING-WHAN
To: INEOS USA LLC
Reel/Frame 022748/0625 →