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United States Department of Agriculture

Agricultural Research Service

Research Project: PROCESS TECHNOLOGIES FOR PRODUCING BIOFUELS AND COPRODUCTS FROM LIGNOCELLULOSIC FEEDSTOCKS

Location: Bioenergy Research Unit

Title: Long-term conversion of n-butyrate to n-butanol with Clostridium saccharoperbutylacetonicum using a two-stage continuous culture and in-situ product removal

Authors
item Richter, Hanno -
item Qureshi, Nasib
item Dien, Bruce
item Cotta, Michael
item Angenent, Largus -

Submitted to: Meeting Abstract
Publication Type: Abstract Only
Publication Acceptance Date: July 28, 2011
Publication Date: May 16, 2011
Citation: Richter, H., Qureshi, N., Dien, B.S., Cotta, M.A., Angenent, L.T. 2011. Long-term conversion of n-butyrate to n-butanol with Clostridium saccharoperbutylacetonicum using a two-stage continuous culture and in-situ product removal [abstract]. Society for Industrial Microbiology. Paper No. 19556.

Technical Abstract: We are operating anaerobic bioreactors with undefined mixed cultures to convert waste lignocellulosic biomass into useful products. A traditional product of anaerobic bioreactors (i.e., anaerobic digesters) is methane. Recently, we modified bioreactor conditions to more efficiently produce a range of carboxylates, including n-butyrate rather than methane. The objective of the present study was to upgrade n-butyrate into the biofuel n-butanol via fermentation, using pure cultures of solventogenic Clostridia. Here, we describe a two-stage continuous fermentation system with Clostridium saccharoperbutylacetonicum strain N1-4 designed for conversion of n-butyrate into n-butanol. In the first stage, glucose was added as a source of energy and reducing equivalents, while in the second stage undissociated n-butyrate was maintained at a concentration of 0.3 g/L with a pH-auxostat to induce a high solventogenic activity (i.e., production of n-butanol). We integrated a gas-stripping and condensation system in the second stage as a strategy for in-situ product removal. The two-stage fermentation successfully minimized metabolic oscillations that are common to n-butanol fermentation carried out by Clostridia. In addition, culture degeneration was avoided by periodical heat shocking and reinoculating stage 1. The average n-butyrate consumption was 0.251 g/(L*h), the conversion efficiency for n-butyrate to n-butanol was 93%, the overall n-butanol production was 0.39 g/(L*h), the molar ratio of butyrate:glucose consumed was 0.358, the molar yield Yn-butanol/n-butyrate was 2.01, the molar yield Yn-butanol/glucose was 0.718, and the yield Yn-butanol/carbon was 0.386. This is the first report of a continuous fermentation system specifically designed and optimized for the conversion of n-butyrate into n-butanol.

Last Modified: 10/1/2014
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