Microbial removal of carboxylic acids from 1,3-propanediol in glycerol anaerobic digestion effluent by PHAs-producing consortium
Anaerobic fermentation of glycerol to 1,3-propanediol (1,3-PDO) is conceived as an economic feasible pathway to handle with increasing crude glycerol from biodiesel industry. However, glycerol anaerobic digestion effluent (ADE) consists of carboxylic acids and 1,3-PDO, imposing difficulties for sepa...
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sg-ntu-dr.10356-866872020-03-07T11:43:36Z Microbial removal of carboxylic acids from 1,3-propanediol in glycerol anaerobic digestion effluent by PHAs-producing consortium Pan, Chaozhi Tan, Giin-Yu Amy Ge, Liya Chen, Chia-Lung Wang, Jing-Yuan School of Civil and Environmental Engineering Nanyang Environment and Water Research Institute Residues and Resource Reclamation Centre Glycerol Anaerobic Digestion Effluent Polyhydroxyalkanoates Anaerobic fermentation of glycerol to 1,3-propanediol (1,3-PDO) is conceived as an economic feasible pathway to handle with increasing crude glycerol from biodiesel industry. However, glycerol anaerobic digestion effluent (ADE) consists of carboxylic acids and 1,3-PDO, imposing difficulties for separation. The objective of this study was, therefore, to investigate microbial removal of carboxylic acids from 1,3-PDO in glycerol ADE by polyhydroxyalkanoates (PHAs) producing consortium. Growth tests on carbon sources showed Corynebacterium hydrocarbooxydans had preference for butyrate while Bacillus megaterium for acetate and glycerol. Consequently, their consortium had a higher cell density and a faster substrate utilization rate than single strain grown in glycerol ADE. Acidic pH at 6.0 and 5.2 strongly inhibited cell growth and activity, while C:N ratio (w/w) at 8:1 could balance nitrogen demand for cell growth and PHA synthesis. Kinetic study further revealed over 80% of fed 1,3-PDO was preserved after depletion of carboxylic acids. Correspondingly, total organic carbon (TOC) contribution from 1,3-PDO rose from initial 55.8% to 84%. Produced PHAs comprised 3-hydroxybutyrate (3-HB) units. The results showed this study as the first attempt to provide a win-win solution to remove carboxylic acids from 1,3-PDO in glycerol ADE and converted them into PHAs as a secondary value-added product. Accepted version 2017-12-15T06:36:48Z 2019-12-06T16:27:21Z 2017-12-15T06:36:48Z 2019-12-06T16:27:21Z 2016 Journal Article Pan, C., Tan, G.-Y. A., Ge, L., Chen, C.-L., & Wang, J.-Y. (2016). Microbial removal of carboxylic acids from 1,3-propanediol in glycerol anaerobic digestion effluent by PHAs-producing consortium. Biochemical Engineering Journal, 112, 269-276. 1369-703X https://hdl.handle.net/10356/86687 http://hdl.handle.net/10220/44151 10.1016/j.bej.2016.04.031 en Biochemical Engineering Journal © 2016 Elsevier. This is the author created version of a work that has been peer reviewed and accepted for publication by Biochemical Engineering Journal, Elsevier. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1016/j.bej.2016.04.031]. 34 p. application/pdf |
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Glycerol Anaerobic Digestion Effluent Polyhydroxyalkanoates Pan, Chaozhi Tan, Giin-Yu Amy Ge, Liya Chen, Chia-Lung Wang, Jing-Yuan Microbial removal of carboxylic acids from 1,3-propanediol in glycerol anaerobic digestion effluent by PHAs-producing consortium |
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Anaerobic fermentation of glycerol to 1,3-propanediol (1,3-PDO) is conceived as an economic feasible pathway to handle with increasing crude glycerol from biodiesel industry. However, glycerol anaerobic digestion effluent (ADE) consists of carboxylic acids and 1,3-PDO, imposing difficulties for separation. The objective of this study was, therefore, to investigate microbial removal of carboxylic acids from 1,3-PDO in glycerol ADE by polyhydroxyalkanoates (PHAs) producing consortium. Growth tests on carbon sources showed Corynebacterium hydrocarbooxydans had preference for butyrate while Bacillus megaterium for acetate and glycerol. Consequently, their consortium had a higher cell density and a faster substrate utilization rate than single strain grown in glycerol ADE. Acidic pH at 6.0 and 5.2 strongly inhibited cell growth and activity, while C:N ratio (w/w) at 8:1 could balance nitrogen demand for cell growth and PHA synthesis. Kinetic study further revealed over 80% of fed 1,3-PDO was preserved after depletion of carboxylic acids. Correspondingly, total organic carbon (TOC) contribution from 1,3-PDO rose from initial 55.8% to 84%. Produced PHAs comprised 3-hydroxybutyrate (3-HB) units. The results showed this study as the first attempt to provide a win-win solution to remove carboxylic acids from 1,3-PDO in glycerol ADE and converted them into PHAs as a secondary value-added product. |
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School of Civil and Environmental Engineering |
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School of Civil and Environmental Engineering Pan, Chaozhi Tan, Giin-Yu Amy Ge, Liya Chen, Chia-Lung Wang, Jing-Yuan |
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Article |
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Pan, Chaozhi Tan, Giin-Yu Amy Ge, Liya Chen, Chia-Lung Wang, Jing-Yuan |
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Pan, Chaozhi |
title |
Microbial removal of carboxylic acids from 1,3-propanediol in glycerol anaerobic digestion effluent by PHAs-producing consortium |
title_short |
Microbial removal of carboxylic acids from 1,3-propanediol in glycerol anaerobic digestion effluent by PHAs-producing consortium |
title_full |
Microbial removal of carboxylic acids from 1,3-propanediol in glycerol anaerobic digestion effluent by PHAs-producing consortium |
title_fullStr |
Microbial removal of carboxylic acids from 1,3-propanediol in glycerol anaerobic digestion effluent by PHAs-producing consortium |
title_full_unstemmed |
Microbial removal of carboxylic acids from 1,3-propanediol in glycerol anaerobic digestion effluent by PHAs-producing consortium |
title_sort |
microbial removal of carboxylic acids from 1,3-propanediol in glycerol anaerobic digestion effluent by phas-producing consortium |
publishDate |
2017 |
url |
https://hdl.handle.net/10356/86687 http://hdl.handle.net/10220/44151 |
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1681040824315412480 |