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Production of hexanoic acid from d-galactitol by a newly isolated Clostridium sp. BS-1

  • Applied Microbial and Cell Physiology
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Abstract

In a study screening anaerobic microbes utilizing d-galactitol as a fermentable carbon source, four bacterial strains were isolated from an enrichment culture producing H2, ethanol, butanol, acetic acid, butyric acid, and hexanoic acid. Among these isolates, strain BS-1 produced hexanoic acid as a major metabolic product of anaerobic fermentation with d-galactitol. Strain BS-1 belonged to the genus Clostridium based on phylogenetic analysis using 16S rRNA gene sequences, and the most closely related strain was Clostridium sporosphaeroides DSM 1294T, with 94.4% 16S rRNA gene similarity. In batch cultures, Clostridium sp. BS-1 produced 550 ± 31 mL L−1 of H2, 0.36 ± 0.01 g L−1 of acetic acid, 0.44 ± 0.01 g L−1 of butyric acid, and 0.98 ± 0.03 g L−1 of hexanoic acid in a 4-day cultivation. The production of hexanoic acid increased to 1.22 and 1.73 g L−1 with the addition of 1.5 g L−1 of sodium acetate and 100 mM 2-(N-morpholino)ethanesulfonic acid (MES), respectively. Especially when 1.5 g L−1 of sodium acetate and 100 mM MES were added simultaneously, the production of hexanoic acid increased up to 2.99 g L−1. Without adding sodium acetate, 2.75 g L−1 of hexanoic acid production from d-galactitol was achieved using a coculture of Clostridium sp. BS-1 and one of the isolates, Clostridium sp. BS-7, in the presence of 100 mM MES. In addition, volatile fatty acid (VFA) production by Clostridium sp. BS-1 from d-galactitol and d-glucose was enhanced when a more reduced culture redox potential (CRP) was applied via addition of Na2S·9H2O.

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References

  • Barker HA, Taha SM (1942) Clostridium kluyveri, an organism concerned in the formation of caproic acid from ethyl alcohol. J Bacteriol 43:347–363

    CAS  Google Scholar 

  • Collins MD, Lawson PA, Willems A, Cordoba JJ, Fernandez-Garayzabal J, Garcia P, Cai J, Hippe H, Farrow JA (1994) The phylogeny of the genus Clostridium: proposal of five new genera and eleven new species combinations. Int J Syst Bacteriol 44:812–826

    Article  CAS  Google Scholar 

  • Dürre P (2005) Handbook on clostridia, Taylor & Francis

  • Felsenstein J (1985) Confidence limits on phylogenies: an approach using the bootstrap. Evolution 39:783–791

    Article  Google Scholar 

  • Genthner BR, Davis CL, Bryant MP (1981) Features of rumen and sewage sludge strains of Eubacterium limosum, a methanol- and H2-CO2-utilizing species. Appl Environ Microbiol 42:12–19

    CAS  Google Scholar 

  • Herrero AA (1983) End-product inhibition in anaerobic fermentations. Trends Biotechnol 1:49–53

    Article  CAS  Google Scholar 

  • Holdeman LV, Cato EP, Moore WEC (1977) Anaerobe laboratory manual, 4th edn. Virginia Polytechnic Institute and State University, Blacksburg

    Google Scholar 

  • Hungate RE (1950) The anaerobic mesophilic cellulolytic bacteria. Bacteriol Rev 14:1–49

    CAS  Google Scholar 

  • Jeon B-S, Um Y, Lee S-M, Lee S-Y, Kim H-J, Kim YH, Gu MB, Sang B-I (2008) Performance analysis of a proton exchange membrane fuel cell (PEMFC) integrated with a trickling bed bioreactor for biological high-rate hydrogen production. Energy Fuels 22:83–86

    Article  CAS  Google Scholar 

  • Kawasaki S, Watamura Y, Ono M, Watanabe T, Takeda K, Niimura Y (2005) Adaptive responses to oxygen stress in obligatory anaerobes Clostridium acetobutylicum and Clostridium aminovalericum. Appl Environ Microbiol 71:8442–8450

    Article  CAS  Google Scholar 

  • Kenealy WR, Cao Y, Weimer PJ (1995) Production of caproic acid by cocultures of ruminal cellulolytic bacteria and Clostridium kluyveri grown on cellulose and ethanol. Appl Microbiol Biotechnol 44:507–513

    Article  CAS  Google Scholar 

  • Kim BH, Gadd GM (2008) Bacterial physiology and metabolism. Cambridge University Press, Cambridge

    Book  Google Scholar 

  • Kim BH, Bellows P, Datta R, Zeikus JG (1984) Control of carbon and electron flow in Clostridium acetobutylicum fermentations: utilization of carbon monoxide to inhibit hydrogen production and to enhance butanol yields. Appl Environ Microbiol 48:764–770

    CAS  Google Scholar 

  • Kleinert M, Barth T (2008) Towards a lignincellulosic biorefinery: direct one-step conversion of lignin to hydrogen-enriched biofuel. Energy Fuels 22:1371–1379

    Article  CAS  Google Scholar 

  • Kohlmiller EF Jr, Gest H (1951) A comparative study of the light and dark fermentations of organic acids by Rhodospirillum rubrum. J Bacteriol 61:269–282

    CAS  Google Scholar 

  • Kumar S, Tamura K, Nei M (2004) MEGA3: Integrated software for molecular evolutionary genetics analysis and sequence alignment. Brief Bioinform 5:150–163

    Article  CAS  Google Scholar 

  • Lane DJ (1991) 16S/23S rRNA sequencing. In: Stackebrandt E, Goodfellow M (eds) Nucleic acid techniques in bacterial systematics. Wiley, New York, pp 115–175

    Google Scholar 

  • Lee S-M, Cho MO, Park CH, Chung Y-C, Kim JH, Sang B-I, Um Y (2008) Continuous butanol production using suspended and immobilized Clostridium beijerinckii NCIMB 8052 with supplementary butyrate. Energy Fuels 22:3459–3464

    Article  CAS  Google Scholar 

  • Marounek M, Fliegrova K, Bartos S (1989) Metabolism and some characteristics of ruminal strains of Megasphaera elsdenii. Appl Environ Microbiol 55:1570–1573

    CAS  Google Scholar 

  • Nath K, Das D (2004) Improvement of fermentative hydrogen production: various approaches. Appl Microbiol Biotechnol 65:520–529

    Article  CAS  Google Scholar 

  • Ragauskas AJ, Williams CK, Davison BH et al (2006) The path forward for biofuels and biomaterials. Science 311:484–489

    Article  CAS  Google Scholar 

  • Robinson JW, Frame EMS, Frame GM (2004) Undergraduate instrumental analysis. Marcel Dekker, New York

    Google Scholar 

  • Roddick FA, Britz ML (1997) Production of hexanoic acid by free and immobilised cells of Megasphaera elsdenii: influence of in-situ product removal using Ion exchange resin. J Chem Technol Biotechnol 69:383–391

    Article  CAS  Google Scholar 

  • Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4:406–425

    CAS  Google Scholar 

  • Smith MV, Pierson MD (1979) Effect of reducing agents on oxidation-reduction potential and the outgrowth of Clostridium botulinum type E spores. Appl Environ Microbiol 37:978–984

    CAS  Google Scholar 

  • Thauer RK, Jungermann K, Henninger H, Wenning J, Decker H (1968) The energy metabolism of Clostridium kluyveri. Eur J Biochem 4:173–180

    Article  CAS  Google Scholar 

  • Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997) The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 25:4876–4882

    Article  CAS  Google Scholar 

  • Wi SG, Kim HJ, Mahadevan SA, Yang DJ, Bae HJ (2009) The potential value of the seaweed Ceylon moss (Gelidium amansii) as an alternative bioenergy resource. Bioresour Technol 100:6658–6660

    Article  CAS  Google Scholar 

  • Wu Z, Yang S-T (2003) Extractive fermentation for butyric acid proruction from glucose by Clostridium tyrobutyricum. Biotechnol Bioeng 82:93–103

    Article  CAS  Google Scholar 

  • Zigova J, Sturdik E (2000) Advances in biotechnological production of butyric acid. J Ind Microbiol Biotechnol 24:153–160

    Article  CAS  Google Scholar 

Download references

Acknowledgment

This work was supported by the New & Renewable Energy of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) grant funded by the Korea government Ministry of Knowledge Economy (No. 2009T100100337).

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Correspondence to Byoung-In Sang.

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Fig. S1

Total ion current chromatogram of VFAs produced in sludge culture broth. Peak no. 3 in the hexane extraction (A) and no 4. in the ethyl acetate extraction (B) are defined as hexanoic acid in a sludge culture utilizing d-galactitol. (PDF 1231 kb)

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Jeon, B.S., Kim, BC., Um, Y. et al. Production of hexanoic acid from d-galactitol by a newly isolated Clostridium sp. BS-1. Appl Microbiol Biotechnol 88, 1161–1167 (2010). https://doi.org/10.1007/s00253-010-2827-5

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