| Peer-Reviewed

Characterization of the Rumen-Mimetic Continuous Cultivation System for Volatile Fatty Acid Production from Lignocellulosic Biomass

Received: 31 January 2021    Accepted: 7 February 2021    Published: 23 February 2021
Views:       Downloads:
Abstract

The rumen-mimetic continuous cultivation system (RMS) was used to produce volatile fatty acids (VFAs), such as acetic, propionic, and butyric acids, from lignocellulosic biomass. Typical 12 species of ruminal bacteria were detected in the culture broth cultivated by RMS using species-specific PCR assay. These species are known to be cellulolytic, hemicellulolytic, proteolytic, amylolytic, and lipolytic bacteria and methanogens. Therefore, RMS was characterized to be ruminal fermentation like the digestive system of roughage in the rumen of cattle. Using RMS, the ruminal bacteria were continuously cultivated for 120 days to produce VFAs. The yield of total VFAs from 20–50 μm rice straw was 167% higher than that from 300–1000 μm rice straw. However, the productivity was not increased by pulverization of the substrate. The yield and productivity of acetic acid from 20–50 μm rice straw were 0.147 g/g and 34.8 mg/L/h, respectively, and those of propionic acid were 0.104 g/g and 24.6 mg/L/h, respectively. The selectivity (P/A ratio) of acetic and propionic acid production from microcrystalline cellulose at pH 6.5 and 7.0 were 0.83±0.07 and 0.31±0.03, respectively. The ruminal bacteria could not continue to produce VFAs at pH 6.0. The yield and productivity of acetic acid from microcrystalline cellulose at pH 6.5 were 0.234 g/g and 51.7 mg/L/h, respectively, and those of propionic acid were 0.223 g/g and 49.3 mg/L/h, respectively. This study proposes that in order to increase the productivity of RMS, it is necessary to increase the ruminal bacterial biomass by recycling biomass (flocs) using a settling tank.

Published in International Journal of Microbiology and Biotechnology (Volume 6, Issue 1)
DOI 10.11648/j.ijmb.20210601.11
Page(s) 1-8
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Rumen, Ruminal Bacteria, Volatile Fatty Acid, Acetic Acid, Propionic Acid, Lignocellulosic Biomass

References
[1] Annamalai, N., Elayaraja, S., Oleskowicz-Popiel, P., Sivakumar, N., and Bahry, S. A. “Volatile fatty acids production during anaerobic digestion of lignocellulosic biomass” in Recent Developments in Bioenergy Research, Gupta, V. K., Treichel, H., Kuhad, R. C., and Rodrigues-Cout, S., Eds. Elsevier B. V., Amsterdam, 2020. pp. 237–251.
[2] Dusselier, M., Mascal, M., and Sels, B. F. (2014). Top chemical opportunities from carbohydrate biomass: A chemist’s view of the biorefinery, Top Curr. Chem., 353.
[3] Baumann, I. and Westermann, P. (2016). Microbial production of short chain fatty acids from lignocellulosic biomass: current processes and market, Biomed Res. Int., 2016: 1–15.
[4] Gonzalez-Garcia, R. A., McCubbin, T., Navone, L., Stowers, C., Nielsen, L. K., and Marcellin, E. (2017). Microbial propionic acid production, Fermentation, 3: 1–21.
[5] Agematu, H., Takahashi, T., and Hamano, Y. (2017). Continuous volatile fatty acid production from lignocellulosic biomass by a novel rumen-mimetic bioprocess, J. Biosci. Bioeng., 124: 528–533.
[6] Agematu, H., Takahashi, T., and Hamano, Y. (2019). An in vitro rumen-mimetic continuous cultivation system for evaluating the nutritional value of micropulverized roughage based on volatile fatty acid production, Anim. Husb. Dairy Vet. Sci., 3: 1–8.
[7] Kocherginskaya, S. A., Aminov, R. I., and White, B. A. (2001). Analysis of the rumen bacterial diversity under two different diet conditions using denaturing gradient gel electrophoresis, random sequencing, and statistical ecology approaches, Anaerobe, 7: 119–134.
[8] Nagaraja, T. G. “Microbiology of the Rumen” in Rumenology, Millen, D. D., De Beni Arrigoni, M. and Lauritano Pacheco, R. D. Eds. Springer-International Publishing, Switzerland, 2016, pp. 39–61.
[9] Takahashi, T. (2019). Scaled-up pulverizing for lignocellulose biomass using a vibratory mill with ring media, Renew. Energy, 144: 77–83.
[10] Takahashi, T., Ito, K., Ito, A., Enda, Y., Gochi, M., Mori, H., and Kobayashi, J. (2014). Tandem-ring mill pulverization benefits for enzymatic saccharification of biomass, Renew. Energy, 65: 146–151.
[11] Denman, S. E. and McSweeney, C. S. (2006). Development of a real-time PCR assay formonitoring anaerobic fungal and cellulolytic bacterial populations within the rumen, FEMS Microbiol. Ecol., 58: 572–582.
[12] Tajima, K., Aminov, R. I., Nagamine, T., Matsui, H., Nakamura, M., and Benno, Y. (2001). Diet-dependent shifts in the bacterial population of the rumen revealed with real-time PCR, Appl. Environ. Microbiol., 67: 2766–2774.
[13] Koike, S., Pan, J., Kobayashi, Y., and Tanaka, K. (2003). Kinetics of in sacco fiber-attachment of representative ruminal cellulolytic bacteria monitored by competitive PCR, J. Dairy Sci., 86: 1429–1435.
[14] Bekele, A. Z., Koike, S., and Kobayashi, Y. (2010). Genetic diversity and diet specificity of ruminal Prevotella revealed by16S rRNA gene-based analysis, FEMS Microbiol. Lett., 305: 49–57.
[15] Ufnar, J. A., Wang, S. Y., Ufnar, D. F., and Ellender, R. D. (2007). Methanobrevibacter ruminantium as an indicator of domesticated-ruminant fecal pollution in surface waters, Appl. Environ. Microbiol., 73: 7118–7121.
[16] Owens, F. N. and Basalan, M. “Ruminal Fermentation” in Rumenology, Millen, D. D., De Beni Arrigoni, M. and Lauritano Pacheco, R. D. Eds. Springer-International Publishing, Switzerland, 2016, pp. 63–102.
[17] Koike, S., Yoshitani, S., Kobayashi, Y., and Tanaka, K. (2003). Phylogenetic analysis of fiber-associated rumen bacterial community and PCR detection of uncultured bacteria, FEMS Microbiol. Lett., 229: 23–30.
[18] Forsberg, C. W., Cheng, K. J., and White, B. A. “Polysaccharide degradation in the rumen and large intestine” in Gastrointestinal Microbiology, Mackie, R. I., and White, B. A. Eds. Chapman and Hall, New York, 1997, pp. 319–379.
[19] Fondevila, M. and Dehority, B. A. (1996). Interactions between Fibrobacter succinogenes, Prevotella ruminicola, and Ruminococcus flavefaciens in the digestion of cellulose from forages, J. Anim. Sci., 74: 678–684.
[20] Sawanon, S., Koike, S., and Kobayashi, Y. (2011). Evidence for the possible involvement of Selenomonas ruminantium in rumen fiber digestion, FEMS Microbiol. Lett., 325: 170–179.
[21] Kudo, H., Cheng, K. J., and Costerton, J. W. (1987). Interactions between Treponema bryantii and cellulolytic bacteria in the in vitro degradation of straw cellulose, Can. J. Microbiol., 33: 244–24.
[22] Goad, D. W., Goad, C. L., and Naganya, T. G. (1998). Ruminai microbial and fermentative changes associated with experimentally induced subacute acidosis in steers, J. Anim. Sci., 76: 234–241.
[23] Kim, J. N., Méndez–García1, C., Geier, R. R. Iakiviak, M., Chang, J., Cann, I., and Mackie, R. I. (2017). Metabolic networks for nitrogen utilization in Prevotella ruminicola 23, Sci. Rep., 7: 1–11.
[24] Rodriguez, F. (2003). Control of lactate accumulation in ruminants using Prevotella bryantii. PhD Thesis. Iowa State University, Ames.
[25] Chiquette, J., Allison, M. J., and Rasmussen, M. A. (2008). Prevotella bryantii 25A used as a probiotic in early-lactation dairy cows: effect on ruminal fermentation characteristics, milk production, and milk composition1, J. Dairy Sci., 91: 3536–3543.
[26] Russell, J. B. and Hino, T. (1985). Regulation of lactate production in Streptococcus bovis: A spiraling effect that contributes to rumen acidosis, J. Dairy Sci., 68: 1712–1721.
[27] Nagaraja, T. G. and Titgemeyer, E. C. (2007). Ruminal acidosis in beef cattle: The current microbiological and nutritional outlook, J. Dairy Sci., 90: 17–38.
[28] Station, T. B. (1984). Glucose metabolism of Treponema bryantii, an anaerobic rumen spirochete, Can. J. Microbiol., 30: 526–531.
[29] Prins, R. A., Lankhorst, A., van der Meer, P,. Van Nevel, C. J. (1975). Some characteristics of Anaerovibrio lipolytica a rumen lipolytic organism, Antonie van Leeuwenhoek, 41: 1–11.
[30] Louis, P., Duncan, S. H. McCrae, S. I., Millar, J., Jackson, M. S., and Flint, H. J. (2004). Restricted distribution of the butyrate kinase pathway among butyrate-producing bacteria from the human colon, J. Bacteriol., 186: 2099–2106.
[31] Singh, K. M., Tripathi, A. K., Pandya, P. R., Parnerkar, S., Kothari, R. K., and Joshi, C. G. (2013). Molecular genetic diversity and quantitation of methanogen in ruminal fluid of buffalo (Bubalus bubalis) fed ration (wheat straw and concentrate mixture diet), Genet. Res. Int., 2013: 1–7.
[32] Balch, W. E., Fox, G. E., Magrum, L. J., Woese, C. R., and Wolfe, R. S. (1979). Methanogens: Reevaluation of a unique biological group, Microbiol. Rev., 43: 260–296.
[33] Taherzadeh, M. J. and Karimi, K. (2008). Pretreatment of lignocellulosic wastes to improve ethanol and biogas production, Int. J. Mol. Sci., 9: 1621–1651.
[34] Russell, J. B. and Wilson, D. B. (1996). Why are ruminal cellulolytic bacteria unable to digest cellulose at low pH?, J. Dairy Sci., 79: 1503–1509.
[35] Wells, J. E. and Russell, J. B. (1996). Why do many ruminal bacteria die and lyse so quickly? J. Dairy Sci., 79: 147–1495.
Cite This Article
  • APA Style

    Hitosi Agematu, Jun Watanabe, Takehiko Takahashi. (2021). Characterization of the Rumen-Mimetic Continuous Cultivation System for Volatile Fatty Acid Production from Lignocellulosic Biomass. International Journal of Microbiology and Biotechnology, 6(1), 1-8. https://doi.org/10.11648/j.ijmb.20210601.11

    Copy | Download

    ACS Style

    Hitosi Agematu; Jun Watanabe; Takehiko Takahashi. Characterization of the Rumen-Mimetic Continuous Cultivation System for Volatile Fatty Acid Production from Lignocellulosic Biomass. Int. J. Microbiol. Biotechnol. 2021, 6(1), 1-8. doi: 10.11648/j.ijmb.20210601.11

    Copy | Download

    AMA Style

    Hitosi Agematu, Jun Watanabe, Takehiko Takahashi. Characterization of the Rumen-Mimetic Continuous Cultivation System for Volatile Fatty Acid Production from Lignocellulosic Biomass. Int J Microbiol Biotechnol. 2021;6(1):1-8. doi: 10.11648/j.ijmb.20210601.11

    Copy | Download

  • @article{10.11648/j.ijmb.20210601.11,
      author = {Hitosi Agematu and Jun Watanabe and Takehiko Takahashi},
      title = {Characterization of the Rumen-Mimetic Continuous Cultivation System for Volatile Fatty Acid Production from Lignocellulosic Biomass},
      journal = {International Journal of Microbiology and Biotechnology},
      volume = {6},
      number = {1},
      pages = {1-8},
      doi = {10.11648/j.ijmb.20210601.11},
      url = {https://doi.org/10.11648/j.ijmb.20210601.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijmb.20210601.11},
      abstract = {The rumen-mimetic continuous cultivation system (RMS) was used to produce volatile fatty acids (VFAs), such as acetic, propionic, and butyric acids, from lignocellulosic biomass. Typical 12 species of ruminal bacteria were detected in the culture broth cultivated by RMS using species-specific PCR assay. These species are known to be cellulolytic, hemicellulolytic, proteolytic, amylolytic, and lipolytic bacteria and methanogens. Therefore, RMS was characterized to be ruminal fermentation like the digestive system of roughage in the rumen of cattle. Using RMS, the ruminal bacteria were continuously cultivated for 120 days to produce VFAs. The yield of total VFAs from 20–50 μm rice straw was 167% higher than that from 300–1000 μm rice straw. However, the productivity was not increased by pulverization of the substrate. The yield and productivity of acetic acid from 20–50 μm rice straw were 0.147 g/g and 34.8 mg/L/h, respectively, and those of propionic acid were 0.104 g/g and 24.6 mg/L/h, respectively. The selectivity (P/A ratio) of acetic and propionic acid production from microcrystalline cellulose at pH 6.5 and 7.0 were 0.83±0.07 and 0.31±0.03, respectively. The ruminal bacteria could not continue to produce VFAs at pH 6.0. The yield and productivity of acetic acid from microcrystalline cellulose at pH 6.5 were 0.234 g/g and 51.7 mg/L/h, respectively, and those of propionic acid were 0.223 g/g and 49.3 mg/L/h, respectively. This study proposes that in order to increase the productivity of RMS, it is necessary to increase the ruminal bacterial biomass by recycling biomass (flocs) using a settling tank.},
     year = {2021}
    }
    

    Copy | Download

  • TY  - JOUR
    T1  - Characterization of the Rumen-Mimetic Continuous Cultivation System for Volatile Fatty Acid Production from Lignocellulosic Biomass
    AU  - Hitosi Agematu
    AU  - Jun Watanabe
    AU  - Takehiko Takahashi
    Y1  - 2021/02/23
    PY  - 2021
    N1  - https://doi.org/10.11648/j.ijmb.20210601.11
    DO  - 10.11648/j.ijmb.20210601.11
    T2  - International Journal of Microbiology and Biotechnology
    JF  - International Journal of Microbiology and Biotechnology
    JO  - International Journal of Microbiology and Biotechnology
    SP  - 1
    EP  - 8
    PB  - Science Publishing Group
    SN  - 2578-9686
    UR  - https://doi.org/10.11648/j.ijmb.20210601.11
    AB  - The rumen-mimetic continuous cultivation system (RMS) was used to produce volatile fatty acids (VFAs), such as acetic, propionic, and butyric acids, from lignocellulosic biomass. Typical 12 species of ruminal bacteria were detected in the culture broth cultivated by RMS using species-specific PCR assay. These species are known to be cellulolytic, hemicellulolytic, proteolytic, amylolytic, and lipolytic bacteria and methanogens. Therefore, RMS was characterized to be ruminal fermentation like the digestive system of roughage in the rumen of cattle. Using RMS, the ruminal bacteria were continuously cultivated for 120 days to produce VFAs. The yield of total VFAs from 20–50 μm rice straw was 167% higher than that from 300–1000 μm rice straw. However, the productivity was not increased by pulverization of the substrate. The yield and productivity of acetic acid from 20–50 μm rice straw were 0.147 g/g and 34.8 mg/L/h, respectively, and those of propionic acid were 0.104 g/g and 24.6 mg/L/h, respectively. The selectivity (P/A ratio) of acetic and propionic acid production from microcrystalline cellulose at pH 6.5 and 7.0 were 0.83±0.07 and 0.31±0.03, respectively. The ruminal bacteria could not continue to produce VFAs at pH 6.0. The yield and productivity of acetic acid from microcrystalline cellulose at pH 6.5 were 0.234 g/g and 51.7 mg/L/h, respectively, and those of propionic acid were 0.223 g/g and 49.3 mg/L/h, respectively. This study proposes that in order to increase the productivity of RMS, it is necessary to increase the ruminal bacterial biomass by recycling biomass (flocs) using a settling tank.
    VL  - 6
    IS  - 1
    ER  - 

    Copy | Download

Author Information
  • Department of Applied Chemistry, Akita National College of Technology, Akita, Japan

  • Department of Agribusiness, Akita Prefectural University, Ohgata, Japan

  • Department of Machine Intelligence and Systems Engineering, Akita Prefectural University, Yurihonjo, Japan

  • Sections