Skip to main content
Log in

Effect of hydrogen on soil bacterial community structure in two soils as determined by terminal restriction fragment length polymorphism

  • Regular Article
  • Published:
Plant and Soil Aims and scope Submit manuscript

Abstract

The metabolism of hydrogen evolved from HUP legume nodules can alter bacterial community structures in the rhizosphere. Our earlier experiments demonstrated increased hydrogen uptake and appearance of white spots within bacterial colonies in H2-treated soil. We were also able to isolate hydrogen-oxidizing bacteria from soil samples exposed to hydrogen, but not from samples exposed to air. To further understand the effect of hydrogen metabolism on soil microbial communities, in this study 16S rRNA terminal restriction fragment (TRF) profiles of different soil samples exposed to hydrogen gas under laboratory, greenhouse, and field conditions were analyzed. Relationships between soil bacterial community structures from hydrogen-treated soil samples and controls, illustrated by UPGMA (unpaired group mathematical averages) dendrograms, indicated a significant contribution of hydrogen metabolism to the variation in bacterial community. The intensity variation of TRF peaks includes both hydrogen-utilizing bacteria, whose growth were stimulated by hydrogen exposure, and other bacterial species whose growth was inhibited. Comparison of TRF profiles between laboratory and greenhouse samples showed that T-RFLP is a useful technique in the detection of root-related effects on soil bacterial community structure.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Bianchi A, Bianchi M (1995) Microbial diversity and ecosystem maintenance: An overview. In: Allsopp RR, Colwell RR (eds) Microbial Diversity and Ecosystem Function. CAB International, Wallingford, UK, pp 185–198

    Google Scholar 

  • Cunningham SD, Kapulnik Y, Phillips DA (1986) Distribution of H2-metabolising bacteria in Alfalfa field soil. Appl Environ Microbiol 52:1091–1095

    PubMed  Google Scholar 

  • Dean CA (2004) Effect of hydrogen metabolism of legume nodules on rhizobacterial communities and plant growth. M.Sc thesis, Dalhousie University, Halifax, NS, Canada

    Google Scholar 

  • Dong Z, Layzell DB (2001) H2 oxidation, O2 uptake and CO2 fixation in hydrogen treated soils. Plant Soil 229:1–12 doi:10.1023/A:1004810017490

    Article  CAS  Google Scholar 

  • Dunbar J, Ticknor LO, Kuske CR (2000) Assessment of microbial diversity in four southwestern United States soils by 16S rRNA gene terminal restriction fragment analyses. Appl Environ Microbiol 66:2943–2950 doi:10.1128/AEM.66.7.2943-2950.2000

    Article  PubMed  CAS  Google Scholar 

  • Dunbar J, Ticknor LO, Kuske CR (2001) Phylogenetic specificity and reproducibility and new methods for analysis of terminal restriction fragment profiles of 16S rRNA genes from bacterial communities. Appl Environ Microbiol 67:190–197 doi:10.1128/AEM.67.1.190-197.2001

    Article  PubMed  CAS  Google Scholar 

  • Kaplan CW, Kitts CL (2003) Variation between observed and true terminal Restriction Fragment length is dependent on true TRF length and purine content. J Microbiol Methods 54:121–125 doi:10.1016/S0167-7012(03)00003-4

    Article  PubMed  CAS  Google Scholar 

  • Kaplan CW, Astaire JC, Sanders ME, Reddy BS, Kitts CL (2001) 16S Ribosome DNA Terminal Restriction Fragment Pattern Analysis of Bacterial Communities in Feces of Rats Fed Lactobacillus acidophilus NCFM. Appl Environ Microbiol 67:1394–1403 doi:10.1128/AEM.67.4.1935-1939.2001

    Article  Google Scholar 

  • Kent AD, Smith DJ, Benson B, Triplett EW (2003) Web-Based phylogenetic assignment tool for analysis of terminal restriction fragment length polymorphism profiles of microbial communities. Appl Environ Microbiol 69:6768–6776 doi:10.1128/AEM.69.11.6768-6776.2003

    Article  PubMed  CAS  Google Scholar 

  • Kitts CL (2001) Terminal restriction fragment patterns: A tool for comparing microbial communities and assessing community dynamics. Curr Issues Intest Microbiol 2:17–25

    PubMed  CAS  Google Scholar 

  • La Favre JS, Focht DD (1983) Conservation in soil of H2 liberated from N2 fixation by HUP nodules. Appl Environ Microbiol 46:304–311

    PubMed  Google Scholar 

  • Lechner S, Conrad R (1997) Detection in soil of aerobic hydrogen-oxidizing bacteria related to Alcaligenes eutrophus by PCR and hybridization assays targeting the gene of the membrane-bound (NiFe) hydrogenase. FEMS Microbiol Ecol 22:193–206 doi:10.1111/j.1574-6941.1997.tb00371.x

    Article  CAS  Google Scholar 

  • Liu WT, Marsh TL, Cheng H, Forney LJ (1997) Characterization of microbial diversity by determining terminal restriction fragment length polymorphisms of genes encoding 16S rRNA. Appl Environ Microbiol 63:4516–4522

    PubMed  CAS  Google Scholar 

  • McLearn N, Dong Z (2002) Microbial nature of the hydrogen-oxidizing agent in hydrogen treated soil. Biol Fertil Soils 35:465–469 doi:10.1007/s00374-002-0495-z

    Article  CAS  Google Scholar 

  • Maimaiti J, Zhang Y, Yang J, Cen YP, Layzell DB, Peoples M, Dong Z (2007) Isolation and Characterization of hydrogen-oxidizing bacteria induced following exposure of soil to hydrogen gas and their impact on plant growth. Environ Microbiol 9:435–444 doi:10.1111/j.1462-2920.2006.01155.x

    Article  PubMed  CAS  Google Scholar 

  • Moeseneder MM, Arrieta JM, Muyzer G, Winter C, Herndle GJ (1999) Optimization of terminal-restriction fragment length polymorphism analysis for complex Marine Bacterioplankton communities and comparison with denaturing Gradient Gel Electrophoresis. Appl Environ Microbiol 65:3518–3525

    PubMed  CAS  Google Scholar 

  • Osborne CA, Rees GN, Bernstein Y, Janssen PH (2006) New threshold and confidence estimates for terminal restriction fragment length polymorphism analysis of complex bacterial communities. Appl Environ Microbiol 72:1270–1278 doi:10.1128/AEM.72.2.1270-1278.2006

    Article  PubMed  CAS  Google Scholar 

  • Peoples MB, McLennan PD, Brockwell J (2008) Hydrogen emission from nodulated soybeans [Glycine max (L.) Merr.] and consequences for the productivity of a subsequent maize (Zea mays L.) crop. Plant Soil 307:67–82 doi:10.1007/s11104-008-9582-8

    Article  CAS  Google Scholar 

  • Popelier F, Liessens J, Verstraete W (1985) Soil hydrogen uptake in relation to soil properties and rhizobial hydrogen production. Plant Soil 85:85–96 doi:10.1007/BF02197803

    Article  CAS  Google Scholar 

  • Sait L, Galic M, Strugnell RA, Janssen PH (2003) Secretory antibodies do not affect the composition of the bacterial microbiota in the terminal ileum of 10-week-old mice. Appl Environ Microbiol 69:2100–2109 doi:10.1128/AEM.69.4.2100-2109.2003

    Article  PubMed  CAS  Google Scholar 

  • Stein S, Selesi D, Schilling R, Pattis I, Schmid M, Hartmann A (2005) Microbial activity and bacterial composition of H2-treated soils with net CO2 fixation. Soil Biol Biochem 37:1938–1945 doi:10.1016/j.soilbio.2005.02.035

    Article  CAS  Google Scholar 

  • Zhang Y (2006) Mechanisms of isolated hydrogen-oxidizing bacteria in plant growth promotion and effects of hydrogen metabolism on rhizobacterial community structure. Msc thesis, St. Mary’s University, Halifax, NS, Canada

Download references

Acknowledgements

This work was supported by the Natural Sciences and Engineering Research Council (NSERC) and industrial and government partners, through the Green Crop Networks (GCN) Research Network and an NSERC Discovery Grant to ZD.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Zhongmin Dong.

Additional information

Responsible Editor: Euan K. James.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zhang, Y., He, X. & Dong, Z. Effect of hydrogen on soil bacterial community structure in two soils as determined by terminal restriction fragment length polymorphism. Plant Soil 320, 295–305 (2009). https://doi.org/10.1007/s11104-009-9894-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11104-009-9894-3

Keywords

Navigation