Skip to main content

Micro-spatial Distribution of Bacteria in the Rhizosphere

  • Conference paper
Biological Resources and Migration
  • 411 Accesses

Abstract

Long-term experimental fields (having either no nitrogen, phosphorus, or potassium fertilizer or with complete application of N, P, and K fertilizers since 1914) were used for the investigation of bacterial habitat distribution in the rhizosphere. From the rhizosphere of Lupinus albus L., we screened rhizobacteria by their utilization ability of phytate as sole carbon (C) and phosphorus (P) source. Though almost all of the isolates were identified as Burkholderia genus, there was a wide variation in their phosphate utilization. By comparing isolates from rhizosphere soil and isolates from the rhizoplane, those isolates from the latter exhibit higher inorganic phosphate uptake ability when compared at the same extracellular phytase level. We propose that phytate-utilizing bacteria may adapt and segregate from their habitat along a spatial gradient of C and P availability in the rhizosphere. That is, rhizobacteria, which live very close to the rhizoplane, utilize phytate mainly as a P source rather than as a C source, because a large amount of C is provided from roots, whereas this may not be true for P. On the other hand, rhizosphere bacteria that live in a remote area from roots utilize phytate as a C source rather than as a P source, because the lack of available C may restrict the growth of bacteria.

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 169.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 219.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Similar content being viewed by others

References

  • Balandereau J, Viallard V, Cournoyer B, Coenye T, Laevens S, Vandamme P (2001) Burkholderia cepacia genomovar III is a common plant-associated bacterium. Appl Environ Microbiol 67: 982–985

    Article  Google Scholar 

  • Coenye T, Schouls LM, Govan JRW, Kersters K, Vandamme P (1999) Identification of Burkholderia species and genomovars from cystic fibrosis patients by AFLP fingerprinting. Int J Syst Bacteriol 49: 1657–1666

    Article  PubMed  CAS  Google Scholar 

  • Dalai RC (1977) Soil organic phosphorus. Adv Agron 29: 83–117

    Article  Google Scholar 

  • Hiltner L (1904) Über neuere Erfahrungen and Probleme auf dem Gebiet der Bodenbakteriologie and unter besonderer Berücksichtingung der Gründüngung and Brache. Arb Dtsch Landw Ges 98: 59–78

    Google Scholar 

  • Hiraishi A (1992) Direct automated sequencing of 16S rDNA amplified by polymerase chain reaction from bacteria cultures without DNA purification. Lett Appl Microb 15: 210–213

    Article  CAS  Google Scholar 

  • Ishizawa S, Suzuki T, Sato O, Toyoda H (1958) Studies on microbial population in the rhizosphere of higher plants with special reference to the method of study. Plant Soil Food 3: 85–94

    Article  Google Scholar 

  • LiPuma JJ (1998) Burkholderia cepaciea. Management issues and new insights. Curr Opin Pulm Med 4:337–341

    Article  PubMed  CAS  Google Scholar 

  • Moulin L, Munive A, Dreyfus B, Boivin-Masson C (2001) Nodulation of legumes by members of beta-subclass of proteobacteria. Nature 411: 948–950

    Article  PubMed  CAS  Google Scholar 

  • Murphy J, Riley JP (1962) A modified single solution method for the determination of phosphate in natural waters. Anal Chim Acta 27: 31–36

    Article  CAS  Google Scholar 

  • Richardson AE, Hadobas PA (1997) Soil isolates of Pseudomonas spp. that utilize inositol phosphates. Can J Microbiol 43: 509–516

    Article  PubMed  CAS  Google Scholar 

  • Sullivan JT, Ronson CW (1998) Evolution of rhizobia by acquisition of a 500-kb symbiosis island that integrates into a phe-tRNA gene. Proc Natl Acad Sci USA 95: 5145–5149

    Article  PubMed  CAS  Google Scholar 

  • Van Elsas JD, Gardener BB, Wolters AC, Smit E (1998) Isolation, characterization, and transfer of cryptic gene-mobilizing plasmids in the wheat rhizosphere. Appl Environ Microbiol 64: 880–889

    PubMed  Google Scholar 

  • Yabuuchi E, Kosako Y, Oyaizu H, Yano I, Hotta H, Hashimoto Y, Ezaki T, Arakawa M (1993) Proposal of Burkholderia gen. nov. and transfer of seven species of the genus Pseudomonas homology group II to the new genus, with the type species Burkholderia cepasia (Palleronhi and Holmes 1981) comb. nov. Microbiol Immunol 36: 1251–1275

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2004 Springer-Verlag Berlin Heidelberg

About this paper

Cite this paper

Unno, Y., Shinano, T., Wasaki, J., Osaki, M. (2004). Micro-spatial Distribution of Bacteria in the Rhizosphere. In: Werner, D. (eds) Biological Resources and Migration. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-06083-4_14

Download citation

  • DOI: https://doi.org/10.1007/978-3-662-06083-4_14

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-05989-6

  • Online ISBN: 978-3-662-06083-4

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics