Skip to main content

Advertisement

Log in

Characterization of the predominant bacterial population of different mangrove rhizosphere soils using 16S rRNA gene-based single-strand conformation polymorphism (SSCP)

  • Original Paper
  • Published:
World Journal of Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

Variations in chemical parameters and bacterial populations in mangrove rhizosphere samples were noted for different sites. The C, N, P and K contents as well as pH, EC and salinity showed variation between sites. Significant differences in soil properties were also found in sampling sites. Two types of soil were noted among sites. Guesthouse had significantly higher organic matter and nutrient content (N) than other three sites suggesting that human discharges, litter deposition and surface runoff were major nutrient inputs. This contaminated site was located at the landward edges. Positive correlations between organic matter, N, P and K contents were found suggesting that these nutrients were from similar input sources. Effects of sampling sites on microbial diversity were also analyzed via SSCP. Porteresia coarctata and Rhizophora mucronata did not show any variation in the banding patterns among replicates sampled in short distance within site. But Sonneratia apetala showed variation among replicates sampled in distance within site. A significant variation was noted in the SSCP profile among replicates between sites. The majority of dominant SSCP band sequences were related to bacterial genera of root and root-free soil environments, namely Bacillus, Planococcus, Planomicrobium, low G+C Gram-positive bacterium, glacial ice bacterium and unidentified bacteria. In the analysis of 16S rRNA sequences, members belonging to the phylum Firmicutes dominated the sequence collection. The phylogenetic analysis of 16S rRNA gene sequences showed close relationships to a wide range of clones or bacterial species of phylum Firmicutes and unidentified bacteria.

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

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

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

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

Explore related subjects

Discover the latest articles and news from researchers in related subjects, suggested using machine learning.

References

  • Atlas RM, Horowitz A, Krichevsky M, Bej AK (1991) Response of microbial populations to environmental disturbance. Microbial Ecol 22:249–256

    Article  Google Scholar 

  • Bashan Y (1998) Inoculants of plant growth-promoting bacteria for use in agriculture. Biotechnol Adv 16:729–770

    Article  CAS  Google Scholar 

  • Bassam BJ, Caetano-Anolles G, Gresshoff PM (1991) Fast and sensitive silver staining of DNA in polyacrylamide gels. Anal Biochem 80:81–84

    Google Scholar 

  • Bouillon S, Dahdouh-Guebas TMNKF, Baeyens W, Dehairs F (2004) Variability in the origin of carbon substrates for bacterial communities in mangrove sediments. FEMS Microbiol Ecol 49:171–179

    Article  CAS  Google Scholar 

  • Caratini C, Blasco F, Thanikaimoni G (1973) Relations between the pollen spectra and the vegetation of a South Indian mangrove. Pollen Spores 15:281–292

    Google Scholar 

  • Cavalcant VA, Dobereiner J (1988) A new acid-tolerant nitrogen fixing bacterium associated with sugar cane. Plant Soil 108:23–31

    Article  Google Scholar 

  • Cragg SM (1983) The mangrove ecosystem of the Purari delta In: Petr T (ed) The purari-tropical environment of a high rain-fall river basin. Dr W Junk, The Hague, pp 295–324

    Google Scholar 

  • Dai X, Wang YN, Wang BJ, Liu SJ, Zhou YG (2005) Planomicrobium chinense sp nov isolated from coastal sediment and transfer of Planococcus psychrophilus and Planococcus alkanoclasticus to Planomicrobium as Planomicrobium psychrophilum comb nov and Planomicrobium alkanoclasticum comb Nov. Int J Syst Evol Microbiol 55:699–702

    Article  CAS  Google Scholar 

  • Davis SE, Corronado-Molina C, Daniel L, Childers, Day JW (2003) Temporally dependent C N and P dynamics associated with the decay of Rhizophora mangle L leaf litter in oligotrophic mangrove wetlands of the Southern Everglades. Aqua Bot 75:199–215

    Article  CAS  Google Scholar 

  • De Troch P, Vanderleyden J (1996) Surface properties and motility of Rhizobium and Azospirillum in relation to plant root attachment. Microbial Ecol 32:149–169

    Article  Google Scholar 

  • Engelhardt MA, Daly K, Swannell RPJ, Head IM (2001) Isolation and characterization of a novel hydrocarbon-degrading Gram-positive bacterium isolated from intertidal beach sediment and description of Planococcus alkanoclasticus sp nov. J Appl Microbiol 90:237–247

    Article  CAS  Google Scholar 

  • Holmer M, Andersen F, Kristensen E, Thongtham N (2001) Spatial and temporal variability in benthic processes along a mangrove—sea grass transect near the Bangrong mangrove. Thailand Wetlands Ecol Manage 9:141–158

    Article  Google Scholar 

  • Holt JG, Krieg NR, Sheath PHA, Staley JT, William T (1994) Bergey’s Manual of Determinative Bacteriology. Williams and Wilkins, Baltimore

    Google Scholar 

  • Kannupandi T, Kannan R (1998) Hundred years of Pichavaram mangrove forest In: An Anthology of Indian mangroves In: ENVIS Special Publication Annamalai University India p 66

  • Kathiresan K, Ravikumar S, Ravichandran D, Sakaravarthy K (1998) Relation between tannin concentration and bacterial counts in a mangrove environment In: A Gaufam (ed) Conservation and management of aquatic. Resources Daya Publishing House, Delhi, pp 97–105

    Google Scholar 

  • Krishnamurthy K (1993) The mangroves. ENVIS Newsletter, Annamalai University 1:1–3

    Google Scholar 

  • Kristensen E, Andersen F, Holmer M, Thongtham N (2000) Carbon and nitrogen mineralization in sediments of the Bangrong mangrove area Phuket Thailand. Aqua Microbial Ecol 22:199–213

    Article  Google Scholar 

  • Kuske CR, Ticknor LO, Miller ME, Dunbar JM, Davis JA, Barns SM, Belna J (2002) Comparison of soil bacterial communities in rhizospheres of three plant species and the interspaces in an arid grassland. Appl Environ Microbiol 68:1854–1863

    Article  CAS  Google Scholar 

  • Lacerda LD, Ittekkot V, Patchineelam SR (1995) Biogeochemistry of Mangrove Soil Organic Matter: a Comparison Between Rhizophora and Avicennia Soils in South-eastern Brazil Estuarine Coastal and Shelf. Science 40:713–720

    CAS  Google Scholar 

  • Lee DH, Zo YG, Kim SJ (1996) Non-radioactive method to study genetic profiles of natural bacterial communities by PCR-single-strand Conformation polymorphism. Appl Environ Microbiol 62:3112–3120

    CAS  Google Scholar 

  • Lopez-Garcia P, Kazmierczak J, Benzerara K, Kempe S, Guyot F, Moreira D (2005) Bacterial diversity and carbonate precipitation in the giant microbialites from the highly alkaline Lake Van Turkey. Extremophiles 9:263–274

    Article  CAS  Google Scholar 

  • Lueders T, Pommerenke B, Friedrich MW (2004) Stable-isotope probing of microorganisms thriving at thermodynamic limits: syntrophic propionate oxidation in flooded soil. Appl Environ Microbiol 70:5778–5786

    Article  CAS  Google Scholar 

  • Mongias AD, Ganeshamurthy AN (1989) Typical differences between the chemical characteristics of Rhizophora and Avicennia mangrove forest soils in South Andamans. Agrochimica 33:1–7

    Google Scholar 

  • Nayak ST (1993) Remote sensing applications in the management of wetland ecosystem with special emphasis on management of mangrove ecosystem and coastal protection. Visakhapatnam India, pp 21

  • Oppong D, King VM, Bowen JA (2003) Isolation and characterization of filamentous bacteria from paper mill slimes. Int Biodeterior Biodegradat 52:53–62

    Article  CAS  Google Scholar 

  • Orita M, Iwahana H, Kanazawa H, Hayashi K, Sekiya T (1989) Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proce Nat Acad Sci 86:2766–2770

    Article  CAS  Google Scholar 

  • Petra M, Crowley D, Yang CH (2004) Development of specific rhizosphere bacterial communities in relation to plant species nutrition and soil type. Plant Soil 261:199–208

    Article  Google Scholar 

  • Pikovskaya RI (1948) Mobilization of phosphorus in soil in connection with the vital activity of some of the microbial species. Mikrobiologiya 17:362–370

    CAS  Google Scholar 

  • Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual 2nd edn. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY

    Google Scholar 

  • Schmalenberger A, Schwieger F, Tebbe CC (2001) Effect of primers hybridizing to different evolutionarily conserved regions of the small-subunit rRNA gene in PCR-based microbial community analyses and genetic profiling. Appl Environ Microbiol 67:3557–3563

    Article  CAS  Google Scholar 

  • Schwieger F, Tebbe CC (1998) A new approach to utilize PCR-single-strand-conformation polymorphism for 16S rRNA gene-based microbial community analysis. Appl Environ Microbiol 64:4870–4876

    CAS  Google Scholar 

  • Semenov AM, van Bruggen AH, Zelenev VV (1999) Moving waves of bacterial populations and total organic carbon along roots of wheat. Microbial Ecol 37:116–128

    Article  CAS  Google Scholar 

  • Smith TJ, Boto KG, Frusher SD, Giddins RL (1991) Keystone species and mangrove forest dynamics: the influence of burrowing by crabs on soil nutrient status and forest productivity Estuarine Coastal Shelf. Science 33:419–432

    CAS  Google Scholar 

  • Steinke TD, Barnabas AD, Samuru R (1990) Structural changes and associated microbial activity accompanying decomposition of mangrove leaves in Mgeni Estuary. South African J Bot 56:39–48

    Google Scholar 

  • Valinsky L, Della VG, Scupham AJ, Alvey S, Figueroa A, Yin B, Hartin RJ, Chrobak M, Crowley DE, Jiang T, Borneman J (2002) Analysis of bacterial community composition by oligonucleotide fingerprinting of rRNA genes. Appl Environ Microbiol 68:3243–3250

    Article  CAS  Google Scholar 

  • Wardle DA, Bonner KI, Nicholson KS (1997) Biodiversity and plant litter: experimental evidence which does not support the view that enhanced species richness improves ecosystem function. Oikos 79:247–258

    Article  Google Scholar 

  • Woitchik AF, Ohowa B, Kazungu JM, Rao RG, Goeyens L, Dehairs F (1997) Nitrogen enrichment during decomposition of mangrove leaf litter in an east African coastal lagoon (Kenya): relative importance of biological nitrogen fixation. Bioqeochemistry 39:15–35

    Article  CAS  Google Scholar 

  • Yoon JH, Weiss N, Kang KH, Oh TK, Park YH (2003) Planococcus maritimus sp nov isolated from sea water of a tidal. Int J Syst Evol Microbiol 53:2013–2017

    Article  CAS  Google Scholar 

  • Zhou J, Xia B, Treves DS, Wu LY, Marsh TL, O’Neill RV, Palumbo AV, Tiedje JM (2002) Spatial and resource factors influencing high microbial diversity in soil. Appl Environ Microbiol 68:326–334

    Article  CAS  Google Scholar 

Download references

Acknowledgement

The financial aid from the Department of Biotechnology, Government of India is gratefully acknowledged.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sudha Nair.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bharathkumar, S., RameshKumar, N., Paul, D. et al. Characterization of the predominant bacterial population of different mangrove rhizosphere soils using 16S rRNA gene-based single-strand conformation polymorphism (SSCP). World J Microbiol Biotechnol 24, 387–394 (2008). https://doi.org/10.1007/s11274-007-9487-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11274-007-9487-3

Keywords