Skip to main content
Log in

Evaluation of fluorescent Pseudomonas spp. with single and multiple PGPR traits for plant growth promotion of sorghum in combination with AM fungi

  • Original paper
  • Published:
Plant Growth Regulation Aims and scope Submit manuscript

Abstract

Traits involved in plant growth promotion by bacteria are ambiguously decided as phytohormones, siderophores, HCN, proteases, chitinases, cellulases, ammonia, exopolysaccharide production and phosphate solubilization or antagonistic activity. A total of 40 fluorescent Pseudomonas strains were isolated from diverse soils of various agro-ecosystems of India. Among these 7 strains viz, P1, P10, P13, P18, P21, P28 and P38 were selected depending on their character of possessing single or multiple PGPR traits. These isolates individually and in combination with AM fungi (Glomus fasciculatum and Glomus aggregatum) were used for treating sorghum seeds. 25 days after sowing, plants were analysed for different plant growth promoting parameters. It was observed that strains in presence of mycorrhizae performed well compared to the strains devoid of mycorrhizae. Pseudomonas sp. P1 possessing GA3, EPS production and ‘P’ solubilization performed well. Pseudomonas sp. P38 which was a volatile (HCN) producer but a good phosphate solubilizer did not perform well. Strain P28 with multiple PGPR traits did not show the expected out come. Results varied when mycorrhizae was used in combination. P10 and P13 which were good in IAA, GA3, EPS, siderophore and ‘P’ solubilization performed well with mycorrhizae, with an overall increase in plant biomass, leaf area, total chlorophyll and mycorrhizal infection compared to other combinations. Here, strain P1 in combination with mycorrhizae did not show significant increase in plant growth compared to P10 and P13. Hence, mere possession of multiple PGPR traits does not confer fluorescent Pseudomonas strains as PGPR. Further studies have to be carried out in order to evaluate the other traits which may be involved in plant growth promotion.

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

Similar content being viewed by others

References

  • Andrade G, Mihara KL, Linderman RG, Bethlenfalvay GJ (1997) Bacteria from rhizosphere and hyphosphere soils of different arbuscular-mycorrhizal fungi. Plant Soil 192:71–79

    Article  CAS  Google Scholar 

  • Antoun H, Beauchamp CJ, Goussard N, Chabot R, Lalande R (1998) Potential of Rhizobium and Bradyrhizobium species as plant growth promoting rhizobacteria on non-legumes: effect on radishes (Raphanus sativus L.). Plant Soil 204:57–67

    Article  CAS  Google Scholar 

  • Artursson V, Finlal RD, Janet KJ (2006) Interactions between arbuscular mycorrhizal fungi and bacteria and their potential for stimulating plant growth. Environ Microbiol 8(1):1–10

    Article  PubMed  CAS  Google Scholar 

  • Atkinson D, Berta G, Hooker JE (1994) Impact of mycorrhizal colonization on root architecture, root longevity, and the formation of growth regulators. In: Gininazzi S, Scheupp H (eds) Impact of arbuscular mycorrhizas on sustainable agriculture and natural ecosystems. Birkhauser Verlag, Basal, pp 89–99

  • Azcon R (1989) Selective interaction between free-living rhizosphere bacteria and vesicular-arbuscular mycorrhizal fungi. Soil Biol Biochem 21:639–644

    Article  Google Scholar 

  • Bakker AW, Schippers B (1987) Microbial cyanide production in the rhizosphere in relation to potato yield reduction and Pseudomonas spp. mediated pant growth stimulation. Soil Biol Biochem 19:451–457

    Article  CAS  Google Scholar 

  • Barea JM, Toutant P, Balazs E, Galante E, Lynch JM, Shepers JS, Werner D, Werry PA (2000) Rhizosphere and mycorrhiza of field crops. INRA and Springer, Berlin

    Google Scholar 

  • Behl RK, Sharma H, Kumar V, Narula N (2003) Interactions amongst mycorrhiza, Azotobacter chroococcum and root characteristics of wheat varieties. J Agron Crop Sci 198:151–155

    Article  Google Scholar 

  • Belimov AA, Safronova VI, Sergeyeva TA, Egorova TN, Matveyeva VA, Tsyganov VE, Borisov AY, Tikhonovich IA, Kluge C, Preisfeld A, Dietz KJ, Stepanok VV (2001) Characterization of plant growth promoting rhizobacteria isolated from polluted soils and containing 1-aminocyclopropane-1-carboxylate deaminase. Can J Microbiol 47:642–652

    Article  PubMed  CAS  Google Scholar 

  • Brick JM, Bostock RM, Silverstone SE (1991) Rapid in situ assay for indole acetic acid production by bacteria immobilized on nitrocellulose membrane. Appl Environ Microbiol 57:535–538

    Google Scholar 

  • Cattelan AJ, Hartel PG, Fuhrmann JJ (1999) Screening for plant growth promoting rhizobacteria to ptomote early soyabean growth. Soil Sci Soc Am J 63:1670–1680

    Article  CAS  Google Scholar 

  • Chaudhry TM, Khan AG (2002) Role of symbiotic organisms in sustainable plant growth on heavy metal contaminated industrial sites. In: Rajak RC (ed) Biotechnology of microbes and sustainable utilization. Scientific Publishers, Jodhpur, pp 270–279

  • Chaudhry TM, Khan AG (2003) Proceedings of the 7th international conference on the biogeochemistry of trace elements. In: Gorban GR, Lepp N (eds) Swedish University of Agricultural Sciences, Uppsala, pp 134–135 (June 15–19)

  • Correa JD, Barrios ML, Galdona RP (2004) Screening for plant growth-promoting rhizobacteria in Chamaecytisus proliferus (tagasaste), a forage tree-shrub legume endemic to the Canary Islands. Plant Soil 266:75–84

    Google Scholar 

  • Dye DW (1962) The inadequacy of the usual determinative tests for identification of Xanthomonas spp. NZT Sci 5:393–416

    Google Scholar 

  • Garbaye J (1994) Helper bacteria: a new dimension to the mycorrhizal symbiosis. New Phytol 128:197–210

    Article  Google Scholar 

  • Hall IR (1983) A summary of the features of endogonaceous taxa. Technical report no. 8, 3rd edn. Intermay Agricultural Research Centre, New Zealand, p 33

    Google Scholar 

  • Han J, Sun L, Dong X, Cai Z, Yang H, Wang Y, Song W (2005) Characterization of a novel plant growth promoting bacteria strain Delftia tsuruhatensis HR4 both as a diazotroph and a potential biocontrol agent against various pathogens. Sys Appl Microbiol 28:66–76

    Article  CAS  Google Scholar 

  • Hirano S, Nagao N (1988) An improved method for the preparation of colloidal chitin by using methanesulfonic acid. Agric Biol Chem 52:2111–2112

    Article  CAS  Google Scholar 

  • Holbrook AA, Edge WJW, Baily F (1961) Spectrophotometric method for determination of gibberellic acid. Adv Chem Ser 28:159–167

    Article  Google Scholar 

  • King EO, Ward MK, Raney DE (1954) Two simple media for the demonstration of pyocyanin and fluorescin. J Lab Clin Med 44:301–307

    PubMed  CAS  Google Scholar 

  • Loper JE, Scroth MN (1986) Influence of bacterial sources on indole-3 acetic acid on root elongation of sugarbeet. Phytopathol 76:386–389

    Article  CAS  Google Scholar 

  • Lynch JM (1990) The rhizosphere. Wiley, West Sussex

    Google Scholar 

  • Marschner P, Baumann K (2003) Changes in bacterial community structure induced by mycorrhizal colonisation in split-root maize. Plant Soil 251:279–289

    Article  CAS  Google Scholar 

  • Meyer RJ, Linderman RG (1986) Response of subterranean clover to dual inoculation with vesicular-arbuscular mycorrhizal fungi and a plant growth-promoting bacterium, Pseudomonas putida. Soil Biol Biochem 18:185–190

    Article  CAS  Google Scholar 

  • Miller KJ, Wood JM (1996) Osmoadoptation by rhizosphere bacteria. Annu Rev Microbiol 50:101–136

    Article  PubMed  CAS  Google Scholar 

  • Mosse B (1962) The establishment of vesicular-arbuscular mycorrhiza under aseptic conditions. J Gen Microbio 27:509–520

    CAS  Google Scholar 

  • Olsen SR, Sommers LE (1982) Phosphorous. In: Page AL, Miller RH (eds) Methods of soil analysis. Part 2, Chemical and Microbiological Properties, 2nd edn. Agronomy Monograph 9. American Society of Agronomy and Soil Science Society of America, Madison, WI, pp 403–430

  • Pal KK, Tilak KVBR, Saxena AK, Dey R, Singh CS (2001) Suppression of maize root diseases caused by, Macrophomina phaseolina, Fusarium moniliformae and Fusarium graminearum by plant growth promoting rhizobacteria. Microbiol Res 156:209–223

    Article  PubMed  CAS  Google Scholar 

  • Pikovskaya RE (1948) Mobilization of phosphorous in soil in connection with vital activity of some microbial species. Mikrobiol 17:362–370

    CAS  Google Scholar 

  • Robert S, William B (1960) Determination of protein-bound carbohydrate in serum by modified anthrone method. Anal Chem 32(7):885–886

    Article  Google Scholar 

  • Rodriguez H, Fraga R (1999) Phosphate solubilizing bacteria and their role in plant growth promotion. Biotechnol Adv 17:319–339

    Article  PubMed  CAS  Google Scholar 

  • Rojas A, Holguin G, Glick BR, Bashan Y (2001) Synergism between Phyllobacterium sp. (N2-fixer) and Bacillus licheniformis (P-solubilizer), both from a semiarid mangrove rhizosphere. FEMS Microbiol Ecol 35:181–187

    Article  PubMed  CAS  Google Scholar 

  • Schwyn B, Neilands JB (1987) Universal chemical assay for the detection and determination of siderophores. Anal Biochem 160:47–56

    Article  PubMed  CAS  Google Scholar 

  • Skidmore AM, Dickinson CH (1976) Colony interactions and hyphal interference between Septoria nodorum and phylloplane fungi. Trans Br Mycol Soc 66:57–64

    Article  Google Scholar 

  • Sun YP, Unestam T, Lucase SD, Johanson KJ, Kenne L, Finlay R (1999) Exudation-reabsorption in a mycorrhizal fungus, the dynamic interface for interaction with soil and soil microorganisms. Mycorr 9:137–144

    Article  CAS  Google Scholar 

  • Vivas A, Marulanda A, Ruiz-Lozana JM, Barea JM, Azcon R (2003) Influence of a Bacillus sp. on physiological activities of two arbuscular mycorrhizal fungi and on plant responses to PEG-induced drought stress. Mycorrhiza 13(5):249–256

    Google Scholar 

  • Vosatka M, Gryndler M (1999) Treatment with culture fractions from Pseudomonas putida modifies the development of Glomus fistulosum mycorrhiza and the response of potato and maize plants to inoculation. App Soil Ecol 11:245–251

    Article  Google Scholar 

Download references

Acknowledgments

Financial support from Indian Council of Agricultural Research, New Delhi under a network project on “Application of Microorganisms in Agriculture and Allied Sectors” (AMAAS) is gratefully acknowledged.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to N. Kishore.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Praveen Kumar, G., Kishore, N., Leo Daniel Amalraj, E. et al. Evaluation of fluorescent Pseudomonas spp. with single and multiple PGPR traits for plant growth promotion of sorghum in combination with AM fungi. Plant Growth Regul 67, 133–140 (2012). https://doi.org/10.1007/s10725-012-9670-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10725-012-9670-x

Keywords

Navigation