Skip to main content

Phosphate solubilizing microorganisms vs. phosphate mobilizing microorganisms: What separates a phenotype from a trait?

  • Conference paper
First International Meeting on Microbial Phosphate Solubilization

Part of the book series: Developments in Plant and Soil Sciences ((DPSS,volume 102))

Abstract

Soils are often high in insoluble mineral phosphates but deficient in the soluble orthophosphate (Pi) essential for the growth of most plants and microorganisms. In agricultural crop production, phosphorous is second only to nitrogen in importance as a fertilizer amendment so that phosphorus fertilizers are the world’s second largest bulk agricultural chemical and, therefore, the second most widely applied chemical on Earth. There is a broad spectrum of mineral phosphate chemistries; but in arid to semiarid soils the predominant forms are the calcium phosphates. Calcium phosphates are soluble to varying degrees in the presence of the wide array of organic acids produced by microorganisms. Other biosolubilization mechanisms exist as well, so that conversion of mineral phosphates to Pi is generically attributed to microorganisms in most representations of global P cycling. With respect to plant growth, some workers have postulated that associations between plant roots and mineral phosphate solubilizing (MPS) microorganisms could play an important role in phosphorus nutrition in many natural and agroecosystems. As a result, an enormous amount of research has been conducted over the last 100 years involving isolation and characterization of MPS microorganisms from many soils with the goal of developing P biofertilizers that would accomplish much the same function as biological nitrogen fixation. To date, the results of these efforts have been problematic. In this review, we will attempt to identify the variables of state with respect to the MPS phenomenon in bacteria and briefly summarize the challenges that confront this field of research. Finally we will discuss our observation that, in Gram-negative rhizobacteria, extracellular oxidation of glucose to gluconic acid and 2-ketogluconic acid via the direct oxidation pathway provides the biochemical basis for highly efficacious calcium phosphate solubilization and may, in fact, be the basis for the evolution of mutualistic plant-bacteria relationships in some phosphate-limited soil ecosystems.

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.

References

  • Adamowicz M, Conway T and Nickerson K W 1991 Nutritional complementation of oxidative glucose metabolism in Escherichia coli via pyrroloquinoline quinone-dependent glucose dehydrogenase and the Entner-Doudoroff pathway. Appl. Environ. Microbiol. 57, 2012–2015.

    PubMed  CAS  Google Scholar 

  • Agnihotri V P 1970 Solubilization of insoluble phosphates by some soil fungi isolated from nursery seed beds. Can. J. Microbiol. 16, 877–880.

    Article  PubMed  CAS  Google Scholar 

  • Asea P, Kucy R M N and Stewart J.W.B. J W B 1988 Inorganic phosphate solubilization by two Penicillium species in solution culture and soil. Soil. Biol. Biochem. 20, 459–464.

    Article  CAS  Google Scholar 

  • Babu-Khan S, Yeo T-C, Martin W L, Duron M, Rogers R D and Goldstein A H 1995 Cloning of a mineral phosphate solubilizing gene from Pseudomonas cepacia. Appl. Environ. Microbiol. 61, 972–978.

    PubMed  CAS  Google Scholar 

  • Bagyaraj D J, Krishnaraj P U and Khanuja S P S 2000 Mineral phosphate solubilization: agronomic implications, mechanism and molecular genetics. Proc. Indian Natl. Sci. Acad. (PINSA) 66, 69–82.

    CAS  Google Scholar 

  • Banik S and Dey B K 1982 Available phosphate content of an alluvial soil as influenced by inoculation of some isolated phosphate-solubilizing microorganisms. Plant Soil 69, 353–364.

    Article  CAS  Google Scholar 

  • Blake F 1993 Organic Food Production in World Agriculture. Cartwright Sterling Publication Ltd, Hong-Kong p. 284.

    Google Scholar 

  • Chabot R, Antoun H and Cescas M P 1993 Stimulation de la croissance du mais et de la laitue romaine par des microorganisms dissolvant de phosphate inorganique. Can. J. Microbiol. 39, 941–947.

    Article  Google Scholar 

  • Cosgrove D J 1977 Microbial transformations in phosphorus cycle. Adv. Microb. Ecol. 1, 95–128.

    CAS  Google Scholar 

  • Duine J A 1991 Quinoproteins: enzymes containing the quinoid cofactor pyrroloquinoline quinone, topaquinone or tryptophan-tryptophan quinone. Eur. J. Biochem. 200, 271–284.

    Article  PubMed  CAS  Google Scholar 

  • Egan S E, Fliege R, Tong S, Shibata A, Wolfe R E Jr and Conway T 1992 Molecular characterization of the Entner-Doudoroff pathway in Escherichia coli: Sequence analysis and localization of promoters for edd-eda operon. J. Bacteriol. 174, 4638–4646.

    PubMed  CAS  Google Scholar 

  • Gaur A C 1990 Phosphate Solubilizing Microorganisms as Biofertilizer. Omega Scientific Publications, New Delhi p. 176.

    Google Scholar 

  • Gerretsen F C 1948 The influence of microorganisms on the phosphate intake by the plant. Plant Soi1 1, 51–81.

    Article  CAS  Google Scholar 

  • Glick B R 1995 The enhancement of plant growth by free living bacteria. Can. J. Microbiol. 32, 145–148.

    Google Scholar 

  • Goldstein A H 1986 Bacterial mineral phosphate solubilization: Historical perspective and future prospects. Am J. Alt. Agric. 1, 57–65.

    Google Scholar 

  • Goldstein A H and Liu S-T 1987 Molecular cloning and regulation of a mineral phosphate solubilizing gene from Erwinia herbicola. Bio/Technology 5, 72–74.

    Article  CAS  Google Scholar 

  • Goldstein A H, Rogers R D and Mead G 1993 Separating phosphate from ores via bioprocessing. Bio/Technology 11, 1250–1254.

    CAS  Google Scholar 

  • Goldstein A H 1994 Involvement of the quinoprotein glucose dehydrogenase in the solubilization of exogenous phosphates by gram-negative bacteria. In Phosphate in Microorganisms: Cellular and Molecular Biology. Eds. A. Torriani-Gorini, E. Yagil and S. Silver. pp. 197–203. ASM Press, Washington, D.C. p. 223.

    Google Scholar 

  • Goldstein A H 1995 Recent progress in understanding the molecular genetics and biochemistry of calcium phosphate solubilization by gram negative bacteria. Biol. Agric. Hortic. 12, 185–193.

    Google Scholar 

  • Goldstein A H, Braverman K E and Osorio N 1999 Evidence for mutualism between a plant growing in a phosphatelimited desert environment and a mineral phosphate solubilizing (MPS) rhizobacteria. FEMS Microbiol. Ecol. 30, 295–300.

    Article  PubMed  CAS  Google Scholar 

  • Goldstein A H 2000 Bioprocessing of rock phosphate ore: essential technical considerations for the development of a successful commercial technology. In Proceedings of the 4th International Fertilizer Association Technical Conference. IFA, Paris, p. 220.

    Google Scholar 

  • Halder A K, Mishra A K and Chakraborthy P K 1991 Solubilizing of inorganic phosphates by Bradyrhizobium. Indian J. Expt. Biol. 29, 28–31.

    CAS  Google Scholar 

  • Hardy G P, Texeria M A, de Mattos M J and Neijssel O M 1993 Energy conservation by pyrroloquinoline quinonelinked xylose oxidation in Pseudomonas putida NCTC10936 during carbon limited growth in chemostat culture. FEMS Microbiol. Lett. 107, 107–110.

    Article  PubMed  CAS  Google Scholar 

  • Hausenbuiller R L 1972 Soil Science, Principles and Practices. Wm. C. Brown Company, Dubuque, Iowa p. 501.

    Google Scholar 

  • Holford I C R 1997 Soil phosphorus its measurement and its uptake by plants. Aust. J. Soil Res. 35, 227–239.

    Article  CAS  Google Scholar 

  • Holt J G, Krieg N R, Sneath P H A, Stanley J T and William S T 1994 Bergey’s Mannual of Determinative Bacteriology, 9th Edition, Williams and Willikins, Baltimore.

    Google Scholar 

  • Illmer P. and Schinner F 1992 Solubilization of inorganic phosphates by microorganisms isolated from forest soils. Soil Biol. Biochem. 24, 389–395.

    Article  Google Scholar 

  • Illmer P and Schinner F 1995 Solubilization of inorganic calcium phosphates-solubilization mechanisms. Soil Biol. Biochem. 27, 257–263.

    Article  CAS  Google Scholar 

  • Jackson ML 1973 Soil Chemical Analysis. Prentice Hall of India (P) Ltd, New Delhi, India. p. 318.

    Google Scholar 

  • Juriank J J, Dudley S C, Allen M F and Knight W G 1986 The role of calcium oxalate in the availability of phosphorus in soils of semiarid regions: Thermodynamic study. Soil Sci. 142, 255–261.

    Article  Google Scholar 

  • Kadrekar S B and Talashilkar S C 1977 Efficiency of applied phosphorus in relation to its saturation in lateritic soils of Konkan. J. Indian Soc. Soil Sci. 25, 269–273.

    Google Scholar 

  • Krishnaraj P U 1987 Studies on beneficial microorganisms in crop plants. M. Sc. (Agri) Thesis, U.A.S., Bangalore.

    Google Scholar 

  • Krishnaraj PU and Gowda T K S 1990 Occurrence of phosphate solubilizing bacteria in the endorhizosphere of crop plants. Curr. Sci. 59, 933–934.

    Google Scholar 

  • Krishnaraj P U 1996 Genetic characterization of mineral phosphate solubilization in Pseudomonas sp. Ph.D. Thesis, I.A.R.I., New Delhi.

    Google Scholar 

  • Kucey R W N, Tanzen H H and Leggett M E 1989 Microbially mediated increases in plant available phosphorus. Adv. Agron. 42, 199–228.

    Article  CAS  Google Scholar 

  • Larsen S 1967 Soil phosphorus. Adv. Agron. 19, 151–210.

    CAS  Google Scholar 

  • Lessie T G, Berka T and Zamanigian S 1979 Pseudomonas cepacia mutants blocked in the direct oxidative pathway of glucose degradation. J. Bacteriol. 139, 323–325.

    PubMed  CAS  Google Scholar 

  • Liu S-T, Lee L-Y, Tai C-Y, Horng C-H, Chang Y-S, Wolfram J H, Rogers R D and Goldstein A H 1992 Cloning of an Erwinia herbicola gene necessary for gluconic acid production and enhanced mineral phosphate solubilization in Escherichia coli HB101. J. Bacteriol. 174, 5814–5819.

    PubMed  CAS  Google Scholar 

  • Luna M F, Mignone C F and Boiardi J L 2000 The carbon source influences the energetic efficiency of the respiratory chain of N2-fixing Acetobacter diazotrophicus. Appl. Microbiol. Biotechnol. 54, 564–569.

    Article  PubMed  CAS  Google Scholar 

  • Maheshkumar K S 1997 Studies on microbial diversity and their activity in soil under bamboo plantation. M.Sc. Thesis, Univ. Agricultural Sciences, Dharwad, India.

    Google Scholar 

  • Maheshkumar K S, Alagawadi A R, Krishnaraj P U, Patil V C 1998 Microbial diversity in the rhizosphere and inoculation effect of selected rhizobacteria on growth of bamboo seedlings. 39th Annual Conference, Association of Microbiologists of India. Dec. 5–7:1998. Mangalore, India.

    Google Scholar 

  • Martin J K and Cunninghum R B 1973 Factors controlling the release of phosphorus from decomposing wheat roots. Aust. J. Biol. Sci. 26, 715–727.

    CAS  Google Scholar 

  • Mehta Y R and Bhide V P 1970 Solubilization of tricalcium phosphate by some soil fungi. Indian J. Exp. Biol. 8, 228–229.

    PubMed  CAS  Google Scholar 

  • Parks E J, Olson G J, Brickman F E and Baldi F 1990 Characterization of high performance liquid chromatography (HPLC) of the solubilization of phosphorus in iron ore by a fungus. J. Indian Microbiol. 5, 183–190.

    Article  CAS  Google Scholar 

  • Pereira AT 1990 Endorhizosphere bacteria of wetland rice, their H2-dependent chemolithotrophy, N2 fixation, P-solubilization and interaction with rice genotypes. Ph.D. Thesis, University of Agricultural Sciences, Bangalore, p. 192.

    Google Scholar 

  • Pikovskaya R I 1948 Mobilization of phosphorus in soil in connection with vital activity of some microbial species. Mikrobiologiya 17, 362–370.

    CAS  Google Scholar 

  • Richardson A E 1994 Soil microoganisms and phosphorus availability. Soil Biota 50, 35–39.

    Google Scholar 

  • Sperber J I 1957 Solution of mineral phosphates by soil bacteria. Nature 180, 994–995.

    Article  PubMed  CAS  Google Scholar 

  • Stevenson F J 1986 Cycles of Soil Carbon, Nitrogen Phosphorus Sulphur and Micronutrients. Wiley, New York. p. 428.

    Google Scholar 

  • Sundara Rao W B and Sinha M K 1963 Phosphate dissolving microorganisms in the soil and rhizosphere. Indian J. Agric. Sci. 33, 272–278.

    Google Scholar 

  • Tinker P B 1980 The role of rhizosphere microorganisms in phosphorus uptake by plants. In The role of phosphorus in agriculture. Ed. F E Khasawneh, American Society for Agronomy Press, Madison. p. 909.

    Google Scholar 

  • Tomar S S, Pathan M A, Gupta K P and Khandar U R 1993 Effect of phosphate solubilizing bacteria at different levels of phosphate on blackgram (Phaseolus mungo). Indian J. Agron. 38, 131–133.

    CAS  Google Scholar 

  • Torriani-Gorini A, Rothman F G, Silver S, Wright A and Yagil E 1987 Phosphate Metabolism and Cellular Regulation in Microorganisms. ASM Press, Washington, D.C p. 307.

    Google Scholar 

  • Torriani-Gorini A, Yagil E and Silver S 1993 Phosphate in Microorganisms: Cellular and Molecular Biology. ASM Press, Washington, D.C. p. 427.

    Google Scholar 

  • van Schie K J, Hellingwerf J P, van Dijken M G L, Elferink J M, van Dijl L S, Kuenen J G and Konings WN 1985 Energy transduction by electron transfer via pyrroloquinoline quinone-dependent glucose dehydrogenase in Escherichia coli, Pseudomonas aeruginosa, and Acinetobacter calcoaceticus (var lwoffii). J. Bacteriol. 163, 493–499.

    PubMed  Google Scholar 

  • Wani P V, More B B and Patil P L 1979 Physiological studies on the activity of phosphorus solublizing microorganisms. Indian J. Microbiol. 19, 23–31.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

E. Velázquez C. Rodríguez-Barrueco

Rights and permissions

Reprints and permissions

Copyright information

© 2007 Springer

About this paper

Cite this paper

Goldstein, A.H., Krishnaraj, P.U. (2007). Phosphate solubilizing microorganisms vs. phosphate mobilizing microorganisms: What separates a phenotype from a trait?. In: Velázquez, E., Rodríguez-Barrueco, C. (eds) First International Meeting on Microbial Phosphate Solubilization. Developments in Plant and Soil Sciences, vol 102. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-5765-6_31

Download citation

Publish with us

Policies and ethics