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REVIEW article

Front. Microbiol., 02 June 2017
Sec. Plant Pathogen Interactions
This article is part of the Research Topic Harnessing Useful Rhizosphere Microorganisms for Pathogen and Pest Biocontrol, Volume II View all 33 articles

Microbial Phosphorus Solubilization and Its Potential for Use in Sustainable Agriculture

\r\nElizabeth T. AloriElizabeth T. Alori1Bernard R. GlickBernard R. Glick2Olubukola O. Babalola*Olubukola O. Babalola3*
  • 1Department of Biological Sciences, Faculty of Agriculture, Science and Technology, North-West University, Mmabatho, South Africa
  • 2Department of Biology, University of Waterloo, Waterloo, ON, Canada
  • 3Food Security and Safety Niche Area, North-West University, Mmabatho, South Africa

The use of excess conventional Phosphorus (P) fertilizers to improve agricultural productivity, in order to meet constantly increasing global food demand, potentially causes surface and ground water pollution, waterway eutrophication, soil fertility depletion, and accumulation of toxic elements such as high concentration of selenium (Se), arsenic (As) in the soil. Quite a number of soil microorganisms are capable of solubilizing/mineralizing insoluble soil phosphate to release soluble P and making it available to plants. These microorganisms improve the growth and yield of a wide variety of crops. Thus, inoculating seeds/crops/soil with Phosphate Solubilizing Microorganisms (PSM) is a promising strategy to improve world food production without causing any environmental hazard. Despite their great significance in soil fertility improvement, phosphorus-solubilizing microorganisms have yet to replace conventional chemical fertilizers in commercial agriculture. A better understanding of recent developments in PSM functional diversity, colonizing ability, mode of actions and judicious application should facilitate their use as reliable components of sustainable agricultural systems. In this review, we discussed various soil microorganisms that have the ability to solubilize phosphorus and hence have the potential to be used as bio fertilizers. The mechanisms of inorganic phosphate solubilization by PSM and the mechanisms of organic phosphorus mineralization are highlighted together with some factors that determine the success of this technology. Finally we provide some indications that the use of PSM will promote sustainable agriculture and conclude that this technology is ready for commercial exploitation in various regions worldwide.

Introduction

Phosphorus (P) is one of the essential elements that are necessary for plant development and growth; it makes up about 0.2% of a plant’s dry weight. It is second only to nitrogen among mineral nutrients most commonly limiting the growth of crops (Azziz et al., 2012; Tak et al., 2012). On average, the phosphorus content of soil is about 0.05% (w/w); however, only 0.1% of this phosphorus is available for plant use (Zhu et al., 2011). Traditionally, the challenge of soil phosphorus deficiency is addressed by the application of phosphorus fertilizers. However, the majority of the applied fertilizer phosphorus is not available to plants and the addition of inorganic fertilizers in excess of the amount that is commonly employed to overcome this effect can lead to environmental problems such as, groundwater contamination and waterway eutrophication (Kang et al., 2011). It is therefore of great interest to investigate management strategies that are capable of improving phosphorus fertilization efficiency, increase crop yields and reduce environmental pollution caused by phosphorus loss from the soil.

Soil microorganisms enhance plant nutrient acquisition. They are involved in a wide range of biological processes including the transformation of insoluble soil nutrients (Babalola and Glick, 2012a). Some are capable of solubilizing and mineralizing insoluble soil phosphorus for the growth of plants. Apart from chemical fertilization, microbial P-solubilization and mineralization is the only possible way to increase plant-available phosphorus. In the natural environment numerous microorganisms in the soil and rhizosphere are effective at releasing phosphorus from total soil phosphorus through solubilization and mineralization (Bhattacharyya and Jha, 2012). This group of microorganisms are referred to as Phosphorus Solubilizing Microorganisms (PSM). Many species of soil fungi and bacteria are able to solubilize phosphorus in vitro and some of them can mobilize phosphorus in plants (Zhu et al., 2011). PSM increases the bioavailability of soil insoluble phosphorus for plant use (Zhu et al., 2011). They solubilize insoluble inorganic (mineral) phosphorus and mineralize insoluble organic phosphorus (Sharma et al., 2013). The salt-tolerant or halophilic soil microorganisms that also exhibit the ability to solubilize insoluble phosphorus facilitate the development of saline-alkali soil-based agriculture (Zhu et al., 2011).

The inoculation of soil or crop with phosphate solubilizing/mineralizing microorganisms is therefore a promising strategy for the improvement of plant absorption of phosphorus and thereby reducing the use of chemical fertilizers that have a negative impact on the environment (Alori et al., 2012).

Phosphorus Solubilizing Microorganisms (PSM)

A large number of microbial organisms including bacteria, fungi, actinomycetes, and algae exhibit P solubilization and mineralization ability. Soil bacteria that have been reported to mobilize poorly available phosphorus via solubilization and mineralization include Pseudomonas spp., Agrobacterium spp., and Bacillus circulans (Babalola and Glick, 2012b). Other phosphorus solubilizing and mineralizing bacteria include various strains of Azotobacter (Kumar et al., 2014), Bacillus (Jahan et al., 2013; David et al., 2014), Burkholderia (Mamta et al., 2010; Zhao et al., 2014; Istina et al., 2015), Enterobacter, Erwinia (Chakraborty et al., 2009), Kushneria (Zhu et al., 2011), Paenibacillus (Fernández Bidondo et al., 2011), Ralstonia, Rhizobium (Tajini et al., 2012), Rhodococcus, Serratia, Bradyrhizobium, Salmonella, Sinomonas, and Thiobacillus (Postma et al., 2010; David et al., 2014).

The microbial fungi that function similarly include strains of Achrothcium, Alternaria, Arthrobotrys, Aspergillus, Cephalosporium, Cladosporium, Curvularia, Cunninghamella, Chaetomium, Fusarium, Glomus, Helminthosporium, Micromonospora, Mortierella, Myrothecium, Oidiodendron, Paecilomyces, Penicillium, Phoma, Pichia fermentans, Populospora, Pythium, Rhizoctonia, Rhizopus, Saccharomyces, Schizosaccharomyces, Schwanniomyces, Sclerotium, Torula, Trichoderma, and Yarrowia (Srinivasan et al., 2012; Sharma et al., 2013).

Soil fungi have been reported to be able to traverse long distances within the soil more easily than bacteria and may be more important to the solubilization of inorganic phosphate in soils as they typically produce and secrete more acids, such as gluconic, citric, lactic, 2-ketogluconic, oxalic, tartaric and acetic acid, than bacteria (Sharma et al., 2013). In addition, approximately 20% of actinomycetes could solubilize P, including those in the genera Actinomyces, Micromonospora, and Streptomyces. Algae such as cyanobacteria have also been reported to show P solubilization activity (Sharma et al., 2013).

Benefits of Phosphorus Solubilizing Microorganism

For better utilization of the phosphorus accumulated in soils, PSMs that are capable of transforming insoluble phosphorus to soluble forms can function as biofertilizers. This increases the soluble phosphorus content (Zhu et al., 2012). The use of phosphorus biofertilizers is a promising approach to improving food production through enhancing agricultural yield as it is better to use an environmentally friendly approach (that is, a paradigm that emphasizes the use of biological soil amendments in place of chemicals) to solve the problems of infertile soil (Babalola and Glick, 2012a). Figure 1 shows the effect of inoculation with a PSM (Pseudomonas sp.) on a maize plant. The growth of maize that was inoculated with PSM was improved compared to the control that was not inoculated. PSM act as biofertilizers by making otherwise unavailable P available to growing plants. Phosphorus solubilizing bacteria may also aid the growth of plants by stimulating the efficiency of biological nitrogen fixation, synthesizing phytohormones and enhancing the availability of some trace elements such as zinc and iron (Wani et al., 2007).

FIGURE 1
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FIGURE 1. Biofertilizer effect of Pseudomonas sp. on maize. (A) Maize not inoculated with a PSM. (B) Maize inoculated with a PSM Pseudomonas sp.

Many PSM inoculation studies have shown both improved plant yield and increased phosphorus uptake both in pot experiments and under field conditions. In a pot experiment where Aspergillus niger was used as a biofertilizer (using wheat husks with 20% perlite as carrier material) the soil colonization rate was 5.6 × 106 spores g-1 soil (Wang et al., 2015). The benefits of adopting microbial management of the rhizosphere for sustainable agriculture production includes enhancing the bioavailability of phosphate to crops, stimulated roots and shoots growth, improved root and shoot length, and increased fresh and dry shoot weights, P-labeled phosphate uptake, and significant improvement of grain and dry matter yields (Rodríguez and Fraga, 1999). Table 1 shows the effect of some PSM on a variety of crops.

TABLE 1
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TABLE 1. Effects of some PSM on crops.

Phosphate Solubilizing Microorganisms have considerable synergistic effect on the growth and development of crops (Tallapragada and Gudimi, 2011). Besides solubilizing P, some PSM also demonstrate potential as biocontrol agents against some plant pathogens. PSM manage the pathogens by producing antifungal compounds (such as PAL, phenolics and flavonoids), siderophores, antibiotics, hydrogen cyanide and lytic enzymes all of which enhance inhibition of the growth of plant pathogens.

Phosphate Solubilizing Microorganisms technology improves the fertility and agricultural use of saline-alkaline soil without causing any environmental or health hazard that accompanies the continuous use of synthetic fertilizers. Kushneria sp. YCWA18, a strain that is capable of solubilizing both inorganic phosphorus and organo-phosphorus has also demonstrated moderate halophilic properties and can be used in the development of saline-alkaline based agriculture (Zhu et al., 2011). Aerococcus sp. strain PSBCRG1-1, Pseudomonas aeruginosa strain PSBI3-1, A. terreus strain PSFCRG2-1 and Aspergillus sp. strain PSFNRH-2 were all shown to solubilize tricalcium phosphate at different NaCl concentrations (Srinivasan et al., 2012). The PSM Burkholderia cepacia promoted the growth of maize plants in the presence of NaCl concentrations of up to 5% (Zhao et al., 2014). These organisms all have potential as biofertilizers in saline-alkaline soil based agriculture. In one set of experiments, for bacterial solubilization, increases in NaCl concentration up to 0.8 M resulted in an increase in the percentage of phosphorus released but it declined thereafter. On the other hand, with increases in NaCl concentration the amount of P released among phosphate solubilizing fungi was found to decrease throughout the incubation periods (Srinivasan et al., 2012).

Mechanisms of Inorganic Phosphate Solubilization by PSM

A number of theories explain the mechanism of inorganic phosphate solubilization. As observed in many experiments, the principal mechanism is the production of mineral dissolving compounds such as organic acids, siderophores, protons, hydroxyl ions and CO2 (Rodríguez and Fraga, 1999; Sharma et al., 2013). Organic acids produced as described in Figure 2 together with their carboxyl and hydroxyl ions chelate cations or reduce the pH to release P (Seshachala and Tallapragada, 2012); The organic acids are produced in the periplasmic space by the direct oxidation pathway (Zhao et al., 2014). The excretion of these organic acids is accompanied by a drop in pH that results in the acidification of the microbial cells and the surroundings, hence, P ions are released by substitution of H+ for Ca2+ (Goldstein, 1994). Surprisingly, Asea et al. (1988) discovered that no correlation exists between the pH and the amount of P solubilized. Hence Illmer and Schinner (1995) proposed the theory of acidification by H+. They explained that H+ released is associated with cation assimilation. For example, assimilation of NH4+ together with H+ excretion brings about P solubilisation (Illmer and Schinner, 1995). An alternative mechanism to organic acid production for solubilization of mineral phosphates is the release of H+ to the outer surface in exchange for cation uptake or with the help of H+ translocation ATPase (Rodríguez and Fraga, 1999). It was also reported that the assimilation of NH4+ within microbial cells is accompanied by the release of protons and this results in the solubilization of phosphorus without the production of any organic acids (Sharma et al., 2013). Of all the organic acids, gluconic acid is the most frequent agent of mineral phosphate solubilization; it chelates the cations bound to phosphate, thus making the phosphate available to plants. Gram-negative bacteria solubilize mineral phosphate by direct oxidation of glucose to gluconic acid (Goldstein, 2000). Pyrroloquinoline quinone (PQQ) acts as a redox cofactor in glucose dehydrogenases (GDH) resulting in phosphate solubilisation (Rodríguez et al., 2000).

FIGURE 2
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FIGURE 2. Schematic representation of the organic acids that may be produced by PSM and used to solubilize inorganic forms of phosphate.

Other mechanisms of mineral phosphate solubilization by microorganisms are the production of inorganic acids (such as sulphuric, nitric, and carbonic acids) and the production of chelating substances. It has, however, been reported that the effectiveness of the inorganic acids and the chelating substances in the release of phosphorus in soil is less than that of the organic acids. Kim et al. (1997b) therefore reiterate that organic acid production in P solubilization by PSM is not the sole reason for the increase in P concentration into culture medium. Furthermore, Mycorrhizal fungi effectively extend plant roots, aiding crop phosphorus nutrition by increasing the volume of soil from which phosphate may be absorbed (Browne et al., 2009).

Another mechanism of microbial phosphate solubilization reported in the literature is the liberation of enzymes or enzymolysis, the mechanism of P solubilization by PSM in a medium containing lecithin where the increase in acidity is caused by enzymes that act on lecithin and produce choline (Zhu et al., 2011).

Mechanisms of Organic Phosphorus Mineralization

The major source of organic phosphorus in soil is the organic matter. The values of organic phosphorus in soil can be as high as 30–50% of the total P and soil organic P is largely in the form of inositol phosphate (soil phytate). Other organic P compounds that have been reported are: phosphomonoesters, phosphodiesters, phospholipids, nucleic acids, and phosphotriesters (Rodríguez and Fraga, 1999). In addition, large quantities of xenobiotic phosphonates (pesticides, detergent additives, antibiotics, and flame retardants) that are regularly released into the environment also contain organic P. Most of these organic compounds are high molecular-weight materials that are generally resistant to chemical hydrolysis and must therefore be bio-converted to either soluble ionic phosphate (Pi, HPO42-, H2PO4-), or low molecular-weight organic phosphate, to be assimilated by the cell (Peix et al., 2001).

Phosphorus mineralization refers to the solubilization of organic phosphorus and the degradation of the remaining portion of the molecule. One important theory proposed by Halvorson et al. (1990) for the solubilisation of organic P is the sink theory. This refers to continuous removal of P that result in the dissolution of Ca-P compounds. Consequently, the decomposition of P in organic substrates is consistently correlated with the P content in the biomass of PSM (Dighton and Boddy, 1989). This biological process plays an important role in phosphorus cycling. Different groups of enzymes are involved in this. The first groups of enzymes are those that dephosphorylate the phosphor-ester or phosphoanhydride bond of organic compounds. They are non-specific acid phosphatases (NSAPs). The most studied among these NSAPs enzymes released by PSM, are the phosphomonoesterases also referred to as phosphatases (Nannipieri et al., 2011). These enzymes can either be acid or alkaline phosphomonoesterases (Jorquera et al., 2011). The pH of most soils where phosphate activities were reported ranges from acidic to neutral values. This signifies that acid phosphatases play the major role in this process (Rodríguez and Fraga, 1999).

Another enzyme produced by PSM in the process of organic P mineralization is phytase. This enzyme is responsible for the release of phosphorus from organic materials in soil (plant seeds and pollen) that are stored in the form of phytate. Phytate degradation by phytase releases phosphorus in a form that is available for plant use. Plants generally cannot acquire phosphorus directly from phytate, however, the presence of PSM within the rhizosphere may compensate for a plant’s inability to otherwise acquire phosphorus directly from phytate (Richardson and Simpson, 2011).

Factors Influencing Microbial Phosphate Solubilization

The ability of PSM to transform insoluble organic and inorganic phosphorus is associated with, the nutritional richness of the soil, and the physiological and growth status of the organism. PSM from soils from environmental extremes such as saline-alkaline soils, soil with a high level of nutrient deficiency, or soil from extreme temperature environments have the tendency to solubilize more phosphate than PSM from soils from more moderate conditions (Zhu et al., 2011). There has been a conflicting report on the influence of temperature on phosphorus solubilization by microbes. White et al. (1997) found 20–25°C as the optimum temperature for maximum microbial phosphorus solubiliztion while 28°C was reported by Kang et al. (2002), and Varsha (2002). In addition, others including Kim et al. (1997a), Rosado et al. (1998), Johri et al. (1999), and Fasim et al. (2002), have recorded 30°C as the best temperature for P solubilization. Nahas (1996) and Nautiyal et al. (2000) reported P solubilization at extreme temperature of 45°C in desert soil while Johri et al. (1999) reported solubilization at a low temperature of 10°C.

Among other factors influencing microbial phosphate solubilization are interactions with other microorganisms in the soil, the extent of vegetation, ecological conditions, climatic zone soil types, plant types, agronomic practices, land use systems, and the soil’s physicochemical properties such as organic matter and soil pH (Seshachala and Tallapragada, 2012). Phosphorus is solubilized faster in warm humid climates and slower in cool dry climates. A well-aerated soil will more readily permit rapid phosphorus solubilisation compared to a saturated wet soil. The land use system is the use that the farmland has been previously committed to, such as cropping or livestock activities or even mixed use. Recently, Zhang et al. (2014) reported that adding small amounts of inorganic phosphorus to the rhizosphere could drive phytic acid mineralization by bacteria and thereby improve plant phosphorus nutrition. Lime and compost, used as a soil improver, also had positive effects on phosphate solubilizers. Phosphorus Solubilizing Bacteria population richness and diversity, according to Azziz et al. (2012), were more abundant and diverse following crop rotation. Soil rich in organic matter will favor microbial growth and therefore favors microbial phosphorus solubilisation. Soil pH values between 6 and 7.5 are best for P-availability, this is because at pH values below 5.5 and between 7.5 and 8.5 limits P from becoming fixed by aluminum, iron, or calcium, and hence, not being available for plant use. A negative correlation was observed between the amount of phosphate solubilized by B. cepacia SCAUK0330 and the pH drop that is associated with this process. The pH drop leads to an increase in phosphate solubilization. At pH 3.12, 452 μg⋅mL-1 of phosphorus was solubilized, and when 154 μg⋅mL-1 of P was solubilized the pH value was 4.95 (Zhao et al., 2014). Research has also shown that microbial phosphate solubilization largely depends on the kinds of metabolite produced and its rate of release (Zhu et al., 2011).

Future Prospects

As additional insights are gained regarding PSM and the mechanisms that they use, there is every reason to believe that the use of PSM as biofertilizers will likely improve their use, as effective and important components in the establishment of sustainable soil management systems. The focus of consumers of agricultural produce is on the health, quality and nutritional value of those products. Thus, the employment of PSM as biofertilizers is an option that can increase food production without imposing any health hazard, and at the same time conserve the environment. It is essential that researchers continue to learn more about PSM and, immediately, translate this knowledge into a form that can readily be used by farmers.

Conclusion

This review has shown that phosphate-solubilizing microorganisms have tremendous potential as Bio-fertilizers. Mobilizing soil inorganic phosphate and increasing its bioavailability for plant use by harnessing soil PSM promotes sustainable agriculture, improves the fertility of the soil, and hence increases crop productivity. The use of PSM as microbial inoculants is a new horizon for better plant productivity. PSM technology can contribute to low-input farming systems and a cleaner environment. However, there is need to develop PSB technologies specific to various regions and this should be communicated to farmers in a relatively short time.

Author Contributions

All authors listed, have made substantial, direct and intellectual contribution to the work, and approved it for publication.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

North-West University granted ETA post-doctoral support. BG and OB would like to thank the Natural Sciences and Engineering Research Council of Canada and National Research Foundation, South Africa for grant (UID81192), respectively, for funds that have supported research in their labs.

Abbreviations

PSM, phosphate solubilizing microorganisms.

References

Alori, E., Fawole, O., and Afolayan, A. (2012). Characterization of arbuscular mycorrhizal spores isolated from Southern Guinea Savanna of Nigeria. J. Agric. Sci. 4, 13–19. doi: 10.5539/jas.v4n7p13

CrossRef Full Text | Google Scholar

Asea, P. E. A., Kucey, R. M. N., and Stewart J. W. B. (1988). Inorganic phosphate solubilization by two Penicillium species in solution culture and soil. Soil Biol. Biochem. 20, 459–464. doi: 10.1016/0038-0717(88)90058-2

CrossRef Full Text | Google Scholar

Azziz, G., Bajsa, N., Haghjou, T., Taulé, C., Valverde, A., Igual, J., et al. (2012). Abundance, diversity and prospecting of culturable phosphate solubilizing bacteria on soils under crop–pasture rotations in a no-tillage regime in Uruguay. Appl. Soil Ecol. 61, 320–326. doi: 10.1016/j.apsoil.2011.10.004

CrossRef Full Text | Google Scholar

Babalola, O. O., and Glick, B. R. (2012a). Indigenous African agriculture and plant associated microbes: current practice and future transgenic prospects. Sci. Res. Essays 7, 2431–2439.

Google Scholar

Babalola, O. O., and Glick, B. R. (2012b). The use of microbial inoculants in African agriculture: current practice and future prospects. J. Food Agric. Environ. 10, 540–549.

Google Scholar

Bhattacharyya, P. N., and Jha, D. K. (2012). Plant growth-promoting rhizobacteria (PGPR): emergence in agriculture. World J. Microbiol. Biotechnol. 28, 1327–1350. doi: 10.1007/s11274-011-0979-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Browne, P., Rice, O., Miller, S. H., Burke, J., Dowling, D. N., Morrissey, J. P., et al. (2009). Superior inorganic phosphate solubilization is linked to phylogeny within the Pseudomonas fluorescens complex. Appl. Soil Ecol. 43, 131–138. doi: 10.1016/j.apsoil.2009.06.010

CrossRef Full Text | Google Scholar

Chakraborty, U., Chakraborty, B. N., Basnet, M., and Chakraborty, A. P. (2009). Evaluation of Ochrobactrum anthropi TRS-2 and its talc based formulation for enhancement of growth of tea plants and management of brown root rot disease. J. Appl. Microbiol. 107, 625–634. doi: 10.1111/j.1365-2672.2009.04242.x

PubMed Abstract | CrossRef Full Text | Google Scholar

David, P., Raj, R. S., Linda, R., and Rhema, S. B. (2014). Molecular characterization of phosphate solubilizing bacteria (PSB) and plant growth promoting rhizobacteria (PGPR) from pristine soils. Int. J. Innov. Sci. Eng. Technol. 1, 317–324.

Dighton, J., and Boddy, L. (1989). “Role of fungi in nitrogen, phosphorus and sulfur cycling in temperate forest ecosystems,” in Nitrogen, Phosphorus and Sulfur Utilization by Fungi, eds L. Boddy, R. Marchant, and D. Read (Cambridge: Cambridge University Press), 269–298.

Fasim, F., Ahmed, N., Parsons, R., and Gadd, G. M. (2002). Solubilization of zinc salts by bacterium isolated by the air environment of tannery. FEMS Microbiol. Lett. 213, 1–6. doi: 10.1111/j.1574-6968.2002.tb11277.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Fernández Bidondo, L., Silvani, V., Colombo, R., Pérgola, M., Bompadre, J., and Godeas, A. (2011). Pre-symbiotic and symbiotic interactions between Glomus intraradices and two Paenibacillus species isolated from AM propagules. In vitro and in vivo assays with soybean (AG043RG) as plant host. Soil Biol. Biochem. 43, 1866–1872. doi: 10.1016/j.soilbio.2011.05.004

CrossRef Full Text | 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 (Washington, DC: ASM Press), 197–203.

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, (Paris: IFA), 220.

Google Scholar

Halvorson, H. O., Keynan, A., and Kornberg, H. L. (1990). Utilization of calcium phosphates for microbial growth at alkaline pH. Soil Biol. Biochem. 22, 887–890. doi: 10.1016/0038-0717(90)90125-J

PubMed Abstract | CrossRef Full Text | Google Scholar

Illmer, P., and Schinner, F. (1995). Solubilization of inorganic calcium phosphates—solubilization mechanisms. Soil Biol. Biochem. 27, 257–263. doi: 10.1016/0038-0717(94)00190-C

CrossRef Full Text | Google Scholar

Istina, I. N., Widiastuti, H., Joy, B., and Antralina, M. (2015). Phosphate-solubilizing microbe from Saprists peat soil and their potency to enhance oil palm growth and P uptake. Proc. Food Sci. 3, 426–435. doi: 10.1016/j.profoo.2015.01.047

CrossRef Full Text | Google Scholar

Jahan, M., Mahallati, M. N., Amiri, M. B., and Ehyayi, H. R. (2013). Radiation absorption and use efficiency of sesame as affected by biofertilizers inoculation in a low input cropping system. Ind. Crops Prod. 43, 606–611. doi: 10.1016/j.indcrop.2012.08.012

CrossRef Full Text | Google Scholar

Jain, R., Saxena, J., and Sharma, V. (2012). Effect of phosphate-solubilizing fungi Aspergillus awamori S29 on mungbean (Vigna radiata cv. RMG 492) growth. Folia Microbiol. 57, 533–541. doi: 10.1007/s12223-012-0167-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Johri, J. K., Surange, S., and Nautiyal, C. S. (1999). Occurrence of salt, pH and temperature tolerant phosphate solubilizing bacteria in alkaline soils. Curr. Microbiol. 39, 89–93. doi: 10.1007/s002849900424

PubMed Abstract | CrossRef Full Text | Google Scholar

Jorquera, M. A., Crowley, D. E., Marschner, P., Greiner, R., Fernandez, M. T., Romero, D., et al. (2011). Identification of β-propeller phytase-encoding genes in culturable Paenibacillus and Bacillus sp. from the rhizosphere of pasture plants on volcanic soils. FEMS Microbiol. Ecol. 75, 163–172. doi: 10.1111/j.1574-6941.2010.00995.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Kang, J., Amoozegar, A., Hesterberg, D., and Osmond, D. L. (2011). Phosphorus leaching in a sandy soil as affected by organic and incomposted cattle manure. Geoderma 161, 194–201. doi: 10.1016/j.geoderma.2010.12.019

CrossRef Full Text

Kang, S. C., Ha, G. C., Lee, T. G., and Maheshwari, D. K. (2002). Solubilization of insoluble inorganic phosphates by a soil inhabiting fungus sp. Ps 102. Curr. Sci. 79, 439–442.

Google Scholar

Kim, K. Y., Jordan, D., and Kirshanan, H. B. (1997a). Rahnella aquatilis, a bacterium isolated from soybean rhizosphere, can solubilize hydroxyapatite. FEMS Micobiol. Lett. 153, 273–277. doi: 10.1016/S0378-1097(97)00246-2

CrossRef Full Text | Google Scholar

Kim, K. Y., McDonald, G. A., and Jordan, D. (1997b). Solubilization of hydroxyapatite by Enterobacter agglomerans and cloned Escherichia coli in culture medium. Biol. Fertil. Soils 24, 347–352. doi: 10.1007/s003740050256

CrossRef Full Text | Google Scholar

Kumar, S., Bauddh, K., Barman, S. C., and Singh, R. P. (2014). Amendments of microbial bio fertilizers and organic substances reduces requirement of urea and DAP with enhanced nutrient availability and productivity of wheat (Triticum aestivum L.). Ecol. Eng. 71, 432–437. doi: 10.1016/j.ecoleng.2014.07.007

CrossRef Full Text | Google Scholar

Mahanta, D., Rai, R. K., Mishra, S. D., Raja, A., Purakayastha, T. J., and Varghese, E. (2014). Influence of phosphorus and biofertilizers on soybean and wheat root growth and properties. Field Crops Res. 166, 1–9. doi: 10.1016/j.fcr.2014.06.016

CrossRef Full Text | Google Scholar

Mamta, R. P., Pathania, V., Gulati, A., Singh, B., Bhanwra, R. K., and Tewari, R. (2010). Stimulatory effect of phosphate-solubilizing bacteria on plant growth, stevioside and rebaudioside-A contents of Stevia rebaudiana Bertoni. Appl. Soil Ecol. 46, 222–229. doi: 10.1016/j.apsoil.2010.08.008

CrossRef Full Text | Google Scholar

Nahas, E. (1996). Factors determining rock phosphate solubilization by microorganisms isolated from soil. World J. Microbiol. Biotechnol. 12, 567–572. doi: 10.1007/BF00327716

PubMed Abstract | CrossRef Full Text | Google Scholar

Nannipieri, P., Giagnoni, L., Landi, L., and Renella, G. (2011). “Role of phosphatase enzymes in soil,” in Phosphorus in Action: Biological Processes in Soil Phosphorus Cycling. Soil Biology, eds E. Bunemann, A. Oberson, and E. Frossard (Berlin: Springer), 215–243.

Google Scholar

Nautiyal, C. S., Bhadauria, S., Kumar, P., Lal, H., Mondal, R., and Verma, D. (2000). Stress induced phosphate solubilization in bacteria isolated from alkaline soils. FEMS Microbiol. Lett. 182, 291–296. doi: 10.1111/j.1574-6968.2000.tb08910.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Peix, A., Mateos, P. F., Rodríguez-Barrueco, C., Martínez-Molina, E., and Velázquez, E. (2001). Growth promotion of common bean (Phaseolus vulgaris L.) by a strain of Burkholderia cepacia under growth chamber conditions. Soil Biol. Biochem. 33, 1927–1935. doi: 10.1016/S0038-0717(01)00119-5

CrossRef Full Text | Google Scholar

Postma, J., Nijhuis, E. H., and Someus, E. (2010). Selection of phosphorus solubilizing bacteria with biocontrol potential for growth in phosphorus rich animal bone charcoal. Appl. Soil Ecol. 46, 464–469. doi: 10.1016/j.apsoil.2010.08.016

CrossRef Full Text | Google Scholar

Richardson, A. E., and Simpson, R. J. (2011). Soil microorganisms mediating phosphorus availability. Plant Physiol. 156, 989–996. doi: 10.1104/pp.111.175448

PubMed Abstract | CrossRef Full Text | Google Scholar

Rodríguez, H., and Fraga, R. (1999). Phosphate solubilizing bacteria and their role in plant growth promotion. Biotechnol. Adv. 17, 319–339. doi: 10.1016/S0734-9750(99)00014-2

CrossRef Full Text | Google Scholar

Rodríguez, H., Rossolini, G. M., Gonzalez, T., Li, J., and Glick, B. R. (2000). Isolation of a gene from Burkholderia cepacia IS-16 encoding a protein that facilitates phosphatase activity. Curr. Microbiol. 40, 362–366. doi: 10.1007/s002840010071

PubMed Abstract | CrossRef Full Text | Google Scholar

Rosado, A. S., De Azevedo, F. S., da Croz, D. W., Van Elas, J. D., and Seldin, L. (1998). Phenotypic and genetic diversity of Paenibacillus azotofixans strains isolated from the rhizosphere soil of different grasses. J. Appl. Microbiol. 84, 216–226. doi: 10.1046/j.1365-2672.1998.00332.x

CrossRef Full Text | Google Scholar

Seshachala, U., and Tallapragada, P. (2012). Phosphate solubilizers from the rhizosphere of Piper nigrum L. in Karnataka, India. Chil. J. Agric. Res. 72, 397–403. doi: 10.4067/S0718-58392012000300014

CrossRef Full Text | Google Scholar

Sharma, S. B., Sayyed, R. Z., Trivedi, M. H., and Gobi, T. A. (2013). Phosphate solubilizing microbes: sustainable approach for managing phosphorus deficiency in agricultural soils. Springerplus 2, 587–600. doi: 10.1186/2193-1801-2-587

PubMed Abstract | CrossRef Full Text | Google Scholar

Srinivasan, R., Yandigeri, M. S., Kashyap, S., and Alagawadi, A. R. (2012). Effect of salt on survival and P-solubilization potential of phosphate solubilizing microorganisms from salt affected soils. Saudi J. Biol. Sci. 19, 427–434. doi: 10.1016/j.sjbs.2012.05.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Swarnalakshmi, K., Prasanna, R., Kumar, A., Pattnaik, S., Chakravarty, K., Shivay, Y. S., et al. (2013). Evaluating the influence of novel cyanobacterial biofilmed biofertilizers on soil fertility and plant nutrition in wheat. Euro. J. Soil Biol. 55, 107–116. doi: 10.1016/j.ejsobi.2012.12.008

CrossRef Full Text | Google Scholar

Tajini, F., Trabelsi, M., and Drevon, J. J. (2012). Combined inoculation with Glomus intraradices and Rhizobium tropici CIAT899 increases phosphorus use efficiency for symbiotic nitrogen fixation in common bean (Phaseolus vulgaris L.). Saudi J. Biol. Sci. 19, 157–163. doi: 10.1016/j.sjbs.2011.11.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Tak, H. I., Ahmad, F., Babalola, O. O., and Inam, A. (2012). Growth, photosynthesis and yield of chickpea as influenced by urban wastewater and different levels of phosphorus. Int. J. Plant Res. 2, 6–13. doi: 10.5923/j.plant.20120202.02

CrossRef Full Text | Google Scholar

Tallapragada, P., and Gudimi, M. (2011). Phosphate solubility and biocontrol activity of Trichoderma harzianum. Turk. J. Biol. 35, 593–600.

Google Scholar

Tani, A., Akita, M., Murase, H., and Kimbara, K. (2011). Culturable bacteria in hydroponic cultures of moss Racomitrium japonicum and their potential as biofertilizers for moss production. J. Biosci. Bioeng. 112, 32–39. doi: 10.1016/j.jbiosc.2011.03.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Varsha, N. H. H. (2002). Aspergillus aculeatus as a rock phosphate solubilizer. Soil Biol. Biochem. 32, 559–565.

Google Scholar

Wang, H., Liu, S., Zhal, L., Zhang, J., Ren, T., Fan, B., et al. (2015). Preparation and utilization of phosphate biofertilizers using agricultural waste. J. Integr. Agric. 14, 158–167. doi: 10.1016/S2095-3119(14)60760-7

CrossRef Full Text | Google Scholar

Wang, S.-L., Hsu, W.-H., and Liang, T.-W. (2010). Conversion of squid pen by Pseudomonas aeruginosa K187 fermentation for the production of N-acetyl chitooligosaccharides and biofertilizers. Carbohydr. Res. 345, 880–885. doi: 10.1016/j.carres.2010.01.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Wani, P. A., Khan, M. S., and Zaidi, A. (2007). Co-inoculation of nitrogen fixing and phosphate solubilizing bacteria to promote growth, yield and nutrient uptake in chickpea. Acta Agron. Hung. 55, 315–323. doi: 10.1556/AAgr.55.2007.3.7

CrossRef Full Text | Google Scholar

White, C., Sayer, J. A., and Gadd, G. M. (1997). Microbial solubilization and immobilization of toxic metals: key biogeochemical processes for treatment of contamination. FEMS Microbiol. Rev. 20, 503–516. doi: 10.1111/j.1574-6976.1997.tb00333.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Xiao, C., Zhang, H., Fang, Y., and Chi, R. (2013). Evaluation for rock phosphate solubilization in fermentation and soil–plant system using a stress-tolerant phosphate-solubilizing Aspergillus niger WHAK1. Appl. Microbiol. Biotechnol. 169, 123–133. doi: 10.1007/s12010-012-9967-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Zayed, M. S. (2012). Improvement of growth and nutritional quality of Moringa oleifera using different biofertilizers. Ann. Agric. Sci. 57, 53–62. doi: 10.1016/j.aoas.2012.03.004

CrossRef Full Text | Google Scholar

Zhang, L., Ding, X., Chen, S., He, X., Zhang, F., and Feng, G. (2014). Reducing carbon: phosphorus ratio can enhance microbial phytin mineralization and lessen competition with maize for phosphorus. J. Plant Interact. 9, 850–856. doi: 10.1080/17429145.2014.977831

CrossRef Full Text | Google Scholar

Zhao, K., Penttinen, P., Zhang, X., Ao, X., Liu, M., Yu, X., et al. (2014). Maize rhizosphere in Sichuan, China, hosts plant growth promoting Burkholderia cepacia with phosphate solubilizing and antifungal abilities. Microbiol. Res. 169, 76–82. doi: 10.1016/j.micres.2013.07.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, F., Qu, L., Hong, X., and Sun, X. (2011). Isolation and characterization of a phosphate solubilizing halophilic bacterium Kushneria sp. YCWA18 from Daqiao Saltern on the coast of yellow sea of China. Evid. Based Complement. Alternat. Med. 2011:615032. doi: 10.1155/2011/615032

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, H. J., Sun, L. F., Zhang, Y. F., Zhang, X. L., and Qiao, J. J. (2012). Conversion of spent mushroom substrate to biofertilizer using a stress-tolerant phosphate-solubilizing Pichia farinose FL7. Bioresour. Technol. 11, 410–416. doi: 10.1016/j.biortech.2012.02.042

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: mineralization, phosphorus, soil nutrient management, soil microbes, solubilization

Citation: Alori ET, Glick BR and Babalola OO (2017) Microbial Phosphorus Solubilization and Its Potential for Use in Sustainable Agriculture. Front. Microbiol. 8:971. doi: 10.3389/fmicb.2017.00971

Received: 04 February 2017; Accepted: 15 May 2017;
Published: 02 June 2017.

Edited by:

Brigitte Mauch-Mani, University of Neuchâtel, Switzerland

Reviewed by:

Oswaldo Valdes-Lopez, National Autonomous University of Mexico, Mexico
Yunuen Tapia Torres, National Autonomous University of Mexico, Mexico

Copyright © 2017 Alori, Glick and Babalola. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Olubukola O. Babalola, olubukola.babalola@nwu.ac.za

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