Open Access Open Access  Restricted Access Subscription Access

Rock Phosphate Solubilization using Oxalic Acid - secreting Laccaria fraterna


Affiliations
1 Methodist Hospital Research Institute, Houston, TX 77030, United States
2 Baylor College of Medicine, Houston, TX 77030,, United States
3 Morgan State University, Baltimore, MD 21251,, United States
 

Laccaria fraterna is an ectomycorrhizal fungus commonly associated with conifers and angiosperms. To check whether L. fraterna possess mechanism to solubilize rock phosphate by secreting organic acids, it was grown in Pikovskaya’s medium with rock phosphate as the main ‘P’ source in the presence of ammonium sulphate. The fungus grew profusely in the medium by secreting oxalic acid which caused a reduction in the pH of the medium. To understand the mechanism behind the rock phosphate solubilization, an attempt was made to clone the fungal genomic DNA. In the Pikovskaya’s medium amended with rock phosphate, the clone MAP 22 released 80 μg/mL of P at the end of 24 h while, L. fraterna released 65 μg/mL of P at the end of 30 days incubation. We used HPTLC to confirm that oxalic acid is the main mineral-transforming agent that was secreted. The wild and the sub-clone MAP 22 released 1,490 and 2,950 μg/mL of oxalic acid, respectively. Therefore, it is possible to use the clone MAP 22 for more efficient inoculum production in vivo.

Keywords

Ectomycorrhizal Fungus, Laccaria fraterna, Phosphate Solubilization, Rock Phosphate
User
Notifications

  • Rodríquez H, Fraga R. Phosphate solubilizing bacteria and their role in plant growth promotion. Biotechnol. Adv. 1999; 17(4–5): 319–339.
  • Vassileva M, Vassilev N et al. Rock phosphate solubilization by Aspergillus niger on olive cake-based medium and its further application in a soil-plant system. W J Microb Biot. 1998; 14(2):281–284.
  • Omar SA. The role of rock-phosphate-solubilizing fungi and Vesicular-Arbusular-Mycorrhiza (VAM) in growth of wheat plants fertilized with rock phosphate. W J Microb Biot. 1998; 14 (2): 211–218.
  • Abd Alla MH. Phosphatases and the utilization of organic phosphorus by Rhizobium leguminosarum biovar viceae. Lett Appl Microbiol. 1994; 18(5):294–296.
  • Cordell D, Drangert JO, White S. The story of phosphorus: Global food security and food for thought. Global Environ Chang. 2009; 19(2):292–305.
  • Gerke L. Phosphate, aluminum, and iron in the soil solution of three different soils in relation to varying concentrations of citric acid. Zeitschrift für Pflanzenernährung und Bodenkunde. 1992; 155(4):339–343.
  • Chellappan P, Christy SAA, Mahadevan A. Multiplication of Arbuscular Mycorrhizal Fungi on ischolar_mains. In: Mukerji KG, Manoharachary C, Chamola BP. editors. Techniques in mycorrhizal studies. Kluwer, Dordrecht, 285–297.
  • Marmeisse R, Guidot A, Gay G, Lambilliotte R, Sentenac H, Combier J-P, Melayah D, Fraissinet-Tachet L, Debaud JC. Hebeloma cylindrosporum- a model species to study ectomycorrhizal symbiosisfrom gene to ecosystem. New Phytol. 2004; 163(3): 481–498.
  • Burford EP, Fomina M, Gadd GM. Fungal involvement in bioweathering and biotransformation of rocks and minerals. Mineral Mag. 2003; 67(6):1127–1155.
  • Liu Q, Loganathan P, Hedleya MJ, Grace LJ. Effect of mycorrhizal inoculation on rhizosphere properties, phosphorus uptake and growth of pine seedlings treated with and without a phosphate rock fertilizer. J Plant Nutr. 2008; 31(1): 137–156.
  • Smits MM, Bonneville S, Haward S, Leake JR. Ectomy-corrhizal weathering, a matter of scale? Mineral Mag. 2008; 72(1):131–134.
  • Dighton J. Acquisition of nutrients from organic resources by mycorrhizal autotrophic plants. Experientia. 1991; 47(4):362–369.
  • Nahas E. Factors determining rock phosphate solubilization by microorganisms isolated from soil. W J Microb Biot. 1996; 12(6):567–572.
  • Lapeyrie F, Ranger J. Phosphate–solubilizing activity of ectomycorrhizal fungi in vitro. Can J Bot. 1991; 69(2): 342–346.
  • Tommerup IC, Bougher NL. Laccaria fraterna, a common ectomycorrhizal fungus with mono-and bi-sporic basidia and multinucleate spore: comparison with the quadristerigmate, binuleate spored Laccaria laccata and the hypogeous relative Hydnangium carneum. Mycol Res. 1991; 95(6):689–698.
  • Marx DH. The influence of ectotrophic mycorrhizal fungi on the resistance of pine ischolar_mains to pathogenic infections. In, Antagonism of mycorrhizal fungi ischolar_main pathogenic fungi and soil bacteria. Phytopathol. 1969; 59:153–163.
  • Pikovskaya RI. Mobilization of phosphorus in soil in connection with the vital activity of some microbial species. Mikrobiologia. 1948; 17:362.
  • Zolan ME, Pukkila PJ. Inheritance of DNA methylation in Coprinus cinereus. Mol Cell Biol. 1986; 6(1): 195–200.
  • Sambrook J, Maniatis T, Fritsch EF. Molecular cloning: A laboratory manual, 2nd ed. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory; 1989.
  • Sternberg N, Tiemeier D, Enquist L. In vitro packaging of a ? Dam vector containing EcoRI DNA fragments of Escherichia coli and phage P1. Gene. 1977; 1(3–4): 255–280.
  • Murphy J, Riley JP. A modified single solution method for determination of phosphate in natural waters. Anal Chim Acta. 1962; 27:31–36.
  • Mahadevan A, Sridhar R. Methods in physiological plant pathology. Chennai, India: Sivakami; 1996.
  • Stahl E. Thin-layer chromatography: A laboratory handbook. 2nd ed. London: Springer-Verlag; 1969.
  • Pradhan M, Shukla LB. Solubilization of inorganic phosphates by fungi isolated from agriculture soil. African J of Biotech. 2005; 5(10):850–854.
  • Narsian V, Patel HH. Aspergillus aculeatus as a rock phosphate solubilizer. Soil Biol Biochem. 2000; 32(4): 559–565.
  • Salsac L, Mention M, Plassard C, Mousain D. Donnees sur la nutrition azotee des champignons ectomycorrhiziens. Colloq. INRA. 1982; 13, 129–140.
  • Goldstein AH, Rogers RD, Mead G. Separating phosphate from ores via. Bioprocessing. Bio/Technology. 1993; 11:1250–1254.
  • Martin F, Tommerup IC Tagu D. (1994). Genetics of ectomycorrhizal fungi: progress and prospects. Plant Soil. 1994; 159(1):159–170.
  • Cornell RM, Schindler PW. Photochemical dissolution of goethite in acid/oxalate solution. Clay Clay Miner. 1987; 35:347–352.
  • Rosling A, Lindahl BD, Finlay RD. Carbon allocation in intact mycorrhizal systems of Pinus sylvestris L. seedlings colonizing different mineral substrates. New Phytol. 2004; 162:795–802.
  • Cessna SG, Sears VE, Dickman MB, Low PS. Oxalic acid, a pathogenicity factor for Sclerotinia sclerotiorum, suppresses the oxidative burst of the host plant. Plant Cell. 2000; 12(11):2191–2200.
  • Dutton MV, Evans CS. Oxalate production by fungi: its role in pathogenicity and ecology in soil environment. Can J Microbiol. 1996; 42(9):881–895.

Abstract Views: 469

PDF Views: 257




  • Rock Phosphate Solubilization using Oxalic Acid - secreting Laccaria fraterna

Abstract Views: 469  |  PDF Views: 257

Authors

S. A. Anithachristy
Methodist Hospital Research Institute, Houston, TX 77030, United States
M. Arunmani
Baylor College of Medicine, Houston, TX 77030,, United States
Viji Sitther
Morgan State University, Baltimore, MD 21251,, United States

Abstract


Laccaria fraterna is an ectomycorrhizal fungus commonly associated with conifers and angiosperms. To check whether L. fraterna possess mechanism to solubilize rock phosphate by secreting organic acids, it was grown in Pikovskaya’s medium with rock phosphate as the main ‘P’ source in the presence of ammonium sulphate. The fungus grew profusely in the medium by secreting oxalic acid which caused a reduction in the pH of the medium. To understand the mechanism behind the rock phosphate solubilization, an attempt was made to clone the fungal genomic DNA. In the Pikovskaya’s medium amended with rock phosphate, the clone MAP 22 released 80 μg/mL of P at the end of 24 h while, L. fraterna released 65 μg/mL of P at the end of 30 days incubation. We used HPTLC to confirm that oxalic acid is the main mineral-transforming agent that was secreted. The wild and the sub-clone MAP 22 released 1,490 and 2,950 μg/mL of oxalic acid, respectively. Therefore, it is possible to use the clone MAP 22 for more efficient inoculum production in vivo.

Keywords


Ectomycorrhizal Fungus, Laccaria fraterna, Phosphate Solubilization, Rock Phosphate

References