Phosphate-solubilizing microbes and their occurrence in the rhizospheres of Piper betel in Karnataka, India

Low phosphate solubility is one of the most important factors limiting the plant growth in Indian soils. Many microorganisms can enhance phosphate solubility, but little is known about the magnitude of their phosphorus-solubilizing ability. The native populations of phosphate-solubilizing bacteria and fungi were studied in different rhizospheric soil samples obtained from betel vine plants (Piper betel L.) in order to compare the results. The present study focuses on the phosphate-solubilizing capacity of bacteria and fungi in rhizospheric soil samples obtained from betel vine plants, revealing the dominance of Aspergillus species (26.1 mm) as major phosphate solubilizers, along with Bacillus subtilis (46.6 mm) among the bacteria that utilize tricalcium phosphate, potassium dihydrogen phosphate, and rock phosphate as phosphate sources. The other phosphorus-solubilizing microorganisms were Bacillus species, Streptomyces, Aspergillus fumigatus, Nocardia, actinomycetes, and certain yeasts. The presence of high numbers of phosphate-solubilizing bacterium Bacillus subtilis (3 × 106 cfu g-1) and fungus Aspergillus niger (3 × 105 cfu g-1) in the rhizospheric zones of Piper betel plants explains how the plants obtain their nutrient requirements. The identity of Aspergillus species and Bacillus with the maximum zone was confirmed using molecular sequencing with 16s rDNA. The sequence data were aligned and analyzed to identify the bacteria along with their closest neighbors.

Phosphate-solubilizing microbes and their occurrence in the rhizospheres of Piper betel in Karnataka, India

Low phosphate solubility is one of the most important factors limiting the plant growth in Indian soils. Many microorganisms can enhance phosphate solubility, but little is known about the magnitude of their phosphorus-solubilizing ability. The native populations of phosphate-solubilizing bacteria and fungi were studied in different rhizospheric soil samples obtained from betel vine plants (Piper betel L.) in order to compare the results. The present study focuses on the phosphate-solubilizing capacity of bacteria and fungi in rhizospheric soil samples obtained from betel vine plants, revealing the dominance of Aspergillus species (26.1 mm) as major phosphate solubilizers, along with Bacillus subtilis (46.6 mm) among the bacteria that utilize tricalcium phosphate, potassium dihydrogen phosphate, and rock phosphate as phosphate sources. The other phosphorus-solubilizing microorganisms were Bacillus species, Streptomyces, Aspergillus fumigatus, Nocardia, actinomycetes, and certain yeasts. The presence of high numbers of phosphate-solubilizing bacterium Bacillus subtilis (3 × 106 cfu g-1) and fungus Aspergillus niger (3 × 105 cfu g-1) in the rhizospheric zones of Piper betel plants explains how the plants obtain their nutrient requirements. The identity of Aspergillus species and Bacillus with the maximum zone was confirmed using molecular sequencing with 16s rDNA. The sequence data were aligned and analyzed to identify the bacteria along with their closest neighbors.

___

  • Sanyal SK, De Datta SK. Chemistry of phosphorus transforma- tions in soil. Adv Soil Sci 16: 1-20, 1991. McLaughlin MJ, Alston AM, Martin JK. Phosphorus cycling in wheat-pasture rotations. I. Th e source of phosphorus taken up by wheat. Aust J Soil Res 26: 323-331, 1988. 3. Gyaneshwar P, Naresh Kumar G, Parekh LJ et al. Role of soil microorganisms in improving P nutrition of plants. Plant and Soil 245: 83-93, 2002.
  • Fankem H, Nwaga D, Deubel A et al. Occurrence and functioning of phosphate solubilizing microorganisms from oil palm tree (Elaeis guineensis) rhizosphere in Cameroon. Afr J Biotech 5: 2450-2460, 2006.
  • Th eodorou ME, Plaxton WC. Metabolic adaptations of plant respiration to nutritional phosphate deprivation. Plant Physiol 101: 339-344, 1993.
  • Vassilev N, Vassileva M. Biotechnological solubilization of rock phosphate on media containing agroindustrial wastes. Appl Microbiol Biotechnol 61: 435-440, 2003. 7. Holford ICR. Soil phosphorus: its measurement and its uptake by plants. Aust J Soil Res 35: 227-239, 1997.
  • Rodriguez H, Fraga R. Phosphate solubilizing bacteria and their role in plant growth promotion. Biotechnol Adv 17: 319- 339, 1999. 9. Vikram A, Alagawadi AR, Hamzehzarghani H et al. Factors related to the occurrence of phosphate solubilizing bacteria and their isolation in vertisols. Int J Agri Res 2: 571-580, 2007.
  • Kundu BS, Nehra K, Yadav R et al. Biodiversity of phosphate solubilizing bacteria in rhizosphere of chickpea, mustard and wheat grown in diff erent regions of Haryana. Ind J Microbiol 49: 120-127, 2009.
  • Kirk JL, Beaudette LA, Hart M et al. Methods of studying soil microbial diversity. J Microbiol Meth 58: 169-188, 2004.
  • Khiari L, Parent LE. Phosphorus transformations in acid light- textured soils treated with dry swine manure. Can J Soil Sci 85: 75-87, 2005.
  • Nahas E. Factors determining rock phosphate solubilization by microorganisms isolated from soil. World J Microb Biotechnol 12: 18-23, 1996.
  • Duebel A, Gransee A, Merbach W. Transformation of organic rhizodeposits by rhizoplane bacteria and its infl uence on the availability of tertiary calcium phosphate. J Plant Nutr Soil Sci 163: 387-392, 2000.
  • Khan AA, Jilani G, Akhtar MS et al. Phosphorus solubilizing bacteria: occurrence, mechanisms and their role in crop production. J Agric Biol Sci 1: 48-58, 2009.
  • Barea JM, Pozo MJ, Azcón R et al. Microbial co-operation in the rhizosphere. J Exp Bot 56: 1761-1778, 2005.
  • Pikovskaya RI. Mobilization of phosphorus in soil in connection with vital activity of some microbial species. Mikrobiologiya 17: 362-370, 1948.
  • Jumaniyazova GI, Tillayev TS, Takhtobin KS et al. Exploring the phosphate solubilizing capacity of soil bacteria through the application of 32P radioisotope techniques and X-RAY diff raction method. 26th Southern Conservation Tillage Conference, 2002.
  • Nenwani V, Doshi P, Saha T et al. Isolation and characterization of a fungal isolate for phosphate solubilization and plant growth promoting activity. J of Yeast and Fungal Res 1: 9-14, 2010.
  • Husen E. Screening of soil bacteria for plant growth promotion activities in vitro. Indonesian J Agri Sci 4: 27-31, 2003.
  • Nopparat C, Jatupornipat M, Rittiboon A. Isolation of phosphate solubilizing fungi in soil from Kanchanaburi, Th ailand. KMITL Sci Technol J 7: 137-146, 2007.
  • Espinosa-Victoria D, López-Reyes L, de la Cruz-Benítez A. Use of 16s RNA gene for characterization of phosphate-solubilizing bacteria associated with corn. Rev Fitotec Mex 32: 31-37, 2009.
  • Suliasih, Widawati S. Isolation and identifi cation of phosphate solubilizing and nitrogen fi xing bacteria from soil in Wamena Biological Garden, Jayawijaya, Papua. Biodiversitas 6: 175-177, 2005.
  • Gupta N, Sabat J, Parida R et al. Solubilization of tricalcium phosphate and rock phosphate by microbes isolated from chromite, iron and manganese mines. Acta Bot Croat 66: 197- 204, 2007.
  • Chailharn M, Chunhaleuchanon S, Kozo A et al. Screening of rhizobacteria for their plant growth promoting activities. KMITL Sci and Tech J 8: 18-23, 2008.
  • Bruno WJ, Socci ND, Halpern AL. Weighted neighbor joining: a likelihood-based approach to distance-based phylogeny reconstruction. Molecular Biological Evolution 17: 189-197, 2000.
  • Hamaki T, Suzuki M, Fudou R et al. Isolation of novel bacteria and actinomycetes using soil-extract agar medium. J Biosc and Bioeng 99: 485-492, 2005. Turan M, Ataoğlu N, Şahin F. Eff ects of Bacillus FS-3 on growth of tomato (Lycopersicon esculentum L.) plants and availability of phosphorus in soil. Plant Soil Environ 53: 58-64, 2007.
  • Hamza S, Srinivasan V, Dinesh R. Nutrient diagnosis of black pepper (Piper nigrum L.) gardens in Kerala and Karnataka. J Spices and Aromatic Crops 16: 77-81, 2007.
  • Rajankar PN, Tambekar DH, Wate SR. Study of phosphate solubilization of fungi and bacteria isolated from saline belt of Purna river basin. Res J Agri Biol Sci 3: 701-703, 2007.
  • Venkateshwarulu B, Rao AV, Raina P. Evaluation of phosphorus solubilization by microorganisms isolated from aridisols. J Ind Soc Soil Sci 32: 273-277, 1984.
  • Gupta RD, Bharadwaj KKR, Marwah BC et al. Occurrence of phosphate dissolving bacteria in some soils of North-West Himalayas under varying biosequence and climosequence. J Ind Soc Soil Sc 34: 498-504, 1986.
  • Illmer P, Schinner F. Solubilization of inorganic phosphates by microorganisms isolated from forest soils. Soil Biol Biochem 24: 89-395, 1992.
  • Chung H, Park M, Madhaiyan M et al. Isolation and characterization of phosphate solubilizing bacteria from the rhizosphere crop plants of Korea. Soil Biol Biochem 37: 1970- 1974, 2005.
  • Chen X, Tang J, Fang Z et al. Phosphate solubilizing microbes in rhizosphere soils of 19 weeds in southeastern China. J Zhejiang University Science 3: 355- 361, 2002.
  • Dave A, Patel HH. Inorganic phosphate solubilizing soil pseudomonads. In J Microbiol 39: 161-164, 1999.
  • Chakraborty BN, Chakraborty U, Saha A et al. Evaluation of phosphate solubilizers from soils of North Bengal and their diversity analysis. J Agri Sci 6: 195-200, 2010.
  • Rashid M, Khalil S, Ayub N et al. Organic acids production and phosphate solubilization by phosphate solubilizing microorganisms (PSM) under in vitro conditions. Pak J Biol Sci 7: 187-196, 2004.
  • Kang SC, Pandey P, Khillon R et al. Process of rock phosphate solubilization by Aspergillus sp PS 104 in amended medium. J Environ Biol 29: 743-746, 2008.
  • Goenadi DH, Siswanto, Sugiarto Y. Bioactivation of poorly soluble phosphate rocks with a phosphorus-solubilizing fungus. Soil Sci Soc Am J 64: 927-932, 2000.
  • Taalab AS, Badr MA. Phosphate availability from compacted rock phosphate with nitrogen to sorghum inoculated with phospho-bacterium. J Appl Sci Res 3: 195-201, 2007.
  • Silva GN, Vipor C. Phosphate solubilizing activity of microorganisms in the presence of nitrogen, iron, calcium and potassium. Pest Agro Bras 36: 1495-1508, 2001.
  • Yu SL, Liu YN, Jing GL et al. Analysis of phosphate accumulating organisms cultivated under diff erent carbon sources with polymerase reaction-denaturing gradient gel electrophoresis assay. J Environ Sc 17: 611-614, 2005.
Turkish Journal of Biology-Cover
  • ISSN: 1300-0152
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Phylogenetic characterization, antimicrobial susceptibilities, and mechanisms of resistance in bacteria isolates from a poultry waste-polluted river, southwestern Nigeria

Olawale Olufemi ADELOWO, Obasola Ezekiel FAGADE

Salvia türünün farklı ekstrelerinin antienfl amatuvar etkileri

Lütfiye Ömür DEMİREZER, Perihan GÜRBÜZ, Elif ÇADIRCI, Zühal GÜVENALP, Halis SÜLEYMAN, KURUÜZÜM Ayşe UZ

Phosphate-solubilizing microbes and their occurrence in the rhizospheres of Piper betel in Karnataka, India

Padmavathi TALLAPRAGADA, Usha SESHACHALA

Protective effects of β-carotene and silymarin on human lymphocytes

Erkan YURTCU, Ezgi KASAPOĞLU, Feride İffet ŞAHİN

Antimicrobial activity of poplar propolis on mutans streptococci and caries development in rats

Soley ARSLAN, Sibel SİLİCİ, Duygu PERÇİN, Ayşe Nedret KOÇ, Özgür ER

Cytotoxic and antibacterial activities of leaf extracts of Astragalus gombiformis Pomel (Fabaceae) growing wild in Tunisia

Hassen TEYEB, Nahla ZANINA, Mohamed NEFFATI, Wahiba DOUKI, Mohamed Fadhel NAJJAR

Protective effects of b-carotene and silymarin on human lymphocytes

Erkan YURTCU, Ezgi KASAPOĞLU, Feride İffet ŞAHİN

Comparison of three Yarrowia lipolytica strains for lipase production: NBRC 1658, IFO 1195, and a local strain

Özgür KEBABCI, Nilüfer CİHANGİR

Folk medicines in the villages of Ilıca District (Erzurum, Turkey)

Ufuk ÖZGEN, Yusuf KAYA, Peter HOUGHTON

Anti-inflammatory effects of different extracts from three Salvia species

Elif ÇADIRCI, Halis SÜLEYMAN, Perihan GÜRBÜZ, Ayşe KURUÜZÜM UZ, Zühal GÜVENALP, Lütfiye Ömür DEMİREZER