Abstract
To grow, both plants and bacteria utilize nutrients that are mainly acquired from the soil environment. In addition to small amounts of a number of different metals, plants and bacteria require fixed nitrogen, iron, and phosphorus. In this chapter, the mechanisms and genes involved in PGPB and plant resource acquisition are discussed in some detail. In fact, one of the major benefits that PGPB provide to their plant partners is that they facilitate the plant’s acquisition of resources from the soil.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Further Reading
Adams MWW, Mortenson LE, Chen JS (1981) Hydrogenase. Biochim Biophys Acta 594:105–176
Ahmad E, Khan MS, Zaidi A (2013) ACC deaminase producing Pseudomonas putida strain PSE3 and Rhizobium leguminosarum strain RP2 in synergism improves growth, nodulation and yield of pea grown in alluvial soils. Symbiosis 61:93–104
Albrecht SL, Maier RJ, Hanus FJ, Russell SA, Emerich DW, Evans HJ (1979) Hydrogenase in Rhizobium japonicum increases nitrogen fixation by nodulated soybeans. Science 203:1255–1257
Brito B, Palacios JM, Imperial J, Ruiz-Argüeso T (2002) Engineering the Rhizobium leguminosarum bv. viciae hydrogenase system for expression in free-living microaerobic cells and increased hydrogenase activity. Appl Environ Microbiol 68:2461–2467
Brito B, Toffanin A, Prieto R-I, Imperial J, Ruiz-Argüeso T, Palacios JM (2008) Host-dependent expression of Rhizobium leguminosarum bv. viciae hydrogenase is controlled at transcriptional and post-transcriptional levels in legume nodules. Molec Plant Microbe Interact 21:597–604
Cantrell MA, Haugland RA, Evans HJ (1983) Construction of a Rhizobium japonicum gene bank and use in isolation of a hydrogen uptake gene. Proc Natl Acad Sci USA 80:181–185
Chaurasia AK, Apte SK (2011) Improved eco-friendly recombinant Anabaena sp. strain PCC7120 with enhanced nitrogen biofertilizer potential. Appl Environ Microbiol 77:395–399
Cheng Q (2008) Perspectives in biological nitrogen fixation. J Integrat Plant Biol 50:784–796
Duan J, Müller KM, Charles TC, Vesely S, Glick BR (2009) 1-Aminocyclopropane-1-carboxylate (ACC) deaminase genes in Rhizobia from southern Saskatchewan. Microb Ecol 57:423–436
Evans HJ, Harker AR, Papen H, Russell SA, Hanus FJ, Zuber M (1987) Physiology, bio-chemistry, and genetics of the uptake hydrogenase in rhizobia. Annu Rev Microbiol 41:335–361
Fernandez-Valiente E, Quesada A (2004) A shallow water ecosystem: rice fields. The relevance of cyanobacteria in the ecosystem. Limnetica 23:95–108
Gresshoff PM, Roth LE, Stacey G, Newton WE (eds) (1990) Nitrogen fixation: achievements and objectives. Chapman and Hall, New York
Hennecke H (1990) Nitrogen fixation genes involved in the Bradyrhizobium japonicum-soybean symbiosis. FEBS Lett 268:422–426
Khan MS, Ahmad E, Zaidi A, Oves M (2013) Functional aspect of phosphate-solubilizing bacteria: importance in crop production. In: Maheshwari DK, Saraf M, Aeron A (eds) Bacteria in agrobiology: crop productivity. Springer, Berlin and Heidelberg, pp 237–263
Lemanceau P, Bauer P, Kraemer S, Briat J-F (2009) Iron dynamics in the rhizosphere as a case study for analyzing interactions between soils, plants and microbes. Plant Soil 321:513–535
Long SR, Buikema WJ, Ausubel FM (1982) Cloning of Rhizobium meliloti nodulation genes by direct complementation of Nod− mutants. Nature 298:485–488
Ma W, Guinel FC, Glick BR (2003a) The Rhizobium leguminosarum bv. viciae ACC deaminase protein promotes the nodulation of pea plants. Appl Environ Microbiol 69:4396–4402
Ma W, Sebestianova S, Sebestian J, Burd GI, Guinel F, Glick BR (2003b) Prevalence of 1-aminocyclopropaqne-1-carboxylate in deaminase in Rhizobia spp. Anton. Van Leeuwenhoek 83:285–291
Ma W, Charles TC, Glick BR (2004) Expression of an exogenous 1-aminocyclopropane-1-carboxylate deaminase gene in Sinorhizobium meliloti increases its ability to nodulate alfalfa. Appl Environ Microbiol 70:5891–5897
Maier RJ, Triplett EW (1996) Toward more productive, efficient, and competitive nitrogen-fixing symbiotic bacteria. Crit Rev Plant Sci 15:191–234
Marroquà S, Zorreguieta A, SantamarÃa C, Temprano F, Soberón M, MegÃas M, Downie JA (2001) Enhanced symbiotic performance by Rhizobium tropici glycogen synthase mutants. J Bacteriol 183:854–864
Marugg JD, van Spanje M, Hoekstra WPM, Schippers B, Weisbeek PJ (1985) Isolation and analysis of genes involved in siderophore biosynthesis in plant-growth-stimulating Pseudomonas putida WCS358. J Bacteriol 164:563–570
Marugg JD, Nielander HB, Horrevoets AJG, van Megen I, van Genderen I, Weisbeek PJ (1988) Genetic organization and transcriptional analysis of a major gene cluster involved in siderophore biosynthesis in Pseudomonas putida WCS358. J Bacteriol 170:1812–1819
Mylona P, Pawlowski K, Bisseling T (1995) Symbiotic nitrogen fixation. Plant Cell 7:869–885
Nap J-P, Bisseling T (1990) Developmental biology of a plant-prokaryote symbiosis: the legume root nodule. Science 250:948–954
Ortiz-Marquez JC, Do Nasciment M, Zehr JP, Curatti L (2013) Genetic engineering of multispecies microbial cell factories as an alternative for bioenergy production. Trends Biotechnol 31:521–529
Peralta H, Mora Y, Salazar E, Encarnación S, Palacios R, Mora J (2004) Engineering the nifH promoter region and abolishing poly-β-hydroxybutyrate accumulation in Rhizobium etli enhance nitrogen fixation in symbiosis with Phaseolus vulgaris. Appl Environ Microbiol 70:3272–3281
Peters JW, Fisher K, Dean DR (1995) Nitrogenase structure and function: a biochemical-genetic perspective. Annu Rev Microbiol 49:335–366
RamÃrez M, Valderrama B, Arrendondo-Peter R, Soberón M, Mora J, Hernández G (1999) Rhizobium etli genetically engineered for the heterologous expression of Vitreoscilla sp. hemoglobin: effects on free-living and symbiosis. Mol Plant-Microbe Interact 12:1008–1015
Scavino AF, Pedraza RO (2013) The role of siderophores in plant growth-promoting bacteria. In: Maheshwari DK, Saraf M, Aeron A (eds) Bacteria in agrobiology: crop productivity. Springer-Verlag, Berlin, pp 265–285
Seefeldt FC, Hoffman BM, Dean DR (2009) Mechanism of Mo-dependent nitrogenase. Annu Rev Biochem 78:701–722
Spaink HP, Wijffelman CA, Pees E, Okker RJH, Lugtenberg BJJ (1987) Rhizobium nodulation gene nodD as a determinant of host specificity. Nature 328:337–340
Sprent JI (1986) Benefits of Rhizobium to agriculture. Trends Biotechnol 4:124–129
Stacey G (1995) Bradyrhizobium japonicum nodulation genetics. FEMS Microbiol Lett 127:1–9
van Rhijn P, Vanderleyden J (1995) The Rhizobium-plant symbiosis. Microbiol Rev 59:124–142
Wang D, Yang S, Tang F, Zhu H (2012) Symbiosis specificity in the legume-rhizobial mutualism. Cell Microbiol 14:334–342
Webb BA, Hildreth S, Helm RF, Scharf BE (2014) Sinorhizobium meliloti chemoreceptor McpU mediates chemotaxis toward plant exudates through direct proline sensing. Appl Environ Micorbiol 80:3404–3415
Yang Z-Y, Moure VR, Dean DR, Seefeldt LC (2012) Carbon dioxide to methane and coupling with acetylene to form propylene catalyzed by remodeled nitrogenase. Proc Natl Acad Sci USA 109:19644–19648
Zafar-ul-Hye M, Ahmad M, Shahzad SM (2013) Synergistic effect of rhizobia and plant growth promoting rhizobacteria on the growth and nodulation of lentil seedlings under axenic conditions. Soil Environ 32:79–86
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
Copyright information
© 2015 Springer International Publishing Switzerland
About this chapter
Cite this chapter
Glick, B.R. (2015). Resource Acquisition. In: Beneficial Plant-Bacterial Interactions. Springer, Cham. https://doi.org/10.1007/978-3-319-13921-0_2
Download citation
DOI: https://doi.org/10.1007/978-3-319-13921-0_2
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-13920-3
Online ISBN: 978-3-319-13921-0
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)