DOI QR코드

DOI QR Code

Use of plant growth-promoting rhizobacteria to control stress responses of plant roots

  • Kang, Bin-Goo (ReSEAT Program, Korea Institute of Science and Technology Information) ;
  • Kim, Woo-Taek (Department of Biology, Yonsei University) ;
  • Yun, Hye-Sup (Department of Biological Sciences, Konkuk University) ;
  • Chang, Soo-Chul (University College, Yonsei University)
  • Received : 2010.03.18
  • Accepted : 2010.03.30
  • Published : 2010.09.30

Abstract

Ethylene is a key gaseous hormone that controls various physiological processes in plants including growth, senescence, fruit ripening, and responses to abiotic and biotic stresses. In spite of some of these positive effects, the gas usually inhibits plant growth. While chemical fertilizers help plants grow better by providing soil-limited nutrients such as nitrogen and phosphate, overusage often results in growth inhibition by soil contamination and subsequent stress responses in plants. Therefore, controlling ethylene production in plants becomes one of the attractive challenges to increase crop yields. Some soil bacteria among plant growth-promoting rhizobacteria (PGPRs) can stimulate plant growth even under stressful conditions by reducing ethylene levels in plants, hence the term "stress controllers" for these bacteria. Thus, manipulation of relevant genes or gene products might not only help clear polluted soil of contaminants but contribute to elevating the crop productivity. In this article, the beneficial soil bacteria and the mechanisms of reduced ethylene production in plants by stress controllers are discussed.

Keywords

References

  1. Abeles FB, Morgan PW, Sltveit ME Jr (1992) Ethylene in plant biology. Academic, New York
  2. Belimov AA, Safronova VI, Sergeyeva TA, Egorova TN, Matveyeva VA, Tsyganov VE, Borisov AY, Tikhonovich IA, Kluge C, Preisfeld A, Dietz K-J, Stepanok VV (2001) Characterization of plant growth promoting rhizobacteria isolated from polluted soils and containing 1-aminocyclopropane-1-carboxylate deaminase. Can J Microbiol 47:642-652 https://doi.org/10.1139/w01-062
  3. Blaha D, Prigent-Combaret C, Mirza MS, Moe¨nne-Loccoz Y (2006) Phylogeny of the 1-aminocyclopropane-1-carboxylic acid deaminase- encoding gene acdS in phytobeneficial and pathogenic Proteobacteria and relation with strain biogeography. FEMS Microbiol Ecol 56:455-470 https://doi.org/10.1111/j.1574-6941.2006.00082.x
  4. Cattelan AJ, Hartel PG, Fuhrmann JJ (1999) Screening for plant growth-promoting Rhizobacteria to promote early soybean growth. Soil Sci Soc Am J 63:1670-1680 https://doi.org/10.2136/sssaj1999.6361670x
  5. Gleba D, Borisjuk NV, Borisjuk LG, Kneer R, Poulev A, Skarzhinskaya M, Dushenkov S, Logendra S, Gleba YY, Raskin I (1999) Use of plant roots for phytoremediation and molecular farming. Proc Natl Acad Sci USA 96:5973-5977 https://doi.org/10.1073/pnas.96.11.5973
  6. Glick BR (2005) Modulation of plant ethylene levels by the bacterial enzyme ACC deaminase. FEMS Microbiol Lett 251:1-7 https://doi.org/10.1016/j.femsle.2005.07.030
  7. Glick BR, Penrose DM, Li J (1998) A model for the lowering of plant ethylene concentrations by plant growth-promoting bacteria. J Theor Biol 190:63-68 https://doi.org/10.1006/jtbi.1997.0532
  8. Glick BR, Cheng Z, Czarny J, Duan J (2007) Promotion of plant growth by ACC deaminase-producing soil bacteria. Eur J Plant Pathol 119:329-339 https://doi.org/10.1007/s10658-007-9162-4
  9. Grichko VP, Glick BR (2001) Amelioration of flooding stress by ACC deaminase-containing plant growth-promoting bacteria. Plant Physiol Biochem 39:11-17 https://doi.org/10.1016/S0981-9428(00)01212-2
  10. Haas D, Keel C (2003) Regulation of antibiotic production in rootcolonizing Pseudomonas spp. and relevance for biological control of plant disease. Annu Rev Phytopathol 41:117-153 https://doi.org/10.1146/annurev.phyto.41.052002.095656
  11. Kamilova F, Lamers G, Lugtenberg B (2008) Biocontrol strain Pseudomonas fluorescens WCS365 inhibits germination of Fusarium oxysporum spores in tomato root exudates as well as subsequent formation of new spores. Environ Microbiol 10:2455-2461 https://doi.org/10.1111/j.1462-2920.2008.01638.x
  12. Kim JH, Kim WT, Kang BG (2001) IAA and N6-benzyladenine inhibit ethylene-regulated expression of ACC oxidase and synthase genes in mungbean hypocotyls. Plant Cell Physiol 42:1056-1061 https://doi.org/10.1093/pcp/pce133
  13. Ma W, Guinel FC, Glick BR (2003) The Rhizobium leguminosarum bv. viciae ACC deaminase protein promotes the nodulation of pea plants. Appl Environ Microbiol 69:4396-4402 https://doi.org/10.1128/AEM.69.8.4396-4402.2003
  14. 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 https://doi.org/10.1128/AEM.70.10.5891-5897.2004
  15. Mayak S, Tirosh T, Glick BR (1999) Effect of wild-type and mutant plant growth-promoting Rhizobacteria on the rooting of mung bean cuttings. J Plant Growth Regul 18:49-53 https://doi.org/10.1007/PL00007047
  16. Mayak S, Tirosh T, Glick BR (2004) Plant growth-promoting bacteria that confer resistance in tomato to salt stress. Plant Physiol Biochem 42:565-572 https://doi.org/10.1016/j.plaphy.2004.05.009
  17. Meharg AA, Killham K (1995) Loss of exudates from the roots of perennial ryegrass inoculated with a range of microorganisms. Plant Soil 170:345-349 https://doi.org/10.1007/BF00010488
  18. Morgan PW, Drew CD (1997) Ethylene and plant responses to stress. Physiol Plant 100:620-630 https://doi.org/10.1111/j.1399-3054.1997.tb03068.x
  19. Reed MLE, Glick BR (2005) Growth of canola (Brassica napus) in the presence of plant growth-promoting bacteria and either copper or polycyclic aromatic hydrocarbons. Can J Microbiol 51:1061-1069 https://doi.org/10.1139/w05-094
  20. Robison MM, Shah S, Tamot B, Pauls KP, Moffatt BA, Glick BR (2001) Reduced symptoms of Verticillium wilt in transgenic tomato expressing a bacterial ACC deaminase. Mol Plant Pathol 2:135-145 https://doi.org/10.1046/j.1364-3703.2001.00060.x
  21. Sisler EC, Serek M (1997) Inhibitors of ethylene responses at the receptor level: recent developments. Physiol Plant 100:577-582 https://doi.org/10.1111/j.1399-3054.1997.tb03063.x
  22. Stearns JC, Shah S, Dixon DG, Greenberg BM, Glick BR (2005) Tolerance of transgenic canola expressing 1-aminocyclopropane- carboxylic acid deaminase to growth inhibition by nickel. Plant Physiol Biochem 43:701-708 https://doi.org/10.1016/j.plaphy.2005.05.010
  23. Uren NC (2007) Types, amounts, and possible functions of compounds released into the rhizosphere by soil-grown plants. In: Pinton T, Varanini Z, Nannipieri P (eds) The rhizosphere, biochemistry and organic substances at the soil-plant interface, 2nd edn. CRC, Boca Raton, pp 1-21
  24. Vessey JK (2003) Plant growth promoting rhizobacteria as biofertilizers. Plant Soil 255:571-586 https://doi.org/10.1023/A:1026037216893
  25. Wang C, Knill E, Glick BR, Defago G (2000) Effect of transferring 1- aminocyclopropane-1-carboxylic acid (ACC) deaminase gene into Pseudomonas fluorenscens strain CHA0 and its gacA derivative CHA96 on their growth promoting and diseasesuppressive capacities. Can J Microbiol 46:898-907 https://doi.org/10.1139/w00-071

Cited by

  1. Manipulation of Ethylene Synthesis in Roots Through Bacterial ACC Deaminase for Improving Nodulation in Legumes vol.30, pp.3, 2010, https://doi.org/10.1080/07352689.2011.572058
  2. Assessment of Pesticide-Tolerance and Functional Diversity of Bacterial Strains Isolated from Rhizospheres of Different Crops vol.1, pp.1, 2010, https://doi.org/10.5567/imicro-ik.2011.8.19
  3. Effect of Pesticides on Plant Growth Promoting Traits of Greengram-Symbiont, Bradyrhizobium sp. strain MRM6 vol.86, pp.4, 2011, https://doi.org/10.1007/s00128-011-0231-1
  4. Evaluation of plant-growth-promoting activities of rhizobacterium Pseudomonas putida under herbicide stress vol.62, pp.4, 2010, https://doi.org/10.1007/s13213-011-0407-2
  5. Effects of pesticides on plant growth promoting traits of Mesorhizobium strain MRC4 vol.11, pp.1, 2012, https://doi.org/10.1016/j.jssas.2011.10.001
  6. Proven and potential involvement of vitamins in interactions of plants with plant growth-promoting bacteria-an overview vol.50, pp.3, 2010, https://doi.org/10.1007/s00374-013-0894-3
  7. The rhizosphere microbiota of plant invaders: an overview of recent advances in the microbiomics of invasive plants vol.5, pp.None, 2010, https://doi.org/10.3389/fmicb.2014.00368
  8. Bacterial community structure and detection of putative plant growth-promoting rhizobacteria associated with plants grown in Chilean agro-ecosystems and undisturbed ecosystems vol.50, pp.7, 2010, https://doi.org/10.1007/s00374-014-0935-6
  9. Current Perspectives on Plant Growth-Promoting Rhizobacteria vol.35, pp.3, 2010, https://doi.org/10.1007/s00344-016-9583-4
  10. Effect of GFP tagging of Paenibacillus polymyxa P2b-2R on its ability to promote growth of canola and tomato seedlings vol.52, pp.3, 2016, https://doi.org/10.1007/s00374-015-1083-3
  11. Biofertilizers: a potential approach for sustainable agriculture development vol.24, pp.4, 2010, https://doi.org/10.1007/s11356-016-8104-0
  12. Adaptation of primocane fruiting raspberry plants to environmental factors under the influence of Bacillus strains in Western Siberia vol.24, pp.8, 2010, https://doi.org/10.1007/s11356-017-8427-5
  13. Phytoremediation of petroleum hydrocarbon-contaminated saline-alkali soil by wild ornamental Iridaceae species vol.19, pp.3, 2010, https://doi.org/10.1080/15226514.2016.1225282
  14. Effects of organochlorine pesticides on plant growth-promoting traits of phosphate-solubilizing rhizobacterium, Paenibacillus sp. IITISM08 vol.25, pp.6, 2018, https://doi.org/10.1007/s11356-017-0940-z
  15. Plant Growth Promoting Rhizobacteria (PGPR) - Prospective and Mechanisms: A Review vol.12, pp.2, 2010, https://doi.org/10.22207/jpam.12.2.34
  16. Perspectives of Microbial Inoculation for Sustainable Development and Environmental Management vol.9, pp.None, 2010, https://doi.org/10.3389/fmicb.2018.02992
  17. Effect of Trichoderma koningiopsis on Chickpea Rhizosphere Activities under Different Fertilization Regimes vol.8, pp.10, 2010, https://doi.org/10.4236/ojss.2018.810020
  18. Mechanistic insights on plant root colonization by bacterial endophytes: a symbiotic relationship for sustainable agriculture vol.1, pp.1, 2010, https://doi.org/10.1007/s42398-018-0011-5
  19. Potential use of rhizobium for vegetable crops growth promotion vol.14, pp.8, 2019, https://doi.org/10.5897/ajar2017.12885
  20. Plant growth promoting rhizobacteria in sustainable agriculture: from theoretical to pragmatic approach vol.78, pp.2, 2010, https://doi.org/10.1007/s13199-019-00602-w
  21. The Interactions of Rhizodeposits with Plant Growth-Promoting Rhizobacteria in the Rhizosphere: A Review vol.9, pp.7, 2019, https://doi.org/10.3390/agriculture9070142
  22. Biological control of the tomato wilt caused by Clavibacter michiganensis subsp. michiganensis using formulated plant growth-promoting bacteria vol.29, pp.1, 2019, https://doi.org/10.1186/s41938-019-0152-6
  23. Soil Bacterial Community and Soil Enzyme Activity Depending on the Cultivation of Triticum aestivum, Brassica napus, and Pisum sativum ssp. arvense vol.11, pp.12, 2019, https://doi.org/10.3390/d11120246
  24. Plant Growth-Promoting Rhizobacteria Isolated from Degraded Habitat Enhance Drought Tolerance of Acacia ( Acacia abyssinica Hochst. ex Benth.) Seedlings vol.2020, pp.None, 2010, https://doi.org/10.1155/2020/8897998
  25. Phylogenetic and Functional Characterization of Culturable Endophytic Actinobacteria Associated With Camellia spp. for Growth Promotion in Commercial Tea Cultivars vol.11, pp.None, 2010, https://doi.org/10.3389/fmicb.2020.00318
  26. Effect of Salinity-NaCl and Pseudomonas fluorescens on the Germination of Wheat Genotypes (Triticum durum L.) Cultivated in Arid Regions of Algeria vol.10, pp.2, 2010, https://doi.org/10.3923/sjsres.2020.182.189
  27. Biodegradation of carbendazim by a potent novel Chryseobacterium sp. JAS14 and plant growth promoting Aeromonas caviae JAS15 with subsequent toxicity analysis vol.10, pp.7, 2010, https://doi.org/10.1007/s13205-020-02319-w
  28. Complementary Dynamics of Banana Root Colonization by the Plant Growth-Promoting Rhizobacteria Bacillus amyloliquefaciens Bs006 and Pseudomonas palleroniana Ps006 at Spatial and Temporal Scales vol.80, pp.3, 2010, https://doi.org/10.1007/s00248-020-01571-0
  29. Fungicide-Tolerant Plant Growth-Promoting Rhizobacteria Mitigate Physiological Disruption of White Radish Caused by Fungicides Used in the Field Cultivation vol.17, pp.19, 2010, https://doi.org/10.3390/ijerph17197251
  30. 중금속 오염 토양 정화를 위한 식물생장촉진세균: 특성, 활용 및 전망 vol.48, pp.4, 2020, https://doi.org/10.48022/mbl.2008.08015
  31. The Effects of Various Doses and Types of Effective Microorganism Applications on Microbial and Enzyme Activity of Medium and the Photosynthetic Activity of Scarlet Sage vol.11, pp.3, 2010, https://doi.org/10.3390/agronomy11030603
  32. Combination of arbuscular mycorrhizal fungi and phosphate solubilizing bacteria on growth and production of Helianthus tuberosus under field condition vol.11, pp.1, 2021, https://doi.org/10.1038/s41598-021-86042-3
  33. Endophytic Community Composition and Genetic-Enzymatic Features of Cultivable Bacteria in Vaccinium myrtillus L. in Forests of the Baltic-Nordic Region vol.12, pp.12, 2010, https://doi.org/10.3390/f12121647