Skip to main content

Azotobacter: PGPR Activities with Special Reference to Effect of Pesticides and Biodegradation

  • Chapter
  • First Online:
Microbial Inoculants in Sustainable Agricultural Productivity

Abstract

Among all the microorganisms, plant growth-promoting rhizobacteria (PGPR) have significant influence on soil physiological and structural properties. PGPR help to replace chemical fertilizer for the sustainable agriculture production by fixing the atmospheric nitrogen and producing growth-promoting substances. Among the PGPR group, Azotobacter are ubiquitous, aerobic, free-living, and N2-fixing bacteria commonly living in soil, water, and sediments. Being the major group of soilborne bacteria, Azotobacter plays different beneficial roles and is known to produce varieties of vitamins, amino acids, plant growth hormones, antifungal substances, hydrogen cyanide, and siderophores. The growth-promoting substances such as indoleacetic acid, gibberellic acid, arginine, etc., produced by Azotobacter have direct influence on shoot and root length as well as seed germination of several agricultural crops. Azotobacter species are efficient in fixation of highest amount of nitrogen (29.21 μg NmL−1day−1), production of indoleacetic acid (24.50μgmL−1) and gibberellic acid (15.2 μg 25 mL−1), and formation of larger phosphate solubilizing zone (13.4 mm). Many species of Pseudomonas, Bacillus, and Azotobacter can grow and survive at extreme environmental conditions, viz., tolerant to higher salt concentration, pH values, and even at dry soils with maximum temperature. Different factors affect Azotobacter population in soil such as pH, phosphorus content, soil aeration and moisture contents, etc. A. chroococcum found tolerant to a maximum NaCl concentration of 6 % with a temperature of 45 ° C and also up to pH of 8. Azotobacter species such as A. vinelandii, A. chroococcum, A. salinestris, A. tropicalis, and A. nigricans are able to produce antimicrobial compounds which inhibit the growth of common plant pathogens, viz., Fusarium, Aspergillus, Alternaria, Curvularia, and Rhizoctonia species. Pesticides used to control pests, insects, and phytopathogens are known to cause direct effect on soil microbiological aspects, environmental pollution, and health hazards in all living beings of the soil ecosystem. The species of Azotobacter are known to tolerate up to 5 % pesticide concentration and also to degrade heavy metals and pesticides. A. chroococcum and A. vinelandii proved their biodegradation efficiency of many commonly used pesticides, viz., endosulfan, chlorpyrifos, pendimethalin, phorate, glyphosate, and carbendazim. From these results, it is clear that the Azotobacter strains not only produce plant growth-promoting substances (PGPS) but are also tolerant to abiotic stress under different physiological conditions.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Agarwal N, Singh HP (2002) Antibiotic resistance and inhibitory effect of Azotobacter on soil borne plant pathogens. Indian J Microbiol 42:245–246

    Google Scholar 

  • Ahmad F, Ahmad I, Khan MS (2005) Indole acetic production by the indigenous isolates of Azotobacter and fluorescent Pseudomonas in the presence and absence of tryptophan. Turk J Biol 29:29–34

    CAS  Google Scholar 

  • Ahmad F, Ahmad I, Khan MS (2008) Screening of free living rhizospheric bacteria for their multiple growth promoting activities. Microbiol Res 163:173–181

    Article  CAS  PubMed  Google Scholar 

  • Akhter MS, Hossain SJ, Hossain SKA, Datta RKD (2012) Isolation and characterization of salinity tolerant Azotobacter species. Gre J Biolo Sci 2(3):43–51

    Google Scholar 

  • Aleem A, Isar J, Malik A (2003) Impact of long term application of industrial wastewater on the emergence of resistance traits of Azotobacter vinelandii isolated from rhizosphere soil. Biores Technol 86:7–13

    Article  CAS  Google Scholar 

  • Almon L (1958) The vitamin B12 content of Azotobacter vinelandii. J Nutr 65:643–648

    CAS  PubMed  Google Scholar 

  • Anupama KS, Paul S (2009) Ex situ and in situ biodegradation of lindane by Azotobacter chroococcum. J Environ Sci Health 45(1):58–66

    Article  Google Scholar 

  • Aquilanti L, Favilli F, Clementi F (2004) Comparison of different strategies for isolation and preliminary identification of Azotobacter from soil samples. Soil Biol Biochem 36:1475–1483

    Article  CAS  Google Scholar 

  • Bagyaraj DJ, Patil RB (1975) Azotobacter research in Karnataka. Curr Res 4:181–184

    Google Scholar 

  • Barazani O, Friedman J (1999) IAA is the major root growth factor secreted from plant growth mediated bacteria. J Chem Ecol 25:2397–2407

    Article  CAS  Google Scholar 

  • Barrera AD, Soto E (2010) Biotechnological uses of Azotobacter vinelandii: current state limits and prospects. Afr J Biotechnol 9(33):5240–5250

    Google Scholar 

  • Becking JH (1981) The family Azotobacteraceae. In: Ballows A, Truper HG, Dworkin M, Harder W, Schleifer KH (eds) The Prokaryotes: a handbook on habitats, isolation, and identification of bacteria. Springer, Heidelberg, pp 795–817

    Chapter  Google Scholar 

  • Bhosale HJ, Kadam TA, Bobade AR (2013) Identification and production of Azotobacter vinelandii and its antifungal activity against Fusarium oxysporum. J Environ Biol 34:177–182

    CAS  PubMed  Google Scholar 

  • Bowen GD, Rovira AD (1999) The rhizosphere and its management to improve plant growth. Adv Agron 66:101–102

    Google Scholar 

  • Burk D, Lineweaver H, Horner CK (1932) Iron in relation to the stimulation of growth by humic acid. Soil Sci 33: 413-454

    Google Scholar 

  • Castillo JM, Casas J, Romero E (2011) Isolation of an endosulfan degrading bacterium from a coffee farm soil: persistence and inhibitory effect on its biological functions. Sci Total Environ 412–413:20–27

    Article  PubMed  Google Scholar 

  • Cavaglieri LR, Andres L, Ibanez M et al (2005) Rhizobacteria and their potential to control Fusarium verticillioides: effect of maize bacterization and inoculum density. Ant Van Leeuwenhoek 87:179–187

    Article  CAS  Google Scholar 

  • Channal HT, Alaganadi AR, Bharamagoudar TD et al (1989) Azotobacter population as influenced by soil properties in some soils of North Karnataka. Curr Sci 52(2):70–71

    Google Scholar 

  • Chennappa G, Adkar-Purushothama CR, Suraj U et al (2013) Pesticide tolerant Azotobacter isolates from paddy growing areas of northern Karnataka, India. World J Microbiol Biotechnol 30:1–7

    Article  PubMed  Google Scholar 

  • Chennappa G, Naik MK, Sreenivasa MY et al (2014a) Antifungal activity of Azotobacter species against plant pathogens isolated from paddy soils. Paper presented in the Karnataka state science and technology academy conference on science and technology for harnessing natural resources towards sustainable development at University of Agricultural Sciences, Raichur 4–5 Jan 2014

    Google Scholar 

  • Chennappa G, Adkar-Purushothama CR, Naik MK et al (2014b) Impact of pesticide on PGPR activity of Azotobacter sp. Isolated from pesticide flooded paddy soils. Gre J Agri Sci 4(4):117–129

    Google Scholar 

  • Das AC, Mukharjee D (1998) Soil application of insecticides influences microorganisms and plant nutrients. Appl Soil Ecol 14:55–62

    Article  Google Scholar 

  • Garg SK, Bhatnagar A, Kalla A et al (2001) In vitro nitrogen fixation, phosphate solubilization, survival and nutrient release by Azotobacter strains in an aquatic system. Biores Technol 80:101–109

    Article  CAS  Google Scholar 

  • Ghosh PG, Sawant NA, Patil SN et al (2010) Microbial biodegradation of organophosphate pesticides. Int J Biotech Biochem 6:871–876

    Google Scholar 

  • Glick BR (1995) The enhancement of plant growth by free living bacteria. Can J Microbiol 41:109–117

    Article  CAS  Google Scholar 

  • Herter S, Schmidt M, Thompson ML et al (2011) A new phenol oxidase produced during melanogenesis and encystment stage in the nitrogen-fixing soil bacterium Azotobacter chroococcum. Appl Microbiol Biotechnol 90:1037–1049

    Article  CAS  PubMed  Google Scholar 

  • Jimenez DJ, Montana JS, Martienz MM (2011) Characterization of free nitrogen fixing bacteria of the genus Azotobacter in organic vegetable grown in Colombian soils. Braz J Microbiol 42:846–858

    PubMed Central  CAS  PubMed  Google Scholar 

  • Johri BN, Sharma A, Virdi JS (2003) Rhizobacterial diversity in India and its influence on soil and plant health. Adv Biochem Eng Biotechnol 84:49–89

    CAS  PubMed  Google Scholar 

  • Kadam TA, Gangawane LV (2005) Degradation of phorate by Azotobacter isolates. Indian J Biotechnol 4:153–155

    CAS  Google Scholar 

  • Kannapiran E, Sriramkumar V (2011) Inoculation effect of nitrogen-fixing and phosphate-solubilizing bacteria to promote growth of black gram (Phaseolus mungo Roxb; Eng). Ann Bio Res 2(5):615–621

    CAS  Google Scholar 

  • Kaushik A, Sethi V (2005) Salinity effects on nitrifying and free diazotrophic bacterial populations in the rhizosphere of rice. Bul Nat Inst Ecol 15:139–144

    Google Scholar 

  • Khan HR, Mohiuddin, Rahman M (2008) Enumeration, isolation and identification of nitrogen fixing bacterial strains at seedling stage in rhizosphere of rice grown in non-calcareous grey flood plain soil of Bangladesh. J Facul Environ Sci Technol 13:97–101

    CAS  Google Scholar 

  • Khanafari A (2007) Alginate biopolymer production by Azotobacter chroococcum from whey degradation. J Environ Sci 4(4):427–432

    CAS  Google Scholar 

  • Kirokasyan A, Karinyan R, Akhinyan M (1955) Distribution of Azotobacter in soils of armyal. Appl Microbiol 5:480–486

    Google Scholar 

  • Kizilkaya R (2009) Nitrogen fixation capacity of Azotobacter spp. strains isolated from soils in different ecosystems and relationship between them and the microbiological properties of soils. J Environ Biol 30:73–82

    CAS  PubMed  Google Scholar 

  • Kloepper JW, Schroth MN (1980) Plant growth promoting rhizobacteria on radishes. Proc Int Conf Plant Pathol Bacteriol 2:879–882

    Google Scholar 

  • Kole RK, Saha J, Pal S et al (1994) Bacterial degradation of herbicide Pendimethalin and activity evaluation of its metabolites. Bul Env Cont Toxicol 52(5):779–786

    CAS  Google Scholar 

  • Kraepiel A, Bellenger J, Wichard T, Morel F (2009) Multiple roles of siderophores in free living nitrogen-fixing bacteria. Biometals 22:573–581

    Article  CAS  PubMed  Google Scholar 

  • Kumar V, Behl RK, Narula N (2000) Establishment of phosphate solubilizing strains of Azotobacter chroococcum in the rhizosphere and their effect on wheat cultivars under green house conditions. Microbiol Res 156:87–93

    Article  Google Scholar 

  • Latifi AM, Khodi S, Mirzaei M et al (2012) Isolation and characterization of five chlorpyrifos degrading bacteria. Afr J Biotechnol 11:3120–3146

    Google Scholar 

  • Lopez JG, Toledo MV, Reina S et al (1981) Root exudates of maize on production of auxins, gibberellins, cytokinins, amino acids and vitamins by Azotobacter chroococcum chemically defined media and dialysed soil media. Toxicol Environ Chem 33:69–78

    Article  Google Scholar 

  • Mali GV, Bodhankar MG (2009) Antifungal and phytohormone production potential of Azotobacter chroococcum isolates from groundnut (Arachis hypogaea L.) rhizosphere. Asia J Exp Sci 23:293–297

    CAS  Google Scholar 

  • Martin XM, Sumathi CS, Kannan VR (2011) Influence of agrochemical and Azotobacter spp. Application on soil fertility in relation to maize growth under nursery conditions. Eurasian J Biosci 5:19–28

    Article  Google Scholar 

  • Mirzakhani M, Ardakani MR, Band AA et al (2009) Response of spring safflower to co-inoculation with Azotobacter chroococcum and Glomus intraradices under different levels of nitrogen and phosphorus. Am J Agri Biol Sci 4:255–261

    Article  Google Scholar 

  • Mishra AK, Dutta S, Dileep Kumar BS (2005) Effect of fluorescent Pseudomonas strains on crop enhancement and suppression of root diseases of tea. Proc Asia Conf Emerging Trends Plant Microbe Interactions 26–30

    Google Scholar 

  • Mollmann U, Heinisch L, Bauernfeind A et al (2009) Siderophores as drug delivery agents: application of the Trojan horse strategy. Biometals 22:615–624

    Article  PubMed  Google Scholar 

  • Moneke AN, Okpala GN, Anyanwu CU (2010) Biodegradation of glyphosate herbicide In vitro using bacterial isolates from four rice fields. Afr J Biotechnol 9:4067–4074

    CAS  Google Scholar 

  • Moreno J, Lopez JG, Vela GR (1986) Survival of Azotobacter spp. in dry soils. App Env Microb 51:123–125

    CAS  Google Scholar 

  • Mrkovacki NB, Cacic NA, Milic VM (2002) Effects of Pesticides on Azotobacter chroococcum. Proc Nat Sci 23–28

    Google Scholar 

  • Mulder EG, Brontonegoro S (1974) Free living heterotrophic nitrogen fixing bacteria. Biol Nitro Fix 57:205–222

    Google Scholar 

  • Murcia R, Rodelas B, Salmeron V et al (1997) Effects of Herbicide simazine on vitamin production by Azotobacter chroococcum and Azotobacter vinelandii. Appl Soil Econ 6:187–193

    Article  Google Scholar 

  • Myresiotis CK, Vryzas Z, Mourkidou EP (2012) Biodegradation of soil applied pesticides by selected strains of plant growth promoting rhizobacteria (PGPR) and their effects on bacterial growth. Biodegradation 23:297–310

    Article  CAS  PubMed  Google Scholar 

  • Naik AT, Eranna N, Suresh CK (2007) Influence of Azotobacter chroococcum strains on growth and biomass of Adhatoda vasica Nees. Karnataka J Agri Sci 20:613–615

    Google Scholar 

  • Naik MK, Rajalaxmi K, Amaresh YS et al (2013) Search for 2, 4 DAPG positive genes in fluorescent Pseudomonas and their exploitation for sustainable disease management. Recent Advances in biofertilizer and bio fungicides (PGPR) for sustainable agriculture. Cambridge Scholar, Proceedings of the 3rd Asian PGPR Conference on Plant growth promoting rhizobacteria (PGPR) and other microbials, pp 21–24

    Google Scholar 

  • Niewiadomska A (2004) Effect of carbendazim, imazetapir and thiram on Nitrogenase activity, the number of microorganisms in soil and yield of red clover (Trifolium pratense L.). Pol J Environ Stud 13:403–410

    CAS  Google Scholar 

  • Page WJ, Shivprasad S (1991) Azotobacter salinestris spp. nov., a sodium dependent, microaerophilic and aeroadaptive nitrogen fixing bacteria. Int J Syst Bacteriol 41:369–376

    Article  Google Scholar 

  • Page W, Von Tigerstrom M (1988) Aminochelin, a catecholamine siderophore produced by Azotobacter vinelandii. J Gen Microbiol 134:453–460

    CAS  Google Scholar 

  • Parker LT, Socolofsky MD (1966) Central body of the Azotobacter cyst. J Bacteriol 91:297–303

    PubMed Central  CAS  PubMed  Google Scholar 

  • Patten CL, Glick BR (2002) Role of Pseudomonas putida indole acetic acid in development of the host plant root system. Appl Environ Microbiol 68:3795–3801

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Polyanskaya LM, Vedina OT, Lysak LV et al (2002) The growth promoting effect of Beijerinck mobilis and Clostridium sp. cultures on some agricultural crops. Microbiology 71(1):109–115

    Article  CAS  Google Scholar 

  • Ramaswami P, Mathan K, Nair K (1977) Azotobacter population in red and black soils of Tamil nadu. Mys J Agri Sci 11:364–366

    Google Scholar 

  • Rangaswamy G, Sadasivan KV (1964) Studies on occurrence of Azotobacter in some soil types. Ind Soc Soil Sci 12:43–49

    Google Scholar 

  • Rao AV, Venkateswarlu B (1982) Occurrence of Azotobacter and nitrogen fixation in the desert soils. Indian J Microbiol 22(4):255–257

    Google Scholar 

  • Reinhardt EL, Ramos PL, Manfio GP et al (2008) Molecular characterization of nitrogen-fixing bacteria isolated from Brazilian agricultural plants at also Paulo state. Braz J Microbiol 39:414–422

    Article  PubMed Central  PubMed  Google Scholar 

  • Revillas JJ, Rodelas B, Pozo C et al (2000) Production of B-group vitamins by two Azotobacter strains with phenolic compounds as sole carbon source under diazotrophic and adiazotrophic conditions. J Appl Microbiol 89(3):486–493

    Article  CAS  PubMed  Google Scholar 

  • Roy DB, Deb B, Sharma GD (2010) Evaluation of carrier based inoculants of Azotobacter chroococcum strain SDSA-12/2 in improving growth and yield summer (ahu) rice cv. IR-36. Biofrontiers 1(2):36–40

    Google Scholar 

  • Rubio MGT, Plata SAV, Castillo JB et al (2000) Isolation of enterobacteria, Azotobacter sp. and Pseudomonas sp., produces of indole acetic acid and siderophores from Colombian rice rhizosphere. Revista Latinoamericana de Microbiologica 42:171–176

    Google Scholar 

  • Sachin DN (2009) Effect of Azotobacter chroococcum (PGPR) on the growth of bamboo (Bambusa bamboo) and maize (Zea mays) plants. Biofront 1:24–31

    Google Scholar 

  • Sakthivel U, Karthikeyan B (2012) Isolation and characterization of plant growth promoting rhizobacteria (PGPR) from the rhizosphere of coleus forskohlii grown soil. Int J Rec Sci Res 3(5):288–296

    Google Scholar 

  • Shafiani S, Malik A (2003) Tolerance of pesticides and antibiotic resistance in bacteria isolated from wastewater irrigated soil. World J Microbiol Biotechnol 19:897–901

    Article  CAS  Google Scholar 

  • Spaepen S, Vanderleyden J, Remans R (2007) Indole-3-acetic acid in microbial and microorganism plant signalling. FEMS Microbiol Rev 31:425–448

    Article  CAS  PubMed  Google Scholar 

  • Subbarao NS (1988) Biofertilizers in agriculture, 2nd edn. IBH Publishing Co. Pvt. Ltd, Oxford/New Delhi, pp 189–202

    Google Scholar 

  • Subhani A, Ayman ME, Changyong H et al (2000) Effects of pesticides on soil microbial biomass. Pak J Bio Sci 3:705–709

    Article  Google Scholar 

  • Tejera N, Lluch C, Toledo MVM et al (2005) Isolation and characterization of Azotobacter and Azospirillum strains from the sugarcane rhizosphere. Plant Soil 270:223–232

    Article  CAS  Google Scholar 

  • Tilak KVBR, Ranganayaki N, Pal KK et al (2005) Diversity of plant growth and soil health supporting bacteria. Curr Sci 89:136–150

    CAS  Google Scholar 

  • Upadhyay SK, Singh DP, Saikia R (2009) Genetic diversity of plant growth promoting rhizobacteria isolated from rhizospheric soil of wheat under saline condition. Curr Microbiol. doi:10.1007/s00284-009-9464-1

    Google Scholar 

  • Waksman SA (1952) Soil microbiology, 1st edn. Wiley, New York, pp 199–200

    Google Scholar 

  • Whipps JM (2001) Microbial interactions and biocontrol in the rhizosphere. J Exp Bot 52:487–512

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgment

The authors are thankful to Dr. M. K. Naik, Professor of Plant Pathology and Dean (Postgraduate Studies), College of Agriculture, UAS, Raichur, Karnataka, and Department of Studies in Microbiology, University of Mysore.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. K. Naik .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2016 Springer India

About this chapter

Cite this chapter

Gurikar, C., Naik, M.K., Sreenivasa, M.Y. (2016). Azotobacter: PGPR Activities with Special Reference to Effect of Pesticides and Biodegradation. In: Singh, D., Singh, H., Prabha, R. (eds) Microbial Inoculants in Sustainable Agricultural Productivity. Springer, New Delhi. https://doi.org/10.1007/978-81-322-2647-5_13

Download citation

Publish with us

Policies and ethics