Production of indole-3-acetic acid via the indole-3-acetamide pathway in the plant-beneficial bacterium pseudomonas chlororaphis O6 is inhibited by ZnO nanoparticles but enhanced by CuO nanoparticles

Applied and Environmental Microbiology

Volumn 78, Issue 5, 2012, Pages 1404-1410

  Dimkpa, Christian O ^a,b   Zeng, Jia ^a   McLean, Joan E ^b   Britt, David W ^a   Zhan, Jixun ^a   Anderson, Anne J ^a,b  

^a Utah State University   (United States)

^b UTAH STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

A PLANTS; B-Y IONS; BENEFICIAL EFFECTS; CONTROL CULTURES; CUO NANOPARTICLES; GENES ENCODING; INDOLE-3-ACETIC ACID; INTERMEDIATE LEVEL; ION RELEASE; PSEUDOMONAS CHLORORAPHIS; SUBLETHAL DOSE; ZNO; ZNO NANOPARTICLES;

ACETIC ACID; AMINO ACIDS; CELL CULTURE; GENES; GROWTH KINETICS; NANOPARTICLES; PH; ZINC OXIDE;

BACTERIA;

ANTIINFECTIVE AGENT; COPPER; CUPRIC OXIDE; INDOLEACETAMIDE; INDOLEACETIC ACID; INDOLEACETIC ACID DERIVATIVE; NANOPARTICLE; TRYPTOPHAN; ZINC OXIDE;

BACTERIUM; CONCENTRATION (COMPOSITION); COPPER; GROWTH REGULATOR; INHIBITION; METABOLISM; NANOTECHNOLOGY; ZINC;

ARTICLE; CHEMISTRY; CULTURE MEDIUM; DRUG EFFECT; METABOLISM; MICROBIOLOGY; PLANT; PSEUDOMONAS;

ANTI-BACTERIAL AGENTS; COPPER; CULTURE MEDIA; INDOLEACETIC ACIDS; NANOPARTICLES; PLANTS; PSEUDOMONAS; TRYPTOPHAN; ZINC OXIDE;

BACTERIA (MICROORGANISMS); PSEUDOMONAS CHLORORAPHIS;

EID: 84857084507     PISSN: 00992240     EISSN: 10985336     Source Type: Journal    
DOI: 10.1128/AEM.07424-11     Document Type: Article

References (42)

1. Andrews M, Hodge S, Raven JA. 2010. Positive plant microbial interactions. Ann. Appl. Biol. 157:317-320
2. 3) to Escherichia coli, Bacillus subtilis, and Streptococcus aureus. Sci. Total Environ. 409:1603-1608
3. Barazani O, Friedman J. 1999. Is IAA the major root growth factor secreted from plant-growth-mediating bacteria? J. Chem. Ecol. 25:2397-2406
4. Beyeler M, Keel C, Michaux P, Haas D. 1999. Enhanced production of indole-3-acetic acid by a genetically modified strain of Pseudomonas fluorescens CHA0 affects root growth of cucumber, but does not improve protection of the plant against Pythium root rot. FEMS Microbiol. Ecol. 28:225-233
5. Bhattacharyya RN, Chakraborty B, Bhunia S, Misra M. 1999. Effect of heavy metals on growth and IAA production of a Rhizobium sp. isolated from the root nodules of Alysicarpus vaginalis DC. Environ. Ecol. 17:873-878
6. Cho SM, et al. 2008. 2R, 3R-butanediol, a bacterial volatile produced by Pseudomonas chlororaphis O6, is involved in induction of systemic tolerance to drought in Arabidopsis thaliana. Mol. Plant Microbe Interact. 8:1067-1077
7. Chung K-R, Shilts T, Erturk U, Timmer LW, Ueng PP. 2003. Indole derivatives produced by the fungus Collectotrichum acutatum causing lime anthracnose and post bloom fruit decrease of citrus. FEMS Microbiol. Lett. 226:23-30
8. Comai L, Kosuge T. 1980. Involvement of plasmid deoxyribonucleic acid in indole acetic acid synthesis in Pseudomonas savastanoi. J. Bacteriol. 143:950-957
9. Costacurta A, Vanderleyden J. 1995. Synthesis of phytohormones by plant-associated bacteria. Crit. Rev. Microbiol. 21:1-18
10. Dimkpa CO, et al. 2011. Interaction of silver nanoparticles with an environmentally beneficial bacterium, Pseudomonas chlororaphis. J. Hazard. Mater. 188:428-435
11. Dimkpa CO, Calder A, McLean JE, Britt DW, Anderson AJ. 2011. Responses of a soil bacterium, Pseudomonas chlororaphis O6 to commercial metal oxide nanoparticles compared with responses to metal ions. Environ. Pollut. 159:1749-1756
12. Dimkpa CO, McLean JE, Britt DW, Anderson AJ. 11 July 2011, posting date. CuO and ZnO nanoparticles differently affect the secretion of fluorescent siderophores in the beneficial root colonizer, Pseudomonas chlororaphis O6. Nanotoxicology doi:10.3109/17435390.2011.598246
13. Dimkpa C, Merten D, Svatoš A, Büchel G, Kothe E. 2008. Hydroxamate siderophores produced by Streptomyces acidiscabies E13 bind nickel and promote growth in cowpea (Vigna unguiculata L.) under nickel stress. Can. J. Microbiol. 54:163-172
14. Dimkpa C, Merten D, Svatoš A, Büchel G, Kothe E. 2009. Metalinduced oxidative stress impacting plant growth in contaminated soil is alleviated by microbial siderophores. Soil Biol. Biochem. 41:154-162
15. Dimkpa CO, et al. 2008. Involvement of siderophores in the reduction of metal-induced inhibition of auxin synthesis in Streptomyces spp. Chemosphere 74:19-25
16. Dimkpa C, Weinand T, Asch F. 2009. Plant-rhizobacteria interactions alleviate abiotic stress conditions. Plant Cell Environ. 32:1682-1694
17. Dodd IC, Zinovkina NY, Safronova VI, Belimov AA. 2010. Rhizobacterial mediation of plant hormone status. Ann. Appl. Biol. 157:361-379
18. Gajjar P, et al. 2009. Antimicrobial activities of commercial nanoparticles against an environmental soil microbe, Pseudomonas putida KT2440. J. Biol. Eng. 3:9
19. Ghanem ME, et al. 2011. Root-targeted biotechnology to mediate hormonal signalling and improve crop stress tolerance. Plant Cell Rep. 30: 807-823
20. Jones N, Ray B, Ranjit KT, Manna AC. 2008. Antibacterial activity of ZnO nanoparticle suspensions on a broad spectrum of microorganisms. FEMS Microbiol. Lett. 279:71-76
21. Joshi P, et al. 2011. Site-specific interaction between ZnO nanoparticles and tryptophan: a first principles quantum mechanical study. Phys. Chem. Chem. Phys. 13:476-479
22. Kamnev AA, et al. 2005. Effects of heavy metals on plant-associated rhizobacteria: comparison of endophytic and non-endophytic strains of Azospirillum brasilense. J. Trace Elem. Med. Biol. 19:91-95
23. Kang BR, et al. 2006. Production of indole-3-acetic acid in the plantbeneficial strain Pseudomonas chlororaphis O6 is negatively regulated by the global sensor kinase, GacS. Curr. Microbiol. 52:473-475
24. Leveau JHJ, Lindow SE. 2005. Utilization of the plant hormone indole-3-acetic acid for growth by Pseudomonas putida strain 1290. Appl. Environ. Microbiol. 71:2365-2371
25. Lindow SE, et al. 1998. Occurrence of indole-3-acetic acid-producing bacteria on pear trees and their association with fruit russet. Phytopathology 88:1149-1157
26. Malhotra M, Srivastava S. 2009. Stress-responsive indole-3-acetic acid biosynthesis by Azospirillum brasilense SM and its ability to modulate plant growth. Eur. J. Soil Biol. 5:73-80
27. Mandal G, Bhattacharya S, Ganguly T. 2009. Nature of interactions of tryptophan with zinc oxide nanoparticles and L-aspartic acid: a spectroscopic approach. Chem. Phy. Lett. 472:128-133
28. Manulis S, Shafrir H, Epstein E, Lichter A, Barash I. 1994. Biosynthesis of indole-3-acetic acid via the indole-3-acetamide pathway in Streptomyces spp. Microbiology 140:1045-1050
29. Oberhänsli T, Defago G, Haas D. 1991. Indole-3-acetic-acid (IAA) synthesis in the biocontrol strain CHA0 of Pseudomonas fluorescens-role of tryptophan side-chain oxidase. J. Gen. Microbiol. 137:2273-2279
30. Oota Y, Tsudzuki T. 1971. Resemblance of growth substances to metal chelators with respect to their actions on duckweed growth. Plant Cell Physiol. 12:619-631
31. Pal S, Tak YK, Song JM. 2007. Does the antibacterial activity of silver nanoparticles depend on the shape of the nanoparticle? A study of the gram-negative bacterium Escherichia coli. Appl. Environ. Microbiol. 73: 1712-1720
32. Patten CL, Glick BR. 2002. Role of Pseudomonas putida indoleacetic acid in development of the host plant root system. Appl. Environ. Microbiol. 68:3795-3801
33. Qu J, Yuan X, Wang X, Shao P. 2011. Zinc accumulation and synthesis of ZnO nanoparticles using Physalis alkekengi L. Environ. Pollut. 159: 1783-1788
34. Ryu C-M, et al. 2007. Tobacco cultivars vary in induction of systemic resistance against Cucumber mosaic virus and growth promotion by Pseudomonas chlororaphis O6 and its gacS mutant. Eur. J. Plant Pathol. 119: 383-390
35. Shvedova AA, Kagan VE, Fadeel B. 2010. Close encounters of the small kind: adverse effects of man-made materials interfacing with the nanocosmos of biological systems. Annu. Rev. Pharmacol. Toxicol. 50:63-88
36. Spaepen S, Vanderleyden J, Remans R. 2007. Indole-3-acetic acid in microbial and microorganism-plant signaling. FEMS Microbiol. Rev. 31: 425-448
37. Spencer M, et al. 2003. Induced defence in tobacco by Pseudomonas chlororaphis strain O6 involves at least the ethylene pathway. Mol. Plant Microbe Interact. 63:27-34
38. Sposito G. 1989. The chemistry of soils, p 277. Oxford University Press, New York, NY
39. Stobrawa K, Lorenc-Plucińska G. 2007. Changes in antioxidant enzyme activity in the fine roots of black poplar (Populus nigra L.) and cottonwood (Populus deltoides Bartr. ex Marsch) in a heavy metal-polluted environment. Plant Soil 298:57-68
40. Vessey JK. 2003. Plant growth promoting rhizobacteria as biofertilizer. Plant Soil 255:571-586
41. Wang X, et al. 2008. Pedological characteristics of Mn mine tailing and metal accumulation by native plants. Chemosphere 72:1260-1266
42. Xie Y, He Y, Irwin PL, Jin T, Shi X. 2011. Antibacterial activity and mechanism of action of zinc oxide nanoparticles against Campylobacter jejuni. Appl. Environ. Microbiol. 77:2325-2331.