References
- Anderson, A. J. and Kim, Y. C. 2018. Biopesticides produced by plant-probiotic Pseudomonas chlororaphis isolates. Crop Prot. 105: 62-69. https://doi.org/10.1016/j.cropro.2017.11.009
- Aslam, S. N., Newman, M. A., Erbs, G., Morrissey, K. L., Chinchilla, D., Boller, T. et al. 2008. Bacterial polysaccharides suppress induced innate immunity by calcium chelation. Curr. Biol. 18: 1078-1083. https://doi.org/10.1016/j.cub.2008.06.061
- Bae, H., Kim, S. H., Kim, M. S., Sicher, R. C., Lary, D., Strem, M. D. et al. 2008. The drought response of Theobroma cacao (cacao) and the regulation of genes involved in polyamine biosynthesis by drought and other stresses. Plant Physiol. Biochem. 46: 174-188. https://doi.org/10.1016/j.plaphy.2007.10.014
- Bakker, P. A. H. M., Doornbos, R. F., Zamioudis, C., Berendsen, R. L. and Pieterse, C. M. J. 2013. Induced systemic resistance and the rhizosphere microbiome. Plant Pathol. J. 29: 136-143. https://doi.org/10.5423/PPJ.SI.07.2012.0111
- Bonebrake, M., Anderson, K., Valiente, J., Jacobson, A., McLean, J. E. Anderson, A. et al. 2018. Biofilms benefiting plants exposed to ZnO and CuO nanoparticles studied with a root-mimetic hollow fiber membrane. J. Agric. Food Chem. 66: 6619-6627. https://doi.org/10.1021/acs.jafc.7b02524
- Cheng, X., Etalo, D. W., van de Mortel, J. E., Dekkers, E., Nguyen, L., Medema, M. H. et al. 2017. Genome-wide analysis of bacterial determinants of plant growth promotion and induced systemic resistance by Pseudomonas fluorescens. Environ. Microbiol. 19: 4638-4656. https://doi.org/10.1111/1462-2920.13927
- Cho, S. M., Kang, B. R., Han, S. H., Anderson, A. J., Park, J. Y., Lee, Y. H. 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. 21: 1067-1075. https://doi.org/10.1094/MPMI-21-8-1067
- Cho, S. M., Kang, B. R., Kim, J. J. and Kim, Y. C. 2012. Induced systemic drought and salt tolerance by Pseudomonas chlororaphis O6 root colonization is mediated by ABA-independent stomatal closure. Plant Pathol. J. 28: 202-206. https://doi.org/10.5423/PPJ.2012.28.2.202
- Cho, S. M., Kang, B. R. and Kim, Y. C. 2013. Transcriptome analysis of induced systemic drought tolerance elicited by Pseudomonas chlororaphis O6 in Arabidopsis thaliana. Plant Pathol. J. 29: 209-220. https://doi.org/10.5423/PPJ.SI.07.2012.0103
- Creelman, R. A. and Mullet, J. E. 1997. Biosynthesis and action of jasmonate in plants. Annu. Rev. Plant Physiol. Plant Mol. Biol. 48: 355-381. https://doi.org/10.1146/annurev.arplant.48.1.355
- Evans, N. H. 2003. Modulation of guard cell plasma membrane potassium currents by methyl jasmonate. Plant Physiol. 131: 8-11. https://doi.org/10.1104/pp.014266
- Han, S. H., Anderson, A. J., Yang, K. Y., Cho, B. H., Kim, K. Y., Lee, M. C. et al. 2006. Multiple determinants influence root colonization and induction of induced systemic resistance by Pseudomonas chlororaphis O6. Mol. Plant Pathol. 7: 463-472. https://doi.org/10.1111/j.1364-3703.2006.00352.x
- Hung, C.-C., Santschi, P. H. and Gillow, J. B. 2005. Isolation and characterization of extracellular polysaccharides produced by Pseudomonas fluorescens Biovar II. Carbohydr. Polym. 61: 141-147. https://doi.org/10.1016/j.carbpol.2005.04.008
- Jiang, C.-H., Fan, Z.-H., Xie, P. and Guo, J.-H. 2016. Bacillus cereus AR156 extracellular polysaccharides served as a novel micro-associated molecular pattern to induced systemic immunity to Pst DC3000 in Arabidopsis. Front. Microbiol. 7: 664.
- Kim, H. J., Nam, H. S., Anderson, A. J., Yang, K. Y., Cho, B. H. and Kim, Y. C. 2007. Mutation in the edd gene encoding the 6-phosphogluconate dehydratase of Pseudomonas chlororaphis O6 impairs root colonization and is correlated with reduced induction of systemic resistance. Lett. Appl. Microbiol. 44: 56-61. https://doi.org/10.1111/j.1472-765X.2006.02029.x
- Kim, Y. C., Leveau, J., McSpadden Gardener, B. B., Pierson, E. A., Pierson III, L. S. and Ryu, C. M. 2011. The multifactorial basis for plant health promotion by plant-associated bacteria. Appl. Environ. Microbiol. 77: 1548-1555. https://doi.org/10.1128/AEM.01867-10
- Kim, Y. C., Glick, B. R., Bashan, Y. and Ryu, C. M. 2012. Enhancement of Plant Drought Tolerance by Microbes. In: Plant Responses to Drought Stress, ed. by R. Aroca, pp. 383-413. Springer, Berlin, Germany.
- Kim, Y. C. and Anderson, A. J. 2018. Rhizosphere pseudomonads as probiotics improving plant health. Mol. Plant Pathol. doi:10.1111/mpp.12693.
- Leung, J. and Giraudat, J. 1998. Abscisic acid signal transduction Annu. Rev. Plant Physiol. Plant Mol. Biol. 49: 199-222. https://doi.org/10.1146/annurev.arplant.49.1.199
- Mayak, S., Tirosh, T. and Glick, B. R. 2004. Plant growth-promoting bacteria confer resistance in tomato plants to salt stress. Plant Physiol. Biochem. 42: 565-572. https://doi.org/10.1016/j.plaphy.2004.05.009
- Melotto, M., Underwood, W., Koczan, J., Nomura, K. and He, S. Y. 2006. Plant stomata function in innate immunity against bacterial invasion. Cell 126: 969-980. https://doi.org/10.1016/j.cell.2006.06.054
- Ortmann, I., Conrath, U. and Moerschbacher, B. M. 2006. Exopolysaccharides of Pantoea agglomerans have different priming and eliciting activities in suspension-cultured cells of monocots and dicots. FEBS Lett. 580: 4491-4494. https://doi.org/10.1016/j.febslet.2006.07.025
- Park, K., Kloepper, J. W. and Ryu, C. M. 2008. Rhizobacterial exopolysaccharides elicit induced resistance on cucumber. J. Microbiol. Biotechnol. 18: 1095-1100.
- Ryu, C. M., Farag, M. A., Hu, C. H., Reddy, M. S., Kloepper, J. W. and Pare, P. W. 2004. Bacterial volatiles induce systemic resistance in Arabidopsis. Plant Physiol. 134: 1017-1026. https://doi.org/10.1104/pp.103.026583
- Sandhya, V., Ali, S. Z., Grover, M., Reddy, G. and Venkateswarlu, B. 2009. Alleviation of drought stress effects in sunflower seedlings by the exopolysaccharides producing Pseudomonas putida strain GAP-P45. Biol. Fert. Soils 46: 17-26. https://doi.org/10.1007/s00374-009-0401-z
- Santaella, C., Schue, M., Berge, O., Heulin, T. and Achouak, W. 2008. The exopolysaccharide of Rhizobium sp. YAS34 is not necessary for biofilm formation on Arabidopsis thaliana and Brassica napus roots but contributes to root colonization. Environ. Microbiol. 10: 2150-2163. https://doi.org/10.1111/j.1462-2920.2008.01650.x
- Schroeder, J. I., Kwak, J. M. and Allen, G. J. 2001. Guard cell abscisic acid signalling and engineering drought hardiness in plants. Nature 410: 327-330. https://doi.org/10.1038/35066500
- Shukla, N., Awasthi, R. P., Rawat, L. and Kumar, J. 2015. Seed biopriming with drought tolerant isolates of Trichoderma harzianum promote growth and drought tolerance in Triticum aestivum. Ann. Appl. Biol. 166: 171-182. https://doi.org/10.1111/aab.12160
- Suhita, D., Raghavendra, A. S., Kwak, J. M. and Vavasseur, A. 2004. Cytoplasmic alkalization precedes reactive oxygen species production during methyl jasmonate- and abscisic acid-induced stomatal closure. Plant Physiol. 134: 1536-1545. https://doi.org/10.1104/pp.103.032250
- Timmusk, S. and Wagner, E. G. 1999. The plant-growth-promoting rhizobacterium Paenibacillus polymyxa induces changes in Arabidopsis thaliana gene expression: a possible connection between biotic and abiotic stress responses. Mol. Plant Microbe Interact. 12: 951-959. https://doi.org/10.1094/MPMI.1999.12.11.951
- Underwood, W., Melotto, M. and He, S. Y. 2007. Role of plant stomata in bacterial invasion. Cell. Microbiol. 9: 1621-1629. https://doi.org/10.1111/j.1462-5822.2007.00938.x
- Wingender, J., Neu, T. R. and Flemming, H.-C. 1999. What are bacterial extracellular polymeric substances? In: Microbial Extracellular Polymeric Substances, eds. by J. Wingender, T. R. Neu and H.-C. Flemming, pp. 1-19. Springer, Berlin, Germany.
- Woo, N. S., Badger, M. R. and Pogson, B. J. 2008. A rapid, non-invasive procedure for quantitative assessment of drought survival using chlorophyll fluorescence. Plant Methods 4: 27. https://doi.org/10.1186/1746-4811-4-27
- Yang, J., Kloepper, J. W. and Ryu, C. M. 2009. Rhizosphere bacteria help plants tolerate abiotic stress. Trends Plant Sci. 14: 1-4. https://doi.org/10.1016/j.tplants.2008.10.004
- Yang, K.-Y., Doxey, S., McLean, J. E., Britt, D., Watson, A., Al Qassy, D. et al. 2017. Remodeling of root morphology by CuO and ZnO nanoparticles: effects on drought tolerance for plants colonized by a beneficial pseudomonad. Botany 96: 175-186.
- Zhang, H., Murzello, C., Sun, Y., Kim, M. S., Xie, X., Jeter, R. M. et al. 2010. Choline and osmotic-stress tolerance induced in Arabidopsis by the soil microbe Bacillus subtilis (GB03). Mol. Plant Microbe Interact. 23: 1097-1104. https://doi.org/10.1094/MPMI-23-8-1097
- Zhu, J. K. 2001. Cell signaling under salt, water and cold stresses. Curr. Opin. Plant Biol. 4: 401-406. https://doi.org/10.1016/S1369-5266(00)00192-8