Research Article
Year 2018,
Volume: 46 Issue: 1, 101 - 111, 01.03.2018
Abstract
References
- M. Pessarakli, I. Szabolcs, Handbook of Plant Crop Stress, NY (1999) USA: CRC Press.
- Food and Agriculture Organization of the United Nations Save and Grow in practice maize rice wheat. A guide to sustainable cereal production, (2016) Rome.
- P.M. Hasegawa, R.A. Bressan, J.K. Zhu, H.J. Bohnert, Plant cellular and molecular responses to high salinity. Ann. Rev. Plant Physiol. Plant Mol. Biol., 51 (2000) 463-499.
- J.K. Zhu, Genetic analysis of plant salt tolerance using arabidopsis, Plant Physiol., 124 (2000) 941-948.
- V. Fotopoulos, A. Christou, C. Antoniou, G. Manganaris, Hydrogen sulphide: a versatile tool for the regulation of growth and defence responses in horticultural crops, J. Hortic. Sci. Biotechnol., 90 (2015) 227-234.
- P. Filippou, C. Antoniou, T. Obata, K. Van Der Kelen, V. Harokopos, L. Kanetis, V. Aidinis, F. Van Breusegem, AR. Fernie, V. Fotopoulos, Kresoximmethyl primes Medicago truncatula plants against abiotic stress factors via altered reactive oxygen and nitrogen species signalling leading to downstream transcriptional and metabolic readjustment, J. Exp. Bot., 67 (2016) 1259-1274.
- A. Sofo, G. Tataranni, A. Scopa, B. Dichio, C. Xiloyannis, Direct effects of Trichoderma harzianum strain T-22 on micropropagated GiSeLa6 (R) (Prunus spp.) rootstocks, Environ. Exp. Bot. 76 (2012) 33-38.
- R. Hermosa, A. Viterbo, I. Chet, E. Monte, Plantbeneficial effects of Trichoderma and of its genes, Microbiology 158 (2012) 17-25.
- S.A. Karaoglu, S. Ulker, Isolation, identification and seasonal distribution of soilborne fungi in tea growing areas of Iyidere-Ikizdere vicinity (Rize-Turkey), J. Basic Microbiol., 46 (2006) 208-218.
- M.S. Goettel, D.G. Inglis Fungi: Hyphomycetes. In: Lacey LA, editor. Manual of techniques in insectpathology, London, UK: Academic Press, (1997) 213-249
- F.J. Castillo, Antioxidative protection in the inducible CAM plant Sedum album L. following the imposition of severe water stress and recovery, Oecologia, 107 (1996) 469-477.
- D.I. Arnon, Copper Enzymes in Chloroplasts, Polyphenoloxidase in Beta vulgaris, Plant Physiol., 24 (1949) 1-15.
- E.M.J. Jaspars, Pigmentation of tobacco crowngall tissues cultured in vitro in dependence of the composition of the medium, Physiol. Plant, 18 (1965) 933-940.
- R.L. Heath, L. Packer, Photoperoxidation in isolated chloroplast, I. Kinetics and stochiometry of fatty acid peroxidation, Arc. Biochem Biophys., 125 (1968) 189- 198.
- L.S. Bates, R.P. Waldren, L.D. Teare, Rapid determination of free proline for water-stress studies, Plant Soil, 39 (1973) 205-207.
- R.S, Dhindsa, W. Matowe, Drought tolerance in two mosses: correlated with enzymatic defence against lipid peroxidation, J. Exp. Bot., 32 (1981) 79-91.
- H. Urbanek, E. Kuzniak-Gebarowska, K. Herka, Elicitation of defense responses in bean leaves by Botrytis cinerea polygalacturanase, Acta. Physiol. Plant, 13 (1991) 43-50.
- H. Aebi, Catalase. In: Bergmeyer H, editor. Methods of Enzymatic Analysis. 3rd ed. Weinheim, Germany: Verlag Chemie, (1983) 273-286.
- C.H. Foyer, B. Halliwell, Presence of glutathione and glutathione reductase in chloroplast: a proposed role in ascorbic acid metabolism, Planta, 133 (1976) 21-25.
- M.M. Bradford, A rapid and sensitive method for the quantitation of microgram quantities protein utilizing the principle of protein-dye binding, Ann. Biochem., 72 (1976) 248-254.
- J.N. Miller, J.C. Miller, Statistics and Chemometrics for Analytical Chemistry, Atlanta, Pearson/Prentice USA, 2005.
- B. Gupta, H. Bingru, Mechanism of salinity tolerance in plants: physiological, biochemical, and molecular characterization, Int. J. Genom., (2014) http://dx.doi. org/10.1155/2014/701596.
- J. Dluzneiwska, Reaction of fungi of Trichoderma genus to selected abiotic factors, E. J. Polish Agric. Uni. Agro., 6 (2003) 239-242.
- G.E. Harman, P.K, Kubicek Trichoderma and Gliocladium: Enzymes, biological control and commercial applications, London, UK (1998) Taylor and Francis.
- H. Bae, R.C. Sicher, M.S. Kim, S.H. Kim, M.D. Strem, RL. Melnick, BA. Bailey, The beneficial endophyte Trichoderma hamatum isolate DIS 219b promotes growth and delays the onset of the drought response in Theobroma cacao, J. Exp. Bot., 60 (2009) 3279-295.
- T. Benitez, A.M. Rincon, M.C. Limon, A.C. Codon, Biocontrol mechanisms of Trichoderma strains, Int. Microbiol., 7 (2004) 249-260.
- G.E. Harman, Myths and dogmas of biocontrolchanges in perceptions derived from research on Trichoderma harzianum T-22, Plant Disease, 84 (2000) 377-393.
- R. Hermosa, L. Botella, M. Montero-Barrientos, A. Alonso-Ramirez, V. Arbona, A. Gomez-Cadenas, C. Nicolas, Biotechnological applications of the gene transfer from the beneficial fungus Trichoderma harzianum to plants, Plant Signal. Behav., 6 (2011) 1235-1236.
- M. Eisendle, H. Oberegger, R. Buttinger, P. Illmer, H. Haas Biosynthesis and uptake of siderophores is controlled by the PacC-mediated ambient-pH Regulatory system in Aspergillus nidulans, Eukaryot. Cell, 3 (2004) 561-563.
- R.K. Behera, PC. Mishra, N.K. Choudhary, High irradiance and water stress induced alterations in pigment composition and chloroplast activities of primary wheat leaves, J. Plant Physiol., 159 (2002) 967-973.
- R. Mittler, Oxidative stress, antioxidants and stress tolerance, Trends in Plant Sci., 7 (2002) 405-410.
- N. Pehlivan, A.M. Yesilyurt, N. Durmus, S.A. Karaoglu, Trichoderma lixii ID11D seed biopriming mitigates dose dependent salt toxicity in maize, Acta Physiol. Plant., (2017) 10.1007/s1738-017-2375-z.
- S.E. Ahmed, M.H. Nawata, Y. Domae, T. Sakuratani, Alterations in photosynthesis and some antioxidant enzymatic activities of mungbean subjected to waterlogging, Plant Sci., 163 (2002) 117-123.
- K. Maxwell, GN. Johnson, Chlorophyll fluorescence-a practical guide, J. Exp. Bot, 51 (2000) 659-668.
- A.F. Lodeyro, M. Giró, H.O. Poli, G. Bettucci, A. Cortadi, A.M Ferri, N. Carrillo, Suppression of reactive oxygen species accumulation in chloroplasts prevents leaf damage but not growth arrest in salt-stressedtobacco plants. PLoS One, 11 (2016). http://doi.org/10.1371/ journal.pone.0159588
- F. Moradi, A.M. Ismail, Responses of photosynthesis, chlorophyll fluorescence and ROS-scavenging systems to salt stress during seedling and reproductive stages in rice, Ann Bot., 99 (2007) 1161-1173.
Year 2018,
Volume: 46 Issue: 1, 101 - 111, 01.03.2018
Abstract
The rapid increase in global population and industrial pollution pose severe environmental threats to
agriculture that are exacerbated by salt stress. Molecular characterization of new fungal isolates and
assessment of their impact on agriculture might be an eco-friendly approach to modulating salt tolerance.
Herein, fungal seed biopriming was conducted on salt (NaCl) stressed maize in a dose-dependent manner.
Genetic lineages of fungi were identified using well-known fungal ITS (internal transcribed spacer) barcodes
that revealed similarity to the Trichoderma citrinoviride (T11C) species. Fv/Fm, ETR and qP were recorded as
close to optimum in bioprimed maize plants after application of salt stress. NPQ (nonphotochemical quenching)
decreased slightly in respective groups. Higher photosynthetic pigment contents were also detected. T11C
seed biopriming decreased the lipid oxidation remarkably under salt stress. SOD, GPX, GR and CAT activities
were not found to be significantly induced in the roots or leaves of T11C after biopriming. However, higher
RWC (relative water content), soluble protein and proline were measured in bioprimed test groups treated
with high salt stress, demonstrating increased osmoregulatory capacity. Our ongoing research is directed
toward developing powdered fungal biopreperations to assay multiple stress tolerances in agriculture for agroeconomically
important cereals such as maize.
agriculture that are exacerbated by salt stress. Molecular characterization of new fungal isolates and
assessment of their impact on agriculture might be an eco-friendly approach to modulating salt tolerance.
Herein, fungal seed biopriming was conducted on salt (NaCl) stressed maize in a dose-dependent manner.
Genetic lineages of fungi were identified using well-known fungal ITS (internal transcribed spacer) barcodes
that revealed similarity to the Trichoderma citrinoviride (T11C) species. Fv/Fm, ETR and qP were recorded as
close to optimum in bioprimed maize plants after application of salt stress. NPQ (nonphotochemical quenching)
decreased slightly in respective groups. Higher photosynthetic pigment contents were also detected. T11C
seed biopriming decreased the lipid oxidation remarkably under salt stress. SOD, GPX, GR and CAT activities
were not found to be significantly induced in the roots or leaves of T11C after biopriming. However, higher
RWC (relative water content), soluble protein and proline were measured in bioprimed test groups treated
with high salt stress, demonstrating increased osmoregulatory capacity. Our ongoing research is directed
toward developing powdered fungal biopreperations to assay multiple stress tolerances in agriculture for agroeconomically
important cereals such as maize.
References
- M. Pessarakli, I. Szabolcs, Handbook of Plant Crop Stress, NY (1999) USA: CRC Press.
- Food and Agriculture Organization of the United Nations Save and Grow in practice maize rice wheat. A guide to sustainable cereal production, (2016) Rome.
- P.M. Hasegawa, R.A. Bressan, J.K. Zhu, H.J. Bohnert, Plant cellular and molecular responses to high salinity. Ann. Rev. Plant Physiol. Plant Mol. Biol., 51 (2000) 463-499.
- J.K. Zhu, Genetic analysis of plant salt tolerance using arabidopsis, Plant Physiol., 124 (2000) 941-948.
- V. Fotopoulos, A. Christou, C. Antoniou, G. Manganaris, Hydrogen sulphide: a versatile tool for the regulation of growth and defence responses in horticultural crops, J. Hortic. Sci. Biotechnol., 90 (2015) 227-234.
- P. Filippou, C. Antoniou, T. Obata, K. Van Der Kelen, V. Harokopos, L. Kanetis, V. Aidinis, F. Van Breusegem, AR. Fernie, V. Fotopoulos, Kresoximmethyl primes Medicago truncatula plants against abiotic stress factors via altered reactive oxygen and nitrogen species signalling leading to downstream transcriptional and metabolic readjustment, J. Exp. Bot., 67 (2016) 1259-1274.
- A. Sofo, G. Tataranni, A. Scopa, B. Dichio, C. Xiloyannis, Direct effects of Trichoderma harzianum strain T-22 on micropropagated GiSeLa6 (R) (Prunus spp.) rootstocks, Environ. Exp. Bot. 76 (2012) 33-38.
- R. Hermosa, A. Viterbo, I. Chet, E. Monte, Plantbeneficial effects of Trichoderma and of its genes, Microbiology 158 (2012) 17-25.
- S.A. Karaoglu, S. Ulker, Isolation, identification and seasonal distribution of soilborne fungi in tea growing areas of Iyidere-Ikizdere vicinity (Rize-Turkey), J. Basic Microbiol., 46 (2006) 208-218.
- M.S. Goettel, D.G. Inglis Fungi: Hyphomycetes. In: Lacey LA, editor. Manual of techniques in insectpathology, London, UK: Academic Press, (1997) 213-249
- F.J. Castillo, Antioxidative protection in the inducible CAM plant Sedum album L. following the imposition of severe water stress and recovery, Oecologia, 107 (1996) 469-477.
- D.I. Arnon, Copper Enzymes in Chloroplasts, Polyphenoloxidase in Beta vulgaris, Plant Physiol., 24 (1949) 1-15.
- E.M.J. Jaspars, Pigmentation of tobacco crowngall tissues cultured in vitro in dependence of the composition of the medium, Physiol. Plant, 18 (1965) 933-940.
- R.L. Heath, L. Packer, Photoperoxidation in isolated chloroplast, I. Kinetics and stochiometry of fatty acid peroxidation, Arc. Biochem Biophys., 125 (1968) 189- 198.
- L.S. Bates, R.P. Waldren, L.D. Teare, Rapid determination of free proline for water-stress studies, Plant Soil, 39 (1973) 205-207.
- R.S, Dhindsa, W. Matowe, Drought tolerance in two mosses: correlated with enzymatic defence against lipid peroxidation, J. Exp. Bot., 32 (1981) 79-91.
- H. Urbanek, E. Kuzniak-Gebarowska, K. Herka, Elicitation of defense responses in bean leaves by Botrytis cinerea polygalacturanase, Acta. Physiol. Plant, 13 (1991) 43-50.
- H. Aebi, Catalase. In: Bergmeyer H, editor. Methods of Enzymatic Analysis. 3rd ed. Weinheim, Germany: Verlag Chemie, (1983) 273-286.
- C.H. Foyer, B. Halliwell, Presence of glutathione and glutathione reductase in chloroplast: a proposed role in ascorbic acid metabolism, Planta, 133 (1976) 21-25.
- M.M. Bradford, A rapid and sensitive method for the quantitation of microgram quantities protein utilizing the principle of protein-dye binding, Ann. Biochem., 72 (1976) 248-254.
- J.N. Miller, J.C. Miller, Statistics and Chemometrics for Analytical Chemistry, Atlanta, Pearson/Prentice USA, 2005.
- B. Gupta, H. Bingru, Mechanism of salinity tolerance in plants: physiological, biochemical, and molecular characterization, Int. J. Genom., (2014) http://dx.doi. org/10.1155/2014/701596.
- J. Dluzneiwska, Reaction of fungi of Trichoderma genus to selected abiotic factors, E. J. Polish Agric. Uni. Agro., 6 (2003) 239-242.
- G.E. Harman, P.K, Kubicek Trichoderma and Gliocladium: Enzymes, biological control and commercial applications, London, UK (1998) Taylor and Francis.
- H. Bae, R.C. Sicher, M.S. Kim, S.H. Kim, M.D. Strem, RL. Melnick, BA. Bailey, The beneficial endophyte Trichoderma hamatum isolate DIS 219b promotes growth and delays the onset of the drought response in Theobroma cacao, J. Exp. Bot., 60 (2009) 3279-295.
- T. Benitez, A.M. Rincon, M.C. Limon, A.C. Codon, Biocontrol mechanisms of Trichoderma strains, Int. Microbiol., 7 (2004) 249-260.
- G.E. Harman, Myths and dogmas of biocontrolchanges in perceptions derived from research on Trichoderma harzianum T-22, Plant Disease, 84 (2000) 377-393.
- R. Hermosa, L. Botella, M. Montero-Barrientos, A. Alonso-Ramirez, V. Arbona, A. Gomez-Cadenas, C. Nicolas, Biotechnological applications of the gene transfer from the beneficial fungus Trichoderma harzianum to plants, Plant Signal. Behav., 6 (2011) 1235-1236.
- M. Eisendle, H. Oberegger, R. Buttinger, P. Illmer, H. Haas Biosynthesis and uptake of siderophores is controlled by the PacC-mediated ambient-pH Regulatory system in Aspergillus nidulans, Eukaryot. Cell, 3 (2004) 561-563.
- R.K. Behera, PC. Mishra, N.K. Choudhary, High irradiance and water stress induced alterations in pigment composition and chloroplast activities of primary wheat leaves, J. Plant Physiol., 159 (2002) 967-973.
- R. Mittler, Oxidative stress, antioxidants and stress tolerance, Trends in Plant Sci., 7 (2002) 405-410.
- N. Pehlivan, A.M. Yesilyurt, N. Durmus, S.A. Karaoglu, Trichoderma lixii ID11D seed biopriming mitigates dose dependent salt toxicity in maize, Acta Physiol. Plant., (2017) 10.1007/s1738-017-2375-z.
- S.E. Ahmed, M.H. Nawata, Y. Domae, T. Sakuratani, Alterations in photosynthesis and some antioxidant enzymatic activities of mungbean subjected to waterlogging, Plant Sci., 163 (2002) 117-123.
- K. Maxwell, GN. Johnson, Chlorophyll fluorescence-a practical guide, J. Exp. Bot, 51 (2000) 659-668.
- A.F. Lodeyro, M. Giró, H.O. Poli, G. Bettucci, A. Cortadi, A.M Ferri, N. Carrillo, Suppression of reactive oxygen species accumulation in chloroplasts prevents leaf damage but not growth arrest in salt-stressedtobacco plants. PLoS One, 11 (2016). http://doi.org/10.1371/ journal.pone.0159588
- F. Moradi, A.M. Ismail, Responses of photosynthesis, chlorophyll fluorescence and ROS-scavenging systems to salt stress during seedling and reproductive stages in rice, Ann Bot., 99 (2007) 1161-1173.
There are 36 citations in total.
Details
| Primary Language | English |
|---|---|
| Journal Section | Articles |
| Authors | |
| Publication Date | March 1, 2018 |
| Acceptance Date | December 6, 2017 |
| Published in Issue | Year 2018 Volume: 46 Issue: 1 |
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HACETTEPE JOURNAL OF BIOLOGY AND CHEMİSTRY
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