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Effects of Bacillus cereus strain BBS7 Rhizobacterium Isolate on the Expression of Heat Shock Genes in Tomato Under Drought Stress

Yıl 2025, , 85 - 93, 30.06.2025
https://doi.org/10.18615/anadolu.1683423

Öz

Drought stress causes significant economic losses in agricultural production due to disruptions in the physiological functions of plants. Tomato plants, which have strategic importance in the agricultural sector, are among the species most severely affected by these stress conditions. Research has demonstrated that root bacteria promoting plant growth enhance drought tolerance by influencing cellular, physiological, and morphological mechanisms. In this study, seeds of tomato were inoculated with Bacillus cereus strain BBS7 and planted in a peat medium. Seedlings at the 2-3 true leaf stage were transferred to a hydroponic system and maintained under control conditions for 7 days before being subjected to drought stress simulated using PEG 6000. The drought stress intensity was gradually increased (¼, ½, ¾, and full dose) every 48 hours until the target water potential (Ψs = -1.0 MPa) was achieved. Plant samples were collected at the 2nd and 12th hours after stress application, and the expression levels of heat shock protein genes (HSP21, HSP70, and HSFA), produced in response to drought stress, were analyzed via qPCR. The results indicate that B. cereus strain BBS7 acts as an effective PGPR (Plant Growth-Promoting Rhizobacterium) by regulating the expression profiles of these genes, thereby enhancing drought resistance in tomato plants.

Proje Numarası

FYL-2021-22622

Kaynakça

  • Altunlu, H. 2011. Aşılamanın Domateste Kuraklık Stresi Üzerine Etkileri. Ege Üniversitesi Fen Bilimleri Enstitüsü Bahçe Bitkileri Anabilim Dalı (Basılmamış) Doktora tezi. İzmir- Türkiye. 206 s.
  • Altunlu, H., G. Aydoner Coban, A. Gul, H. Ozaktan. 2024. Effect of Rhizobacteria On Drought Stress Tolerance of Tomato Plants at Vegetative and Fruiting Growth Stages. Journal of Crop Health 76: 195–208. https://doi.org/10.1007/s 10343-023-00941-1.
  • Altunlu, H., G. Aydöner Çoban, ve A. Gül. 2022. Domates genotiplerinin kuraklık stresine tolerans açısından tohum çimlendirme ve vegetatif gelişme aşamalarında hızlı taranmasına uygun testlerin optimizasyonu. Journal of Agriculture Faculty of Ege University 59(4): 697-707. https://doi.org/10.20289/zfdergi.1117366
  • Aranda, M.A., M. Escaler, D. Wang, A.J. Maule. 1996. Induction of HSP70 and polyubiquitin expression associated with plant virus replication. Proc Natl Acad Sci. 93:15289–15293.
  • Baniwal, S.K., K. Bharti, K.Y. Chan et al. 2004. Heat stress response in plants: a complex game with chaperones and more than twenty heat stress transcription factors. J Biosci. 29:471–487
  • Bray, E. A. 1988. Drought- and ABA-Induced Changes in Polypeptide and mRNA Accumulation in Tomato Leaves. Plant Physiology. 88(4): 1210- 1214. doi: 10.1104/pp.88.4.1210
  • Bukau, B., A.L. Horwich. 1998. The Hsp70 and Hsp60 chaperone machines. Cell 92(3):351–366.
  • Cho, S.M., R. Beom, K. Yong, Y. Ang, C. oung, K. Heol. 2013. Transcriptomeanalysis of induced systemic Drought Tolerance Elicited by Pseudomonaschlororaphis O6 in Arabidopsis thaliana. Plant Pathol J. 29: 209–220.
  • Dimkpa, C., T. Weinand, F. Asch. 2009. Plant-rhizobacteria interactions alleviateabiotic stress conditions. Plant Cell Environ. 32: 1682–1694.
  • Djordjevic, MA., DW. Gabriel, BG. Rolfe. 1987. Rhizobium the Refined Parasite of Legumes. Annual review of phytopathology, 25(1), 145-168.
  • Ferreira MCB, MS. Fernandes, J. Döbereiner. 1987. Role of Azospirillum Brasilense Nitrate Reductase in Nitrate Assimilation by Wheat Plants. Biology and fertility of soils 4(1): 47-53.
  • Fragkostefanakis, S., S. Roth, E. Schleiff, K.D. Scharf. 2015. Prospects of engineering thermotolerance in crops through modulation of heat stress transcription factor and heat shock protein networks. Plant Cell Environ. 38: 1881–1895.
  • Guerra, D., C. Crosatti, H.H. Khoshro, A. M. Mastrangelo, E. Mica, Mazzucotelli, E. 2015. Post-transcriptional and post-translational regulations of drought and heat response in plants: a spider’s web of mechanisms. Front Plant Sci. 6:57.
  • Gul, A., H. Ozaktan, L. Yolageldi, H. Altunlu, G. Aydoner Coban , G. Eryigit, O. Unay. 2021. In vitro selection of rhizobacteria for increasing drought tolerance of tomato plants. 1320:429-436. https://doi.org/10.17660/ActaHortic. 2021. 1320.57.
  • Jones, H.G. 2006. Monitoring plant and soil water status: established and novel methods revisited and their relevance to studies of drought tolerance. J Exp Bot. 58:119–130.
  • Kaldenhoff, R. and M. Fischer. 2006. Aquaporins in plants. Acta Physiol. 187:169–176.
  • Katiyar-Agarwal, S., M. Agarwal, and A. Grover. 2003. Heat-tolerant basmati rice engineered by over-expression of hsp101 . Plant Mol Biol 51:677–686. https://doi.org/10.1023/A:1022561926 676
  • Kim, Y.C., B. Glick, Y. Bashan, C.M. Ryu. 2013. Enhancement of plant drought tolerance by microbes. In: Aroca, R. (Ed.), Plant Responses to Drought Stress.Springer Verlag, Berlin.
  • Kotak, S., J. Larkindale, U Lee, P. von Koskull-Döring, E. Vierling, K. D. Scharf. 2007. Complexity of the heat stressresponse in plants. Curr Opin Plant Biol. 10:310–316.
  • Kregel, K.C. 2002. Invited review: heat shock proteins: modifying factors in physiological stress responses and acquired thermotolerance. J Appl Physiol. 92:2177–2186.
  • Kumar, R.R., S. Goswami, S.K. Sharma, K. Singh, K. A. Gadpayle, N, Kumar, G. K. Rai, M. Singh, R. D. Rai. 2012 Protection against heat stress in wheat involves change in cell membrane stability, antioxidant enzymes, osmolyte, H2O2 and transcript of heat shock protein. Int J. Plant Physiol Biochem. 4:83–91.
  • Lata, C., and M. Prasad. 2011. Role of DREBs in regulation of abiotic stress responses in plants. J Exp Bot. 62:4731–4748.
  • Latif, F., F. Ullah, S. Mehmood, A. Khattak, A. Khan, S. Khan, I. Husain. 2016. Effects of salicylic acid on growth and accumulation of phenolics in Zea mays L. under drought stress. Acta Agric Scand Sect B Soil Plant Sci. 66:325–332.
  • Leborgne-Castel, N., E.P. Jelitto-Van Dooren, A.J. Crofts, J. Denecke. 1999. Overexpression of BiP in tobacco alleviates endoplasmic reticulum stress. Plant Cell. 11:459–470.
  • Liberek, K., A. Lewandowska, S. Ziętkiewicz. 2008. Chaperones in control of protein disaggregation. EMBO J. 27:328–335.
  • Lim, J.H., S.D. Kim. 2013. Induction of drought stress resistance by multi-functionalPGPR Bacillus licheniformis K11 in Pepper. Plant Pathol. J. 29: 201–208.
  • Mittler, R., A. Finka, P. Goloubinoff. 2012. How do plants feel the heat? Trends Biochem Sci. 37: 118–125.
  • Nouri, M.Z., S. Komatsu. 2013. Subcellular protein overexpression to develop abiotic stress tolerant plants. Front Plant Sci. 4:2.
  • Peremyslov, V.V., Y. Hagiwara, V.V. Dolja. 1999. HSP70 homolog functions in cell-to-cell movement of a plant virus. Proc Natl Acad Sci. 96:14771–14776.
  • Pérez-Clemente, R.M., V. Vives, S.I. Zandalinas et al 2013. Biotechnological approaches to study plant responses to stress. Biomed Res Int. https ://doi.org/10.1155/2013/65412 0
  • Priya, M., O.P. Dhanker, K.H.M. Siddique, B. HanumanthaRao, R.M. Nair, S. Pandey, S. Singh, RK. Varshney, PVV. Prasad, H. Nayyar. 2019. Drought and heat stress-related proteins: an update about their functional relevance in imparting stress tolerance in agricultural crops. Theor Appl Genet. 132(6):1607-1638. doi: 10.1007/s00122-019-03331-2. Epub 2019 Apr 2. PMID: 30941464.
  • Rosenzweig, C., J. Elliott, D. Deryng, A.C. Ruane, C. Müller, A. Arneth, K.J. Boote, C. Folberth, M. Glotter, N. Khabarov, K. Neumann, F. Piontek, T.A. Pugh, E. Schmid, E. Stehfest, H. Yang, J.W. Jones. 2014. Assessing agricultural risks of climate change in the 21st century in a global gridded crop model intercomparison. Proc Natl Acad Sci. 111:3268–3273.
  • Sable, A., and S.K. Agarwal. 2018. Plant heat shock protein families: essential machinery for development and defense. Int J Biol Sci. 4:51–64.
  • Sarkar, N.K., P. Kundnani, A. Grover. 2013. Functional analysis of Hsp70 superfamily proteins of rice (Oryza sativa). Cell Stress Chaperones. 18: 427–437.
  • Sarma, R. K., and R. Saikia. 2014. Alleviation of drought stress in mung bean by strain Pseudomonas aeruginosa GGRJ21, Plant and Soil, 377(1): 111-126. doi: 10.1007/s11104-013-1981-9.
  • Sewelam, N., Y. Oshima, N. Mitsuda, M. OHME-TAKAGI. 2014. A step towards understanding plant responses to multiple environmental stresses: a genome-wide study. Plant Cell Environ. 37:2024–2035.
  • Timmusk, S., A. Islam, D. Abd El, C. Lucian, T. Tanilas, A. Kannaste, L. Behers, E. Nevo, G. Seisenbaeva, E. Stenström, Ü. Niinemets . 2014. Drought-tolerance of wheat improved by rhizosphere bacteria from harshenvironments: Enhanced biomass production and reduced emissions of stressvolatiles. PLoS One 9:1–13.
  • Timmusk, S., and E. Nevo. 2011. Plant root associated biofilms. pp. 285–300. In: Maheshwari, D.K.(Ed.). Bacteria in Agrobiology. Plant Nutrient Management. 3. Springer Verlag, Berlin.
  • Timmusk, S., and E.G. Wagner. 1999. The plant-growth-promoting rhizobacterium Paenibacillus polymyxa induces changes in Arabidopsis thaliana geneexpression: a possible connection between biotic and abiotic stress responses.Mol. Plant Microb. Interact. 12, 951.
  • Tuteja, N., and S.S. Gill. 2016. Abiotic stress response in plants. Environmental Science, Biology, Agricultural and Food Sciences, Wiley, Hoboken. https://api.semanticscholar.org/CorpusID:90643900
  • Udvardi, M.K., K. Kakar, M. Wandrey, O. Montanari, J. Murray, A. Andriankaja, J-Y. Zhang, V. Benedito, J.M.I. Hofer, F. Chueng, D. 2007. Christopher. Legume transcription factors: global regulators of plant development and response to the environment. Plant Physiol. 144:538–549.
  • ul Haq, S., A. Khan, A. M. Khattak, W. X. Gai, H. X. Zhang, Z. H. Gong. 2019. Heat shock proteins: dynamic biomolecules to counter plant biotic and abiotic stresses. International Journal of Molecular Sciences. 20(21): 5321-5352.
  • Vishwakarma, K., N. Upadhyay, N. Kumar, G. Yadav, J. Singh, R.K. Mishra, V. Kumar, R. Verma, R.G. Upadhyay, M. Pandey, S. Sharma. 2017. Abscisic acid signaling and abiotic stress tolerance in plants: a review on current knowledge and future prospects. Front Plant Sci. 8:161.
  • Vurukonda S. S. K. P., S. Vardharajula, M. Shrivastava, A. SkZ. 2016. Enhancement of drought stress tolerance in crops by plant growth promoting rhizobacteria, Microbiological Research 184: 13-24. ISSN 0944-5013, https://doi.org/10.1016/j.micres.2015.12.003.
  • Wahid, A., S. Gelani, M. Ashraf, M.R. Foolad. 2007. Heat tolerance in plants: an overview. Environ Exp Bot 61:199–223
  • Wang, J., N. Sun, T. Deng, L. Zhang, K. Zuo. 2014. Genome-wide cloning, identification, classification and functional analysis of cotton heat shock transcription factors in cotton (Gossypium hirsutum). BMC Genom 15:961
  • Wang, W., B. Vinocur, O. Shoseyov, A. Altman. 2004. Role of plant heatshock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci. 9:244–252.
  • Yang, J., J.W. Kloepper, C.M. Ryu. 2009. Rhizosphere bacteria help plants tolerateabiotic stress. Trends Plant Sci. 14: 1–4.
  • Ye, Y., Y. Ding, Q. Jiang, F. Wang, J. Sun, C. Zhu. 2017. The role of receptor-like protein kinases (RLKs) in abiotic stress response in plants. Plant Cell Rep. 36:235–242.
  • Zandalinas, S.I., R. Mittler, D. Balfagón, V. Arbona, A. Gómez-Cadenas. 2018. Plant adaptations to the combination of drought and high temperatures. Physiol Plant. 162:2–12.
  • Zhang, J., Y. Li, H-X Jia, J.B. Li, J. Huang, M.Z. Lu, J.J. Hu. 2015. The heat shock factor gene family in Salix suchowensis: a genome-wide survey and expression profiling during development and abiotic stresses. Front Plant Sci 6:74.

Bacillus cereus Strain BBS7 Kök Bakterisi İzolatının Kuraklık Stresi Altında Domateste Isı Şok Genlerinin İfadesi Üzerine Etkileri

Yıl 2025, , 85 - 93, 30.06.2025
https://doi.org/10.18615/anadolu.1683423

Öz

Kuraklık stresi, bitkilerin fizyolojik işlevlerinde meydana gelen değişimler nedeniyle tarımsal üretimde önemli ekonomik kayıplara neden olmaktadır. Tarım sektöründe stratejik bir öneme sahip olan domates bitkisi de bu stres koşullarından en fazla etkilenen türler arasında yer almaktadır. Bitki gelişimini artıran kök bakterilerinin hücresel, fizyolojik ve morfolojik mekanizmaları etkileyerek bitkilerin kuraklık toleransını artırdığı belirlenmiştir. Bu çalışmada, domates tohumları Bacillus cereus strain BBS7 kök bakterisi ile sardırıldıktan sonra torf ortamına ekilmiştir. Fideler 2-3 gerçek yapraklı döneme ulaştıktan sonra su kültürüne alınmış ve 7 gün boyunca kontrol uygulamasında tutulduktan sonra PEG 6000 ile kuraklık stresine tabi tutulmuştur. Kuraklık stresinin etkisi (Ψs = -1.0 MPa) kademeli olarak artırılarak (¼, ½, ¾ ve tam doz) uygulanmış, her bir doz artışı 48 saatlik aralıklarla gerçekleştirilmiştir. Stres uygulamasının ardından 2. ve 12. saatlerde alınan bitki örneklerinde, kuraklık stresine yanıt olarak üretilen HSP21, HSP70 ve HSFA gibi ısı şok protein genlerinin ekspresyon seviyeleri qPCR yöntemiyle analiz edilmiştir. Sonuçlar, B. cereus strain BBS7 kök bakterisinin bu genlerin ekspresyon profillerini düzenleyerek domates bitkilerinde kuraklık direncini artıran etkili bir PGPR türü olduğunu göstermiştir.

Etik Beyan

Etik beyan gerekmemektedir

Destekleyen Kurum

Ege Üniversitesi Bilimsel Araştırma Projeleri Koordinasyon Birimi

Proje Numarası

FYL-2021-22622

Teşekkür

Bu çalışma, Macide Elif Güçlüer’in Yüksek Lisans tez çalışması kapsamında gerçekleştirilmiş ve Ege Üniversitesi Bilimsel Araştırma Projeleri Koordinasyon Birimi tarafından desteklenmiştir (Proje Numarası: FYL-2021-22622).

Kaynakça

  • Altunlu, H. 2011. Aşılamanın Domateste Kuraklık Stresi Üzerine Etkileri. Ege Üniversitesi Fen Bilimleri Enstitüsü Bahçe Bitkileri Anabilim Dalı (Basılmamış) Doktora tezi. İzmir- Türkiye. 206 s.
  • Altunlu, H., G. Aydoner Coban, A. Gul, H. Ozaktan. 2024. Effect of Rhizobacteria On Drought Stress Tolerance of Tomato Plants at Vegetative and Fruiting Growth Stages. Journal of Crop Health 76: 195–208. https://doi.org/10.1007/s 10343-023-00941-1.
  • Altunlu, H., G. Aydöner Çoban, ve A. Gül. 2022. Domates genotiplerinin kuraklık stresine tolerans açısından tohum çimlendirme ve vegetatif gelişme aşamalarında hızlı taranmasına uygun testlerin optimizasyonu. Journal of Agriculture Faculty of Ege University 59(4): 697-707. https://doi.org/10.20289/zfdergi.1117366
  • Aranda, M.A., M. Escaler, D. Wang, A.J. Maule. 1996. Induction of HSP70 and polyubiquitin expression associated with plant virus replication. Proc Natl Acad Sci. 93:15289–15293.
  • Baniwal, S.K., K. Bharti, K.Y. Chan et al. 2004. Heat stress response in plants: a complex game with chaperones and more than twenty heat stress transcription factors. J Biosci. 29:471–487
  • Bray, E. A. 1988. Drought- and ABA-Induced Changes in Polypeptide and mRNA Accumulation in Tomato Leaves. Plant Physiology. 88(4): 1210- 1214. doi: 10.1104/pp.88.4.1210
  • Bukau, B., A.L. Horwich. 1998. The Hsp70 and Hsp60 chaperone machines. Cell 92(3):351–366.
  • Cho, S.M., R. Beom, K. Yong, Y. Ang, C. oung, K. Heol. 2013. Transcriptomeanalysis of induced systemic Drought Tolerance Elicited by Pseudomonaschlororaphis O6 in Arabidopsis thaliana. Plant Pathol J. 29: 209–220.
  • Dimkpa, C., T. Weinand, F. Asch. 2009. Plant-rhizobacteria interactions alleviateabiotic stress conditions. Plant Cell Environ. 32: 1682–1694.
  • Djordjevic, MA., DW. Gabriel, BG. Rolfe. 1987. Rhizobium the Refined Parasite of Legumes. Annual review of phytopathology, 25(1), 145-168.
  • Ferreira MCB, MS. Fernandes, J. Döbereiner. 1987. Role of Azospirillum Brasilense Nitrate Reductase in Nitrate Assimilation by Wheat Plants. Biology and fertility of soils 4(1): 47-53.
  • Fragkostefanakis, S., S. Roth, E. Schleiff, K.D. Scharf. 2015. Prospects of engineering thermotolerance in crops through modulation of heat stress transcription factor and heat shock protein networks. Plant Cell Environ. 38: 1881–1895.
  • Guerra, D., C. Crosatti, H.H. Khoshro, A. M. Mastrangelo, E. Mica, Mazzucotelli, E. 2015. Post-transcriptional and post-translational regulations of drought and heat response in plants: a spider’s web of mechanisms. Front Plant Sci. 6:57.
  • Gul, A., H. Ozaktan, L. Yolageldi, H. Altunlu, G. Aydoner Coban , G. Eryigit, O. Unay. 2021. In vitro selection of rhizobacteria for increasing drought tolerance of tomato plants. 1320:429-436. https://doi.org/10.17660/ActaHortic. 2021. 1320.57.
  • Jones, H.G. 2006. Monitoring plant and soil water status: established and novel methods revisited and their relevance to studies of drought tolerance. J Exp Bot. 58:119–130.
  • Kaldenhoff, R. and M. Fischer. 2006. Aquaporins in plants. Acta Physiol. 187:169–176.
  • Katiyar-Agarwal, S., M. Agarwal, and A. Grover. 2003. Heat-tolerant basmati rice engineered by over-expression of hsp101 . Plant Mol Biol 51:677–686. https://doi.org/10.1023/A:1022561926 676
  • Kim, Y.C., B. Glick, Y. Bashan, C.M. Ryu. 2013. Enhancement of plant drought tolerance by microbes. In: Aroca, R. (Ed.), Plant Responses to Drought Stress.Springer Verlag, Berlin.
  • Kotak, S., J. Larkindale, U Lee, P. von Koskull-Döring, E. Vierling, K. D. Scharf. 2007. Complexity of the heat stressresponse in plants. Curr Opin Plant Biol. 10:310–316.
  • Kregel, K.C. 2002. Invited review: heat shock proteins: modifying factors in physiological stress responses and acquired thermotolerance. J Appl Physiol. 92:2177–2186.
  • Kumar, R.R., S. Goswami, S.K. Sharma, K. Singh, K. A. Gadpayle, N, Kumar, G. K. Rai, M. Singh, R. D. Rai. 2012 Protection against heat stress in wheat involves change in cell membrane stability, antioxidant enzymes, osmolyte, H2O2 and transcript of heat shock protein. Int J. Plant Physiol Biochem. 4:83–91.
  • Lata, C., and M. Prasad. 2011. Role of DREBs in regulation of abiotic stress responses in plants. J Exp Bot. 62:4731–4748.
  • Latif, F., F. Ullah, S. Mehmood, A. Khattak, A. Khan, S. Khan, I. Husain. 2016. Effects of salicylic acid on growth and accumulation of phenolics in Zea mays L. under drought stress. Acta Agric Scand Sect B Soil Plant Sci. 66:325–332.
  • Leborgne-Castel, N., E.P. Jelitto-Van Dooren, A.J. Crofts, J. Denecke. 1999. Overexpression of BiP in tobacco alleviates endoplasmic reticulum stress. Plant Cell. 11:459–470.
  • Liberek, K., A. Lewandowska, S. Ziętkiewicz. 2008. Chaperones in control of protein disaggregation. EMBO J. 27:328–335.
  • Lim, J.H., S.D. Kim. 2013. Induction of drought stress resistance by multi-functionalPGPR Bacillus licheniformis K11 in Pepper. Plant Pathol. J. 29: 201–208.
  • Mittler, R., A. Finka, P. Goloubinoff. 2012. How do plants feel the heat? Trends Biochem Sci. 37: 118–125.
  • Nouri, M.Z., S. Komatsu. 2013. Subcellular protein overexpression to develop abiotic stress tolerant plants. Front Plant Sci. 4:2.
  • Peremyslov, V.V., Y. Hagiwara, V.V. Dolja. 1999. HSP70 homolog functions in cell-to-cell movement of a plant virus. Proc Natl Acad Sci. 96:14771–14776.
  • Pérez-Clemente, R.M., V. Vives, S.I. Zandalinas et al 2013. Biotechnological approaches to study plant responses to stress. Biomed Res Int. https ://doi.org/10.1155/2013/65412 0
  • Priya, M., O.P. Dhanker, K.H.M. Siddique, B. HanumanthaRao, R.M. Nair, S. Pandey, S. Singh, RK. Varshney, PVV. Prasad, H. Nayyar. 2019. Drought and heat stress-related proteins: an update about their functional relevance in imparting stress tolerance in agricultural crops. Theor Appl Genet. 132(6):1607-1638. doi: 10.1007/s00122-019-03331-2. Epub 2019 Apr 2. PMID: 30941464.
  • Rosenzweig, C., J. Elliott, D. Deryng, A.C. Ruane, C. Müller, A. Arneth, K.J. Boote, C. Folberth, M. Glotter, N. Khabarov, K. Neumann, F. Piontek, T.A. Pugh, E. Schmid, E. Stehfest, H. Yang, J.W. Jones. 2014. Assessing agricultural risks of climate change in the 21st century in a global gridded crop model intercomparison. Proc Natl Acad Sci. 111:3268–3273.
  • Sable, A., and S.K. Agarwal. 2018. Plant heat shock protein families: essential machinery for development and defense. Int J Biol Sci. 4:51–64.
  • Sarkar, N.K., P. Kundnani, A. Grover. 2013. Functional analysis of Hsp70 superfamily proteins of rice (Oryza sativa). Cell Stress Chaperones. 18: 427–437.
  • Sarma, R. K., and R. Saikia. 2014. Alleviation of drought stress in mung bean by strain Pseudomonas aeruginosa GGRJ21, Plant and Soil, 377(1): 111-126. doi: 10.1007/s11104-013-1981-9.
  • Sewelam, N., Y. Oshima, N. Mitsuda, M. OHME-TAKAGI. 2014. A step towards understanding plant responses to multiple environmental stresses: a genome-wide study. Plant Cell Environ. 37:2024–2035.
  • Timmusk, S., A. Islam, D. Abd El, C. Lucian, T. Tanilas, A. Kannaste, L. Behers, E. Nevo, G. Seisenbaeva, E. Stenström, Ü. Niinemets . 2014. Drought-tolerance of wheat improved by rhizosphere bacteria from harshenvironments: Enhanced biomass production and reduced emissions of stressvolatiles. PLoS One 9:1–13.
  • Timmusk, S., and E. Nevo. 2011. Plant root associated biofilms. pp. 285–300. In: Maheshwari, D.K.(Ed.). Bacteria in Agrobiology. Plant Nutrient Management. 3. Springer Verlag, Berlin.
  • Timmusk, S., and E.G. Wagner. 1999. The plant-growth-promoting rhizobacterium Paenibacillus polymyxa induces changes in Arabidopsis thaliana geneexpression: a possible connection between biotic and abiotic stress responses.Mol. Plant Microb. Interact. 12, 951.
  • Tuteja, N., and S.S. Gill. 2016. Abiotic stress response in plants. Environmental Science, Biology, Agricultural and Food Sciences, Wiley, Hoboken. https://api.semanticscholar.org/CorpusID:90643900
  • Udvardi, M.K., K. Kakar, M. Wandrey, O. Montanari, J. Murray, A. Andriankaja, J-Y. Zhang, V. Benedito, J.M.I. Hofer, F. Chueng, D. 2007. Christopher. Legume transcription factors: global regulators of plant development and response to the environment. Plant Physiol. 144:538–549.
  • ul Haq, S., A. Khan, A. M. Khattak, W. X. Gai, H. X. Zhang, Z. H. Gong. 2019. Heat shock proteins: dynamic biomolecules to counter plant biotic and abiotic stresses. International Journal of Molecular Sciences. 20(21): 5321-5352.
  • Vishwakarma, K., N. Upadhyay, N. Kumar, G. Yadav, J. Singh, R.K. Mishra, V. Kumar, R. Verma, R.G. Upadhyay, M. Pandey, S. Sharma. 2017. Abscisic acid signaling and abiotic stress tolerance in plants: a review on current knowledge and future prospects. Front Plant Sci. 8:161.
  • Vurukonda S. S. K. P., S. Vardharajula, M. Shrivastava, A. SkZ. 2016. Enhancement of drought stress tolerance in crops by plant growth promoting rhizobacteria, Microbiological Research 184: 13-24. ISSN 0944-5013, https://doi.org/10.1016/j.micres.2015.12.003.
  • Wahid, A., S. Gelani, M. Ashraf, M.R. Foolad. 2007. Heat tolerance in plants: an overview. Environ Exp Bot 61:199–223
  • Wang, J., N. Sun, T. Deng, L. Zhang, K. Zuo. 2014. Genome-wide cloning, identification, classification and functional analysis of cotton heat shock transcription factors in cotton (Gossypium hirsutum). BMC Genom 15:961
  • Wang, W., B. Vinocur, O. Shoseyov, A. Altman. 2004. Role of plant heatshock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci. 9:244–252.
  • Yang, J., J.W. Kloepper, C.M. Ryu. 2009. Rhizosphere bacteria help plants tolerateabiotic stress. Trends Plant Sci. 14: 1–4.
  • Ye, Y., Y. Ding, Q. Jiang, F. Wang, J. Sun, C. Zhu. 2017. The role of receptor-like protein kinases (RLKs) in abiotic stress response in plants. Plant Cell Rep. 36:235–242.
  • Zandalinas, S.I., R. Mittler, D. Balfagón, V. Arbona, A. Gómez-Cadenas. 2018. Plant adaptations to the combination of drought and high temperatures. Physiol Plant. 162:2–12.
  • Zhang, J., Y. Li, H-X Jia, J.B. Li, J. Huang, M.Z. Lu, J.J. Hu. 2015. The heat shock factor gene family in Salix suchowensis: a genome-wide survey and expression profiling during development and abiotic stresses. Front Plant Sci 6:74.
Toplam 51 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Bitki Biyoteknolojisi, Sebze Yetiştirme ve Islahı, Biyoteknolojinin Genetik Modifikasyonsuz Kullanımı
Bölüm Makaleler
Yazarlar

Birsen Çakır Aydemir 0000-0003-4268-8547

Macide Elif Güçlüer 0000-0001-7660-5880

Proje Numarası FYL-2021-22622
Yayımlanma Tarihi 30 Haziran 2025
Gönderilme Tarihi 25 Nisan 2025
Kabul Tarihi 2 Haziran 2025
Yayımlandığı Sayı Yıl 2025

Kaynak Göster

APA Çakır Aydemir, B., & Güçlüer, M. E. (2025). Bacillus cereus Strain BBS7 Kök Bakterisi İzolatının Kuraklık Stresi Altında Domateste Isı Şok Genlerinin İfadesi Üzerine Etkileri. ANADOLU Ege Tarımsal Araştırma Enstitüsü Dergisi, 35(1), 85-93. https://doi.org/10.18615/anadolu.1683423
AMA Çakır Aydemir B, Güçlüer ME. Bacillus cereus Strain BBS7 Kök Bakterisi İzolatının Kuraklık Stresi Altında Domateste Isı Şok Genlerinin İfadesi Üzerine Etkileri. ANADOLU. Haziran 2025;35(1):85-93. doi:10.18615/anadolu.1683423
Chicago Çakır Aydemir, Birsen, ve Macide Elif Güçlüer. “Bacillus Cereus Strain BBS7 Kök Bakterisi İzolatının Kuraklık Stresi Altında Domateste Isı Şok Genlerinin İfadesi Üzerine Etkileri”. ANADOLU Ege Tarımsal Araştırma Enstitüsü Dergisi 35, sy. 1 (Haziran 2025): 85-93. https://doi.org/10.18615/anadolu.1683423.
EndNote Çakır Aydemir B, Güçlüer ME (01 Haziran 2025) Bacillus cereus Strain BBS7 Kök Bakterisi İzolatının Kuraklık Stresi Altında Domateste Isı Şok Genlerinin İfadesi Üzerine Etkileri. ANADOLU Ege Tarımsal Araştırma Enstitüsü Dergisi 35 1 85–93.
IEEE B. Çakır Aydemir ve M. E. Güçlüer, “Bacillus cereus Strain BBS7 Kök Bakterisi İzolatının Kuraklık Stresi Altında Domateste Isı Şok Genlerinin İfadesi Üzerine Etkileri”, ANADOLU, c. 35, sy. 1, ss. 85–93, 2025, doi: 10.18615/anadolu.1683423.
ISNAD Çakır Aydemir, Birsen - Güçlüer, Macide Elif. “Bacillus Cereus Strain BBS7 Kök Bakterisi İzolatının Kuraklık Stresi Altında Domateste Isı Şok Genlerinin İfadesi Üzerine Etkileri”. ANADOLU Ege Tarımsal Araştırma Enstitüsü Dergisi 35/1 (Haziran 2025), 85-93. https://doi.org/10.18615/anadolu.1683423.
JAMA Çakır Aydemir B, Güçlüer ME. Bacillus cereus Strain BBS7 Kök Bakterisi İzolatının Kuraklık Stresi Altında Domateste Isı Şok Genlerinin İfadesi Üzerine Etkileri. ANADOLU. 2025;35:85–93.
MLA Çakır Aydemir, Birsen ve Macide Elif Güçlüer. “Bacillus Cereus Strain BBS7 Kök Bakterisi İzolatının Kuraklık Stresi Altında Domateste Isı Şok Genlerinin İfadesi Üzerine Etkileri”. ANADOLU Ege Tarımsal Araştırma Enstitüsü Dergisi, c. 35, sy. 1, 2025, ss. 85-93, doi:10.18615/anadolu.1683423.
Vancouver Çakır Aydemir B, Güçlüer ME. Bacillus cereus Strain BBS7 Kök Bakterisi İzolatının Kuraklık Stresi Altında Domateste Isı Şok Genlerinin İfadesi Üzerine Etkileri. ANADOLU. 2025;35(1):85-93.
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