آمار
| تعداد نشریات | 28 |
| تعداد شماره‌ها | 391 |
| تعداد مقالات | 3,806 |
| تعداد مشاهده مقاله | 6,234,114 |
| تعداد دریافت فایل اصل مقاله | 4,571,346 |
Investigating Effective Factors in Improving Plant Growth by Native Phosphate-dissolving Bacteria Isolated from Wheat | ||
| Journal of Genetic Resources | ||
| مقالات آماده انتشار، پذیرفته شده، انتشار آنلاین از تاریخ 13 تیر 1402 اصل مقاله (551.97 K) | ||
| نوع مقاله: Research Article | ||
| شناسه دیجیتال (DOI): 10.22080/jgr.2023.25663.1364 | ||
| نویسندگان | ||
| Hossein Mirzaei Najafgholi* 1؛ Ehsan Hasanvand1؛ Samira Pakbaz1؛ Neda Rouhani2 | ||
| 1Department of Plant Protection, Faculty of Agriculture, Lorestan University, Lorestan, Iran | ||
| 2Department of Plant Protection, Faculty of Agriculture, Ferdowsi University of Mashhad, Khorasan Razavi, Iran | ||
| تاریخ دریافت: 02 اردیبهشت 1402، تاریخ بازنگری: 18 مرداد 1402، تاریخ پذیرش: 01 تیر 1402 | ||
| چکیده | ||
| Wheat is one of the most important strategic products in providing food security for the growing world population. The purpose of this research is to isolate and identify plant growth-promoting bacteria from the wheat rhizosphere and their inhibitory effect on the growth of the pathogenic fungus Fusarium sp. isolated from wheat. The initial screening of 100 bacterial strains isolated from wheat roots was done based on their ability to dissolve phosphate. The effective factors in plant growth and inhibition of fungal pathogens, such as the ability to produce IAA, siderophores, protease, biofilm, bacterial swarming motility, tolerance to salt, seed germination, and seed vigor tests, were investigated. In the initial screening, four bacterial isolates with the highest amount of phosphate dissolution were identified based on morphological and biochemical characteristics as well as the sequence of 16S rRNA region belonging to Curtobacterium sp., Arthrobacter sp., Acinetobacter calcoaceticus, and Cellulosimicrobium sp.; Curtobacterium sp. had the highest amount of IAA (6.14μg/ml), siderophore (2.25cm), protease (1.4cm), and the highest tolerance to salinity (20%) and phosphate dissolution (375.3mg/ml). In the swarming motility test, the highest values were related to Arthrobacter sp. and Curtobacterium sp. at 2.7 and 2.2cm, respectively. The highest amount of biofilm formation was associated with Acinetobacter calcoaceticus and Curtobacterium sp. with an average absorption coefficient of 0.153 and 0.139, respectively. The highest and lowest average values of percentage inhibition of pathogenic fungus colony growth were evaluated in Curtobacterium sp. isolate with a value of 57.3%, and Cellulosimicrobium sp. isolate with 33%, respectively. | ||
| کلیدواژه‌ها | ||
| Arthrobacter sp؛ Biofilm Formation؛ Curtobacterium sp؛ PGPR | ||
| مراجع | ||
|
Abdul-Baki, A. A., & Anderson, J. D. (1973). Vigor determination in soybean seed by multiple criteria 1. Crop Science, 13(6), 630-633. http://dx.doi.org/10.2135/cropsci1973. 0011183X001300060013x
Aeini, M., Khodakaramian, G., & Mirzaei Najafgholi, H. (2018). Sugar beet leaf culturable endophytic bacterial composition from the major sugar beet growing areas in the west of Iran. Journal of Genetic Resources, 4(2), 105-113. https://dx.doi.org/10.22080/jgr.2019.15537.1118
Alexander, D. B., & Zuberer, D. A. (1991). Use of chrome azurol S reagents to evaluate siderophore production by rhizosphere bacteria. Biology and Fertility of Soils, 12, 39-45. https://doi.org/10.1007/BF00369386
Alori, E. T., Glick, B. R., & Babalola, O. O. (2017). Microbial phosphorus solubilization and its potential for use in sustainable agriculture. Frontiers in Microbiology, 8, 971. https://doi.org/10.3389/fmicb.2017.00971
Alsharif, W., Saad, M. M., & Hirt, H. (2020). Desert microbes for boosting sustainable agriculture in extreme environments. Frontiers in Microbiology, 11, 496411. https://doi.org/10.3389/fmicb.2020.01666.
Ansari, F. A., & Ahmad, I. (2018). Biofilm development, plant growth promoting traits and rhizosphere colonization by Pseudomonas entomophila FAP1: a promising PGPR. Advances in Microbiology, 8(03), 235-251. https://doi.org/10.4236/aim.2018.83016
Bano, A., & Fatima, M. (2009). Salt tolerance in Zea mays (L). following inoculation with Rhizobium and Pseudomonas. Biology and Fertility of Soils, 45, 405-413. http://dx.doi.org/10.1007/s00374-008-0344-9
Aydi-Ben Abdallah, R., Mejdoub-Trabelsi, B., Jabnoun-Khiareddine, H., & Daami-Remadi, M. (2017). Use of endophytic bacteria naturally associated with Cestrum nocturnum for Fusarium wilt biocontrol and enhancement of tomato growth. Tunisian Journal of Plant Protection, 12, 15-40. https://doi.org/10.4172/1948-5948.1000259
Bhattacharyya, P. N., & Jha, D. K. (2012). Plant growth-promoting rhizobacteria (PGPR): emergence in agriculture. World Journal of Microbiology and Biotechnology, 28, 1327-1350. https://doi.org/10.1007/s11274-011-0979-9
Bric, J. M., Bostock, R. M., & Silverstone, S. E. (1991). Rapid in situ assay for indoleacetic acid production by bacteria immobilized on a nitrocellulose membrane. Applied and Environmental Microbiology, 57(2), 535-538. https://doi.org/10.1128/aem.57.2.535-538.1991
CGIAR report .2018. Research program on wheat. https://hdl.handle.net/10568/103691
Díez-Méndez, A., & Rivas, R. (2017). Improvement of saffron production using Curtobacterium herbarum as a bioinoculant under greenhouse conditions. AIMS Microbiology, 3(3), 354-364. http://dx.doi.org/10.3934/microbiol.2017.3.354
Eisendle, M., Oberegger, H., Buttinger, R., Illmer, P., & Haas, H. (2004). Biosynthesis and uptake of siderophores is controlled by the PacC-mediated ambient-pH regulatory system in Aspergillus nidulans. Eukaryotic Cell, 3(2), 561-563. https://doi.org/10.1128/EC.3.2.561-563.2004
Glick, B. R. (2012). Plant growth-promoting bacteria: mechanisms and applications. Scientifica, 2012: 963401. https://doi.org/10.6064/2012/963401
Glickmann, E., & Dessaux, Y. (1995). A critical examination of the specificity of the Salkowski reagent for indolic compounds produced by phytopathogenic bacteria. Applied and Environmental Microbiology, 61(2), 793-796. https://doi.org/10.1128/aem.61.2.793-796.1995
González-Lamothe, R., El Oirdi, M., Brisson, N., & Bouarab, K. (2012). The conjugated auxin indole-3-acetic acid-aspartic acid promotes plant disease development. Plant Cell, 24(2), 762-777. https://doi.org/10.1105/tpc.111.095190
Goswami, D., Thakker, J. N., & Dhandhukia, P. C. (2016). Portraying mechanics of plant growth promoting rhizobacteria (PGPR): A review. Cogent Food and Agriculture, 2(1), 1127500. https://doi.org/10.1080/23311932.2015.1127500
Idris, R., Trifonova, R., Puschenreiter, M., Wenzel, W. W., & Sessitsch, A. (2004). Bacterial communities associated with flowering plants of the Ni hyperaccumulator Thlaspi goesingense. Applied and Environmental Microbiology, 70(5), 2667-2677. https://doi.org/10.1128/aem.70.5.2667-2677.2004
Kasim, W. A., Gaafar, R. M., Abou-Ali, R. M., Omar, M. N., & Hewait, H. M. (2016). Effect of biofilm forming plant growth promoting rhizobacteria on salinity tolerance in barley. Annals of Agricultural Sciences, 61(2), 217-227. https://doi.org/10.1016/j.aoas.2016.07.003
Khan, M. A., Asaf, S., Khan, A. L., Ullah, I., Ali, S., Kang, S. M., & Lee, I. J. (2019). Alleviation of salt stress response in soybean plants with the endophytic bacterial isolate Curtobacterium sp. SAK1. Annals of Microbiology, 69(8), 797-808. https://doi.org/10.1007/s13213-019-01470-x
Kloepper, J. W., Leong, J., Teintze, M., & Schroth, M. N. (1980). Enhanced plant growth by siderophores produced by plant growth-promoting rhizobacteria. Nature, 286(5776), 885-886. https://doi:10.1038/286885a0
Maguire, J. D. (1962). Speed of germination-aid in selection and evaluation for seedling emergence and vigor. Crop Science, 2, 176-177. https://doi.org/10.2135/cropsci1962. 0011183X000200020033x
Moreira, R. R., Nesi, C. N., & De Mio, L. L. M. (2014). Bacillus spp. and Pseudomonas putida as inhibitors of the Colletotrichum acutatum group and potential to control Glomerella leaf spot. Biological Control, 72, 30-37. http://dx.doi.org/10.1016%2Fj.biocontrol. 2014.02.001
Narimani, S., Bazgir, E., Mirzaei Najafgholi, H. (2017). Evaluation of effective factors on survival and activity of petroleum degradation bacteria in bioremediation process. Cellular and Molecular Researches, 30:91-99. https://dorl.net/dor/20.1001.1.23832738.1396.30.1.8.7
Pal, K. K., & Gardener, B. M. (2006). Biological control of plant pathogens. Plant Health Instructor, https://doi.org/10.1094/PHI-A-2006-1117-02
Patel, M., Patel, K., Al-Keridis, L. A., Alshammari, N., Badraoui, R., Elasbali, A. M., ... & Adnan, M. (2022). Cadmium-tolerant plant growth-promoting bacteria Curtobacterium oceanosedimentum improves growth attributes and strengthens antioxidant system in chili (Capsicum frutescens). Sustainability, 14(7), 4335. https://doi.org/10.3390/su14074335
Pratika, M., Ananda, M., & Suwastika, I. N. (2021). Protease activity from bacterial isolates of Nepenthes maxima reinw. ex nees. Journal of Physics: Conference Series, 1763 (1), 012092. http://dx.doi.org/10.1088/1742-6596/1763/1/012092
Presta, L., Fondi, M., Perrin, E., Maida, I., Miceli, E., Chiellini, C., ... & Fani, R. (2016). Arthrobacter sp. EpRS66 and Arthrobacter sp. EpRS71: draft genome sequences from two bacteria isolated from Echinacea purpurea Rhizospheric Soil. Frontiers in Microbiology, 7, 1417. https://doi.org/10.3389/fmicb.2016.01417
Rosenblueth, M., & Martínez-Romero, E. (2006). Bacterial endophytes and their interactions with hosts. Molecular Plant-Microbe Interactions, 19(8), 827-837. https://doi.org/10.1094/MPMI-19-0827
Schaad, N. W., Jones, J. B., & Chun, W. (2001). Laboratory guide for the identification of plant pathogenic bacteria. American Phytopathological Society, 50, 812-814. https://doi.org/10.1046/j.1365-3059.2001.00635.x
Siah, A., Deweer, C., Morand, E., Reignault, P., & Halama, P. (2010). Azoxystrobin resistance of French Mycosphaerella graminicola strains assessed by four in vitro bioassays and by screening of G143A substitution. Crop Protection, 29(7), 737-743. https://doi.org/10.1016/j.cropro.2010.02.012
Sperber, J. I. (1958). The incidence of apatite-solubilizing organisms in the rhizosphere and soil. Australian Journal of Agricultural Research, 9(6), 778-781. https://doi.org/10.1071/AR9580778
Vanissa, T. T. G., Berger, B., Patz, S., Becker, M., Turečková, V., Novák, O., ... & Ruppel, S. (2020). The response of maize to inoculation with Arthrobacter sp. and Bacillus sp. in phosphorus-deficient, salinity-affected soil. Microorganisms, 8(7), 1005. https://doi.org/10.3390/microorganisms8071005
Van Hamme, J. D., Singh, A., & Ward, O. P. (2003). Recent advances in petroleum microbiology. Microbiology and Molecular Biology Reviews, 67(4), 503-549. https://doi.org/10.1128/MMBR.67.4.503-549. 2003
Weisburg, W. G., Barns, S. M., Pelletier, D. A., & Lane, D. J. (1991). 16S ribosomal DNA amplification for phylogenetic study. Journal of Bacteriology, 173(2), 697-703. https://doi.org/10.1128/jb.173.2.697-703.1991
Yasmin, S., Hafeez, F. Y., Mirza, M. S., Rasul, M., Arshad, H. M., Zubair, M., & Iqbal, M. (2017). Biocontrol of bacterial leaf blight of rice and profiling of secondary metabolites produced by rhizospheric Pseudomonas aeruginosa BRp3. Frontiers in Microbiology, 8, 1895. https://doi.org/10.3389/fmicb.2017.01895 | ||
|
آمار تعداد مشاهده مقاله: 10 تعداد دریافت فایل اصل مقاله: 50 |
||