References
-
Lewinski, N., Colvin, V. & Drezek, R. Cytotoxicity of nanoparticles. Small 4, 26–49. https://doi.org/10.1002/smll.200700595 (2008).
-
Hasan, S. A review on nanoparticles: their synthesis and types. Res. J. Recent. Sci. 2277, 2502 (2015).
-
Altammar, K. A. A review on nanoparticles: characteristics, synthesis, applications, and challenges. Front. Microbiol. 14, 1155622. https://doi.org/10.3389/fmicb.2023.1155622 (2023).
-
Wang, Y. et al. Transcriptome analysis reveals differentially expressed genes (DEGs) related to lettuce (Lactuca sativa) treated by TiO2/ZnO nanoparticles. Plant. Growth Regul. 83, 13–25. https://doi.org/10.1007/s10725-017-0280-5 (2017).
-
Hirpara, D. G. & Gajera, H. P. Green synthesis and antifungal mechanism of silver nanoparticles derived from chitin-induced exometabolites of trichoderma interfusant. Appl. Organomet. Chem. 34, 5407. https://doi.org/10.1002/aoc.5407 (2020).
-
Savani, K. R., Gajera, H. P., Hirpara, D. G., Savaliya, D. D. & Kandoliya, U. K. Salicylic acid-functionalised Chitosan nanoparticles restore impaired sucrose metabolism in the developing anther of cotton (Gossypium hirsutum) under heat stress, Funct. Plant. Biol. 50, 736–751. https://doi.org/10.1071/FP22309 (2023).
-
Hirapara, K. M., Gajera, H. P., Hirpara, D. G. & Savaliya, D. D. Deciphering metabolomic responses and signaling pathways for augmented osmotic stress tolerance under nanosilicon influence in Chickpea (Cicer arietinum L.), S. Afr. J. Bot. 171, 768–779. https://doi.org/10.1016/j.sajb.2024.06.046 (2024).
-
Singh, J. et al. The potential of green synthesized zinc oxide nanoparticles as nutrient source for plant growth. J. Clean. Prod. 214, 1061–1070. https://doi.org/10.1016/j.jclepro.2019.01.018 (2019).
-
Sirelkhatim, A. et al. Review on zinc oxide nanoparticles: antibacterial activity and toxicity mechanism. Nano-Micro Lett. 7, 219–242. https://doi.org/10.1007/s40820-015-0040-x (2015).
-
Prasad, T. N. V. K. V. et al. Effect of nanoscale zinc oxide particles on the germination, growth and yield of peanut. J. Plant. Nutr. 35, 905–927. https://doi.org/10.1080/01904167.2012.663443 (2012).
-
Harish, M. S., Gowda, R. & Nethra, N. Standardization of nanoparticles for enhancing groundnut seed quality Cv. ICGV-91114. J. Pharmacogn Phytochem. 8, 2208–2212 (2019).
-
Ge, S. X., Jung, D. & Yao, R. ShinyGO: a graphical gene-set enrichment tool for animals and plants. Bioinformatics 36, 2628–2629. https://doi.org/10.1093/bioinformatics/btz931 (2020).
-
Sharma, D., Sharma, S., Kaith, B. S., Rajput, J. & Kaur, M. Synthesis of ZnO nanoparticles using surfactant free in-air and microwave method. Appl. Surf. Sci. 257, 9661–9672. https://doi.org/10.1016/j.apsusc.2011.06.094 (2011).
-
Houmiao, W. et al. Functional genomic analysis of Aspergillus flavus interacting with resistant and susceptible peanut. Toxins 8, 46–62. https://doi.org/10.3390/toxins8020046 (2016).
-
Hamid, R. et al. Transcriptome profiling and cataloguing differential gene expression in floral buds of fertile and sterile lines of cotton (Gossypium hirsutum L). Genes 660, 80–91. https://doi.org/10.1016/j.gene.2018.03.070 (2018).
-
Wang, T. et al. Transcriptome identification of the resistance-associated genes (RAGs) to Aspergillus flavus infection in pre-harvested peanut (Arachis hypogaea), Funct. Plant. Biol. 40, 292–303. https://doi.org/10.1071/FP12143 (2013).
-
Dolezal, A. L. et al. Localization, morphology and transcriptional profile of Aspergillus flavus during seed colonization, mol. Plant. Pathol. 14, 898–909. https://doi.org/10.1111/mpp.12056 (2013).
-
Liu, S., Liu, C., Li, Y. & Liu, Y. Determination of Zn responsive genes involved in Zn fertilization in peanuts based on transcriptome analysis. Plant. Growth Regul. 42, 3162–3172. https://doi.org/10.1007/s00344-022-10781-4 (2023).
-
Gulluoglu, L., Bakal, H., Onat, B., Kurt, C. & Arioglu, H. The effect of harvesting date on some agronomic and quality characteristics of peanut grown in the mediterranean region of Turkey. Turk. J. Field Crops. 21, 224–232. https://doi.org/10.17557/tjfc.20186 (2016).
-
Fu, S., Wang, G., Xia, S. & Liu, L. A multi-granularity representation learning framework for user identification across social networks, in: rough sets: IJCRS 2019. Springer Int. Publ Debrecen Hung. 507–521. https://doi.org/10.1007/978-3-030-22815-6_39 (2019).
-
Ashwini, M. N., Gajera, H. P., Hirpara, D. G., Savaliya, D. D. & Kandoliya, U. K. Comparative impact of seed priming with zinc oxide nanoparticles and zinc sulphate on biocompatibility, zinc uptake, germination, seedling vitality, and antioxidant modulation in groundnut. J. Nanopart. Res. 26, 235. https://doi.org/10.1007/s11051-024-06141-w (2024).
-
Navas, D., Ibañez, A., González, I., Palma, J. L. & Dreyse, P. Controlled dispersion of ZnO nanoparticles produced by basic precipitation in solvothermal processes. Heliyon 6, 65–68. https://doi.org/10.1016/j.heliyon.2020.e05821 (2020).
-
Sarma, H. & Sarma, K. C. X-ray peak broadening analysis of ZnO nanoparticles derived by precipitation method. Int. J. Sci. Res. 4, 1–7 (2014).
-
Golthi, V., Kommu, J. & Ramesh, A. V. A green and sustainable approach to the fabrication of ZnO nanoparticles via Jatropha Podagrica leaf extract for effective dye degradation and antibacterial applications. Colloid Polym. Sci. 302, 183–197. https://doi.org/10.1007/s00396-023-05187-x (2024).
-
Jeevarathinam, M. & Asharani, I. V. Synthesis of CuO, ZnO nanoparticles, and CuO-ZnO nanocomposite for enhanced photocatalytic degradation of Rhodamine B: a comparative study. Sci. Rep. 14, 9718. https://doi.org/10.1038/s41598-024-60008-7 (2024).
-
Da-Costa, M. V. J., Kevat, N. & Sharma, P. K. Copper oxide nanoparticle and copper (II) ion exposure in Oryza sativa reveals two different mechanisms of toxicity. Water Air Soil. Pollut. 231, 1–16. https://doi.org/10.1007/s11270-020-04592-0 (2020).
-
Jiang, C. et al. Comparative transcriptome analysis of genes involved in the drought stress response of two peanut (Arachis Hypogaea L.) varieties. BMC Plant. Biol. 21, 1–14. https://doi.org/10.1186/s12870-020-02761-1 (2021).
-
Soneson, C. et al. A comprehensive examination of nanopore native RNA sequencing for characterization of complex transcriptomes. Nat. Commun. 10, 3359. https://doi.org/10.1038/s41467-019-11272-z (2019).
-
Xie, S. et al. Applications and potentials of nanopore sequencing in the (epi)genome and (epi)transcriptome era. Innov. (Camb). 2, 25–28. https://doi.org/10.1016/j.xinn.2021.100153 (2021).
-
Liu, Z. M., Faizan, M., Chen, C., Zheng, L. H. & Yu, F. Y. The combined analysis of transcriptome and antioxidant enzymes revealed the mechanism of EBL and ZnO NPs enhancing Styrax tonkinensis seed abiotic stress resistance. Genes 13, 2170. https://doi.org/10.3390/genes13112170 (2022).
-
Xue, H. et al. A near complete genome of Arachis monticola, an allotetraploid wild peanut. Plant. Biotechnol. J. 5, 1–3. https://doi.org/10.1111/pbi.14331 (2024).
-
Anjum, A. et al. Identification of differentially expressed genes in RNA-seq data of Arabidopsis thaliana: a compound distribution approach. J. Comput. Biol. 23, 239–247. https://doi.org/10.1089/cmb.2015.0205 (2016).
-
Wang, Z. et al. Zinc oxide nanoparticles alleviated vanadium-induced Inhibition by regulating plant hormone signal transduction and phenylpropanoid biosynthesis in maize seedlings (Zea Mays L). Environ. Technol. Innov. 103696. https://doi.org/10.2139/ssrn.4760246 (2024).
-
Starnes, D. et al. Toxicogenomic responses of Caenorhabditis elegans to pristine and transformed zinc oxide nanoparticles. Environ. Pollut. 247, 917–926. https://doi.org/10.1016/j.envpol.2019.01.077 (2019).
-
Zeeshan, M. et al. Insights into the ameliorative effect of ZnONPs on arsenic toxicity in soybean mediated by hormonal regulation, transporter modulation, and stress responsive genes, front. Plant. Sci. 15, 1427367. https://doi.org/10.3389/fpls.2024.1427367 (2024).
-
Zarasvand, A. A. Comparative analysis of zinc oxide nanoparticles induced transcriptomic responses in Arabidopsis, M.Sc. thesis, North Dakota State Univ., United States, (2020).
-
Zou, Z. et al. Isoprene acts as a signaling molecule in gene networks important for stress responses and plant growth. Plant. Physiol. 180, 124–152. https://doi.org/10.1104/pp.18.01391 (2019).
-
Fini, A. et al. Isoprene responses and functions in plants challenged by environmental pressures associated to climate change, front. Plant. Sci. 8, 1281. https://doi.org/10.3389/fpls.2017.01281 (2017).
-
Vranova, E., Coman, D. & Gruissem, W. Network analysis of the MVA and MEP pathways for isoprenoid synthesis. Annu. Rev. Plant. Biol. 64, 665–700. https://doi.org/10.1146/annurev-arplant-050312-120116 (2013).
-
Carrigan, C. N. & Poulter, C. D. Zinc is an essential cofactor for type I isopentenyl diphosphate: dimethylallyl diphosphate isomerase. J. Am. Chem. Soc. 125, 9008–9009. https://doi.org/10.1021/ja0350381 (2003).
-
Movahedi, A. et al. Isoprenoid biosynthesis regulation in poplars by Methylerythritol phosphate and mevalonic acid pathways, front. Plant. Sci. 13, 968780. https://doi.org/10.3389/fpls.2022.968780 (2022).
-
Bhardwaj, P., Goswami, N., Narula, P., Jain, C. K. & Mathur, A. Zinc oxide nanoparticles (ZnO NP) mediated regulation of bacosides biosynthesis and transcriptional correlation of HMG-CoA reductase gene in suspension culture of Bacopa monnieri, plant physiol. Biochem 130, 148–156. https://doi.org/10.1016/j.plaphy.2018.07.001 (2018).
-
Cakmak, I. Possible roles of zinc in protecting plant cells from damage by reactive oxygen species. New. Phytol. 146, 185–205. https://doi.org/10.1046/j.14698137.2000.00630.x (2000).
-
Tejaswini, K. S. et al. Studies on efficacy of nanoparticles in improving seed physiological parameters in groundnut (Arachis Hypogaea L). Int. J. Chem. Stud. 7, 1786–1791 (2019).
-
Prasad, T. N. V. K. V. et al. Combined effect of nanoscale nutrients (Zinc, Calcium, and Silica) on growth and yield of groundnut (Arachis Hypogaea L.), Lett. Appl. Nano Bio Sci. 12, 1–12 (2023).
-
Lv, W. et al. The behavior, transport, and positive regulation mechanism of ZnO nanoparticles in a plant-soil-microbe environment. Environ. Pollut. 315, 120368 (2022).
