Biosynthesis uses, and defensive mechanisms of kauralexins and zealexins against fungi that attack maize (Zea mays) crops- An Review
Biosynthesis uses, and defensive mechanisms of kauralexins and zealexins against fungi that attack maize (Zea mays) crops
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https://doi.org/10.15625/2525-2518/18104Keywords:
Phytoalexin, fungal disease, kauralexin biosynthesis, secondary metabolites, metabolomics, plant-fungus interactionAbstract
Fungal pathogens have a high effect on maize crops, where it leads to heavy loss of yield production globally. Secondary metabolites are biochemical compounds that play a crucial role in the stress and defense mechanism of plants. It controls several biotic and abiotic stresses and their related side effects. The fungi cause high-impact diseases to bio-organisms such as plants, animals, and humans. Evidently, throughout the world, a notable feed and used industrial product source is "Corn". Earlier studies have shown diverse approaches in plant defense mechanisms for plant growth and development. Here, we can see short-overview about the phytoalexin derivatives namely labdane-type diterpenoids kauralexins and acidic sesquiterpenoids zealexins biosynthesis, mode of action against fungal pathogens in maize crops. Additionally, past and current trend approach on plant-pathogen interactions used bioinformatics and metabolomic tools approach for disease resistance, database tools of plant metabolomics, and especially focused on resources database tools of plant-fungus interactions. Furthermore, this review is to pointout the “Phytoalexins” derivative bioactive diterpenoid compounds of kauralexins & zealexins antifungal defense mechanisms in maize (Z.mays) crops.
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1. Godfray H. C., Mason-D'Croz D., and Robinson S. - Food system consequences of a fungal disease epidemic in a major crop, Philos Trans R Soc. Lond B Biol. Sci. 371 (1709). https://doi.org/10.1098/rstb.2015.0467
2. Tyanova S., Temu T., and Cox J. - The MaxQuant computational platform for mass spectrometry-based shotgun proteomics, Nat. Protoc. 11 (12) (2016) 2301-2319. https://doi.org/10.1038/nprot.2016.136
3. Ranum P., Pena-Rosas J. P., and Garcia-Casal M. N. - Global maize production, utilization, and consumption, Ann. N. Y. Acad. Sci. 1312 (2014) 105-112. https://doi.org/ 10.1111/nyas.12396
4. FAO - Crop Prospects and Food Situation - Quarterly Global Report No. 1, March 2020. Rome. https://doi.org/10.4060/ca8032en
5. George N. Agrios - PlantPathology, Fifth Edition, Elsevier Academic Press, London, U.K., 2005.
6. Pusztahelyi T., Holb I. J., and Pocsi I. - Secondary metabolites in fungus-plant interactions, Front Plant Sci. 6 (2015) 573. https://doi.org/10.3389/fpls.2015.00573
7. Hiruma K. - Roles of Plant-Derived Secondary Metabolites during Interactions with Pathogenic and Beneficial Microbes under Conditions of Environmental Stress, Microorganisms 7 (9) (2019). https://doi.org/10.3390/microorganisms7090362
8. Pusztahelyi T., Holb I. J., and Pócsi I. - Plant-Fungal Interactions: Special Secondary Metabolites of the Biotrophic, Necrotrophic, and Other Specific Interactions, In: Fungal Metabolites (2016) 1-58. https://doi.org/10.1007/978-3-319-19456-1_39-1
9. Murphy K. M. and Zerbe P. - Specialized diterpenoid metabolism in monocot crops: Biosynthesis and chemical diversity, Phytochemistry 172 (2020) 112289. https://doi.org/ 10.1016/j.phytochem.2020.112289
10. Anna K., Jager S. H. F. - Correlation between Plant Secondary Metabolites and Their Antifungal Mechanisms A Review, Medicinal & Aromatic Plants 03 (02) (2014). https://doi.org/10.4172/2167-0412.1000154
11. Ahuja I., Kissen R., and Bones A. M. - Phytoalexins in defense against pathogens, Trends Plant Sci. 17 (2) (2012) 73-90. https://doi.org/10.1016/j.tplants.2011.11.002
12. Pusztahelyi T., Holb I. J., Pócsi I. - Plant-Fungal Interactions: Special Secondary Metabolites of the Biotrophic, Necrotrophic, and Other Specific Interactions, In: Mérillon JM., Ramawat K. (Eds.), Fungal Metabolites, Reference Series in Phytochemistry, Springer, Cham., 2017. https://doi.org/10.1007/978-3-319-25001-4_39
13. Castro-Moretti F. R., Gentzel I. N., Mackey D., and Alonso A. P. - Metabolomics as an Emerging Tool for the Study of Plant-Pathogen Interactions, Metabolites 10 (2) (2020). https://doi.org/10.3390/metabo10020052
14. Manoj et.al. - Chapter 8-Omics Technology: Role and Futurein Providing Biotic and Abiotic StressTolerance to PlantsA. Sharma (Ed.), Microbes and Signaling Biomolecules Against Plant Stress, Rhizosphere Biology, 2021, https://doi.org/10.1007/978-981-15-7094-0_8
15. Erb M. and Kliebenstein D. J. - Plant Secondary Metabolites as Defenses, Regulators, and Primary Metabolites: The Blurred Functional Trichotomy, Plant Physiol 184 (1) (2020) 39-52. https://doi.org/10.1104/pp.20.00433
16. Jain A., Sarsaiya S., Wu Q., Lu Y., and Shi J. - A review of plant leaf fungal diseases and its environment speciation, Bioengineered 10 (1) (2019) 409-424. https://doi.org/ 10.1080/21655979.2019.1649520
17. Redkar A., Matei A., and Doehlemann G. - Insights into Host Cell Modulation and Induction of New Cells by the Corn Smut Ustilago maydis, Front Plant Sci. 8 (2017) 899. https://doi.org/10.3389/fpls.2017.00899
18. Strange R. N. and Scott P. R. - Plant disease: a threat to global food security, Annu Rev. Phytopathol 43 (2005) 83116. https://doi.org/10.1146/annurev.phyto.43.113004.1338396
19. Singh R. and Chandrawat K. S. - Role of Phytoalexins in Plant Disease Resistance, International Journal of Current Microbiology and Applied Sciences 6 (1) (2017) 125-129. https://doi.org/10.20546/ijcmas.2017.601.016
20. Lee J., Hilgers F., Loeschke A., Jaeger K. E., and Feldbrugge M. - Ustilago maydis Serves as a Novel Production Host for the Synthesis of Plant and Fungal Sesquiterpenoids, Front Microbiol 11 (2020) 1655. https://doi.org/10.3389/fmicb.2020.01655
21. Mazid M., KhanT.A. and Mohammad F. (2011): Role of secondary metabolites in defense mechanismsof plants. Biology and Medicine3: 232-249.
22. Andersen E. J., Ali S., Byamukama E., Yen Y., and Nepal M. P. - Disease ResistanceMechanisms in Plants, Genes 9 (7) (2018) 339. https://doi.org/10.3390/ genes9070339
23. Ramírez-Gómez S. X. N., Jiménez-García S., Beltrán Campos V., and Lourdes García Campos Ma. - Plant Metabolites in Plant Defense Against Pathogens, Intech Open (2020). doi: 10.5772/intechopen.87958
24. Soares M. B., Pontes-De-Carvalho L., and Ribeiro-Dos-Santos R. - The pathogenesis of Chagas' disease: when autoimmune and parasite-specific immune responses meet, Anais da Academia Brasileira de Ciencias 73 (4) (2001) 547-559. https://doi.org/10.1590/s0001-37652001000400008
25. Xiao Y., Liu H., Wu L., Warburton M., and Yan J. - Genome-wide Association Studies in Maize: Praise and Stargaze, Molecular plant 10 (3) (2017) 359-374. https://doi.org/ 10.1016/j.molp.2016.12.008
26. Schmelz E. A., Kaplan F., Huffaker A., Dafoe N. J., Vaughan M. M., Ni X., Rocca J. R., Alborn H. T., and Teal P. E. - Identity, regulation, and activity of inducible diterpenoid phytoalexins in maize, Proc. Nat. Acad Sci. USA 108 (13) (2011) 5455-5460. https://doi.org/10.1073/pnas.1014714108
27. Huffaker A., Kaplan F., Vaughan M. M., Dafoe N. J., Ni X., Rocca J. R., Alborn H. T., Teal P. E., and Schmelz E. A. - Novel acidic sesquiterpenoids constitute a dominant class of pathogen-induced phytoalexins in maize, Plant Physiol 156 (4) (2011) 2082-2097. https://doi.org/10.1104/pp.111.179457
28. Matthews D. E., Lazo G. R., Anderson O. D. - Plant and crop databases, Methods Mol. Biol. 513 (2009) 243-262. doi:10.1007/978-1-59745-427-8_13
29. Horai H., Arita M., Kanaya S., Nihei Y., Ikeda T., Suwa K., Ojima Y., Matsuura F., Soga T., Taguchi R., Saito K., and Nishioka T. - MassBank: a public repository for sharing mass spectral data for life sciences, J. Mass. Spectrom 45 (7) (2010) 703-714. https://doi.org/10.1002/jms.1777
30. Rahman, M., Shaheen, T., Rahman, M., Iqbal, M. A., & Zafar, Y. (2016). Bioinformatics: A Way Forward to Explore “Plant Omics”. InTech. doi: 10.5772/64043
31. Razzaq, A., Sadia, B., Raza, A., Khalid Hameed, M., & Saleem, F. (2019, Dec 14). Metabolomics: A Way Forward for Crop Improvement. Metabolites, 9(12). https://doi.org/10.3390/metabo9120303
32. Kusano M. and Saito K. - Role of Metabolomics in Crop Improvement, Journal of Plant Biochemistry and Biotechnology 21 (S1) (2012) 24-31. https://doi.org/10.1007/s13562-012-0131-4
33. Kumar R., Bohra A., Pandey A. K., Pandey M. K., and Kumar A. - Metabolomics for Plant Improvement: Status and Prospects, Front Plant Sci. 8 (2017) 1302. https://doi.org/10.3389/fpls.2017.01302
34. Dixon R. A., Gang D. R., Charlton A. J., Fiehn O., Kuiper H. A., Reynolds T. L., and Seiber J. N. - Applications of metabolomics in agriculture, Journal of agricultural and food chemistry 54 (24) (2006) 8984-8994.
35. Upadhyay J., Joshi R., Singh B., Bohra A., Vijayan R., Bhatt M., ... and Wani S. H. - Application of bioinformatics in understanding of plant stress tolerance, Plant Bioinformatics: Decoding the Phyta (2017) 347-374.
36. Wishart D. S. - Current progress in computational metabolomics, Brief Bioinform 8 (5) (2007) 279-293. https://doi.org/10.1093/bib/bbm030
37. Srivastava M., Malviya N., and Dandekar T. - Application of Biotechnology and Bioinformatics Tools in Plant–Fungus Interactions, In: Plant Biology and Biotechnology, 2015, pp. 49-64. https://doi.org/10.1007/978-81-322-2283-5_3
38. Orchard S., Ammari M., Aranda B., Breuza L., Briganti L., Iannuccelli M., Jagannathan S., Jimenez Cesareni G., and Hermjakob H. - The MIntAct project--IntAct as a common curation platform for 11 molecular interaction databases, Nucleic Acids Res. 42 (Database issue) (2014) D358-363. https://doi.org/10.1093/nar/gkt1115
39. Licata L., Briganti L., Peluso D., Perfetto L., Iannuccelli M., Galeota E., Sacco F., Palma A., Nardozza A. P., Santonico E., Castagnoli L., and Cesareni G. - MINT, the molecular interaction database: 2012 update, Nucleic Acids Res. 40 (Database issue) (2012) D857-861. https://doi.org/10.1093/nar/gkr930
40. Jeandet P. - Phytoalexins: Current Progress and Future Prospects, Molecules 20 (2) (2015) 2770-2774. https://doi.org/10.3390/molecules20022770
41. Bizuneh G. K. - The chemical diversity and biological activities of phytoalexins, Adv. Tradit Med. (ADTM) 21 (2021) 31-43. https://doi.org/10.1007/s13596-020-00442-w
42. Onaga G. and Wydra K. - Advances in Plant Tolerance to Biotic Stresses, In: Plant Genomics, 2016. https://doi.org/10.5772/64351
43. Jeandet P., Hébrard C., Deville M. A., Cordelier S., Dorey S., Aziz A., and Crouzet J. - Deciphering the role of phytoalexins in plant-microorganism interactions and human health, Molecules, Basel, Switzerland, 19 (11) (2014) 18033-18056. https://doi.org/ 10.3390/molecules191118033
44. Ejike C. E. C. C., Gong M., and Udenigwe C. C. - Phytoalexins from the Poaceae: Biosynthesis, function and prospects in food preservation, Food Research International 52 (1) (2013) 167-177. https://doi.org/10.1016/j.foodres.2013.03.012
45. Zaynab M., Fatima M., Abbas S., Sharif Y., Umair M., Zafar M. H., and Bahadar K. - Role of secondary metabolites in plant defense against pathogens, Microb Pathog 124 (2018) 198-202. https://doi.org/10.1016/j.micpath.2018.08.034
46. Cruickshank I. A. M. and Perrin D. R. - Isolation of a phytoalexin from Pisum sativum L, Nature 187 (1960) 799-800.
47. Anna K., Jager S. H. F. - Correlation between Plant Secondary Metabolites and Their Antifungal Mechanisms A Review, Medicinal & Aromatic Plants 03 (02) (2014). https://doi.org/10.4172/2167-0412.1000154
48. Arruda R. L., Paz A. T. S., Bara M. T. F., Côrtes M. V. D. C. B., Filippi M. C. C. D., and Conceição E. C. D. - An approach on phytoalexins: function, characterization and biosynthesis in plants of the family Poaceae, Ciência Rural 46 (2016) 1206-1216.
49. Huffaker A., Kaplan F., Vaughan M. M., Dafoe N. J., Ni X., Rocca J. R., Alborn H. T., Teal P. E., and Schmelz E. A. - Novel acidic sesquiterpenoids constitute a dominant class of pathogen-induced phytoalexins in maize, Plant Physiol 156 (4) (2011) 2082-2097. https://doi.org/10.1104/pp.111.179457
50. Lambarey H., Moola N., Veenstra A., Murray S., and Suhail Rafudeen M. - Transcriptomic Analysis of a Susceptible African Maize Line to Fusarium verticillioides Infection, Plants (Basel) 9 (9) (2020). https://doi.org/10.3390/plants9091112
51. Xu M., Wilderman P. R., Morrone D., Xu J., Roy A., Margis-Pinheiro M., Upadhyaya N. M., Coates R. M., and Peters R. J. - Functional characterization of the rice kaurene synthase-like gene family, Phytochemistry 68 (3) (2007) 312-326. https://doi.org/ 10.1016/j.phytochem.2006.10.016
52. Poloni A. and Schirawski J. - Red card for pathogens: phytoalexins in sorghum and maize, Molecules 19 (7) (2014) 9114-9133. https://doi.org/10.3390/molecules19079114
53. Schnee C., Kollner T. G., Held M., Turlings T. C., Gershenzon J., and Degenhardt J. - The products of a single maize sesquiterpene synthase form a volatile defense signal that attracts natural enemies of maize herbivores, Proc. Natl. Acad. Sci. USA 103 (4) (2006) 1129-1134. https://doi.org/10.1073/pnas.0508027103
54. Mao H., Liu J., Ren F., Peters R. J., and Wang Q. - Characterization of CYP71Z18 indicates a role in maize zealexin biosynthesis, Phytochemistry 121 (2016) 4-10. https://doi.org/10.1016/j.phytochem.2015.10.003
55. Peters R. J. - Uncovering the complex metabolic network underlying diterpenoid phytoalexin biosynthesis in rice and other cereal crop plants, Phytochemistry 67 (21) (2006) 2307-2317. https://doi.org/10.1016/j.phytochem.2006.08.009
56. Schmelz E. A., Kaplan F., Huffaker A., Dafoe N. J., Vaughan M. M., Ni X., Rocca J. R., Alborn H. T., and Teal P. E. - Identity, regulation, and activity of inducible diterpenoid phytoalexins in maize, Proceedings of the National Academy of Sciences of the United States of America 108 (13) (2011) 5455-5460. https://doi.org/10.1073/pnas.1014714108
57. Ding Y., Weckwerth P. R., Poretsky E., Murphy K. M., Sims J., Saldivar E., ... and Huffaker A. - Genetic elucidation of interconnected antibiotic pathways mediating maize innate immunity, Nature plants 6 (11) (2020) 1375-1388.
58. Christensen S. A., Huffaker A., Sims J., Hunter C. T., Block A., Vaughan M. M., Willett D., Romero M., Mylroie J. E., Williams W. P., and Schmelz E. A. - Fungal and herbivore elicitation of the novel maize sesquiterpenoid, zealexin A4, is attenuated by elevated CO2, Planta 247 (4) (2018b) 863-873. https://doi.org/10.1007/s00425-017-2830-5
59. Block A. K., Vaughan M. M., Schmelz E. A., and Christensen S. A. - Biosynthesis and function of terpenoid defense compounds in maize (Zea mays), Planta 249 (2019) 21-30.
Meyer J., Berger D. K., Christensen S. A., and Murray S. L. - RNA-Seq analysis of resistant and susceptible sub-tropical maize lines reveals a role for kauralexins in resistance to grey leaf spot disease, caused by Cercospora zeina, BMC Plant Biol. 17 (1) (2017) 197. https://doi.org/10.1186/s12870-017-1137-9
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