PLANT BIOLOGY
ANIMAL BIOLOGY
SUBSCRIPTION
E-SUBSCRIPTION
 
MAP
MAIN PAGE

 

 

 

 

Prasad S.S., Singh A., Murali N.V., Chimmalagi U., Jeevitha D., Das U., Adishesha K., Sutradhar M. Enzyme dynamics in aerobic plants under flood stress (review). Sel'skokhozyaistvennaya Biologiya [Agricultural Biology], 2025, Vol. 60, № 5, p. 792-809.
(how to cite this article)

doi: 10.15389/agrobiology.2025.5.792eng

UDC: 631:58.02

 

ENZYME DYNAMICS IN AEROBIC PLANTS UNDER FLOOD STRESS (review)

S.S. Prasad1 ✉, A. Singh1, N.V. Murali2, U. Chimmalagi3,
D. Jeevitha3, U. Das4, K. Adishesha5, M. Sutradhar

1Department of Agriculture, Koneru Lakshmaiah Education Foundation, Vaddeswaram, AP, India, e-mail 5257shiv@gmail.com (✉ corresponding author), singhatul9415@gmail.com, Monoj.gene.enggnr@gmail.com;
2Department of Food science and technology, School of agriculture sciences, Mallareddy University, Maisamagudda, Hyderabad, Telangana 500043, e-mail drmurali.nv@mallareddyuniversity.ac.in;
3Department of Agriculture, Karunya Institute of Technology and Sciences, Coimbatore-641 114, Tamil Nadu, India, e-mail hortiumeshbc850@gmail.com, jeevitha@karunya.edu;
4VIT School of Agricultural Innovations& Advanced Learning (VAIAL), Vellore Institute of Technology, Vellore-632014, Tamil Nadu, India, e-mail utpaldashorts14@gmail.com;
5Department of Plant Physiology, School of Agriculture, Mohan Babu University, Sree Sainath Nagar, Tirupati, Andhra Pradesh-517102, e-mail adishesha1144@gmail.com

ORCID:
Prasad S.S. orcid.org/0000-0002-5537-0565
Jeevitha D. orcid.org/0000-0003-4357-0815
Singh A. orcid.org/0000-0002-1032-4442
Das U. orcid.org/0000-0003-2239-7400
Murali N.V. orcid.org/0000-0001-7133-2465
Adishesha K. orcid.org/0009-0007-1063-0400
Chimmalagi U. orcid.org/0000-0002-3316-1770
Sutradhar M. orcid.org/0000-0002-0408-2096

Final revision received March 15, 2025
Accepted April 25, 2025

Flood stress is a prevalent abiotic stress condition that affects plant growth, development, and overall productivity. Under such conditions, plants activate various defence mechanisms, including enzyme-mediated responses, to cope with the adverse effects of excess water and oxygen deprivation. It triggers the inhibition of mitochondrial respiration and prompts plants to switch from aerobic to anaerobic metabolism. These enzymatic adaptations enable plants to survive and thrive in waterlogged conditions by promoting anaerobic respiration. Understanding the intricate mechanisms of enzyme responses to flood stress can aid in developing flood-tolerant crop varieties and implementing effective management strategies to mitigate the adverse effects of flooding on plant productivity and agriculture.

Keywords: anti-oxidants, SOD, ROS, scavenger, osmolyte, flood, enzyme.

 

REFERENCES

  1. Khan M.I.R., Trivellini A., Chhillar H., Chopra P., Ferrante A., Khan N.A., Ismail A.M. The significance and functions of ethylene in flooding stress tolerance in plants. Environmental and Experimental Botany, 2020, 179: 104188 CrossRef
  2. Busari T.I., Senzanje A., Odindo A.O., Buckley C.A. Evaluating the effect of irrigation water management techniques on (taro) madumbe (Colocasia esculenta (L.) Schott) grown with anaerobic filter (AF) effluent at Newlands, South Africa. Journal of Water Reuse and Desalination, 2019, 9(2): 203-212 CrossRef
  3. Zhou W., Chen F., Meng Y., Chandrasekaran U., Luo X., Yang W., Shu K. Plant waterlogging/flooding stress responses: From seed germination to maturation. Plant Physiology and Biochemistry, 2020, 148: 228-236 CrossRef
  4. Kim Y., Shahzad R., Lee I.J. Regulation of flood stress in plants. In: Plant life under changing environment: responses and management. Tripathi D.K., Singh V.P., Chauhan D.K., Sharma S., Prasad S.M., Dubey N.K., Ramawat N. (eds.). Academic Press, 2020: 157-173 CrossRef
  5. Krishna R.N., Ronan K., Spencer C., Alisic E. The lived experience of disadvantaged communities affected by the 2015 South Indian floods: Implications for disaster risk reduction dialogue. International Journal of Disaster Risk Reduction, 2021, 54: 102046 CrossRef
  6. Lehman J., Kinchy A. Bringing climate politics home: lived experiences of flooding and housing insecurity in a natural gas boomtown. Geoforum, 2021, 121: 152-161 CrossRef
  7. Kim N. How much more exposed are the poor to natural disasters? Global and regional measurement. Disasters, 2012, 36(2): 195-211 CrossRef
  8. Sundaram S., Devaraj S., Yarrakula K. Modeling, mapping and analysis of urban floods in India — a review on geospatial methodologies. Environmental Science and Pollution Research, 28: 67940-67956 CrossRef
  9. Davydov R., Antonov V., Molodtsov D., Cheremisin A., Korablev V. The simulation model for a flood management by flood control facilities. MATEC Web of Conferences, 2018, 245: 15002 CrossRef
  10. Wang X., Komatsu S. Review: Proteomic techniques for the development of flood-tolerant soybean. International Journal of Molecular Sciences,2020, 21(20): 7497 CrossRef
  11. Khan M., Jannat A., Munir F., Fatima N., Amir R. Biochemical and molecular mechanisms of abiotic stress tolerance. In: Plant ecophysiology and adaptation under climate change: mechanisms and perspectives II. M. Hasanuzzaman (ed.).Springer, Singapore 2020: 187-230 CrossRef
  12. Oladosu Y., Rafii M.Y., Arolu F., Chukwu S.C., Muhammad I., Kareem I., Salisu M.A., Arolu I.W. Submergence tolerance in rice: review of mechanism, breeding and, future prospects. Sustainability,2020, 12(4): 1632 CrossRef
  13. Bailey-Serres J., Lee S.C., Brinton E. Waterproofing crops: effective flooding survival strategies. Plant Physiology, 2012, 160(4): 1698-1709 CrossRef
  14. Sadhukhan A., Prasad S.S., Mitra J., Siddiqui N., Sahoo L., Kobayashi Y., Koyama H. How do plants remember drought? Planta, 2022, 256(1): 7 CrossRef
  15. Blom C.W.P.M., Voesenek L.A.C.J. Flooding: the survival strategies of plants. Trends in Ecology & Evolution, 1996, 11(7): 290-295 CrossRef
  16. Agarwal S., Grover A. Molecular biology, biotechnology and genomics of flooding-associated low O2 stress response in plants. Critical Reviews in Plant Sciences, 2006, 25(1): 1-21 CrossRef
  17. Komatsu S., Hiraga S., Yanagawa Y. Proteomics techniques for the development of flood tolerant crops. Journal of Proteome Research, 2012, 11(1): 68-78 CrossRef
  18. Dat J.F., Capelli N., Folzer H., Bourgeade P., Badot P.-M. Sensing and signalling during plant flooding. Plant Physiology and Biochemistry, 2004, 42(4): 273-282 CrossRef
  19. Manghwar H., Hussain A., Alam I., Khoso M.A., Ali Q., Liu F. Waterlogging stress in plants: Unraveling the mechanisms and impacts on growth, development, and productivity. Environmental and Experimental Botany, 2024, 224: 105824 CrossRef
  20. Grichko V.P., Glick B.R. Flooding tolerance of transgenic tomato plants expressing the bacterial enzyme ACC deaminase controlled by the 35S, rolD or PRB-1b promoter. Plant Physiology and Biochemistry, 2001, 39(1): 19-25 CrossRef
  21. Zhao Y., Zhang W., Abou-Elwafa S.F., Shabala S., Xu L. Understanding a mechanistic basis of ABA involvement in plant adaptation to soil flooding: the current standing. Plants, 2021, 10(10): 1982 CrossRef
  22. Aigner H., Wilson R.H., Bracher A., Calisse L., Bhat J.Y., Hartl F.U., Hayer-Hartl M. Plant RuBisCo assembly in E. coli with five chloroplast chaperones including BSD2. Science, 2017, 358(6368): 1272-1278 CrossRef
  23. Arbona V., Hossain Z., López-Climent M.F., Pérez-Clemente R.M., Gómez-Cadenas A. Antioxidant enzymatic activity is linked to waterlogging stress tolerance in citrus. Physiologia Plantarum, 2008, 132(4): 452-466 CrossRef
  24. Salla S., Sunkara R., Ogutu S., Walker L.T., Verghese M. Antioxidant activity of papaya seed extracts against H2O2 induced oxidative stress in HepG2 cells. LWT — Food Science and Technology, 2016, 66: 293-297 CrossRef
  25. Thabet S.G., Alomari D.Z., Alqudah A.M. Exploring natural diversity reveals alleles to enhance antioxidant system in barley under salt stress. Plant Physiology and Biochemistry, 2021, 166: 789-798 CrossRef
  26. Yordanova R., Christov K.N., Popova L.P. Antioxidative enzymes in barley plants subjected to soil flooding. Environmental and Experimental Botany, 2004, 51(2): 93-101 CrossRef
  27. Singh A., Prasad S.S., Das U., Ingle K.P., Patil K., Shukla P.K., et al. Regulation of nucleotide metabolism in response to salt stress. In: Genetics of salt tolerance in plants. CABI, GB, 2024: 9-23.
  28. Hurng W.P., Kao C.H. Lipid peroxidation and antioxidative enzymes in senescing tobacco leaves during post-flooding. Plant Science, 1994, 96(1-2): 41-44 CrossRef
  29. Verma K.K., Singh M., Gupta R.K., Verma C.L. Photosynthetic gas exchange, chlorophyll fluorescence, antioxidant enzymes, and growth responses of Jatropha curcas during soil flooding. Turkish Journal of Botany, 2014, 38(1): 130-140 CrossRef
  30. Koppitz H. Effects of flooding on the amino acid and carbohydrate patterns of Phragmites australis. Limnologica, 2004, 34(1-2): 37-47 CrossRef
  31. Ruprecht C., Blaukopf M., Pfrengle F. Synthetic fragments of plant polysaccharides as tools for cell wall biology. Current Opinion in Chemical Biology, 2022, 71: 102208 CrossRef
  32. Pociecha E., Rapacz M., Dziurka M., Kolasińska I. Mechanisms involved in the regulation of photosynthetic efficiency and carbohydrate partitioning in response to low- and high-temperature flooding triggered in winter rye (Secale cereale) lines with distinct pink snow mold resistances. Plant Physiology and Biochemistry, 2016, 104: 45-53 CrossRef
  33. Pomraning K.R., Dai Z., Munoz N., Kim Y.-M., Gao Y., Deng S., Kim J, Hofstad B.A., Swita M.S., Lemmon T., Collett J.R., Panisko E.A., Webb-Robertson B.-J.M., Zucker J.D., Nicora C.D., De Paoli H., Baker S.E., Burnum-Johnson K.E., Hillson N.J., Magnuson J.K. Integration of proteomics and metabolomics into the design, build, test, learn cycle to improve 3-hydroxypropionic acid production in Aspergillus pseudoterreus. Frontiers in Bioengineering and Biotechnology, 2021, 9: 603832 CrossRef
  34. Thapa B., Shrestha A. Protein metabolism in plants to survive against abiotic stress. In: Plant defense mechanisms. J.N. Kimatu (ed.). IntechOpen, 2022 CrossRef
  35. Ferguson D.L., Guikema J.A., Paulsen G.M. Ubiquitin pool modulation and protein degradation in wheat roots during high temperature stress. Plant Physiology, 1990, 92(3): 740-746 CrossRef
  36. Cui F., Liu L., Zhao Q., Zhang Z., Li Q., Lin B., Wu Y., Tang S., Xie Q. Arabidopsis ubiquitin conjugase UBC32 is an ERAD component that functions in brassinosteroid-mediated salt stress tolerance. The Plant Cell, 2012, 24(1): 233-244 CrossRef
  37. Hamilton E.S., Schlegel A.M., Haswell E.S. United in diversity: mechanosensitive ion channels in plants. Annual Review of Plant Biology, 2015, 66(1): 113-137 CrossRef
  38. Dobson C.M., Šali A., Karplus M. Protein folding: a perspective from theory and experiment. Angewandte Chemie International Edition, 1998, 37(7): 868-893 CrossRef
  39. Chen Y., Chen X., Wang H., Bao Y., Zhang W. Examination of the leaf proteome during flooding stress and the induction of programmed cell death in maize. Proteome Science, 2014, 12(1): 33 CrossRef
  40. Voesenek L., Bailey-Serres J. Flooding tolerance: O2 sensing and survival strategies. Current Opinion in Plant Biology, 2013, 16(5): 647-653 CrossRef
  41. Kamal A.H.M., Komatsu S. Involvement of reactive oxygen species and mitochondrial proteins in biophoton emission in roots of soybean plants under flooding stress. Journal of Proteome Research, 2015, 14(5): 2219-2236 CrossRef
  42. Denness L., McKenna J.F., Segonzac C., Wormit A., Madhou P., Bennett M., Mansfield J., Zipfel C., Hamann T. Cell wall damage-induced lignin biosynthesis is regulated by a reactive oxygen species- and jasmonic acid-dependent process in Arabidopsis. Plant Physiology, 2011, 156(3): 1364-1374 CrossRef
  43. Surówka E., Latowski D., Dziurka M., Rys M., Maksymowicz A., Żur I., Olchawa-Pajor M., Desel C., Krzewska M., Miszalski Z. ROS-scavengers, osmoprotectants and violaxanthin de-epoxidation in salt-stressed Arabidopsis thaliana with different tocopherol composition. International Journal of Molecular Sciences, 2021, 22(21): 11370 CrossRef
  44. Yan B., Dai Q., Liu X., Huang S., Wang Z. Flooding-induced membrane damage, lipid oxidation and activated oxygen generation in corn leaves. Plant and Soil, 1996, 179(2): 261-268 CrossRef
  45. Park S.-U., Lee C.-J., Park S.-C., Nam K.J., Lee K.-L., Kwak S.-S., Kim H.S., Kim Y.-H. Flooding tolerance in sweet potato (Ipomoea batatas (L.) Lam) is mediated by reactive oxygen species and nitric oxide. Antioxidants, 2022, 11(5): 878 CrossRef
  46. Shone M.G.T., Flood A.V. Effects of periods of localized water stress on subsequent nutrient uptake by barley roots and their adaptation by osmotic adjustment. New Phytologist, 1983, 94(4): 561-572 CrossRef
  47. Naidoo G. Effects of flooding on leaf water potential and stomatal resistance in Bruguiera gymnorrhiza (L.) LAM. New Phytologist, 1983, 93(3): 369-376 CrossRef
  48. Wahab A., Abdi G., Saleem M.H., Ali B., Ullah S., Shah W., Mumtaz S., Yasin G., Muresan C.C., Marc R.A. Plants’ physio-biochemical and phyto-hormonal responses to alleviate the adverse effects of drought stress: a comprehensive review. Plants, 2022, 11(13): 1620 CrossRef
  49. Singh M., Kumar J., Singh S., Singh V.P., Prasad S.M. Roles of osmoprotectants in improving salinity and drought tolerance in plants: a review. Reviews in Environmental Science and Bio/Technology, 2015, 14(3): 407-426 CrossRef
  50. Yeung E., van Veen H., Vashisht D., Sobral Paiva A.L., Hummel M., Rankenberg T., Steffens B., Steffen-Heins A., Sauterf M., de Vries M., Schuurink R.C., Bazinh J., Bailey-Serres J., Voesenek L.A.C.J., Sasidharan R. A stress recovery signaling network for enhanced flooding tolerance in Arabidopsis thaliana. Proceedings of the National Academy of Sciences, 2018, 115(26): E6085-E6094 CrossRef
  51. Nemat Alla M.M., Younis M.E., El-Shihaby O.A., El-Bastawisy Z.M. Kinetin regulation of growth and secondary metabolism in waterlogging and salinity treated Vigna sinensis and Zea mays. Acta Physiologiae Plantarum, 2002, 24(1): 19-27 CrossRef
  52. Aschi-Smiti S., Chaibi W., Brouquisse R., Ricard B., Saglio P. Assessment of enzyme induction and aerenchyma formation as mechanisms for flooding tolerance in Trifolium subterraneum “Park”. Annals of Botany, 2003, 91(2): 195-204 CrossRef
  53. Bradford K.J. Effects of soil flooding on leaf gas exchange of tomato plants. Plant Physiology, 1983, 73(2): 475-479 CrossRef
  54. Jackson M.B., Hall K.C. Early stomatal closure in waterlogged pea plants is mediated by abscisic acid in the absence of foliar water deficits. Plant, Cell and Environment, 1987, 10(2): 121-130 CrossRef
  55. Bradford K.J., Yang S.F. Xylem transport of 1-aminocyclopropane-1-carboxylic acid, an ethylene precursor, in waterlogged tomato plants. Plant Physiology, 1980, 65(2): 322-326 CrossRef
  56. Bacanamwo M., Purcell L.C. Soybean root morphological and anatomical traits associated with acclimation to flooding. Crop Science, 1999, 39(1): 143-149 CrossRef
  57. Castonguay Y., Nadeau P., Simard R.R. Effects of flooding on carbohydrate and ABA levels in roots and shoots of alfalfa. Plant, Cell & Environment, 1993, 16(6): 695-702 CrossRef
  58. Taymaz-Nikerel H., Cankorur-Cetinkaya A., Kirdar B. Genome-wide transcriptional response of Saccharomyces cerevisiae to stress-induced perturbations. Frontiers in Bioengineering and Biotechnology, 2016, 4: 17 CrossRef
  59. Mohapatra S., Panda A.K., Bastia A.K., Mukherjee A.K., Sanghamitra P., Meher J., Mohanty S.P., Pradhan S.K. Development of submergence-tolerant, bacterial blight-resistant, and high-yielding near isogenic lines of popular variety, ‘swarna’ through marker-assisted breeding approach. Frontiers in Plant Science, 2021, 12 CrossRef
  60. Raghu P.T., Veettil P.C., Das S. Smallholder adaptation to flood risks: adoption and impact of Swarna-Sub1 in Eastern India. Environmental Challenges, 2022, 7: 100480 CrossRef
  61. Park S.-U., Lee C.-J., Kim S.-E., Lim Y.-H., Lee H.-U., Nam S.-S., Kim H.S., Kwak S.-S. Selection of flooding stress tolerant sweetpotato cultivars based on biochemical and phenotypic characterization. Plant Physiology and Biochemistry, 2020, 155: 243-251 CrossRef
  62. Collaku A., Harrison S.A. Losses in wheat due to waterlogging. Crop Science, 2002, 42(2): 444 CrossRef
  63. Liu H., Able A.J., Able J.A. Priming crops for the future: rewiring stress memory. Trends in Plant Science, 2022, 27(7): 699-716 CrossRef
  64. Tripepi R.R., Mitchell C.A. Stem hypoxia and root respiration of flooded maple and birch seedlings. Physiologia Plantarum, 1984, 60(4): 567-571 CrossRef
  65. Topa M.A., Cheeseman J.M. Effects of root hypoxia and a low P supply on relative growth, carbon dioxide exchange rates and carbon partitioning in Pinus serotina seedlings. Physiologia Plantarum, 1992, 86(1): 136-144 CrossRef
  66. Wu C., Zeng A., Chen P., Florez-Palacios L., Hummer W., Mokua J., Klepadlo M., Yan L., MA Q., Cheng Y. An effective field screening method for flood tolerance in soybean. Plant Breeding, 2017, 136(5): 710-719 CrossRef
  67. Luan H., Guo B., Shen H., Pan Y., Hong Y., Lv C., Xu R. Overexpression of barley transcription factor HvERF2.11 in Arabidopsis enhances plant waterlogging tolerance. International Journal of Molecular Sciences, 2020, 21(6): 1982 CrossRef
  68. Li C., Bai T., Ma F., Han M. Hypoxia tolerance and adaptation of anaerobic respiration to hypoxia stress in two Malus species. Scientia Horticulturae, 2010, 124(2): 274-279 CrossRef
  69. Singh A., Septiningsih E.M., Balyan H.S., Singh N.K., Rai V. Genetics, physiological mechanisms and breeding of flood-tolerant rice (Oryza sativa L.). Plant and Cell Physiology, 2017, 58(2): 185-197 CrossRef
  70. Hashiguchi A., Sakata K., Komatsu S. Proteome analysis of early-stage soybean seedlings under flooding stress. Journal of Proteome Research, 2009, 8(4): 2058-2069 CrossRef
  71. Barabaschi D., Tondelli A., Desiderio F., Volante A., Vaccino P., Valè G., Cattivelli L. Next generation breeding. Plant Science, 2016, 242: 3-13 CrossRef
  72. Bassi F.M., Bentley A.R., Charmet G., Ortiz R., Crossa J. Breeding schemes for the implementation of genomic selection in wheat (Triticum spp.). Plant Science, 2015, 242: 23-36 CrossRef
  73. Kim C., Guo H., Kong W., Chandnani R., Shuang L.S., Paterson A.H. Application of genotyping by sequencing technology to a variety of crop breeding programs. Plant Science, 2016, 242: 14-22 CrossRef
  74. De Oliveira M.R., Wu C., Harrison D., Florez‐Palacios L., Acuna A., Da Silva M.P., Ravelombola S.F., Winter J., Rupe J., Shakiba E., Wood L.S., Chen P., Nguyen H., Mozzoni L.A. Response to selection to different breeding methods for soybean flood tolerance. Crop Science, 2022, 62(2): 648-660 CrossRef
  75. Yu N., Gan G., Li D., Li W., Jiang Y., Yang Q., Wang P., Li W., Wang Y. Genetic changes in F1 hybrids of the genetically divergent Solanum L., Solanum melongena L. ½ Solanum aethiopicum L. Plant Growth Regulation, 2023, 99(3): 539-552 CrossRef
  76. Huang C.-F., Miki D., Tang K., Zhou H.-R., Zheng Z., Chen W., Ma Z.-Y., Yang L., Zhang H., Liu R., He X.-J., Zhu J.-K. A pre-mRNA-splicing factor is required for RNA-directed DNA methylation in Arabidopsis. PLoS Genetics, 2013, 9(9): e1003779 CrossRef
  77. Bhat J.A., Ali S., Salgotra R.K., Mir Z.A., Dutta S., Jadon V., Tyagi A., Mushtaq M., Jain N., Singh P.K., Singh G.P., Prabhu K.V. Genomic selection in the era of next generation sequencing for complex traits in plant breeding. Frontiers in Genetics, 2016, 7: 221 CrossRef
  78. Zhang M., Lu Q., Wu W., Niu X., Wang C., Feng Y., Xu Q., Wang S., Yuan X., Yu H., Wang Y., Wei X. Association mapping reveals novel genetic loci contributing to flooding tolerance during germination in Indica rice. Frontiers in Plant Science, 2017, 8: 678 CrossRef
  79. Wang X., Zhao Y., Jiang C., Wang L., Chen L., Li F., Zhang Y., Pan Y., Zhang T. Evolution of different rice ecotypes and genetic basis of flooding adaptability in Deepwater rice by GWAS. BMC Plant Biology, 2022, 22(1): 526 CrossRef
  80. Fu D., Mason A.S., Xiao M., Yan H. Effects of genome structure variation, homeologous genes and repetitive DNA on polyploid crop research in the age of genomics. Plant Science, 2016, 242: 37-46 CrossRef
  81. Soltani A., MafiMoghaddam S., Oladzad-Abbasabadi A., Walter K., Kearns P.J., Vasquez-Guzman J., Mamidi S., Lee R., Shade A.L., Jacobs J.L., Chilivers M.I., Lowry D.B., McClean P., Osorno J.M. Genetic analysis of flooding tolerance in an andean diversity panel of dry bean (Phaseolus vulgaris L.). Frontiers in Plant Science, 2018, 9: 767 CrossRef
  82. Gepts P. Crop domestication as a long-term selection experiment. In: Plant breeding reviews. Vol. 24. Part 2: Long‐term selection: crops, animals, and bacteria. J. Janick (ed.). John Wiley & Sons, Inc., 2010: 1-44 CrossRef
  83. de Brito G.G., Campos A.D., de Melo C.L.P., Bertagnoli P.F., Klumb E.K., da Silva Porto F.G., de Magalhães Jr. A.M., Fagundes P.R.R., Parfitt J.M.B., Theisen G., Nunes C.D.M. Integrating Non-photochemical Quenching (NPQ) measurements for identifying flood-tolerant soybean genotypes in the era of climate change. Journal of Agricultural Science, 2023, 15(10): 39-57 CrossRef
  84. Prasad S.S. Enhancing the throughput of design—build—test—learn cycle for the future perspective of synthetic biology in plants (review). Sel’skokhozyaistvennaya Biologiya, 2024, 59(5): 831-846 CrossRef
  85. Schwender J. Walking the ‘design—build—test—learn’ cycle: flux analysis and genetic engineering reveal the pliability of plant central metabolism. New Phytologist, 2023, 239(5): 1539-1541 CrossRef
  86. Lv Y., Wang W. Metabolic design–build–test–learn cycle used for the biosynthesis of plant-derived bioactive compounds. In: Engineering biology for microbial biosynthesis of plant-derived bioactive compounds. Y. Wei, X.-J. Ji, M. Cao (eds.). Academic Press, 2024.
  87. Vozhzhova N.N., Zhogaleva O.S., Dubina A.Yu., Kostilev P.I. Zernovoe khozyaystvo Rossii, 2022, 5: 15-19 CrossRef (in Russ.).
  88. Chertkova N.G., Usatov A.V., Kostilev P.I., Dupliy N.G. Sotsial’no-ekologicheskie tekhnologii, 2023, 13(4): 366-383 CrossRef (in Russ.).
  89. Zaidi P.H., Rashid Z., Vinayan M.T., Almeida G.D., Phagna R.K., Babu R. QTL mapping of agronomic waterlogging tolerance using recombinant inbred lines derived from tropical maize (Zea mays L) germplasm. PLoS ONE, 2015, 10(4): e0124350 CrossRef
  90. Wang X., Niu L., Liu H., Jia X., Zhao Y., Wang Q., Lu G., Zhao Y., Dong P., Zhang M., Li H., An P., Li Z., Mu X., Zhang Y., Li C.. Integrated transcriptomics and metabolomics analysis provide insights into the alleviation of waterlogging stress in maize by exogenous spermidine application. Journal of Integrative Agriculture, 2024 CrossRef
  91. Cheng L., Zou Y., Ding S., Zhang J., Yu X., Cao J., et al. Polyamine accumulation in transgenic tomato enhances the tolerance to high temperature stress. Journal of Integrative Plant Biology, 2009, 51(5): 489-499 CrossRef
  92. Geldhof B., Pattyn J., Van de Poel B. From a different angle: genetic diversity underlies differentiation of waterlogging-induced epinasty in tomato. Frontiers in Plant Science, 2023, 14: 1178778 CrossRef
  93. Xu K., Xu X., Fukao T., Canlas P., Maghirang-Rodriguez R., Heuer S., Ismail A.M., Bailey-Serres J., Ronald P.C., Mackill D.J. Sub1A is an ethylene-response-factor-like gene that confers submergence tolerance to rice. Nature, 2006, 442: 705-708 CrossRef
  94. Hu J., Ren B., Dong S., Liu P., Zhao B., Zhang J. Comparative proteomic analysis reveals that exogenous 6-benzyladenine (6-BA) improves the defense system activity of waterlogged summer maize. BMC Plant Biology, 2020, 20(1): 44 CrossRef
  95. Yu F., Han X., Geng C., Zhao Y., Zhang Z., Qiu F. Comparative proteomic analysis revealing the complex network associated with waterlogging stress in maize (Zea mays L.) seedling root cells. Proteomics, 2015, 15(1): 135-147 CrossRef
  96. Yan M., Xue C., Xiong Y., Meng X., Li B., Shen R., Lan P. Proteomic dissection of the similar and different responses of wheat to drought, salinity and submergence during seed germination. Journal of Proteomics, 2020, 220: 103756 CrossRef
  97. Zeng N., Yang Z., Zhang Z., Hu L., Chen L. Comparative transcriptome combined with proteome analyses revealed key factors involved in alfalfa (Medicago sativa) response to waterlogging stress. International Journal of Molecular Sciences, 2019, 20(6): 1359 CrossRef
  98. Yiu J.-C., Tseng M.-J., Liu C.-W. Exogenous catechin increases antioxidant enzyme activity and promotes flooding tolerance in tomato (Solanum lycopersicum L.). Plant and Soil, 2011, 344(1-2): 213-225 CrossRef
  99. Sarker K.K., Quamruzzaman A.K.M., Uddin M.N., Rahman A., Quddus A., Biswas S.K., Gaber A., Hossain A. Evaluation of 10 eggplant (Solanum melongena L.) genotypes for development of cultivars suitable for short-term waterlogged conditions. Gesunde Pflanzen, 2023, 75(1): 179-192 CrossRef
  100. Zhao Q., Feng Y., Shao Y., Huang J., Chen Z. Response mechanism of Cynodon dactylon to flooding stress based on integrating metabonomics and transcriptomics analysis. Environmental and Experimental Botany, 2024, 225: 105846 CrossRef

 

back

 


CONTENTS

 

Full article PDF (Rus)