Menu
×
Baxter-Patrick James Island
9 a.m. - 5 p.m.
Phone: (843) 795-6679
West Ashley Library
9 a.m. - 5 p.m.
Phone: (843) 766-6635
Wando Mount Pleasant Library
9 a.m. - 5 p.m.
Phone: (843) 805-6888
Village Library
9 a.m. - 1 p.m.
Phone: (843) 884-9741
St. Paul's/Hollywood Library
9 a.m. - 5 p.m.
Phone: (843) 889-3300
Otranto Road Library
9 a.m. - 5 p.m.
Phone: (843) 572-4094
Mt. Pleasant Library
9 a.m. – 5 p.m.
Phone: (843) 849-6161
McClellanville Library
9 a.m. – 1 p.m.
Phone: (843) 887-3699
Keith Summey North Charleston Library
9 a.m. - 5 p.m.
Phone: (843) 744-2489
John's Island Library
9 a.m. - 5 p.m.
Phone: (843) 559-1945
Hurd/St. Andrews Library
9 a.m. - 5 p.m.
Phone: (843) 766-2546
Folly Beach Library
9 a.m. - 2 p.m.
*open the 2nd and 4th Saturday
*open the 2nd and 4th Saturday
Phone: (843) 588-2001
Edisto Island Library
9 a.m. - 1 p.m.
Phone: (843) 869-2355
Dorchester Road Library
9 a.m. - 5 p.m.
Phone: (843) 552-6466
John L. Dart Library
9 a.m. - 5 p.m.
Phone: (843) 722-7550
Main Library
9 a.m. - 5 p.m.
Phone: (843) 805-6930
Bees Ferry West Ashley Library
9 a.m. - 5 p.m.
Phone: (843) 805-6892
Edgar Allan Poe/Sullivan's Island Library
Closed for renovations
Phone: (843) 883-3914
Mobile Library
Closed
Phone: (843) 805-6909
Today's Hours
Baxter-Patrick James Island
9 a.m. - 5 p.m.
Phone: (843) 795-6679
West Ashley Library
9 a.m. - 5 p.m.
Phone: (843) 766-6635
Wando Mount Pleasant Library
9 a.m. - 5 p.m.
Phone: (843) 805-6888
Village Library
9 a.m. - 1 p.m.
Phone: (843) 884-9741
St. Paul's/Hollywood Library
9 a.m. - 5 p.m.
Phone: (843) 889-3300
Otranto Road Library
9 a.m. - 5 p.m.
Phone: (843) 572-4094
Mt. Pleasant Library
9 a.m. – 5 p.m.
Phone: (843) 849-6161
McClellanville Library
9 a.m. – 1 p.m.
Phone: (843) 887-3699
Keith Summey North Charleston Library
9 a.m. - 5 p.m.
Phone: (843) 744-2489
John's Island Library
9 a.m. - 5 p.m.
Phone: (843) 559-1945
Hurd/St. Andrews Library
9 a.m. - 5 p.m.
Phone: (843) 766-2546
Folly Beach Library
9 a.m. - 2 p.m.
*open the 2nd and 4th Saturday
*open the 2nd and 4th Saturday
Phone: (843) 588-2001
Edisto Island Library
9 a.m. - 1 p.m.
Phone: (843) 869-2355
Dorchester Road Library
9 a.m. - 5 p.m.
Phone: (843) 552-6466
John L. Dart Library
9 a.m. - 5 p.m.
Phone: (843) 722-7550
Main Library
9 a.m. - 5 p.m.
Phone: (843) 805-6930
Bees Ferry West Ashley Library
9 a.m. - 5 p.m.
Phone: (843) 805-6892
Edgar Allan Poe/Sullivan's Island Library
Closed for renovations
Phone: (843) 883-3914
Mobile Library
Closed
Phone: (843) 805-6909
Patron Login
menu
Item request has been placed!
×
Item request cannot be made.
×
Processing Request
Heat stress-mediated effects on the morphophysiological, biochemical, and ultrastructural parameters of germinating Melanoxylon brauna Schott. seeds.
Item request has been placed!
×
Item request cannot be made.
×
Processing Request
- Author(s): Reis LP;Reis LP; de Lima E Borges EE; de Lima E Borges EE; Brito DS; Brito DS; Bernardes RC; Bernardes RC; Dos Santos Araújo R; Dos Santos Araújo R
- Source:
Plant cell reports [Plant Cell Rep] 2021 Sep; Vol. 40 (9), pp. 1773-1787. Date of Electronic Publication: 2021 Jun 28.- Publication Type:
Journal Article- Language:
English - Source:
- Additional Information
- Source: Publisher: Springer Country of Publication: Germany NLM ID: 9880970 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-203X (Electronic) Linking ISSN: 07217714 NLM ISO Abbreviation: Plant Cell Rep Subsets: MEDLINE
- Publication Information: Original Publication: Berlin ; New York : Springer, 1981-
- Subject Terms: Fabaceae/*physiology ; Heat-Shock Response/*physiology ; Plant Proteins/*metabolism ; Seeds/*physiology ; Seeds/*ultrastructure; Antioxidants/metabolism ; Carotenoids/metabolism ; Enzymes/metabolism ; Fabaceae/ultrastructure ; Fatty Acids/metabolism ; Germination ; Glucose/metabolism ; Hydrogen Peroxide/metabolism ; Malondialdehyde/metabolism ; Mitochondria/metabolism ; Mitochondria/ultrastructure ; Oxidative Stress ; Superoxides/metabolism
- Abstract: Key Message: The present study showed that the heat stress (40 °C) caused changes in morphophysiological, biochemical, and ultrastructural parameters to the seeds Melanoxylon brauna, ultimately leading to loss of germination capacity. Temperature is an abiotic factor that influences seed germination. In the present study, we investigated morphophysiological, biochemical, and ultrastructural changes during the germination of Melanoxylon brauna seeds under heat stress. Seed germination was evaluated at constant temperatures of 25 and 40 °C. The samples consisted of seeds soaked in distilled and ionized water for 48 and 96 h at both temperatures. For the evaluation of internal morphology, the seeds were radiographed. Ultrastructural parameters were assessed using transmission electron microscopy (TEM). The production of reactive oxygen species (ROS), content of malondialdehyde (MDA) and glucose, carbonylated proteins, and activity of the enzymes (superoxide dismutase-SOD, ascorbate peroxidase-APX, catalase-CAT, peroxidase-POX, glucose-6-phosphate dehydrogenase-G6PDH, lipase, α- and β-amylase, and protease) were measured by spectrophotometric analysis. An 82% reduction in the germination of M. brauna seeds was observed at 25 °C, and 0% at 40 °C. TEM showed that seeds submitted to heat stress (40 °C) had poorly developed mitochondria and significantly reduced respiration rates. The content of ROS and protein carbonylation in seeds subjected to 40 °C increased compared to that at 25 °C. The activity of antioxidant enzymes, namely SOD, APX, CAT, and POX, was significantly reduced in seeds subjected to heat stress. Glucose content, G6PDH, and lipase activity also decreased when the seeds were exposed to heat stress. Conversely, α- and β-amylase enzymes and the protease increased due to the increase in temperature. Our data showed that the increase in temperature caused an accumulation of ROS, increasing the oxidative damage to the seeds, which led to mitochondrial dysfunction, ultimately leading to loss of germination.
(© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.) - References: Able AJ, Guest DI, Sutherland MW (1998) Use of a new tetrazolium-based assay to study the production of superoxide radicals by tobacco cell cultures challenged with avirulent zoospores of Phytophthora parasitica var nicotianae. Plant Physiol 117:491–499. https://doi.org/10.1104/pp.117.2.491. (PMID: 10.1104/pp.117.2.491962570234969)
Ahmad P, Jaleel CA, Salem MA, Nabi G, Sharma S (2010) Roles of enzymatic and nonenzymatic antioxidants in plants during abiotic stress. Crit Rev Biotechnol 30(3):161–175. https://doi.org/10.3109/07388550903524243. (PMID: 10.3109/0738855090352424320214435)
Ahmad P, Tripathi DK, Deshmukh R, Singh VP, Corpas FJ (2019) Revisiting the role of ROS and RNS in plants under changing environment. Environ Exp Bot 161:1–3. https://doi.org/10.1016/j.envexpbot.2019.02.017. (PMID: 10.1016/j.envexpbot.2019.02.017)
Alamri S, Siddiqui MH, Kushwaha BK, Singh VP, Ali HM (2021) Mitigation of arsenate toxicity by indole-3-acetic acid in brinjal roots: plausible association with endogenous hydrogen peroxide. J Hazard Mater 405:124336. https://doi.org/10.1016/j.jhazmat.2020.124336. (PMID: 10.1016/j.jhazmat.2020.12433633153795)
Bailly C (2019) The signalling role of ROS in the regulation of seed germination and dormancy. Biochem J 476:3019–3032. https://doi.org/10.1042/BCJ20190159. (PMID: 10.1042/BCJ2019015931657442)
Bailly C, Kranner I (2011) Analyses of reactive oxygen species and antioxidants in relation to seed longevity and germination. Methods Mol Biol 773:343–367. https://doi.org/10.1007/978-1-61779-231-1_20. (PMID: 10.1007/978-1-61779-231-1_2021898265)
Balogh G, Péter M, Glatz A, Gombos I, Török Z, Horváth I, Harwood JL, Vígh L (2013) Key role of lipids in heat stress management. FEBS Lett 587:1970–1980. https://doi.org/10.1016/j.febslet.2013.05.016. (PMID: 10.1016/j.febslet.2013.05.01623684645)
Bernfeld P (1955) α- and β- Amylases. Meth Enzym 1:149–158. (PMID: 10.1016/0076-6879(55)01021-5)
Bewley JD, Bradford KJ, Hilhorst HWM, Nonogaki H (2013) Seeds: Physiology of development, germination and dormancy, 3rd edn. Springer, Berlin, p 392. https://www.springer.com/gp/book/9781461446927.
Bhattacharjee S (2013) Heat and chilling induced disruption of redox homeostasis and its regulation by hydrogen peroxide in germinating rice seeds (Oryza sativa L., Cultivar Ratna). Physiol Mol Biol Plants 19:199–207. https://doi.org/10.1007/s12298-012-0159-x. (PMID: 10.1007/s12298-012-0159-x244314873656194)
Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254. https://doi.org/10.1006/abio.1976.9999. (PMID: 10.1006/abio.1976.9999942051)
Buttar ZA, Wu SN, Arnao MB, Wang C, Ullah I, Wang C (2020) Melatonin suppressed the heat stress-induced damage in wheat seedlings by modulating the antioxidant machinery. Plants 9:809. https://doi.org/10.3390/plants907080. (PMID: 10.3390/plants9070807412093)
Carrie C, Murcha MW, Giraud E, Ng S, Zhang MF, Narsai R, Whelan J (2013) How do plants make mitochondria? Planta 237:429–439. https://doi.org/10.1007/s00425-012-1762-3. (PMID: 10.1007/s00425-012-1762-322976451)
Carvalho PER (2010) Espécies arbóreas brasileiras. 21. ed. Brasília: Embrapa Informação Tecnológica, pp 644.
Chen K, Arora R (2011) Dynamics of the antioxidant system during seed osmopriming, postpriming germination, and seedling establishment in Spinach (Spinacia oleracea). Plant Sci 180:212–220. https://doi.org/10.1016/j.plantsci.2010.08.007. (PMID: 10.1016/j.plantsci.2010.08.00721421363)
Ciacka K, Tymiński M, Gniazdowska A, Krasuska U (2020) Carbonylation of proteins—an element of plant ageing. Planta 252:1–13. https://doi.org/10.1007/s00425-020-03414-1. (PMID: 10.1007/s00425-020-03414-1)
Cupp-Enyard C (2008) Sigma’s non-specific protease activity assay-casein as a substrate. J vis Exp 19:e899. https://doi.org/10.3791/899. (PMID: 10.3791/899)
Dai VuL, Gevaert K, De Smet I (2019) Feeling the heat: searching for plant thermosensors. Trends Plant Sci 24:210–219. https://doi.org/10.1016/j.tplants.2018.11.004. (PMID: 10.1016/j.tplants.2018.11.004)
Del Longo OT, Goinz׳zlez CA, Pastori GM, Trippi VS (1993) Antioxidant defenses under hyperoxygenic and hyperosmotic conditions in leaves of two lines of maize with differential to drought. Plant Cell Physiol Oxf 37:1023–1028. https://doi.org/10.1093/oxfordjournals.pcp.a078515. (PMID: 10.1093/oxfordjournals.pcp.a078515)
Dong S, Beckles DM (2019) Dynamic changes in the starch-sugar interconversion within plant source and sink tissues promote a better abiotic stress response. J Plant Physiol 234:80–93. https://doi.org/10.1016/j.jplph.2019.01.007. (PMID: 10.1016/j.jplph.2019.01.00730685652)
Dunn JD, Alvarez LAJ, Zhang X, Soldati T (2015) Reactive oxygen species and mitochondria: a nexus of cellular homeostasis. Redox Biol 6:472–485. https://doi.org/10.1016/j.redox.2015.09.005. (PMID: 10.1016/j.redox.2015.09.005)
Dvorak P, Krasylenko Y, Zeiner A, Samaj J, Takac T (2020) Signaling toward ROS-scavenging enzymes in plants. Front Plant Sci 11:2178. https://doi.org/10.3389/fpls.2020.618835. (PMID: 10.3389/fpls.2020.618835)
Felix FC, Araújo FS, Silva MD, Ferrari CS, Pacheco MV (2018) Water and thermal stress on the germination Leucaena leucocephala (Lam.) de Wit seeds. Rev Bras Cienc Agrar. https://doi.org/10.5039/agraria.v13i2a5515. (PMID: 10.5039/agraria.v13i2a5515)
Folch J, Lees M, Stanle GHS (1957) A simple method for the isolation and purification of total lipides from animal tissues. J Bio Chem 226:497–509. PMID: 13428781. https://pubmed.ncbi.nlm.nih.gov/13428781/.
Gadge PP, Madhikar SD, Yewle JN, Jadhav UU, Chougale AD, Zambare VP, Padul MV (2011) Biochemical studies of lipase from germinating oil seeds (Glycine max). Am J Biochem Biotechnol 73:141–145. https://doi.org/10.3844/ajbbsp.2011.141.145. (PMID: 10.3844/ajbbsp.2011.141.145)
Gimbi DM, Kitabatak N (2002) Changes in alpha-and beta-amylase activities during seed germination of African finger millet. Inter J Food Sci Nutri 53:481–488. https://doi.org/10.1080/09637480220164361. (PMID: 10.1080/09637480220164361)
Gomes JP, Oliveira LM, Ferreira PI, Batista F (2016) Substrates and temperatures for germination test of myrtaceae seeds. Ciê Flor 26:285–293. https://doi.org/10.5902/1980509821120. (PMID: 10.5902/1980509821120)
Hanif S, Saleem MF, Sarwar M, Irshad M, Shakoor A, Wahid MA, Khan HZ (2021) Biochemically triggered heat and drought stress tolerance in rice by proline application. J Plant Gro Reg 40:305–312. https://doi.org/10.1007/s00344-020-10095-3. (PMID: 10.1007/s00344-020-10095-3)
Harsh A, Sharma YK, Joshi U, Rampuria S, Singh G, Kumar S, Sharma R (2016) Effect of short-term heat stress on total sugars, proline and some antioxidant enzymes in moth bean (Vigna aconitifolia). Ann Agric Sci 61:57–64. https://doi.org/10.1016/j.aoas.2016.02.001. (PMID: 10.1016/j.aoas.2016.02.001)
He Xu, Kermode R (2010) Programmed cell death of the megagametophyte during post-germinative growth of white spruce (Picea glauca) seeds is regulated by reactive oxygen species and the ubiquitin-mediated proteolytic system. Plant and Cell Physiol 51:1707–1720. https://doi.org/10.1093/pcp/pcq130. (PMID: 10.1093/pcp/pcq130)
He Q, Li P, Zhang W, Bi Y (2020) Cytoplasmic glucose-6-phosphate dehydrogenase plays an important role in the silicon-enhanced alkaline tolerance in highland barley. Func Plant Biol 48:119–130. https://doi.org/10.1071/FP20084. (PMID: 10.1071/FP20084)
Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198. https://doi.org/10.1016/0003-9861(68)90654-1. (PMID: 10.1016/0003-9861(68)90654-15655425)
Heymann T, Heinz P, Glomb MA (2015) Lycopene inhibits the isomerization of β-carotene during quenching of singlet oxygen and free radicals. J Agric Food Chem 63:3279–3287. https://doi.org/10.1021/acs.jafc.5b00377. (PMID: 10.1021/acs.jafc.5b0037725803572)
Ihsan MZ, Daur I, Alghabari F, Alzamanan S, Rizwan S, Ahmad M, Shafqat W (2019) Heat stress and plant development: role of sulphur metabolites and management strategies. Acta Agric Scand 69:332–342. https://doi.org/10.1080/09064710.2019.1569715. (PMID: 10.1080/09064710.2019.1569715)
Ishibashi Y, Kasa S, Sakamoto M, Aoki N, Kai K (2015) A role for reactive oxygen species produced by NADPH oxidases in the embryo and aleurone cells in barley seed germination. PLoS ONE 10:e0143173. https://doi.org/10.1371/journal.pone.0143173. (PMID: 10.1371/journal.pone.0143173265797184651353)
Janecek S, Baláz S (1992) α-Amylases and approaches leading to their enhanced stability. FEBS Lett 304:1–3. https://doi.org/10.1016/0014-5793(92)80575-2. (PMID: 10.1016/0014-5793(92)80575-21618293)
Ju C, Song Y, Kong D (2020) Arabidopsis GLR3. 5-modulated seed germination involves GA and ROS signaling. Plant Sig Behav 15:1729537. https://doi.org/10.1080/15592324.2020.1729537. (PMID: 10.1080/15592324.2020.1729537)
Junglee S, Urban L, Sallanon H, Lopez-Lauri F (2014) Optimized assay for hydrogen peroxide determination in plant tissue using potassium iodide. Am J Anal Chem 5:730–736. https://doi.org/10.4236/ajac.2014.511081. (PMID: 10.4236/ajac.2014.511081)
Kar M, Mishra D (1976) Catalase, peroxidase and polyphenoloxidase activities during rice leaf senescence. Plant Physiol 57:315–319. https://doi.org/10.1104/pp.57.2.315. (PMID: 10.1104/pp.57.2.31516659474542015)
Keunen E, Remans T, Bohler S, Vangronsveld J, Cuypers A (2011) Metal-induced oxidative stress and plant mitochondria. Int J Mol Sci 12:6894–6918. https://doi.org/10.3390/ijms12106894. (PMID: 10.3390/ijms12106894220729263211017)
Kohli SK, Khanna K, Bhardwaj R, AbdAllah EF, Ahmad P, Corpas FJ (2019) Assessment of subcellular ROS and NO metabolism in higher plants: multifunctional signaling molecules. Antioxidants 8(12):641. https://doi.org/10.3390/antiox8120641. (PMID: 10.3390/antiox81206416943533)
Krasensky J, Jonak C (2012) Drought, salt, and temperature stress-induced metabolic rearrangements and regulatory networks. J Exp Bot 63:1593–1608. https://doi.org/10.1093/jxb/err460. (PMID: 10.1093/jxb/err46022291134)
Krishnan HB, Kim WS, Oehrle NW, Smith JR, Gillman JD (2020) Effect of heat stress on seed protein composition and ultrastructure of protein storage vacuoles in the cotyledonary parenchyma cells of soybean genotypes that are either tolerant or sensitive to elevated temperatures. Inter J Mol Sci 21:4775. https://doi.org/10.3390/ijms21134775. (PMID: 10.3390/ijms21134775)
Laghmouchi Y, Belmehdi O, Bouyahya A, Senhaji NS, Abrin J (2017) Effect of temperature, salt stress and pH on seed germination of medicinal plant Origanum compactum. Bioc Agric Biot 10:156–160. https://doi.org/10.1016/j.bcab.2017.03.002. (PMID: 10.1016/j.bcab.2017.03.002)
Liu Y, Li J, Zhu Y, Jones A, Rose RJ, Song Y (2019) Heat stress in legume seed setting: effects, causes, and future prospects. Front Plant Sci 10:938. https://doi.org/10.3389/fpls.2019.00938. (PMID: 10.3389/fpls.2019.00938314175796684746)
Logan DC, Millar AH, Sweetlove LJ, Hill SA, Leaver CJ (2001) Mitochondrial biogenesis during germination in maize embryos. Plant Physiol 125:662–672. https://doi.org/10.1104/pp.125.2.662. (PMID: 10.1104/pp.125.2.6621116102464868)
Lu J, Xu Y, Wang J, Singer SD, Chen G (2020) The role of triacylglycerol in plant stress response. Plants 9(4):472. https://doi.org/10.3390/plants9040472. (PMID: 10.3390/plants90404727238164)
Martinelli G, Moraes MD (2013) Livro vermelho da flora do Brasil.1ª ed. Rio de Janeiro: Andrea Jakobsson, Instituto de Pesquisas Jardim Botânico do Rio de Janeiro, CNCFlora.
Matos ACB, Borges EEL, Sekita MC (2014) Production of reactive oxygen species in Dalbergia nigra seeds under thermal stress. J Seed Sci 36:282–289. https://doi.org/10.1590/2317-1545v36n3973. (PMID: 10.1590/2317-1545v36n3973)
Meyer EH, Welchen E, Carrie C (2019) Assembly of the complexes of the oxidative phosphorylation system in land plant mitochondria. Ann Rev Plant Biol 70:23–50. https://doi.org/10.1146/annurev-arplant-050718-100412. (PMID: 10.1146/annurev-arplant-050718-100412)
Nagata M, Yamashita I (1992) Simple method for simultaneous determination of chlorophyll and carotenoids in tomato fruit. Nippon Sho K Gak 39:925–928. https://doi.org/10.3136/nskkk1962.39.925. (PMID: 10.3136/nskkk1962.39.925)
Ozden E, Light ME, Demir I (2021) Alternating temperatures increase germination and emergence in relation to endogenous hormones and enzyme activities in aubergine seeds. S Afr J Bot 139:130–139. https://doi.org/10.1016/j.sajb.2021.02.015. (PMID: 10.1016/j.sajb.2021.02.015)
PBMC (2014) Impactos, vulnerabilidades e adaptação às mudanças climáticas. In: Assad ED, Magalhães AR (eds) Contribuição do Grupo de Trabalho 2 do Painel Brasileiro de Mudanças Climáticas ao Primeiro Relatório de Avaliação Nacional sobre Mudanças Climáticas. COPPE. Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brasil, p 414.
Rani K (2013) Immobilization of glycine max amylase onto variety of chlorinated and nitrated fabrics (Silk, Nylon and Cotton). J BioSci 2:8–12. https://doi.org/10.5176/2251-3140_3140_2.2.34. (PMID: 10.5176/2251-3140_3140_2.2.34)
Rashid M, Hampton JG, Rolston MP, Khan KM, Saville DJ (2018) Heat stress during seed development affects forage brassica (Brassica napus L.) seed quality. J Agron Crop Sci 204:147–154. https://doi.org/10.1111/jac.12251. (PMID: 10.1111/jac.12251)
Rashid M, Hampton JG, Shaw ML, Rolston MP, Khan KM, Saville DJ (2020) Oxidative damage in forage rape (Brassica napus L.) seeds following heat stress during seed development. J Agron Crop Sci 206:101–117. https://doi.org/10.1111/jac.12372. (PMID: 10.1111/jac.12372)
Ratajczak E, Małecka A, Ciereszko I, Staszak AM (2019) Mitochondria are important determinants of the aging of seeds. Int J Mol Sci 20:1568. https://doi.org/10.3390/ijms20071568. (PMID: 10.3390/ijms200715686479606)
Reis LP, Borges EEL, Souza GA, Brito D (2020) Relationships between substrate and the mobilization of reserve with temperature during seed germination of Ormosia coarctata Jack. J Seed Sci 42:e202042017. https://doi.org/10.1590/2317-1545v42223509. (PMID: 10.1590/2317-1545v42223509)
Ribeiro MZ, Silva DP, Vitolo M, Roberto IC, Pessoa Junior A (2007) Partial purification of glucose-6- phosphate dehydrogenase by aqueous two-phase poly (ethyleneglycol)/phosphate systems. Braz J Microbiol 38:78–83. https://doi.org/10.1590/S1517-83822007000100016. (PMID: 10.1590/S1517-83822007000100016)
Santiago JP, Soltani A, Bresson MM, Preiser AL, Lowry DB, Sharkey TD (2021) Contrasting anther glucose-6-phosphate dehydrogenase activities between two bean varieties suggest an important role in reproductive heat tolerance. P Cell Environ. https://doi.org/10.1111/pce.14057. (PMID: 10.1111/pce.14057)
Santos MM, Borges EEL, Ataíde GDM, Souza GAD (2017) Germination of seeds of Melanoxylon brauna Schott. under heat stress: production of reactive oxygen species and antioxidant activity. Forests 8:1–13. https://doi.org/10.3390/f8110405. (PMID: 10.3390/f8110405)
Santos MM, Borges EEDL, Ataíde GDM, Pires RMDO, Rocha DK (2020) Enzyme activity in the micropylar region of Melanoxylon brauna Schott seeds during germination under heat stress conditions. J Seed Sci 42:1–10. https://doi.org/10.1590/2317-1545v42229988. (PMID: 10.1590/2317-1545v42229988)
Siddiqui MH, Alamri S, Khan MN, Corpas FJ, Al-Amri AA, Alsubaie QD, Ahmad P (2020) Melatonin and calcium function synergistically to promote the resilience through ROS metabolism under arsenic-induced stress. J Haz Mat. https://doi.org/10.1016/j.jhazmat.2020.122882. (PMID: 10.1016/j.jhazmat.2020.122882)
Sun JL, Li JY, Wang MJ, Song ZT, Liu JX (2020) Protein quality control in plant organelles: current progress and future perspectives. Mol Plant 14:1. https://doi.org/10.1016/j.molp.2020.10.011. (PMID: 10.1016/j.molp.2020.10.011)
UNDRR (2020) United Nations Office of disaster risk reduction. In: The human cost of disasters: an overview of the last 20 years (2000–2019), Geneva.
Wang TY, Libardo MDJ, Angeles-Boza AM, Pellois JP (2017) Membrane oxidation in cell delivery and cell killing applications. ACS Chem Biol 12:1170–1182. https://doi.org/10.1021/acschembio.7b00237. (PMID: 10.1021/acschembio.7b00237283550595905413)
Xia Q, El-Maarouf-Bouteau H, Bailly C, Meimoun P (2016) Determination of protein carbonylation and proteasome activity in seeds. In: Plant proteostasis. Humana Press, Totowa, pp 205–212. https://doi.org/10.1007/978-1-4939-3759-2_16.
Xin X, Tian Q, Yin G, Chen X, Zhang J, Ng S, Lu X (2014) Reduced mitochondrial and ascorbate–glutathione activity after artificial ageing in soybean seed. J Plant Physiol 171:140–147. https://doi.org/10.1016/j.jplph.2013.09.016. (PMID: 10.1016/j.jplph.2013.09.01624331429)
Yalcinkaya T, Uzilday B, Ozgur R, Turkan I, Mano JI (2019) Lipid peroxidation-derived reactive carbonyl species (RCS): Their interaction with ROS and cellular redox during environmental stresses. Environ Exp Bot 165:139–149. https://doi.org/10.1016/j.envexpbot.2019.06.004. (PMID: 10.1016/j.envexpbot.2019.06.004)
Yoshida K, Terashima I, Noguchi K (2007) Up-regulation of mitochondrial alternative oxidase concomitant with chloroplast over-reduction by excess light. Plant Cell Physiol 48:606–614. https://doi.org/10.1093/pcp/pcm033. (PMID: 10.1093/pcp/pcm03317339232)
Zhang K, Zhang Y, Sun J, Meng J, Tao J (2021) Deterioration of orthodox seeds during ageing: influencing factors, physiological alterations and the role of reactive oxygen species. Plant Phys Biochem. https://doi.org/10.1016/j.plaphy.2020.11.031. (PMID: 10.1016/j.plaphy.2020.11.031)
Zhou J, Wang J, Yu JQ, Chen Z (2014) Role and regulation of autophagy in heat stress responses of tomato plants. Front Plant Sci 5:174. https://doi.org/10.3389/fpls.2014.00174. (PMID: 10.3389/fpls.2014.00174248178754012191) - Contributed Indexing: Keywords: Anti-oxidative enzymes; High temperatures; Mitochondria; Reserve enzymes; Respiratory rate
- Accession Number: 0 (Antioxidants)
0 (Enzymes)
0 (Fatty Acids)
0 (Plant Proteins)
11062-77-4 (Superoxides)
36-88-4 (Carotenoids)
4Y8F71G49Q (Malondialdehyde)
BBX060AN9V (Hydrogen Peroxide)
IY9XDZ35W2 (Glucose) - Publication Date: Date Created: 20210628 Date Completed: 20210831 Latest Revision: 20221117
- Publication Date: 20231215
- Accession Number: 10.1007/s00299-021-02740-2
- Accession Number: 34181045
- Source:
Contact CCPL
Copyright 2022 Charleston County Public Library Powered By EBSCO Stacks 3.3.0 [350.3] | Staff Login
No Comments.