journal article·2022-12

Cerium-doped carbon quantum dots trigger mung bean seeds to help mitigate salt stress by increasing the degree of stomata opening

Zihao Dong, Yan Gong, Jie Zhao

Carbon Letters· Volume 32· Issue 7
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Abstract

Since soil salinization imposes various adverse effects on plants, research on how to relieve salt stress from plants is extremely urgent. We synthesized a new type of cerium-doped carbon quantum dots by a hydrothermal synthesis method. Characterization shows that the carbon quantum dots have a small and uniform particle size, high stability, high water solubility and biocompatibility. Mung bean seeds were soaked in CDs:Ce solutions under a concentration gradient (0.25, 0.5, 1, 2, 3 mg/mL) and germinated under salt stress (150 mM NaCl). Compared with salt stress, the addition of CDs solutions effectively enhanced the ability of plants to relieve salt stress. The relieving effect on mung bean plants was the most significant after treatment with 2 mg/mL CDs:Ce, and the main root length, plant height and leaf length in comparison with the case of salt stress increased by 83%, 80%, and 60%, respectively. Chlorophyll content, peroxidase activity, superoxide dismutase activity and catalase activity, total protein content increased by 90%, 77%, 76%, 77% and 76%, respectively, malondialdehyde and proline The content decreased by 83% and 77%. Inductively coupled plasma mass spectroscopy proved mung bean plants absorbed CDs:Ce, but the absorption of NaCl decreased by 21.8%. Fluorescence imaging showed CDs:Ce was absorbed by roots, and transferred from the vascular system and apoplastic pathways to stems and leaf veins, and mainly aggregated in intercellular gaps, the vascular system, leaf veins, cilia and stomata. Stereomicroscopy showed that CDs:Ce induction increased the stomatal opening by 15.7%, and improved metabolic efficiency and NaCl excretion from the plants. Hence, CDs:Ce shows great potential in protecting crops from abiotic stress.
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Research context

OpenAlex topics: Carbon and Quantum Dots Applications · Selenium in Biological Systems · Heavy Metal Exposure and Toxicity

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (61)

Show source-provided references
1. Arzani A (2008) Improving salinity tolerance in crop plants: a biotechnological view. In Vitro Cell Dev Biol-Plant 44(5):373–38310.1007/s11627-008-9157-7 ↗
2. Hailu B, Mehari H (2021) Impacts of soil salinity/sodicity on soil-water relations and plant growth in dry land areas: a review. J Nat Sci Res 12(3):1–10
3. Abogadallah GM (2010) Insights into the significance of antioxidative defense under salt stress. Plant Signal Behav 5(4):369–37410.4161/psb.5.4.10873 ↗
4. Khan MA, Ungar IA, Showalter AM (2000) Effects of salinity on growth, water relations and ion accumulation of the subtropical perennial halophyte. Atriplex griffithii var stocksii Ann Bot 85(2):225–232
5. Chang CC, Locy RD, Smeda R, Sahi SV, Singh NK (1997) Photoautotrophic tobacco cells adapted to grow at high salinity. Plant Cell Rep 16(7):495–50210.1007/BF01092773 ↗
6. Zhang L, Ma H, Chen T, Pen J, Yu S, Zhao X (2014) Morphological and physiological responses of cotton (Gossypium hirsutum L.) plants to salinity. PLoS One 9(11): e112807.10.1371/journal.pone.0112807 ↗
7. Mja A, Ah A, Ms A, Mr B, Fa C (2021) Mungbean Wild Genetic Resource: A Potential Source of Genetic Improvement for Biotic and Abiotic Stress Tolerance. Wild Germplasm for Genetic Improvement in Crop Plants: 299–319.10.1016/B978-0-12-822137-2.00016-3 ↗
8. Ondrasek G, Rengel Z, Kondres N, Tanaskovik V (2021) Growth and Element Uptake by Salt-Sensitive Crops under Combined NaCl and Cd Stresses.10.3390/plants10061202 ↗
9. Friedman R a, Altman A, Levin N (1989) The effect of salt stress on polyamine biosynthesis and content in mung bean plants and in halophytes. Physiol. Plant. 76(3): 295-30210.1111/j.1399-3054.1989.tb06194.x ↗
10. Fatma M, Iqbal N, Gautam H, Sehar Z, Khan NA (2021) Ethylene and sulfur coordinately modulate the antioxidant system and ABA accumulation in mustard plants under salt stress. Plants 10(1):18010.3390/plants10010180 ↗
11. Sheoran IS, Garg OP (1979) Quantitative and qualitative changes in peroxidase during germination of mung bean under salt stress. Physiol Plant 46(2):147–15010.1111/j.1399-3054.1979.tb06547.x ↗
12. Rossi L, Zhang W, Ma X (2017) Cerium oxide nanoparticles alter the salt stress tolerance of Brassica napus L. by modifying the formation of root apoplastic barriers. Environ Pollut 229:132–13810.1016/j.envpol.2017.05.083 ↗
13. Hu H, Shan C (2018) Effect of cerium (Ce) on the redox states of ascorbate and glutathione through ascorbate-glutathione cycle in the roots of maize seedlings under salt stress. Cereal Res Commun 46(1):31–4010.1556/0806.45.2017.057 ↗
14. An J, Hu P, Li F, Wu H, Shen Y, White JC, Tian X, Li Z, Giraldo JP (2020) Emerging investigator series: molecular mechanisms of plant salinity stress tolerance improvement by seed priming with cerium oxide nanoparticles. Environ Sci Nano 7(8):2214–222810.1039/D0EN00387E ↗
15. Kang Z, Liu Y, Bioimaging nanomaterials based on carbon dots, Near-infrared Nanomaterials2016, pp. 70–100.10.1039/9781782623939-00070 ↗
16. Mirtchev P, Henderson EJ, Soheilnia N, Yip CM, Ozin GA (2012) Solution phase synthesis of carbon quantum dots as sensitizers for nanocrystalline TiO2 solar cells. JMCh 22(4):1265–1269
17. Wang H, Zhang M, Song Y, Li H, Huang H, Shao M, Liu Y, Kang Z (2018) Carbon dots promote the growth and photosynthesis of mung bean sprouts. Carbon 136:94–10210.1016/j.carbon.2018.04.051 ↗
18. Zhang M, Hu L, Wang H, Song Y, Liu Y, Li H, Shao M, Huang H, Kang Z (2018) One-step hydrothermal synthesis of chiral carbon dots and their effects on mung bean plant growth. Nanoscale 10(26):12734–1274210.1039/C8NR01644E ↗
19. Xiao L, Guo H, Wang S, Li J, Wang Y, Xing B (2019) Carbon dots alleviate the toxicity of cadmium ions (Cd2+) toward wheat seedlings. Environ Sci Nano 6(5):1493–150610.1039/C9EN00235A ↗
20. Li Y, Gao J, Xu X, Wu Y, Zhuang J, Zhang X, Zhang H, Lei B, Zheng M, Liu Y (2020) Carbon Dots as a Protective Agent Alleviating Abiotic Stress on Rice (Oryza sativa L.) through Promoting Nutrition Assimilation and the Defense System. ACS Applied Materials & Interfaces 12(30): 33575–33585.10.1021/acsami.0c11724 ↗
21. Li J, Xiao L, Cheng Y, Cheng Y, Wang Y, Wang X, Ding L (2019) Applications of carbon quantum dots to alleviate Cd2+ phytotoxicity in Citrus maxima seedlings. Chemosphere 236:12438510.1016/j.chemosphere.2019.124385 ↗
22. Li F, Liu C, Yang J, Wang Z, Liu W, Tian F (2014) Mg/N double doping strategy to fabricate extremely high luminescent carbon dots for bioimaging. RSC Adv 4(7):3201–320510.1039/C3RA43826K ↗
23. Bruuinsma J (1963) The quantitative analysis of chlorophylls a and b in plant extracts. PcPb 2(2):241–249
24. Kostka P, Kwan CY (1989) Instability of malondialdehyde in the presence of H2O2: implications for the thiobarbituric acid test. Lipids 24(6):545–54910.1007/BF02535136 ↗
25. Qiu R-L, Zhao X, Tang Y-T, Yu F-M, Hu P-J (2008) Antioxidative response to Cd in a newly discovered cadmium hyperaccumulator. Arabis paniculata F Chemosphere 74(1):6–1210.1016/j.chemosphere.2008.09.069 ↗
26. Kochba J, Lavee S, Spiegel-Roy P (1977) Differences in peroxidase activity and isoenzymes in embryogenic ane non-embryogenic ‘Shamouti’orange ovular callus lines. PCPhy 18(2):463–467
27. Sequeira L, Mineo L (1966) Partial purification and kinetics of indoleacetic acid oxidase from tobacco roots. Plant Physiol 41(7):1200–120810.1104/pp.41.7.1200 ↗
28. Ma C, Liu H, Guo H, Musante C, Coskun SH, Nelson BC, White JC, Xing B, Dhankher OP (2016) Defense mechanisms and nutrient displacement in Arabidopsis thaliana upon exposure to CeO2 and In2O3 nanoparticles. Environ Sci Nano 3(6):1369–137910.1039/C6EN00189K ↗
29. Bates LS, Waldren RP, Teare ID (1973) Rapid determination of free proline for water-stress studies. Plant Soil 39(1):205–20710.1007/BF00018060 ↗
30. Zhang M, Zhao L, Du F, Wu Y, Cai R, Xu L, Jin H, Zou S, Gong A, Du F (2019) Facile synthesis of cerium-doped carbon quantum dots as a highly efficient antioxidant for free radical scavenging. Nanot 30(32):32510110.1088/1361-6528/ab12ef ↗
31. Deshpande S, Patil S, Kuchibhatla SVNT, Seal S (2005) Size dependency variation in lattice parameter and valency states in nanocrystalline cerium oxide. ApPhL 87(13):133113
32. Zou S, Guo F, Wu L, Ju H, Sun M, Cai R, Xu L, Gong Y, Gong A, Zhang M (2020) One-pot synthesis of cerium and praseodymium co-doped carbon quantum dots as enhanced antioxidant for hydroxyl radical scavenging. Nanot 31(16):16510110.1088/1361-6528/ab5b40 ↗
33. Parida AK, Das AB (2005) Salt tolerance and salinity effects on plants: a review. Ecotoxicol Environ Saf 60(3):324–34910.1016/j.ecoenv.2004.06.010 ↗
34. Odukoya O, Sofidiya M, Ilori O, Gbededo M, Ajadotuigwe J, Olaleye O, Bouskela E, Cyrino F, Marcelon G, Brinkhaus B (1994) Malondialdehyde determination as index of lipid peroxidation. Int J Biol Chem 3:281–285
35. Wang Y, Ding M, Gu X, Wang J, Pang Y, Gao L, Xia T (2013) Analysis of interfering substances in the measurement of Malondialdehyde content in plant leaves. Am J Biochem Biotechnol 9(3):235–24210.3844/ajbbsp.2013.235.242 ↗
36. Wu H, Tito N, Giraldo JP (2017) Anionic cerium oxide nanoparticles protect plant photosynthesis from abiotic stress by scavenging reactive oxygen species. ACS Nano 11(11):11283–1129710.1021/acsnano.7b05723 ↗
37. Wu H, Shabala L, Shabala S, Giraldo JP (2018) Hydroxyl radical scavenging by cerium oxide nanoparticles improves Arabidopsis salinity tolerance by enhancing leaf mesophyll potassium retention. Environ Sci Nano 5(7):1567–158310.1039/C8EN00323H ↗
38. Ellouzi H, Sghayar S, Abdelly C (2017) H2O2 seed priming improves tolerance to salinity; drought and their combined effect more than mannitol in Cakile maritima when compared to Eutrema salsugineum. J Plant Physiol 210:38–5010.1016/j.jplph.2016.11.014 ↗
39. Özdemir F, Bor M, Demiral T, Türkan İ (2004) Effects of 24-epibrassinolide on seed germination, seedling growth, lipid peroxidation, proline content and antioxidative system of rice (Oryza sativa L.) under salinity stress. Plant growth regulation 42(3): 203–211.10.1023/B:GROW.0000026509.25995.13 ↗
40. Latef AAHA, Alhmad MFA, Abdelfattah KE (2017) The possible roles of priming with ZnO nanoparticles in mitigation of salinity stress in lupine (Lupinus termis) plants. J Plant Growth Regul 36(1):60–7010.1007/s00344-016-9618-x ↗
41. Paparella S, Araújo SS, Rossi G, Wijayasinghe M, Carbonera D, Balestrazzi A (2015) Seed priming: state of the art and new perspectives. Plant Cell Rep 34(8):1281–129310.1007/s00299-015-1784-y ↗
42. Ibrahim EA (2016) Seed priming to alleviate salinity stress in germinating seeds. J Plant Physiol 192:38–4610.1016/j.jplph.2015.12.011 ↗
43. Krishnaraj C, Jagan E G, Ramachandran R, Abirami S M, Mohan N, Kalaichelvan P T (2012) Effect of biologically synthesized silver nanoparticles on Bacopa monnieri (Linn.) Wettst. plant growth metabolism. Process Biochem. 47(4): 651–658.10.1016/j.procbio.2012.01.006 ↗
44. Larue C, Castillo-Michel H, Sobanska S, Cécillon L, Bureau S, Barthes V, Ouerdane L, Carrière M, Sarret G (2014) Foliar exposure of the crop Lactuca sativa to silver nanoparticles: evidence for internalization and changes in Ag speciation. J Hazard Mater 264:98–10610.1016/j.jhazmat.2013.10.053 ↗
45. Delauney AJ, Verma DPS (1993) Proline biosynthesis and osmoregulation in plants. PlJ 4(2):215–223
46. Kiyosue T, Yoshiba Y, Yamaguchi-Shinozaki K, Shinozaki K (1996) A nuclear gene encoding mitochondrial proline dehydrogenase, an enzyme involved in proline metabolism, is upregulated by proline but downregulated by dehydration in Arabidopsis. Plant Cell 8(8):1323–1335
47. Strizhov N, Ábrahám E, Ökrész L, Blickling S, Zilberstein A, Schell J, Koncz C, Szabados L (1997) Differential expression of two P5CS genes controlling proline accumulation during salt-stress requires ABA and is regulated by ABA1, ABI1 and AXR2 in Arabidopsis. PlJ 12(3):557–569
48. Lutts S, Majerus V, Kinet JM (1999) NaCl effects on proline metabolism in rice (Oryza sativa) seedlings. Physiol Plant 105(3):450–45810.1034/j.1399-3054.1999.105309.x ↗
49. Markiewicz B, Sajnóg A, Lorenc W, Hanć A, Komorowicz I, Suliburska J, Kocyłowski R, Barałkiewicz D (2017) Multielemental analysis of 18 essential and toxic elements in amniotic fluid samples by ICP-MS: Full procedure validation and estimation of measurement uncertainty. Talanta 174:122–13010.1016/j.talanta.2017.05.078 ↗
50. Tokalıoğlu Ş (2012) Determination of trace elements in commonly consumed medicinal herbs by ICP-MS and multivariate analysis. Food Chem 134(4):2504–250810.1016/j.foodchem.2012.04.093 ↗
51. Carpita N, Sabularse D, Montezinos D, Delmer DP (1979) Determination of the pore size of cell walls of living plant cells. Sci 205(4411):1144–114710.1126/science.205.4411.1144 ↗
52. Li J, Hu J, Ma C, Wang Y, Wu C, Huang J, Xing B (2016) Uptake, translocation and physiological effects of magnetic iron oxide (γ-Fe2O3) nanoparticles in corn (Zea mays L.). Chemosphere 159:326–33410.1016/j.chemosphere.2016.05.083 ↗
53. Scott P, Physiology and behaviour of plants, John Wiley & Sons2013.
54. Navarro DA, Bisson MA, Aga DS (2012) Investigating uptake of water-dispersible CdSe/ZnS quantum dot nanoparticles by Arabidopsis thaliana plants. J Hazard Mater 211:427–43510.1016/j.jhazmat.2011.12.012 ↗
55. Annie RW, Xu H, Dixon J, Zoraida PA (2009) Observation of uptake and distribution of quantum dots in plants. MRS Online Proc Libr 1209(1):1–6
56. Geisler-Lee J, Brooks M, Gerfen JR, Wang Q, Fotis C, Sparer A, Ma X, Berg RH, Geisler M (2014) Reproductive toxicity and life history study of silver nanoparticle effect, uptake and transport in Arabidopsis thaliana. Nanomaterials 4(2):301–31810.3390/nano4020301 ↗
57. Li W, Zheng Y, Zhang H, Liu Z, Su W, Chen S, Liu Y, Zhuang J, Lei B (2016) Phytotoxicity, uptake, and translocation of fluorescent carbon dots in mung bean plants. ACS Appl Mater Interfaces 8(31):19939–1994510.1021/acsami.6b07268 ↗
58. Tripathi DK, Tripathi A, Singh S, Singh Y, Vishwakarma K, Yadav G, Sharma S, Singh VK, Mishra RK, Upadhyay RG (2017) Uptake, accumulation and toxicity of silver nanoparticle in autotrophic plants, and heterotrophic microbes: a concentric review. Front Microbiol 8:710.3389/fmicb.2017.00007 ↗
59. Rossi L, Zhang W, Lombardini L, Ma X (2016) The impact of cerium oxide nanoparticles on the salt stress responses of Brassica napus L. Environ Pollut 219:28–3610.1016/j.envpol.2016.09.060 ↗
60. Gonzalez Gomez H, Ramirez Godina F, Ortega Ortiz H, Benavides Mendoza A, Robledo Torres V, Cabrera De la Fuente M (2017) Use of chitosan-PVA hydrogels with copper nanoparticles to improve the growth of grafted watermelon. Molecules 22(7):103110.3390/molecules22071031 ↗
61. Kim J-H, Oh Y, Yoon H, Hwang I, Chang Y-S (2015) Iron nanoparticle-induced activation of plasma membrane H+-ATPase promotes stomatal opening in Arabidopsis thaliana. Environ Sci Technol 49(2):1113–111910.1021/es504375t ↗