4.7 Article

Influence of Cd toxicity on subcellular distribution, chemical forms, and physiological responses of cell wall components towards short-term Cd stress in Solanum nigrum

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 28, Issue 11, Pages 13955-13969

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-020-11505-5

Keywords

Cadmium; Solanum nigrum; Cell wall polysaccharides; Subcellular distribution; Chemical forms

Funding

  1. National Nature Science Foundations of China [31702003, 31902105]
  2. National Key Research and Development Program [2016YFD0800807, 2016YFD0800803]
  3. Young Elite Scientists Sponsorship Program by CAST [2017QNRC001]
  4. Chenguang Program - Shanghai Education Development Foundation [17CG07]
  5. Shanghai Municipal Education Commission [17CG07]
  6. China Postdoctoral Science Foundation [2019M651505]

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The study found that cadmium stress led to growth inhibition in Solanum nigrum plants and that cadmium was primarily accumulated in the cell wall of the plant. The results also showed that the percentage of cadmium concentration increased in different plant tissues and cell wall components, except for pectin and cellulose. Additionally, the activity of pectin methylesterase was significantly increased under cadmium stress, indicating the important role of cell wall components in cadmium fixation.
Solanum nigrum is a well-documented cadmium (Cd) hyperaccumulator; however, its Cd-induced tolerance capability and detoxification mechanism remain elusive. Hence, a short-term hydroponic experiment was performed in a multiplane glasshouse to determine the influence of Cd toxicity on subcellular distribution, chemical forms, and the physiological responses of cell wall towards Cd stress in a 4-week-old plant. The experiment was conducted following completely randomized design (CRD) with five treatments (n = 4 replicates). The results showed that Cd stress showed dose-dependent response towards growth inhibition. The subcellular distribution of Cd in S. nigrum was in the order of cell wall > soluble fractions > organelles, and Cd was predominantly extracted by 1 M NaCl (29.87 similar to 43.66%). The Cd contents in different plant tissues and cell wall components including pectin, hemicellulose 1 (HC1), hemicellulose 2 (HC2), and cellulose were increased with the increase in Cd concentrations; however, the percentage of Cd concentration decreased in pectin and cellulose. Results of the polysaccharide components such as uronic acid, total sugar contents, and pectin methylesterase (PME) activity showed Cd-induced dose-dependent increase relative to exposure Cd stress. The pectin methylesterase (PME) activity was significantly (p < 0.05) enhanced by 125.78% at 75 mu M Cd in root, 105.78% and 73.63% at 100 mu M Cd in stem and leaf, respectively. In addition, the esterification, amidation, and pectinase treatment of cell wall and Fourier transform infrared spectroscopy (FTIR) assay exhibited many functional groups that were involved in cell wall retention Cd, especially on carboxyl and hydroxyl groups of cell wall components that indicated that the -OH and -COOH groups of S. nigrum cell wall play a crucial role in Cd fixation. In summary, results of the current study will add a novel insight to understand mobilization/immobilization as well as detoxification mechanism of cadmium in S. nigrum.

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