4.7 Article

Acute cadmium toxicity and post-stress recovery: Insights into coordinated and integrated response/recovery strategies of Anabaena sp. PCC 7120

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 411, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2020.124822

Keywords

Acute Cd stress; BN-SDS PAGE; Cd chelators and efflux transporters; Cyclic electron flow; IEF-SDS PAGE

Funding

  1. Department of Science and Technology-Innovation of Science Pursuit for Inspire Research (DST-INSPIRE) fellowship, New Delhi, India
  2. Council of Scientific & Industrial Research (CSIR), New Delhi, India
  3. University Grant Commission (UGC), New Delhi, India

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The study revealed that acute Cd stress induced Cd accumulation and ROS production in Anabaena cells, leading to reduced photosynthetic efficiency. During post-stress recovery, Anabaena reprogrammed the expression pattern of proteins/genes involved in cellular defense and repair in a coordinated manner, facilitating detoxification of Cd and repair of cellular damage.
Cyanobacteria, the first photoautotrophs have remarkable adaptive capabilities against most abiotic stresses, including Cd. A model cyanobacterium, Anabaena sp. PCC 7120 has been commonly used to understand cyanobacterial plasticity under different environmental stresses. However, very few studies have focused on the acute Cd toxicity. In this context, Anabaena was subjected to 100 ?M Cd for 48 h (acute Cd stress, ACdS) and then transferred into the fresh medium for post-stress recovery (PSR). We further investigated the dynamics of morpho-ultrastructure, physiology, cytosolic proteome, thylakoidal complexes, chelators, and transporters after ACdS, as well as during early (ER), mid (MR), and late (LR) phases of PSR. The findings revealed that ACdS induced intracellular Cd accumulation and ROS production, altered morpho-ultrastructure, reduced photosynthetic pigments, and affected the structural organization of PSII, which subsequently hindered photosynthetic efficiency. Anabaena responded to ACdS and recovered during PSR by reprogramming the expression pattern of proteins/genes involved in cellular defense and repair; CO2 access, Calvin-Benson cycle, glycolysis, and pentose phosphate pathway; protein biosynthesis, folding, and degradation; regulatory functions; PSI-based cyclic electron flow; Cd chelation; and efflux. These modulations occurred in an integrated and coordinated manner that facilitated Anabaena to detoxify Cd and repair ACdS-induced cellular damage.

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