A transporter Slr1512 involved in bicarbonate and pH-dependent acclimation mechanism to high light stress in Synechocystis sp. PCC 6803

Biochim Biophys Acta Bioenerg. 2021 Jan 1;1862(1):148336. doi: 10.1016/j.bbabio.2020.148336. Epub 2020 Nov 9.

Abstract

High light (HL) exposure leads to photoinhibition and excess accumulation of toxic reactive oxygen species (ROS) in photosynthetic organisms, negatively impacting the global primary production. In this study, by screening a mutant library, a gene related with bicarbonate transport, slr1512, was found involved in HL acclimation in model cyanobacterium Synechocystis sp. PCC 6803. Comparative growth analysis showed that the slr1512 knockout mutant dramatically enhanced the tolerance of Synechocystis towards long-term HL stress (200 μmol photons m-2 s-1) than the wild type, achieving an enhanced growth by ~1.95-folds after 10 d. The phenotype differences between Δslr1512 and the wild type were analyzed via absorption spectrum and chlorophyll a content measurement. In addition, the accessible bicarbonate controlled by slr1512 and decreased PSII activity were demonstrated, and they were found to be the key factors affecting the tolerance of Synechocystis against HL stress. Further analysis confirmed that intracellular bicarbonate can significantly affect the activity of photosystem II, leading to the altered accumulation of toxic ROS under HL. Finally, a comparative transcriptomics was applied to determine the differential responses to HL between Δslr1512 and the wild type. This work provides useful insights to long-term acclimation mechanisms towards HL and valuable information to guide the future tolerance engineering of cyanobacteria against HL.

Keywords: Bicarbonate transport; Cyanobacteria; High light stress; PSII electron transport; Synechocystis sp. PCC 6803; Transcriptomics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acclimatization*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Bicarbonates / metabolism*
  • Chlorophyll A / genetics
  • Chlorophyll A / metabolism
  • Gene Expression Regulation, Bacterial
  • Hydrogen-Ion Concentration
  • Light*
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism*
  • Stress, Physiological*
  • Synechocystis / genetics
  • Synechocystis / metabolism*

Substances

  • Bacterial Proteins
  • Bicarbonates
  • Membrane Transport Proteins
  • Chlorophyll A