Essential Role of Acyl-ACP Synthetase in Acclimation of the Cyanobacterium Synechococcus elongatus Strain PCC 7942 to High-Light Conditions

Plant Cell Physiol. 2015 Aug;56(8):1608-15. doi: 10.1093/pcp/pcv086. Epub 2015 Jun 10.


Most organisms capable of oxygenic photosynthesis have an aas gene encoding an acyl-acyl carrier protein synthetase (Aas), which activates free fatty acids (FFAs) via esterification to acyl carrier protein. Cyanobacterial aas mutants are often used for studies aimed at photosynthetic production of biofuels because the mutation leads to intracellular accumulation of FFAs and their secretion into the external medium, but the physiological significance of the production of FFAs and their recycling involving Aas has remained unclear. Using an aas-deficient mutant of Synechococcus elongatus strain PCC 7942, we show here that remodeling of membrane lipids is activated by high-intensity light and that the recycling of FFAs is essential for acclimation to high-light conditions. Unlike wild-type cells, the mutant cells could not increase their growth rate as the light intensity was increased from 50 to 400 µmol photons m(-2) s(-1), and the high-light-grown mutant cells accumulated FFAs and the lysolipids derived from all the four major classes of membrane lipids, revealing high-light-induced lipid deacylation. The high-light-grown mutant cells showed much lower PSII activity and Chl contents as compared with the wild-type cells or low-light-grown mutant cells. The loss of Aas accelerated photodamage of PSII but did not affect the repair process of PSII, indicating that PSII is destabilized in the mutant. Thus, Aas is essential for acclimation of the cyanobacterium to high-light conditions. The relevance of the present finding s to biofuel production using cyanobacteria is discussed.

Keywords: Acyl-ACP synthetase; Biofuel production; Cyanobacteria; High-light acclimation; Photoinhibition of PSII.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acclimatization
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Carbon-Sulfur Ligases / genetics
  • Carbon-Sulfur Ligases / metabolism*
  • Fatty Acids, Nonesterified / metabolism
  • Light
  • Membrane Lipids / metabolism
  • Mutation
  • Photosynthesis / physiology
  • Photosynthesis / radiation effects
  • Photosystem II Protein Complex / physiology
  • Photosystem II Protein Complex / radiation effects
  • Synechococcus / enzymology*
  • Synechococcus / genetics
  • Synechococcus / physiology
  • Synechococcus / radiation effects


  • Bacterial Proteins
  • Fatty Acids, Nonesterified
  • Membrane Lipids
  • Photosystem II Protein Complex
  • Carbon-Sulfur Ligases
  • long-chain-fatty-acid-(acyl-carrier-protein) ligase