4.4 Article

The siderophilic cyanobacterium Leptolyngbya sp strain JSC-1 acclimates to iron starvation by expressing multiple isiA-family genes

Journal

PHOTOSYNTHESIS RESEARCH
Volume 128, Issue 3, Pages 325-340

Publisher

SPRINGER
DOI: 10.1007/s11120-016-0257-7

Keywords

Cyanobacteria; Fe homeostasis; Photosystem; IsiA; Light harvesting; Supercomplexes

Categories

Funding

  1. National Science Foundation [MCB-1021725]
  2. Photosynthetic Antenna Research Center (PARC), an Energy Frontier Research Center - DOE, Office of Science, Office of Basic Energy Sciences [DE-SC 0001035]
  3. Direct For Biological Sciences
  4. Div Of Molecular and Cellular Bioscience [1021725] Funding Source: National Science Foundation

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In the evolution of different cyanobacteria performing oxygenic photosynthesis, the core complexes of the two photosystems were highly conserved. However, cyanobacteria exhibit significant diversification in their light-harvesting complexes and have flexible regulatory mechanisms to acclimate to changes in their growth environments. In the siderophilic, filamentous cyanobacterium, Leptolyngbya sp. strain JSC-1, five different isiA-family genes occur in two gene clusters. During acclimation to Fe limitation, relative transcript levels for more than 600 genes increased more than twofold. Relative transcript levels were similar to 250 to 300 times higher for the isiA1 gene cluster (isiA1-isiB-isiC), and similar to 440- to 540-fold for the isiA2-isiA3-isiA4-cpcG2-isiA5 gene cluster after 48 h of iron starvation. Chl-protein complexes were isolated and further purified from cells grown under Fe-replete and Fe-depleted conditions. A single class of particles, trimeric PSI, was identified by image analysis of electron micrographs of negatively stained PSI complexes from Fe-replete cells. However, three major classes of particles were observed for the Chl-protein supercomplexes from cells grown under iron starvation conditions. Based on LC-MS-MS analyses, the five IsiA-family proteins were found in the largest supercomplexes together with core components of the two photosystems; however, IsiA5 was not present in complexes in which only the core subunits of PSI were detected. IsiA5 belongs to the same clade as PcbC proteins in a phylogenetic classification, and it is proposed that IsiA5 is most likely involved in supercomplexes containing PSII dimers. IsiA4, which is a fusion of an IsiA domain and a C-terminal PsaL domain, was found together with IsiA1, IsiA2, and IsiA3 in complexes with monomeric PSI. The data indicate that horizontal gene transfer, gene duplication, and divergence have played important roles in the adaptive evolution of this cyanobacterium to iron starvation conditions.

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