A nanopore array in the septal peptidoglycan hosts gated septal junctions for cell-cell communication in multicellular cyanobacteria

Int J Med Microbiol. 2019 Dec;309(8):151303. doi: 10.1016/j.ijmm.2019.03.007. Epub 2019 Mar 26.

Abstract

Some filamentous cyanobacteria are phototrophic bacteria with a true multicellular life style. They show patterned cell differentiation with the distribution of metabolic tasks between different cell types. This life style requires a system of cell-cell communication and metabolite exchange along the filament. During our study of the cell wall of species Nostoc punctiforme and Anabaena sp. PCC 7120 we discovered regular perforations in the septum between neighboring cells, which we called nanopore array. AmiC-like amidases are drilling the nanopores with a diameter of 20 nm, and are essential for communication and cell differentiation. NlpD-like regulators of AmiC activity and septum localized proteins SepJ, FraC and FraD are also involved in correct nanopore formation. By focused ion beam (FIB) milling and electron cryotomography we could visualize the septal junctions, which connect adjacent cells and pass thru the nanopores. They consist of cytoplasmic caps, which are missing in the fraD mutant, a plug inside the cytoplasmic membrane and a tube like conduit. A destroyed membrane potential and other stress factors lead to a conformational change in the cap structure and loss of cell-cell communication. These gated septal junctions of cyanobacteria are ancient structures that represent an example of convergent evolution, predating metazoan gap junctions.

Keywords: Amidase; Cell-cell communication; Filamentous cyanobacterium; Gated septal junctions; Nanopore; Nostoc.

Publication types

  • Review

MeSH terms

  • Amidohydrolases / metabolism
  • Anabaena / cytology*
  • Anabaena / enzymology
  • Cell Communication*
  • Gene Expression Regulation, Bacterial
  • Nanopores*
  • Nostoc / cytology*
  • Nostoc / enzymology
  • Peptidoglycan / metabolism*
  • Tight Junctions / metabolism

Substances

  • Peptidoglycan
  • Amidohydrolases