Slr4, a newly identified S-layer protein from marine Gammaproteobacteria, is a major biofilm matrix component

Mol Microbiol. 2020 Dec;114(6):979-990. doi: 10.1111/mmi.14588. Epub 2020 Sep 15.

Abstract

S-layers are paracrystalline proteinaceous lattices that surround prokaryotic cells, forming a critical interface between the cells and their extracellular environment. Here, we report the discovery of a novel S-layer protein present in the Gram-negative marine organism, Pseudoalteromonas tunicata D2. An uncharacterized protein (EAR28894) was identified as the most abundant protein in planktonic cultures and biofilms. Bioinformatic methods predicted a beta-helical structure for EAR28894 similar to the Caulobacter S-layer protein, RsaA, despite sharing less than 20% sequence identity. Transmission electron microscopy revealed that purified EAR28894 protein assembled into paracrystalline sheets with a unique square lattice symmetry and a unit cell spacing of ~9.1 nm. An S-layer was found surrounding the outer membrane in wild-type cells and completely removed from cells in an EAR28894 deletion mutant. S-layer material also appeared to be "shed" from wild-type cells and was highly abundant in the extracellular matrix where it is associated with outer membrane vesicles and other matrix components. EAR28894 and its homologs form a new family of S-layer proteins that are widely distributed in Gammaproteobacteria including species of Pseudoalteromonas and Vibrio, and found exclusively in marine metagenomes. We propose the name Slr4 for this novel protein family.

Keywords: Pseudoalteromonas tunicata; S-layer; biofilms; extracellular matrix; marine bacteria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aquatic Organisms / genetics
  • Bacterial Outer Membrane Proteins / genetics
  • Bacterial Outer Membrane Proteins / isolation & purification
  • Bacterial Outer Membrane Proteins / ultrastructure
  • Biofilms*
  • Extracellular Polymeric Substance Matrix / metabolism
  • Membrane Glycoproteins / genetics*
  • Membrane Glycoproteins / isolation & purification
  • Membrane Glycoproteins / ultrastructure
  • Phylogeny
  • Protein Conformation
  • Pseudoalteromonas / genetics*

Substances

  • Bacterial Outer Membrane Proteins
  • Membrane Glycoproteins
  • S-layer proteins

Supplementary concepts

  • Pseudoalteromonas tunicata

Associated data

  • figshare/10.6084/m9.figshare.11993505.v1