| Literature DB >> 32949024 |
Ning Zhang1, Yong-Gang Chang1,2, Roger Tseng1,3, Sergey Ovchinnikov4, Rakefet Schwarz5, Andy LiWang1,6,7.
Abstract
Biofilms are accumulations of microorganisms embedded in extracellular matrices that protect against external factors and stressful environments. Cyanobacterial biofilms are ubiquitous and have potential for treatment of wastewater and sustainable production of biofuels. But the underlying mechanisms regulating cyanobacterial biofilm formation are unclear. Here, we report the solution NMR structure of a protein, Se0862, conserved across diverse cyanobacterial species and involved in regulation of biofilm formation in the cyanobacterium Synechococcus elongatus PCC 7942. Se0862 is a class α+β protein with ααββββαα topology and roll architecture, consisting of a four-stranded β-sheet that is flanked by four α-helices on one side. Conserved surface residues constitute a hydrophobic pocket and charged regions that are likely also present in Se0862 orthologs.Entities:
Keywords: NMR spectroscopy; S. elongatus PCC 7942; biofilm; cyanobacteria; protein structure
Year: 2020 PMID: 32949024 PMCID: PMC7586914 DOI: 10.1002/pro.3952
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725