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FusC, a member of the M16 protease family acquired by bacteria for iron piracy against plants
- Source :
- PLoS Biology, PLoS Biology, Vol 16, Iss 8, p e2006026 (2018)
- Publication Year :
- 2018
- Publisher :
- Public Library of Science (PLoS), 2018.
-
Abstract
- Iron is essential for life. Accessing iron from the environment can be a limiting factor that determines success in a given environmental niche. For bacteria, access of chelated iron from the environment is often mediated by TonB-dependent transporters (TBDTs), which are β-barrel proteins that form sophisticated channels in the outer membrane. Reports of iron-bearing proteins being used as a source of iron indicate specific protein import reactions across the bacterial outer membrane. The molecular mechanism by which a folded protein can be imported in this way had remained mysterious, as did the evolutionary process that could lead to such a protein import pathway. How does the bacterium evolve the specificity factors that would be required to select and import a protein encoded on another organism’s genome? We describe here a model whereby the plant iron–bearing protein ferredoxin can be imported across the outer membrane of the plant pathogen Pectobacterium by means of a Brownian ratchet mechanism, thereby liberating iron into the bacterium to enable its growth in plant tissues. This import pathway is facilitated by FusC, a member of the same protein family as the mitochondrial processing peptidase (MPP). The Brownian ratchet depends on binding sites discovered in crystal structures of FusC that engage a linear segment of the plant protein ferredoxin. Sequence relationships suggest that the bacterial gene encoding FusC has previously unappreciated homologues in plants and that the protein import mechanism employed by the bacterium is an evolutionary echo of the protein import pathway in plant mitochondria and plastids.<br />Author summary Earth’s carbon cycle depends on saprophytic microbes to rot old or diseased plant matter and recycle carbon from that biomass. Some bacteria (phytopathogens) have evolved to cause disease and rot in even healthy plants and may have utility as biological control agents against noxious weeds. To understand the mechanisms driving each of these scenarios has significance in environmental engineering and agriculture. Access to iron is a limiting factor for bacteria-mediated plant rot. Here, we show how a plant-pathogenic bacteria has reevolved a mechanism, analogous to the protein import pathways that evolved in plant plastids and mitochondria, to import the plant iron–bearing protein ferredoxin from plant tissue. The study is based on structural and biophysical characterization of a key M16 family protease, FusC, resident inside the bacterial outer membrane.
- Subjects :
- 0106 biological sciences
0301 basic medicine
Cell Membranes
Pectobacterium
Markov models
Plant Science
Biochemistry
01 natural sciences
Small-Angle Scattering
Scattering
Hidden Markov models
Biology (General)
Ferredoxin
Phylogeny
Plant Proteins
2. Zero hunger
Crystallography
Plant Bacterial Pathogens
Membrane transport protein
Physics
General Neuroscience
food and beverages
Metalloendopeptidases
Proteases
Plants
Condensed Matter Physics
Enzymes
Cell biology
Transport protein
Protein Transport
Plant protein
Physical Sciences
Crystal Structure
Ferredoxins
Cellular Structures and Organelles
General Agricultural and Biological Sciences
Bacterial outer membrane
Research Article
Bacterial Outer Membrane Proteins
Mitochondrial processing peptidase
Protein family
QH301-705.5
Materials by Structure
Iron
Materials Science
Plant Pathogens
Biology
Crystals
General Biochemistry, Genetics and Molecular Biology
03 medical and health sciences
Bacterial Proteins
Solid State Physics
Plastid
General Immunology and Microbiology
Bacteria
fungi
Biology and Life Sciences
Proteins
Membrane Proteins
Membrane Transport Proteins
Probability theory
Cell Biology
Plant Pathology
Outer Membrane Proteins
030104 developmental biology
Enzymology
biology.protein
Mathematics
010606 plant biology & botany
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- PLoS Biology, PLoS Biology, Vol 16, Iss 8, p e2006026 (2018)
- Accession number :
- edsair.doi.dedup.....fcd2c409ebdc1da15815e094507cb682