Difference between revisions of "Biofilm formation"
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==Labs working on biofilm formation== | ==Labs working on biofilm formation== | ||
* [[Daniel Kearns]] | * [[Daniel Kearns]] | ||
| + | * [[Roberto Kolter]] | ||
* [[Oscar Kuipers]] | * [[Oscar Kuipers]] | ||
* [[Beth Lazazzera]] | * [[Beth Lazazzera]] | ||
* [[Richard Losick]] | * [[Richard Losick]] | ||
* [[Nicola Stanley-Wall]] | * [[Nicola Stanley-Wall]] | ||
| + | * [[Jörg Stülke]] | ||
==Key genes and operons involved in biofilm formation== | ==Key genes and operons involved in biofilm formation== | ||
Revision as of 22:12, 10 February 2012
Biofilms are the result of the multicellular lifestyle of B. subtilis. They are characterized by the formation of a matrix polysaccharide and an amyloid-like protein, TasA. Correction of sfp, epsC, swrAA, and degQ as well as introduction of rapP from a plasmid present in NCIB3610 results in biofilm formation in B. subtilis 168 PubMed.
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Contents
Biofilm formation in SubtiPathways
Labs working on biofilm formation
- Daniel Kearns
- Roberto Kolter
- Oscar Kuipers
- Beth Lazazzera
- Richard Losick
- Nicola Stanley-Wall
- Jörg Stülke
Key genes and operons involved in biofilm formation
- matrix polysaccharide synthesis:
- amyloid protein synthesis, secretion and assembly
- regulation
- biofilm disassembly
- other proteins required for biofilm formation
Important original publications
Key reviews
Additional reviews: PubMed
