Unit

You have free access to this content

UNIT 1B.1 Growing and Analyzing Static Biofilms

  1. Judith H. Merritt1,
  2. Daniel E. Kadouri2,
  3. George A. O'Toole3

Published Online: 1 AUG 2011

DOI: 10.1002/9780471729259.mc01b01s22

Current Protocols in Microbiology

Current Protocols in Microbiology

How to Cite

Merritt, J. H., Kadouri, D. E. and O'Toole, G. A. 2011. Growing and Analyzing Static Biofilms. Current Protocols in Microbiology. 22:B:1B.1:1B.1.1–1B.1.18.

Author Information

  1. 1

    Glycobia Inc., Ithaca, New York

  2. 2

    University of Medicine and Dentistry of New Jersey, Newark, New Jersey

  3. 3

    Dartmouth Medical School, Hanover, New Hampshire

Publication History

  1. Published Online: 1 AUG 2011
  2. Published Print: AUG 2011
Table 1B.1.1. Typical Conditions for Developing and Performing Microtiter Plate Biofilm Assays
OrganismIncubation temperature (°C)Solvent for solubilization of stained biofilmsReference
Agrobacterium tumefaciens28100% dimethyl sulfoxide (DMSO)Danhorn et al., 2004
Escherichia coli2580% ethanol/20% acetoneO'Toole et al., 1999
Pseudomonas aeruginosa25-3795% ethanolO'Toole et al., 1999
Pseudomonas aeruginosa25-3730% acetic acidZegans et al., 2009
Pseudomonas fluorescens25-3095% ethanolO'Toole et al., 1999
Staphylococcus aureus3733% glacial acetic acidStepanovic et al., 2001
Streptococcus mutans3795% ethanol or 100% DMSOO'Toole et al., 1999
Vibrio cholerae25-30100% DMSOO'Toole et al., 1999