4.6 Article

A new easy method for determination of surface adhesion of phototrophic biofilms

Journal

BIOTECHNOLOGY AND BIOENGINEERING
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1002/bit.28536

Keywords

adhesion; flow chamber; optical coherence tomography; phototrophic biofilms; rotational rheometer

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An easy-to-implement method for analyzing biofilm adhesion was developed using a flow chamber combined with optical coherence tomography and computational fluid dynamics simulation. The cultivation time of the biofilms was found to be positively correlated with adhesion strength. The role of extracellular polymeric substances in surface adhesion was evaluated. The comparability of results obtained from the flow chamber with other methods was successfully tested using a rotational rheometer.
Terrestrial cyanobacteria grow as phototrophic biofilms and offer a wide spectrum of interesting products. For cultivation of phototrophic biofilms different reactor concepts have been developed in the last years. One of the main influencing factors is the surface material and the adhesion strength of the chosen production strain. In this work a flow chamber was developed, in which, in combination with optical coherence tomography and computational fluid dynamics simulation, an easy analysis of adhesion forces between different biofilms and varied surface materials is possible. Hereby, differences between two cyanobacteria strains and two surface materials were shown. With longer cultivation time of biofilms adhesion increased in all experiments. Additionally, the content of extracellular polymeric substances was analyzed and its role in surface adhesion was evaluated. To test the comparability of obtained results from the flow chamber with other methods, analogous experiments were conducted with a rotational rheometer, which proved to be successful. Thus, with the presented flow chamber an easy to implement method for analysis of biofilm adhesion was developed, which can be used in future research for determination of suitable combinations of microorganisms with cultivation surfaces on lab scale in advance of larger processes.

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