Abstract
Biofilm formation on biotic or abiotic surfaces has unwanted consequences in medical, clinical, and industrial settings. Treatments with antibiotics or biocides are often ineffective in eradicating biofilms. Promising alternatives to conventional agents are biofilm-inhibiting compounds regulating biofilm development without toxicity to growth. Here, we screened a biofilm inhibitor, raffinose, derived from ginger. Raffinose, a galactotrisaccharide, showed efficient biofilm inhibition of Pseudomonas aeruginosa without impairing its growth. Raffinose also affected various phenotypes such as colony morphology, matrix formation, and swarming motility. Binding of raffinose to a carbohydrate-binding protein called LecA was the cause of biofilm inhibition and altered phenotypes. Furthermore, raffinose reduced the concentration of the second messenger, cyclic diguanylate (c-di-GMP), by increased activity of a c-di-GMP specific phosphodiesterase. The ability of raffinose to inhibit P. aeruginosa biofilm formation and its molecular mechanism opens new possibilities for pharmacological and industrial applications.
Original language | English |
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Article number | 25318 |
Journal | Scientific reports |
Volume | 6 |
DOIs | |
Publication status | Published - 2016 May 4 |
Bibliographical note
Funding Information:We would like to thank Professor You-Hee Cho in Cha University for kindly providing PA14 mutants (ΔwspF and ΔlecA), and Joo Hee Chung for performing HPLC analysis and Dr. Eunha Hwang for performing ITC experiments at the Korea Basic Science Institute. In addition, we sincerely thank Professor Arnold Demain in Drew University for critical reading of the manuscript and his advice. This research was funded by National Research Foundation of Korea grants (2015R1D1A1A09057657 and 2014R1A4A1007304).
Publisher Copyright:
© 2016, Nature Publishing Group. All rights reserved.
ASJC Scopus subject areas
- General