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      Dispersing biofilms with engineered enzymatic bacteriophage.

      Proceedings of the National Academy of Sciences of the United States of America
      Bacteriophage T3, enzymology, genetics, Bacteriophage T7, Biofilms, growth & development, Escherichia coli, physiology, virology, Extracellular Matrix, Genetic Engineering, methods

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          Abstract

          Synthetic biology involves the engineering of biological organisms by using modular and generalizable designs with the ultimate goal of developing useful solutions to real-world problems. One such problem involves bacterial biofilms, which are crucial in the pathogenesis of many clinically important infections and are difficult to eradicate because they exhibit resistance to antimicrobial treatments and removal by host immune systems. To address this issue, we engineered bacteriophage to express a biofilm-degrading enzyme during infection to simultaneously attack the bacterial cells in the biofilm and the biofilm matrix, which is composed of extracellular polymeric substances. We show that the efficacy of biofilm removal by this two-pronged enzymatic bacteriophage strategy is significantly greater than that of nonenzymatic bacteriophage treatment. Our engineered enzymatic phage substantially reduced bacterial biofilm cell counts by approximately 4.5 orders of magnitude ( approximately 99.997% removal), which was about two orders of magnitude better than that of nonenzymatic phage. This work demonstrates the feasibility and benefits of using engineered enzymatic bacteriophage to reduce bacterial biofilms and the applicability of synthetic biology to an important medical and industrial problem.

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          Author and article information

          Journal
          17592147
          1899193
          10.1073/pnas.0704624104

          Chemistry
          Bacteriophage T3,enzymology,genetics,Bacteriophage T7,Biofilms,growth & development,Escherichia coli,physiology,virology,Extracellular Matrix,Genetic Engineering,methods

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