A joint project of the Graduate School, Peabody College, and the Jean & Alexander Heard Library

Title page for ETD etd-11302011-163338

Type of Document Master's Thesis
Author Schroeder, Kaitlin Alayna
URN etd-11302011-163338
Title Examining the Efficacy of Antibiotics and the Proteomic Response in the Treatment of Staphylococcus aureus Biofilms Grown In-Vitro.
Degree Master of Science
Department Chemistry
Advisory Committee
Advisor Name Title
Richard Caprioli Committee Chair
Eric Skaar Committee Co-Chair
  • Mass spectrometry
  • Biofilms
  • Staphylococcus aureus
  • Chemistry
Date of Defense 2011-12-02
Availability unrestricted
The proteomic response of Staphylococcus aureus bacteria in a biofilm is examined using MALDI Imaging Mass Spectrometry (IMS) and Liquid-Chromatography Tandem Mass Spectrometry (LC-MS/MS). S. aureus biofilms grown in-vitro and exposed to ampicillin were imaged in order to demonstrate the diffusion pattern of the antibiotic treatment as well as the molecular response of the bacteria. Identification of defensive bacterial proteins resulted in relative quantitation of penicillin-binding proteins (PBPs), cell division proteins, general stress proteins, and methicillin resistance factors across six sections taken from S. aureus biofilm.

Quantitation and identification of said proteins suggest that S. aureus bacteria grown in a biofilm up-regulate methicillin resistance factors and penicillin-binding protein 4 in regions exposed to the drug in an attempt to survive treatment. Cell division proteins as well as penicillin-binding protein 1 are up-regulated in unexposed regions of the film, likely due to cell-to-cell signaling which alerts them to the oncoming drug treatment.

  Filename       Size       Approximate Download Time (Hours:Minutes:Seconds) 
 28.8 Modem   56K Modem   ISDN (64 Kb)   ISDN (128 Kb)   Higher-speed Access 
  KaitlinAlaynaSchroeder120111.pdf 4.38 Mb 00:20:16 00:10:25 00:09:07 00:04:33 00:00:23

Browse All Available ETDs by ( Author | Department )

If you have more questions or technical problems, please Contact LITS.