4.7 Article

Leveraging Stereoelectronic Effects in Biofilm Eradication: Synthetic β-Amino Human Milk Oligosaccharides Impede Microbial Adhesion As Observed by Scanning Electron Microscopy

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 85, Issue 24, Pages 16128-16135

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.0c01958

Keywords

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Funding

  1. National Institutes of Health [R35GM133602, R01HD090061]
  2. College of Arts & Science at Vanderbilt University
  3. Cell Imaging Shared Resource at Vanderbilt University
  4. Vanderbilt Institute for Clinical and Translational Research program
  5. National Center for Research Resources [UL1 RR024975-01]
  6. National Center for Advancing Translational Sciences [2 UL1 TR000445-06]

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Alongside Edward, Lemieux was among the earliest researchers studying negative hyperconjugation (i.e., the anomeric effect) or the preference for gauche conformations about the C1-O5 bond in carbohydrates. Lemieux also studied an esoteric, if not controversial, theory known as the reverse anomeric effect (RAE). This theory is used to rationalize scenarios where predicted anomeric stabilization does not occur. One such example is the Kochetkov amination where reducing end amines exist solely as the beta-anomer. Herein, we provide a brief account of Lemieux's contributions to the field of stereoelectronics and apply this knowledge toward the synthesis of beta-amino human milk oligosaccharides (beta Alpha-HMOs). These molecules were evaluated for their ability to inhibit growth and biofilm production in Group B Streptococcus (GBS) and Staphylococcus aureus. While the parent HMOs lacked antimicrobial and antibiofilm activity, their beta-amino derivatives significantly inhibited biofilm formation in both species. Field emission gun-scanning single electron microscopy (FEG-SEM) revealed that treatment with beta-amino HMOs significantly inhibits bacterial adherence and eliminates the ability of both microbes to form biofilms.

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