The use of glycopolymer-functionalized resins (Resin-Glc), as a solid support, in column mode for bacterial/protein capture and quantification is explored. The Resin-Glc is synthesized from commercially available chloromethylated polystyrene resin and glycopolymer, and is characterized by fourier transform infrared spectroscopy, thermogravimetry, and elemental analysis. The percentage of glycopolymer functionalized on Resin-Glc is accounted to be 5 wt%. The ability of Resin-Glc to selectively capture lectin, Concanavalin A, over Peanut Agglutinin, reversibly, is demonstrated for six cycles of experiments. The bacterial sequestration study using SYBR (Synergy Brands, Inc.) Green I tagged Escherichia coli/Staphylococcus aureus reveals the ability of Resin-Glc to selectively capture E. coli over S. aureus. The quantification of captured cells in the column is carried out by enzymatic colorimetric assay using methylumbelliferyl glucuronide as the substrate. The E. coli capture studies reveal a consistent capture efficiency of 10 CFU (Colony Forming Units) g over six cycles. Studies with spiked tap water samples show satisfactory results for E. coli cell densities ranging from 10 to 10 CFU mL . The method portrayed can serve as a basis for the development of a reusable solid support in capture and detection of proteins and bacteria.
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http://dx.doi.org/10.1002/mabi.202000342 | DOI Listing |
Macromol Biosci
March 2021
Bio-Organic Division, Bhabha Atomic Research Centre, Trombay, Mumbai, 400085, India.
The use of glycopolymer-functionalized resins (Resin-Glc), as a solid support, in column mode for bacterial/protein capture and quantification is explored. The Resin-Glc is synthesized from commercially available chloromethylated polystyrene resin and glycopolymer, and is characterized by fourier transform infrared spectroscopy, thermogravimetry, and elemental analysis. The percentage of glycopolymer functionalized on Resin-Glc is accounted to be 5 wt%.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2020
Department of Chemistry & Biochemistry, University of California Los Angeles, Los Angeles, California 90095, United States.
Using glycopolymer surfaces, we have stimulated bacterial colonization and induced where the bacteria attach on a molecular pattern. When adherent bacteria were rinsed with methyl α-d-mannopyranoside, the glycopolymer-functionalized surfaces retained more cells than self-assembled monolayers terminated by a single mannose unit. These results suggest that the three-dimensional multivalency of the glycopolymers both promotes and retains bacterial attachment.
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