Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Entrapment of Living Bacterial Cells in Low-Concentration Silica Materials Preserves Cell Division and Promoter Regulation

Eleftheriou, Nikolas LU ; Ge, Xin ; Kolesnik, Julia ; Falconer, Shannon B. ; Harris, Robert J. ; Khursigara, Cezar ; Brown, Eric D. and Brennan, John D. (2013) In Chemistry of Materials 25(23). p.4798-4805
Abstract
The entrapment of bacterial cells within inorganic silica materials was reported almost 20 years ago. However, almost all studies to date have shown that these entrapped cells are unable to divide and thus should be expected to have reduced promoter activity. In view of the importance of bacteria as model systems for both fundamental and applied biological studies, it is crucial that immobilized cells retain solutionlike properties, including the ability to divide and display normal promoter activity. Herein we report on a method to immobilize bacterial cells within low-density inorganic silica-based materials, where the cells retain both cell division and promoter activity. Sol gel processing was used to entrap Escherichia coli cells... (More)
The entrapment of bacterial cells within inorganic silica materials was reported almost 20 years ago. However, almost all studies to date have shown that these entrapped cells are unable to divide and thus should be expected to have reduced promoter activity. In view of the importance of bacteria as model systems for both fundamental and applied biological studies, it is crucial that immobilized cells retain solutionlike properties, including the ability to divide and display normal promoter activity. Herein we report on a method to immobilize bacterial cells within low-density inorganic silica-based materials, where the cells retain both cell division and promoter activity. Sol gel processing was used to entrap Escherichia coli cells carrying a variety of green fluorescent protein-linked promoters into sodium silicate-derived materials that were formed in microwell plates. Using a series of assays, we were able to demonstrate that (1) the entrapped cells can divide within the pores of the silica matrix, (2) cellular pathways are regulated in a similar manner in both solution and the sol-gel-derived materials, and (3) promoters in entrapped cells can be specifically induced with small molecules (e.g., antimicrobial compounds) in a concentration-dependent manner to allow assessment of both potency and mode of action. This solid-phase assay system was tested using multiple antimicrobial pathways and should enable the development of solid-phase assays for the discovery of new small molecules that are active against bacteria. (Less)
Please use this url to cite or link to this publication:
author
; ; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
encapsulation, sol-gel, biosensor, screening, green fluorescent protein, silica, cell entrapment
in
Chemistry of Materials
volume
25
issue
23
pages
4798 - 4805
publisher
The American Chemical Society (ACS)
external identifiers
  • wos:000328437300020
  • scopus:84890408463
ISSN
0897-4756
DOI
10.1021/cm403198z
language
English
LU publication?
yes
id
18a96809-2922-4a86-89a2-873c781983a9 (old id 4272366)
date added to LUP
2016-04-01 10:38:29
date last changed
2022-04-12 08:14:23
@article{18a96809-2922-4a86-89a2-873c781983a9,
  abstract     = {{The entrapment of bacterial cells within inorganic silica materials was reported almost 20 years ago. However, almost all studies to date have shown that these entrapped cells are unable to divide and thus should be expected to have reduced promoter activity. In view of the importance of bacteria as model systems for both fundamental and applied biological studies, it is crucial that immobilized cells retain solutionlike properties, including the ability to divide and display normal promoter activity. Herein we report on a method to immobilize bacterial cells within low-density inorganic silica-based materials, where the cells retain both cell division and promoter activity. Sol gel processing was used to entrap Escherichia coli cells carrying a variety of green fluorescent protein-linked promoters into sodium silicate-derived materials that were formed in microwell plates. Using a series of assays, we were able to demonstrate that (1) the entrapped cells can divide within the pores of the silica matrix, (2) cellular pathways are regulated in a similar manner in both solution and the sol-gel-derived materials, and (3) promoters in entrapped cells can be specifically induced with small molecules (e.g., antimicrobial compounds) in a concentration-dependent manner to allow assessment of both potency and mode of action. This solid-phase assay system was tested using multiple antimicrobial pathways and should enable the development of solid-phase assays for the discovery of new small molecules that are active against bacteria.}},
  author       = {{Eleftheriou, Nikolas and Ge, Xin and Kolesnik, Julia and Falconer, Shannon B. and Harris, Robert J. and Khursigara, Cezar and Brown, Eric D. and Brennan, John D.}},
  issn         = {{0897-4756}},
  keywords     = {{encapsulation; sol-gel; biosensor; screening; green fluorescent protein; silica; cell entrapment}},
  language     = {{eng}},
  number       = {{23}},
  pages        = {{4798--4805}},
  publisher    = {{The American Chemical Society (ACS)}},
  series       = {{Chemistry of Materials}},
  title        = {{Entrapment of Living Bacterial Cells in Low-Concentration Silica Materials Preserves Cell Division and Promoter Regulation}},
  url          = {{http://dx.doi.org/10.1021/cm403198z}},
  doi          = {{10.1021/cm403198z}},
  volume       = {{25}},
  year         = {{2013}},
}