Engineered living materials based on adhesin-mediated trapping of programmable cells

Shuaiqi Guo (Corresponding author), Emilien Dubuc, Yahav Rave, Mick Verhagen, Simone A.E. Twisk, Tim van der Hek, Guido J.M. Oerlemans, Maxime C.M. van den Oetelaar, Laura S. van Hazendonk, Mariska Brüls, Bruno V. Eijkens, Pim L. Joostens, Sander R. Keij, Weizhou Xing, Martijn Nijs, Jitske Stalpers, Manoj Sharma, Marieke Gerth, Roy J.E.A. Boonen, Kees VerduinMaarten Merkx, Ilja K. Voets (Corresponding author), Tom F.A. De Greef (Corresponding author)

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41 Citaten (Scopus)
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Samenvatting

Engineered living materials have the potential for wide-ranging applications such as biosensing and treatment of diseases. Programmable cells provide the functional basis for living materials; however, their release into the environment raises numerous biosafety concerns. Current designs that limit the release of genetically engineered cells typically involve the fabrication of multilayer hybrid materials with submicrometer porous matrices. Nevertheless the stringent physical barriers limit the diffusion of macromolecules and therefore the repertoire of molecules available for actuation in response to communication signals between cells and their environment. Here, we engineer a novel living material entitled "Platform for Adhesin-mediated Trapping of Cells in Hydrogels" (PATCH). This technology is based on engineered E. coli that displays an adhesion protein derived from an Antarctic bacterium with a high affinity for glucose. The adhesin stably anchors E. coli in dextran-based hydrogels with large pore diameters (10-100 μm) and reduces the leakage of bacteria into the environment by up to 100-fold. As an application of PATCH, we engineered E. coli to secrete the bacteriocin lysostaphin which specifically kills Staphyloccocus aureus with low probability of raising antibiotic resistance. We demonstrated that living materials containing this lysostaphin-secreting E. coli inhibit the growth of S. aureus, including the strain resistant to methicillin (MRSA). Our tunable platform allows stable integration of programmable cells in dextran-based hydrogels without compromising free diffusion of macromolecules and could have potential applications in biotechnology and biomedicine. ©

Originele taal-2Engels
Pagina's (van-tot)475-485
Aantal pagina's11
TijdschriftACS Synthetic Biology
Volume9
Nummer van het tijdschrift3
DOI's
StatusGepubliceerd - 20 mrt. 2020

Financiering

The authors would like to acknowledge the financial support for this research of the STW-foundation, the EPSRC-NSFC Joint Research Project (No. 51461135005), the European Union (ERC-StG No. 635928 & 677313), the Dutch Science Foundation (NWO ECHO Grant No. 712.016.002 and NWO-VIDI Grant No. 723.016.003), and the Dutch Ministry of Education, Culture and Science (Gravity Program 024.001.035). Dextran was kindly provided by Pharmacosmos A/S. We thank Ingeborg Schreur-Piet for her support for SEM imaging. We thank Prof. Peter Sebo for generously providing the plG575 plasmid for amplifying the HlyB/HlyD genes. We thank Bas Rosier for his help and valuable advice with Figure 3 b. We thank Mathijs F.J. Mabesoone for his help with acquiring and interpreting NMR and IR data. We are indebted to Prof. Luc Brunsveld for his important guidance and financial support while supervising the Tue 2018 iGEM team. Molecular graphics and analyses were performed with UCSF Chimera, developed by the Resource for Biocomputing, Visualization, and Informatics at the University of California, San Francisco, with support from NIH P41-GM103311.

FinanciersFinanciernummer
EPSRC-NSFC51461135005
STW
National Institute of General Medical SciencesP41GM103311
European Commission677313, 635928
Ministerie van OCW024.001.035
Nederlandse Organisatie voor Wetenschappelijk Onderzoek712.016.002, 723.016.003

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