Chemical Modification of Polyhydroxyalkanoates (PHAs) for the Preparation of Hybrid Biomaterials

FH - HES

Authors

  • Mònica Bassas-Galià HES-SO Valais, Institute of Life Technologies, Route du Rawyl 47, CH-1950 Sion 2, Switzerland. marc.mathieu@hevs.ch
  • Adolfo Gonzalez HES-SO Valais, Institute of Life Technologies, Route du Rawyl 47, CH-1950 Sion 2, Switzerland
  • Fabrice Micaux HES-SO Valais, Institute of Life Technologies, Route du Rawyl 47, CH-1950 Sion 2, Switzerland
  • Vanessa Gaillard HES-SO Valais, Institute of Life Technologies, Route du Rawyl 47, CH-1950 Sion 2, Switzerland
  • Umberto Piantini HES-SO Valais, Institute of Life Technologies, Route du Rawyl 47, CH-1950 Sion 2, Switzerland
  • Silvia Schintke HEIG-VD, Laboratory of Applied NanoSciences, CH-1401 Yverdon-les-Bains, Switzerland
  • Manfred Zinn HES-SO Valais, Institute of Life Technologies, Route du Rawyl 47, CH-1950 Sion 2, Switzerland
  • Marc Mathieu HES-SO Valais, Institute of Life Technologies, Route du Rawyl 47, CH-1950 Sion 2, Switzerland

DOI:

https://doi.org/10.2533/chimia.2015.627

Keywords:

Biosynthesis, Epoxidation, Kinetic monitoring, Nuclear magnetic resonance, Polyhydroxyalkanoates

Abstract

Polyhydroxyalkanoates (PHAs) are biopolyesters produced by bacteria as intracellular granules under metabolic stress conditions. Many carbon sources such as alkanes, alkenes, alcohols, sugars, fatty acids can be used as feedstock and thus a wide variety of polyesters and monomer units can be potentially synthetized. The work presented here describes the process to chemically modify such biopolymers in order to render them readily available for the preparation of bio-molecular conjugates as promising new classes of biocompatible biomaterials. Such hybrid biomaterials belong to the rapidly growing class of biocompatible polymers, which are of great interest for medical and therapeutic applications. In this work, the biosynthesis of a new PHA homopolymer and the chemical modification, an epoxidation reaction, are described.

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Published

2015-10-28

How to Cite

[1]
M. Bassas-Galià, A. Gonzalez, F. Micaux, V. Gaillard, U. Piantini, S. Schintke, M. Zinn, M. Mathieu, Chimia 2015, 69, 627, DOI: 10.2533/chimia.2015.627.