Tailoring Trehalose for Biomedical and Biotechnological Applications
Document Type
Article
Publication Date
9-2017
Publication Title
Pure Applied Chemistry
Keywords
Trehalose, analogue, chemical synthesis, chemoenzymatic synthesis, biocatalysis, imaging, inhibitors, mycobacteria, biopreservation
Abstract
Trehalose is a non-reducing sugar whose ability to stabilize biomolecules has brought about its widespread use in biological preservation applications. Trehalose is also an essential metabolite in a number of pathogens, most significantly the global pathogen Mycobacterium tuberculosis, though it is absent in humans and other mammals. Recently, there has been a surge of interest in modifying the structure of trehalose to generate analogues that have applications in biomedical research and biotechnology. Non-degradable trehalose analogues could have a number of advantages as bioprotectants and food additives. Trehalose-based imaging probes and inhibitors are already useful as research tools and may have future value in the diagnosis and treatment of tuberculosis, among other uses. Underlying the advancements made in these areas are novel synthetic methods that facilitate access to and evaluation of trehalose analogues. In this review, we focus on both aspects of the development of this class of molecules. First, we consider the chemical and chemoenzymatic methods that have been used to prepare trehalose analogues and discuss their prospects for synthesis on commercially relevant scales. Second, we describe ongoing efforts to develop and deploy detectable trehalose analogues, trehalose-based inhibitors, and non-digestible trehalose analogues. The current and potential future uses of these compounds are discussed, with an emphasis on their roles in understanding and combatting mycobacterial infection.
Recommended Citation
O’Neill, M.K., Piligian, B.F., Olson, C.D., Woodruff, P.J., & Swarts, B.M. (2017). Tailoring trehalose for biomedical and biotechnological applications. Pure Applied Chemistry. 89(9), 1223-1249. doi:10.1515/pac-2016-1025