| Literature DB >> 30788782 |
James Jeffryes1,2, Jonathan Strutz1, Chris Henry2, Keith E J Tyo3.
Abstract
There is a growing consensus that enzymes are capable of catalyzing not just one canonical reaction but entire families of related reactions. These capacities often go unnoticed in the enzyme's native context but can become apparent in engineered metabolism when the enzyme is exposed to novel substrates or high concentrations of pathway intermediates. This chapter describes how to use metabolic in silico network expansion (MINE) databases to predict novel biotransformations and their resulting metabolites. In particular, searching MINEs by structural similarity or with metabolomics data allows scientists to detect, exploit, or avoid these predicted transformations.Keywords: Enzyme promiscuity; Feature annotation; Metabolite damage; Untargeted metabolomics
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Year: 2019 PMID: 30788782 DOI: 10.1007/978-1-4939-9142-6_2
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745