Rapid characterization of the activities of lignin-modifying enzymes based on nanostructure-initiator mass spectrometry (NIMS).
Kai DengJijiao ZengGang ChengJian GaoKenneth L SaleBlake A SimmonsAnup K SinghPaul D AdamsTrent R NorthenPublished in: Biotechnology for biofuels (2018)
A new assay procedure has been developed for studying lignin-modifying enzymes by nanostructure-initiator mass spectrometry. Enzyme assays of a laccase and a MnP on phenolic and nonphenolic β-aryl ether substrates revealed different primary reaction pathways due to the availability of the phenoxy radical intermediates. Our assay provides a wealth of information on bond cleavage events not available using conventional colorimetric assays and can easily be carried out in microliter volumes and the quantitative analysis of product formation and kinetics is rapidly achieved by NIMS. This is the first time that NIMS technology was applied to study the activities of lignin-modifying enzymes. Unlike other previous works, our use of amphiphilic guaiacylglycerol β-O-4 substrate (I) enables the formation of micelles. This approach helps avoid the re-polymerization of the resulting monomeric product. As a result, our assay can clearly demonstrate the degradation pathways of phenolic guaiacylglycerol β-O-4 type of molecules with laccase and MnP.
Keyphrases
- high throughput
- mass spectrometry
- ionic liquid
- high resolution
- liquid chromatography
- single cell
- gold nanoparticles
- drug delivery
- gas chromatography
- high performance liquid chromatography
- hydrogen peroxide
- healthcare
- minimally invasive
- nitric oxide
- cancer therapy
- health information
- sensitive detection
- dna binding
- living cells
- social media
- simultaneous determination