| Literature DB >> 25984987 |
Paul D Sainsbury1, Yelena Mineyeva1, Zoe Mycroft1, Timothy D H Bugg2.
Abstract
Bacterial lignin degradation could be used to generate aromatic chemicals from the renewable resource lignin, provided that the breakdown pathways can be manipulated. In this study, selective inhibitors of enzymatic steps in bacterial degradation pathways were developed and tested for their effects upon lignin degradation. Screening of a collection of hydroxamic acid metallo-oxygenase inhibitors against two catechol dioxygenase enzymes, protocatechuate 3,4-dioxygenase (3,4-PCD) and 2,3-dihydroxyphenylpropionate 1,2-dioxygenase (MhpB), resulted in the identification of selective inhibitors D13 for 3,4-PCD (IC50 15μM) and D3 for MhpB (IC50 110μM). Application of D13 to Rhodococcus jostii RHA1 in minimal media containing ferulic acid led to the appearance of metabolic precursor protocatechuic acid at low concentration. Application of 1mM disulfiram, an inhibitor of mammalian aldehyde dehydrogenase, to R. jostii RHA1, gave rise to 4-carboxymuconolactone on the β-ketoadipate pathway, whereas in Pseudomonas fluorescens Pf-5 disulfiram treatment gave rise to a metabolite found to be glycine betaine aldehyde.Entities:
Keywords: Aldehyde dehydrogenase; Catechol dioxygenase; Disulfiram; Enzyme inhibition; Hydroxamic acid; Lignin valorization
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Year: 2015 PMID: 25984987 DOI: 10.1016/j.bioorg.2015.05.002
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275