| Literature DB >> 28407946 |
Jana Rückriemen1, Oliver Klemm1, Thomas Henle2.
Abstract
Manuka honey (Leptospermum scoparium) exerts a strong antibacterial effect. Bacterial enzymes are an important target for antibacterial compounds. The enzyme urease produces ammonia and enables bacteria to adapt to an acidic environment. A new enzymatic assay, based on photometric detection of ammonia with ninhydrin, was developed to study urease activity. Methylglyoxal (MGO) and its precursor dihydroxyacetone (DHA), which are naturally present in manuka honey, were identified as jack bean urease inhibitors with IC50 values of 2.8 and 5.0mM, respectively. Urease inhibition of manuka honey correlates with its MGO and DHA content. Non-manuka honeys, which lack MGO and DHA, showed significantly less urease inhibition. MGO depletion from manuka honey with glyoxalase reduced urease inhibition. Therefore, urease inhibition by manuka honey is mainly due to MGO and DHA. The results obtained with jack bean urease as a model urease, may contribute to the understanding of bacterial inhibition by manuka honey.Entities:
Keywords: Dihydroxyacetone; Dihydroxyacetone (PubChem CID: 670); Helicobacter pylori; Jack bean urease; Manuka honey; Methylglyoxal; Methylglyoxal (PubChem CID: 880); Ninhydrin
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Year: 2017 PMID: 28407946 DOI: 10.1016/j.foodchem.2017.03.075
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514