Haloperoxidase mediated quorum quenching by Nitzschia cf pellucida: study of the metabolization of N-Acyl Homoserine Lactones by a benthic diatom
Syrpas, M.; Ruysbergh, E.; Blommaert, L.; Vanelslander, B.; Sabbe, K.; Vyverman, W.; De Kimpe, N.; Mangelinckx, S. (2014). Haloperoxidase mediated quorum quenching by Nitzschia cf pellucida: study of the metabolization of N-Acyl Homoserine Lactones by a benthic diatom. Mar. Drugs 12(1): 352-367. dx.doi.org/10.3390/md12010352
In: Marine Drugs. Molecular Diversity Preservation International (MDPI): Basel. ISSN 1660-3397; e-ISSN 1660-3397
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| Keywords |
Nitzschia pellucida Grunow, 1880 [WoRMS]
Marine/Coastal |
| Author keywords |
quorum sensing; haloperoxidase; degradation pathway; AHL; referencecompounds; diatom-bacteria interactions |
| Authors | | Top |
- Syrpas, M.
- Ruysbergh, E.
- Blommaert, L.
- Vanelslander, B.
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- Sabbe, K., more
- Vyverman, W., more
- De Kimpe, N.
- Mangelinckx, S.
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| Abstract |
Diatoms are known to produce a variety of halogenated compounds, which were recently shown to have a role in allelopathic interactions between competing species. The production of these compounds is linked to haloperoxidase activity. This research, has shown that this system may also be involved in diatom-bacteria interactions via the H2O2 dependent inactivation of a type of quorum sensing (QS) molecule, i.e., N-ß-ketoacylated homoserine lactones (AHLs), by a natural haloperoxidase system from the benthic diatom Nitzschia cf pellucida. The AHL degradation pathway towards corresponding halogenated derivatives was elucidated via HPLC-MS analysis and the synthesis of a broad series of novel halogenated AHL analogues as reference compounds. Furthermore, their biological activity as quorum sensing modulators was directly compared and evaluated against a series of naturally occurring ß-keto-AHLs. It has been demonstrated that the loss of the QS activity results from the final cleavage of the halogenated N-acyl chain of the signal molecules. |
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