| Literature DB >> 30508325 |
Chien-Chi Hsiao1, Simon Sieber1, Antri Georgiou2, Aurélien Bailly2, Despina Emmanouilidou1, Aurélien Carlier2, Leo Eberl2, Karl Gademann1.
Abstract
The plant Psychotria kirkii hosts an obligatory bacterial symbiont, Candidatus Burkholderia kirkii, in nodules on their leaves. Recently, a glucosylated derivative of (+)-streptol, (+)-streptol glucoside, was isolated from the nodulated leaves and was found to possess a plant growth inhibitory activity. To establish a structure-activity relationship study, a convergent strategy was developed to obtain several pseudosugars from a single synthetic precursor. Furthermore, the glucosylation of streptol was investigated in detail and conditions affording specifically the α or β glucosidic anomer were identified. Although (+)-streptol was the most active compound, its concentration in P. kirkii plant leaves extract was approximately ten-fold lower than that of (+)-streptol glucoside. These results provide compelling evidence that the glucosylation of (+)-streptol protects the plant host against the growth inhibitory effect of the compound, which might constitute a molecular cornerstone for this successful plant-bacteria symbiosis.Entities:
Keywords: Psychotria kirkii; glucosylation; natural products; streptol; streptol glucoside; structure-activity relationships
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Year: 2019 PMID: 30508325 DOI: 10.1002/chem.201805693
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236