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海绵体中溴酪氨酸生物碱生物合成中的对映体差异?

Enantiodivergence in the Biosynthesis of Bromotyrosine Alkaloids from Sponges?

作者信息

Ragini Kavita, Fromont Jane, Piggott Andrew M, Karuso Peter

机构信息

Department of Chemistry and Biomolecular Sciences, Macquarie University , Sydney, NSW 2109, Australia.

Department of Aquatic Zoology, Western Australian Museum , Western Australia 6106, Australia.

出版信息

J Nat Prod. 2017 Jan 27;80(1):215-219. doi: 10.1021/acs.jnatprod.6b01038. Epub 2017 Jan 13.

Abstract

The isolation of bromotyrosine alkaloids, some of which are enantiomers of previously isolated compounds, has highlighted a possible enantiodivergence in their biosynthesis. Two new (1, 2) and six known bromotyrosine alkaloids (4-9), and the enantiomer (10) of a known compound, have been isolated from a Western Australian marine sponge, Pseudoceratina cf. verrucosa. The compounds inhibited the growth of multidrug-resistant and methicillin-resistant Staphylococcus aureus with comparable activity to vancomycin. In addition, one possible artifact of extraction (3) containing an ethoxy group was isolated. From analysis of the known bromotyrosine alkaloids, a biogenesis is proposed that explains the formation of antipodal natural products within this family of sponges.

摘要

溴酪氨酸生物碱的分离,其中一些是先前分离出的化合物的对映体,这突出表明它们的生物合成中可能存在对映体差异。从西澳大利亚的一种海洋海绵Pseudoceratina cf. verrucosa中分离出了两种新的(1, 2)和六种已知的溴酪氨酸生物碱(4 - 9),以及一种已知化合物的对映体(10)。这些化合物对耐多药和耐甲氧西林金黄色葡萄球菌的生长具有抑制作用,其活性与万古霉素相当。此外,还分离出了一种可能的含有乙氧基的提取产物(3)。通过对已知溴酪氨酸生物碱的分析,提出了一种生物合成过程,该过程解释了这类海绵中对映体天然产物的形成。

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