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迈向对海藻毒素生物合成更好的理解。

Towards a Better Understanding of Toxin Biosynthesis in Seaweeds.

机构信息

Univ Angers, Univ Brest, IRF, SFR ICAT, 49000, Angers, France.

School of the Biological and Chemical Sciences, Ryan Institute, National University of Ireland Galway, H91TK33, Galway, Republic of Ireland.

出版信息

Chembiochem. 2022 Aug 17;23(16):e202200223. doi: 10.1002/cbic.202200223. Epub 2022 Jun 21.

Abstract

Harmful algal blooms (HABs) represent both ecological and public health hazards in the marine environment. Indeed, some algae can produce metabolites that have negative effects on marine ecosystems and mammals. Kainoid derivatives such as kainic acid (KA) and domoic acid (DA) are considered some of the most toxic metabolites of marine origin biosynthesized by a limited number of micro- and macroalgae. While recent works have provided the first insights into the biosynthetic route of KA in red algae and DA in diatoms, the DA biosynthetic pathway has remained uncharacterized for red algae. In a recent work, the research groups of Chekan and Moore have not only elucidated the biosynthetic pathway of DA in the red alga Chondria armata but also shed light on its complex evolution among marine species. We discuss here the importance of pursuing active research in this area to gain insights into secondary biosynthetic pathways in marine organisms for diagnostic and metabolic engineering perspectives.

摘要

有害藻华(HABs)在海洋环境中既代表生态危害,也代表公共健康危害。事实上,一些藻类可以产生对海洋生态系统和哺乳动物有负面影响的代谢物。石房蛤毒素衍生物,如石房蛤毒素(KA)和软骨藻酸(DA),被认为是由少数微藻和巨藻生物合成的最具毒性的海洋来源代谢物之一。虽然最近的研究工作为红藻中的 KA 和硅藻中的 DA 的生物合成途径提供了初步的见解,但 DA 的生物合成途径在红藻中仍未得到描述。在最近的一项研究中,Chekan 和 Moore 的研究小组不仅阐明了红藻 Chondria armata 中 DA 的生物合成途径,还揭示了其在海洋物种中的复杂进化。我们在这里讨论了在这一领域开展积极研究的重要性,以便从诊断和代谢工程的角度深入了解海洋生物中的次生生物合成途径。

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