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普遍存在的儿茶酚部分在链霉菌中引发铁载体和安古环素的产生。

The ubiquitous catechol moiety elicits siderophore and angucycline production in Streptomyces.

作者信息

van Bergeijk Doris A, Elsayed Somayah S, Du Chao, Santiago Isabel Nuñez, Roseboom Anna M, Zhang Le, Carrión Victor J, Spaink Herman P, van Wezel Gilles P

机构信息

Institute of Biology, Leiden University, Sylviusweg 72, 2333 BE, Leiden, The Netherlands.

Netherlands Institute of Ecology, NIOO-KNAW, Droevendaalsesteeg 10, 6708 PB, Wageningen, The Netherlands.

出版信息

Commun Chem. 2022 Feb 3;5(1):14. doi: 10.1038/s42004-022-00632-4.

Abstract

Actinobacteria are a rich source of bioactive molecules, and genome sequencing has shown that the vast majority of their biosynthetic potential has yet to be explored. However, many of their biosynthetic gene clusters (BGCs) are poorly expressed in the laboratory, which prevents discovery of their cognate natural products. To exploit their full biosynthetic potential, better understanding of the signals that promote the expression of BGCs is needed. Here, we show that the human stress hormone epinephrine (adrenaline) elicits siderophore production by Actinobacteria. Catechol was established as the likely eliciting moiety, since similar responses were seen for catechol and for the catechol-containing molecules dopamine and catechin but not for related molecules. Exploration of the catechol-responsive strain Streptomyces sp. MBT84 using mass spectral networking revealed elicitation of a BGC that produces the angucycline glycosides aquayamycin, urdamycinone B and galtamycin C. Heterologous expression of the catechol-cleaving enzymes catechol 1,2-dioxygenase or catechol 2,3-dioxygenase counteracted the eliciting effect of catechol. Thus, our work identifies the ubiquitous catechol moiety as a novel elicitor of the expression of BGCs for specialized metabolites.

摘要

放线菌是生物活性分子的丰富来源,基因组测序表明其绝大多数生物合成潜力尚未得到探索。然而,它们的许多生物合成基因簇(BGCs)在实验室中表达不佳,这阻碍了其同源天然产物的发现。为了充分发挥其生物合成潜力,需要更好地了解促进BGCs表达的信号。在这里,我们表明人类应激激素肾上腺素( adrenaline )能引发放线菌产生铁载体。邻苯二酚被确定为可能的引发部分,因为邻苯二酚以及含邻苯二酚的分子多巴胺和儿茶素都有类似反应,而相关分子则没有。利用质谱网络对邻苯二酚响应菌株链霉菌属MBT84进行探索,发现一个产生安古霉素类糖苷水谷霉素、乌达霉素酮B和加尔他霉素C的BGC被激活。邻苯二酚裂解酶邻苯二酚1,2-双加氧酶或邻苯二酚2,3-双加氧酶的异源表达抵消了邻苯二酚的引发作用。因此,我们的工作确定普遍存在的邻苯二酚部分是一种用于特殊代谢物的BGCs表达的新型诱导剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993f/9814775/fae379272023/42004_2022_632_Fig1_HTML.jpg

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