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鉴定真菌产生蓝绿色色素木林菌素的生物合成基因簇。

Identification of a Biosynthetic Gene Cluster for the Production of the Blue-Green Pigment Xylindein by the Fungus .

作者信息

Guo Yanfang, Navarro-Muñoz Jorge, Rodenbach Caroline, Dwars Elske, Dieleman Chendo, van den Hout Bart, Sanders Bazante, Zhou Miaomiao, Arogunjo Ayodele, Cox Russell J, Driessen Arnold J M, Collemare Jérôme

机构信息

Fungal Natural Products Group, Westerdijk Fungal Biodiversity Institute, 3584 CT Utrecht, Netherlands.

Department of Molecular Microbiology, University of Groningen, 9747 AG Groningen, Netherlands.

出版信息

J Nat Prod. 2025 Feb 28;88(2):233-244. doi: 10.1021/acs.jnatprod.4c00350. Epub 2025 Jan 23.

DOI:10.1021/acs.jnatprod.4c00350
PMID:39847046
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11877519/
Abstract

Xylindein is a blue-green pigment produced by the fungi and Its stunning color and optoelectronic properties make xylindein valuable for textiles and as a natural semiconductor material. However, producing xylindein from culture broths remains challenging because of the slow growth of the species and the poor solubility of xylindein in organic solvents. An alternative production route for obtaining pure xylindein is heterologous expression of the xylindein biosynthetic genes. Here, we resequenced the genome of and , and subsequent genome mining and phylogenetic dereplication identified a unique candidate biosynthetic gene cluster with a nonreducing polyketide synthase (nrPKS). RNA sequencing during xylindein production revealed that the core gene is co-regulated with eight other genes at the locus. Among those, and encode a putative fatty acid synthase, which likely provides the starter unit to XLNpks. Attempts to heterologously express in alone or in combination with and did not yield any intermediate, but expression of the closely related viriditoxin nrPKS (VdtA) produced the expected intermediate. Based on our results, we propose a biosynthetic route to xylindein and suggest that the obtained transformants open ways to further study xylindein biosynthesis.

摘要

木林菌素是一种由真菌产生的蓝绿色色素,其惊人的颜色和光电特性使木林菌素在纺织品领域以及作为一种天然半导体材料具有重要价值。然而,由于该菌种生长缓慢且木林菌素在有机溶剂中的溶解度较差,从培养液中生产木林菌素仍然具有挑战性。获得纯木林菌素的另一种生产途径是木林菌素生物合成基因的异源表达。在此,我们对[具体菌种1]和[具体菌种2]的基因组进行了重测序,随后的基因组挖掘和系统发育去重复鉴定出一个具有非还原聚酮合酶(nrPKS)的独特候选生物合成基因簇。木林菌素生产过程中的RNA测序显示,核心基因[具体基因名称]与该位点的其他八个基因共同受到调控。其中,[具体基因1]和[具体基因2]编码一种推定的脂肪酸合酶,其可能为XLNpks提供起始单元。单独或与[具体基因1]和[具体基因2]组合在[具体宿主菌]中进行异源表达的尝试均未产生任何中间体,但密切相关的绿脓菌素nrPKS(VdtA)的表达产生了预期的中间体。基于我们的结果,我们提出了一条木林菌素的生物合成途径,并表明所获得的[具体宿主菌]转化体为进一步研究木林菌素生物合成开辟了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/83aea0e14c9c/np4c00350_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/f36ee1bb2f52/np4c00350_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/ea7cba6757c0/np4c00350_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/23daa7d15f72/np4c00350_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/817923c933d7/np4c00350_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/9be6fbc81c1e/np4c00350_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/da6ad7c1a493/np4c00350_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/83aea0e14c9c/np4c00350_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/f36ee1bb2f52/np4c00350_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/ea7cba6757c0/np4c00350_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/23daa7d15f72/np4c00350_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/817923c933d7/np4c00350_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/9be6fbc81c1e/np4c00350_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/da6ad7c1a493/np4c00350_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efc/11877519/83aea0e14c9c/np4c00350_0007.jpg

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