转录组学发现柠檬酸盐输出是黑曲霉缺锰引起的关键事件。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2024-11-05 Epub Date: 2024-10-08 DOI:10.1128/spectrum.01906-24
Erzsébet Fekete, Vivien Bíró, Alexandra Márton, István Bakondi-Kovács, Erzsébet Sándor, Béla Kovács, Nicholas Geoffrion, Adrian Tsang, Christian P Kubicek, Levente Karaffa
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引用次数: 0

摘要

一个多世纪以来,丝状子囊菌黑曲霉在柠檬酸的工业化生产中发挥了举足轻重的作用。维持高产柠檬酸积累的一个关键发酵参数是,在工艺的早期阶段,培养液中锰(II)离子的浓度不达标。然而,人们尚未从功能基因组学的角度研究这种缺乏的原因。在本研究中,我们比较了柠檬酸高产菌 A. niger NRRL2270 菌株在 6 升生物反应器中柠檬酸生产条件下,在锰离子缺乏(5 ppb)和锰离子充足(100 ppb)条件下三个早期培养时间点的转录组。在基因组中的 11,846 个基因中,有 963 个基因(占总数的 8.1%)在这些条件下有显著差异表达。大量差异调控基因编码预测的细胞外蛋白和膜蛋白。在 Mn2+ 离子缺乏条件下上调最多的基因组编码作用于多糖的酶。相反,编码次生代谢物的六个基因簇在缺锰条件下出现下调。Mn2+ 缺乏还引发了编码柠檬酸盐输出器的 cexA 基因的上调。我们提供的功能性证据表明,柠檬酸或乙酰-CoA的胞内积累导致了cexA基因的上调,并且是引发柠檬酸溢出的主要因素:柠檬酸是通过丝状真菌黑曲霉的批量发酵进行工业化生产的。高产柠檬酸的生产需要在 6 升规模的生物反应器中,在 Mn2+ 离子缺乏(5 ppb)和 Mn2+ 离子充足(100 ppb)的条件下,在三个早期培养时间点培养低产(黑曲霉菌株在柠檬酸生产条件下生长)的菌株。我们观察到,Mn2+ 缺乏会引发柠檬酸盐输出基因 cexA 的上调,并提供了功能性证据,证明这一事件是柠檬酸盐溢出的原因。除了工业相关性之外,这是首次在全基因组范围内研究 Mn2+ 离子缺乏在异养真核细胞中的作用。
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Transcriptomics identify the triggering of citrate export as the key event caused by manganese deficiency in Aspergillus niger.

For over a century, the filamentous Ascomycete fungus Aspergillus niger has played a pivotal role in the industrial production of citric acid. A critical fermentation parameter that sustains high-yield citric acid accumulation is the suboptimal concentration of manganese(II) ions in the culture broth at the early stages of the process. However, the requirement for this deficiency has not been investigated on a functional genomics level. In this study, we compared the transcriptome of the citric acid hyper-producer A. niger NRRL2270 strain grown under citric acid-producing conditions in 6-L scale bioreactors at Mn2+ ion-deficient (5 ppb) and Mn2+ ion-sufficient (100 ppb) conditions at three early time points of cultivation. Of the 11,846 genes in the genome, 963 genes (8.1% of the total) were identified as significantly differentially expressed under these conditions. Disproportionately high number of differentially regulated genes encode predicted extracellular and membrane proteins. The most abundant gene group that was upregulated in Mn2+ ion deficiency condition encodes enzymes acting on polysaccharides. In contrast, six clusters of genes encoding secondary metabolites showed downregulation under manganese deficiency. Mn2+ deficiency also triggers upregulation of the cexA gene, which encodes the citrate exporter. We provide functional evidence that the upregulation of cexA is caused by the intracellular accumulation of citrate or acetyl-CoA and is a major factor in triggering citrate overflow.

Importance: Citric acid is produced on industrial scale by batch fermentation of the filamentous fungus Aspergillus niger. High-yield citric acid production requires a low (<5 ppb) manganese(II) ion concentration in the culture broth. However, the requirement for this deficiency has not been investigated on a functional genomics level. Here, we compared the transcriptome of a citric acid hyper-producer A. niger strain grown under citric acid-producing conditions in 6-L scale bioreactors at Mn2+ ion-deficient (5 ppb) and Mn2+ ion-sufficient (100 ppb) conditions at three early time points of cultivation. We observed that Mn2+ deficiency triggers an upregulation of the citrate exporter gene cexA and provides functional evidence that this event is responsible for citrate overflow. In addition to the industrial relevance, this is the first study that examined the role of Mn2+ ion deficiency in a heterotrophic eukaryotic cell on a genome-wide scale.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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