Erzsébet Fekete, Vivien Bíró, Alexandra Márton, István Bakondi-Kovács, Erzsébet Sándor, Béla Kovács, Nicholas Geoffrion, Adrian Tsang, Christian P Kubicek, Levente Karaffa
{"title":"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。","authors":"Erzsébet Fekete, Vivien Bíró, Alexandra Márton, István Bakondi-Kovács, Erzsébet Sándor, Béla Kovács, Nicholas Geoffrion, Adrian Tsang, Christian P Kubicek, Levente Karaffa","doi":"10.1128/spectrum.01906-24","DOIUrl":null,"url":null,"abstract":"<p><p>For over a century, the filamentous Ascomycete fungus <i>Aspergillus niger</i> 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 <i>A. niger</i> NRRL2270 strain grown under citric acid-producing conditions in 6-L scale bioreactors at Mn<sup>2+</sup> ion-deficient (5 ppb) and Mn<sup>2+</sup> 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 Mn<sup>2+</sup> ion deficiency condition encodes enzymes acting on polysaccharides. In contrast, six clusters of genes encoding secondary metabolites showed downregulation under manganese deficiency. Mn<sup>2+</sup> deficiency also triggers upregulation of the <i>cexA</i> gene, which encodes the citrate exporter. We provide functional evidence that the upregulation of <i>cexA</i> is caused by the intracellular accumulation of citrate or acetyl-CoA and is a major factor in triggering citrate overflow.</p><p><strong>Importance: </strong>Citric acid is produced on industrial scale by batch fermentation of the filamentous fungus <i>Aspergillus niger</i>. 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 <i>A. niger</i> strain grown under citric acid-producing conditions in 6-L scale bioreactors at Mn<sup>2+</sup> ion-deficient (5 ppb) and Mn<sup>2+</sup> ion-sufficient (100 ppb) conditions at three early time points of cultivation. We observed that Mn<sup>2+</sup> 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 Mn<sup>2+</sup> ion deficiency in a heterotrophic eukaryotic cell on a genome-wide scale.</p>","PeriodicalId":18670,"journal":{"name":"Microbiology spectrum","volume":null,"pages":null},"PeriodicalIF":3.7000,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11537073/pdf/","citationCount":"0","resultStr":"{\"title\":\"Transcriptomics identify the triggering of citrate export as the key event caused by manganese deficiency in <i>Aspergillus niger</i>.\",\"authors\":\"Erzsébet Fekete, Vivien Bíró, Alexandra Márton, István Bakondi-Kovács, Erzsébet Sándor, Béla Kovács, Nicholas Geoffrion, Adrian Tsang, Christian P Kubicek, Levente Karaffa\",\"doi\":\"10.1128/spectrum.01906-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>For over a century, the filamentous Ascomycete fungus <i>Aspergillus niger</i> 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 <i>A. niger</i> NRRL2270 strain grown under citric acid-producing conditions in 6-L scale bioreactors at Mn<sup>2+</sup> ion-deficient (5 ppb) and Mn<sup>2+</sup> 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 Mn<sup>2+</sup> ion deficiency condition encodes enzymes acting on polysaccharides. In contrast, six clusters of genes encoding secondary metabolites showed downregulation under manganese deficiency. Mn<sup>2+</sup> deficiency also triggers upregulation of the <i>cexA</i> gene, which encodes the citrate exporter. We provide functional evidence that the upregulation of <i>cexA</i> is caused by the intracellular accumulation of citrate or acetyl-CoA and is a major factor in triggering citrate overflow.</p><p><strong>Importance: </strong>Citric acid is produced on industrial scale by batch fermentation of the filamentous fungus <i>Aspergillus niger</i>. 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 <i>A. niger</i> strain grown under citric acid-producing conditions in 6-L scale bioreactors at Mn<sup>2+</sup> ion-deficient (5 ppb) and Mn<sup>2+</sup> ion-sufficient (100 ppb) conditions at three early time points of cultivation. We observed that Mn<sup>2+</sup> 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 Mn<sup>2+</sup> ion deficiency in a heterotrophic eukaryotic cell on a genome-wide scale.</p>\",\"PeriodicalId\":18670,\"journal\":{\"name\":\"Microbiology spectrum\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2024-11-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11537073/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microbiology spectrum\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/spectrum.01906-24\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/10/8 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology spectrum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/spectrum.01906-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/8 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
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.
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.