Department of Biochemical Engineering, Faculty of Science and Technology, University of Debrecen, Debrecen, Hungary.
University of Debrecen, Juhász-Nagy Pál Doctoral School of Biology and Environmental Sciences, Debrecen, Hungary.
Microbiol Spectr. 2024 Nov 5;12(11):e0190624. doi: 10.1128/spectrum.01906-24. Epub 2024 Oct 8.
For over a century, the filamentous Ascomycete fungus 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 NRRL2270 strain grown under citric acid-producing conditions in 6-L scale bioreactors at Mn ion-deficient (5 ppb) and Mn 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 ion deficiency condition encodes enzymes acting on polysaccharides. In contrast, six clusters of genes encoding secondary metabolites showed downregulation under manganese deficiency. Mn deficiency also triggers upregulation of the gene, which encodes the citrate exporter. We provide functional evidence that the upregulation of is caused by the intracellular accumulation of citrate or acetyl-CoA and is a major factor in triggering citrate overflow.
Citric acid is produced on industrial scale by batch fermentation of the filamentous fungus . 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 strain grown under citric acid-producing conditions in 6-L scale bioreactors at Mn ion-deficient (5 ppb) and Mn ion-sufficient (100 ppb) conditions at three early time points of cultivation. We observed that Mn 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 ion deficiency in a heterotrophic eukaryotic cell on a genome-wide scale.
一个多世纪以来,丝状子囊菌真菌一直 在柠檬酸的工业生产中发挥着关键作用。在发酵过程的早期阶段,维持高产柠檬酸积累的一个关键发酵参数是培养基中锰(II)离子的亚最佳浓度。然而,这种缺乏的需求尚未在功能基因组学水平上进行研究。在这项研究中,我们比较了柠檬酸高产菌 NRRL2270 菌株在柠檬酸生产条件下,在 Mn 离子缺乏(5 ppb)和 Mn 离子充足(100 ppb)条件下,在培养的三个早期时间点,在 6-L 规模生物反应器中的转录组。在基因组的 11846 个基因中,有 963 个基因(总基因的 8.1%)在这些条件下被鉴定为显著差异表达。差异调节基因的数量不成比例地高,编码预测的细胞外和膜蛋白。在 Mn 离子缺乏条件下上调的最丰富的基因组编码作用于多糖的酶。相比之下,六个编码次级代谢物的基因簇在锰缺乏时下调。Mn 缺乏还触发了 基因的上调,该基因编码柠檬酸外排蛋白。我们提供了功能证据,证明 基因的上调是由细胞内柠檬酸或乙酰辅酶 A 的积累引起的,是触发柠檬酸溢出的主要因素。
柠檬酸是通过丝状真菌的分批发酵在工业规模上生产的。高产柠檬酸生产需要培养基中锰(II)离子浓度低(<5 ppb)。然而,这种缺乏的需求尚未在功能基因组学水平上进行研究。在这里,我们比较了柠檬酸高产菌 菌株在柠檬酸生产条件下,在 6-L 规模生物反应器中,在 Mn 离子缺乏(5 ppb)和 Mn 离子充足(100 ppb)条件下,在培养的三个早期时间点的转录组。我们观察到,Mn 缺乏会触发柠檬酸外排蛋白基因 cexA 的上调,并提供了功能证据,证明这一事件是导致柠檬酸溢出的原因。除了工业相关性外,这是第一项在全基因组范围内研究 Mn 离子缺乏对异养真核细胞的作用的研究。