Fritsche Susanne, Ellena Valeria, Demirbas-Uzel Güler, Steiger Matthias G
acib - Austrian Centre of Industrial Biotechnology, Vienna, Austria.
Institute of Chemical, Environmental and Bioscience Engineering, Research Group Biochemistry, Technische Universität Wien, Vienna, Austria.
PLoS One. 2025 Apr 24;20(4):e0321363. doi: 10.1371/journal.pone.0321363. eCollection 2025.
Glycolysis in A. niger, a key organism in industrial biotechnology, provides essential precursors for efficient citric acid production. Glucose-6-phosphate dehydrogenase (G6PD), encoded by the gene gsdA, is a critical point in the cellular metabolism as it determines the metabolic fate of glucose-6-phosphate by redirecting it into the pentose phosphate pathway (PPP). Despite its decisive position in the metabolic network the functional role of G6PD and its impact on citric acid synthesis and growth is not fully understood. Here, we present an A. niger strain expressing a ptet-on regulated version of gsdA at the pyrG locus. The native gene was disrupted and hence, gsdA expression was based on a single copy level. Under non-inducing conditions, the strain was not growing on glucose. On gluconate, a precursor for an intermediate of the oxidative PPP, growth was restored but delayed compared to the control strain expressing gsdA under the native promoter. Furthermore, citric acid production was monitored in dependency of different gsdA induction levels using doxycycline. At low induction levels, the yield on glucose was enhanced by 49% compared to the control strain, albeit with reduced growth leading to lower titers. Through supplementation of the medium with gluconate, we anticipated to provide precursors for biomass production for efficient metabolization of glucose to citric acid. Without the native regulation of the gsdA gene growth and citric acid production were time delayed. However, the yield of the gsdA-regulated strain was higher compared to the control after 120 h of cultivation and was positively influenced with an increasing proportion of gluconate in the medium. The findings of this study underscore the dependency of growth and citric acid production on gsdA expression in A. niger.
黑曲霉是工业生物技术中的关键生物,其糖酵解为高效柠檬酸生产提供了必需的前体物质。由基因gsdA编码的葡萄糖-6-磷酸脱氢酶(G6PD)是细胞代谢中的一个关键点,因为它通过将葡萄糖-6-磷酸重定向到磷酸戊糖途径(PPP)来决定其代谢命运。尽管G6PD在代谢网络中处于决定性地位,但其功能作用及其对柠檬酸合成和生长的影响尚未完全了解。在此,我们展示了一种在pyrG位点表达ptet-on调控版本gsdA的黑曲霉菌株。天然基因被破坏,因此,gsdA的表达基于单拷贝水平。在非诱导条件下,该菌株在葡萄糖上无法生长。在葡萄糖酸盐(氧化PPP中间体的前体)上,生长得以恢复,但与在天然启动子下表达gsdA的对照菌株相比有所延迟。此外,使用强力霉素监测了不同gsdA诱导水平下的柠檬酸生产情况。在低诱导水平下,与对照菌株相比,葡萄糖产率提高了49%,尽管生长减少导致滴度降低。通过在培养基中添加葡萄糖酸盐,我们预期为生物质生产提供前体物质,以便将葡萄糖高效代谢为柠檬酸。没有gsdA基因的天然调控,生长和柠檬酸生产会出现时间延迟。然而,在培养120小时后,gsdA调控菌株的产率高于对照菌株,并且培养基中葡萄糖酸盐比例增加对其有积极影响。本研究结果强调了黑曲霉中生长和柠檬酸生产对gsdA表达的依赖性。