Thermodynamic limitations of PHB production from formate and fructose in Cupriavidus necator

钩虫贪铜菌 格式化 生物塑料 代谢工程 化学 生物化学 代谢网络 柠檬酸合酶 柠檬酸循环 延胡索酶 细菌 生物 羟基烷酸 生态学 遗传学 催化作用
作者
Markus Janasch,Nick Crang,Johannes Asplund‐Samuelsson,Emil Sporre,Manuel Bruch,Arvid H. Gynnå,Michael Jahn,Elton P. Hudson
出处
期刊:Metabolic Engineering [Elsevier]
卷期号:73: 256-269 被引量:8
标识
DOI:10.1016/j.ymben.2022.08.005
摘要

The chemolithotroph Cupriavidus necator H16 is known as a natural producer of the bioplastic-polymer PHB, as well as for its metabolic versatility to utilize different substrates, including formate as the sole carbon and energy source. Depending on the entry point of the substrate, this versatility requires adjustment of the thermodynamic landscape to maintain sufficiently high driving forces for biological processes. Here we employed a model of the core metabolism of C. necator H16 to analyze the thermodynamic driving forces and PHB yields from formate for different metabolic engineering strategies. For this, we enumerated elementary flux modes (EFMs) of the network and evaluated their PHB yields as well as thermodynamics via Max-min driving force (MDF) analysis and random sampling of driving forces. A heterologous ATP:citrate lyase reaction was predicted to increase driving force for producing acetyl-CoA. A heterologous phosphoketolase reaction was predicted to increase maximal PHB yields as well as driving forces. These enzymes were then verified experimentally to enhance PHB titers between 60 and 300% in select conditions. The EFM analysis also revealed that PHB production from formate may be limited by low driving forces through citrate lyase and aconitase, as well as cofactor balancing, and identified additional reactions associated with low and high PHB yield. Proteomics analysis of the engineered strains confirmed an increased abundance of aconitase and cofactor balancing. The findings of this study aid in understanding metabolic adaptation. Furthermore, the outlined approach will be useful in designing metabolic engineering strategies in other non-model bacteria.
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