4.7 Article

H-2 drives metabolic rearrangements in gas-fermenting Clostridium autoethanogenum

期刊

BIOTECHNOLOGY FOR BIOFUELS
卷 11, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s13068-018-1052-9

关键词

Acetogen; Clostridium autoethanogenum; Gas fermentation; H-2 metabolism; Genome-scale modelling; Quantitative proteomics; Metabolomics

资金

  1. Australian Research Council [ARC LP140100213]
  2. Queensland Node of Metabolomics Australia
  3. National Biologics Facility
  4. Novo Nordisk Fonden [NNF10CC1016517] Funding Source: researchfish
  5. NNF Center for Biosustainability [Quantitative Modeling of Cell Metab] Funding Source: researchfish

向作者/读者索取更多资源

Background: The global demand for affordable carbon has never been stronger, and there is an imperative in many industrial processes to use waste streams to make products. Gas-fermenting acetogens offer a potential solution and several commercial gas fermentation plants are currently under construction. As energy limits acetogen metabolism, supply of H-2 should diminish substrate loss to CO2 and facilitate production of reduced and energy-intensive products. However, the effects of H-2 supply on CO-grown acetogens have yet to be experimentally quantified under controlled growth conditions. Results: Here, we quantify the effects of H-2 supplementation by comparing growth on CO, syngas, and a high-H-2 CO gas mix using chemostat cultures of Clostridium autoethanogenum. Cultures were characterised at the molecular level using metabolomics, proteomics, gas analysis, and a genome-scale metabolic model. CO-limited chemostats operated at two steady-state biomass concentrations facilitated co-utilisation of CO and H-2. We show that H-2 supply strongly impacts carbon distribution with a fourfold reduction in substrate loss as CO2 (61% vs. 17%) and a proportional increase of flux to ethanol (15% vs. 61%). Notably, H-2 supplementation lowers the molar acetate/ethanol ratio by fivefold. At the molecular level, quantitative proteome analysis showed no obvious changes leading to these metabolic rearrangements suggesting the involvement of post-translational regulation. Metabolic modelling showed that H-2 availability provided reducing power via H-2 oxidation and saved redox as cells reduced all the CO2 to formate directly using H-2 in the Wood-Ljungdahl pathway. Modelling further indicated that the methylene-THF reductase reaction was ferredoxin reducing under all conditions. In combination with proteomics, modelling also showed that ethanol was synthesised through the acetaldehyde: ferredoxin oxidoreductase (AOR) activity. Conclusions: Our quantitative molecular analysis revealed that H-2 drives rearrangements at several layers of metabolism and provides novel links between carbon, energy, and redox metabolism advancing our understanding of energy conservation in acetogens. We conclude that H-2 supply can substantially increase the efficiency of gas fermentation and thus the feed gas composition can be considered an important factor in developing gas fermentation-based bioprocesses.

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