Engineering new-to-nature biochemical conversions by combining fermentative metabolism with respiratory modules.
Helena Schulz-MirbachJan Lukas KrüsemannTheofania AndreadakiJana Natalie NerlichEleni MavrothalassitiSimon BoeckerPhilipp SchneiderMoritz WeresowOmar AbdelwahabNicole PacziaBeau DronsellaTobias J ErbArren Bar-EvenSteffen KlamtSteffen N LindnerPublished in: Nature communications (2024)
Anaerobic microbial fermentations provide high product yields and are a cornerstone of industrial bio-based processes. However, the need for redox balancing limits the array of fermentable substrate-product combinations. To overcome this limitation, here we design an aerobic fermentative metabolism that allows the introduction of selected respiratory modules. These can use oxygen to re-balance otherwise unbalanced fermentations, hence achieving controlled respiro-fermentative growth. Following this design, we engineer and characterize an obligate fermentative Escherichia coli strain that aerobically ferments glucose to stoichiometric amounts of lactate. We then re-integrate the quinone-dependent glycerol 3-phosphate dehydrogenase and demonstrate glycerol fermentation to lactate while selectively transferring the surplus of electrons to the respiratory chain. To showcase the potential of this fermentation mode, we direct fermentative flux from glycerol towards isobutanol production. In summary, our design permits using oxygen to selectively re-balance fermentations. This concept is an advance freeing highly efficient microbial fermentation from the limitations imposed by traditional redox balancing.
Keyphrases
- saccharomyces cerevisiae
- highly efficient
- microbial community
- escherichia coli
- wastewater treatment
- lactic acid
- respiratory tract
- high resolution
- type diabetes
- high throughput
- network analysis
- skeletal muscle
- blood pressure
- candida albicans
- biofilm formation
- high intensity
- cystic fibrosis
- metabolic syndrome
- amino acid
- weight loss
- multidrug resistant