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Hoyt, K. O.

Publications and source records attributed to Hoyt, K. O..

2 recordsLinked to original sources

Exploring C1 substrate cofeeding in Eubacterium limosum with AneVO, a low-cost anaerobic parallel bioreactor platform

Acetogenic bacteria have emerged as attractive biocatalysts for renewable biochemical production, using the highly efficient Wood-Ljungdahl pathway to convert a range of sustainable single-carbon (C1) feedstocks. The major challenge is their energy-constrained anaerobic lifestyle, which results in slow growth and limits the product spectrum. To overcome this limitation, here we investigate substrate co-metabolism in the acetogen Eubacterium limosum, cofeeding either carbon monoxide (CO) or glucose alongside the primary C1 substrate (methanol or formate). To increase experimental throughput, we developed AneVO, a parallel mini bioreactor system based on eVOLVER that enables benchtop anaerobic batch and fed-batch cultivation, along with continuous delivery of anaerobic gas blends. With all substrate pairs tested, E. limosum grew faster and reached 52-254% higher cell densities with cofeeding, while maintaining or improving the volumetric uptake rate of the main C1 substrate. Product formation also improved, with an increase in volumetric acetate productivity from glucose cofeeding of 2.2-fold with formate and 2.4-fold with methanol, and 3-fold from CO cofeeding with methanol. Together these results validate AneVO as a low-cost platform for convenient benchtop cultivation of strict anaerobic microbes in multiple growth modes, and present a strategy for enhancing C1 bioconversion rates in E. limosum, an emerging model acetogen.

microbiology↗

Development of a Transcriptional Biosensor for Hydrogen Sulfide that Functions under Aerobic and Anaerobic Conditions

Hydrogen sulfide (H2S) is a gaseous gut metabolite with disputed effects on gastrointestinal health. Monitoring H2S concentration in the gut would provide insight into its role in disease, but is complicated by sulfides reactivity and volatility. Here we develop a transcriptional sulfide biosensor in E. coli. The sensor relies on enzymatic oxidation of sulfide catalyzed by a sulfide:quinone reductase (Sqr) to polysulfides, which bind to the repressor SqrR, triggering unbinding from the promoter and transcription of the reporter. Through promoter engineering and improving soluble SqrR expression, we optimized the system to provide an operational range of 50 {micro}M - 750 {micro}M and dynamic range of 18 aerobically. To enable sensing in anaerobic environments, we identified an Sqr from Wolinella succinogenes that uses menaquinone, facilitating reoxidation through the anaerobic electron transport chain by fumarate or nitrate. Use of this homolog resulted in an anaerobic H2S response up to 750 {micro}M. This sensor could ultimately enable spatially and temporally resolved measurements of H2S in the gastrointestinal tract to elucidate the role of this metabolite in disease, and potentially as a non-invasive diagnostic.

synthetic biology↗