# Engineering Clostridium thermocellum for production of 2,3-butanediol from cellulose

## TL;DR

Scientists engineered a bacterium to produce a valuable chemical from cellulose, improving its efficiency and understanding of the process.

## Contribution

The study introduces a thermophilic 2,3-butanediol pathway in Clostridium thermocellum and identifies key metabolic limitations using cell-free systems.

## Key findings

- A 23BD titer of 19.7 mM was achieved from cellulose with a 24% metabolic yield.
- Exogenous BDH activity was essential, while native ALS and ALDC activities were limiting.
- Adding acetate improved 23BD yield by addressing redox balance limitations.

## Abstract

Clostridium thermocellum is a promising host for consolidated bioprocessing due to its ability to directly ferment cellulose into fuels and chemicals. However, natural product formation in this organism is limited. Here, we report engineering C. thermocellum for the production of 2,3-butanediol (23BD), a valuable industrial chemical. We functionally expressed a thermophilic 23BD pathway in this organism resulting in a 23BD titer of 19.7 mM from cellulose, representing a metabolic yield of 24%. We used a cell-free systems biology approach to identify limiting steps in the 23BD pathway, revealing that exogenous 23BD dehydrogenase (BDH) activity was essential for production, while native acetolactate synthase (ALS) and acetolactate decarboxylase (ALDC) activities were present but limiting in the parent strain. This approach also revealed redox balance limitations. We demonstrated that this improved understanding of redox balance limitations could be used to increase 23BD titer in vivo, showing that adding acetate could be used to increase 23BD yield. This work establishes a foundation for developing C. thermocellum into a robust platform for 23BD production directly from cellulose and highlights the utility of cell-free systems for guiding metabolic engineering in non-model organisms.