Abstract
Acetic acid is one of the main inhibitors of lignocellulosic hydrolysates and acetic acid tolerance is crucial for the development of robust cell factories for conversion of biomass. As a precursor of acetyl-coenzyme A, it also plays an important role in central carbon metabolism. Thus, monitoring acetic acid levels is a crucial aspect when cultivating yeast. Transcription factor-based biosensors represent useful tools to follow metabolite concentrations. Here, we present the development of an acetic acid biosensor based on the Saccharomyces cerevisiae transcription factor Haa1 that upon binding to acetic acid relocates to the nucleus. In the biosensor, a synthetic transcription factor consisting of Haa1 and BM3R1 from Bacillus megaterium was used to control expression of a reporter gene under a promoter containing BM3R1 binding sites. The biosensor did not drive expression under a promoter containing Haa1 binding sites and responded to acetic acid over a linear range spanning from 10 to 60 mM. To validate its applicability, the biosensor was integrated into acetic acid-producing strains. A direct correlation between biosensor output and acetic acid production was detected. The developed biosensor enables high-throughput screening of strains producing acetic acid and could also be used to investigate acetic acid-tolerant strain libraries.
Original language | English |
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Article number | foab049 |
Journal | FEMS Yeast Research |
Volume | 21 |
Issue number | 6 |
DOIs | |
Publication status | Published - 1 Sept 2021 |
MoE publication type | A1 Journal article-refereed |
Keywords
- acetic acid
- biosensor
- Haa1
- synthetic transcription factor
- Acetic Acid
- Biosensing Techniques
- Saccharomyces cerevisiae Proteins/genetics
- Transcription Factors/genetics
- Saccharomyces cerevisiae/genetics