Biosensors for the detection of chorismate and cis,cis-muconic acid in Corynebacterium glutamicum

• Published in: Journal of industrial microbiology & biotechnology Vol. 51
• Main Authors: Velasquez-Guzman, Jeanette C, Huttanus, Herbert M, Morales, Demosthenes P, Werner, Tara S, Carroll, Austin L, Guss, Adam M, Yeager, Chris M, Dale, Taraka, Jha, Ramesh K
• Format: Journal Article
• Language: English
• Published: Germany Oxford University Press 09.01.2024
• Subjects: Acinetobacter - genetics; Acinetobacter - metabolism; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Biosensing Techniques - methods; Chorismic Acid - metabolism; Corynebacterium glutamicum - genetics; Corynebacterium glutamicum - metabolism; Promoter Regions, Genetic; Sorbic Acid - analogs & derivatives; Sorbic Acid - metabolism; Transcription Factors - genetics; Transcription Factors - metabolism; Flow cytometry; Promoter optimization; muconic acid; Tool transfer; Chorismate; Biosensor; High-throughput screening; Biomanufacturing; Non-model organism; cis,cis-muconic acid
• ISSN: 1367-5435; 1476-5535; 1476-5535
• DOI: 10.1093/jimb/kuae024

Abstract   Corynebacterium glutamicum ATCC 13032 is a promising microbial chassis for industrial production of valuable compounds, including aromatic amino acids derived from the shikimate pathway. In this work, we developed two whole-cell, transcription factor based fluorescent biosensors to track cis,cis-muconic acid (ccMA) and chorismate in C. glutamicum. Chorismate is a key intermediate in the shikimate pathway from which value-added chemicals can be produced, and a shunt from the shikimate pathway can divert carbon to ccMA, a high value chemical. We transferred a ccMA-inducible transcription factor, CatM, from Acinetobacter baylyi ADP1 into C. glutamicum and screened a promoter library to isolate variants with high sensitivity and dynamic range to ccMA by providing benzoate, which is converted to ccMA intracellularly. The biosensor also detected exogenously supplied ccMA, suggesting the presence of a putative ccMA transporter in C. glutamicum, though the external ccMA concentration threshold to elicit a response was 100-fold higher than the concentration of benzoate required to do so through intracellular ccMA production. We then developed a chorismate biosensor, in which a chorismate inducible promoter regulated by natively expressed QsuR was optimized to exhibit a dose-dependent response to exogenously supplemented quinate (a chorismate precursor). A chorismate–pyruvate lyase encoding gene, ubiC, was introduced into C. glutamicum to lower the intracellular chorismate pool, which resulted in loss of dose dependence to quinate. Further, a knockout strain that blocked the conversion of quinate to chorismate also resulted in absence of dose dependence to quinate, validating that the chorismate biosensor is specific to intracellular chorismate pool. The ccMA and chorismate biosensors were dually inserted into C. glutamicum to simultaneously detect intracellularly produced chorismate and ccMA. Biosensors, such as those developed in this study, can be applied in C. glutamicum for multiplex sensing to expedite pathway design and optimization through metabolic engineering in this promising chassis organism. One-Sentence Summary High-throughput screening of promoter libraries in Corynebacterium glutamicum to establish transcription factor based biosensors for key metabolic intermediates in shikimate and β-ketoadipate pathways.