| Literature DB >> 29087704 |
Chang Liu1,2, Bo Zhang1,3, Yi-Ming Liu1, Ke-Qian Yang1, Shuang-Jiang Liu1.
Abstract
The quantitative monitoring of intracellular metabolites with in vivo biosensors provides an efficient means of identifying high-yield strains and observing product accumulation in real time. In this study, a shikimic acid (SA) biosensor was constructed from a LysR-type transcriptional regulator (ShiR) of Corynebacterium glutamicum. The SA biosensor specifically responded to the increase of intracellular SA concentration over a linear range of 19.5 ± 3.6 to 120.9 ± 1.2 fmole at the single-cell level. This new SA biosensor was successfully used to (1) monitor the SA production of different C. glutamicum strains; (2) develop a novel result-oriented high-throughput ribosome binding site screening and sorting strategy that was used for engineering high-yield shikimate-producing strains; and (3) engineer a whole-cell biosensor through the coexpression of the SA sensor and a shikimate transporter shiA gene in C. glutamicum RES167. This work demonstrated that a new intracellular SA biosensor is a valuable tool facilitating the fast development of microbial SA producer.Entities:
Keywords: Corynebacterium glutamicum; high-throughput screening; shikimic acid biosensor; single-cell sorting; transcriptional regulator; whole-cell biosensor
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Year: 2017 PMID: 29087704 DOI: 10.1021/acssynbio.7b00339
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110