Abstract
Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙L−1 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙L−1). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an OD600 of 40,150 mg∙L−1 naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-L−1 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain.[Figure not available: see fulltext.]
Original language | English |
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Pages (from-to) | 793-801 |
Number of pages | 9 |
Journal | Frontiers of Chemical Science and Engineering |
Volume | 14 |
Issue number | 5 |
DOIs | |
State | Published - 1 Oct 2020 |
Keywords
- 1-naphthol
- 4-aminoantipyrine
- ARTP mutagenesis
- Bacillus cereus QCG
- high-throughput screening
- naphthalene