| 论文题目: | Development of an anhydrotetracycline-inducible gene expression system for solvent-producing Clostridium acetobutylicum: A useful tool for strain engineering |
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| 作者: | Dong, HJ; Tao, WW; Zhang, YP; Li, Y |
| 联系作者: | Li, Y |
| 刊物名称: | METABOLIC ENGINEERING |
| 期: | 1 |
| 卷: | 14 |
| 页: | 59-67 |
| 年份: | 2012 |
| 影响因子: | 5.614 |
| 论文下载: | 下载地址 |
| 摘要: | Clostridium acetobutylicum is an important solvent (acetone-butanol-ethanol) producing bacterium. However, a stringent, effective, and convenient-to-use inducible gene expression system that can be used for regulating the gene expression strength in C acetobutylicum is currently not available. Here, we report an anhydrotetracycline-inducible gene expression system for solvent-producing bacterium C acetobutylicum. This system consists of a functional chloramphenicol acetyltransferase gene promoter containing tet operators (tetO), Pthl promoter (thiolase gene promoter from C acetobutylicum) controlling TetR repressor expression cassette, and the chemical inducer anhydrotetracycline (aTc). The optimized system, designated as pGusA2-2tetO1, allows gene regulation in an inducer aTc concentration-dependent way, with an inducibility of over two orders of magnitude. The stringency of TetR repression supports the introduction of the genes encoding counterselective marker into C acetobutylicum, which can be used to increase the mutant screening efficiency. This aTc-inducible gene expression system will thus increase the genetic manipulation capability for engineering C acetobutylicum. (C) 2011 Elsevier Inc. All rights reserved. |
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