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使用正向和反向遗传工具操作丁醇产生菌拜氏梭菌 NCIMB 14988。

The Butanol Producing Microbe Clostridium beijerinckii NCIMB 14988 Manipulated Using Forward and Reverse Genetic Tools.

机构信息

Clostridia Research Group, BBSRC/EPSRC Synthetic Biology Research Centre (SBRC), University of Nottingham, University Park, Nottingham NG7 2RD, UK.

出版信息

Biotechnol J. 2018 Nov;13(11):e1700711. doi: 10.1002/biot.201700711. Epub 2018 Apr 29.

DOI:10.1002/biot.201700711
PMID:29660854
Abstract

The solventogenic anaerobe Clostridium beijerinckii has potential for use in the sustainable bioconversion of plant-derived carbohydrates into solvents, such as butanol or acetone. However, relatively few strains have been extensively characterised either at the genomic level or through exemplification of a complete genetic toolkit. To remedy this situation, a new strain of C. beijerinckii, NCIMB 14988, is selected from among a total of 55 new clostridial isolates capable of growth on hexose and pentose sugars. Chosen on the basis of its favorable properties, the complete genome sequence of NCIMB 14988 is determined and a high-efficiency plasmid transformation protocol devised. The developed DNA transfer procedure allowed demonstration in NCIMB 14988 of the forward and reverse genetic techniques of transposon mutagenesis and gene knockout, respectively. The latter is accomplished through the successful deployment of both group II intron retargeting (ClosTron) and allelic exchange. In addition to gene inactivation, the developed allelic exchange procedure is used to create point mutations in the chromosome, allowing for the effect of amino acid changes in enzymes involved in primary metabolism to be characterized. ClosTron mediated disruption of the currently unannotated non-coding region between genes LF65_05915 and LF65_05920 is found to result in a non-sporulating phenotype.

摘要

产溶剂厌氧细菌凝结芽孢杆菌有望用于可持续地将植物来源的碳水化合物转化为溶剂,如丁醇或丙酮。然而,只有相对较少的菌株在基因组水平或通过完整遗传工具包的范例得到了广泛的表征。为了改善这种情况,从总共 55 种能够在己糖和戊糖上生长的新型梭菌分离株中选择了一株新型凝结芽孢杆菌 NCIMB 14988。基于其有利的特性选择了 NCIMB 14988,确定了其完整基因组序列并设计了高效质粒转化方案。开发的 DNA 转移程序允许在 NCIMB 14988 中分别展示转座子诱变和基因敲除的正向和反向遗传技术。后者是通过成功部署 II 类内含子重定向(ClosTron)和等位基因交换来实现的。除了基因失活外,开发的等位基因交换程序还用于在染色体上产生点突变,从而可以表征参与初级代谢的酶中的氨基酸变化的影响。发现 ClosTron 介导的 LF65_05915 和 LF65_05920 基因之间未注释的非编码区的破坏导致不产孢子的表型。

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