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BglBrick vectors and datasheets: A synthetic biology platform for gene expression.BglBrick 载体和数据表:用于基因表达的合成生物学平台。
J Biol Eng. 2011 Sep 20;5:12. doi: 10.1186/1754-1611-5-12.
2
Driving forces enable high-titer anaerobic 1-butanol synthesis in Escherichia coli.在大肠杆菌中,驱动因素使高浓度厌氧 1-丁醇的合成成为可能。
Appl Environ Microbiol. 2011 May;77(9):2905-15. doi: 10.1128/AEM.03034-10. Epub 2011 Mar 11.
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Targeted proteomics for metabolic pathway optimization: application to terpene production.靶向蛋白质组学在代谢途径优化中的应用:萜类化合物生产的应用。
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Simultaneous consumption of pentose and hexose sugars: an optimal microbial phenotype for efficient fermentation of lignocellulosic biomass.同时消耗戊糖和己糖:木质纤维素生物质高效发酵的最佳微生物表型。
Appl Microbiol Biotechnol. 2010 Nov;88(5):1077-85. doi: 10.1007/s00253-010-2839-1. Epub 2010 Sep 14.
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Microbial production of fatty-acid-derived fuels and chemicals from plant biomass.利用植物生物质生产脂肪酸衍生燃料和化学品。
Nature. 2010 Jan 28;463(7280):559-62. doi: 10.1038/nature08721.
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Regulation of arabinose and xylose metabolism in Escherichia coli.大肠杆菌中阿拉伯糖和木糖代谢的调控。
Appl Environ Microbiol. 2010 Mar;76(5):1524-32. doi: 10.1128/AEM.01970-09. Epub 2009 Dec 18.
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Quantification and monosaccharide composition of hemicelluloses from different plant functional types.不同植物功能类型中半纤维素的定量和单糖组成。
Plant Physiol Biochem. 2010 Jan;48(1):1-8. doi: 10.1016/j.plaphy.2009.09.008. Epub 2009 Oct 9.
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Transcriptional effects of CRP* expression in Escherichia coli.CRP* 在大肠杆菌中的转录效应。
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Deletion of methylglyoxal synthase gene (mgsA) increased sugar co-metabolism in ethanol-producing Escherichia coli.甲基乙二醛合酶基因(mgsA)的缺失增加了产乙醇大肠杆菌中的糖共代谢。
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Enzymatic assembly of DNA molecules up to several hundred kilobases.长达数百千碱基的DNA分子的酶促组装。
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细胞内 XylR 的补充导致半纤维素糖的共利用。

Supplementation of intracellular XylR leads to coutilization of hemicellulose sugars.

机构信息

Joint BioEnergy Institute, Emeryville, California, USA.

出版信息

Appl Environ Microbiol. 2012 Apr;78(7):2221-9. doi: 10.1128/AEM.06761-11. Epub 2012 Jan 27.

DOI:10.1128/AEM.06761-11
PMID:22286982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3302627/
Abstract

Escherichia coli has the potential to be a powerful biocatalyst for the conversion of lignocellulosic biomass into useful materials such as biofuels and polymers. One important challenge in using E. coli for the transformation of biomass sugars is diauxie, or sequential utilization of different types of sugars. We demonstrate that, by increasing the intracellular levels of the transcription factor XylR, the preferential consumption of arabinose before xylose can be eliminated. In addition, XylR augmentation must be finely tuned for robust coutilization of these two hemicellulosic sugars. Using a novel technique for scarless gene insertion, an additional copy of xylR was inserted into the araBAD operon. The resulting strain was superior at cometabolizing mixtures of arabinose and xylose and was able to produce at least 36% more ethanol than wild-type strains. This strain is a useful starting point for the development of an E. coli biocatalyst that can simultaneously convert all biomass sugars.

摘要

大肠杆菌有可能成为一种强大的生物催化剂,可将木质纤维素生物质转化为有用的材料,如生物燃料和聚合物。在利用大肠杆菌将生物质糖转化为有用物质的过程中,一个重要的挑战是双重营养期现象,即顺序利用不同类型的糖。我们证明,通过增加转录因子 XylR 的细胞内水平,可以消除阿拉伯糖优先于木糖的消耗。此外,必须对 XylR 的增强进行精细调整,以实现这两种半纤维素糖的稳健共利用。我们使用一种无痕基因插入的新技术,将额外的 xylR 拷贝插入到 araBAD 操纵子中。结果表明,该菌株在共代谢阿拉伯糖和木糖混合物方面表现出色,比野生型菌株能够多生产至少 36%的乙醇。该菌株是开发能够同时转化所有生物质糖的大肠杆菌生物催化剂的一个有用起点。