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本文引用的文献

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MEME SUITE: tools for motif discovery and searching.MEME套件:用于基序发现和搜索的工具。
Nucleic Acids Res. 2009 Jul;37(Web Server issue):W202-8. doi: 10.1093/nar/gkp335. Epub 2009 May 20.
2
Constitutive mutations in the Escherichia coli AraC protein.大肠杆菌AraC蛋白的组成型突变
J Bacteriol. 2009 Apr;191(8):2668-74. doi: 10.1128/JB.01529-08. Epub 2009 Feb 13.
3
Carbon catabolite repression in bacteria: many ways to make the most out of nutrients.细菌中的碳分解代谢物阻遏:充分利用营养物质的多种方式。
Nat Rev Microbiol. 2008 Aug;6(8):613-24. doi: 10.1038/nrmicro1932.
4
Role of xylose transporters in xylitol production from engineered Escherichia coli.木糖转运蛋白在工程化大肠杆菌生产木糖醇中的作用。
J Biotechnol. 2008 Apr 30;134(3-4):246-52. doi: 10.1016/j.jbiotec.2008.02.003. Epub 2008 Feb 15.
5
The mechanisms of carbon catabolite repression in bacteria.细菌中碳分解代谢物阻遏的机制。
Curr Opin Microbiol. 2008 Apr;11(2):87-93. doi: 10.1016/j.mib.2008.02.007. Epub 2008 Mar 21.
6
RegulonDB (version 6.0): gene regulation model of Escherichia coli K-12 beyond transcription, active (experimental) annotated promoters and Textpresso navigation.RegulonDB(版本6.0):大肠杆菌K-12超越转录的基因调控模型、活跃(实验性)注释启动子及Textpresso导航
Nucleic Acids Res. 2008 Jan;36(Database issue):D120-4. doi: 10.1093/nar/gkm994. Epub 2007 Dec 23.
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Quantifying similarity between motifs.量化基序之间的相似性。
Genome Biol. 2007;8(2):R24. doi: 10.1186/gb-2007-8-2-r24.
8
RegTransBase--a database of regulatory sequences and interactions in a wide range of prokaryotic genomes.RegTransBase——一个包含多种原核生物基因组调控序列及相互作用的数据库。
Nucleic Acids Res. 2007 Jan;35(Database issue):D407-12. doi: 10.1093/nar/gkl865. Epub 2006 Nov 16.
9
Engineering Escherichia coli for xylitol production from glucose-xylose mixtures.工程改造大肠杆菌以利用葡萄糖-木糖混合物生产木糖醇。
Biotechnol Bioeng. 2006 Dec 20;95(6):1167-76. doi: 10.1002/bit.21082.
10
Global physiological analysis of carbon- and energy-limited growing Escherichia coli confirms a high degree of catabolic flexibility and preparedness for mixed substrate utilization.对碳和能量受限条件下生长的大肠杆菌进行的全局生理学分析证实,其具有高度的分解代谢灵活性以及对混合底物利用的准备状态。
Environ Microbiol. 2005 Oct;7(10):1568-81. doi: 10.1111/j.1462-2920.2005.00846.x.

大肠杆菌中阿拉伯糖和木糖代谢的调控。

Regulation of arabinose and xylose metabolism in Escherichia coli.

机构信息

Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 600 S. Mathews Ave., Urbana, IL 61810, USA.

出版信息

Appl Environ Microbiol. 2010 Mar;76(5):1524-32. doi: 10.1128/AEM.01970-09. Epub 2009 Dec 18.

DOI:10.1128/AEM.01970-09
PMID:20023096
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2832368/
Abstract

Bacteria such as Escherichia coli will often consume one sugar at a time when fed multiple sugars, in a process known as carbon catabolite repression. The classic example involves glucose and lactose, where E. coli will first consume glucose, and only when it has consumed all of the glucose will it begin to consume lactose. In addition to that of lactose, glucose also represses the consumption of many other sugars, including arabinose and xylose. In this work, we characterized a second hierarchy in E. coli, that between arabinose and xylose. We show that, when grown in a mixture of the two pentoses, E. coli will consume arabinose before it consumes xylose. Consistent with a mechanism involving catabolite repression, the expression of the xylose metabolic genes is repressed in the presence of arabinose. We found that this repression is AraC dependent and involves a mechanism where arabinose-bound AraC binds to the xylose promoters and represses gene expression. Collectively, these results demonstrate that sugar utilization in E. coli involves multiple layers of regulation, where cells will consume first glucose, then arabinose, and finally xylose. These results may be pertinent in the metabolic engineering of E. coli strains capable of producing chemical and biofuels from mixtures of hexose and pentose sugars derived from plant biomass.

摘要

当同时提供多种糖时,细菌(如大肠杆菌)通常会一次消耗一种糖,这个过程被称为碳分解代谢物阻遏。经典的例子涉及葡萄糖和乳糖,大肠杆菌首先会消耗葡萄糖,只有当它消耗完所有的葡萄糖后,才会开始消耗乳糖。除了乳糖之外,葡萄糖还会抑制其他许多糖的消耗,包括阿拉伯糖和木糖。在这项工作中,我们描述了大肠杆菌中的第二个层次,即阿拉伯糖和木糖之间的层次。我们表明,当在两种戊糖的混合物中生长时,大肠杆菌会先消耗阿拉伯糖,然后再消耗木糖。与涉及分解代谢物阻遏的机制一致,在阿拉伯糖存在的情况下,木糖代谢基因的表达受到抑制。我们发现这种抑制是依赖于 AraC 的,并且涉及一种机制,其中阿拉伯糖结合的 AraC 结合到木糖启动子上并抑制基因表达。总的来说,这些结果表明,大肠杆菌中的糖利用涉及多个层次的调节,细胞首先消耗葡萄糖,然后是阿拉伯糖,最后是木糖。这些结果在代谢工程中可能是相关的,代谢工程旨在利用源自植物生物质的己糖和戊糖混合物来生产化学品和生物燃料。