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Construction of a genome scale metabolic model of Mycobacterium tuberculosis to investigate growth-regulated modulation of metabolism.

Construction of a genome scale metabolic model of Mycobacterium tuberculosis to investigate growth-regulated modulation of metabolism.
构建结核分枝杆菌基因组规模的代谢模型,以研究代谢的生长调节。
批准号:
BB/D007208/1
负责人:
Johnjoe McFadden
金额:
$55.53万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2006
资助国家:
英国
项目状态:
已结题
起止时间:
2006 至 --

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中文摘要
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英文摘要
The TB bacillus is an important pathogen of man and animals that kills about three million people each year. This proposal is to develop a virtual model of the BCG vaccine strain of the TB bacillus in a computer. The model will provide important insight into how this pathogen grows and replicates. The model may also be used to perform virtual experiments that would be very hard or impossible to perform in the real world. For instance, it is difficult to study the behaviour of the TB bacillus when it is growing inside patient's lungs. But if we can identify the metabolic pathways that are active then we can perform easily virtual experiments that will, for instance, investigate how the bacillus will respond to a new antibiotic whilst it is living in the patient's lungs. The virtual TB may also be used to screen new compounds for activity against the TB bacillus: the effect of various antibiotics can be tested in the virtual TB cell far more quickly than with live cells (and with no possibility of the experimenter catching TB). But probably most importantly, the virtual TB cell can be used to invent new antibiotics, by identifying pathways, or groups of pathways, that are essential for growth. This model will first be built using DNA sequence data from the genome. However, to make the virtual cell more realistic, we must incorporate biological data. We will therefore grow the real life organism (actually the vaccine strain of the TB bacillus) in highly defined conditions in the laboratory and perform chemical analysis of what goes in and what comes out of the cell. A remarkable mathematical technique, known as metabolic flux analysis, can then be used to estimate the flux of metabolites through each central metabolism pathway inside the cell. This information will be incorporated into the virtual cell to make its behaviour correspond more closely with the biological organism. The next stage of the project is testing our virtual cell. To do this we will identify which pathways are essential in the virtual cell and then inactivate those pathways in living cells. We will then see if the growth (or absence of growth) of the real life cells matches the predictions of the model. These tests will be used to refine and improve the model that may thereafter be used in drug development.
期刊论文(8)
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会议论文
DOI: 10.1371/journal.ppat.1002091
发表时间: 2011-07
期刊: PLoS pathogens
影响因子: 6.7
作者: [Beste DJ, Bonde B, Hawkins N, Ward JL, Beale MH, Noack S, Nöh K, Kruger NJ, Ratcliffe RG, McFadden J]
通讯作者: McFadden J
DOI: 10.1186/gb-2007-8-5-r89
发表时间: 2007
期刊: GENOME BIOLOGY
影响因子: 12.3
作者: [Beste, Dany J V, Hooper, Tracy, Stewart, Graham, Bonde, Bhushan, Avignone-Rossa, Claudio, Bushell, Michael E, Wheeler, Paul, Klamt, Steffen, Kierzek, Andrzej M, McFadden, Johnjoe]
通讯作者: McFadden, Johnjoe
DOI: 10.1371/journal.pone.0005349
发表时间: 2009-04-28
期刊: PloS one
影响因子: 3.7
作者: [Beste DJ, Espasa M, Bonde B, Kierzek AM, Stewart GR, McFadden J]
通讯作者: McFadden J
DOI: 10.1371/journal.pcbi.1002060
发表时间: 2011-06
期刊: PLoS computational biology
影响因子: 4.3
作者: [Bonde BK, Beste DJ, Laing E, Kierzek AM, McFadden J]
通讯作者: McFadden J
Systems-based screen of compounds that target nitrogen metabolism of Mycobacterium tuberculosis.
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    BB/V010611/1
  • 项目类别:
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    $95.88万
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    2021
  • 负责人:
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Newton001: Identification of host and pathogen glucose metabolism modulation during Mycobacterium leprae infection of human macrophages and Schwann ce
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    BB/L022869/1
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    2014
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  • 项目类别:
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  • 财政年份:
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  • 负责人:
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  • 依托单位:
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