A systems approach to understanding metabolic switching in Streptomyces coelicolor
A systems approach to understanding metabolic switching in Streptomyces coelicolor
批准号:
BB/F003498/1
负责人:
Elizabeth Wellington
金额:
$159.47万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2007
资助国家:
英国
项目状态:
已结题
起止时间:
2007 至 --
中文摘要
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英文摘要
Bacteria found in soil have been exploited for their ability to produce antibiotics for over 60 years. This resulted in the effective treatment of diseases such as TB, bacterial pneumonia, sepsis and a wide range of infections which previously resulted in death or had a very low survival rate. Recently the alarming rise in antibiotic resistant pathogens especially those acquired in hospitals has reduced the efficacy of our existing armoury of drugs and new antibiotics are badly needed. In addition there are a number of emerging pathogens for which existing drugs are not effective. Antibiotics are made during the second phase of growth when there is a transition in metabolism from primary metabolism to secondary metabolism. Primary metabolism is growth related and involves all the normal cellular activities associated with cell growth and division. Whereas secondary metabolism is non-growth linked and is non-essential but many important activities occur during this phase which help the bacterium survive and compete in its natural environment. One of these activities is antibiotic production and is widespread in streptomycetes found in most soils. These bacteria have a fascinating life history and are abundant producers of biologically active compounds many of which have been exploited for their anti-tumour, anti-bacteria and anti-fungal activity. Our research will greatly improve our understanding of how these bacteria regulate the transitions from primary to secondary metabolism and provide mathematical models to simulate the metabolic switch of life styles. The overall approach is regarded as a 'systems' analysis where a model is built of the whole metabolism and it can predict outcomes that will not have been determined previously by experimental methods. A range of modelling tools will be provided and these will be available for use with many other projects involved in a systems approach to biology. The fuller understanding of the metabolic switch and the elucidation of how and why certain antibiotics are made under defined growth conditions will be vital for the full exploitation of these bacteria. Many tools are available to manipulate bacterial genomes and with an understanding of the metabolism it will be possible to discover and manipulate growth in order to produce novel antibiotics.
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DOI:
10.1186/1471-2164-11-202
发表时间:
2010-03-26
期刊:
BMC genomics
影响因子:
4.4
作者:
[Alam MT, Merlo ME, STREAM Consortium, Hodgson DA, Wellington EM, Takano E, Breitling R]
通讯作者:
Breitling R
DOI:
10.1093/nar/gks205
发表时间:
2012-07
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Iqbal M, Mast Y, Amin R, Hodgson DA, STREAM Consortium, Wohlleben W, Burroughs NJ]
通讯作者:
Burroughs NJ
Software Tools and Algorithms for Biological Systems
生物系统的软件工具和算法
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[Arabnia, Hamid R., Tran, Quoc-Nam Professor]
通讯作者:
Tran, Quoc-Nam Professor
DOI:
10.1371/journal.pone.0035756
发表时间:
2012
期刊:
PloS one
影响因子:
3.7
作者:
[Laskaris P, Sekine T, Wellington EM]
通讯作者:
Wellington EM
DOI:
10.1186/1471-2164-11-10
发表时间:
2010-01-06
期刊:
BMC genomics
影响因子:
4.4
作者:
[Nieselt K, Battke F, Herbig A, Bruheim P, Wentzel A, Jakobsen ØM, Sletta H, Alam MT, Merlo ME, Moore J, Omara WA, Morrissey ER, Juarez-Hermosillo MA, Rodríguez-García A, Nentwich M, Thomas L, Iqbal M, Legaie R, Gaze WH, Challis GL, Jansen RC, Dijkhuizen L, Rand DA, Wild DL, Bonin M, Reuther J, Wohlleben W, Smith MC, Burroughs NJ, Martín JF, Hodgson DA, Takano E, Breitling R, Ellingsen TE, Wellington EM]
通讯作者:
Wellington EM
共 6 条
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国内基金
海外基金
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