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Elucidation of bacterial glycosylytransferase specificity

Elucidation of bacterial glycosylytransferase specificity
细菌糖基转移酶特异性的阐明
批准号:
DP0559665
负责人:
Prof Peter Reeves
金额:
$15.94万
依托单位:
依托单位国家:
澳大利亚
项目类别:
Discovery Projects
财政年份:
2005
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2005-03-03 至 2008-12-01

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英文摘要
The benefits are involvement in the growth area of polysaccharide research, with potential for major industrial spin off. Polysaccharides are critical in all organisms as signalling, structural and storage compounds. Bacteria make a wide variety with extensive use of unusual sugars, some with uses from oil emulsifiers to food thickeners. The project is on the enzymes that assemble bacterial polysaccharides. We are world leaders in genetics of the gene clusters especially synthesis of the unusual sugars. We now aim to fill a major gap by determining which enzymes make which bonds, leading to options for new gene combinations and novel structures. We have a lead in research in this area and Australia gains if we maintain that lead.
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Importance of Wzx flippase specificity for O-antigen diversity
  • 批准号:
    DP140104068
  • 项目类别:
    Discovery Projects
  • 资助金额:
    $25.84万
  • 财政年份:
    2014
  • 负责人:
    Prof Peter Reeves
  • 依托单位:
Major upgrade of the computing hardware and software for the widely used BioManager bioinformatic service
  • 批准号:
    LE0668549
  • 项目类别:
    Linkage Infrastructure, Equipment and Facilities
  • 资助金额:
    $18.67万
  • 财政年份:
    2006
  • 负责人:
    Prof Peter Reeves
  • 依托单位:
Synthesis and assembly of bacterial repeat unit polysaccharides
  • 批准号:
    DP0452629
  • 项目类别:
    Discovery Projects
  • 资助金额:
    $15.67万
  • 财政年份:
    2004
  • 负责人:
    Prof Peter Reeves
  • 依托单位:
Genetics and evolution of Shigella O antigens
  • 批准号:
    ARC : DP0210675
  • 项目类别:
    Discovery Projects
  • 资助金额:
    $17.6万
  • 财政年份:
    2002
  • 负责人:
    Prof Peter Reeves
  • 依托单位:
国内基金
海外基金
中国棉铃虫核多角体病毒基因组库和分子进化
  • 批准号:
    30540076
  • 项目类别:
    专项基金项目
  • 资助金额:
    8.0万元
  • 批准年份:
    2005
  • 负责人:
    王汉中
  • 依托单位:
细菌脂蛋白(BLP)诱导LPS交叉耐受的分子机理研究