A genomics based strategy for the discovery and study of new signaling systems...
A genomics based strategy for the discovery and study of new signaling systems...
批准号:
7670727
负责人:
SEAN F BRADY
金额:
$69.8万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-05-01 至 2014-02-28
关键词:
AnabolismAzidesBacterial GenomeBacterial InfectionsBacterial ModelBiological FactorsBurkholderia malleiChemistryCodeComplexFermentationGene ClusterGenomeGenomicsGrowthHealthHumanInfectionLaboratoriesOperonPathway interactionsPeptide SynthesisPlayRoleSignal TransductionSignaling MoleculeSystemToxinWorkbasebiodefensefollow-upinsightnovelpathogenpromotersmall molecule
中文摘要
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英文摘要
Small molecules play important roles in both the establishment and propagation of bacterial infections.
Although the characterization of small molecules produced by bacterial pathogens grown under controlled
conditions in the laboratory has led to the discovery of many important signaling molecules and toxins,
laboratory fermentation conditions are not representative of the growth conditions under which an infection
occurs. Laboratory based fermentation studies are therefore unlikely to have provided access to the full
repertoire of molecules used by bacterial pathogens during an infection. Cryptic small molecule biosynthetic
gene clusters, gene clusters that do not appear to encode the biosynthesis of any known metabolites, are
routinely found in sequenced bacterial genomes. These cryptic pathways represent the pool of pathways
from which additional signaling systems and toxins will be found in bacterial pathogens. The work outlined in
this proposal will provide access to previously unknown molecules encoded by the cryptic biosynthetic
pathways found in the genomes of biodefense relevant bacterial pathogens. A detailed analysis of the
genomes of many biodefense relevant pathogens suggests that they contain numerous previously unknown
gene clusters that likely code for the biosynthesis of, as yet, unidentified small molecules. The genomics
based approaches that we are using for the discovery of small molecules should result in a more complete
description of the complex networks of small molecule signals and toxins that are used by biodefense
relevant bacterial pathogens; and as a result, provide novel insights into how best to disrupt key steps in the
establishment and propagation of bacterial infections.
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