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Summary/Abstract The University of California, San Diego was awarded a R01 with PI, Hwa based on the following Project Summary: This project aims to elucidate the physiological origin of the growth inhibitory effect of short-chain fatty acids (SCFA) such as acetate, propionate, and butyrate on exemplary bacterial species in the gut microbiota. Our preliminary data indicate that the affectors of SCFA toxicity are a reduction in intracellular pH and an accumulation of the anion form of these acids in the cytoplasm. A battery of high-throughput methods (quantitative metabolomics, quantitative proteomics, tRNA aminoacylation arrays, ratiometric fluorescence) are proposed together with classical biochemical approaches to identify the locations of the growth bottlenecks, and link their growth inhibitory effects quantitatively to the two identified affectors. These methods will be combined with orthogonal perturbations, one creating “overdose of useless metabolites” but not affecting intracellular pH, the other reducing intracellular pH but not affecting metabolite abundances, to quantify the effect of each perturbation on bacterial growth. The results obtained will be used to develop quantitative models that predict the % growth-reduction for a given SCFA level in the environment. The above studies will be done for each of the three major SCFAs and for four exemplary gut bacterial species: the best characterized model organism Echerichia coli, a pathogenic strain of Salmonella Typhimurium, and Bacteroides thetaiotaomircon and Eubacteria rectale, abundant members from the respective phyla of Bacteroidetes and Firmicutes which comprise the vast majority of the gut microbiota. We will additionally characterize key mutants that exhibit reduced SCFA-sensitivity. Comparisons of results for these different species and mutants will provide us with a comprehensive picture for strategies gut bacteria use to cope with SCFA toxicity, as well as the compromises these strategies impose on the growth physiology of the organisms in unstressed conditions. An important piece of equipment for the research, an epi-fluorescence microscope, is broken, and we are requesting an emergency equipment supplement to replace key components of the microscope so that measurements that depend on the microscope can be completed.
期刊论文(14)
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会议论文
DOI: 10.1128/msphere.00095-18
发表时间: 2018-04-25
期刊: mSphere
影响因子: 4.8
作者: [Zhu M, Dai X]
通讯作者: Dai X
DOI: 10.1016/j.mib.2021.07.008
发表时间: 2021-10
期刊: CURRENT OPINION IN MICROBIOLOGY
影响因子: 5.4
作者: [Okano, Hiroyuki, Hermsen, Rutger, Hwa, Terence]
通讯作者: Hwa, Terence
On the optimality of the enzyme-substrate relationship in bacteria.
关于细菌中酶 - 基底关系的最佳性。
DOI: 10.1371/journal.pbio.3001416
发表时间: 2021-10
期刊: PLoS biology
影响因子: 9.8
作者: [Dourado H, Mori M, Hwa T, Lercher MJ]
通讯作者: Lercher MJ
DOI: 10.1038/nature12446
发表时间: 2013-08-15
期刊: Nature
影响因子: 64.8
作者: []
通讯作者:
8
    Training Program in Quantitative Integrative Biology
    Training Program in Quantitative Integrative Biology
    Quantitative studies of metabolic switches in enteric bacteria
    Quantitative Studies of Metabolic Switches in enteric bacteria
    国内基金
    海外基金
    具有抗癌活性的天然产物金霉酸(Aureolic acids)全合成与选择性构建2-脱氧糖苷键
    • 批准号:
      22007039
    • 项目类别:
      青年科学基金项目
    • 资助金额:
      24.0万元
    • 批准年份:
      2020
    • 负责人:
      王黎明
    • 依托单位:
    海洋放线菌来源聚酮类化合物Pteridic acids生物合成机制研究
    手性Lewis Acids催化的分子内串联1,5-氢迁移/环合反应及其在构建结构多样性手性含氮杂环化合物中的应用
    对空气稳定的新型的有机金属Lewis Acids催化剂制备、表征与应用研究
    • 批准号:
      21172061
    • 项目类别:
      面上项目
    • 资助金额:
      30.0万元
    • 批准年份:
      2011
    • 负责人:
      许新华
    • 依托单位: