BACTERIAL CELL SURFACE STRUCTURE FUNCTIONS & BIOGENESIS

细菌细胞表面结构功能

基本信息

  • 批准号:
    2459330
  • 负责人:
  • 金额:
    $ 16.77万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1980
  • 资助国家:
    美国
  • 起止时间:
    1980-08-01 至 1998-12-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION: (adapted from investigator's abstract) A rapidly increasing number of membrane proteins in bacteria have been found to contain an N- terminal lipoamino acid, N-acyl-diacylglycerylcysteine, the hallmark of all bacterial lipoproteins. As of 1993, more than 130 lipoproteins have been identified in both gram positive and gram negative bacteria covering a wide spectrum of genera and species. The biosynthesis of lipoproteins in bacteria is both temporally and spatially related to the export of these membrane proteins across the cytoplasmic membranes. These proteins are made as precursor proteins with N-terminal signal sequences which contain a "lipobox" sequence at the junction of the signal sequences and the mature proteins. Following the interaction of the precursor proteins with the export machinery defined by the SecA, SecY SecD and SecF proteins, the prolipoproteins are modified and processed by three enzymes located in the cytoplasmic membrane. These three enzymes are prolipoprotein diacylglyceral transferase, prolipoprotein signal peptidase and apolipoprotein N- acyltransferase encoded by the lgt, lsp, and lnt genes, respectively, in Escherichia coli and Salmonella typhimurium. Mutants defective in any of these three genes are conditionally lethal. In addition, lnt mutants are also copper sensitive, and the lnt gene is allelic with the cutE gene, one of six genes postulated to be involved in copper transport and homeostasis in E. coli. Using the E. coli major outer membrane lipoprotein as the model system, the investigator proposes; (i) to elucidate the biochemical basis for the essential nature of the lipoprotein biosynthetic pathway in E. coli or S. typhimurium; (ii) to identify the gene encoding lipoprotein:peptidoglycan ligase in E. coli; (iii) to study the structure, function and assembly of the prolipoprotein modification and processing enzymes; and (iv) to study the interrelationship between apolipoprotein N-acylation and the transport and homeostasis of divalent cations such as Cu++ in E. coli. The results of the proposed studies will provide new information regarding the structures, functions and biogenesis of lipoproteins in bacteria. These studies will also provide a rational basis for the search or design of antibacterial agents which utilize the enzymes of this pathway as targets.
描述:(改编自研究者的摘要)A迅速

项目成果

期刊论文数量(45)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Prolipoprotein signal peptidase in Escherichia coli is distinct from the M13 procoat protein signal peptidase.
  • DOI:
    10.1016/s0021-9258(18)33964-4
  • 发表时间:
    1982-09
  • 期刊:
  • 影响因子:
    0
  • 作者:
    M. Tokunaga;J. Loranger;P. Wolfe;H. C. Wu
  • 通讯作者:
    M. Tokunaga;J. Loranger;P. Wolfe;H. C. Wu
Alterations of the carboxyl-terminal amino acid residues of Escherichia coli lipoprotein affect the formation of murein-bound lipoprotein.
大肠杆菌脂蛋白羧基末端氨基酸残基的改变影响胞壁质结合脂蛋白的形成。
Isolation and characterization of a temperature-sensitive mutant of Salmonella typhimurium defective in prolipoprotein modification.
前脂蛋白修饰缺陷的鼠伤寒沙门氏菌温度敏感突变体的分离和表征。
Isolation and characterization of a new globomycin-resistant dnaE mutant of Escherichia coli.
大肠杆菌新的球霉素抗性 dnaE 突变体的分离和表征。
  • DOI:
    10.1128/jb.169.8.3400-3408.1987
  • 发表时间:
    1987
  • 期刊:
  • 影响因子:
    3.2
  • 作者:
    Sakka,K;Watanabe,T;Beers,R;Wu,HC
  • 通讯作者:
    Wu,HC
Neither lipid modification nor processing of prolipoprotein is essential for the formation of murein-bound lipoprotein in Escherichia coli.
脂质修饰和前脂蛋白加工对于大肠杆菌中胞壁质结合脂蛋白的形成都不是必需的。
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PAUL D RICK其他文献

PAUL D RICK的其他文献

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{{ truncateString('PAUL D RICK', 18)}}的其他基金

Male Fertility & Protein Expression in Spermatogenesis
男性生育能力
  • 批准号:
    6788832
  • 财政年份:
    2001
  • 资助金额:
    $ 16.77万
  • 项目类别:
BIOSYNTHESIS OF ENTEROBACTERIAL COMMON ANTIGEN
肠杆菌共同抗原的生物合成
  • 批准号:
    2444866
  • 财政年份:
    1984
  • 资助金额:
    $ 16.77万
  • 项目类别:
BIOSYNTHESIS OF ENTEROBACTERIAL COMMON ANTIGEN
肠杆菌共同抗原的生物合成
  • 批准号:
    3131285
  • 财政年份:
    1984
  • 资助金额:
    $ 16.77万
  • 项目类别:
BIOSYNTHESIS OF ENTEROBACTERIAL COMMON ANTIGEN
肠杆菌共同抗原的生物合成
  • 批准号:
    2192074
  • 财政年份:
    1984
  • 资助金额:
    $ 16.77万
  • 项目类别:
BIOSYNTHESIS OF ENTEROBACTERIAL COMMON ANTIGEN
肠杆菌共同抗原的生物合成
  • 批准号:
    6019067
  • 财政年份:
    1984
  • 资助金额:
    $ 16.77万
  • 项目类别:
BIOSYNTHESIS OF ENTEROBACTERIAL COMMON ANTIGEN
肠杆菌共同抗原的生物合成
  • 批准号:
    3131288
  • 财政年份:
    1984
  • 资助金额:
    $ 16.77万
  • 项目类别:
BIOSYNTHESIS OF ENTEROBACTERIAL COMMON ANTIGEN
肠杆菌共同抗原的生物合成
  • 批准号:
    3131290
  • 财政年份:
    1984
  • 资助金额:
    $ 16.77万
  • 项目类别:
BIOSYNTHESIS OF ENTEROBACTERIAL COMMON ANTIGEN
肠杆菌共同抗原的生物合成
  • 批准号:
    2734768
  • 财政年份:
    1984
  • 资助金额:
    $ 16.77万
  • 项目类别:
BIOSYNTHESIS OF ENTEROBACTERIAL COMMON ANTIGEN
肠杆菌共同抗原的生物合成
  • 批准号:
    2061463
  • 财政年份:
    1984
  • 资助金额:
    $ 16.77万
  • 项目类别:
BIOSYNTHESIS OF ENTEROBACTERIAL COMMON ANTIGEN
肠杆菌共同抗原的生物合成
  • 批准号:
    3131291
  • 财政年份:
    1984
  • 资助金额:
    $ 16.77万
  • 项目类别:

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