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Studies of the productivity and maintenance of cell functions in the stationary-phase cells of bacteria

Studies of the productivity and maintenance of cell functions in the stationary-phase cells of bacteria
细菌静止期细胞的生产力和细胞功能维持的研究
批准号:
07556089
负责人:
TAKAHASHI Hideo
金额:
$1.6万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (A)
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1996

项目摘要

项目成果

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中文摘要
翻译
本研究旨在阐明大肠杆菌稳定期特异性功能的sigma^蛋白的结构与功能关系<38>,了解sigma^<38>蛋白在氨基酸生产细胞中的特性。得到的结果如下:(1)删除了区域4.2的sigma^的导数<38>比原始sigma^保留了更高的活性<38>,表明区域4.2具有调节活性的功能。(2)在产氨基酸的大肠杆菌细胞的培养物中(苏氨酸生产),sigma β蛋白的水平<38>在培养的前3至5小时迅速增加,然后在10- 20小时稳定在较低水平,并且之后再次增加。通过碳源向氨基酸的转化效率估计的氨基酸生产率在培养的20小时最高,然后下降。这些结果表明,可以通过监测细胞中sigma^蛋白的水平来指示高效生产氨基酸的临界时间<38>。
英文摘要
This research project was aimed to clarify the relationship between structure and function of sigma^<38> protein which functions specifically in the stationary phase of E.coli, and to know the properties of sigma^<38> protein in the amino acid-producing cells. The results obtained are as follows : (1) A derivative of sigma^<38> which has deleted the region 4.2 retained a higher activity than the original sigma^<38>, indicating that the region 4.2 has a function to moderate the activity. (2) In the culture of amino acid-producing E.coli cells (threonine production), the level of sigma^<38> protein increased rapidly in the first 3 to 5 hr cultivation, then settled down to a lower level at 10-20hr, and increased again afterward Amino acid productivity estimated by the conversion efficiency of carbon source to amino acid was highest at 20 hr cultivation and then decreased. These results indicate that the critical time for efficient production of amino acid can be pointed by monitoring the level of sigma^<38> protein in the cells.
期刊论文(12)
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会议论文
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作者: []
通讯作者:
Asayama, M.et al.: "A new set of PCR primers for specific detection of the gene encoding the principal sigma factor in cyanobacteria" J.Gen. Appl. Microbiol.42. 511-515 (1996)
Asayama, M.等人:“一套新的 PCR 引物,用于特异性检测编码蓝藻中主要 Sigma 因子的基因”J.Gen。
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通讯作者:
Chibazakura, T: "Effects of spoOA promoter switching at the initiation of sporulation in Bacillus subtilis" J. Bacteriol.177. 4520-4523 (1995)
Chibazakura, T:“枯草芽孢杆菌孢子形成起始时 spoOA 启动子转换的影响”J. Bacteriol.177。
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通讯作者:
K.Tanaka: "Identification and analysis of the rpoS-depndent promoter of katE,encoding catalase HPIIin Escherichia coli" Biochem.Biophys.Acta. (印刷中). (1997)
K. Tanaka:“大肠杆菌中编码过氧化氢酶 HPII 的 rpoS 依赖性启动子的鉴定和分析”Biochem.Biophys.Acta(出版中)。
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通讯作者:
共 11 条
    Basic study of the niche function improvement medicine development that targeted a homeodynamics-related mediator
    • 批准号:
      18K06905
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.75万
    • 财政年份:
      2018
    • 负责人:
      TAKAHASHI Hideo
    • 依托单位:
    Research for homeodynamics regeneration-promoting drug discovery
    • 批准号:
      15K08253
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.16万
    • 财政年份:
      2015
    • 负责人:
      TAKAHASHI Hideo
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    Basic scientific research for formulating drugs for treatment of hypertension
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      24590337
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.49万
    • 财政年份:
      2012
    • 负责人:
      TAKAHASHI Hideo
    • 依托单位:
    Fundamental research for NMR structural analysis of human membrane proteins
    • 批准号:
      24370048
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $11.4万
    • 财政年份:
      2012
    • 负责人:
      TAKAHASHI Hideo
    • 依托单位:
    国内基金
    海外基金
    基于hTERT promoter突变的脑胶质瘤分子异质性可视化及靶向的研究
    • 批准号:
      82373403
    • 项目类别:
      面上项目
    • 资助金额:
      48万元
    • 批准年份:
      2023
    • 负责人:
      程也
    • 依托单位: