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1996 Fiscal Year Final Research Report Summary

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

Research Project

Project/Area Number 07556089
Research Category

Grant-in-Aid for Scientific Research (A)

Allocation TypeSingle-year Grants
Section試験
Research Field 応用微生物学・応用生物化学
Research InstitutionThe University of Tokyo

Principal Investigator

TAKAHASHI Hideo  University of Tokyo, Institute of Molecular and Cellular Biosciences, Professor, 分子細胞生物学研究所, 教授 (90013333)

Co-Investigator(Kenkyū-buntansha) KOJIMA Hiroyuki  Ajinomoto Co. ; Central Research Institute ; Principal Researcher, 中央研究所, 主任研究員
Project Period (FY) 1995 – 1996
Keywordsstationary phase, / promoter, / sigma^<38> / E.coli / major-type sigma factors, / rpoS gene
Research Abstract

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.

  • Research Products

    (6 results)

All Other

All Publications (6 results)

  • [Publications] Asayama,M: "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)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] K.Tanaka: "Identification and analysis of the rpoS-depndent promoter of katE,encoding catalase HPIIin Escherichia coli" Biochem.Biophys.Acta. (印刷中). (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 高橋秀夫: "分業する転写開始因子と細菌の生残戦略" イオン・クラスター・エア-. 3. 2-11 (1996)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 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)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Tanaka, K.et al.: "Identification and analysis of the ropS-dependent promoter of katE encoding catalase HPII in Escherichia coli." Biocehm. Biophys. Acta. (in printing). (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takahashi, H.: "Transcriptional initiation factors which divide up the works and a surviving strategy of eubacterial cells (in Japanese)." Ion Cluster and Air 3. 2-11 (1996)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 1999-03-09  

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