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Functional Analysis of Butyrolactone Autoregulator Receptor from Streptomyces virginiae

Research Project

Project/Area Number 07680684
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Functional biochemistry
Research InstitutionOsaka University

Principal Investigator

NIHIRA Takuya  Osaka University, Dept.Biotechnology Associate Professor, 工学部, 助教授 (70144441)

Co-Investigator(Kenkyū-buntansha) IHARA Fumio  Osaka University, Dept.Biotechnology Assistant Professor, 工学部, 助手 (70252583)
Project Period (FY) 1995 – 1996
Project Status Completed (Fiscal Year 1996)
Budget Amount *help
¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1996: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1995: ¥1,500,000 (Direct Cost: ¥1,500,000)
Keywordsbutyrolactone autoregulator / receptor / Streptomyces / virginiae butanolide / 放線菌 / autoregulator / リセプター / 大量発現
Research Abstract

To roughly determine the essential regions on the butyrolactone autoregulator receptor, we at first prepared several deletion mutants by means of PCR.However, the one lacking N-terminal 47 amino acid residues formed high-molecular weight aggregates, while the ones lacking either C-terminal 49 or 96 amino acid resildues formed inclusion bodies when expressed in E.coli. Fusion proteins with thioredoxin also showed the same phenomena, indicating that both the N-terminal and C-terminal 50 amino acid residues are important in maintaining the higher structure of the receptor protein.
Next, to identify the essential amino acid residues, we modified the receptor by chemical reagents. DTNB which can specifically react with Cys residues could modify two Cys residues of the receptor. However, the resulting receptor retained the full ligand binding activity and also showed the intact dimeric structure as revealed by gel-filtration experiments, indicating that Cys residues did not play any important roles in the receptor. Dye-sensitized photooxidation resulted in the loss of ligand binding activity, but the modified receptor was present as high-molecular weight aggregates, indicating that the modified residues participate in structure stability.

Report

(3 results)
  • 1996 Annual Research Report   Final Research Report Summary
  • 1995 Annual Research Report

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Published: 1995-04-01   Modified: 2016-04-21  

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