• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Discovery and functional analysis of the novel protein derived from microorganism that shows damaging activity on cultured cancer cells

Research Project

Project/Area Number 17K07780
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Bioorganic chemistry
Research InstitutionSojo University

Principal Investigator

EKINO Keisuke  崇城大学, 生物生命学部, 教授 (30310030)

Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2019: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2018: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2017: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
KeywordsBacillus thuringiensis / parasporin / 結晶性タンパク質 / パラスポリン / 細胞損傷タンパク質 / 応用微生物
Outline of Final Research Achievements

It was found that a protein having a cell-damaging activity exists in the culture medium of Bacillus thuringiensis (BT). After protein purification, the 297_1_00946 gene present on the A297 strain genome was considered to be a target protein candidate. Moreover, since the condition showing no activity was found depending on the culture conditions, a comparative analysis of gene expression levels under both culture conditions was performed. As a result, it was found that there are differences in the expression levels of genes related to the production of two secondary metabolites and one type of enterotoxin, and further analysis is being conducted. In addition, analysis of cell-damaging activity using a fluorescent probe strongly suggested that it acts on the cell membrane of cultured cells.

Academic Significance and Societal Importance of the Research Achievements

Bacillus thuringiensis(BT)は殺虫タンパク質を生成することから、これまで微生物殺虫剤や遺伝子組換え作物に利用されてきた。21世紀に入り、BTが作る結晶性タンパク質の中に培養細胞に対して損傷活性を示すタンパク質が発見され、パラスポリンとよばれている。現在6種類に分類されているこれらのタンパク質は既知タンパク質との配列相同性が低く、新規な生物活性タンパク質である。本研究課題の成果は、これらBTの生物活性タンパク質の新たな知見を提供する可能性がある。

Report

(4 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (7 results)

All 2020 2019 2017

All Journal Article (5 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 5 results,  Open Access: 4 results) Presentation (2 results)

  • [Journal Article] Systematic approach for assessing whether undeletable chromosomal regions in Saccharomyces cerevisiae are required for cell viability.2020

    • Author(s)
      Hassan N, Easmin F, Sasano Y, Ekino K, Taguchi H, Harashima S.
    • Journal Title

      AMB Express

      Volume: 10 Issue: 1 Pages: 73-73

    • DOI

      10.1186/s13568-020-01001-x

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] CRISPR-PCDup: a novel approach for simultaneous segmental chromosomal duplication in Saccharomyces cerevisiae2020

    • Author(s)
      Hassan Naim、Sasano Yu、Kimura Shunta、Easmin Farhana、Ekino Keisuke、Taguchi Hisataka、Harashima Satoshi
    • Journal Title

      AMB Express

      Volume: 10 Issue: 1 Pages: 27-27

    • DOI

      10.1186/s13568-020-0957-4

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] CRISPR-PCD and CRISPR-PCRep: Two novel technologies for simultaneous multiple segmental chromosomal deletion/replacement in Saccharomyces cerevisiae2020

    • Author(s)
      Easmin Farhana、Sasano Yu、Kimura Shunta、Hassan Naim、Ekino Keisuke、Taguchi Hisataka、Harashima Satoshi
    • Journal Title

      Journal of Bioscience and Bioengineering

      Volume: 129 Issue: 2 Pages: 129-139

    • DOI

      10.1016/j.jbiosc.2019.08.004

    • NAID

      40022159677

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] gRNA-transient expression system for simplified gRNA delivery in CRISPR/Cas9 genome editing.2019

    • Author(s)
      Easmin F, Hassan N, Sasano Y, Ekino K, Taguchi H, Harashima S.
    • Journal Title

      J Biosci Bioeng

      Volume: 印刷中 Issue: 3 Pages: 373-378

    • DOI

      10.1016/j.jbiosc.2019.02.009

    • NAID

      40022010876

    • Related Report
      2019 Annual Research Report 2018 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Cloning, Purification, and Characterization of Tripeptidyl Peptidase from Streptomyces herbaricolor TY-212017

    • Author(s)
      Ekino Keisuke、Yonei Shinichi、Oyama Hiroshi、Oka Takuji、Nomura Yoshiyuki、Shin Takashi
    • Journal Title

      Applied Biochemistry and Biotechnology

      Volume: 184 Issue: 1 Pages: 239-252

    • DOI

      10.1007/s12010-017-2547-8

    • Related Report
      2017 Research-status Report
    • Peer Reviewed
  • [Presentation] PCR-based quick methodto deliver gRNA for CRISPR/Cas9 in yeast2019

    • Author(s)
      Farhana Easmin, Naim Hassan, Yu Sasano, Keisuke Ekino, Hisataka Taguchi, and Satoshi Harashima
    • Organizer
      日本農芸化学会西日本支部大会(熊本)
    • Related Report
      2018 Research-status Report
  • [Presentation] Bacillus subtilis NBRC13719由来抗菌ペプチドの解析2017

    • Author(s)
      前山 諒、岡 拓二、原島 俊、浴野圭輔
    • Organizer
      第24回日本生物工学会九州支部沖縄大会
    • Related Report
      2017 Research-status Report

URL: 

Published: 2017-04-28   Modified: 2021-02-19  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi