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2017 Fiscal Year Final Research Report

Development of an antibacterial activity enhancer that restores lost antibacterial activity

Research Project

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Project/Area Number 15K07932
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Biological pharmacy
Research InstitutionHiroshima University (2016-2017)
Okayama University (2015)

Principal Investigator

Kuroda Teruo  広島大学, 医歯薬保健学研究科(薬), 教授 (80304327)

Project Period (FY) 2015-04-01 – 2018-03-31
Keywordstopoisomerase / vancomycin / キノロン
Outline of Final Research Achievements

The action mechanism of compound K on MRSA and VRE was investigated. Compound K inhibited topoisomerase IV of Staphylococcus aureus. However, this action mechanism was different from both ciprofloxacin and novobiocin, already known inhibitors of topoisomerase IV. Compound K also showed the combined effect with vancomycin. Expression of vancomycin resistant cluster genes was not inhibited with compound K, and exposure to compound K restored D-alanyl-D-alanine in VRE cells.

Free Research Field

微生物学

URL: 

Published: 2019-03-29  

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