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      KCI등재 SCIE SCOPUS

      Antimicrobial Effects of a Hexapetide KCM21 against Pseudomonas syringae pv. tomato DC3000 and Clavibacter michiganensis subsp. michiganensis

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      https://www.riss.kr/link?id=A103805939

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      다국어 초록 (Multilingual Abstract)

      Antimicrobial peptides (AMPs) are small but effectivecationic peptides with variable length. In previous study, four hexapeptides were identified that showed antimicrobial activities against various phytopathogenicbacteria. KCM21, the most effective a...

      Antimicrobial peptides (AMPs) are small but effectivecationic peptides with variable length. In previous study, four hexapeptides were identified that showed antimicrobial activities against various phytopathogenicbacteria. KCM21, the most effective antimicrobial peptide, was selected for further analysis to understand its modes of action by monitoring inhibitory effects of various cations, time-dependent antimicrobial kinetics, and observing cell disruption by electron microscopy. The effects of KCM21 on Gram-negative strain, Pseudomonassyringae pv. tomato DC3000 and Gram-positive strain, Clavibacter michiganensis subsp. michiganensis were compared. Treatment with divalent cations such as Ca2+ and Mg2+ inhibited the bactericidal activities of KCM21 significantly against P. syringae pv. tomato DC3000. The bactericidal kinetic study showed that KCM21 killed both bacteria rapidly and the process was faster against C. michiganensis subsp. michiganensis.
      The electron microscopic analysis revealed that KCM21 induced the formation of micelles and blebs on the surface of P. syringae pv. tomato DC3000 cells, while it caused cell rupture against C. michiganensis subsp. michiganensis cells. The outer membrane alterationand higher sensitivity to Ca2+ suggest that KCM21 interact with the outer membrane of P. syringae pv. tomatoDC3000 cells during the process of killing, but not with C. michiganensis subsp. michiganensis cells that lack outer membrane. Considering that both strains had similar sensitivity to KCM21 in LB medium, outer membrane could not be the main target of KCM21, instead common compartments such as cytoplasmic membrane or internal macromolecules might be a possibletarget(s) of KCM21.

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      참고문헌 (Reference)

      1 Reddy, K. V., "peptides: Premises and promises" 24 : 536-547, 2004

      2 Vidaver, A. K., "Uses of antimicrobials in plant agriculture" 34 : 107-110, 2002

      3 Houghten, R. A., "The use of synthetic peptide combinatorial libraries for the identification of bioactive peptides" 13 : 412-421, 1992

      4 Lemaitre, B., "The host defense of Drosophila melanogaster" 25 : 697-743, 2007

      5 Blondelle, S. E., "Synthetic combinatorial libraries: Novel discovery strategy for identification of antimicrobial agents" 40 : 1067-1071, 1996

      6 Concannon, S. P., "Susceptibility of oral bacteria to an antimicrobial decapeptide" 52 : 1083-1093, 2003

      7 Blondelle, S. E., "Rapid identification of compounds with enhanced antimicrobial activity by using conformationally defined combinatorial libraries" 313 : 141-147, 1996

      8 Sal-Man, N., "Preassembly of membrane-active peptides is an important factor in their selectivity toward target cells" 41 : 11921-11930, 2002

      9 Hancock, R. E., "Peptide antibiotics" 43 : 1317-1323, 1999

      10 Houghten, R. A., "Parallel array and mixture-based synthetic combinatorial chemistry: Tools for the next millennium" 40 : 273-282, 2000

      1 Reddy, K. V., "peptides: Premises and promises" 24 : 536-547, 2004

      2 Vidaver, A. K., "Uses of antimicrobials in plant agriculture" 34 : 107-110, 2002

      3 Houghten, R. A., "The use of synthetic peptide combinatorial libraries for the identification of bioactive peptides" 13 : 412-421, 1992

      4 Lemaitre, B., "The host defense of Drosophila melanogaster" 25 : 697-743, 2007

      5 Blondelle, S. E., "Synthetic combinatorial libraries: Novel discovery strategy for identification of antimicrobial agents" 40 : 1067-1071, 1996

      6 Concannon, S. P., "Susceptibility of oral bacteria to an antimicrobial decapeptide" 52 : 1083-1093, 2003

      7 Blondelle, S. E., "Rapid identification of compounds with enhanced antimicrobial activity by using conformationally defined combinatorial libraries" 313 : 141-147, 1996

      8 Sal-Man, N., "Preassembly of membrane-active peptides is an important factor in their selectivity toward target cells" 41 : 11921-11930, 2002

      9 Hancock, R. E., "Peptide antibiotics" 43 : 1317-1323, 1999

      10 Houghten, R. A., "Parallel array and mixture-based synthetic combinatorial chemistry: Tools for the next millennium" 40 : 273-282, 2000

      11 Crandall, A. D., "Nisin resistance in Listeria monocytogenes ATCC 700302 is a complex phenotype" 64 : 231-237, 1998

      12 Abee, T., "Mode of action of nisin z against Listeria monocytogenes scott a grown at high and low temperatures" 60 : 1962-1968, 1994

      13 Houghten, R. A., "Mixture-based synthetic combinatorial libraries" 42 : 3743-3778, 1999

      14 Yeaman, M. R., "Mechanisms of antimicrobial peptide action and resistance" 55 : 27-55, 2003

      15 Miyasaki, K. T., "Killing of Fusobacterium nucleatum, Porphyromonas gingivalis and Prevotella intermedia by protegrins" 33 : 91-98, 1998

      16 Lopez-Garcia, B., "Identification of novel hexapeptides bioactive against phytopathogenic fungi through screening of a synthetic peptide combinatorial library" 68 : 2453-2460, 2002

      17 최재혁, "Identification of Novel Bioactive Hexapeptides Against Phytopathogenic Bacteria Through Rapid Screening of a Synthetic Combinatorial Library" 한국미생물·생명공학회 19 (19): 792-802, 2009

      18 Lopez-Garcia, B., "Identification and characterization of a hexapeptide with activity against phytopathogenic fungi that cause postharvest decay in fruits" 13 : 837-846, 2000

      19 Wei, G. X., "Human salivary mucin muc712-mer-l and 12-mer-d peptides: Antifungal activity in saliva, enhancement of activity with protease inhibitor cocktail or edta, and cytotoxicity to human cells" 49 : 2336-2342, 2005

      20 Houghten, R. A., "Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery" 354 : 84-86, 1991

      21 Anderson, P. K., "Emerging infectious diseases of plants: Pathogen pollution, climate change and agrotechnology drivers" 19 : 535-544, 2004

      22 Sugiarto, H., "Effects of cations on antimicrobial activity of ostricacins-1 and 2 on E. coli O157:H7 and S. aureus 1056MRSA" 55 : 36-41, 2007

      23 Sundin, G. W., "Ecological and genetic analysis of copper and streptomycin resistance in Pseudomonas syringae pv. syringae" 59 : 1018-1024, 1993

      24 Kim, K. S., "Deficient autolytic enzyme activity in antibiotic-tolerant lactobacilli" 36 : 582-585, 1982

      25 Hancock, R. E., "Cationic peptides: A new source of antibiotics" 16 : 82-88, 1998

      26 Munoz, A., "Antimicrobial properties of derivatives of the cationic tryptophan-rich hexapeptide paf26" 354 : 172-177, 2007

      27 Brogden, K. A., "Antimicrobial peptides: Pore formers or metabolic inhibitors in bacteria?" 3 : 238-250, 2005

      28 Yedery, R. D., "Antimicrobial peptides as microbicidal contraceptives: Prophecies for prophylactics--a mini review. Eur" 10 : 32-42, 2005

      29 Hancock, R. E., "Antimicrobial and hostdefense peptides as new anti-infective therapeutic strategies" 24 : 1551-1557, 2006

      30 Lawyer, C., "Antimicrobial activity of a 13 amino acid tryptophan-rich peptide derived from a putative porcine precursor proten of a novel family of atibacterial prptides" 390 : 95-98, 1996

      31 Hancock, R. E., "Antibacterial peptides and the outer membranes of gram-negative bacilli" 46 : 1-3, 1997

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2003-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2000-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.14 0.32 0.84
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.69 0.57 0.477 0.17
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