• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1998년도 Proceedings of UNESCO-internetwork Cooperative Regional Seminar and Workshop on Bioassay Guided Isolation of Bioactive Substances from Natural Products and Microbial Products
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• pp.163-165
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• 1998

The use of synthetic pesticides in crop production, brings the possibility of a nonselective toxicity and accumulation of toxic compounds in the environment. As an alternative, bioactive compounds from actinomycetes can provide a rich source for biodegradable pesticides. A variety of biological activities such as antibacterial, antifungal, herbicidal, insecticidal and anticoccidial are associated with these microbial metabolites. Studies on the production of bioactive compounds from marine-derived actinomycetes have been very few, compared to the terrestrial actinomycetes. With their unique metabolic and physiological capabilities, the marine actinomycetes can be useful producers of novel metabolites.

• 한국식품과학회지
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• 제38권2호
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• pp.268-272
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• 2006

본 연구에서는 단메밀과 쓴메밀에 Viscozyme L과 Alcalase 2.4L 효소를 첨가하여 가수분해물을 제조하고, 이들의 항균, 항곰팡이, 항고혈압 활성을 조사하였다. 그 결과 효소를 첨가하지 않은 단메밀과 쓴메밀의 수율은 각각 7.92, 3.17%로 낮은 가수분해율을 보었으며 Viscozyme L을 첨가한 단메밀과 쓴메밀의 경우 18.70, 19.45% 그리고 Alcalase 2.4L을 첨가한 단메밀과 쓴메밀의 경우 24.65, 22.10%로 가장 높은 수율을 보였다. 메밀 가수분해물을 E. coli, S. typhimurium, P. aeruginosa, B. subtilis, S. aureus 및 L. monocytogences 균주에 대해 항균 활성을 조사한 결과, Viscozyme L을 첨가한 단메밀 가수분해물이 L. monocytogences, S. typhimurium에 대해 3-7.2 mm의 clear zone으로 항균 활성을 나타내었으며 쓴메밀 가수분해물이 S. typhimurium에 대해 5.7 mm의 clear zone으로 낮은 항균 활성을 나타내었다. A. niger, M. miehei, P. rugullosum, A. oryzae, T. reesei 균주의 항곰팡이 활성은 Viscozyme L을 첨가한 단메밀 가수분해물이 T. reesei에 대해 3.7-12 mm의 clear zone으로 강한 활성을 나타내었다. ACE 저해 활성은 효소를 첨가하지 않은 단메밀은 45.82%, 쓴메밀은 73.06%으로 나타났다. Viscozyme L을 첨가한 가수분해물의 경우 단메밀은 39.39%, 쓴메밀은 46.83%로 효소를 첨가하지 않은 메밀 가수분해물에 비해 낮은 ACE 저해활성을 보였다. 반면 Alcalase 2.4 L을 첨가한 가수분해물의 경우 단메밀 61.19%, 쓴메밀 94.48%로 가장 높은 ACE 저해활성을 나타내었다.

• 대한수의사회지
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• 제13권6호
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• pp.393-395
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• 1977

Ranunculus species, a poisonous plant that grow in the field and the dales throughout the country has been recommended in folklore for the therapy of traumatic inflammation. A chloroform extract of this plant has been shown to inhibit the growth of severa

• Journal of Microbiology and Biotechnology
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• 제18권5호
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• pp.990-996
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• 2008

In a previous study, we found an antifungal effect on human pathogenic fungi by the cell-penetrating peptide Tat (47-58) derived from HIV-1. Tat (47-58) immediately entered into the fungal nucleus and affected some physiological changes on the intracellular condition. In this study, Tat (47-58) showed a broad spectrum of antibacterial activity against pathogenic bacteria including bacterial clinical isolates. To improve resistance against proteases for use in vivo, we synthesized an analog of Tat (47-58) by substituting the L-amino acid for the D-amino acid. The D-enantiomer of Tat (47-58) also exhibited a broad spectrum of antibacterial activity at almost the same level of L-Tat (47-58) concentration. Unlike L-Tat (47-58), D-Tat (47-58) showed a significant proteolytic resistance against all proteases tested and antimicrobial activities in the presence of trypsin. Moreover, D-Tat (47-58) inhibited MRSA infection in human HeLa cells whereas L-Tat (47-58) partially allowed MRSA infection, and the results were due to the proteolytic resistance of D-Tat (47-58).

• Journal of Microbiology
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• 제35권1호
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• pp.21-24
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• 1997

The hybrid peptides, CA-ME, CA-MA and CA-BO, with the N-terminal sequence 1-8 of cecropin A and the N-terminal sequences 1-12 of melittin, magainin 2 and bombinin, respectively, have more improved antibacterial activities. CA-MA was found to have stronger antifungal activity against Trichoderma sp than other hybrid peptides and their parental peptides. In order to elucidate the relationships between the peptide structure and antifungal activity, several analogues of CA-MA or CA-BO were also designed and synthesized by the solid phase method. An tifungal activity was measured against T. reesei and T. viride, and hemolytic activity was measured by a solution method against human red blood cells. The residue 16 of CA-MA, Ser, was found to be important for antifungal activity. When the residue was substituted with Leu, showed powerful antifungal activity was dramatically decreased. CA-MA, P1, P4 and P5 designed in this study showed powerful antifungal activity against T. reesei and T. viride with low hemolytic activity against human red blood cells. These hybrid peptides will be potentially useful model to further design peptides with powerful antifungal activity for the effective therepy of fungal infection and understand the mechanisms of antifungal actions of hybrid peptides.

• 대한화학회지
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• 제56권3호
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• pp.341-347
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• 2012

A series of 2-(4-chlorophenylimino)-5-((3-(p-substituted phenyl)-1-phenyl-1H-pyrazol-4-yl) methylene) thiazolidin-4-one ($\mathbf{3a-h}$) compounds were prepared from the 2-(4-chlorophenylimino) thiazolidin-4-one ($\mathbf{1}$) and 1-phenyl-3-(p-substituted phenyl)-1H-pyrazole-4-carbaldehyde ($\mathbf{2a-h}$). All compounds were characterized by elemental (C, H, N) analysis and spectral (FT-IR, $^1H$ NMR and GC-MS) analysis. These newly synthesized compounds were screened for their antibacterial and antifungal activities. Antimicrobial activity was observed and evaluated against the bacterial strains like Eschericha coli (MTCC 443), Pseudomonas aeruginosa (MTCC 1688), Staphylococcus aureus (MTCC 96), Streptococcus pyogenes (MTCC 442) and against the fungal strains like Candida albicans (MTCC 227), Aspergillus niger (MTCC 282) and Aspergillus clavatus (MTCC 1323). All the synthesized compounds were found to possess moderate to excellent antimicrobial activity against above selected strains.

• 대한화학회지
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• 제65권2호
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• pp.93-105
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• 2021

Mononuclear Cu(II), Ni(II), Co(II), Mn(II), Zn(II), Fe(III), Ru(III), and UO2(II) complexes of 2-hydroxy-4-(p-tolyldiazenyl)benzylidene)-2-(p-tolylamino)acetohydrazide (H2L) were prepared by direct method. The ligand and its complexes were isolated in solid state and characterized by analytical techniques such as elemental and thermal analyses, molar conductance, magnetic susceptibility measurements and spectroscopic techniques such as UV-Visible, IR, 1H-NMR and 13C-NMR. The spectral data indicated that the ligand acted as neutral/monobasic bidentate or monobasic/dibasic tridentate ligand bonded to the metal ions through the oxygen atom of ketonic or enolic carbonyl group, azomethine nitrogen atom and deprotonated/protonated phenolic oxygen atom forming either tetragonally distorted octahedral or octahedral. Antimicrobial activities of the ligand and its complexes were evaluated against Escherichia coli, Bacillus subtilis and Aspergillus niger by well diffusion method. The results of antifungal activity showed that the Fe(III) complex (10) exhibited higher antifungal against Aspergillus niger than the other complexes. However, the results of antibacterial activity revealed that Cu(II) complex (4) is the most active against Escherichia coli while the Cu(II) complex (5) and Fe(III) complex (10) exhibited higher antibacterial effect on Bacillus subtilis than the other complexes.

• 한국균학회지
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• 제23권2호통권73호
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• pp.176-189
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• 1995

98종의 한국산버섯의 그람음성균에 대한 항균활성을 검색한 결과 20종의 버섯의 80% 에탄올(E) 및 증류수(H) 추출물이 Klebsiella pneumoniae, Proteus mirabilis, Serratia marcescens, Shiegella sonnei, Shiegella dysenteiae, Salmonella typhi, Salmonella typhimurium 및 Pseudomonas aeruginosa에 대하여 항균력을 나타내며, 특히 R. sinuatus, S. luteus, B. umbriniporus, 그리고 A. tabescens의 E 추출물은 다른 버섯에 비하여 여러 종류의 그람음성균에 대하여 다양한 항균활성을 보였다. Abortiporus biennis, Phellinus gilvus, 및 Polyporus dispansus의 E 추출물은 S. typhi에 대하여 강력한 항균력을 나타내었으며 이들의 MIC는 $10\;{\mu}g/ml$이었다. 25종 버섯의 곰팡이균에 대한 항균활성을 검색한 결과 Armillariella tabescens의 E 추출물이 Trichopyton mentagrophytes에 대하여 항균력을 가지며 이의 MIC는 $300\;{\mu}g/ml$이었다.

• Applied Biological Chemistry
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• 제42권2호
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• pp.176-179
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• 1999

지칭개, 구절초 및 산국에서 분리한 9종류의 sesquiterpene lactones에 대한 생리활성 실험의 일환으로, 10종의 세균에 대한 항세균활성과 6종의 식물병원균에 대한 항진균활성을 조사하였다. 항세균 활성실험에서는 지칭개에서 분리한 hemistepsin A와 B 그리고 산국에서 분리한 tulipinolide가 시험균주 전반에 대하여 강한 활성을 보였으며, 항진균 활성실험에서는 hemistepsin B, angeloylcumambrin B, tigloylcumambrin B, 그리고 costunolide가 광범위한 활성을 보였다. 또한, 항세균 활성실험과 항진균 활성실험 모두 비교적 뚜렷한 균주특이성을 나타내었다.

• 한국미생물·생명공학회지
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• 제21권1호
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• pp.59-65
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• 1993

방선균 분리주 GMT 1153로부터 ts/NRK 세포의 형태를 변형된 세포형태에서 정상세포의 형태로 전환하는 활성물질을 분리, 정제하였다. 활성물질 MT 1155는 UV, IR, 1H-NMR, 13C-NMR, mass,원소분석 등의 기기분석을 통하여 항진균성 항암물질인 toyocamycin으로 동정되었다. MT 1155는 ts/NRK 세포의 형태전환에 대한 활성외에도 PKA 효소활성 저해와 CTLL 세포에 대한 세포독성이 있으나 K562 소포형성 억제 및 PKC 효소활성에 대한 저해효과도 없었다.