• 한국환경농학회지
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• 제34권2호
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• pp.139-148
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• 2015

BACKGROUND: The aim of this study was to isolate and identify algicidal bacterium that tends to kill the toxic dinoflagellate Alexandrium catenella, and to determine the algicidal activity and algicidal range of algicide. METHODS AND RESULTS: Among of algicidal bacteria isolated in this study, NH-3 isolate was the strongest algicidal activity against A. catenella. NH-3 isolate was identified on the basis of biochemical characteristics and analysis of 16S rRNA gene sequences. The NH-3 isolate showed over 99% homology with Arthrobacter oxydans, and was designated as Arthrobacter sp. NH-3. The optimal culture conditions were $25^{\circ}C$, initial pH 7.0, and 2.0% (w/v) NaCl concentration. The algicidal activity of Arthrobacter sp. NH-3 was significantly increased to maximum value in the late of logarithmic phase. Arthrobacter sp. NH-3 showed algicidal activity through indirect attack, which excreted active substance into the culture filtrate. When 10% culture filtrate of NH-3 was applied to A. catenella, 100% of algal cells were destroyed within 30 h. In addition, the algicidal activities were increased in dose and time dependent manners. The pure algicide was isolated from the ethyl acetate extract of the culture filtrate of NH-3 by using silica gel column chromatography and high performance liquid chromatography (HPLC). We investigated the algicidal activity of this algicide on the growth of harmful algal bloom (HAB) species, including A. catenella. As a result, it showed algicidal activity against several HAB species at a concentration of $100{\mu}g/mL$ and had a relatively wide host range. CONCLUSION: Taken together, our results suggest that Arthrobacter sp. NH-3 and its algicide could be a candidate for controlling of toxic and harmful algal blooms.

• The Plant Pathology Journal
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• 제21권3호
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• pp.262-269
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• 2005

An antiviral producing bacterial strain was isolated from a ginseng rhizosphere in Kangwon province of Republic of Korea. In order to identify the bacterial strain, microbiological, physiological and biochemical tests were performed, along with RAPD, 16S rRNA, 16S-23S rRNA ITS (intergenic spacer region) and DNA-DNA hybridization analyses. The bacterium was found to be a strain of Pseudomonas fluorescens, which was designated as Gpf01. The strain was grown in Muller-Hinton (MH) broth, and the culture supernatant obtained was filtered through a $0.45{\mu}l$ filter. It was further boiled at $100^{\circ}C$ and tested in two experiments for its ability to control a yellow strain of Cucumber mosaic virus (CMV-Y). In the first experiment, boiled culture filtrate (RCF) was treated on one half of the leaves of Chenopodium amaranticolor followed by CMV- Y inoculation on both halves. In the second experiment, BCF was treated on the lower leaves of Nicotiana tobacum var. Xanthi-nc, with the CMV-Y mechanically inoculated onto the upper untreated leaves. In the first experiment, BCF treatment was able to considerably reduce the number of viral lesion, and in the second experiment, plants treated with BCF showed no visible viral symptoms compared to the Muller-Hinton (MH) media treated controls 15 days post inoculation (dpi), and remained symptomless throughout the study period. Thus, Gpf01, identified as P. fluorescence, was able to produce an antiviral component in the culture filtrate, which was found to be heat stable, non-phytotoxic and effective in local as well as systemic hosts of CMV.

• 한국식품위생안전성학회지
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• 제14권3호
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• pp.270-276
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• 1999

Alteromonas sp. SR-14의 배양여액을 사용하여 C. calcitrans의 증식에 미치는 영향과 조류 증식저해 물질의 특성을 살펴보았다. Alteromonas sp. SR-14의 peptone broth 배양여액은 C. calcitrans에 대하여 증식 저해 활성을 나타내었으며, 이 균에 의한 조류 증식 저해 물질은 온도 $15~20^{\circ}C$, pH 7.0~9.0, 염분 농도 $23~30{\textperthousand}$의배양 조건에서 강한 활성으로 생성되었으며, 이러한 조건(온도 $20^{\circ}C$, pH 8.0, 염분 농도 $30\textperthousand$)에서는 정지기부터 활성이 증가하였다. Alteromonas sp. SR-14가 peptone broth에서 생산하는 조류 증식 저해 물질의 분자량은 약 3KDa~12KDa의 복합 물질이었는데, $100^{\circ}C$에서 10분간 열처리하였을 때 3~10KDa 이하의 물질은 내열성이 있었으나 10KDa 이상의 물질은 불활성 되었다.

• Mycobiology
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• 제35권4호
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• pp.210-214
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• 2007

Antibacterial and antifungal activities of liquid culture filtrate, water and ethanol extract (solid culture) of Stereum ostrea were evaluated against 5 bacteria and 3 plant pathogenic fungi. To determine the minimal inhibitory concentration (MIC), we studied $5{\sim}300\;mg/ml$ concentrations against bacteria and fungi separately. The MIC was 10 mg/ml for Bacillus subtilis and 40 mg/ml for Colletotrichum gloeosporioides and Colletotrichum miyabeanus. Liquid culture filtrate was more effective against Gram positive than Gram negative bacteria, and Staphylococcus aureus was the most inhibited (20.3 mm) bacterium. Water and ethanol extracts were effective against both Gram positive and Gram negative bacteria, and water extract was better than ethanol extract. In water and ethanol extract, inhibition zones were 23.6 and 21.0 mm (S. aureus) and 26.3 and 22.3 mm (Pseudomonas aeruginosa), respectively. For plant pathogenic fungi, the highest and lowest percent inhibition of mycelial growth (PIMG) was found 82.8 and 14.4 against C. miyabeanus and Botrytis cinerea in liquid culture filtrate, respectively. In water extract, the PIMG was found to be the highest 85.2 and lowest 41.7 for C. miyabeanus and C. gloeosporioides, respectively. The inhibitory effect of ethanol extract was better against C. miyabeanus than C. gloeosporioides and B. cinerea. Among 3 samples, water extract was the best against tested pathogenic fungi. This study offers that the extracts isolated from S. ostrea contain potential compounds which inhibit the growth of both bacteria and fungi.

• 한국균학회지
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• 제24권1호통권76호
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• pp.49-55
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• 1996

살충성진균 Metarhizium anisopliae가 시들음병을 일으키는 Fusarium oxysporum, 잿빛곰팡이 병을 일으키는 Botrytis cinerea, 겹둥근무늬병을 일으키는 Alternaria solani 등에 대하여 항진균활성을 갖는지 알아보았다. 그 결과 Plate상에서 균사생장저해 실험과 inhibition rate실험을 했을 때 항진균활성이 검정되었으며 또한 YPD배지에서 배양된 M. anisopliae로부터 얻은 배양여액을 식물병원균에 30%농도로 첨가했을 때 이들의 포자발아율은 B. cinerea, F. oxysporum에서 각각 21.5%(control: 88.2%), 53.0%(control: 78.6%)로 감소하였으며 발아개시 시간도 8시간 정도 지연되었다. 또한 현미경을 통한 미세구조관찰에서는 10% 배양여액을 첨가했을 때 F. oxysporum의 균사로부터 후막포자가 생성되고 생장저해가 일어나는 것이 확인되었다. 이상의 결과로부터 M. anisopliae의 항진균활성은 fungistatic effect를 나타냄을 알 수 있었다.

• Journal of Microbiology and Biotechnology
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• 제12권6호
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• pp.895-900
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• 2002

A soil microorganism producing ${\alpha}$- and ${\beta}$-glucosidase inhibitors was identified as Bacillus lentimorbus, based on the fatty acid and morphological analyses, along with biochemical and physiological tests. The ${\alpha}$-glucosidase inhibitor was highly produced by this strain in a culture medium containing $0.25\%$ of sodium glutamate and $0.5\%$ of glucose, pH 8.0 at $30^{\circ}C$ for 2 days. The ${\alpha}$-glucosidase inhibitor from culture filtrate of his strain was identified as water soluble, organic solvent nonextractable, and heat stable. In addition to ${\alpha}$-glucosidase inhibitor, this strain also produced ${\beta}$-glucosidase inhibitor in he same culture medium and this inhibitor showed an antifugal activity against Botrytis cinerea. While the production of ${\alpha}$- glucosidase inhibitor was decreased by a glucose concentration higher than $1\%$, the production of ${\beta}$-glucosidase inhibitor was lot Influenced by a glucose concentration higher than $20\%$. The ${\alpha}$-glucosidase inhibitor from culture filtrate of this strain was separated from the ${\beta}$-glucosidase inhibitor through Sephadex G-100 column chromatography.

• BMB Reports
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• 제36권2호
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• pp.185-189
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• 2003

Chitinase (EC 3.2.1.14) was isolated from the culture filtrate of Streptomyces sp. M-20 and purified by ammonium sulfate precipitation, DEAE-cellulose ion-exchange chromatography, and Sephadex G-100 gel filtration. No exochitinase activity was found in the culture filtrate. The molecular mass of the purified chitinase was 20 kDa, estimated by a sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and was confirmed by activity staining with Calcofluor White M2R. Chitinase was optimally active at pH of 5.0 and at $30^{\circ}C$. The enzyme was stable from pH 4 to 8, and up to $40^{\circ}C$. Among the metals and inhibitors that were tested, the $Hg^+$, $Hg^{2+}$, and p-chloromercuribenzoic acid completely inhibited the enzyme activity. The chitinase activity was high on colloidal chitin, chitotriose, and chitooligosaccharide. The purified chitinase showed antifungal activity against Botrytis cinerea, and lysozyme activity against the cell wall of Botrytis cinerea.

• 한국미생물·생명공학회지
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• 제24권5호
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• pp.540-545
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• 1996

A facultative anaerobe Enterococcus faecium 19-46-4 was used to study the production of an antimicrobial substance in anaerobic conditions. Major part of the antibiotic activity was found in the culture filtrate of the bacterium. The active compound was extracted by an equal volume of iso-butanol and concentrated in vacuo (at 50$\circ$C) before purification by C-18 liguid column chromatography and HPLC. A chromatographically pure compound was obtained by two passages of HPLC columns, The compound appeared as a pale-yellow powder. The yield was about 2.5 mg 1$^{-1}$ culture filtrate. The compound was named as KIST 194. KIST 194 were identified as cholic acid (3$\alpha$, 7$\alpha$, 12$\alpha$-trihydroxy-5$\beta$-cholan 24-oic acid) based on its physico-chemical properties determined by UV, IR, $^{1}H-NMR, $^{13}$C-NMR, El-MS and LC-MS.

• 한국미생물·생명공학회지
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• 제32권4호
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• pp.371-374
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• 2004

A bacterium producing the $\beta$-mannosidase was isolated from intestine of fresh fish. The isolate YB-29 has been identified as Chryseomeningosepticum on the basis on its 16S rRNA sequence, morphology and biochemical proper The $\beta$-mannosdiase activity was detected in both the culture filtrate and the cell extract of C. meningosepticum YB-29. The $\beta$-mannosidase of culture filtrate showed the maximum activity for hydrolysis of para-nitrophenyl-$\beta$-D-mannopyranoside at pH 5.0-6.0 and 55-$60^{\circ}C$. The enzyme was able to hydrolyze the oligomeric substrates such as mannobiose and mannotriose with higher activity for mannotriose than mannobiose.

• 한국수산과학회지
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• 제33권4호
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• pp.339-347
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• 2000

적조생물을 살조시키는 해양세균 Microcorcus sp. LG-5가 생산하는 세포외 분비 살조물질의 최적 생성조건, 살조물질의 특성과 한외여과 분획별 살조활성 및 해양생물에 미치는 영향을 조사함으로서 자연생태 조화형, 환경 친화적 적조방제 기술개발의 기초 자료를 제공하고자 연구한 결과를 요약하면 다음과 같다. Micrococcus sp. LG-5의 살조물질 생성 최적온도는 $20{\~}30^{\circ}C$로 살조활성이 $100{\%}$였으며, 살조물질 생성 최적 pH는 7.0, 최저 염농도는 $3.0{\%}$였다. 또한 세포외 분비 살조물질의 $IC_(50)$ 값은 $0.482{\%}$였다. 세포외 분비 살조물질의 열 안정성을 실험한 결과, 열처리한 배양여과액 $1{\%}$ 첨가시 12시간 후에 $31.4{\%}$, 24시간 후 $79.7{\%}$, 36시간 후 $94.6{\%}$의 살조활성을 보였고 $5{\%}, 10{\%}$의 경우 각자 36시간, 24시간 후에 $100{\%}$ 살조되었으며, 열처리하지 않은 배양여과액을 넣었을 때와 비교해볼 때 살조력에 유의한 차이는 없었다. 이와 같이 Micrococcus sp. LG-5가 생산, 분비하는 살조물질은 열에 안정한 내열성 물질로 판단된다. 또한 대사산물의 pH 안정성은 $pH 6.0{\~}8.0$에서 거의 $100{\%}$의 살조활성을 보였으며 $pH 5.0{\~}10.0$에서 살조활성이 $85{\%}$ 이상으로 나타나 살조물질은 약산성과 알카리에서 살조활성이 안정하였다. 또한 한외여과의 결과, 분자량 $>10,000, 10,000{\~}1,000, <1,000$의 3개의 분획 모두 살조활성이 있었으며, 각 분획 모두 열에 대단히 안정하였다. 각 분획별 $IC_(50)$ 값은 분자량 1,000 이상에서 강한 살조활성이 나타났으며 분자량 1,000 이하에서는 상대적으로 낮은 살조활성을 보였다. Micrococcus sp. LG-5가 해양세균에 미치는 영향은 E. faecalis, E. coli, K. pneumoniae 및 V. alginolyticus에 대해서는 항균력을 보였으나, P. aeruginosa, P. fluorescens, S. typhi, S. aureus, V. cholerae 및 V parahaemolyticus에 대해서는 전혀 항균력을 보이지 않았다. 그리고 적조생물에 미치는 영향은 A. tamarense, E. gymnastica, G. catenatum, G. niikimotoi, G. sanguineum, G. impudicum, H. triquetra, H akashiwo, P. micans와 Pyramimonas sp.에 대해서는 살조활성을 보였으나 Chlamydomonas sp., C. closterium, P. mininum, P. triestimum, Pseudonitzschia sp.와 S. trochoidea에 대해서는 살조활성을 보이지 않았다. 즉, 적조생물에 따라 살조활성이 다양하게 나타나 종 특이성이 낮았다. 먹이생물에 미치는 영향은 1 galbana를 제외하고 실험한 모든 먹이생물에 별다른 영향이 없거나 오히려 성장을 촉진시켰고, 또한 살조세균 배양여과액을 넙치 사육수에 $10{\%}$까지 투여하였을 때 양식 넙치에 미치는 유해한 생리학적 영향은 없었다. 이상의 연구 결과 살조세균 Micrococcus sp. LG-5의 배양여과액은 조사된 적조생물을 제외한 해양세균, 치${\cdot}$자어의 먹이생물 및 양식 넙치에 유해한 영향은 미치지 않을 것으로 판단된다.