• 제목/요약/키워드: bacillus amyloliquefaciens

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어병균 Vibrio anguillarum 생육 저해 인자를 생산하는 Bacillus amyloliquefaciens H41의 분리 (Isolation of Bacillus amyloliquefaciens H41 Producing Growth Inhibition Factor against Vibrio anguillarum)

  • 김영희;정영기;정경태;류은주;정유정
    • 생명과학회지
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    • 제16권4호
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    • pp.605-611
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    • 2006
  • 양식 산업의 문제점인 어병균을 방제하기 위한 생물 전구체의 개발을 목적으로 해산어의 내장 추출물에서 어병균인 Vibrio anguillarum의 생육을 저해하는 새로운 균주를 분리, 동정하여 Bacillus amyloliquefaciens H41으로 명명하고 생육특성 및 생육저해인자 생성 조건을 검토하였다. 분리 균의 생육 최적 조건은 기본배지로 1% peptone, 질소원으로 1.5% yeast extract, 탄소원으로 1% sucrose, 0.5% NaCl, 금속이온으로는 0.05% $MgSO_4{\cdot}7H_20$이었으며 pH는 7.0-8.0, 온도는 $28-35^{\circ}C$에서 20시간의 진탕배양이었다. V. anguillarum 생육 저해물질은 B. amyloliquefaciens H41의 배양 상등 액에서 볼 수 있었는데 paper-disk 법으로 투명환의 생성여부로 확인하였다. 분리 균에 의한 생육저해 물질 생산 최적 조건은 1% peptone, 1.5% yeast extract, 1% NaCl, 0.05% $MgSO_4{\cdot}7H_20$, 1%의 sucrose이었으며 최적 pH는 7.5, 최적온도는 $35^{\circ}C$이었다. 분리 균은 최적 배양조건하에서 저해물질을 배양 후 16시간부터 24시간대에 가장 높은 활성을 나타내었다. 저해 활성반응은 분리 균에서는 저해 활성을 나타내었으나 B. amyloliquefaciens KCTC1724 표준균주에는 저해활성을 나타나지 않는 대조를 보였다. 또한 분리 균에 의해 생산된 저해물질은 V. anguillarum 에는 생육 억제 효과를 나타내었으나 다른 인체 병원성 Vibrio에는 전혀 영향을 미치지 않는 것으로 나타나 균주 선택성이 특이적이었다.

Bacillus amyloliquefaciens ISP-5 균주의 배지 최적화 및 상추를 이용한 식물 생장 촉진 평가 (Medium optimization for growth of Bacillus amyloliquefaciens ISP-5 strain and evaluation of plant growth promotion using lettuce)

  • 최강현;서선일;박해성;임지환;김평일
    • Journal of Plant Biotechnology
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    • 제49권4호
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    • pp.356-361
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    • 2022
  • 본 연구에서는 Bacillus amyloliquefaciens ISP-5 균주의 최적배지조성을 확인하기 위해 5종의 탄소원(glucose, fructose, sucrose, maltose, corn starch)과 5종의 질소원(yeast extract, peptone, tryptone, soytone, soy bean flour)을 이용하여 각각의 생육을 측정하였다. 그 결과 glucose와 soy bean flour를 각각 최적 탄소원과 질소원으로 확립하였으며 최적 배지를 이용하였을 때 상업용 배지(TSB)에 비해 약 2500배의 생육을 확인할 수 있었다. B. amyloliquefaciens ISP-5 배양액을 상추에 엽면 살포하였을 때 상추의 엽폭과 엽장은 대조군에 비해 8.6%, 12.9%의 증가하였으며, 생체중과 건물중은 대조군에 비해 각각 24.2%, 23.9% 증가하였다. 이러한 결과들을 종합해보았을 때 B. amyloloiquefaciens ISP-5 균주를 이용한 미생물 제제는 상추용 식물생장촉진제로써 활용할 수 있을 것이라 기대된다.

YRp7 vector를 이용한 Bacillus amyloliquefaciens amylase gene의 cloning I I. Saccharomyces cerevisiae에서 발현 (Cloning of Bacillus amyloliquefaciens amylase gene using YRp7 as a vector II. Expression of cloned amylase gene in Saccharomyces cerevisiae)

  • 서정훈;김영호;전도연;배영석;홍순덕;이종태
    • 한국미생물·생명공학회지
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    • 제14권3호
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    • pp.213-218
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    • 1986
  • B. amyloliquefaciens의 $\alpha$-amylase 유전자가 S. cerevisiae 내에서 형질발현하는 가를 조사하기 위하여 본, 연구에서 YRp7 plasmid에 B. amyloliquefaciens amylase유전자를 cloning하여 만든 pEA24를 형질전환시켰다. 먼저 YRp7 plasmid를 이용하여 형질전환 최적 조건을 검토하여 본 바, PH 7과 8사이, 반응온도 3$0^{\circ}C$에서 40%의 polyethylene glycol(MW 4,000)을 처리한 후 2 %의 agar를 함유한 재생배지에 중층도말 하였을 때 형질전환율이 가장 높았다. 형질전환주로부터 생성된 amylase의 활성을 측정한 결과, S. cerevisiae에서 약간의 amylase활성을 나타내어 최고 B. amyloliquefaciens의 2% 정도였고, 세포외효소는 검출되지 않았다. 이들 형질전환 주가 가지고 있는 pEA24 plasmid의 안정성을 조사한 결과 YRp7보다 불안정하였으며, 추출한 DNA를 전기영동하여 그 band를 확인하였다.

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Complete genome sequence of the acidic cellulase producer Bacillus amyloliquefaciens ATC6

  • Kim, Sang Hoon;Oh, Ju Kyoung;Kim, Yong Ho;Kang, Dae-Kyung
    • Journal of Animal Science and Technology
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    • 제62권5호
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    • pp.761-763
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    • 2020
  • Here we report the complete genome sequence of Bacillus amyloliquefaciens ATC6, which produces acidic cellulase, isolated from pig feces. The genome is 4,062,817 bp in length and has a guanine-cytosine (GC) content of 46.27%. Among the predicted 3,913 protein-coding genes, two glucanase genes, which are involved in lichenan and cellulose degradation, were found. This genome analysis helps clarify the mechanism involved in cellulose biodegradation and support its application for efficient use of livestock feeds.

Lipopeptides Extract from Bacillus Amyloliquefaciens Induce Human Oral Squamous Cancer Cell Death

  • Kuo, Chen-Hui;Lin, Yun-Wei;Chen, Ruey-Shyang
    • Asian Pacific Journal of Cancer Prevention
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    • 제16권1호
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    • pp.91-96
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    • 2015
  • A lipopeptide extract of Bacillus amyloliquefaciens BACY1 (BLE) was found to induce cell death in human oral squamous cell carcinoma (OSCC) cell lines, SCC4 and SCC25, in this study. The results of MTT assay showed that BLE inhibited OSCC cell proliferation in a dose-dependent manner. BLE was also effective in increasing the sub-G1 phases. Furthermore, when membrane damage in SCC4 cells treated with BLE was monitored by LDH assay, release of LDH was significantly increased. The protein and mRNA levels of pro-apoptotic Bax, and caspase-3 were up-regulated by BLE. Taken together, these results suggest that BLE induces apoptosis and then inhibits the cell proliferation of human OSCC cells.

Multicatalytic Alkaline Serine Pretense from the Psychrotrophic Bacillus amyloliquefaciens S94

  • Son, Eui-Sun;Kim, Jong-Il
    • Journal of Microbiology
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    • 제41권1호
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    • pp.58-62
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    • 2003
  • An extracellular pretense of Bacillus amyloliquefaciens S94 was purified to apparent homogeneity. The enzyme activity was strongly inhibited by general inhibitor for serine protease, PMSF, suggesting that the enzyme is a serine pretense. The purified enzyme activity was inhibited by leucine peptidase inhibitor, bestatin, suggesting that the enzyme is a leucine endopeptidase. The maximum proteolytic activity against different protein substrates occurred at pH 10, 45$^{\circ}C$ (protein substrate) and pH 8, 45$^{\circ}C$ (synthetic substrate). The purified enzyme was specific in that it readily hydrolyBed substrates with Leu or Lys residues at P$_1$ site. The pretense had characteristics of a cold-adapted protein, which was more active for the hydrolysis of synthetic substrate in the range of 15$^{\circ}C$ to 45$^{\circ}C$, specially at low temperature.

Calcite Production by Bacillus amyloliquefaciens CMB01

  • Lee, Young-Nam
    • Journal of Microbiology
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    • 제41권4호
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    • pp.345-348
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    • 2003
  • The bio-mediated production of calcite crystals by calcinogenic bacteria has great applicable value for the restoration of deteriorated calcareous monuments, because of its high purity and coherency. An investigation of the conditions for calcite production by an alkalophilic Bacillus amyloliquefaciens CMB01 strain was made. Optimal calcite precipitation occurred when the bacterium was cultured at pH 8.0 and 30$^{\circ}C$, and in B4 medium that consisted of 0.4% yeast extract, 0.5% glucose, and 1.5% calcium acetate. Calcium ion of the bacterially induced calcite was analyzed by an inductively coupled plasma (ICP) spectrophotometer. Optical and scanning electron microscopy (SEM) of the calcite revealed a typical rombohedral polycrystalline structure.

Isolation and Characterization of a Protease-Producing Bacterium, Bacillus amyloliquefaciens P27 from Meju as a Probiotic Starter for Fermented Meat Products

  • Lee, Mi-Sun;Lee, Na-Kyoung;Chang, Kyung-Hoon;Choi, Shin-Yang;Song, Chi-Kwang;Paik, Hyun-Dong
    • 한국축산식품학회지
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    • 제30권5호
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    • pp.804-810
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    • 2010
  • This study was performed to select protease-producing Bacillus sp. as a potential probiotic starter for fermented meat products. In order to isolate protease-producing bacterium from meju, measured the diameter of the clear zone on agar plate (TSA, 1% (w/v) skim milk) and analyzed for intracellular protease activity, then 10 Bacillus-like strains were isolated. Three Bacillus-like strains (P19, P27, and P33) among 10 strains were able to tolerate in acidic condition (TSB, pH 2.5, 2 h incubation). These 3 strains were showed antimicrobial activity against food-borne pathogenic bacteria. These vegetative cells of 3 strains were showed a survival rate of 0.04% to 0.08% under the artificial gastric acidic condition (TSB, pH 2.5 with 1% (w/v) pepsin), but spore-forming cells were 56.29% to 84.77%. Vegetative cells of 3 strains were the least bile-resistant, while spore-forming cells of 3 strains showed higher survival rate more than 76% under artificial bile condition (TSB, 0.1% (w/v) oxgall bile). In these strains, P27 strain was finally selected as a good probiotic strain. P27 strain was tentatively identified as Bacillus amyloliquefaciens by API CHB kit and 16S rDNA sequence analysis. The results of this study suggest that B. amyloliquefaciens P27 can be used as a potential probiotic starter for fermented meat product.

PGPR균 EXTN-1 처리에 의한 벼의 생육촉진 및 벼줄무늬잎마름병(RSV)에 대한 유도저항성 발현 (Rice Plant Growth Promotion and Induced Systemic Resistance Against Rice strip tenuivirus by a Selected PGPR, Bacillus amyloliquefaciens)

  • 박진우;박경석;이기운
    • 농약과학회지
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    • 제15권4호
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    • pp.485-489
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    • 2011
  • Bacillus amyloliquefaciens strain EXTN-1 처리에 의해 생육촉진 효과와 함께 광범위한 식물 병 방제효과가 보고되었다. EXTN-1의 PGPR 효과는 생육초기에 PR-1a, PDF1.2 등의 저항성 관련 유전자 발현에 의한 oxidative burst의 증가나 SA, JA나 ethylene 대사에 의한 유도저항성의 발현에 기인한다. 이 연구의 목표는 B. amyloliquefaciens EXTN-1가 기존에 보고된 다른 작물의 경우에서와 마찬가지로 벼의 생육촉진이나 벼줄무늬잎마름병에 대한 저항성에 관여하는지를 확인하기 위해 수행되었다. 벼 종자를 B. amyloliquefaciens EXTN-1에 침지한 후 파종하였을 때 생육촉진 효과와 병에 대한 저항성 발현이 확인되었다. B. amyloliquefaciens EXTN-1을 처리한 30일묘에서 벼의 초장, 생물중, 뿌리길이는 무처리구에 비해 각각 12.6%, 9.8%, 16.0% 증가하여 PGPR 효과가 나타남을 확인할 수 있었다. RSV 접종구에서도 B. amyloliquefaciens EXTN-1 20일묘는 초장, 생물중, 뿌리길이는 무처리구에 비해 각각 12.6%, 9.8%, 16.0% 증가하였다. 유도저항성 발현효과는 감수성 품종에서 저항성 품종에서 상대적으로 뚜렷하게 나타났다.

Bacillus amyloliquefaciens CHP-12에 의한 대두 발효물의 Cyclo-His-Pro (CHP) 함량 증진 및 항당뇨 효과 (Enhancement of Cyclo-His-Pro (CHP) Content from Soybean Fermented with Bacillus amyloliquefaciens CHP-12 and Its Anti-diabetic Effect)

  • 나경수;최장원
    • KSBB Journal
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    • 제26권1호
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    • pp.41-48
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    • 2011
  • To enhance cyclo-His-Pro (CHP) content, soybean hydrolysate was obtained using the strains isolated from Chungkukjang and further purified by various purification steps. First, twenty two strains were screened from Chungkukjang containing high level of CHP. Among them, the strain No. 12, which showed higher productivity of CHP from soybean ferment and have homologous sequence with 16S rDNA of Bacillus amyloliquefaciens, was named B. amyloliquefaciens CHP-12. Through various purification processes, CHP was concentrated from soybean ferment using ultrafiltration, which showed the best efficiency of CHP production, with the yield (71.3%) and CHP content (2.14 mg/g). Moreover, when glucose tolerance test was performed in Type I Sprague-Dawley rat induced by streptozotocin using the soybean ferments [0.5 g soybean ferment/kg body weight (CHP-0.5 group)] and 1.0 g soybean ferment/kg body weight (CHP-1.0 group), there were significant differences in glucose levels between diabetes-control group (265.3 mg/dL) and soybean ferment-treated groups (CHP-0.5 group: 84.3 mg/dL and CHP-1.0 group: 85.3 mg/dL) 120 min after glucose injection (2 g/kg body weight) (p < 0.05). Accordingly, it is suggested that the soybean ferment containing high level of CHP might be a candidate material as an anti-diabetic supplement for manufacturing functional healthy foods.