• 제목/요약/키워드: Citrobacter freundii

검색결과 63건 처리시간 0.03초

Production of methionine γ- lyase in recombinant Citrobacter freundii bearing the hemoglobin gene

  • Kahraman, Huseyin;Aytan, Emel;Kurt, Ash Giray
    • BMB Reports
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    • 제44권9호
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    • pp.590-594
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    • 2011
  • The production of antileukemic enzyme methionine ${\gamma}$-lyase (MGL) in distinctly related bacteria, Citrobacter freundii and in their recombinants expressing the Vitresocilla hemoglobin (VHb) has been studied. This study concerns the potential of Citrobacter freundii expressing the Vitreoscilla hemoglobin gene (vgb) for the methionine ${\gamma}$- liyase production. Methionine ${\gamma}$- liyase production by Citrobacter freundii and its $vgb^-$ and $vgb^+$ bearing recombinant strain was studied in shake-flasks under 200 rpm agitation, culture medium and $30^{\circ}C$ in a time-course manner. The $vgb^+$ and especially the carbon type had a dramatic effect on methionine ${\gamma}$- liyase production. The $vgb^+$ strain of C. freundii had about 2-fold and 3.1-fold higher levels of MGL than the host and $vgb^-$ strain, respectively.

Citrobacter freundii 분리주를 감염시키는 용균 박테리오파지 CF1의 유전체 염기서열 초안 (Draft genome sequence of lytic bacteriophage CF1 infecting Citrobacter freundii isolates)

  • 김영주;고세영;연영은;임재원;한범구;김현일;안정근;김동혁
    • 미생물학회지
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    • 제54권1호
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    • pp.79-80
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    • 2018
  • 본 연구에서는 돼지 축사 근처 하수 오물에서 분리된 그람 음성균이자 항생제 내성을 쉽게 획득하여 병원성을 띄는 균주인 Citrobacter freundii를 host로 하는 박테리오파지의 유전체 분석을 수행하였다. 본 박테리오파지는 G + C 비율이 42.65%이며, 50,339 bp로 구성된 유전체 DNA를 지니고 있었다. 이러한 유전체 DNA에서 89개의 단백질 코딩 유전자가 확인 되었으며, 이 중 55개의 유전자는 BLASTP 분석으로부터 기능을 가지고 있다고 추정되었다. 또한 RNA는 확인되지 않았다.

Citrobacter freundii 감염에 의한 Doctor fish(Garra rufa obtusa)의 집단 폐사 (Mass Mortality of Doctor Fish(Garra rufa obtusa) Caused by Citrobacter freundii Infection)

  • 백근욱;김지형;카시아노 초레스카;데니스 고메즈;신상필;한지은;박세창
    • 한국임상수의학회지
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    • 제26권2호
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    • pp.150-154
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    • 2009
  • 최근 doctor fish(Gara rufa obtusa)를 이용한 Ichthyotherapy는 인간 피부질환의 대체 치료법으로 각광받고 있으며, 근래 doctor fish의 국내 증식 성공으로 인하여 이러한 추세는 증가되고 있다. 그러나 doctor fish의 질병과 생태에 대해서는 아직 연구가 미미한 실정이다. 본 보고는 국내에서 증식되던 doctor fish가 Citrobacter freundii에 감염되어 집단 폐사한 예로서, 병어에 대한 외부 및 내부 진단, 분리된 세균의 형태학적, 생화학적 동정을 통하여 C. freundii를 확정하였으며, 분리된 C. freundii에 대한 항생제 감수성 검사를 수행하였다. 또한 살아남은 병어에 대한 집단 치료를 시도하여 성공적인 치료 효과를 얻을 수 있었다.

Cytosine 정량을 위한 Proteus mirabilis와 Citrobacter freundii 박테리아전극의 개발과 그 비교 (Preparation and Comparison of Proteus mirabilis and Citrobacter freundii Bacterial Electrodes for the Determination of Cytosine)

  • 인권식;김봉원
    • 대한화학회지
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    • 제32권4호
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    • pp.333-341
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    • 1988
  • Cytosine에 대한 bio-electrode는 $NH_3$ 기체감응기에 Proteus mirabilis 와 Citrobacter freundii 박테리아를 고정하여 조립하였다. cytosine deaminase를 포함하는 박테리아는 cytosine 1분자를 $NH_3$ 1분자로 전환시킨다. Proteus mirabilis 박테리아 전극의 감응은 0.2M phosphate 완충용액, pH 8.4에서 $1.0{\times}10^{-3}\;-\;7.0{\times}10^{-3}$M직선범위와 45-48 mV/decade의 감응기울기를 가진다. Citrobacter freundii박테리아 전극의 감응은 0.05M phosphate완충용액, pH 7.6에서 $7.0{\times}10^{-5}\;-\;7.0{\times}10^{-3}$M 직선범위와 48 mV/decade의 감응기울기를 가진다. 이 전극을 pH, 온도, 완충용액, 박테리아의 양, 방해물질, 무기염류의 영향과 전극의 수명을 조사하였다.

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Cloning, Sequence Analysis, and Characterization of the astA Gene Encoding an Arylsulfate Sulfotransferase from Citrobacter freundii

  • Kang, Jin-Wook;Jeoung, Yeon-Joo;Kwon, Ae-Ran;Yun, Hee-Jeong;Kim, Dong-Hyun;Choi, Eung-Chil
    • Archives of Pharmacal Research
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    • 제24권4호
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    • pp.316-322
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    • 2001
  • Arylsulfate sulfotransferase (ASST) transfers a sulfate group from a phenolic sulfate ester to a phenolic acceptor substrate. In the present study, the gene encoding ASST was cloned from a genomic library copy of Citrobacter freundii, subcloned into the vector pGEM3Zf(-) and sequenced. Sequencing revealed two contiguous open reading frames (ORF1 and ORF2) on the same strand and based on amino acid sequence homologyl they were designated as astA and dsbA, respectively. The amino acid sequence of astA deduced from C. freundii was highly similar to that of the Salmonella typhimurium, Enterobacter amnigenus, Klebsiella, Pseudomonas putida, and Campylobacter jejuni, encoded by the astA genes. However, the ASST activity assay revealed different acceptor specificities. Using p-nitrophenyl sulfate (PNS) as a donor substrate, $\alpha$-naphthol was found to be the best acceptor substrate, followed by phenol, resorcinol, p-acetaminophen, tyramine and tyrosine.

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Glucose 정량을 위한 Citrobacter freundii Bio-Sensor의 개발과 그 응용 (Preparation of the Citrobacter freundii Bio-Sensor for the Determination of Glucose and Its Applications)

  • 인권식;홍영석;김의락;장세용;손무정
    • 대한화학회지
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    • 제34권5호
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    • pp.424-429
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    • 1990
  • Citrobacter freundii와 그의 organelle을 CO$_2$ gas-sensor에 고정시켜서 glucose 정량을 위한 biosensor를 조립하였다. 박테리아의 경우가 organelle 보다 감응은 우수하였으나 감응시간은 organelle의 경우가 훨씬 짧았다. 박테리아 전극은 30$^{\circ}C$의 온도에서 pH 7.0 인 0.2M tris-HCl 완충용액을 사용하면 7.0 ${\times}\;10^{-4}$ - 1.0 ${\times}\;10^{-2}$ M glucose 농도범위에서 42.2 mV/decade의 감응기울기를 나타냈다. 이 전극은 glucose에 대해서 선택성이 매우 우수하였으며, 혈청속의 glucose 정량에 사용한 결과 routine analyzer와 좋은 일치를 보였다.

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수용성 프로폴리스의 항균성 (Antimicrobial Activity of Water Soluble Propolis)

  • 박헌국;김상범;심창환
    • 한국식품영양학회지
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    • 제21권1호
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    • pp.15-21
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    • 2008
  • In this study, the minimum inhibition concentration(MIC), growth inhibition activity, and colony forming inhibitory activity of water soluble propolis against Bacillus cereus, Bacillus subtilis, Listeria monocytogenes, Staphylococcus aureus, Streptococcus mutans, Citrobacter freundii, Enterobacter aerogenes, Escherichia coli, Klebsiella pneumoniae and Salmonella enteritidis were tested. The MICs of the water soluble propolis against Bacillus cereus, Bacillus subtilis, Listeria monocytogenes, Staphylococcus aureus, Streptococcus mutans, Citrobacter freundii, Enterobacter aerogenes, Escherichia coli, Klebsiella pneumoniae, and Salmonella enteritidis were 312.5 ppm, below 156.3 ppm, 625 ppm, 10,000 ppm, above 10,000 ppm, 10,000 ppm, above 10,000 ppm, above 10,000 ppm, 10,000 ppm, and above 10,000 ppm, respectively. The growth inhibition concentrations against Bacillus cereus, Bacillus subtilis, Listeria monocytogenes, Staphylococcus aureus, Streptococcus mutans, Citrobacter freundii, Enterobacter aerogenes, Escherichia coli, and Klebsiella pneumoniae were 156.3 ppm, below 156.3 ppm, 625 ppm, 5,000 ppm, 10,000 ppm, 10,000 ppm, 10,000 ppm, 10,000 ppm, and 5,000 ppm, respectively. However, 10,000 ppm did not inhibit the growth of Salmonella enteritidis. Finally, the colony forming inhibitory activities against Bacillus cereus, Bacillus subtilis, Listeria monocytogenes, Staphylococcus aureus, Streptococcus mutans, Citrobacter freundii, Enterobacter aerogenes, Escherichia coli, Klebsiella pneumoniae, and Salmonella enteritidis were 98.0%, 99.8%, 69.8%, 98.1%, 62.0%, 63.1%, 79.5%, 61.9%, 79.6%, and 0.0%, respectively.

Prevention of Citrobacter freundii (MW279218) infection in Nile tilapia, Oreochromis niloticus using zinc oxide nanoparticles

  • Korni, Fatma M. M.;Moawad, Usama K.;Mohammed, Asmaa N.;Edrees, Asmaa
    • 한국어병학회지
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    • 제35권1호
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    • pp.77-92
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    • 2022
  • Aquaculture development is based on the ideas of increasing production while reducing economic losses. Bacterial diseases are the leading source of fish cases. Citrobacter freundii has been linked to septicemia and mortality all over the world. In the current study, the cause of mortality in O. niloticus was C. freundii MW279218. External hemorrhages were seen on the affected fish, as well as paleness in the liver and kidney congestion. C. freundii MW279218 had a median lethal dosage of 1.5×105 CFU/mL. Zinc oxide and zinc oxide nanoparticles (ZnO-NPs) were tested for their biocidal effectiveness against C. freundii MW279218. The lethal effect of ZnO-NPs for C. freundii MW279218 was 100% when compared to zinc oxide compound, and the inhibition zone width was 2.31.1mm at the highest tested concentrations (70 mg/L) compared to the lowest (35 and 45 mg/L, respectively). Fish were fed three different diets for 28 days: diet 1 (no additives), diet 2 (100 mg of ZnO-NPs/kg of feed), and diet 3 (200 mg of ZnO-NPs/kg of feed). Organs were also collected for histopathology 96 hours after injection (P<0.05). In the groups given 200 mg of ZnO-NPs, there was 10% mortality and 80% RPS. The group fed 100 mg of ZnO-NPs/kg, on the other hand, had 20% mortality and 60% RPS, compared to 50% mortality in the control positive group. Histopathological examinations demonstrated significant alterations in the control positive group and mild lesions in the hepatopancreas of the groups administered 100 mg ZnO-NPs/kg of feed. The groups fed 200 mg of ZnO-NPs/kg diet, on the other hand, showed no histological alterations. ZnO-NPs were found to be effective in the up regulation of both IL-10 and complement 5 immune-related genes.

Isolation of Dibutyl Phthalate-Degrading Bacteria and Its Coculture with Citrobacter freundii CD-9 to Degrade Fenvalerate

  • Wu, Min;Tang, Jie;Zhou, Xuerui;Lei, Dan;Zeng, Chaoyi;Ye, Hong;Cai, Ting;Zhang, Qing
    • Journal of Microbiology and Biotechnology
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    • 제32권2호
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    • pp.176-186
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    • 2022
  • Continued fenvalerate use has caused serious environmental pollution and requires large-scale remediation. Dibutyl phthalate (DBP) was discovered in fenvalerate metabolites degraded by Citrobacter freundii CD-9. Coculturing is an effective method for bioremediation, but few studies have analyzed the degradation pathways and potential mechanisms of cocultures. Here, a DBP-degrading strain (BDBP 071) was isolated from soil contaminated with pyrethroid pesticides (PPs) and identified as Stenotrophomonas acidaminiphila. The optimum conditions for DBP degradation were determined by response surface methodology (RSM) analysis to be 30.9 mg/l DBP concentration, pH 7.5, at a culture temperature of 37.2℃. Under the optimized conditions, approximately 88% of DBP was degraded within 48 h and five metabolites were detected. Coculturing C. freundii CD-9 and S. acidaminiphila BDBP 071 promoted fenvalerate degradation. When CD-9 was cultured for 16 h before adding BDBP 071, the strain inoculation ratio was 5:5 (v/v), fenvalerate concentration was 75.0 mg/l, fenvalerate was degraded to 84.37 ± 1.25%, and DBP level was reduced by 5.21 mg/l. In addition, 12 fenvalerate metabolites were identified and a pathway for fenvalerate degradation by the cocultured strains was proposed. These results provide theoretical data for further exploration of the mechanisms used by this coculture system to degrade fenvalerate and DBP, and also offer a promising method for effective bioremediation of PPs and their related metabolites in polluted environments.