• 제목/요약/키워드: r-DNA.

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한반도 중부지방의 벼 뿌리로부터 내생 세균의 분리와 특성 분석 (Isolation and Characterization of Endophytic Bacteria from Rice Root Cultivated in Korea)

  • 박수영;양성현;최수근;김지현;김종국;박승환
    • 한국미생물·생명공학회지
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    • 제35권1호
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    • pp.1-10
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    • 2007
  • 한반도 중부지방인 충청남북도 7개 지역에서 재배되고 있는 벼 시료 21점을 채집하여 이들의 뿌리를 표면살균 한 후 내생균을 44주 분리하고 내생성 검정 시스템을 통해 정착력이 상대적으로 우수한 균주를 최종 16주 확보 하였다. 이들의 분리빈도는 뿌리 생체중 1g당 $10^{3-5}$ CFU로 나타났다. 흥미롭게도 이중 7주가 Eurkholderia 속 균으로 동정되어 기존의 다른 벼 내생세균 연구 결과와는 다른 특징을 보였다. 또한 GFP tagging 방법을 이용하여 분리균주 중 하나인 Enterobacter sp. KJ001 균주에 대해 뿌리조직 내 colonization 위치를 확인해본 결과 뿌리 조직 중 관다발 주변에 군락을 이루고 있음을 관찰하였다. Burkholderia 분리주들은 국내 재배 벼에서 높은 빈도로 분리되며 in vitro상에서 광범위한 진균성 식물병원균에 대해 우수한 길항력과 더불어 대부분 질소고정 관련 유전자인 nifH를 가지는 점으로 보아 질소고정에 의해 식물생육에 도움을 줄 수 있을 것으로 예측되며 실제로 오이 유묘의 생장을 30% 이상 촉진하는 효과를 보여 식물병 억제 및 감소와 더불어 작물의 생장 촉진 및 생산성 증대에 활용가치가 높은 내생균으로 사료된다.

Enterococcus faecium LKE12 Cell-Free Extract Accelerates Host Plant Growth via Gibberellin and Indole-3-Acetic Acid Secretion

  • Lee, Ko-Eun;Radhakrishnan, Ramalingam;Kang, Sang-Mo;You, Young-Hyun;Joo, Gil-Jae;Lee, In-Jung;Ko, Jae-Hwan;Kim, Jin-Ho
    • Journal of Microbiology and Biotechnology
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    • 제25권9호
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    • pp.1467-1475
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    • 2015
  • The use of microbial extracts containing plant hormones is a promising technique to improve crop growth. Little is known about the effect of bacterial cell-free extracts on plant growth promotion. This study, based on phytohormonal analyses, aimed at exploring the potential mechanisms by which Enterococcus faecium LKE12 enhances plant growth in oriental melon. A bacterial strain, LKE12, was isolated from soil, and further identified as E. faecium by 16S rDNA sequencing and phylogenetic analysis. The plant growth-promoting ability of an LKE12 bacterial culture was tested in a gibberellin (GA)-deficient rice dwarf mutant (waito-C) and a normal GA biosynthesis rice cultivar (Hwayongbyeo). E. faecium LKE12 significantly improved the length and biomass of rice shoots in both normal and dwarf cultivars through the secretion of an array of gibberellins (GA1, GA3, GA7, GA8, GA9, GA12, GA19, GA20, GA24, and GA53), as well as indole-3-acetic acid (IAA). To the best of our knowledge, this is the first study indicating that E. faecium can produce GAs. Increases in shoot and root lengths, plant fresh weight, and chlorophyll content promoted by E. faecium LKE12 and its cell-free extract inoculated in oriental melon plants revealed a favorable interaction of E. faecium LKE12 with plants. Higher plant growth rates and nutrient contents of magnesium, calcium, sodium, iron, manganese, silicon, zinc, and nitrogen were found in cell-free extract-treated plants than in control plants. The results of the current study suggest that E. faecium LKE12 promotes plant growth by producing GAs and IAA; interestingly, the exogenous application of its cell-free culture extract can be a potential strategy to accelerate plant growth.

메주로부터 지질분해 효소 생산 균주의 분리 및 배양학적 특성 (The Isolation and Culture Characterization of a Lipolytic Enzyme Producing Strain from Meju)

  • 윤혜주;이유정;여수환;최혜선;박혜영;박희동;백성열
    • 한국미생물·생명공학회지
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    • 제40권2호
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    • pp.98-103
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    • 2012
  • 경기도 일대에서 수집한 메주 시료에서 지질분해 활성을 나타내는 균주 Y124를 분리하여 동정한 결과 Yarrowia lipolytica와 100% 상동성을 보였다. 분리 균주가 생산하는 lipase의 조효소에 대한 일반적인 특성을 조사한 결과, 탄소원으로 olive oil을 단독으로 사용한 YPO 배지에서 8시간 배양하였을 때 lipase 활성이 가장 높게 나타났다. YPD 배지에서는 lipase 활성이 거의 없었으며, olive oil과 glucose를 모두 포함하는 YPDO 배지에서는 lipase 활성이 YPO 배지 보다 낮았다. 그리고 olive oil 농도에 따른 lipase 활성을 측정한 결과, olive oil 무첨가보다 0.7% 첨가하여 8시간 배양했을 때 lipase 활성이134 U/mL으로 가장 높게 나타나 lipase의 생산이 olive oil의 첨가에 의해 유도되는 것으로 생각된다. 생육온도에 따른 lipase 활성 측정한 결과, $30^{\circ}C$에 배양하였을 때 배양 8시간에 가장 높은 활성이 나타났고, $25^{\circ}C$$37^{\circ}C$에 배양하였을 때는 배양 12시간에 활성이 가장 높게 나타났으며, Y124균주의 lipase 활성 최적 온도는 $30^{\circ}C$로 나타났다. 그리고 lipase의 기질 친화도를 확인한 결과 Y124균주가 생산하는 lipase의 경우 p-nitrophenyl octanoate ($C_8$)에서 가장 높은 활성이 나타났다.

Impact of a Glyphosate-Tolerant Soybean Line on the Rhizobacteria, Revealed by Illumina MiSeq

  • Lu, Gui-Hua;Zhu, Yin-Ling;Kong, Ling-Ru;Cheng, Jing;Tang, Cheng-Yi;Hua, Xiao-Mei;Meng, Fan-Fan;Pang, Yan-Jun;Yang, Rong-Wu;Qi, Jin-Liang;Yang, Yong-Hua
    • Journal of Microbiology and Biotechnology
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    • 제27권3호
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    • pp.561-572
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    • 2017
  • The global commercial cultivation of transgenic crops, including glyphosate-tolerant soybean, has increased widely in recent decades with potential impact on the environment. The bulk of previous studies showed different results on the effects of the release of transgenic plants on the soil microbial community, especially rhizosphere bacteria. In this study, comparative analyses of the bacterial communities in the rhizosphere soils and surrounding soils were performed between the glyphosate-tolerant soybean line NZL06-698 (or simply N698), containing a glyphosate-insensitive EPSPS gene, and its control cultivar Mengdou12 (or simply MD12), by a 16S ribosomal RNA gene (16S rDNA) amplicon sequencing-based Illumina MiSeq platform. No statistically significant difference was found in the overall alpha diversity of the rhizosphere bacterial communities, although the species richness and evenness of the bacteria increased in the rhizosphere of N698 compared with that of MD12. Some influence on phylogenetic diversity of the rhizosphere bacterial communities was found between N698 and MD12 by beta diversity analysis based on weighted UniFrac distance. Furthermore, the relative abundances of part rhizosphere bacterial phyla and genera, which included some nitrogen-fixing bacteria, were significantly different between N698 and MD12. Our present results indicate some impact of the glyphosate-tolerant soybean line N698 on the phylogenetic diversity of rhizosphere bacterial communities together with a significant difference in the relative abundances of part rhizosphere bacteria at different classification levels as compared with its control cultivar MD12, when a comparative analysis of surrounding soils between N698 and MD12 was used as a systematic contrast study.

Study of pathogenicity and severity of Lactococcus garvieae isolated from rainbow trout (Oncorhynchus mykiss) farms in Kohkilooieh and Boyerahmad province

  • Karami, Esmaeil;Alishahi, Mojtaba;Molayemraftar, Taravat;Ghorbanpour, Masoud;Tabandeh, Mohammad Reza;Mohammadian, Takavar
    • Fisheries and Aquatic Sciences
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    • 제22권10호
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    • pp.21.1-21.7
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    • 2019
  • Background: Lactococcus garvieae is one of the most important risk factors in the rainbow trout culture. Therefore, the purpose of this study was to identify and detect strains isolated from rainbow trout suspected of having Lactococcus garvieae using biochemical characteristics and PCR and determination of the degree of severity of isolated strains. Methods: In this study, the cause of lactococcosis in selected rainbow trout farms in Kohkilooieh and Boyerahmad province was assayed. Gram-positive and catalase-negative bacterial isolates were first obtained from selected trout fish farms using conventional biochemical tests and PCR assay. The 10-day LD50 method (concentration causing 50% mortality in 10 days) was used to determine the severity of the isolated bacteria. Results: One bacterial isolate was detected from all sampled fish which confirmed as Lactococcus garvieae using a specific PCR assay based on the 16S rDNA gene by producing a single band of 1107 bp. Analysis of the rate of mortality showed that the 10-day LD50 was 4.6 × 105 CFU/fish. The results of this study showed that isolated bacteria had high severity for rainbow trout. The presence of bacteria in internal organs of suspected fish showed a severe systemic infection in challenged fish. Antibiogram assay also indicated that the isolated Lactococcus garvieae were resistant to some mostly used antibiotics in rainbow trout. Conclusions: According to current research, it can be concluded that the condition of lactococcosis in the studied area is not suitable, and despite the presence of disease, there is no proper action to control and prevent the disease. Unfortunately, isolated bacteria from the studied area have a very high severity compared to bacteria isolated from other regions of the country or other countries. Therefore, further investigation is needed to determine the cause of this difference and possibly in the design of the vaccine.

Roles of p53 and Caspases in Induction of Apoptosis in MCF-7 Breast Cancer Cells Treated with a Methanolic Extract of Nigella Sativa Seeds

  • Alhazmi, Mohammed I.;Hasan, Tarique N.;Shafi, Gowhar;Al-Assaf, Abdullah H.;Alfawaz, Mohammed A.;Alshatwi, Ali A.
    • Asian Pacific Journal of Cancer Prevention
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    • 제15권22호
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    • pp.9655-9660
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    • 2014
  • Background: Nigella Sativa (NS) is an herb from the Ranunculaceae family that exhibits numerous medicinal properties and has been used as important constituent of many complementary and alternative medicines (CAMs). The ability of NS to kill cancer cells such as PC3, HeLa and hepatoma cells is well established. However, our understanding of the mode of death caused by NS remains nebulous. The objective of this study was to gain further insight into the mode and mechanism of death caused by NS in breast cancer MCF-7 cells. Materials and Methods: Human breast cancer cells (MCF-7) were treated with a methanolic extract of NS, and a dose- and time-dependent study was performed. The $IC_{50}$ was calculated using a Cell Titer $Blue^{(R)}$ viability assay assay, and evidence for DNA fragmentation was obtained by fluorescence microscopy TUNEL assay. Gene expression was also profiled for a number of apoptosis-related genes (Caspase-3, -8, -9 and p53 genes) through qPCR. Results: The $IC_{50}$ of MCF-7 cells was $62.8{\mu}L/mL$. When MCF-7 cells were exposed to $50{\mu}L/mL$ and $100{\mu}L/mL$ NS for 24h, 48h and 72h, microscopic examination (TUNEL assay) revealed a dose- and time-dependent increase in apoptosis. Similarly, the expression of the Caspase-3, -8, -9 and p53 genes increased significantly according to the dose and time. Conclusions: NS induced apoptosis in MCF-7 cells through both the p53 and caspase pathways. NS could potentially represent an alternative source of medicine for breast cancer therapy.

Biphenyl의 Sphingobium yanoikuyae BK-10에 의한 분해 특성 (Biodegradation of Biphenyl by Sphingbium yanoikuyae BK-10)

  • 이중복;김동걸;최충식;손호용;김장억;권기석
    • 한국미생물·생명공학회지
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    • 제34권2호
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    • pp.174-179
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    • 2006
  • PCBs(polychlorinated biphenyl)는 난분해성 물질로써, 환경호르몬으로 분류된 유독한 화합물이다. 이런 유독한 화합물인 PCBs 화합물이 오염된 토양 및 수계를 회복하기 위해 PCBs의 모체인 biphenyl을 효과적으로 분해하는 미생물을 토양으로부터 분리 선별하여 S. yanoikuyae BK10 (AF406817)와 같이 분해능이 우수한 균주를 분리하였다. 분리된 S. yanoikuyae BK10의 특성을 조사하기 위하여 자연계의 토양 조건인 pH 5.0$\sim$8.0에서 99%이상의 높은 biphenyl 분해효율을 보였다. 또한, 온도를 달리하여 실험 한 결과, 10$\sim$50$^{\circ}C$의 범위에서 모두 70%이상의 높은 분해효율을 보여줌으로써 실제 biphenyl/PCBs로_오염된 토양에서 온도의 영향을 덜 받고 biphenyl을 효과적으로 분해 할 수 있을 것으로 생각된다. S. yanoikuyae BK10는 biphenyl이 500 $\mu$g/ml으로 처리된 mineral salt 배지에서 48시간동안 99% 이상의 biphenyl을 분해하는 높은 분해활성을 보이며, biphenyl을 mineralization 시키는 것으로 판단된다. 또한 biphenyl 분해효소 유도 실험결과는 기질을 biphenyl로 사용하여 증식한 균체가 다른 기질을 사용해서 증식한 균체보다 약 2배가량 biphenyl을 빨리 분해시켰다. 그렇지만, cell-mass를 많이 얻을 수 있는 당을 탄소원으로 사용하여 배양하였을 때에도 단시간 내에 biphenyl분해 효소를 분비하여 biphenyl을 분해하는 것으로 보아, S. yanoikuyae BK10는 실제 biphenyl/PCBs에 오염된 토양 적용 할 경우 안정적으로 균주의 제공이 가능하다고 판단된다. 이상의 결과를 토대로, 토양에서부터 분리한 S. yanoikuyae BK10는 자연계에서 유해화합물인 biphenyl/PCBs을 효과적으로 분해 할 수 있다고 생각되며, 분리균주인 S. yanoikuyae BK10의 분자 생물학적 특성을 조사하여 biphenyl과 PCBs를 분해하는 유전자 탐색에 유용한 정보를 얻을 수 있을 것으로 사료된다.

생마 저온부패 원인세균의 분리 및 부패균의 특성 (Isolation and Characterization of Yam-Putrefactive Psychrotrophic Bacteria from Rotted Yam)

  • 류희영;김영숙;박상조;이봉호;권순태;손호용
    • 한국미생물·생명공학회지
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    • 제34권2호
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    • pp.109-114
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    • 2006
  • 본 연구는 부패 생마로부터 저온성 부패균을 분리, 동정하고 분리균의 생육특성과 다양한 효소의 부패관련성을 조사하여, 생마 저온 장기저장 및 생마 가공식품 개발을 위한 기초자료를 제시할 목적으로 수행되었다. 저온 장기저장중의 부패생마로부터 서로 다른 13종의 저온세균을 분리, 동정하였으며, 다양한 온도에서 생마 절편을 이용한 부패력 측정 결과 분리균주 중 YAM-10및 YAM-12균주가 저온부패에 직접적으로 관련됨을 확인하였으며, 이들은 각각 Pseudomonas cepacia 및 Pseudomonas rhodesiae 동정되었다. 이들 균주는 20$^{\circ}C$에서도 우수한 amylase, CMCase, xylanase 활성을 나타내었으며 , 특히 amylase 활성은 생마 부패에 중요한 역할을 하는 것으로 판단되었다. YAM-10 및 YAM-12균주는 양파절편을 부패시키지는 못하였으며, 4$\sim$12$^{\circ}C$의 온도에서도 생육가능하며, pH 5 이하 및 pH 10 이상에서는 생육이 급격히 억제되었다. 현재 생마의 저온 장기저장 및 부패억제를 위한 저온성 Pseudomonas sp.의 제어와 생마부패에 관련되는 효소들의 특성과 저해에 대한 연구 및 저장성, 관능성이 강화된 산장, 염장 등을 통한 생마 가공식품 개발이 진행 중이다.

ISOLATION, IDENTIFICATION AND CHARACTERIZATION OF AN IMMOBILIZED BACTERIUM PRODUCING N2 FROM NH4+ UNDER AN AEROBIC CONDITION

  • Park, Kyoung-Joo;Cho, Kyoung-Sook;Kim, Jeong-Bo;Lee, Min-Gyu;Lee, Byung-Hun;Hong, Young-Ki;Kim, Joong-Kyun
    • Environmental Engineering Research
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    • 제10권5호
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    • pp.213-226
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    • 2005
  • To treat wastewater efficiently by a one-step process of nitrogen removal, a new bacterial strain producing $N_2$ gas from ${NH_4}^+$ under an aerobic condition was isolated and identified. The cell was motile and a Gram-negative rod, and usually occurred in pairs. By 16S-rDNA analysis, the isolated strain was identified as Enterobacter asburiae with 96% similarity. The isolate showed that the capacity of $N_2$ production under an oxic condition was approximately three times higher than that under an anoxic condition. Thus, the consumption of ${NH_4}^+$ by the isolate was significantly different in the metabolism of $N_2$ production under the two different environmental conditions. The optimal conditions of the immobilized isolate for $N_2$ production were found to be pH 7.0, $30^{\circ}C$ and C/N ratio 5, respectively. Under all the optimum reaction conditions, $N_2$ production by the immobilized isolate resulted in reduction of ORP with both the consumption of DO and the drop of pH. The removal efficiencies of $COD_{Cr}$, and TN were 56.1 and 60.9%, respectively. The removal rates of $COD_{Cr}$, and TN were the highest for the first 2.5 hrs with the removal $COD_{Cr}/TN$ ratios of 32.1, and afterwards the rates decreased as reaction proceeded. For application of the immobilized isolate to a practical process of ammonium removal, a continuous operation was executed with a synthetic medium of a low C/N ratio. The continuous bioreactor system exhibited a satisfactory performance at 12.1 hrs of HRT, in which the effluent concentrations of ${NH_4}^+$-N was measured to be 15.4 mg/L with its removal efficiency of 56.0%. The maximum removal rate of ${NH_4}^+$-N reached 1.6 mg ${NH_4}^+$-N/L/hr at 12.1 hrs of HRT(with N loading rate of $0.08\;Kg-N/m^3$-carrier/d). As a result, the application of the immobilized isolate appears a viable alternative to the nitrification-denitrification processes.

PKA-Mediated Regulation of B/K Gene Transcription in PC12 Cells

  • Choi, Mi-Hyun;Kim, Ho-Shik;Choi, Sung-Ho;Kim, Mi-Young;Jang, Yoon-Seong;Jang, Young-Min;Lee, Jeong-Hwa;Jeong, Seong-Whan;Kim, In-Kyung;Kwon, Oh-Joo
    • The Korean Journal of Physiology and Pharmacology
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    • 제9권6호
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    • pp.333-339
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    • 2005
  • B/K protein is a novel protein containing double C2-like domains. We examined the specific signaling pathway that regulates the transcription of B/K in PC12 cells. When the cells were treated with forskolin ($50{\mu}M$), B/K mRNA and protein levels were time-dependently decreased, reaching the lowest level at 3 or 4 hr, and thereafter returning to the control level. Chemicals such as dibutyryl-cAMP, cellpermeable cyclic AMP (cAMP) analogue and CGS21680, adenosine receptor $A_{2A}$ agonist, also repressed the B/K transcription. However, 1,9-dideoxyforskolin did not show inhibitory effect on B/K transcription, suggesting direct involvement of cAMP in the forskolin-induced inhibition of B/K transcription. Effect of forskolin, dibutyryl cAMP and CGS21680 was significantly reduced in PKA-deficient PC12 cell line (PC12-123.7). One cAMP-response element (CRE)-like sequence (B/K CLS) was found in the promoter region of B/K DNA, and electrophoretic mobility shift assay indicated its binding to CREM and CREB. Forskolin significantly suppressed the promoter activity in CHO-K1 cells transfected with the constructs containing B/K CLS, but not with the construct in which B/K CLS was mutated (AC:TG). Taken together, we suggest that the transcription of B/K gene in PC12 cells may be regulated by PKA-dependent mechanism.