• 생물환경조절학회지
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• 제14권4호
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• pp.275-279
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• 2005

백침계 오이는 측지착과형으로 주지착과형인 국내용 오이와 차이가 있어 백침계 오이의 수량을 증가시키기 위해서는 측지발생을 높여야 가능하다. 그러나 백질계 오이의 재배시기는 대부분 동절기로 저온 및 일조부족 등의 불량한 환경조건 때문에 측지발생이 떨어진다. 본 연구는 생장조정제를 이용하여 백침계 오이의 측지발생을 촉진하기 위하여 BA의 농도 및 살포시기를 구명하고자 하였다 BA $30mg{\cdot}L^{-1}$을 살포한 것은 농도 장해증상이 억제작형에서는 나타났으나, 반촉성작형에서는 경미하게 나타났다. 측지발생은 BA $10mg{\cdot}L^{-1}$ 살포하는 것이 BA $30mg{\cdot}L^{-1}$ 살포하는 것 보다 많았고, 처리시기는 본엽 10매, 15매 전개되었을 메 살포한 것이 본엽 5매 전개되었을 때 살포한 것보다 많았다.

• 한국습지학회지
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• 제16권1호
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• pp.11-18
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• 2014

증가된 이산화탄소 농도와 온도상승에 따른 멸종위기 수생식물 독미나리의 생태학적 반응을 알아보기 위해 대조구, 온도상승구, 그리고 $CO_2$+온도상승구에서 생육시킨 결과를 비교하였다. 독미나리의 지상부 길이는 대조구, 온도상승구 그리고 $CO_2$+온도상승구간에 차이가 없었지만, 분얼 수는 대조구, 온도상승구, $CO_2$+온도상승구 순으로 증가했다. 복산형화서의 수는 대조구와 온도상승구에서 같았고, $CO_2$+온도상승구에서 감소했다. 소산형화서의 수는 대조구와 온도상승구, $CO_2$+온도상승구간에 차이가 없었다. 종자형성률은 온도상승구와 $CO_2$+온도상승구가 대조구보다 감소했고, 온도상승구와 $CO_2$+온도상승구간에 차이가 없었다. 이상으로 보면, $CO_2$농도와 온도상승은 길이생장에 영향을 주지 않은 반면, 분얼 수는 증가시키고 종자생산은 감소시킨다. 그러므로 독미나리는 지구 온난화 조건이 되면 종자생산보다 분얼을 늘려 무성번식 경향이 증가될 것이며, 이러한 개체군 생장을 연구하는 것은 멸종위기종 연구에 중요한 자료로 활용될 것이다.

• Journal of Ginseng Research
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• 제39권3호
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• pp.213-220
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• 2015

Background: Korean ginseng (Panax ginseng Meyer) is a perennial herb prone to various root diseases, with Phytophthora cactorum being considered one of the most dreaded pathogens. P. cactorum causes foliar blight and root rot. Although chemical pesticides are available for disease control, attention has been shifted to viable, eco-friendly, and cost-effective biological means such as plant growth-promoting rhizobacteria (PGPR) for control of diseases. Methods: Native Bacillus amyloliquefaciens strain HK34 was isolated from wild ginseng and assessed as a biological control agent for ginseng. Leaves from plants treated with HK34 were analyzed for induced systemic resistance (ISR) against P. cactorum in square plate assay. Treated plants were verified for differential expression of defense-related marker genes using quantitative reverse transcription polymerase chain reaction. Results: A total of 78 native rhizosphere bacilli from wild P. ginseng were isolated. One of the root-associated bacteria identified as B. amyloliquefaciens strain HK34 effectively induced resistance against P. cactorum when applied as soil drench once (99.1% disease control) and as a priming treatment two times in the early stages (83.9% disease control). A similar result was observed in the leaf samples of plants under field conditions, where the percentage of disease control was 85.6%. Significant upregulation of the genes PgPR10, PgPR5, and PgCAT in the leaves of plants treated with HK34 was observed against P. cactorum compared with untreated controls and only pathogen-treated plants. Conclusion: The results of this study indicate HK34 as a potential biocontrol agent eliciting ISR in ginseng against P. cactorum.

• 한국토양비료학회지
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• 제32권1호
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• pp.57-61
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• 1999

본 연구는 밀양 23호와 내풍벼 볍씨를 Brassino-steroids에 24시간 침종 후 인공산성비에 7일간 발아시킨 후 생육, 발아율, 유기산 함량 등 몇 가지 조사를 수행하였던 바 얻어진 결과를 요약하면 인공 산성비의 조성은 sulfate가 $427.9mg\;kg^{-1}$으로 가장 많았고 그 다음이 nitrate로 $130.6mg\;kg^{-1}$이었다. 초장은 밀양 23호에서 인공 산성비 처리구보다 식물생장조절제 처리구가 길었으나 내풍벼에서는 식물생장조절제의 종류와는 무관하게 감소하였고 근장은 밀양 23호에서 인공 산성비 처리구보다 식물생장조절제 처리구에서 높은 뿌리의 신장 효과를 보였다. 발아율은 밀양 23호에서는 인공산성비 단일 처리구가 84.3%인 것보다 모든 생장조절제 처리에서 88.3%의 발아율을 보였으며 유기산 함량은 밀양 23호에서는 인공 산성비 처리구에서 succinic acid와 acetic acid가 각각 $878,419{\mu}g$으로 가장 높은 농도를 보였고 hBR처리에서는 농도가 낮은 $10^{-3}mg\;kg^{-1}$에서 succinic acid와 acetic acid가 가장 높은 함량을 나타내었으나 epiBR처리에서는 acetic acid는 농도가 높을 때, succinic acid는 농도가 낮을 때 함량이 증가하였다.

• 한국미생물·생명공학회지
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• 제36권4호
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• pp.326-335
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• 2008

Bacillus subtilis AH18균주는 auxin, siderophore 그리고 cellulase를 동시에 생산하는 PGPR 균주이자 생물방제균주로 항진균성 siderophore의 특성을 확인한 결과 catechol type의 siderophore로 확인하였다. $Siderophore_{AH18}$ 의 정제는 Amberlite XAD-2, sephadex LH-20 column chromatography 그리고 HPLC를 통해 정제 및 정제여부를 확인하였으며, GC-MS, $^1H$-NMR, 그리고 $^{13}C$-NMR을 통해 구조 및 분자량을 확인하였다. 그 결과 B. subtilis AH18이 생산하는 siderophore은 분자량 883의 bacillibactin임을 확인하였으며, 포자발아억제활성을 나타냄을 확인하였다. B. subtilis AH18은 P. capsici에 의한 고추역병을 효과적으로 방제하였으며(방제력 55%), 이는 bacillibactin에 의한 효과가 포함되리라 추측된다.

• 한국미생물·생명공학회지
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• 제35권4호
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• pp.357-363
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• 2007

249 fungal strains were isolated from the roots of 26 plants, and the production of GAs was spectrophotometric ally examined. As a result 76 fungal strains were shown to produce GAs. Bioassay of culture broth from seventy six fungal strains producing GAs was carried out with waito-c rice, that is dwarf rice. The seventy six fungi with GAs-producing activity were incubated for seven days in 40 mL of Czapek's liquid medium at $30^{\circ}C$ and 180 rpm, and the culture broth of fungi were treated on the 2-leaf rice sprout. Fifteen of these showed plant growth promoting activity and the amount of each GAs in the medium was measured by Gas chromatographymass spectrometer (GC-MS). Nine of these fungi were also identified by genetic analysis of the nucleotide sequences in the internal transcribed spacer region of the ribosomal DNA.

• 한국토양비료학회지
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• 제49권2호
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• pp.144-156
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• 2016

Soil is a dynamic biological system, in which it is difficult to determine the composition of microbial communities. Knowledge of microbial diversity and function in soils are limited because of the taxonomic and methodological limitations associated with studying the organisms. In this review, approaches to measure microbial diversity in soil were discussed. Research on soil microbes can be categorized as structural diversity, functional diversity and genetic diversity studies, and these include cultivation based and cultivation independent methods. Cultivation independent technique to evaluate soil structural diversity include different techniques such as Phospholipid Fatty Acids (PLFA) and Fatty Acid Methyl Ester (FAME) analysis. Carbon source utilization pattern of soil microorganisms by Community Level Physiological Profiling (CLPP), catabolic responses by Substrate Induced Respiration technique (SIR) and soil microbial enzyme activities are discussed. Genetic diversity of soil microorganisms using molecular techniques such as 16S rDNA analysis Denaturing Gradient Gel Electrophoresis (DGGE) / Temperature Gradient Gel Electrophoresis (TGGE), Terminal Restriction Fragment Length Polymorphism (T-RFLP), Single Strand Conformation Polymorphism (SSCP), Restriction Fragment Length Polymorphism (RFLP) / Amplified Ribosomal DNA Restriction Analysis (ARDRA) and Ribosomal Intergenic Spacer Analysis (RISA) are also discussed. The chapter ends with a final conclusion on the advantages and disadvantages of different techniques and advances in molecular techniques to study the soil microbial diversity.

• 한국토양비료학회지
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• 제45권5호
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• pp.817-821
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• 2012

Soil samples collected from abounded mines of Boryeong area in South Korea were used in isolating bacterial strains and their capacity to solubilize inorganic phosphates and heavy metal tolerance were assessed in vitro. Three different inorganic phosphate sources (Ca phosphate, Fe phosphate, and Al phosphate) and four different heavy metals (Co, Cd, Pb and Zn) each with three concentrations ($100{\mu}g\;mL^{-1}$, $200{\mu}g\;mL^{-1}$, and $400{\mu}g\;mL^{-1}$) were used. The bacterial isolates PSB-1, PSB-2, PSB-3, and PSB-4 solubilized significantly higher amount of Ca phosphate during the first five days of incubation though subsequent drop in soluble phosphorus level in the medium was observed at the later stage (after 5 days) of the incubation. Solubilization of Ca phosphate and Fe phosphate was concomitant with the acidification of the culture medium compared to the control where it remained constant. Isolated strains could solubilize Fe phosphate to certain extent ($25-45{\mu}g\;mL^{-1}$) though solubilization of Al phosphate was found negligible. All the isolates were tolerant to heavy metals (Cd, Pb, and Zn) up to the concentration of $400{\mu}g\;mL^{-1}$ except PSB-1 and PSB-8, which were shown to be vulnerable to Co even at $100{\mu}g\;mL^{-1}$. Heavy metal tolerant strains should be further evaluated for plant growth promoting activities also under field conditions in order to assess their agricultural and environmental significance.

• 한국토양비료학회지
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• 제43권4호
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• pp.522-527
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• 2010

지베렐린산은 곰팡이 및 세균으로부터 생산되는 주요 식물생장촉진물질이며 다양한 산업에서 이용되고 있다. 본 연구는 Methylobacterium oryzae CBMB20을 이용하여 GA3를 생산하기 위해 탄소원 및 질소원을 선발하였으며, 선발된 탄소원 및 질소원의 최적 농도와 최적 비율을 조사하였다. 탄소원으로는 Na-succinate가 methanol, glucose, maltose, sucrose, fructose, lactose에 비해 가장 우수하였으며, 질소원으로는 $NH_4Cl$가 $NO_3$, $NaNO_3$, glycine 등에 비해 우수하였다. 배양액에서 Nasuccinate와 $NH_4Cl$를 각각 5 및 0.4 g $L^{-1}$ 농도 비율로 사용하였을 때 $CA_3$의 생산량이 가장 높았다. 또한 ammonium mineral salt 배지의 pH를 7로 유지하고 $30^{\circ}C$의 조건으로 96시간 배양하였을 때 $CA_3$의 생산이 최대로 나타나는 것을 확인하였다.

• Asian Pacific Journal of Cancer Prevention
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• 제15권18호
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• pp.7527-7532
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• 2014

Saussurea involucrata is a Mongolian medicinal plant well known for its effects in promoting blood circulation, and anti-inflammation and analgesic functions. Earlier studies reported that Saussurea involucrata has anticancer activity. The purpose of this study was to confirm the anticancer activity of an ethanol extract of Saussurea involucrata against hepatic cancer and elucidate its mechanisms of action. Hepatocellular carcinoma cells were tested in vitro for cytotoxicity, AO/EB staining for apoptotic cells, apoptotic DNA fragmentation and cell cycle distribution in response to Saussurea involucrata extract (SIE). The mRNA expression of caspase-3,-9 and Cdk2 and protein expression of caspase-3,-9, PARP, XIAP, Cdk2 and p21 were analyzed through real time PCR and Western blotting. Treatment with SIE inhibited HepG2 cell proliferation dose- and time-dependently, but SIE only exerted a modest cytotoxic effect on a viability of Chang human liver cells. Cells exposed to SIE showed typical hallmarks of apoptotic cell death. Cell cycle analysis revealed that SIE caused G1-phase arrest in HepG2 cells. In conclusion, Saussurea involucrata ethanol extract has potential cytotoxic and apoptotic effects on human hepatocellular carcinoma cells. Its mechanism of action might be associated with the inhibition of DNA synthesis, cell cycle (G1) arrest and apoptosis induction through up-regulation of the protein expressions of caspase-3,-9 a nd p21, degradation of PARP and down-regulation of the protein expression of Cdk2 and XIAP.