본 연구는 유칼립투스(Eucalyptus pulverulenta) 잎에서 치료적 효과가 큰 α-pinene과 1,8-cineole 함량증가에 미치는 H2O2와 SA 처리의 영향에 대해 알아보기 위하여 수행하였다. 유칼립투스가지를 H2O2 수용액(0.3, 0.5, 1%)과 SA 수용액(0.1, 1mM)에 침지하거나 잎에 엽면살포(0.1mM SA, 1% H2O2)한 뒤 시간흐름(0, 0.5, 1, 2, 4시간)에 따른 α-pinene과 1,8-cineole의 함량변화를 분석한 결과, 침지처리에서 유칼립투스 잎의 α-pinene 함량(mg･L-1)은 0.1mM SA에 2시간 침지 후 1.62에서 5.48로 크게 증가하였으며(238.27%, p=0.012), 1,8-cineole 함량(mg･L-1)은 1mM SA에 4시간 침지 후 44.44에서 78.96으로 크게 증가하였다(77.66%, p=0.026). 살포처리에서는 0.1mM SA를 엽면살포 30분 후 α-pinene 함량(mg･L-1)은 1.62에서 3.91로(141.36%, p=0.007), 1,8-cineole 함량(mg･L-1)은 44.44에서 87.91로 증가하였다(97.82%, p=0.001). α-pinene과 1,8-cineole 모두 살포처리 30분 뒤 크게 증가하여, 엽면살포가 짧은 시간내에 방향화합물을 증가시키는데 침지처리보다 효과적이었으며, H2O2와 SA 처리는 α-pinene과 1,8-cineole의 함량증가에 유의한 영향이 있었다. 또한, SA의 처리가 H2O2보다 방향화합물 함량증가에 더 효과적이었으며, 유칼립투스 가지의 경우 원예치료 2시간 전에 0.1mM SA 용액에 담그거나 30분 전에 잎에 살포하면 monoterpene의 유칼립투스 함량이 크게 증가되었다.

대부분의 세균은 표면에서 바이오필름을 형성한 상태로 존재하며, 식품 가공시설이나 주방 배수구 등의 경우 식품 접촉표면에서 잔류하는 음식물 찌꺼기와 미생물 세포의 정착으로 바이오필름을 형성한다. 표면에서 형성된 바이오필름은 제품 및 기기․기구의 교차 오염의 원인이 되며 식품을 매개로 한 식중독 발병의 가능성이 있어 식품 안전성의 잠재적 위해 요소가 된다. 본 연구는 식중독 발생 원인균인 E. coli에 의해 형성되는 바이오필름을 조사하기 위하여 수행되었으며, 바이오필름은 스테인리스 스틸 쿠폰 표면에 형성되어 부착된 세균수로 측정하였다. 연구 결과 Tryptic soy broth 배지에서 37℃에서 7일간 배양 할 때 쿠폰 표면에 대장균으로 인한 바이오필름이 형성되며, 이 때 대장균수는 3.98 log CFU/cm2로 측정되었다.

Stream of afterglow of an atmospheric pressure plasma can conveniently be used for large scale decontamination operations. In the present study, an afterglow dielectric-barrier discharge air plasma (ADDAP) was used to inactivate Escherichia coli O157:H7 as a model microorganism for studying the plasma inactivation effect. The plasma was generated at current levels in the range of 0.4 - 0.8 A. The power consumption of ADDAP generation system ranged 169.5 - 221.9 W with respect to the current intensity range. At this current level, the temperature observed in the treatment chamber remained less than 30℃. Regarding chemical composition of ADDAP in the treatment chamber, NOx species were predominantly generated. The levels of NOx species increased as the current intensity increases and the maximum NO and NO2, concentrations noted were 6 and 4 ppm, respectively, but that of CO was less than 1 ppm level at 0.8 A. Upon treating with the ADDAP generated at 0.4 - 0.8 A for 180 min, E. coli O157:H7 showed 1.24 – 2.71 log reductions. The inactivation patterns exhibited better fit to Weibull-tail model. The comparison of delta values indicated that superior inactivation effects were observed as the current intensity increased.

The outbreaks of foodborne diseases associated with bacterial contamination are still critical issues all over the world. To ensure food safety, the diagnosis of pathogenic bacteria on site at early state of contamination are required. Escherichia coli O157:H7 (E. Coli O157:H7) is one of the major factor causing foodborne diseases. We introduce a sandwich type colorimetric detection method integrated with chitosan-coated starch magnetic polymer beads(CS@SMBs) that can separate and concentrate bacteria in aqueous environment. For signal amplification, horseradish peroxidase-conjugated antibody (HRP-Antibody) and 3,3',5,5'- tetramethylbenzidine (TMB) were employed as enzyme label and chromogenic substrate, respectively. We demonstrate that CS@SMBs not only show a good magnetic sensitivity, but also can capture a variety of bacteria regardless of Gram-negative and Gram-positive, which offer possibility for separation of the broad range of bacteria from food matrix. Our approach successfully captures E. coli O157:H7 with detection limit of 101 CFU/mL through naked eye, making promise of fast, on-site, and sensitive detection of pathogenic bacteria.

H2O maser emission at 22 GHz in the circumstellar envelope is one of the good tracers of detailed physics and kinematics in the mass loss process of asymptotic giant branch stars. Long-term monitoring of an H2O maser spectrum with high time resolution enables us to clarify acceleration processes of the expanding shell in the stellar atmosphere. We monitored the H2O maser emission of the semi-regular variable R Crt with the Kagoshima 6-m telescope, and obtained a large data set of over 180 maser spectra over a period of 1.3 years with an observational span of a few days. Using an automatic peak detection method based on least-squares fitting, we exhaustively detected peaks as significant velocity components with the radial velocity on a 0.1 km s−1 scale. This analysis result shows that the radial velocity of redshifted and blue-shifted components exhibits a change between acceleration and deceleration on the time scale of a few hundred days. These velocity variations are likely to correlate with intensity variations, in particular during flaring state of H2O masers. It seems reasonable to consider that the velocity variation of the maser source is caused by shock propagation in the envelope due to stellar pulsation. However, it is difficult to explain the relationship between the velocity variation and the intensity variation only from shock propagation effects. We found that a time delay of the integrated maser intensity with respect to the optical light curve is about 150 days.

Due to the globalization of food supply have been growing, there have been a great demands for food safety and quality assuarance for on-site detection. On-site detetction isuue is the process should be fast, simple, user-friendly and require minimal equipments. Herein, we developed a Radial chromatography (RC) biosensor integrated with the immuno-gold nanoparticles-coated magnetic nanoparticle (AuNPs@Fe3O4) for specific separation and detection of the target bacteria, E. coli O157:H7, in sample. The immuno-AuNPs@Fe3O4 specifically binds to E.coli O157:H7 creating AuNP@Fe3O4-E.coli complexes and captured bacteria were concentrated by magnet. The complex can be identified with inner ring derived from the difference of mobility of free AuNPs@Fe3O4 on the RC sensor. Our results show that AuNPs@Fe3O4 based RC sensor has high sensitivity to the target bacteria over non-target bacteria with a detection limit of 103 CFU/ml. Our system offers a rapid and sensitive means of detecting E.coli O157:H7 with naked eyes, which can be applied to the field diagnosis.

Rapid, simple, and sensitive detection of pathogen bacteria is a highly topical research area due to increasingly concerning of food safety and public health. Surface-enhanced Raman spectroscopy (SERS) is a promising and attractive technique offering fast, sensitive, comparatively low-cost, and in-suit detection of pathogenic bacteria. However, this technique requires the preparation step for reducing the noise derived from heterogeneous matrixes of food sample. Immunomagnetic separation (IMS) is widely used technique enabling separation and concentration of the target analyte. It can be used not only laboratory scale but also field diagnosis easily. Here, we synthesized gold-shelled starch magnetic microparticles (GS@SMMPs) for effective separation and concentration of Escherichia coli O157:H7, which were subsequently subjected to SERS integrated with gold-coated 3D-well substrate for bacterial detection in aqueous solution. GS@SMMPs were labelled by Anti-E. coli O157 monoclonal antibody through gold binding protein and staphylococcal protein G (GBP-SPG) fusion protein. In IMS experiment, the immuno-GS@SMMPs showed high capture efficiency over 90% to E. coli O157:H7, which resulted in 10 times decrease in detection limit in PCR assay. Through SERS assay, E. coli O157:H7 concentrated by immuno-GS@SMMPs were successfully detected even at an extremely low concentration of 101 CFU/ml the subjected to SERS. Moreover, by using sandwich method using SERS reporter consisting of GBP-SPG, we found that E. coli O157:H7 were able to be detected by SERS quantitatively through measuring the SERS intensity of GBP-SPG. This novel strategy combining SERS and IMS could be meaningful for extending the application in SERS for in-suit sensitive detection of pathogenic bacteria.

최근 기능성과 친환경 화장품에 대한 관심이 증가하고 있으며, 이에 따라 안전하면서 효능이 우수한 식물 추출물을 활용한 소재 개발이 이루어지고 있는 실정이다. 따라서 본 연구에서도 주로 건강 기능성 소재로써 다양한 효능이 있는 것으로 알려진 그라비올라 추출물이 기능성 화장품 소재로써의 가 능성을 확인하고자 하였다. 그라비올라 추출물의 항산화 활성을 확인하고자 총 폴리페놀과 총 플라보노 이드 함량, DPPH radical 소거 활성을 측정하였고, HDF 세포에서의 세포 독성을 확인한 후 적정 농도 에서 HDF 세포에 과산화수소(H2O2)를 처리하여 산화적 스트레스에 대한 ROS 활성 억제 효과와 세포 보호 효과를 측정하였다. 본 실험 결과, 그라비올라 추출물은 항산화 지표가 되는 총 폴리페놀과 플라보 노이드의 100g당 26.6 mg(CA)/100g, 14.3 mg(CA)/100g의 높은 함량을 확인하였으며, 높은 radical 소 거 활성을 확인하였다. HDF 세포에 대한 세포 생존율을 측정한 결과, 모든 농도에서 유의한 세포 독성 이 나타나지 않았으며, 추후 100 μg/mL 농도에서 실험하였다. H2O2로 유도된 HDF 세포에 ROS 활성 억제를 측정한 결과, 농도 의존적인 ROS 활성 억제 효과를 확인하였고, H2O2를 4 시간, 24 시간, 48 시간 동안 처리 후 그라비올라 추출물의 세포 보호 효과를 측정한 결과, 25 μg/mL 농도에서 24시간까 지 89.92%의 높은 세포 보호 효과를 확인하였다. 이와 같은 결과를 통하여 그라비올라 추출물은 항산 화 활성이 우수하고, HDF 세포에 대한 독성이 거의 없으며, H2O2에 의해 발생하는 활성산소에 대한 효과적인 활성 억제 효과와 세포 보호 효과가 우수한 것으로 확인됨에 따라 항산화 및 세포 보호 효과 를 가진 다양한 기능성 소재로서의 가능성을 확인하였다.

Although anti-aging activities of melatonin, a hormone secreted by the pineal gland, have been reported in senescence-accelerated mouse models and several types of cells, its impact and mechanism on the senescence of human dental pulp cells (HDPCs) remains unknown. In this study, we examined the impact of melatonin on cellular premature senescence of HDPCs. Here, we found that melatonin markedly inhibited senescent characteristics of HDPCs after exposure to hydrogen peroxide (H2O2), including the increase in senescence-associated β-galactosidase (SA-β-gal)-positive HDPCs and the upregulation of p21 protein, an indicator for senescence. In addition, as melatonin attenuated H2O2-stimulated phosphorylation of c-Jun N-terminal kinase (JNK), while selective inhibition of JNK activity with SP600125 significantly attenuated H2O2-induced increase in SA-beta-gal activity. Results reveal that melatonin antagonizes premature senescence of HDPCs via JNK pathway. Thus, melatonin may have therapeutic potential to prevent stress-induced premature senescence, possibly correlated with development of dental pulp diseases, and to maintain oral health across the life span.

본 연구는 정향추출물의 E. coli O157:H7에 대한 항균 효과와 E. coli O157:H7 감염 마우스에 대한 치료효과를 평가하기 위해 수행되었다. 정향 메탄올 추출물(FSAE)을 이용하여 E. coli O157:H7 에 대한 항균효과 확인 시험을 수행한 결과, 배양 후 24 시간째에, FSAE를 첨가한 모든 군들에서 E. coli O157:H7 의 생존율이 무투여 대조군에 비해 통계적으로 유의성 있게 감소하는 결과를 보여(0.269 mg/ml, p < 0.05; 0.538과 1.075 mg/ml, p < 0.001), FSAE가 E. coli O157:H7의 증식 억제 효과가 뛰어난 것으로 확인되었다. 또한, E. coli O157:H7을 감염시킨 마우스에 FSAE를 경구로 투여한 결과, 투여 후 3일째에, FSAE를 1.075 (p < 0.05)와 2.15 mg/ ml (p < 0.01)로 투여한 군들에서 대조군과 비교하여 분변 내 E. coli O157:H7의 균수가 유의성 있게 감소하였으며, 투여 7일째에는, 모든 FSAE 투여군들에서 대조군과 비교 하여 E. coli O157:H7의 균수가 통계적으로 유의성 있게 감소하였다(0.538 mg/ml, p < 0.05; 1.075와 2.15 mg/ml, p < 0.001). 이상의 연구결과로부터, FSAE를 E. coli O157: H7에 감염된 마우스에 경구로 투여할 경우, 감염증상을 완화 시킬 수 있을 것으로 기대된다.

We performed temperature dependent current-voltage (I-V) measurements to characterize the electrical properties of Au/Al2O3/n-Ge metal-insulator-semiconductor (MIS) diodes prepared with and without H2O prepulse treatment by atomic layer deposition (ALD). By considering the thickness of the Al2O3 interlayer, the barrier height for the treated sample was found to be 0.61 eV, similar to those of Au/n-Ge Schottky diodes. The thermionic emission (TE) model with barrier inhomogeneity explained the final state of the treated sample well. Compared to the untreated sample, the treated sample was found to have improved diode characteristics for both forward and reverse bias conditions. These results were associated with the reduction of charge trapping and interface states near the Ge/Al2O3 interface.

본 연구에서는 배가스 내 존재하는 오염물질인 NO의 처리효율을 증대시키기 위하여 NO 산화 공정을 연구하였으며, 강력한 산화력의 건식산화제를 제조하는 방법으로 H2O2 촉매분해가 도입되었다. H2O2 분해공정 상에서 적용 가능한 K-Mn/Fe2O3 불균일계 촉매가 제조되었으며, 이들이 가지는 물리화학 적 특성이 H2O2 분해반응에 미치는 영향이 조사되었다. 제조된 건식산화제는 NO가 포함된 모사 배가스를 처리하기 위한 NO 산화공정에 적용되었으며, 다양한 모사 배가스의 유량(5, 10, 20 L/min)에서 약 100% 가까운 NO 전환율을 확인 하였다.

We study CO2/H2O ice abundance ratios in nearby galaxies using AKARI near-infrared slit spec- troscopy. Past studies of the ices intensively examined CO2/H2O ratios mainly in our Galaxy, and found that there were considerable variations in the CO2/H2O ratios from object to object. The cause of the variations is, however, still under debate. As a result of the analysis of our sample that includes 1031 regions in 158 galaxies, the CO2/H2O ratios are in a range of 0.05-0.30. In the dataset, we nd that the CO2/H2O ratios positively correlate with the Brα/PAH 3.3 μm ratios which re ect the massive star formation activity. Furthermore, we find that the CO2/H2O ratios positively correlate with the specific star formation rates of the galaxies where the ices are detected, that re ect the evolutionary stage of a galaxy. These results suggest that the CO2/H2O ratios are enhanced in active star-forming regions and young galaxies.

This study was conducted to investigate the effect of cold plasma combined with UV-C irradiation against Escherichia coli O157:H7, Salmonella enterica serovar Typhimurium, and Listeria monocytogenes on lettuce. E. coli O157:H7, S. Typhimurium, and L. monocytogenes, corresponding to approximately 5.82, 5.09, 5.65 log CFU/ g, were inoculated on lettuce, respectively. Then, the lettuce was treated with cold plasma, UV-C and combination (cold plasma + UV-C), respectively. The treated lettuce was stored for 9 days at 4oC for microbiological analysis and sensory evaluation. Cold plasma reduced the populations of E. coli O157:H7, S. Typhimurium, and L. monocytogenes by 0.26, 0.65, and 0.93 log CFU/g, respectively. Each microorganism were reduced by 0.87, 0.88, and 1.14 log CFU/ g after UV-C treatment. And, the combined treatment that was treated by cold plasma after UV-C treatment reduced the populations of inoculated microorganisms by 1.44, 2.70, 1.62 log CFU/g, respectively. The all treatment significantly (p < 0.05) reduced the populations of all inoculated bacteria compared to untreated lettuce. UV-C combined with cold plasma was the most effective for reducing the pathogenic bacteria on lettuce, by showing log-reductions of ≥ 2.0 log CFU/g. All treatment was not significantly different until 6 day storage compared to control group in terms of appearance, texture and overall acceptability. Therefore, the combined treatment will be an effective intervention method to control the bacteria on lettuce.

We present the results of simultaneous monitoring observations of H2O 61,6–52,3 (22GHz) and SiO J=1–0, 2–1, 3–2 maser lines (43, 86, 129GHz) toward five post-AGB (candidate) stars, using the 21-m single-dish telescopes of the Korean VLBI Network. Depending on the target objects, 7 – 11 epochs of data were obtained. We detected both H2O and SiO maser lines from four sources: OH16.1−0.3, OH38.10−0.13, OH65.5+1.3, and IRAS 19312+1950. We could not detect H2O maser emission toward OH13.1+5.1 between the late OH/IR and post-AGB stage. The detected H2O masers show typical double- peaked line profiles. The SiO masers from four sources, except IRAS 19312+1950, show the peaks around the stellar velocity as a single peak, whereas the SiO masers from IRAS 19312+1950 occur above the red peak of the H2O maser. We analyzed the properties of detected maser lines, and investigated their evolutionary state through comparison with the full widths at zero power. The distribution of observed target sources was also investigated in the IRAS two-color diagram in relation with the evolutionary stage of post-AGB stars. From our analyses, the evolutionary sequence of observed sources is suggested as OH65.5+1.3! OH13.1+5.1! OH16.1−0.3! OH38.10−0.13, except for IRAS 19312+1950. In addition, OH13.1+5.1 from which the H2O maser has not been detected is suggested to be on the gateway toward the post-AGB stage. With respect to the enigmatic object, IRAS 19312+1950, we could not clearly figure out its nature. To properly explain the unusual phenomena of SiO and H2O masers, it is essential to establish the relative locations and spatial distributions of two masers using VLBI technique. We also include the 1.2 – 160 μm spectral energy distribution using photometric data from the following surveys: 2MASS, WISE, MSX, IRAS, and AKARI (IRC and FIS). In addition, from the IRAS LRS spectra, we found that the depth of silicate absorption features shows significant variations depending on the evolutionary sequence, associated with the termination of AGB phase mass-loss.

Various methods for the detection of E. coli O157:H7 in food have been developed in the past decades. However, current detection methods require specialized instruments and lengthy preparation time. In an effort to achieve a rapid and sensitive detection, we developed a radial chromatography (RC) biosensor integrated with gold nanoparticle (AuNP) conjugated with antibody for the detection of E. coli O157:H7. The immuno-AuNP binds to E. coli O157:H7 creating AuNP-E. coli O157:H7 complexes by specific antigen-antibody interaction. The AuNP-E. coli O157:H7 complexes can be identified clearly from free AuNP by RC based on their mobility on porous matrix. Thus, the AuNP complexed with target bacteria, E. coli O157:H7 could be discriminated from free AuNP by radial chromatography. The results showed that the developed RC biosensor is highly selective to E. coli O157:H7 over non-target bacteria, including Bacillus cereus, Staphylococcus aureus and Vibrio cholerae with a detection limit of 105 CFU/ml. When combined with a pre-concentration step using immunomagnetic beads, we could further enhance the detection limit down to 103 CFU/ml. In this study, we developed a novel method that is rapid, sensitive and applicable for qualitative and quantitative detection of E. coli O157:H7. The detection procedure is simple and the results can be easily determined by naked eyes, suggesting that this system is practical and can be applied to the field diagnosis in food industry for the detection of pathogenic bacteria.

Aluminum oxide (Al2O3) thin films were grown by atomic layer deposition (ALD) using a new Al metalorganic precursor, dimethyl aluminum sec-butoxide (C12H30Al2O2), and water vapor (H2O) as the reactant at deposition temperatures ranging from 150 to 300 oC. The ALD process showed typical self-limited film growth with precursor and reactant pulsing time at 250 oC; the growth rate was 0.095 nm/cycle, with no incubation cycle. This is relatively lower and more controllable than the growth rate in the typical ALD-Al2O3 process, which uses trimethyl aluminum (TMA) and shows a growth rate of 0.11 nm/ cycle. The as-deposited ALD-Al2O3 film was amorphous; X-ray diffraction and transmission electron microscopy confirmed that its amorphous state was maintained even after annealing at 1000 oC. The refractive index of the ALD-Al2O3 films ranged from 1.45 to 1.67; these values were dependent on the deposition temperature. X-ray photoelectron spectroscopy showed that the ALD-Al2O3 films deposited at 250oC were stoichiometric, with no carbon impurity. The step coverage of the ALD-Al2O3 film was perfect, at approximately 100%, at the dual trench structure, with an aspect ratio of approximately 6.3 (top opening size of 40 nm). With capacitance-voltage measurements of the Al/ALD-Al2O3/p-Si structure, the dielectric constant of the ALDAl2O3 films deposited at 250 oC was determined to be ~8.1, with a leakage current density on the order of 10−8 A/cm2 at 1 V.