The present study aimed to analyze the metaproteome of the microbial community comprising harmful algal bloom (HAB) in the Daechung reservoir, Korea. HAB samples located at GPS coordinates of 36°29’N latitude and 127°28’E longitude were harvested in October 2013. Microscopic observation of the HAB samples revealed red signals that were presumably caused by the autofluorescence of chlorophyll and phycocyanin in viable cyanobacteria. Metaproteomic analysis was performed by a gelbased shotgun proteomic method. Protein identification was conducted through a two-step analysis including a forward search strategy (FSS) (random search with the National Center for Biotechnology Information (NCBI), Cyanobase, and Phytozome), and a subsequent reverse search strategy (RSS) (additional Cyanobase search with a decoy database). The total number of proteins identified by the two-step analysis (FSS and RSS) was 1.8-fold higher than that by one-step analysis (FSS only). A total of 194 proteins were assigned to 12 cyanobacterial species (99 mol%) and one green algae species (1 mol%). Among the species identified, the toxic microcystin-producing Microcystis aeruginosa NIES-843 (62.3%) species was the most dominant. The largest functional category was proteins belonging to the energy category (39%), followed by metabolism (15%), and translation (12%). This study will be a good reference for monitoring ecological variations at the meta-protein level of aquatic microalgae for understanding HAB.

포인세티아(Euphorbia pulcherrima Willd. Ex Klotzch) ‘Flame’ 은 국립원예특작과학원에서 2015년에 육성한 품종이다. ‘Flame’ 은 단일감응기간이 짧은 적색 포엽의 깊은 열편을 가진 ‘Eckalba’ 와 밝은 적색의 포엽을 가진 국내 육성 품종 ‘Candle Light’를 2013년에 교배하여 획득한 실생 계통을 선발 육성하였다. 2014 년부터 2015년까지 생육 및 개화 특성, 균일성에 대하여 1, 2차 특성검정을 실시하였으며, 2015년에 3차 특성검정을 실시하여 최종선발한 후 직무육성품종심의회에 상정하여 ‘Flame’으로 명명하였다. ‘Flame’ 품종의 포엽은 밝은 적색을 띠며 열편이 깊다. 초장과 초폭은 중간이나 적심하지 않아도 많은 분지가 발생하여 풍성한 수형을 이룬다. 단일처리후 약 7.5주가 경과하면 완전히 착색되어 출하가 가능하다. 이 품종은 2018년 1월 24일에 국립 종자원에 품종등록(등록번호 6921호)되었다.

본 실험은 장미의 삽목시 증산억제제와 생장억제제를 활용 하여 미스트나 밀폐시설 없이 삽목발근 효율을 증가시킬 목적으로 수행하였다. 절화장미 ‘M-Red’ 줄기 삽목 후 증산억제제 ‘Wilt Pruf’ 및 ‘Cloud Cover’ 1, 2, 4, 8%와 생장억제제 paclobutrazole 10, 20, 40, 80mg･L-1, diniconazole 100, 200, 400, 800mg･L-1를 각각 엽면살포 하였다. 증산억제제의 효과 는 종류에 따라 달랐는데, Wilt Pruf는 생존율, 신초 발생율, 발근율을 모두 향상시켰으나 신초수, 뿌리수, 뿌리길이에는 영향을 미치지 않았다. Cloud Cover는 생존율과 발근율을 향상시키는 효과가 없었으나 신초 발생율이 처리농도와 비례하여 높아져 4, 8% 처리시 가장 높게 나타났다. 생장억제제 처리효과도 종류에 따라 달라 paclobutrazol은 생존율과 발근율 향상에 영향을 미치지 않았으나 신초 발생율을 높였으며 1% 처리시에 신초발생이 가장 높았다가 농도가 높아지면서 낮아졌다. Diniconazole은 100, 200mg･L-1 처리시 생존율과 발근율을 향상시켰으나 800mg･L-1의 고농도에서는 생존율과 발근율 모두 낮게 나타났다.

본 연구는 제비꽃과 남산제비꽃 종자의 종자휴면을 구명하고 종자 저장에 따른 발아 특성을 알아보는 것을 목표로 하고 있다. 먼저 장기 저장 종자를 대상으로 다양한 배양 온도, 저온층적처리, GA3처리를 수행하였다. 휴면의 유무를 판단하기 위해 종자를 25/15, 20/10, 15/6°C 온도에서 배양하였고 제비 꽃 종자의 최종 발아율이 각각 86, 66, 66%으로 나타났다. 이는 제비꽃 종자에 휴면이 없는 것으로 여겨진다. 남산제비꽃은 최종 발아율이 50% 이하이며, 4주 이내에 거의 발아를 하지 않아 생리적휴면이 있다고 판단된다. 남산제비꽃 종자에 GA3 1000mg･L-1를 처리했을 때 최종 발아율이 100%로 나타났다. 또한 저온층적처리 실험 결과 남산제비꽃 종자가 저온 층적처리 기간이 증가할수록 최종발아율도 증가하였다. 앞의 실험은 장기 저장이 되었던 종자를 사용한 것이며 채종 직후의 제비꽃, 남산제비꽃의 발아양상도 살펴보았다. 제비꽃은 25/15°C에서 1주 만에 모두 발아를 하여 종자 휴면이 없는 것을 다시 확인하였다. 장기 저장 종자에 비해 평균발아일수가 줄어들고 발아속도가 증가하여 제비꽃 종자는 장기 저장 중에 종자의 활력이 감소됨을 알 수 있었다. 바로 채종한 남산제비 꽃 종자도 4주만에 발아가 거의 이루어지지 않고 저온층적처리를 통해 발아율이 향상 되는 것으로 보아 생리적휴면을 가지고 있다고 재확인되었다. 따라서 제비꽃과 남산제비꽃은 장기 저장에 따라 종자의 휴면 유형은 변하지 않지만 종자 활력 에 따라서 최종발아율, 평균 발아일수, 발아속도, 발아균일도가 달라질 수 있다.

Cryopreservation is used for blastocyst preservation of most mammalian embryos and is an important technique for breeding. We aimed to compare the efficiency of the cryopreservation method using the standard Cryotop device and the ReproCarrier device, a domestic product manufactured in Korea. The efficacy of the two devices was analyzed based on the survival rate, intracellular levels of reactive oxygen species (ROS), and apoptosis of the vitrified bovine blastocysts. The survival rates of the vitrified-warmed blastocysts were similar between the ReproCarrier group (58.4 ± 17.7%) and Cryotop group (59.9 ± 14.1%). Intracellular ROS levels and apoptotic index were determined by DCFDA staining and TUNEL assay. Changes in intracellular ROS levels, number of total nuclei, and cellular apoptosis of vitrified blastocysts after cryopreservation were not significantly different between the two groups. These results indicate that the ReproCarrier device method is as effective as the standard Cryotop method for vitrification of bovine blastocysts in vitro.

Radioisotope ADME (RI-ADME) studies are enabling visualization of the biodistribution in molecular imaging. We applied RI-ADME to investigate the tumor targeting capacity and biodistribution of trastuzumab-monomethyl auristatin F (LCB14-0110) in JIMT-1 xenograft mice and healthy marmoset. The LCB14-0110 was labelled with 125I. 125I-LCB14-0110 was intravenously administered to the animals. The gamma-count and single-photon emission computed tomography/computed tomography (SPECT/CT) was conducted for biodistributioon and bioimaging of the biopharmaceutics. Tumor uptake in xenograft mice was highest at three-day after 125I-LCB14-0110 administration in both the biodistribution and SPECT/CT bioimaging. Alternatively, blood and organ tissues showed gradual decrease in radioactivity over time. In marmosets, radioactivity in all organ tissues rapidly reduced and no specific targeting of organs was observed in the biodistribution study and SPECT/CT imaging. Hence, 125ILCB14- 0110 demonstrated effective tumor targeting capacity and accumulated in JIMT-1 cell-bearing mice. However, accumulation did not occur in the organs of xenograft mice. Additionally, marmosets showed rapidly decrease in radioactivity throughout the entire body without accumulation in the normal organs. We also confirmed that the drug distribution was similar in normal organs between the two experimental animal species except spleen. Therefore, 125I is expected to be a useful tool in the study of RI-ADME in biopharmaceuticals through minimal antibody modification.

After the permanent shutdown of K1 in 2017, decommissioning processes have attracted great attention. According to the current decommissioning roadmap, the dismantling of the activated components of K1 may start in 2026, following the removal of its spent fuel. Since the reactor vessel (RV) and reactor vessel internal (RVI) of K1 contain massive components and are relatively highly activated, their decommissioning process should be conducted carefully in terms of radiological and industrial safety. For achieving maximum efficiency of nuclear waste management processes for K1, we present activation analysis of the segmentation process and waste classification of the RV and RVI components of K1. For RVI, the active fuel regions and some parts of the upper and lower active regions are classified as intermediate-level waste (ILW), while other components are classified as low-level waste (LLW). Due to the RVI’s complex structure and high activation, we suggest various underwater segmentation techniques which are expected to reduce radiation exposure and generate approximately nine ILW and nineteen very low level waste (VLLW)/LLW packages. For RV, the active fuel region and other components are classified as LLW, VLLW, and clearance waste (CW). In this case, we suggest in-situ remote segmentation in air, which is expected to generate approximately forty-two VLLW/LLW packages.

Interferon tau (IFNT) regulation, an anti-luteolytic factor produced by conceptuses of the ruminant ungulates, is essential for the maintenance of early pregnancy, but a definitive mechanism for its temporal transcription has not been elucidated. We and others have observed the T-box protein eomesodermin (EOMES) exhibited high mRNA expression in the ovine embryonic trophectoderm; thus, both caudal-relatedhomeobox-2 (CDX2) and EOMES coexist during the early stages of conceptus development. Objective of this study was to examine the effect of EOMES on ovine IFNT gene transcription when evaluated with CDX2, ETS2 and AP1 transcription factors implicated in the control of cell differentiation in the trophectoderm. In this study, quantitatively via reverse transcription-polymerase chain reaction (RT-PCR) analysis between ovine trophoblast cells was initially performed, finding that transcription factors CDX2 and ‘EOMES transcription factor mRNAs’ were specific to trophectoderm cells. These mRNAs were also found in days 15, 17, and 21 ovine conceptuses. Furthermore, human choriocarcinoma JEG3 cells (trophoblast cell line) were cotransfected with an ovine IFNT (-654bp)-luciferase reporter (-654-oIFNT-Luc) construct and several transcription factor expression plasmids. Cotransfection of the reporter construct with CDX2, ETS2 and AP1 increased transcription of -654-oIFNT-Luc by about 11-fold compared with transfection of the construct alone. When cells were initially transfected with EOMES followed by transfection with CDX2, ETS2 and/or AP1, the expression of -654-oIFNT-Luc was decreased. Also, EOMES factor inhibited the stimulatory activity of CDX2 alone. These results suggest that when conceptuses attach to the uterine epithelium, ovine IFNT gene transcription is down-regulated by an increase of EOMES factor expression in the attached ovine trophoblast cells.

Clear cell odontogenic carcinoma (CCOC), a very rare neoplasm located mostly in the mandible, has been regarded as a benign tumor. However, due to the accumulation of case reports, CCOC has been reclassified as a malignant entity by the World Health Organization. Patients with CCOC present with regional swelling and periodontal indications with variable pain, often remaining misdiagnosed for a long period. CCOC has slow growth but aggressive behavior, requiring radical resection. Histologic analysis revealed the monophasic, biphasic, and ameloblastic types of CCOC with clear cells and a mixed combination of polygonal and palisading cells. At the molecular level, CCOC shows the expression of cytokeratin and epithelial membrane antigen, along with markers that assign CCOC to the sarcoma family. At the genetic level, Ewing sarcoma breakpoint region 1-activating transcription factor 1 fusion is regarded as the key feature for identification. Nevertheless, the scarcity of cases and dependence on histological data delay the development of an efficient therapy. Regarding the high recurrence rate and the potential of distant metastasis, further characterization of CCOC is necessary for an early and accurate diagnosis.

The purpose of this study was to evaluate the effect of addition of ethylene glycol, glycerol and sucrose to TCG (Tris, Citric Acid, Glucose, Egg Yolk) and DMSO Frozen. The extender containing Egg yolk concentration (10%, 20%) affects viability and acrosome morphology of rabbit sperm. Sperm viability was then assessed for the freezing extenders TCGD (Tris + Citricacid + Glucose + DMSO), TCGED (Tris + Citricacid + Glucose + Egg yolk + DMSO), TCGGD (Tris + Citricacid + Glucose + Glycerol + DMSO) and TCGSD Tris + Citricacid + Glucose + Sucrose + DMSO) during thawing at 38oC. for 20 seconds, respectively. TCG + 10% egg yolk (viability: 77.0 ± 0.8, NAI: 73.3 ± 0.9) was significantly (sperm viability and normal acrosome interaction (NAI)) higher than TCG + 20% egg yolk (70.7 ± 1.1, 70.0 ± 0.9) in the sperm normalcy analysis according to the yolk concentration. TCGGD (53.4 ± 0.1, 62.3 ± 0.4), TCGSD (61.3 ± 0.0, 67.1 ± 0.1) sperm viability and normal acrosome interaction (NAI) in frozen spermatozoa are TCGD (46.4 ± 2.8 and 56.3 ± 1. 4) and TCGED (23.0 ± 1.1 and 54.6 ± 1.4) extenders was thawed at 38oC for 20 seconds. According to the results from each frozen bulking agent, sperm membrane integrity by hypotonic swelling test (HOST) analysis in TCGGD (59.8 ± 0.7), TCGSD (59.3 ± 0.5) was significantly high compared to other experimental groups (p < 0.05). In conclusion, these results suggested that TCGGD and TCGSD extenders enhance survivability of rabbit sperm after frozen-thawing.