현대의 방탄 장갑은 우수한 관통 저항성을 갖추어야할 뿐만 아니라 군인과 군용차량의 기동성이 확보되어야 하기 때문에 경량화가 중요한 개발 요소가 되었다. 이종 적층 평판 구조의 방탄 장갑의 방탄 성능은 동일 중량 대비 구성 재료의 배열에 따라 달라진다. 본 논 문에서는 케블라, 초고분자량 폴리에틸렌 그리고 에바 폼으로 구성된 방탄 장갑의 적층 배열에 따른 방탄 성능을 분석한다. 구성 재료 의 두께가 5mm와 6.5mm인 두 가지 경우에서 6가지 적층 배열에 대하여 7.62 × 51mm NATO 탄환의 M80 탄을 856m/s의 속도로 충돌 시키는 피탄 해석을 수행하였다. 방탄 성능을 평가하기 위해 이종 적층 평판을 관통한 발사체의 잔류 속도와 잔류 에너지를 측정하였 다. 시뮬레이션 결과를 통해 케블라, 초고분자량 폴리에틸렌, 에바 폼의 배열 순서를 갖는 적층 구조가 동일 중량에 대해 가장 우수한 방탄 성능을 가짐을 확인하였다.

The long-tailed goral (Naemorhedus caudatus) is classified as 'vulnerable' by the International Union for Conservation of Nature and has been designated an endangered species requiring conservation and management in Korea. The sex determination region of the Y (SRY) gene is a useful marker for the study of paternal lineages; however, the SRY gene of the goral has not yet been sequenced. In this study, the nucleotide sequence of the SRY gene of long-tailed gorals was determined based on the sequence of the SRY gene of goats (Capra hircus). The obtained sequences were aligned with those of other species in the Bovidae family. The long-tailed goral SRY gene comprised 720 base pairs, and its nucleotide and protein sequences were identical to those of goats, sheep (Ovis aries), and cattle (Bos taurus) by 96%, 97%, and 93%, respectively. The results of phylogenetic insights obtained from this study constitute important references for genetic diversity and pedigrees studies of male long-tailed gorals and closely related species.

최근 자기공명영상 획득을 위한 시뮬레이션 도구가 개발되어 오랜 시간이 소요되는 임상 연구를 대체할 수 있게 되었다. 이에 본 연구에서는 MRiLab 시뮬레이션을 사용하여 부가인자인 에코 시간의 변화에 따라 경사에코 펄스 시퀀스가 적용된 뇌 T2 강조 영상을 획득하여 영상의 신호 및 노이즈의 변화를 정량적으로 평가하고 경향성을 파악하고자 한다. 이를 위해 실제 MRI 장비를 기반으로 새롭게 개발된 MRiLab simulation tool을 사용하여 모든 파라미터를 같게 고정한 후 TE만을 20~95 ms범위에서 5 ms 간격으로 각각 설정하여 경사에코 펄스 시퀀스가 적용된 뇌 T2 강조 영상을 획득하였다. 획득된 영상들의 신호 및 노이즈 특성 변화를 정량적으로 평가하기 위해 신호대잡음비 및 대조대잡음비를 측정하였다. 결과적으로, TE가 증가할수록 SNR은 감소하고 CNR은 증가하는 경향을 보였다. 이는 TE가 증가할수록 관심 영역으로 설정된 뇌척 수액 신호는 일정하게 유지되는 반면 노이즈는 증가하였으며, 백그라운드로 설정된 백질의 경우 신호가 감소함과 동시에 노이즈가 증가한 것이 원인으로 분석된다. 결론적으로, 진단에 용이한 경사에코 펄스 시퀀스가 적용된 뇌 T2 강조 영상을 획득하기 위해서는 그 목적에 따라 적합한 TE를 설정하는 것이 중요함을 확인하였다.

The purpose of this study is to explore inter-grade dividing criteria of the 2015 grade group elementary English textbooks. Elementary English textbooks consist of two grade groups: the 3rd and 4th grade group and the 5th and 6th grade group. L2 Syntactic Complexity Analyzer(L2SCA) is utilized to investigate the dividing criteria of the communicative functions implemented in these textbooks. Subjects of the analysis were the listening dialogues for their structural sequencing of 3rd to 4th graders and 5th to 6th graders separately within their own grade groups. Data were processed and analyzed using SPSS 25.0 and independent sample t tests for inter-grade textbooks for 14 L2SCA statistical indices. The findings are: 6 indices out of the 14 L2SCA statistical indices turn out to be critical for dividing the 2015 grade group elementary English textbooks. The 6 indices are mean clause length, mean sentence length, mean t-unit length, mean complex noun phrasal number per phrase and per t-unit and mean number of verb phrases per t-unit. Based on the findings, it is suggested that a standardized criteria derived from these 6 indices can be provided as an inter-grade dividing criteria of the 2015 grade group elementary English textbooks.

리그닌 분해 담자균류로 알려져 있는 느타리버섯균 No.42는 망간퍼옥시데이즈(MnP) 및 락게이즈(Lac)를 생산하였으나 글루코오스-펩톤-이스트-밀기울(GPYW)배지를 이용한 정치배양조건하에서 리그닌퍼옥시데이즈(LiP)활성은 검출 되지 않았다. 한편, 동일배지에서 망간퍼옥시데이즈 활성은 11일째 80(3.6) U/flask(ml)의 최대 생산되었다. 망간퍼옥시 데이즈 분리정제는 Sepha-ros CL-6B 및 Mono-Q 컬럼순으로 수행하였으며 주요 망간퍼옥시데이즈 isozyme은 단일밴 드로 분자량은 36.4KDa이였다. N-말단으로부터 19개의 아 미노산 배열은 단백질 자동 분석 장치로 분석한 결과 ATCADGRTTANAACCVLFP를 나타내었다. 느타리버섯균 No.42의 정치배양조건 하에서 세포외로 생산되는 중요한 망간퍼옥시데이즈 isozyme의 N-말단 아미노산 배열은 이전에 보고된 MnP3의 아미노산 배열과 동일하였다.

멸구과(Delphacidae) 8종의 internal transcribed spacer 2 (ITS2) DNA 염기서열로 종간 차이 추정값을 비교하고 분자계통수를 추론하였다. ITS2 DNA 염기서열 길이는 종(species)마다 550 bp (흰등멸구)에서 699 bp (겨풀멸구)까지 차이를 보였다. 같은 Nilaparvata 속의 겨풀멸구와 벼멸구붙이 사이 의 염기서열 차이 추정값(d ± S.E.)은 0.001 ± 0.001로 가장 낮았으며, 사슴멸구와 일본멸구 사이는 0.579 ± 0.021로 가장 높았다. 벼멸구와 다른 멸구류들 과의 종간 염기서열 차이 추정값은 0.056 ± 0.008 (겨풀멸구)에서부터 0.548 ± 0.021 (일본멸구)로 구분되었다. 반면, Neighbor-joining 방법으로 추론된 분자계통수에서는 겨풀멸구와 벼멸구붙이를 제외하고 나머지 멸구류들은 독립된 다른 그룹으로 분지되었다. 벼멸구의 ITS2 염기서열을 참고하여 벼멸구 특이 고리매개등온증폭(loop-mediated isothermal amplification, LAMP) 프라이머 4 세트(BPH-38, BPH-38-1, BPH-207 및 BPH-92)를 제작하였다. 이들 각각을 벼멸구, 흰등멸구 및 애멸구의 게놈 DNA와 65°C에서 60분간 반응시켰을 때, 벼멸구 시료에서만 증폭 산물들이 관찰되었다. BPH-92 LAMP 프라이머 세트로 65°C에서 벼멸구 DNA의 양(0.1 ng, 1 ng, 10 ng, 100 ng)과 반응시간(20분, 30분, 40분, 60분)을 달리하여 형광반응을 관찰하였을 때, 20분과 30분 반응에서는 100 ng 까지에서도 발광여부 구별이 어려웠다. 그러나 40분 반응에서는 10 ng 이상에서, 60분 반응에서는 0.1 ng 이상에서 발광여 부가 명확히 구별되었다.

Through data mining of the Cordyceps militaris genome, a lectin-encoding gene, CMLec3, was identified. In this study, the CMLec3 sequence was analyzed using bioinformatics approaches, and the gene was heterologously expressed in Escherichia coli BL21 cells. The biological activity of the product was examined. In addition, CMLec3 gene expression levels were assessed. The results showed that the CMLec3 protein contained a lectin domain structure and was successfully expressed. The CMLec3 protein partly inhibited HeLa cell proliferation. CMLec3 exhibited the highest gene expression in the primordium at a level 5.19 times that of the mycelium and 1.35 times that of the fruiting body. This suggests that the gene may be related to fruiting body development.

Occurrence spontaneous mushrooms in eastern Jeju Muryeongarioreum, Sillyecheon-Iseungak, Kyoraegotjawal, Geomunoreum were examined in 2016. The collected mushrooms were classified by 15 order 56 family 149 genera 317 species. Among the collected mushrooms, 87 species of mushrooms were successfully incubated in mushroom complete medium in which DNA of 25 species were completely extracted and amplified using universal primers ITS1 (5’-CTTG GTCA TTTA GAGG AAGT AA-3’) and ITS4 (5’-TCCT CCGC TTAT TGAT ATGC-3’). Four species of them were differently identified between the classification by morphological observation and by analysis of DNA sequences i.e. by morphological identification Ganoderma applanatum, Armillaria gallica, Macrolepiota procera and Trametes gibbosa were identified as G. gibbosum, A. cepistipes, M. detersa and T. elegans by analysis of DNA sequences, respectively. Based on these results both identification ways might be necessary for correct classification of mushrooms. On the other hand, among the collected 317 mushrooms, 48 species could be identified to genus but not to species by the morphological observations. However, by the analysis of DNA sequences, 15 species were identified to species in which 6 species were unregistered mushrooms in Korea. Therefore, the analysis of DNA sequence may be useful to identify the mushrooms which are difficult to recognize by morphological observation.

A. bisporus is the fifth most cultivated mushroom in Korea, and approximately 10,757 tons were cultivated in 2015. The genetic diversity of collected strains in Korea and commercial cultivars was analyzed using inter-simple sequence repeat (ISSR) markers. ISSR markers known to be comparable among A. bisporus spp. were selected from various markers. Totally, 16 markers, namely the ISSR markers 807, 808, 810, 811, 834, 835, 836, 841, 842, P3, P8, P17, P22, P30, P38, and P39, were evaluated to discriminate between ASI 1110, 1114, 1115, 1238, 1246, 1365, 1366, and 1369 for selecting suitable markers in 16 markers. The ISSR markers P31, P38 and P39 exhibited various fingerprints that could help classify the strains in species. Using the three markers, genetic relationships among 39 strains, including commercial cultivars, such as SaeA and SaeYeon, were analyzed using the UPGMA method. The results of the analysis of the genetic relationships between commercial cultivars and collected strains in Korea confirmed that the commercial cultivars were different from the collected strains in Korea. These results suggested that the ISSR markers P31, P38, and P30 could be used for selecting the commercial cultivars of A. bisporus.

The JpL species is one of the 31 species belonging to the Bemisia tabaci complex and is distributed in two countries, Korea and Japan. To clarify genetic relationships among different populations of the JpL species in Korea, 83 cytochrome oxidase subunit I (COI) sequences generated from 83 individuals collected from eight Korean provinces were analyzed together with published 16 Korean COI sequences. A total of eight haplotypes were detected from the 99 COI sequences, and 82 COI sequences shared one haplotype, hap-2. The remaining 17 COI sequences were assigned to seven haplotypes, hap-1, 3, 4, 5, 6, 7, and 8. The median-joining networks of the eight haplotypes revealed that the Korean JpL species has undergone genetic variations separately according to two groups, Korean Peninsula and Jeju Island. In addition, the phylogenetic trees constructed based on the 99 COI sequences and published seven Japanese COI sequences were divided into two clades: clade(A) consisted of 97 COI sequences from the Korean Peninsula group, and clade(B) consisted of 19 COI sequences from the Jeju Island and Japan groups. Our study suggests that the Korean populations of the JpL species might have spread and be undergoing genetic variations separately according to the two groups, Korean Peninsula and Jeju Island.

Twenty Inter simple sequence repeat (ISSR) and 30 SSR primers were used to assess genetic diversity of 64 Agaricus strains including 45 A. bisporus strains and other 19 Agaricus spp. Of them, four ISSR primers, (GA)₈T, (AG)₈YC, (GA)₈C and (CTC)₆and seven SSR markers produced PCR polymorphic bands between the Agaricus species or within A. bisporus strains. PCR polymorphic bands were inputted for UPGMA cluster analysis. Forty five strains of A. bisporus are genetically clustered into 6 groups, showing coefficient similarity from 0.75 to 0.9 among them. The varieties, Saea, saedo, Saejeong and Saeyeon that have recently been developed in Korea were involved in the same group with closely genetic relationship of coefficient similarity over 0.96, whereas, other strains were genetically related to A. bisporus strains that were introduced from USA, Eroupe and Chinese.

Phospholipase A2 (PLA2) catalyzes an ester hydrolysis at sn-2 position of phospholipids. Various PLA2 genes are classified into at least 15 groups. However, on the basis of physiological functions, PLA2 genes are classified into calcium dependent cellular PLA2 (cPLA2), calcium independent cellular PLA2 (iPLA2) and secretary PLA2 (sPLA2). In insects, several sPLA2 genes are known to be associated with venom or immune functions. However, no known cellular PLA2 genes are identified. This study reports an iPLA2 (SeiPLA2) encoded in Spodoptera exigua. SeiPLA2 has an open reading frame of 2448 bp encoding a sequence of 816 amino acid residues. Its predicted protein is 89.55 KDa and 6.15 pI. SeiPLA2 is expressed in egg, larva, pupa and adult stages. In larval stage, SeiPLA2 is expressed in hemocytes, fat body, epidermis, gut, malpighian tubules and salivary gland. To understand its physiological function, its RNA interference is under investigation.