• 제목/요약/키워드: NADH dehydrogenase subunit

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캐비어를 생산하는 철갑상어의 신속 종판별을 위한 SNP 기반 KASP 분석에 관한 연구 (A Study on KASP Analysis Based on SNP to Rapidly Identify Caviar-Producing Sturgeon Species)

  • 이선희;박보름;김형일;조수열;손경훈
    • 한국식품위생안전성학회지
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    • 제39권3호
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    • pp.209-220
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    • 2024
  • 캐비어에 대한 수요가 증가하면서 캐비어 종류의 진위여부를 확인 할 수 있는 분석법 마련이 필요해졌다. 본 연구에서는 캐비어 종류을 나누는 철갑상어 종 특이 KASP 마커를 개발하였고 모니터링을 통해 국내 유통중인 불법 캐비어 제품을 확인하고자 하였다. 본 연구에서는 16S ribosomal RNA gene, cytochrome b gene, cytochrome coxidase subunit I gene, cytochrome c oxidase subunit II gene, NADH dehydrogenase subunit 5 gene에서 철갑상어종 특이적인 SNP를 선정하고 이를 표적하는 KASP 마커 11종을 개발하였다. 개발한 KASP 마커를 이용하여 한국의 온라인 마켓에서 유통중인 캐비어 10종을 모니터링 분석한 결과 2개의 제품에서 제품에 표기된 철갑상어 종과 다른 것으로 확인하였으며 두 제품 모두 실제보다 더 비싼 캐비어로 둔갑하여 판매한 것으로 확인되었다. 본 연구를 통해 제작한 KASP 분석방법으로 유통되는 캐비어 종류 분류가 가능하였고 모니터링을 통해 국내 유통되고 있는 불법 캐비어 제품도 확인하였다. 이에 따라 본 연구에서 개발한 SNP기반 KASP 분석법으로 불법 캐비어 제품 유통 근절에 기여 할 수 있을 것으로 기대한다.

COG pathways에서 원핵생물 1,309종의 대사경로 (Metabolic Pathways of 1309 Prokaryotic Species in Relation to COGs)

  • 이동근;김주희;이상현
    • 생명과학회지
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    • 제32권3호
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    • pp.249-255
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    • 2022
  • 대사는 생존과 번식에 필수적이다. 2020년에 업그레이드된 COG (cluster of orthologous proteins) 데이터베이스에는 "pathways" 항목이 있다. 본 연구에서는 COG pathways를 이용하여 1,309개의 원핵생물의 대사 경로를 분석하였다. 63개의 대사경로와 관련된 822개의 COG가 있었고, 각 분류단위의 대사관련 COG의 평균은 200.50개(phylum Mollicutes)에서 527.07개(phylum Cyanobacteria)의 사이였다. MPCR을 대사경로구성율(하나의 게놈에 존재하는 COG 수 / 각 대사 경로를 구성하는 COG의 총 수)로 정의하였다. MPCR이 100%인 대사경로의 수는 원핵생물에 따라 0에서 26의 범위였다. 다수의 원핵생물에서 100% MPCR인 대사경로는 세포벽 합성과 관련된 murein biosynthesis (922종), glycine cleavage (918종), ribosome 30S subunits (903종) 등이었다. MPCR이 0%인 대사경로(종의 수)는 photosystem I (1,263종), A/V (archaea/vacuolar)-type ATP synthase (1,028종) 및 Na+-translocation NADH dehydrogenase (976종) 등이었다. 원핵생물에 따라 3~49개의 대사경로를 전혀 수행할 수 없었다. MPCR의 보존성이 높은 대사경로의 순서는 ribosome 30S subunit (1,309종의 96.1%), murein biosynthesis (86.8%), arginine biosynthesis (80.4%), serine biosynthesis (80.3%) 및 aminoacyl-tRNA synthetases (82.2%) 등이었다. 단백질과 세포벽 합성이 원핵생물에서 중요한 대사경로인 것을 알 수 있었다. 본 연구의 결과와 원핵생물 사이의 대사경로와 관련된 COG는 항생제 및 인공세포의 개발 등에 활용될 수 있을 것이다.

Molecular Identification of Diphyllobothrium nihonkaiense from 3 Human Cases in Heilongjiang Province with a Brief Literature Review in China

  • Zhang, Weizhe;Che, Fei;Tian, Song;Shu, Jing;Zhang, Xiaoli
    • Parasites, Hosts and Diseases
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    • 제53권6호
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    • pp.683-688
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    • 2015
  • Human diphyllobothriasis is a widespread fish-borne zoonosis caused by the infection with broad tapeworms belonging to the genus Diphyllobothrium. In mainland China, so far 20 human cases of Diphyllobothrium infections have been reported, and the etiologic species were identified as D. latum and D. nihonkaiense based on morphological characteristics or molecular analysis. In the present study, proglottids of diphyllobothriid tapeworms from 3 human cases that occurred in Heilongjiang Province, China were identified as D. nihonkaiense by sequencing mitochondrial cytochrome c oxidase subunit I (cox1) and NADH dehydrogenase subunit 5 (nad5) genes. Two different cox1 gene sequences were obtained. One sequence showed 100% homology with those from humans in Japan. The remaining cox1 gene sequence and 2 different nad5 gene sequences obtained were not described previously, and might reflect endemic genetic characterizations. D. nihonkaiense might also be a major causative species of human diphyllobothriasis in China. Meanwhile, the finding of the first pediatric case of D. nihonkaiense infection in China suggests that infants infected with D. nihonkaiense should not be ignored.

Infection by a Filarial Nematode from the Family Onchocercidae in the Wild Bird Anas falcata

  • Kim, Young Ji;Jang, Jin Ho;Kim, Min Chan;Park, Young-Seok;Kim, Hye Kwon
    • Proceedings of the National Institute of Ecology of the Republic of Korea
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    • 제3권4호
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    • pp.221-226
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    • 2022
  • A filarial nematode was found in a blood sample of an Anas falcata individual collected in South Korea in 2018. Phylogenetic analysis based on partial cytochrome C oxidase subunit I (COI) sequences placed the nematode as a novel genus of the family Onchocercidae and as closely related to Mansonella species, Chandlerella quiscali, and filarial nematodes recently reported in avian species. However, different phylogenetic relationship was observed in the NADH dehydrogenase subunit 5 and 12S rRNA-based phylogenetic trees, which might indicate the filarial nematode found in this study was not defined to belong to the known specific genera of the family Onchocercidae. The screening of 105 additional avian blood samples retrieved only one 12S rRNA-targeting polymerase chain reaction (PCR)-positive sample, which indicates that filarial nematode infection is rare in wild birds or that it occurs below the detection limit of PCR in blood samples. Nevertheless, considering the recent findings about ancient interactions between birds and human pathogenic filarial nematodes and their pathogenic potential in several avian species, additional exploration of novel filarial nematodes in wild birds remains necessary.

Isolation and Properties of Cytoplasmic α-Glycerol 3-Phosphate Dehydrogenase from the Pectoral Muscle of the Fruit Bat, Eidolon helvum

  • Agboola, Femi Kayode;Thomson, Alan;Afolayan, Adeyinka
    • BMB Reports
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    • 제36권2호
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    • pp.159-166
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    • 2003
  • Cytoplasmic $\alpha$-glycerol-3-phosphate dehydrogenase from fruit-bat-breast muscle was purified by ion-exchange and affinity chromatography. The specific activity of the purified enzyme was approximately 120 units/mg of protein. The apparent molecular weight of the native enzyme, as determined by gel filtration on Sephadex G-100 was $59,500{\pm}650$ daltons; its subunit size was estimated to be $35,700{\pm}140$ by SDS-polyacrylamide gel electrophoresis. The true Michaelis-Menten constants for all substrates at pH 7.5 were $3.9{\pm}0.7\;mM$, $0.65{\pm}0.05\;mM$, $0.26{\pm}0.06\;mM$, and $0.005{\pm}0.0004\;mM$ for L-glycerol-3-phosphate, $NAD^+$, DHAP, and NADH, respectively. The true Michaelis-Menten constants at pH 10.0 were $2.30{\pm}0.21\;mM$ and $0.20{\pm}0.01\;mM$ for L-glycerol-3-phosphate and $NAD^+$, respectively. The turnover number, $k_{cat}$, of the forward reaction was $1.9{\pm}0.2{\times}10^4\;s^{-1}$. The treatment of the enzyme with 5,5'-dithiobis-2-nitrobenzoic acid (DTNB) under denaturing conditions indicated that there were a total of eight cysteine residues, while only two of these residues were reactive towards DTNB in the native enzyme. The overall results of the in vitro experiments suggest that $\alpha$-glycerol-3-phosphate dehydrogenase of the fruit bat preferentially catalyses the reduction of dihydroxyacetone phosphate to glycerol-3-phosphate.

제주도 큰발윗수염박쥐(Myotis macrodactylus)의 유전적 집단 구조와 계통 유연관계 (Genetic Population Structure and Phylogenetic Relationship of the Large-footed Bat (Myotis macrodactylus) on Jeju Island)

  • 김유경;박수곤;한상훈;한상현;오홍식
    • 생명과학회지
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    • 제26권7호
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    • pp.749-757
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    • 2016
  • 본 연구는 미토콘드리아 DNA (mtDNA) cytochrome B (CYTB)와 NADH dehydrogenase subunit 1 (ND1) 유전자 서열의 다형성을 근거로 제주도 큰발윗수염박쥐 집단의 유전적 집단 구조와 계통 유연관계를 조사하는 데 목적이 있다. 동아시아 박쥐에서 CYTB 유전자 haplotype은 14개의 haplotype들이 발견되었고, ND1은 9개의 haplotype 들이 발견되었다. 집단별 haplotype의 분포는 지역-특이적인 양상을 보였다. ND1 haplotype 분석결과에서 제주도 집단은 4개의 haplotype을 나타내고, 한라산 소집단과 서부지역 소집단은 3개 haplotype을 나타내었으나, 동부지역 소집단에서는 제주도 전체에서 공통으로 발견되는 1개(Nd03)의 haplotype만 출현하였다. NJ tree에서 제주도 집단은 강원도 집단보다 일본 집단과 더 근연으로 확인되었다. 중국과 일본의 모계선조 계보 사이의 분화 시점은 0.789±0.063 MYBP으로 추정되었고, 제주도와 일본의 모계선조는 약 17만 년(0.168±0.013 MYBP) 전에 분리된 것 으로 판단된다. 제주도 집단은 적어도 5만 년 이전에 이주한 것으로 보인다. 또한 ND1 haplotype 분석결과는 제주도 집단이 이주 후에도 지역 내에서의 적어도 2회 이상의 유전적 분화를 겪었다는 것을 보여주고 있다. 본 연구 결과는 동아시아 큰발윗수염박쥐의 계통 유연관계를 이해하는 데 중요한 기초자료가 될 것이며, 향후 한반도의 남부와 중국, 러시아 등에서 시료 확보를 통해 집단 간 진화적 상관관계를 이해하는 데 필요한 설득력 있는 자료가 마련되어야 할 것이다.

Relationship between Endurance Performance and Genetic Polymorphisms of Mitochondrial DNA in Korean Male Elite Athletes

  • Jang Dai-Ho;Kang Byung-Yong;Jung In-Geun;Oh Sang-Duk;Lee Kang-Oh
    • 대한의생명과학회지
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    • 제11권2호
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    • pp.227-235
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    • 2005
  • It has been reported that endurance performance is influenced by various environmental and genetic factors. In view of an important role of human mitochondrial DNA (mtDNA) as a candidate for endurance performance, this study focused on the relationships between $VO_{2max}$ value as a measure of endurance performance or other associated phenotypes and four mtDNA restriction fragment length polymorphisms (RFLPs) (Bam HI, Hinc II1, Hinc II2 and Nci I) in the NADH dehydrogenase subunit 5 and one (Kpn I) in the D-loop region of mtDNA. MtDNA was purified from buffy coat in human peripheral blood, and PCR-RFLP analysis was performed to estimate the allele frequencies of each polymorphism in the mtDNA. There were no significant differences in allele distributions of all polymorphisms studied between male athletes and controls, respectively (P>0.05). However, the Kpn I polymorphism was significantly associated with diastolic blood pressure level in male athletes, respectively (P<0.05). Therefore, our results suggest that this polymorphism might be one of the factors modifying inter-individual difference in cardiovascular risk. Further studies using larger sample size will be required to generalize these results from the study described herein.

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Genetic Differentiation among the Mitochondrial ND2 Gene and $tRNA^{Trp}$ Gene Sequences of Genus Rana (Anura) in Korea

  • Lee, Hyuk;Yang, Suh-Yung;Lee, Hei-Yung
    • Animal cells and systems
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    • 제4권1호
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    • pp.31-37
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    • 2000
  • The genetic variations among six species of Rana from Korea (R. nigro-maculata, R. piancyi, R. dybowskii, R. sp, R. rugosa type A, B and R. amurensis) were investigated using 499 bases of mitochondrial DNA sequences for ND2 (NADH dehydrogenase subunit 2) gene and $tRNA^{Trp}$ gene. Partial sequences of ND2 gene (427 bp) and full sequences of $tRNA^{Trp}$ gene (73 bp) were identified. The level of sequence divergences ranged from 0.2 to 5.2% within species and 4.9-28.0% among 6 species of the genus Rana. The $tRNA^{Trp}$ gene of the genus Rana was composed of 77 nucleotides which showed a two dimensional "cloverleaf" structure. The secondary structure of $tRNA^{Trp}$ was not found compensatory changes which could potentially confound phylogenetic inference. In the neighborjoining tree, brown frogs were clustered first with the level of sequence divergence of 13.20% between R. amurensis and R. dybowskii, and 9% between R. dybowskii and R. sp. supported by 99% bootstrap iterations, respectively. R. nigromaculata and R. plancyi were clustered into another group with 5.1% divergence supported by 100% bootstrap iteration. R. rugosa A 8nd B types were grouped by 4.9% divergence and clustered into the last group with other two groups with 100% bootstrap iterations.

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Analysis of genetic differentiation and population structure of the Korean-peninsula-endemic genus, Semisulcospira, using mitochondrial markers

  • Eun-Mi Kim;Yeon Jung Park;Hye Min Lee;Eun Soo Noh;Jung-Ha Kang;Bo-Hye Nam;Young-Ok Kim;Tae-Jin Choi
    • Fisheries and Aquatic Sciences
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    • 제25권12호
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    • pp.601-618
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    • 2022
  • The genus Semisulcospira is an economically and ecologically valuable freshwater resource. Among the species, Semisulcospira coreana, Semisulcospira forticosta and Semisulcospira tegulata are endemic to the Korean peninsula and Semisulcospira gottschei is widespread in Asia. Therefore, maintenance and conservation of wild populations of these snails are important. We investigated the genetic diversity and population structure of Semisulcospira based on the mitochondrial cytochrome c oxidase subunit I (COI), NADH dehydrogenase subunit 4 (ND4), and combined mitochondrial DNA (COI + ND4) sequences. All four species and various genetic makers showed a high level of haplotype diversity and a low level of nucleotide diversity. In addition, Fu's Fs and Tajima's D neutrality tests were performed to assess the variation in size among populations. Neutrality tests of the four species yielded negative Fu's Fs and Tajima's D values, except for populations with one haplotype. The minimum spanning network indicated a common haplotype for populations of S. coreana, S. tegulata and S. gottschei, whereas S. forticosta had a rare haplotype. Also, genetic differences and gene flows between populations were assessed by analysis of molecular variance and using the pairwise fixation index. Our findings provided insight into the degree of preservation of the species' genetic diversity and could be utilized to enhance the management of endemic species.

Molecular Authentication of Morus Folium Using Mitochondrial nad7 Intron 2 Region

  • Jin, Chi-Gyu;Kim, Min-Kyeung;Kim, Jin-Young;Sun, Myung-Suk;Kwon, Woo-Saeng;Yang, Deok-Chun
    • 한국자원식물학회지
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    • 제26권3호
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    • pp.397-402
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    • 2013
  • Morus Folium (Sang-yeop in Korean) is one of the most important Oriental medicinal plants. In Korea, both M. alba and M. cathayana are regarded as the botanical sources for Morus Folium. In order to discriminate M. alba and M. cathayana from their adulterant, M. tricuspidata, mitochondrial NADH dehydrogenase subunit 7 (nad7) intron 2 region was targeted for molecular analysis with universal primers. DNA polymorphisms, including SNP sites, insertions, and deletions, were detected among these three species sequencing data. Based on these DNA polymorphisms, specific primers were designed for the three species respectively. Multiplex PCR was conducted for molecular authentication of M. alba, M. cathayana, and M. tricuspidata with specific primers. The present results indicate that it is possible to identify Morus Folium from its adulterant using mitochondrial nad7 intron 2 region. The established multiplex-PCR system was proved to be effective for identification of Morus Folium. The results indicate that mitochondrial introns can be used for inter-specific polymorphic study, and the described method can be applied for molecular identification of medicinal materials.