• 제목/요약/키워드: genebank

검색결과 50건 처리시간 0.024초

Morphological diversity in kidney bean(Phaseolus vulgaris L.) germplasm

  • Han, Sea-Hee;Choi, Yu-Mi;Lee, Gi-An;Cho, Yang-Hee;Ma, Kyung-Ho;Lee, Jung-Ro
    • 한국작물학회:학술대회논문집
    • /
    • 한국작물학회 2017년도 9th Asian Crop Science Association conference
    • /
    • pp.83-83
    • /
    • 2017
  • The National Agrobiodiversity Center (NAS, RDA, Republic of Korea) has continually collected new valuable genetic resources. In this study, we regenerated conserved kidney bean (Phaseolus vulgaris L.) germplasm which couldn't be available because of seed quantity and quality, and we also surveyed their morphological characters for the sustainable utilization. A total of 431 kidney bean accessions were regenerated and 18 morphological traits were surveyed according to the characterization guideline of RDA Genebank. Among the surveyed traits, flowering time ranged from May 23 to September 4 and 73.8% of tested accessions were mainly flowering in June. The maturity time ranged from July 1 to October 15 and main flowering time was July (91.4%). For plant type, 270 accs (62.6%) were climbing type followed by medium type of 86 accs (20.0%) and dwarf type of 65 accs (15.1%). The seed coat colors were various; yellow (34.6%), white (22.3%), brown (17.9%), red (10.7%), black (5.8%), violet (11%), pink (1.4%), navy (0.9%). Principal component analysis indicated that five principal components (PCs) with Eigen values >1 accounted for more than 65.8% variability. The first PC was more related to growth habits such as growth type, flowering time, and plant type. The second and third PCs showed higher values of the pigment characters such as seed coat color, flower color, and pod color. In fourth and fifty PCs, there were the higher positive values of the pod shapes. Our results provided insight into the characteristics kidney beans, thus the utilization basis of kidney beans might be elevated for bio-industry.

  • PDF

Development and Evaluation of Core Collection Using Qualitative and Quantitative Trait Descriptor in Sesame (Sesamum indicum L.) Germplasm

  • Park, Jong-Hyun;Suresh, Sundan;Raveendar, Sebastin;Baek, Hyung-Jin;Kim, Chung-Kon;Lee, Sokyoung;Cho, Gyu-Taek;Ma, Kyung-Ho;Lee, Chul-Won;Chung, Jong-Wook
    • 한국작물학회지
    • /
    • 제60권1호
    • /
    • pp.75-84
    • /
    • 2015
  • Sesame (Sesamum indicum L.) is one of the most important oilseed crops with high oil contents and rich nutrient value. The development of a core collection could facilitate easier access to sesame genetic resources for their use in crop improvement programs and simplify the genebank management. The present study was initiated to the development and evaluation of a core collection of sesame based on 5 qualitative and 10 quantitative trait descriptors on 2,751 sesame accessions. The accessions were different countries of origin. About 10.1 percent of accessions were selected by using the power core program to constitute a core collection consisting of 278 accessions. Mean comparisons using t-test, Nei's diversity index of 10 morphological descriptors and correlation coefficients among traits indicated that the existing genetic variation for these traits in the entire collection has been preserved in the core collection. The results from this study will provide effective information for future germplasm conservation and improvement programs in sesame.

설사 자돈으로부터 분리한 Escherichia coli의 특성에 관한 연구 ; 항균제 감수성, 장독소 및 섬모의 유전형의 분포 및 plasmid profiles (Characteristics of Escherichia coli isolated from piglets with diarrhea ; antimicrobial susceptibility, genotypes of enterotoxins and pili and plasmid profiles)

  • 박주연;신나리;박용호;유한상
    • 대한수의학회지
    • /
    • 제40권2호
    • /
    • pp.301-310
    • /
    • 2000
  • The antimicrobial susceptibility, genotypes of enterotoxins(LT, STa) and pili(K88, 987P), and plasmid profiles were investigated with 102 Escherichia coli isolated from piglets showing diarrhea in Korea. Almost of them were susceptible to ceftiofur(99%), cefquinone(97.1%). However they showed resistance to bacitracin(100%), streptomycin(98%), vancomycin(97%), trimethoprim/sulfamethoxazole(87.2%), tetracycline(84.3%) in antimicrobial susceptibility test. Moreover, all of the isolates demonstrated resistance to more than 2, and 78% of them were resistant to more than 8 of total 17 drugs. Multiplex PCRs for genotyping of enterotoxins(LT, STa) and pili(K88, 987P) were established with primers designed based on sequences from Genebank. Seventeen strains(16.6%) of the isolates had STa gene, 11 strains(10.8%) of them had both STa and LT genes, and 18 strains(17.8%) had K88 gene. But none of the isolates harbored a gene exclusively encoding LT. The gene encoding 987P pili was not found in all isolates. Fifty-four strains of 102 isolates(52.9%) had plasmid with various sizes ranging from 125kb to 1.1kb. Numbers of plasmid per isolates were also various, from 1 to 9. Distinctive relationship between plasmid profiles and genotypes of enterotoxins and pili in the isolates was not found. These results might provide the basic knowledge to establish strategies for the treatment and prevention of colibacillosis in piglets.

  • PDF

Morphological and Genetic Stability of Dormant Apple Winter Buds After Cryopreservation

  • Yi, JungYoon;Lee, GiAn;Chung, JongWook;Lee, YoungYi;Kwak, JaeGyun;Lee, SeokYoung
    • 한국자원식물학회지
    • /
    • 제28권6호
    • /
    • pp.697-703
    • /
    • 2015
  • Twenty apple germplasm accessions from the Korean Genebank were successfully cryopreserved using two-step freezing to back up genetic resources maintained by field collections. This study examined the morphological and genetic stability of cryopreserved dormant apple buds that were stored in liquid nitrogen, and then rewarmed and regrown. Whole plants were regenerated directly from dormant buds through budding without an intermediary callus phase. The cryopreserved buds produced high levels of shoot formation (76.2-100%), similar to those of noncryopreserved buds (91.3-100%), with no observed differences between cryopreserved and noncryopreserved materials. Three of the twenty cryopreserved apple germplasm accessions were used to assess morphological and genetic stability. No differences in morphological characteristics including shoot length, leaf shape, leaf width/length ratio, and root length were observed between controls (fresh control and noncryopreserved) and cryopreserved plantlets. The genetic stability of regenerants (before and after cryopreservation) was investigated using inter simple sequence repeat (ISSR) markers. The ISSR markers produced 253 bands using four primers, ISSR 810, SSR 835, ISSR 864, and ISSR 899. These markers showed monomorphic banding patterns and revealed no polymorphism between the mother plant and regenerants before and after cryopreservation, suggesting that cryopreservation using two-step freezing does not affect the genetic stability of apple germplasm. These results show that two-step freezing cryopreservation is a practical method for long-term storage of apple germplasms.

Differential Display Analysis of 2,3,7,8-Tetrachlorodibenzo-p-dioxin Identified Induction of Ras-related Nuclear Protein Binding Protein2 (RanBP2) Gene

  • Kim, Dong-Hak;Lim, Young-Ran;Park, Hyoung-Goo;Kim, Beom-Joon;Chun, Young-Jin
    • Toxicological Research
    • /
    • 제25권1호
    • /
    • pp.35-40
    • /
    • 2009
  • TCDD (2,3,7,8-tetrachlorodibenzo-p-dioxin) and related halogenated aromatic hydrocarbons elicit a diverse spectrum of biochemical and toxic responses in laboratory animals and mammalian cells in culture. Toxicity and carcinogenicity of TCDD is well established but the molecular mechanism is still poorly understood. Here, we found the noble responsive genes to TCDD using the differential display analysis. Treatment of HepG2 cells with TCDD showed a significantly different mRNA expression pattern from the untreated cells in differential display analysis. The differentially displayed bands were isolated and used as probes in dot blot and Northern blot analyses. Of thirty-five isolated differentially displayed bands, only two bands were confirmed as positive in dot blot and Northern blot analyses. The nucleotides sequences of these clones were analyzed and the search of Genebank database revealed that one clone is highly homologous with RanBP2 (Ras-related nuclear protein binding protein2; 92%) and the other is an unknown gene. RanBP2 is a nucleoporin with SUMO E3 ligase activity that functions in both nucleocytoplasmic transport and mitosis and its role as a novel tumor suppressor has been recently proposed. Thus, these results may suggest the clue elucidating the toxic mechanism of TCDD through RanBP2.

Genetic diversity analysis of tea (Camellia sinensis (L.) O. Kuntze) germplasm in Korea genebank

  • 현도윤;이정로;조규택;;신명재;이경준
    • 한국자원식물학회:학술대회논문집
    • /
    • 한국자원식물학회 2019년도 춘계학술대회
    • /
    • pp.63-63
    • /
    • 2019
  • Tea plant (Camellia sinensis (L.) O. Kuntze) has been cultivated widely in many developing Asian, African, and South American countries, where it is the most widely consumed beverage in the world next to water. It has critical importance to understand the genetic diversity and population sturcutre for effective collection, conservation, and utilization of tea germplasm. In this study, 410 tea accessions collected from South Korea were analyzed using 21 SSR markers. Among 410 tea accessions, 85.4% (310 accessions) accessions were collected from Jeollanam-do. A total of 286 alleles were observed, and the genetic diversity and evenness were estimated to be averagely 0.79 and 0.61, respectively, across all the tested samples. Using discriminant analysis of principal components, the four clusters were detected in 410 tea accessions. Among them, cluster 1 showed higher frequency of rare alleles (less than 1%) than other clusters. Using calculation of the index of association and rbaD value, each cluster showed a clonal mode of reproduction. The result of AMOVA showed that most of the variation observed was within populations (99%) rather than among populations (1%). Our results might contribute to provide data about genetic diversity for the conservation of tea germplasm and for future breeding programs.

  • PDF

푸른곰팡이 대치배양에 의한 꽃송이버섯 균사 생장 특성 및 계통간 교잡균주의 rDNA 분석 (Characteristic of mycelial growth of cauliflower mushroom (Sparassis latifolia) using replacement culture with Trichoderma and rDNA analysis in genealogy of crossbreeding strain)

  • 오득실;김현석;김영;위안진;윤병선;박화식;박형호;왕승진
    • 한국버섯학회지
    • /
    • 제12권1호
    • /
    • pp.41-51
    • /
    • 2014
  • ${\beta}$-glucan 함량이 높다고 알려진 꽃송이버섯의 농가재배 활성화를 위하여 푸른곰팡이 내성균주를 선발하고자 푸른곰팡이 대치배양에 의한 꽃송이버섯 균사생장 특성을 확인하였으며, 또한 생장이 우수한 신품종을 개발하고자 교잡육종 균주에 대한 유전 다양성을 분석하였다. 먼저 푸른곰팡이 대치배양에 의한 꽃송이버섯 균사의 생장 특성을 확인한 결과, 6951 (T. viride) 균주에서는 대치선을 형성한 후 별다른 변화를 보이지 않았고, 6952 (T. spp.) 균주에서는 대치선을 형성한 다음 보다 많은 포자를 형성하는 것이 관찰되었다. 그러나 6426 (T. harzianum) 균주에서는 꽃송이버섯 균사가 생장하고 있던 부분까지 모두 덮어버리는 것이 확인되었다. 그 중 특이하게도 구례에서 채집선발한 균주인 JF02-06 균주에서는 다른 균주에 비해 푸른곰팡이 포자가 형성되지 않는 것을 확인되어 다소 푸른곰팡이에 대한 저항성을 갖는 것으로 사료되었다. 전남 산림자원연구소에서 보유 중인 균주 중 생장 및 자실체 발생이 우수한 모균주를 선발하여 교잡을 실시하여 생장특성을 조사한 결과, 미송톱밥배지에서 JF02-47, 49, 50 균주의 균사생장량이 우수한 것으로 확인되었다. 이러한 교잡육종 균주의 유전 다양성을 분석하기 위하여 ITS1, 5.8S와 ITS4 영역에 대한 염기서열을 분석한 결과 Genebank에 등록된 다른 꽃송이버섯 균주와 높은 유의성을 갖는 것으로 확인되었다. 이러한 꽃송이버섯의 포자 및 균사를 현미경으로 관찰하여 생장 특성을 확인한 결과, 포자의 크기는 장경 $6{\mu}m$, 단경 $5{\mu}m$의 물방울 모양으로 확인되었고, 균사에서 3가지 형태의 꺽쇠가 관찰되었다. 균사의 폭은 $3{\mu}m$이며 꽃송이버섯 균사의 특징으로는 약 50% 정도 꺽쇠에서 균사가 뻗어나가는 특성을 갖고 있음이 확인되었다. 균사의 생장 속도는 $0.507{\mu}m/min$이며, 2차 균사는 $0.082{\mu}m/min$의 속도로 생장하다가 모균사와 평행을 이루는 시점에서는 모균사의 생장속도와 유사한 속도로 생장하였다. 꺽쇠발생은 약 5시간 동안 균사 내부 전해질의 이동이 관찰된 후 작은 꺽쇠를 형성하였다. 약 3시간 후 격막이 형성되기 시작하였으며, 그로부터 2시간 후 최종적으로 완성되었다. 이러한 특성을 갖는 꽃송이버섯의 푸른곰팡이 저항성을 확인하고, 교잡균주의 유전 다양성 및 균사의 생장 특성을 확인하여 꽃송이버섯에 대한 기초적인 이해를 높이고, 더 나아가 버섯산업 발전에 이바지하고자 한다.

근적외선 분광분석법을 이용한 벼 유전자원의 아밀로스 함량과 단백질 함량 정량분석 (Quantitative Analysis of Amylose and Protein Content of Rice Germplasm in RDA-Genebank by Near Infrared Reflectance Spectroscopy)

  • 김정순;조양희;곽재균;마경호;최유미;김정봉;이정희;김태산;조종구;이석영
    • 한국작물학회지
    • /
    • 제53권2호
    • /
    • pp.217-223
    • /
    • 2008
  • 본 시험은 종자은행이 보유하고 있는 다양한 벼 유전자원의 활용을 촉진하기 위하여 비파괴적인 분석방법의 하나인 근적외선 분광분석법을 이용한 유용유전자원의 대량 선발체계 구축을 위해 실시하였다. 1. NIR스펙트럼은 700 nm 이하의 가시광선 범위에서 다양한 범위의 spectrum을 보였으며, 700 nm에서 2500 nm의 근적외선 파장에서도 spectrum의 차이가 크게 나타났고, 1400 nm에서 전체 spectrum의 정점을 나타냈으며 그 이상의 spectrum에서는 포화현상을 나타내었다. 2. NIR 검량식 작성에 이용된 144점의 선발자원이 가지는 단백질함량의 범위는 $6.5{\sim}9.5%$였으며, 134점의 선발자원이 가지는 아밀로스함량의 범위는 $18.1{\sim}21.7%$이었다. 3. 단백질함량과 아밀로스함량의 실험치(Lab data)와 NIR 데이터의 모집단 분포의 해석과 상관관계에 관한 통계분석 결과, 단백질함량과 아밀로스함량의 $R^2$(RSQ) 값은 각각 0.786과 0.865로 높게 보였으며, 검량식 표준오차(SEC)는 각각 0.442와 2.078로 유의한 값을 보였고, 또한 검량식 검정 표준오차(SECV)도 각각 0.541과 3.106으로 유의한 값을 보였지만 검증시 상관정도(1-VR)는 0.68과 0.70로 검량식 작성시보다 낮은 유의성을 보였다.

한국식물병명목록 6.1판(2023 개정본) (Introduction of List of Plant Diseases in Korea 6.1st Edition (2023 Revised Version))

  • 김선희;최재혁;최영준;박병용;이수헌;김경희;공현기;김동근;김순옥;김영호;백창기;변희성;서장균;유준명;윤주연;이동현;이승열;임승모;전용호;전재용;최인수;최인영;최효원;홍진성;홍승범
    • 식물병연구
    • /
    • 제29권4호
    • /
    • pp.331-344
    • /
    • 2023
  • 한국식물병명목록 6판이 2022년 4월에 발행된 이후에 1년이 경과하였다. 목록 6판에서 발견된 오류사항을 수정하고 6판 이후에 보고된 병을 추가하여 한국식물병명목록 6.1판(2023)을 작성하였다. 기존 6판의 수정사항은 397건으로 대부분은 단순 오탈자나 경미한 사항이었으나, 12개의 병은 중복이나 근거가 명확하지 않아 삭제하였고, 2개의 병은 병명을 바꾸었다. 2021년 이전에 보고되었으나 6판에 수록되지 않았거나, 6판 발행 이후에 보고된 158개의 병을 추가하였다. 결국 목록 6.1판에는 6판에 보고된 병 6,534개에 146개 병이 추가되어 총 6,680개의 병이 수록되었다. 기주 분류군도 30개가 더해져 목록 6판의 1,390개에서 6.1판에는 1,420개가 되었다. 병원체는 목록 6판의 2,400개에서 62개가 더해져 6.1판에는 2,462 분류군이 되었다. 결국 한국식물병명목록 6.1판(2023)은 1,420개의 기주에, 2,462 분류군의 병원체가 일으키는 6,680개의 병을 수록하고 있다. 목록 6.1판은 책으로 인쇄되지는 않고 온라인 한국식물병명목록(https://genebank.rda.go.kr/kplantdisease.do)을 통하여 제공되고 있다.

General Primer를 이용한 무균성뇌막염 원인 바이러스 분석 (General Primer-Mediated PCR Detection of Enteroviruses Causing Aseptic Meningitis)

  • 김문보;김기순;배유병;송철용;윤재득;이광호;신학균
    • 대한바이러스학회지
    • /
    • 제26권2호
    • /
    • pp.215-225
    • /
    • 1996
  • Aseptic meningits, an acute inflammation of the meninges, is a common illness during childhood. Virus is the most important cause of aseptic meningitis. Especially enterovirus causes approximately above 85% of all cases of aseptic meningitis. In 1993, there was a big epidemic of aseptic meningitis by ECHO 9 and ECHO 30 viruses. And ECHO 3 virus was isolated as a causative agent of aseptic meningitis in 1994. This study was aimed to detect the causative agent of aseptic meningitis in 1995 and to analyze the 5'-noncoding region which was used to detect virus. Virus was isolated from 87 stools and cerebrospinal fluid specimens of the patients by cultured RD and HEp-2 cell. Neutralizing antibody tests using enterovirus serum pool were performed on the specimens with cytopathic effect. 3 of ECHO 7 viruses and 5 of Coxsackie B3 viruses were isolated from stool specimens and 1 of ECHO 7 and Coxsackie B3 mixed type was confirmed from cerebrospinal fluid specimens. RNA was isolated from the culture supernatants of infected cells and general primers were selected in highly conserved part of the 5'-noncoding region of the enteroviral genome for RT-PCR. PCR product from this virus showed a 152bp band on gel electrophoresis. Sequence of obtained DNA was compared with prototype sequences by accessing to the Genebank database. 5'-noncoding region of isolated Coxsackie B3 virus, which has point mutations in nucleotide sequence positions 493, 497, 502, 523, was closely related to that of polio virus type 1, Mahoney strain. In case of isolated ECHO 7 virus, nucleotide has been changed from cytosine to thymine at position 581 and from thymine to cytosine at position 583. We concluded the causative agents of the outbreak of aseptic meningitis during June to July in 1995 were both ECHO 7 and Coxsackie B3 virus, and the primer used in this study could allow a rapid diagnosis of enteroviruses by PCR.

  • PDF