• Title/Summary/Keyword: spSac3

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Construction of spSac3 Null Mutants Defective in mRNA Export (mRNA의 핵에서 세포질로의 이동에 관여하는 spSac3 유전자의 결실돌연변이 제조와 특성 조사)

  • Kang Sook-Hee;Yoon Jin-Ho
    • Korean Journal of Microbiology
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    • v.42 no.2
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    • pp.153-155
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    • 2006
  • We constructed the null mutants of fission yeast Schizosaccharomyces pombe spSac3 gene that is homologous to budding yeast Saccharomyces cerevisiae SAC3 involved in mRNA export out of nucleus. Tetrad analysis showed that the spSac3 is essential for vegetative growth. The spSac3 mutants harboring pREP81X-spSac3 plasmid showed poly(A)+ RNA export defect in the presence of thiamine. These results suggest that spSac3 is also involved in mRNA export from the nucleus.

Characteristics of Sn-1.7Bi-0.7Cu-0.6In Lead-free Solder (Sn-1.7Bi-0.7Cu-0.6In 솔더의 특성 연구)

  • Park, Ji-Ho;Lee, Hee-Yul;Jhun, Ji-Heon;Cheon, Chu-Seon;Jung, Jae-Pil
    • Journal of Welding and Joining
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    • v.26 no.5
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    • pp.43-48
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    • 2008
  • Characteristics of Sn-1.7%Bi-0.7%Cu-0.6%In (hereafter, SBIC) lead-free solder was investigated in this study. The results from SBIC were compared to other lead-free solders such as Sn-3.5%Ag-0.7%Cu (hereafter, SAC), Sn-0.7%Cu (hereafter, SC), and lead-bearing Sn-37%Pb (hereafter, SP) alloy. Tensile properties of bulk solder, wettability, spreading index, bridge and dross were evaluated. As experimental results, tensile strength and elongation of SBIC was 62.5MPa and 21.5%, respectively. The tensile strength was comparable to that of SP solder. The wetting time of SBIC was 1.2 sec at $250^{\circ}C$, and its wetting properties including wetting force were as good as the SAC alloy. However, wettability of the SC was not so good as the SBIC and SAC. The spreading index of SBIC at $250^{\circ}C$ was 71 %, and it was similar level to those of SAC and SC solders. Bridging was not found for all solders of SBIC, SAC and SC in the range from 240 to $260^{\circ}C$. In dross test at $250^{\circ}C$ for an hour, the amount of dross produced from SBIC was about 57% compared to that from SAC.

Molecular Cloning of nifHD from Rhizobium sp. SNU003 (Rhizobium sp. SNU003의 nifHD 클로닝)

  • 강명수;안정선
    • Korean Journal of Microbiology
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    • v.31 no.2
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    • pp.123-128
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    • 1993
  • Genes for dinitrogenase reductase (nifH) and dinitogenase a subunit (nifD) were found to be located on 7.9 kb of EcoRI, 6.5 kb of Sail, 7.3 kb of HindlII and 4.4 kb of Pstl fragments of the genomic blot of Rhizobium sp. SNU003. a symbiotic strain from root nodule of Canavalia lineata. Nine recombinant phage nif-clones were selected from the genomic library constructed by using EMBL-3 BamHI arms of bacteriophage lambda. Among them. Rnif-6 had insert DNA of 15.3 kb. in which 7.6 kb of BamHI!SacI fragment contained nifHD region. Therefore, the 7.6 kb fragment was subcloned into pUC19 and partial restriction map was constructed. As the results, nifH and nifD were found to be located continuously on 4.5 kb of BamHI/BglIl in the genome of Rhizobium sp. SNU003 strain.

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Ostrich chick fading syndrome(OCFS) caused by bacterial infection of farmed ostrich chicks (세균감염에 의한 초생타조(Struthio camelus camelus)의 쇠약 증후군의 발생 증례)

  • 육현수;김영진;도홍기;노수일;김범석;임채웅
    • Korean Journal of Veterinary Service
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    • v.22 no.2
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    • pp.113-119
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    • 1999
  • The most common cause of death is ostrich chick fading syndrome(OCFS), which is due to bacterial infection during artificial incubation and hatching. Six farmed ostrich chicks aged 3 and 10 days in Chonbuk province, were submitted to Chonbuk Livestock Development and Research Institute for necropsy, Clinically, birds showed hair loss, ocular exudate, lethargy, diarrhea, and subsequently died 3-5 days after onset of clinical signs. Grossly, umbilicus was enlarged. White-yellowish purulent nodules were scattered on the lung and the membrane of air-sac was thickened and had inflamed exudate on the surface in two chicks that died 3 days after hatching. In 10 days-old chick, intestine was shown rodding segmentally. Yolk sac was still retarded and its surface was partially hemorrahgic. The synovial fluid of the leg was yellowish. Microscopically, multifocal purulent exudates were scattered on the lung. Capillary microthrombi in the glomerulus were prominent and tubular epithelia were necrotic. Necrotic hepatocytes were scattered and intestine were congested. Microbiologically, Pseudomonas sp and/or E coli were isolated from air-sac, lung and/or liver. This case suggests that poor hygiene during artificial incubation, hatching or in the first week after hatching may cause high mortality of the ostrich chicks.

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Two New and Two First Recorded Species of Predatory Soil Nematodes (Nematoda : Mononchida) from Korea (한국산 포식선충 (Nematoda : Mononchida) 의 2신종 및 2미기록종기재)

  • Khan Zakaullah;Park, So-Deuk;Bae, Su-Go;Shin, Yong-Seub
    • The Korean Journal of Soil Zoology
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    • v.7 no.1_2
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    • pp.51-57
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    • 2002
  • Two new and two known species of mononchid nematodes from Korea are described and illustrated. lotonchus cucumis sp. n. is characterized by 2.9-3.2 ㎜ long body, presence of 3 each pre- and post-vulval papillae, vagina with cuticularized pieces, a long tail with terminal spinneret. Mylonchulus unicus sp. n. has 1.1-1.2 ㎜ long body, and is characterized by having 2 pairs of teeth on subventral walls of buccal cavity; submedian denticles arranged in 2-3 rows, very short post-vulval sac and terminal spinneret. Mononchus sinensis Soni and Nama (1983) and Mononchus aquaticus Coetzee (1968) are reported for the first time from Korea.

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Stictodora sp. (Trematoda: Heterophyidae) Recovered from a Man in Korea (Stictodoyu sp. (Trematoda; Heterophyidae)의 인체기생 1례)

  • 채종일;홍성종
    • Parasites, Hosts and Diseases
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    • v.26 no.2
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    • pp.127-132
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    • 1988
  • Two adult specimens of heterophyid cuke, which belong to the genus Stictodora, were collected from the stool of a 24-year old man after chemotherapy. The nukes were morphologically characterized by their small body siRe (0.90~0.98mm long and 0.38 mm wide) and peculiar structure of ventrogenital sac with armed gonotyl (with about 12~I5 spines) not enveloping genital pore. Species identification is deferred until more worms are obtained, although they closely resemble Stictadora fuscatum (Onji and Nishio, 1916). The Patient used to eat raw flesh of mullets and gobies, which are regarded as the infection source of Stictodora sp., together with 3 other kinds of heterophyids described elsewhere. This is the first record of human Stictodora infection in the literature.

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Studies on cercariae from the Kuwait Bay. VI. Description and surface topography of Cercaria kuwaitae VI sp. n. (Trematoda: Haplosplanchnidae)

  • Jasem ABDUL-SALAM;Bhaskaran Nair Saralamma SREELATHA
    • Parasites, Hosts and Diseases
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    • v.33 no.3
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    • pp.147-154
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    • 1995
  • A new haplosplanchnid cercaria, Cercaria kuwaitae VI sp. n., was found in the prosobranch snail Cerithidea cincingulata in the Kuwait Bay Details are presented on the morphology and behavior of the cercaria and the encystment process. The new cercaria is a biocellate, distome, with a prominent single sac-like intestinal cecum extending well posterior to the ventral sucker and develops in simple sporocysts. It differs from known haplosplanchnid cercariae in the absence of finger-like processes on the tail, and the presence of V-shaped excretory vesicle extending beyond ventral sucker and the presence of cervical glands. The surface topography of the cercaria and its sporocyst is examined by scanning electron microscopy. This is the first haplosplanchnid cercaria to be described from a Cerithidea species.

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Aspergillosis in an Ostrich (Struthio camelus) (타조(Struthio camelus)에서 발생한 아스퍼질러스증)

  • 조경오;박남용;강문일;이근우
    • Journal of Veterinary Clinics
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    • v.18 no.2
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    • pp.174-177
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    • 2001
  • A nine-month-old male ostrich (Struthio camelus) exhibited loss of appetite and dyspnea for 10 days, followed by emaciation and death. Grossly, multiple white nodules measuring 1-3 mm in diameter were observed in the surface of and inside of the lung and in the mucosa of the air sac. Microscopically, the granuloma formations were observed in the lung and air sac. The core of granuloma consisted mainly of macrophages and fibroblasts. The thin layer comprising the giant cells and macrophages surrounded the granuloma. By Periodic acid Schiff reaction, mycelia were detected especially in the core of granuloma. From the present results, the causative agent inducing the death of an ostrich was thought to be Aspergillus sp. This is the first report of the occurrence of acute Aspergillus pneumonia (brooder pneumonia) in an adult male ostrich in Korea.

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Molecular Cloning of nod Genes from Bradyrhizobium sp. SNU001 (Bradyrhizobium sp. SNU001 nod 유전자 클로닝)

  • 고세리;심웅섭;안정선
    • Korean Journal of Microbiology
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    • v.30 no.4
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    • pp.246-251
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    • 1992
  • Molccular cloning of nod genes from Bradvrhizobium sp. SNU001, a nitrogen-fixing symbiont isolated from thc root nodules of soybean (Clycine trim) . was carried out. nod genes were found to be located on thc genome of the symbiont by gcnomic hybridization with 4.5 kb EcoRI/HndIII fragment (nod DABC) of Rhizohium meliloti as probe. Genomic library of this symbiont was constructed using h phage EMBL3-BanlHI vector. from which five nod positive clones were sclectcd by primary and secondary screening methods. The partial restriction map of inserted genomic DNA of h CNS-l(c1one 2) was constructed. and 3.9 kh Bun7HI fragment. which showed strong hybridization signal to the probe, was subcloned into pBS KS(+) plasmid vector. Partial restriction inap ot' a selected subclone (pBjCNS-I) was constructed and nod DABC was found to be located on the 1.8 kb KpnI/Sacl fragment of this subclone.

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Cloning of Autoregulator Receptor Gene form Saccharopolyspora erythraea IFO 13426 (Saccharopolyspora erythraea IFO 13426으로부터 Autoregulator Receptor Protein Gene의 Cloning)

  • 김현수;이경화;조재만
    • Microbiology and Biotechnology Letters
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    • v.31 no.2
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    • pp.117-123
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    • 2003
  • For screening of autoregulator receptor gene from Saccharopolyspora erythraea, PCR was performed with primers of receptor gene designed on the basis of amino acid sequences of autoregulator receptor proteins with known function. PCR products were subcloned into the BamHI site of pUC19 and transformed into the E. coli DH5$\alpha$. The isolated plasmid from transformant contained the fragment of 120 bp, which was detected on 2% gel after BamHI treatment. The insert, 120 bp PCR product, was confirmed as the expected internal segment of gene encoding autoregulator receptor protein by sequencing. Southern and colony hybridization using Saccha. erythraea chromosomal DNA were performed with the insert as probe. The plasmid (pEsg) having 3.2 kbp SacI DNA fragment from Saccha. erythraea is obtained. The 3.2 kbp SacI DNA fragment was sequenced by the dye terminator sequencing. The nucleotide sequence data was analyzed with GENETYX-WIN (ver 3.2) computer program and DNA database. frame analyses of the nucleotide sequence revealed a gene encoding autoregulator receptor protein which is a region including KpnI and SalI sites on 3.2 kbp SacI DNA fragment. The autoregulator receptor protein consisting of 205 amino acid was named EsgR by author. In comparison with known autoregulator receptor proteins, homology of EsgR showed above 30%.