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A study on The Effect of Antibiotics Usage too The Efficiency of Biological Piggery Wastewater Treatment (축산물에 사용되는 항생제가 축산폐수의 처리효율에 미치는 영향)

  • Cho, Mi Kyeong;Tran, Hung Thuan;Kim, Dae Hee;Jia, Yu Hong;Oh, Se Jin;Ann, Dae Hee
    • Journal of the Korea Organic Resources Recycling Association
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    • v.15 no.1
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    • pp.123-133
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    • 2007
  • The presence of antibiotics in the wastewater from livestock farm due to its over-application should be concerned because they could change microbial ecology, increase the proliferation of antibiotic resistant pathogens, provoke toxic effect on aquatic species. In addition, these antibiotics can cause negative effect on the performance of biological wastewater treatment due to its antibacterial properties. In this study, our aim is to evaluate the effect of some common used antibiotic in Korea piggery farm such as oxytetracycline (OTC) to nitrification efficiency as well as organic compounds removal rate in biological system for treating piggery wastwater. The experiment was conducted in aeration batch reactor and lab-scale $A_2/O$(Anoxic-Anoxic-Oxic) system. From this study, it would be suggested that the piggery wastewater characterization should be examined in order to assess the fraction of common used antibiotics. The alternative treatment processes for piggery wastewater having high-strength antibiotics might be suggested in the future work.

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Morphological, Molecular, and Biochemical Characterization of Monounsaturated Fatty Acids-Rich Chlamydomonas sp. KIOST-1 Isolated from Korea

  • Jeon, Seon-Mi;Kim, Ji Hyung;Kim, Taeho;Park, Areumi;Ko, Ah-Ra;Ju, Se-Jong;Heo, Soo-Jin;Oh, Chulhong;Affan, Md. Abu;Shim, Won-Bo;Kang, Do-Hyung
    • Journal of Microbiology and Biotechnology
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    • v.25 no.5
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    • pp.723-731
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    • 2015
  • Microalgae hold promise as producers of sustainable biomass for the production of biofuels and other biomaterials. However, the selection of strains with efficient and robust production of desirable resources remains challenging. In this study, we isolated a green microalga from Korea and analyzed its morphological, molecular, and biochemical characteristics. Microscopic and phylogenetic analyses demonstrated that the isolate could be classified into the genus Chlamydomonas, and we designated the isolate Chlamydomonas sp. KIOST -1. Compositions of protein, lipid, and carbohydrate in the microalgal cells were estimated to be 58.8 ± 0.2%, 22.7 ± 1.2%, and 18.5 ± 1.0%, respectively. Similar to other microalgae belonging to Chlorophyceae, the dominant amino acid and monosaccharide in Chlamydomonas sp. KIOST-1 were glutamic acid and glucose. On the other hand, the proportions of saturated fatty acids, monounsaturated fatty acids, and polyunsaturated fatty acids clearly differed from other species in the genus Chlamydomonas, and monounsaturated fatty acids accounted for a large portion (41.3%) of the total fatty acids in the isolate. Based on these results, Chlamydomonas sp. KIOST-1 has advantageous characteristics for biomass production.

Molecular Cloning and Expression of DMRT Gene in Protogynous Wrasse, Halichoeres tenuispinis

  • Jeong, Hyung-Bok;Park, Ji-Gweon;Park, Jin-Young;Jin, Young-Jun;Yang, Myung-Cheon;Hyun, Kyung-Man;Kim, Gi-Ok;Kim, Se-Jae
    • Proceedings of the Korean Society of Developmental Biology Conference
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    • 2003.10a
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    • pp.64-64
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    • 2003
  • The sex differentiation of fishes occurs under the control of genetic and various environmental factors. DM-domain containing genes are novel zinc finger transcription factors and play key roles in sex determination. In order to isolate the wrasse DMRT (wDMRT) cDNA from the protogynous wrasse (Halichoeres tenuispinnis), the wrasse testis cDNA library was screened using the $^{32}$ P-labeled PCR products, which were amplified with the degenerate primers from conserved DM-domain regions of several DMRT genes. Among a few positives obtained through screening, the full length wDMRT cDNA of 2.9kb size encoding a predicted 300 amino acid residues was isolated. The sequence analysis exhibited 60%, 43% sequence identity with rainbow trout and tilapia DMRT1, respectively. RT-PCR assay showed that wDMRT was expressed specifically in male testis. Also, wDMRT gene was strongly expressed in May during reproductive season, when the reproductivity of wrasse is most active. This results suggested that wDMRT gene function in testis differentiation The conserved DM-domain regions were amplified using PCR from DMRT genes of several species among Labridae, and their sequences were determined. The sequence of DM-domain region of Halichoeres. tenuispinis was identical to those of Pseudolabrus japonicus, Pteragogus flagellifera, and showed 94% identity with that of Halichoeres poecioptrerus.

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Incidence of Major Diseases on Paeonia lactiflora PALLAS (작약(芍藥)의 주요병해(主要病害) 발생(發生))

  • Park, So-Deuk;Kim, Ki-Jae;You, Oh-Jong;Kim, Se-Jong;Kim, Jae-Chul;Shin, Jong-Hee
    • Korean Journal of Medicinal Crop Science
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    • v.4 no.3
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    • pp.236-240
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    • 1996
  • 1. The pathogenic fungi which infect to shoot of peony was 7 species. The infected parts were as followed, leaf spot disease was in leaf, leaf blotch was stem, powdery mildew was whole aeri­al part of both leaf and stem. 2. The major diseases were leaf spot and powdery mildew, and begin to occur from late April to mid­dle May, and then rapidly heavy infected. The 'Euiseongpeony' variety was more susceptible to those diseases than the 'Yeongcheonpeony' variety. 3. The blight of top part by seasonal in 1995 was begun at late May and increased rapidly 50.6% in Early August.

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Study on development of DNA probe for identification of Prevotella intermedia G8-9-3 (Prevotella intermedia G8-9K-3을 동정할 수 있는 DNA 프로브의 개발에 관한 연구)

  • Bak, Jong-Sung;Kim, Se-Hoon;kim, Dong-Ki;Seong, Jin-Hyo;Kim, Byung-Ock;Kim, Jung-Ki
    • Journal of Periodontal and Implant Science
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    • v.32 no.2
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    • pp.281-290
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    • 2002
  • The purpose of this study is to develop species-specific DNA probe for detection and identification of Prevotella intermedia (P. intermedia) G8-9K-3. This study procedure includes (1) whole-genomic DNA extraction of P. intermedia G8-9K-3 (2) construction of the genomic DNA library, (3) screening of strain-specific DNA probe by reverse dot hybridization, (4) confirmation of strain-specific DNA probe by Southern blot hybridization, (5) determination of nucleotide sequences of strain-specific DNA probe. Twenty-eight recombinant plasmids containing Hind III-digested DNA fragments of P. intermedia G8-9K-3 were obtained. Reverse Dot Hybridization and Southern blot analysis data showed that one of them, Pig3, could be P. intermedia G8-9K-3-specific DNA probe. This datum indicates that this Pig3 DNA probe could be useful in detection and identification of the P. intermedia G8-9K-3 strain.

Occurrence Patterns of Three Planthopper Species in Rice Fields in Bangladesh, Cambodia, Thailand and Vietnam (방글라데시, 캄보디아, 태국, 베트남 벼 포장에서 멸구류 3종의 발생 양상)

  • Park, Bue-Yong;Lee, Sang-Ku;Park, Hong-Hyun;Jeon, Sung-Wook;Jeong, In-Hon;Park, Se-Keun;Hossain, Md. M.;Sovandeth, C.;Rattanakarng, W.;Vuong, P.T.;Chien, H.V.
    • Korean Journal of Organic Agriculture
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    • v.26 no.3
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    • pp.489-500
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    • 2018
  • Rural Development Administration (RDA) is promoting the AFACI IPM (Asian Food & Agricultural Cooperation Initiative program). AFACI consist of 12 countries including Bangladesh, Cambodia, Thailand, Vietnam and so on. The main goal of the AFACI IPM project is 'Establishment of an international cooperative network for the best management of migratory rice planthoppers and setting data-base of pests occurrence information. As a result of the suvey, Planthoppers were increasing all the way from tillering stage to ripe stage and do not appear to be peak of one or two like korea case. In detail, 1,673 of BPH (Nilaparvata lugens) occurred in survey site of Svay Reang, Cambodia, followed by 1.237 at Dobila, Bangladesh. In the case of White backed planthopper (Sogatella furcifera), 1,163 of WBPH occurred in survey site of Dobila, Bangladesh and 849 WBPH were collected at Hamkuria, Bangladesh. It is expected to verify the occurrence and movement patterns of hoppers among member countries in the future.

Antitumor Effect of the Cotreatment of Gagamsibjeondaebo-tang and $As_2O_3$ in Human Lung Cancer Cell Line H-460 (인간 폐암세포주 H-460 세포에서 가감십전대보탕과 $As_2O_3$의 병용처리에 의한 항종양 증진효과)

  • Hur Jong Chan;Won Jin Hee;Kim Dong Woung;Han Se Hee;Moon Goo
    • Journal of Physiology & Pathology in Korean Medicine
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    • v.18 no.4
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    • pp.1089-1097
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    • 2004
  • This study was designed to elucidate the synergistic cytotoxic mechanisms of the cotreatment of Gagamsibjeondaebo-tang (GSD) and AS₂O₃ in human lung cancer cell line, H-460. The combination of GSD and AS₂O₃ synergistically augmented the cytotoxicity of GSD and AS₂O₃ in H-460 cells. The nature of cytotoxicity was revealed as apoptosis which was characterized by chromatin condensation and fragmentaton in DAPI staining. The apoptotic cytotoxicity of GSD and AS₂O₃ was accompanied by the cleavage of PARP. Of note, the expression of pro-apoptotic BclXS protein was increased, but the expressions of Sax and BclXL was not affected in H-460 cells treated with GSD and AS₂O₃. In addition, antioxidant NAC completely blocked the apoptotic death of H-460 cells by GSD and AS₂O₃. In conclusion, this results suggest that the cotreatment of GSD and AS203 induces the synergistic apoptotis of human large cell lung cancer cell line, H-460 via the induction of BclXS and reactive oxygen species (ROS).

Korean Mistletoe (Viscum album var. coloratum) Inhibits Amyloid β Protein (25-35)-induced Cultured Neuronal Cell Damage and Memory Impairment

  • Jang, Ji Yeon;Kim, Se-Yong;Song, Kyung-Sik;Seong, Yeon Hee
    • Natural Product Sciences
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    • v.21 no.2
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    • pp.134-140
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    • 2015
  • The present study aims to investigate the effect of methanol extract of Korean mistletoe (KM; Viscum album var. coloratum), on amyloid $\beta$ protein ($A\beta$) (25-35), a synthetic 25-35 amyloid peptide, -induced neurotoxicity in cultured rat cerebral cortical neurons and memory impairment in mice. Exposure of cultured neurons to $10{\mu}M$ $A\beta$ (25-35) for 24 h induced a neuronal cell death, which was measured by a 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl-tetrazolium bromide (MTT) assay and Hoechst 33342 staining. KM (10, 30 and $50{\mu}g/ml$) significantly inhibited the $A\beta$ (25-35)-induced apoptotic neuronal death. KM ($50{\mu}g/ml$) inhibited 10 μM Aβ (25-35)-induced elevation of intracellular calcium concentration ([Ca2+]i), which was measured by a fluorescent dye, Fluo-4 AM. Glutamate release into medium and generation of reactive oxygen species (ROS) induced by $10{\mu}M$ $A\beta$ (25-35) were also inhibited by KM (10, 30 and $50{\mu}g/ml$). These results suggest that KM may mitigate the $A\beta$ (25-35)-induced neurotoxicity by interfering with the increase of [Ca2+]i and then inhibiting glutamate release and generation of ROS in cultured neurons. In addition, orally administered KM (25 and 50 mg/kg, 7 days) significantly prevented memory impairment induced by intracerebroventricular injection of $A\beta$ (25-35) (8 nmol). Taken together, it is suggested that anti-dementia effect of KM is due to its neuroprotective effect against $A\beta$ (25-35)-induced neurotoxicity and that KM may have therapeutic role in prevention of the progression of Alzheimer's disease.

Molecular Analysis of the 3'-Terminal Region of Lily Latent Carlavirus from Lilium lancitoium

  • Ryu, Ji-Hwan;Park, Hye-Won;Park, Won-Mok;Lee, Se-Yong;Ryu, Ki-Hyun
    • The Plant Pathology Journal
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    • v.16 no.4
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    • pp.231-235
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    • 2000
  • The 3,000 nucleotides of 3'-terminal region of the genomic RNA of a new isolate of carlavirus from a Korean native lily (Lilum lancitoium) was cloned and its nucleotide sequences were determined. The coat protein (CP) gene of the virus showed 72.0% to 72.8% nucleotide sequence identities and 86.9% to 88.0% amino acid sequence identities with those of the four strains (two Korean, one Dutch, and one Japanese isolates) of lily symptomless virus (LSV). Interestingly, different amino acid sequences between the new isolate and LSV strains were located at the N-terminal region of the CP. Pairwise amino acid sequence comparison of the CP gene revealed sequence identities of 22.0% to 71.1% between the virus and other 9 carlavirus species. The 25 kDa and 12 kDa proteins genes of the virus share 30.7% to 76.3% and 31.1% to 85.8% amino acid sequence identities, respectively, with those of 8 other carlaviruses. The 16 kDa protein gene of the virus shares 16.7% to 72.9% amino acid sequence identities with that of 9 other carlaviruses. These data indicate that the virus, designated as lily latent virus (LiLV), is a distinct of the Carlavirus genus and distinguished from the known strains of LSV.

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Extracellular Signal-Regulated Kinase Is a Major Enzyme in Korean Mistletoe Lectin-Mediated Regulation of Macrophage Functions

  • Byeon, Se-Eun;Lee, Jae-Hwi;Yu, Tao;Kwon, Moo-Sik;Hong, Sung-Youl;Cho, Jae-Youl
    • Biomolecules & Therapeutics
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    • v.17 no.3
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    • pp.293-298
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    • 2009
  • Korean mistletoe lectin (KML) is the major component found in Viscum album var. (coloratum), displaying anti-cancer and immunostimulating activities. Even though it has been shown to boost host immune defense mechanisms, the regulatory roles of KML on the functional activation of macrophages have not been fully elucidated. In this study, regulatory mechanism of KML on macrophage-mediated immune responses was examined in terms of KML-mediated signaling event. KML clearly induced mRNA expression of tumor necrosis factor (TNF)-$\alpha$, the generation of reactive oxygen species (ROS) and phagocytic uptake in RAW264.7 cells. All of these events were strongly suppressed by U0126, whereas TNF-$\alpha$ mRNA was not diminished by SB203580 and SP600125, indicating ERK as a central enzyme managing KML-induced up-regulation of macrophage functions. Indeed, KML strongly induced the phosphorylation of ERK in a time-dependent manner without altering its total level. Therefore, these data suggest that ERK may be a major signaling enzyme with regulatory property toward various KML-mediated macrophage responses.