• 제목/요약/키워드: Protein isolate

검색결과 604건 처리시간 0.023초

입원 치료한 무균성 뇌막염 환아의 임상적 검토 : 1996년~1998년 (A Clinical Study of Aseptic Meningitis from 1996 to 1998)

  • 이용희;김애숙
    • Pediatric Infection and Vaccine
    • /
    • 제8권2호
    • /
    • pp.168-174
    • /
    • 2001
  • 목 적 : 1996년부터 1998년까지 3년 동안 포항지역에서 집중 발생한 무균성 뇌막염의 역학 및 임상 양상을 알아보고자 본 연구를 시행하였다. 방 법 : 1996년부터 1998년까지 포항성모병원에 입원하여 무균성 뇌막염으로 진단 후 치료받은 192례의 환아를 대상으로 임상 증상, 검사 소견에 관해 검토하였다. 결 과 : 남녀 환아의 비는 1.91 : 1이었으며, 유행시기는 1996년은 주로 8월(75.7%) 1997년과 1998년은 주로 7, 8월에 집중되어 발생하였다. 말초 혈액 소견상 백혈구 수는 $5,001{\sim}20,000/mm^3$ 사이가 93.3%로 대부분을 차지하였고 적혈구침강속도는 약간 증가된 소견을 보였으며, CRP는 2+ 이하가 93.2%로 대부분을 차지하였다. 뇌척수액 백혈구 수는 $500/mm^3$ 이하가 88.0%, 뇌척수액 단백은 40 mg/dL 미만이 61.5%, 뇌척수액 당은 40 mg/dL 초과가 94.3%로 대부분이 정상 범위이었다. 임상 증상의 빈도는 발열, 구토, 두통, 복통의 순이었다. 평균 발열 기간은 3.8일이었으며 임상 경과는 전 예가 특별한 후유증이나 합병증 없이 회복되었다. 요추천자 후 요통 발생 빈도는 31.2%이었고, 요통의 평균 지속 기간은 1.87일이었다. 결 론 : 포항성모병원에서 1996년부터 1998년까지 입원 치료받은 무균성 뇌막염 환아를 검토한 결과, 원인 바이러스는 밝혀내지 못했으나 무균성 뇌막염의 임상 증상 및 발생 연령, 발생 시기, 뇌척수액 검사 소견, 요추천자 후 요통 발생 빈도 등은 다른 연구와 비교하여 볼 때 큰 차이가 없었다.

  • PDF

부루세라백신(RB51)의 안전성에 관한 연구 I. Brucella abortus RB51 백신균주의 생화학적 및 유전학적 성상비교 (Studies on the safety of Brucella abortus RB51 vaccine I. Comparison of the biochemical and genetic characteristics of Brucella abortus RB51 vaccine strains)

  • 김종만;우승룡;이지연;정석찬;강승원;김종염;윤용덕;조상래;유한상
    • 대한수의학회지
    • /
    • 제40권3호
    • /
    • pp.533-541
    • /
    • 2000
  • Biochemical and genetic analysis were carried out to investigate the potential recovery of pathogenecity or related mutations of Brucella abortus RB51 vaccine strains. RB51 strains were recovered from commercial vaccines, including related seed stocks from private companies in Republic of Korea, strain from USA, a reference strain from C university and a field isolate (Daehungjin) from aborted dairy cow after RB51 vaccination were compared with two identified virulent wild strains (S2308 and a field strain isolated from dairy cow in Korea) at the same conditions. All the strains examined, except identified pathogenic strains, revealed the identical characteristics to the original RB51 in biochemical properties, antigen and bacteriophage typing. Outer membrane protein (OMP) profiles from strains of RB51 showed the same patterns with standard RB51 in SDS-PAGE. In addition, Western blotting with the brucella specific monoclonal antibody also indicated that all the vaccine strains were completely deficient in their LPS compared to the pathogenic Br abortus strains. The differences in DNA structures among strains were also possible to detect after PCR. All vaccine strains, except S19, S1119-3, S1075, S544 and Br suis, were amplified a 178bp DNA fragment of eri-gene, and 364bp of IS711 elements. In contrast, 498bp DNA product was only found with Br abortus. Overall evidences in the present study confirmed that the RB51 strains for vaccine production in Korea did not originated from the phenomena of possible recovery of pathogenicity or related to any potential mutation event at all.

  • PDF

Analysis of nucleotide sequence of a novel plasmid, pILR091, from Lactobacillus reuteri L09 isolated from pig

  • Lee, Deog-Yong;Kang, Sang-Gyun;Rayamajhi, Nabin;Kang, Milan;Yoo, Han Sang
    • 대한수의학회지
    • /
    • 제48권4호
    • /
    • pp.441-449
    • /
    • 2008
  • The genus Lactobacillus is the largest of the genera included in lactic acid bacteria and is associated with mucosal membranes of human and animal. Only a few Lactobacillus plasmid-encoded functions have been discovered and used. In this study, a novel plasmid (pILR091) was isolated from a wild L. reuteri isolated from pig and described the characteristics of its replicons, genetic organization, and relationship with other plasmids. After digestion of the plasmid, pILR091, with SalI, plasmid DNA was cloned into the pQE-30Xa vector and sequenced. The complete sequence was confirmed by the sequencing of PCR products and analyzed with the Genbank database. The isolate copy number and stability were determined by quantitative-PCR. The complete sequence of L. reuteri contained 7,185 nucleotides with 39% G-C content and one cut site by two enzymes, SalI and HindIII. The similar ori sequence of the pC194- rolling circle replication family (TTTATATTGAT) was located 63 bp upstream of the protein replication sequence, ORF 1. Total of five ORFs was identified and the coding sequence represented 4,966 nucleotides (70.4%). ORF1 of pILR091 had a low similarity with the sequence of pTE44. Other ORFs also showed low homology and E-values. The average G-C content of pILR091 was 39%, similar with that of genomic DNA. The copy number of pILR091 was determined at approximately 24 to 25 molecules per genomic DNA. These results suggested that pILR091 might be a good candidate to construct a new vector, which could be used for cloning and expression of foreign genes in lactobacilli.

DETERMINATION OF MOISTURE AND NITROGEN ON UNDRIED FORAGES BY NEAR INFRARED REFLECTANCE SPECTROSCOPY(NIRS)

  • Cozzolino, D.;Labandera, M.;Inia La Estanzuela
    • 한국근적외분광분석학회:학술대회논문집
    • /
    • 한국근적외분광분석학회 2001년도 NIR-2001
    • /
    • pp.1620-1620
    • /
    • 2001
  • Forages, both grazed and conserved, provide the basis of ruminant production systems throughout the world. More than 90 per cent of the feed energy consumed by herbivorous animals world - wide were provided by forages. With such world - wide dependence on forages, the economic and nutritional necessity of been able to characterize them in a meaningful way is vital. The characterization of forages for productive animals is becoming important for several reasons. Relative to conventional laboratory procedures, Near Infrared Reflectance Spectroscopy (NIRS) offers advantages of simplicity, speed, reduced chemical waste, and more cost-effective prediction of product functionality. NIR spectroscopy represents a radical departure from conventional analytical methods, in that entire sample of forage is characterized in terms of its absorption properties in the near infrared region, rather than separate subsamples being treated with various chemicals to isolate specific components. This forces the analyst to abandon his/her traditional narrow focus on the sample (one analyte at a time) and to take a broader view of the relationship between components within the sample and between the sample and the population from which it comes. forage is usually analysed by NIRS in dry and ground presentation. Initial success of NIRS analysis of coarse forages suggest a need to better understand the potential for analysis of minimally processed samples. Preparation costs and possible compositional alterations could be reduced by samples presented to the instrument in undried and unground conditions. NIRS has gained widespread acceptance for the analysis of forage quality constituents on dry material, however little attention has been given to the use of NIRS for chemical determinations on undried and unground forages. Relatively few works reported the use of NIRS to determine quality parameters on undried materials, most of them on both grass and corn silage. Only two works have been found on the determination of quality parameters on fresh forages. The objectives of this paper were (1) to evaluate the use of NIRS for determination of nitrogen and moisture on undried and unground forage samples and (2) to explore two mathematical treatments and two NIR regions to predict chemical parameters on fresh forage. Four hundred forage samples (n: 400) were analysed in a NIRS 6500 instrument (NIR Systems, PA, USA) in reflectance mode. Two mathematical treatments were applied: 1,4,4,1 and 2,5,5,2. Predictive equations were developed using modified partial least squares (MPLS) with internal cross - validation. Coefficient of determination in calibration (${R^2}_{CAL}$) and standard error in cross-validation (SECV) for moisture were 0.92 (12.4) and 0.92 (12.4) for 1,4,4,1 and 2,5,5,2 respectively, on g $kg^{-1}$ dry weight. For crude protein NIRS calibration statistics yield a (${R^2}_{CAL}$) and (SECV) of 0.85 (19.8) and 0.85 (19.6) for 1,4,4,1 and 2,5,5,2 respectively, on a dry weight. It was concluded that NIRS is a suitable method to predict moisture and nitrogen on fresh forage without samples preparation.

  • PDF

한국 Chlorella에 대한 연구 (Studies on the chlorella in Korea)

  • 이주식;심종호
    • 미생물학회지
    • /
    • 제1권1호
    • /
    • pp.38-44
    • /
    • 1963
  • According to the experiment on pure-isolation and the related contaminants of Chlorella, the phenomena of the ecological distributions of Chlorella in Korea have been manifested in several areas and also the aim that in going to do culture, biological and physiological study of Chlorella is carried out. Contaminants very oftenly occupied on the colony of the strains taken in order to fulfil pure-isolation of Chlorella, but in accordance with being piled up the minute research on this subject, I can obtain the desirable results as follows: 1. For the pure-isolation, the duration chose the time from May to September 1957 so that may easily isolate from contaminant water with utilizing the antibiotic substances. 2. To take long time, 36-48 hours until growth of nascent through the non-sporulated, it originates from the difference of the cultured media. In addition to the above mention, the mechanism of growth until nascent through the sporulated must not always require the ligh. However the supply of metabolic energy depend upon its nutritional conditions per phase. 3. The culture of Chlorella should be based on the lower culturing except adding especial conditions such as reagent concentration of media, artifical shake of media and other facts due to the natural conditions. And also these strains grew not only in distilled water but 2% NaCl solution without any abnormality in cell it self. I, therefore, guess it is possible to culture in sea-water under phasic environment. 4. In the experiment of ammonia detection, it is caused by the sampling surroundings to contain the minute quantity of ammonia in strain No. M 918; that is the place to be plenty of Carbohydrate on behalf of protein. 5. To compare the absorption curve of chlorophyll of higher plant with that of Chlorella, the absorption zone made mostly the Same ones each other but a little absorption grade dose not clearly appear. The colony which formed giant type grows with intensive colour and green band on surrounding of the colony and after that it was changed into all the green colour and developed up to end. 6. At first phase for a week, the development of Chlorella suspends the normal condition as in vivo but after a few days, the colour of chlorophyll gradually changed into blue-yellow which secrete the mucous substances on the agar media. The cell was flew out the contained substances itself on leaving the cell wall only, or the various micro-organism diffused on the outer-region of the cell.

  • PDF

국내에서 분리된 포도상구균의 Vancomycin 내성빈도 및 특성 (Characterization and Frequency of Vancomycin Resistance in Staphylococcus aureus Isolated in Korea)

  • 박성언;김종배
    • 대한의생명과학회지
    • /
    • 제6권3호
    • /
    • pp.201-208
    • /
    • 2000
  • Vancomycin은 세포벽의 합성을 억제하여 세균에 대한 항균효과를 나타내는 glycopeptide 계 항생물질로서 그람양성세균으로 인한 감염치료에 광범위하게 사용되며, 특히 methicillin 내성 포도상구균의 선택적 치료제로 쓰이고 있다. 그러나 최근 임상검체에서도 중등도의 내성을 가지는 포도상구균 (Mu50: MIC 8 $\mu\textrm{g}$/ml)이 나타나기 시작하였고 여러 가지 여건상 국내에서도 내성균주가 분리될 가능성이 높다고 사료되어 임상검체 중 methcillin 내성 포도상구균을 대상으로 vancomycin 감수성 및 내성빈도 조사를 실시하고 이에 따른 내성기전을 알아보고자 하였다. 본 실험 결과 107주 (株)의 methicillin 내성균주 중 23.3%가 vancomycin에 대하여 내성을 보였으며 vancomycin 내성을 나타내는 표준균주인 Mu50과 Mu3의 중간 정도의 내성빈도를 보였다. 중합효소 연쇄반응을 통해 장구균의 vancomycin 내성에 관여하는 vanA, vanB, vanC1, vanC2, vanH 특이 유전자는 증폭되지 않았다. SDS-PAGE를 실시하여 81 kDa, 58 kDa, 33 kDa, 28 kDa 등의 주요 단백 분획을 확인하였고, Mu50에서 45 kDa의 특징적인 단백 분획을 관찰하였다. LDH enzyme assay에서는 한 개의 검체가 Mu50과 함께 높은 LDH 활성을 보였다.

  • PDF

Streptomyces sp. YB-9가 생산하는 균체외 ${\beta}-galactosidase$의 특성 (Characterization of the Extracellular ${\beta}-Galactosidase$ Produced from Streptomyces sp. YB-9)

  • 이경섭;김창진;윤기홍
    • Applied Biological Chemistry
    • /
    • 제46권4호
    • /
    • pp.299-304
    • /
    • 2003
  • 토양으로부터 lactose의 가수분해를 촉매하는 균체외 ${\beta}-galactosidase$를 생산하는 YB-9가 분리되었다. 분리균 YB-9는 분리균의 배양, 형태, 생리적 특성을 조사한 결과 Streptomyces속 균주로 동정되었다. 분리균의 배양상등액을 ammonium $sulfate(15{\sim}70%)$로 처리하고 투석하여 부분정제된 ${\beta}-galactosidase$$para-nitrophenyl-{\beta}-D-galactopyranoside(pNP-{\beta}Gal)$와 lactose를 기질로 하여 반응특성을 분석하기 위해 조효소액으로 사용하였다. ${\beta}-Galactosidase$는 pH $6.0{\sim}6.5$$60^{\circ}C$에서 최대활성을 보였다. $pNP-{\beta}Gal$과 lactose에 대한 ${\beta}$-galactosidase의 가수분해 활성은 galactose에 의해 감소되었다. Lactose에 대한 가수분해 활성은 glucose에 의해 미미하게 감소하였으나, glucose에 의해 $pNP-{\beta}Gal$에 대한 활성은 1.3배 증가하였다. 특히, xylose에 의한 lactose의 가수분해 활성에는 영향이 없었고, $pNP-{\beta}Gal$에 대한 활성은 1.6배 증가시켰다.

상지에 배양한 상황버섯 균사체로부터 분리된 다당류의 면역증강 효과 (Immune-Enhancing Effects of Polysaccharides Isolated from Phellinus linteus Mycelium on Mori ramulus)

  • 박혜미;홍주헌
    • 한국식품영양과학회지
    • /
    • 제46권1호
    • /
    • pp.26-33
    • /
    • 2017
  • 본 연구에서는 상지에 배양한 상황버섯 균사체 유래 다당류의 기능성 식품 소재로의 활용 가능성을 확인하기 위해 조다당류의 분리 및 정제를 통해 분획을 얻었으며, 다양한 면역증강 효과를 확인하였다. 건조된 조다당류를 DEAE-sepharose CL-6B를 이용하여 크로마토그래피한 후 340 nm에서의 흡광도, 단백질, 당 및 uronic acid 함량을 분석한 결과, 증류수로 용출되는 비흡착 분획(PF-1, 분획번호 3~15)과 흡착된 후 NaCl 용액에 의해 용출되는 분획(PF-2, 분획번호 24~33)을 얻었다. 분획물 PF-1 및 PF-2의 유용성분 함량으로 총당 함량은 각각 75.51%, 52.38%, 총단백질 함량은 1.63%, 8.41%, uronic acid 함량은 17.53%, 15.04% 및 ${\beta}-glucan$ 함량은 28.33%, 25.04%로 나타났다. PF-1 및 PF-2에 대해 대식세포주에 처리하여 세포생존율을 확인한 결과 $100{\mu}g/mL$ 농도까지 유의적으로 세포사멸이 나타나지 않아 세포독성이 없음을 확인할 수 있었다. Nitric oxide 생성량은 PF-1 $100{\mu}g/mL$에서는 nitric oxide 생성량이 $23.11{\mu}M$로 나타나 양성대조군으로 사용된 LPS 100 ng/mL 처리군($30.30{\mu}M$)의 약 76%의 효과가 있는 것으로 확인되었으며, cytokine 생성량($TNF-{\alpha}$ 및 IL-6) 또한 무처리군에 비하여 높은 생성량을 나타내었다. Polymerase chain reaction을 통한 면역 관련 유전자 발현분석 결과, iNOS, COX-2, $TNF-{\alpha}$, IL-6에서 PF-1 분획에서 높은 발현량을 나타내어 면역 증강을 목적으로 한 기능성 식품 개발에 활용 가능하다고 판단된다.

등수국 잎 추출물 유래 항염 및 항균 활성 성분 (Anti-inflammatory and Anti-bacterial Active Ingredients Derived from the Extract of the Leaves of Hydrangea Petiolaris)

  • 조성미;김정은;이남호
    • 대한화장품학회지
    • /
    • 제46권3호
    • /
    • pp.207-218
    • /
    • 2020
  • 본 연구에서는 등수국 잎 추출물의 항염 및 항균 활성을 확인하고 유효성분을 분리하여 화학구조를 동정하였다. RAW 264.7 세포를 이용한 항염 활성 실험 결과, n-hexane (Hex) 및 ethyl acetate (EtOAc) 분획물이 세포 독성 없이 nitric oxide (NO)의 생성 및 iNOS 단백질의 발현을 농도의존적으로 억제시키는 것을 확인하였다. 추가적인 항염 기전 연구 결과, n-Hex 및 EtOAc 분획물이 전염증성 cytokine (TNF-α, IL-1β, IL-6)의 생성을 억제하는 것을 확인하였다. 또한 표피포도상구균과 여드름균을 이용한 활성 실험 결과, 추출물 및 n-Hex, EtOAc, n-butanol (BuOH) 분획물에서 항균 활성이 나타났다. n-Hex 및 EtOAc 분획물의 활성 성분을 규명하기 위해 컬럼 크로마토그래피를 수행하여 4 개의 화합물을 분리하였다; phytol (1), corosolic acid (2), asiatic acid (3) 및 1-O-p-coumaroyl-β-D-glucopyranoside (4). 이들 화합물은 모두 등수국에서 처음으로 분리된 물질이다. 또한 HPLC 분석을 통해 등수국 잎 추출물에서 분리된 화합물의 함량을 측정한 결과 phytol (1) 이 27.8 mg/g 함유되어 있는 것으로 확인되었다. 이상의 연구 결과를 바탕으로 등수국 잎 추출물을 이용한 항염 및 항균 효과를 갖는 천연 화장품 소재로의 개발이 가능할 것이라 사료된다.

Identification of Genes Involved in Primordial-primary Follicle Transition by Suppression Subtractive Hybridization

  • Park, Chang-Eun;Yoon, Se-Jin;Jeon, Eun-Hyun;Kim, Young-Hoon;Lee, Sook-Hwan;Lee, Kyung-Ah
    • 한국수정란이식학회:학술대회논문집
    • /
    • 한국수정란이식학회 2002년도 국제심포지엄
    • /
    • pp.98-98
    • /
    • 2002
  • Recruitment of primordial follicles(PMF) is crucial for female fertility. however, factors and mechanisms that regulate this process is poorly understood. The present study was conducted to obtain an inclusive view of the gene expression and to identify novel factors and their pathways of regulating PMF arrest and/or growth initiation. Ovaries from one-day neonatal(consists of oocyte and PMF) and five-day old(consists of PMF and primary follicles, PRIF) mice were collected, either total RNA or mRNA was isolated, and suppression subtractive hybridization(SSH) was used to isolate and clone genes that differentially expressed in day 1 and day 5 ovaries. Confirmation that some of these genes are differentially expressed in PMF and/or in PRIF was accomplished by using laser captured microdissection(LCM), RT-PCR. in situ hybridization(ISH) and/or immunohistochemistry(IHC). In toto, 357 clones were sequenced and analyzed by BLAST and RIKEN program. Sequences of 330 clones significantly matched database entries while 27 clones were novel. Forty-two and 47 different genes were identified as differentially expressed in day 1 and day 5 ovaries, respectively, while 7 genes were expressed in both stages of ovaries. Day 5-subtracted library included several genes known as markers far growing follicles, such as ZP2, MATER, and fetuin. Among the genes with assigned functions, 23.8% was associated with cell cycle/apoptosis regulation, 7.1% with cellular structure, 11.9% with metabolism, 26.2% with signal transduction, and 31.0% with gene/protein expression in day 1; while 10.6%, 17.0%, 23.5%, 25.5%, and 23.4% in day 5, respectively. Genes such as GDF-8, Lats2, Septin2, and Weel were the highly expressed genes in PMF, while HSP84, Laminin2, MATER, MTi7, PTP, and Wrn were highly expressed genes in PRIF. We have successfully discovered list of genes expressed in day 1 and day 5 ovaries and confirmed that some of them are differentially expressed in PMF and/or PRIF. Gene expression profile from the present study would provide insight for the future study on the mechanism(s) involved in primordial-primary follicular transition. This work was Supported by Korean Health 21 RND Project, Ministry of Health and Welfare, Korea (01-PJ10-PG6-01GN13-0002).

  • PDF