• Title/Summary/Keyword: 반점화

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Reduction of Antigenicity of Bovine Casein by Microbial Enzymes (미생물효소에 의한 우유 casein의 항원성 저감화)

  • Choe, Hyeon-Seok;Ahn, Jong-Nam;Jeong, Seok-Geun;Ham, Jun-Sang;In, Yeong-Min;Kim, Dong-Un
    • Journal of Dairy Science and Biotechnology
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    • v.21 no.2
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    • pp.97-104
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    • 2003
  • It is extremely important to destroy the antigenicity of milk proteins for dietetic treatment of infants with milk allergy. Enzymatic digestion of milk protein is not only effective for destroying antigenicity, but it also is less liable to alter the nutritive value. Bovine casein was hydrolyzed with eight different commercial proteases derived from bacterias or fungi, either individually or in combination to eliminate protein allergenicity. The average molecular weight of casein hyrdolysates determined by size exclusion chromatography is about 550${\sim}$2,300 dalton range. Antigenicity of the casein hyrdolysates was not detected by heterologous passive cutaneous anaphylaxis in guinea pig-rabbit antiserum system. The inhibition test on the enzyme-linked immunosorbent assay(ELISA) showed that the antigenicity of casein hydrolysates is lowed up to 1/8,000 than that of intact bovine casein. As the enzyme reaction was carried out by the combination of bacterial and fungal protease, casein hydrolysates showed much lower bitterness and antigenicity. It suggests that these hydrolysates will be applied to many kinds of foods including the development of hypo-allergenic infant formula.

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The Crystal and Molecular Structure of Niclosamide monohydrate, $C_{13}H_8Cl_2N_2O_4\cdotH_2O$ (Niclosamide monohydrate, $C_{13}H_8Cl_2N_2O_4\cdotH_2O$의 결정 및 분자구조)

  • 김의성;신현소
    • Korean Journal of Crystallography
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    • v.4 no.1
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    • pp.1-5
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    • 1993
  • The crystal structure of N-(2'-chloro-4'-vitrophenyl)-5-chlorosalicylamide( Niclosamide ) monohydrate has been determined from 1976 sig- nificant independent reflections collected on an automated CAD4 diffractometer using graphitemonochromated Mo-Ka radiation. The crystal is monoclinic, space group P211c, with unit cell dimensions, a=11.331 (3), b=16.964(2), c=7.347(4)A , P =98.20(3)° and Z=4 at T=293k. The structure was solved by direct method using seminvariants of ggg Parity group and refined by the full-matrix least-square method, resulting model with reliability factor, R=0.046. The feature of the molecule show planar structure in parallel to the ab crystal plane.

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Development of watermark free drying process on hydrophobic wafer surface for single wafer process tool

  • Im, Jeong-Su;Choe, Seung-Ju;Seong, Bo-Ram-Chan;Gu, Gyo-Uk;Jo, Jung-Geun
    • Proceedings of the Korean Society Of Semiconductor Equipment Technology
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    • 2007.06a
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    • pp.19-22
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    • 2007
  • 반도체 산업은 회로의 고밀도화, 고집적화에 따라 웨이퍼 표면의 입자, 금속, 금속 이온, 유기물 등 오염물의 크기가 미세해 지고 세정에 대한 요구 조건이 더욱 엄격해지고 있다. 현재 세정 공정은 반도체 제조공정 전체에서 약 30%를 차지하고 있으며, 습식 세정 방식이 주로 사용되고 있다.[1] 습식 세정방식은 탈이온수로 린스하고 건조하는 공정이 필연적으로 따르며, 기판 표면에 건조과정에서 물반점이 남는 문제가 가장 큰 이슈로 남아 있다. 본 연구는 웨이퍼의 습식 세정 공정에 사용되는 DHF Final Clean Process후 IPA Vapor를 이용한 건조 방법을 기술 하였다. Single wafer spin process를 이용하였으며, 웨이퍼 Process 공간을 밀폐 후 N2가스를 충진하여 대기중의 산소 오염원 유입을 차단하고 수세 및 건조 가스를 이용하여 건조시킴으로써 SiFx의 SiOx로의 치환을 방지 하여 건조 효율 향상을 목적으로 한다. Bare 웨이퍼에서 65nm 이상 오염 발생 증가량을 측정 하였으며, 공정 후 웨이퍼 오염 발생량을 35개 이하로 확보 하였다.

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First Record of a Bandfish, Acanthocepola indica (Cepolidae: Perciformes) from Korea (한국산 농어목(Perciformes) 홍갈치과(Cepolidae) 어류 1 미기록종, Acanthocepola indica)

  • Park, Jeong-Ho;Ryu, Jung Hwa;Lee, Jun Mo;Kim, Jin Koo
    • Korean Journal of Ichthyology
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    • v.20 no.3
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    • pp.220-223
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    • 2008
  • A single specimen (220.4 mm SL) of the bandfish Acanthocepola indica was collected near Maemul Island, off southeastern Korea. This species is characterized by having a serrated posterior margin of preopercle and a black blotch on anterior part of dorsal fin. It differs from two other species, A. limbata and A. krusensternii, in having a deeper body, 88 dorsal fin rays, and 101 anal fin rays. Our specimen of A. indica is the first record of the species from Korea, for which we propose the new Korean name "Nam-bang-hong-gal-chi."

A new variety of Hosta (Liliaceae): Hosta clausa var. geumgangensis M. Kim & H. Jo (비비추속(백합과)의 신변종: 금강비비추(Hosta clausa var. geumgangensis M. Kim & H. Jo))

  • Jo, Hyun;Kim, Muyeol
    • Korean Journal of Plant Taxonomy
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    • v.46 no.3
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    • pp.306-313
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    • 2016
  • A new variety, Hosta clausa Nakai var. geumgangensis M. Kim & H. Jo, was found in Geumgang River in Korea. This variety shares several characteristics (rhizomes with underground stolon, smooth scape and purple-colored anthers) with the $re{\acute{o}}lated$ varieties H. clausa Nakai var. clausa and H. clausa var. normalis F. Maekawa. However, H. clausa var. normalis has open flowers, capsules with seeds, purple-spotted petioles, long pistils, and long narrow perianth tubes, whereas this new variety has open flowers, seedless capsules, green-colored petioles, short pistils, and short narrow perianth tubes. Hosta clausa Nakai var. clausa has closed flowers and seedless capsules.

Analysis on the Components of Brown Spot occurred in the Papers (지류에 발생하는 얼룩반점의 성분분석에 관하여)

  • Park, Seh-Youn;Lee, Kyu-Shik;Han, Sung-Hee;Ahn, Hee-Kyun
    • 보존과학연구
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    • s.13
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    • pp.81-95
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    • 1992
  • The old books which have been colored to brown spots were analyzed chemically to compare with white part. The original raw materials were paper mulberry (Broussonetia Kazine) and woodpulp. White part contained58.8%($\alpha$-37.2%,$\beta$-8.6%, $\gamma$-12.7%)cellulose, 21.7% hemicellulose, 19.8% lignin,4.4% pentosan and brown sopt part contained 49.1%($\alpha$-19.8%, $\beta$-14.5%,$\gamma$-14.8%) cellulose, 27.1% hemicellulose, 23.8% lignin, 4.8% pentosan. Both of brown spot and white parts contained starch without protein. The pH was 4.9 in brown and 5.0 in white part respecitively. The brown spot parts were more solidified than white parts according to SEM observation. Difference of organiccompinent in brown part came from white part were 2-hydroxy-benzaldehydeand phenol.

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Synthesis and Structure of [Cu(L)](ClO4)2 (L;3,5,10,12-Tetramethyl-1,4,8,11-tetraazacyclotetradecane) ([Cu(L)](ClO4)2 (L:3,5,10-12-Tetramethyl-1,4,8,11-tetraazacyclotetradecane) 착물의 합성 및 구조)

  • 최기영;홍청표
    • Korean Journal of Crystallography
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    • v.9 no.1
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    • pp.6-10
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    • 1998
  • The complex[Cu(L)](ClO4)2 (1) (L:3,5,10,12-Tetramethyl-1,4,8,11-tetraazacyclotetradecane) has been synthesized and structurally characterized. The complex 1 crystallizes in the monoclinic system, space group P21/n with cell parameters a=8.208(2)Å, b=13.339(6) Å, c=10.752(5) Å, β=111.02(4)˚ Z=2. Least-squares refinement of 1 led to a R(RW)factor of 0.073 (0.142) for 617 observed reflections of F0>40(F0). The crystal structure of 1 has a square-planar geometry and adopts the trans-III conformation.

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Crystal Structure of Macrocyclic Tetraamine Thiocyanate Copper(II) Complex (거대고리 Tetraamine Thiocyanate Copper(II) 착물의 결정구조)

  • Choe, Gi-Yeong;Kim, Chang-Seok;Seo, Il-Hwan
    • Korean Journal of Crystallography
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    • v.9 no.1
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    • pp.11-14
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    • 1998
  • The synthesis and characterization of [Cu(L)](NCS)2 (1) (L:2,5,9,12-Tetramethyl-1,4,8,11-tetraazacyclotetradecane) are described. Crystal structure of 1 crystallizes in the monoclinic system, space group P21/a, a=7.622(2)Å, b=17.645(2) Å, c=8.223(3) Å, β=109.99(2)˚ Z=2. Least-squares refinement of 1 led to a R(Rw) factor of 0.087 (0.158) for 1535 observed reflections of F0>40(F0). The complex 1 has a square planar geometry with average Cu-N (secondary amines) bond distance of 2.030(4)Å. The axially disposed thiocyanate anions are not coordinated with Cu-N distances of 2.842(7) Å.

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Crystal Structure of Three-Dimensional Nickel(II) Tetraaza Macrocyclic Complex Linked by Hydrogen-Bonds (수소 결합에 의한 이차원의 Nickel(II) Tetraaza 거대 고리 착물 결합구조)

  • Park, Ki-Young;Choo, Geum-Hong;Suh, Il-Hwan
    • Korean Journal of Crystallography
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    • v.13 no.1
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    • pp.12-16
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    • 2002
  • The complex [Ni(L)](BDC)·4H₂O (1) (L = 3,14-dimethyl-2,6,13,17-tetraazatricyclo[16,4,O/sup 1.18/,O/sup 7.12/] docosane; BDC = 1,3-benzenedicarboxylate) has been synthesized and characterized by X-ray crystallography. Compound 1 crystallizes in the orthorhombic space group Pcnb, with a = 8.764(2) , b = 17.687(2) , c = 19.475(1) , V = 3018.7(8) ³, Z = 4, R₁, (wR₂) for 2148 observed reflections of [1>2σ(I) was 0.0822 (0.2236). Compound 1 is interconnected to give a three-dimensional network through weak hydrogen-bonding interactions.

Crystal Structure of Two-Dimensional Bis(isonicotinato)tet-raaquazinc(II) Complex Linked by Hydrogen-Bonds (수소 결합에 의한 이차원의 Bis(isonicotinato)tetraaquazinc(II) 착물의 결정구조)

  • Park, Ki-Young;Kim, Moon-Jip;Suh, Il-Hwan
    • Korean Journal of Crystallography
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    • v.13 no.1
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    • pp.17-20
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    • 2002
  • The complex [Zn(L)₂(H₂O)₄] (1) (L = isonicotinate) has been prepared and characterized by X-ray crystallography. Compound 1 crystallizes in the triclinic space group P1, with a = 6.9062(4) , b = 9.2618(7) , c = 6.3313(3) , α = 104.986(6)°, β = 112.865(4)°, γ = 96.213(6)°, V = 350.41(4) , Z = 1, R₁(wR₂) for 1225 observed reflections of [I > 2σ(I)] was 0.0209 (0.0591). The coordination environment of the zinc atom can be described as an octahedron in which the isonicotinato ligands are mutually trans. Compound 1 is also connected into a two-dimensional chain via hydrogen-bonds.