• 제목/요약/키워드: Ion exchange chromatography(IEC)

검색결과 9건 처리시간 0.025초

양이온 교환 크로마토그래피와 HPLC에서의 L-arabinose와 D-ribose의 분리 및 등온 흡착곡선 결정 (Determination of Adsorption Isotherms and Separation of L-arabinose and D-ribose in Cation Exchange Chromatography and HPLC)

  • 전영주;김인호
    • KSBB Journal
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    • 제23권1호
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    • pp.31-36
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    • 2008
  • The use of L-carbohydrates and their corresponding nucleosides in medicinal application has greatly increased. For example L-ribose has been much in demand as the starting material for curing hepatitis B. High performance liquid chromatography (HPLC) method was studied for the analysis of ribose and arabinose fractions from ion exchange chromatography (IEC). Dowex Monosphere 99 Ca/320 resin was packed in IEC to separate ribose and arabinose under various operating conditions. $NH_{2}$ and sugar HPLC columns were then used to analyze the fractions from the IEC column. Pulse input method (PIM) was also used to measure adsorption isotherms of ribose and arabinose in the Dowex column and HPLC columns. Experimental results and simulations by ASPEN chromatography were compared with fair agreement.

참치자숙액 추출물 중의 히스티딘계 저분자 펩타이드 및 산화촉진물질 함량에 미치는 추출방법의 영향 (Effects of Extraction Method on the Histidine Containing Low Molecular Weight Peptide and Pro-oxidants Contents of Tuna Boiled Extracts)

  • 강옥주
    • 한국식품조리과학회지
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    • 제24권3호
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    • pp.349-357
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    • 2008
  • In an effort to augment extractability of carnosine and anserine at the levels of pro-oxidants such as iron and protein in Tuna boiled extracts(Skipjack, Yellowfin and Bigeye), we assessed the effects of heated and ion exchange chromatography(IEC) and ultrafiltration(UF) using a MW 500 cut-off(500 MWCO). We also evaluated the antioxidant activity of these extracts processed as free radical scavengers and reducing agents. Tuna boiled extracts of dark and ordinary muscle protein and total iron were reduced, whereas carnosine and anserine concentrations and antioxidant activity were increased. The carnosine and anserine concentrations of the ion exchange and permeate UF(IEC-UF) extracts were higher than those observed in the heated and permeate UF(heat-UF), whereas the protein and total iron contents were lower than that observed in the heat-UF. The quantity of carnosine and anserine in ordinary muscle was higher than that detected in dark muscle. HPLC analysis and SDS-PAGE were shown to removes the effect of UF on high molecular weight impurities in the tuna boiled extracts. The major free amino acids(FFAs) from Skipjack, Yellowfin and Bigeye tuna IEC-UF extracts were anserine, histidine and carnosine. These three peptides constituted more than 80~85%. of the detected amino acid. The IEC-UF treated ordinary muscle extracts evidenced the highest levels of DPPH radical scavenging activity and the highest levels of reducing power among the various extracts. The IEC-UF extracts evidenced a DPPH radical scavenging effect equal to that of 1mM ascorbic acid.

다랑어(Thunnus) 추출물 중의 Histidine 함유 저분자 펩타이드 및 산화촉진물질 함량에 미치는 추출방법의 영향 (Effects of Extraction Methods on Histidine-containing Low-molecular Weight Peptides and Pro-oxidants Contents in Tuna Thunnus Extracts)

  • 김홍길;송호수
    • 한국수산과학회지
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    • 제50권6호
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    • pp.684-693
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    • 2017
  • We investigated methods for extracting histidine-containing low-molecular-weight (LMW) peptides such as anserine, carnosine and histidine from the edible meat of tuna byproducts. Extracts were treated by several methods including heat treatment ($80^{\circ}C$, 10 min), DOWEX ion exchange (IEC), ultrafiltration (UF), and carboxymethyl (CM)-cellulose column chromatography (IEC+CMC); then the levels of protein, total iron, histidine, carnosine, and anserine were measured. Extracts treated with IEC+CMC using CM-cellulose were analyzed for total iron, protein, histidine, and anserine content, which were $6.27{\pm}0.26mg/mL$, $5.20{\pm}0.21{\mu}g/mL$, 0.80 mg/mL, 0.208 mg/mL, and 4.40 mg/mL, respectively, in yellowfin tuna; and $9.05{\pm}0.82mg/mL$, $4.06{\pm}0.20{\mu}g/mL$, 1.62 mg/mL, 0.012 mg/mL, and 7.28 mg/mL in bigeye tuna. By comparison in IEC-UF treated extracts, protein, total iron, and histidine content decreased by 43%, 73%, and 27% in yellowfin and 0.4%, 54%, and 23% in bigeye tuna, wheres carnosine and anserine content increased by 22% and 17%, respectively. Freeze-dried (FD) extracts exhibited similar trends as non-dried extracts, i.e., dipeptide content increased with purification steps, whereas pro-oxidant (total iron and protein) content decreased. IEC+CMC treated FD extracts had the highest anserine, content, and the greatest reductuion in pro-oxidants.

Purification of fusion ferritin using silica powder and DEAE chromatography

  • 허윤석;김성규;정은미;김인호
    • 한국생물공학회:학술대회논문집
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    • 한국생물공학회 2002년도 생물공학의 동향 (X)
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    • pp.510-513
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    • 2002
  • Iron is an essential nutrient for most organisms, which supplied to them in a protein-iron complex known as ferritin. Ferritins are multimeric proteins those are consisted of spherical shell of 24 subunits defining a cavity of about 8nm in diameter. Soluble form of ferritin was separated from disrupted cells, followed by silica powder adsorption. Ferritin was recovered from silica-poweder by distiiled water, which was applied to DEAE anion exchage chromatography. Collected fractions from the DEAE column were assayed to gain the amount and the purity of ferritin by using GF-HPLC.

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Fractionation and Enzymatic Characterization of Endoprotease and Exopeptidase from Crude Extracts of Cuttlefish Sepia officinalis Hepatopancreas

  • Kim, Min Ji;Kim, Hyeon Jeong;Kim, Ki Hyun;Heu, Min Soo;Lee, Jung Suck;Kim, Jin-Soo
    • Fisheries and Aquatic Sciences
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    • 제15권4호
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    • pp.283-291
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    • 2012
  • This study examines the optimal fractionation method and conditions for the isolation of endoprotease- and exopeptidase-active fractions from crude extracts of cuttlefish hepatopancreas (HP) using four fractionation methods: ammonium sulfate fractionation (ASF), polyethylene glycol fractionation (PGF), ion exchange chromatography (IEC), and gel filtration chromatography (GFC). Total endoprotease activity highest in the fraction II (concentrate of fractions 34-42; 842.60 U) of GFC, followed by fraction III (40-60% ammonium sulfate fraction; 670.25 U) of ASF, fraction I (concentrate of fractions 8-12; 436.89 U) of IEC, and fraction II (10-20% polyethylene glycol; 307.31 U) of PGF. Total exopeptidase activity of these fractions was highest in fraction II (2,704.70 U) of GFC, fraction III (2,110.50 U) of ASF, fraction III (1,605.60 U) of PGF, and fraction II (concentrate of fractions 38-44; 1,196.22 U) of IEC. These results showed that fraction II of GFC had the highest activity toward both exopeptidase and endoprotease, with exopeptidase activity being 3.21 times higher than of endoprotease. These results suggest cuttlefish HP could be used as a potential source for the extraction of exopeptidase, an enzyme capable of catalyzing the cleavage of N- and C-terminal amino acids in polypeptides, Like endoprotease, the most efficient method for separating exopeptide-active fractions was GFC.

고분자전해질 막을 위한 나프탈렌 단위를 포함하는 디 및 트리 블록공중합체의 합성 및 특성분석 (Synthesis and Characterization of Di and Triblock Copolymers Containing a Naphthalene Unit for Polymer Electrolyte Membranes)

  • 김애란
    • 한국수소및신에너지학회논문집
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    • 제27권6호
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    • pp.660-669
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    • 2016
  • A fluorinated-sulfonated, hydrophobic-hydrophilic copolymer was planed subsequently synthesized using typical nucleophilic substitution polycondensation reaction. A novel AB and ABA (or BAB) block copolymers were synthesized using sBCPSBP (sulfonated 4,4'-bis[4-chlorophenyl)sulfonyl]-1,1'-biphenyl), DHN (1,5-dihydroxynaphthalene), DFBP (decafluorobiphenyl) and HFIP (4,4'-hexafluoroisopropylidenediphenol). All block copolymers were easily cast and made into clear films. The structure and synthesized copolymers and corresponding membranes were analyzed using GPC (gel permeation chromatography), $^1H$-NMR ($^1H$ nuclear magnetic resonance) and FT-IR (Fourier transform infrared). TGA (Thermogravimetric analysis) and DSC (differential scanning calorimetry) analysis showed that the prepared membranes were thermally stable, so that elevated temperature fuel cell operation would be possible. Hydrophobic/hydrophilic phase separation and clear ionic aggregate block morpology was confirmed in both triblock and diblock copolymer in AFM (atomic force microscopy), which may be highly related to their proton transport ability. A sulfonated BAB triblock copolymer membrane with an ion-exchange capacity (IEC) of 0.6 meq/g has a maximum ion conductivity of 40.3 mS/cm at $90^{\circ}C$ and 100% relative humidity.

뱀장어(Anguilla japonica) 추출 Carnosine이 과산화수소로 유도된 인체 백혈구의 DNA 손상과 Repair에 미치는 효과 (The Effect of Carnosine Extracted from Eels Anguilla japonica on Oxidative DNA Damage Induced by Hydrogen Peroxide and the DNA Repair Capacity of Human Leukocytes)

  • 송호수
    • 한국수산과학회지
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    • 제50권5호
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    • pp.520-526
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    • 2017
  • Carnosine was recently reported to protect against the DNA damage induced by oxidative stress. In this study, we investigated the protective effect of eel Anguilla japonica carnosine extracts prepared using different methods (heat treatment extracts, HTEs; ion exchange chromatography, IEC; ultrafiltration permeation, UFP) on leukocyte DNA damage using the comet assay. Human leukocytes were incubated with extracts of eel carnosine at concentrations (of 10, 50, $100{\mu}g/mL$), and then subjected to an oxidative stimulus [$200{\mu}M$ hydrogen peroxide ($H_2O_2$)]. Pretreatment of the cells for 30 min with carnosine significantly reduced the genotoxicity of $H_2O_2$ measured as DNA strand breaks. The protective effects of the three types of extract (HTE, IEC, and UFP) increased with concentration. At the highest concentration (100 g/mL). there were no statistical differences in oxidative damage between each extract treatment and PBS-treated negative controls. When leukocytes were incubated with carnosine for 30 min after exposure to $H_2O_2$. the protective ability of each extract changed. Therefore, eel carnosine inhibits the $H_2O_2$ induced damage to cellular DNA in human leukocytes, supporting the protective effect of this compound against oxidative damage.

연어(Oncorhynchus keta) 추출 anserine의 항산화 효과 (Antioxidant Effect of Anserine Extracted from Salmon (Oncorhynchus keta))

  • 민혜옥;송호수
    • 한국식품위생안전성학회지
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    • 제34권4호
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    • pp.396-403
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    • 2019
  • 연어로부터 추출한 anserine의 항산화능 평가를 위해 1차 이온교환 후 한외여과 및 2차 이온교환 추출물인 IEC-B 실험구와 합성 anserine, ${\beta}-alanine$, 1-methylhistidine, taurine, ascorbic acid, BHT를 대조구로 DPPH 라디칼 소거능, 환원력, 금속 킬레이트능, SOD 유사활성 실험을 하였다. DPPH 라디칼 소거능 결과 대조구와 anserine 모두 농도 증가에 따라 라디칼 소거능이 증가하였으며 BHT가 가장 높은 소거능을 나타냈다. 합성 anserine은 농도 증가에 따라 $9.30{\pm}0.65{\sim}28.23{\pm}0.24%$를 나타냈으며 연어 추출 anserine인 IEC-B 추출물은 $7.30{\pm}1.13{\sim}31.05{\pm}0.17%$를 나타내 BHT, ascorbic acid에 비해 소거능이 낮으나 두 실험구와 비교했을 때 약 37%, 49% 정도의 소거능을 나타냈다. 환원력 또한 첨가농도에 따라 증가하였으며 BHT와 ascorbic acid가 높은 환원력을 나타냈고, 그 외 실험구 중에서는 합성 anserine과 연어 추출 anserine인 IEC-B 실험구가 높았으며 유의적으로 동일한 환원력을 나타냈다. 금속 킬레이트능은 BHT, ascorbic acid 순으로 높았으며 합성 anserine과 연어 추출 anserine의 경우 ascorbic acid와 유사한 금속 킬레이트능을 나타냈다. 또한 SOD 유사활성에서는 연어 추출 anserine이 BHT와 ascorbic acid에 비해 낮았으나 농도 증가에 따라 증가하는 경향을 나타내었으며, 합성 anserine, 연어 추출 anserine, ascorbic acid, BHT를 이용하여 과산화물가와 TBARS를 실험하였다. 저장기간 중 linoleic acid의 과산화물가는 큰 폭으로 증가한 반면 연어 추출 anserine을 첨가한 경우 과산화물가의 증가가 억제되는 경향이 나타났으며, 이는 TBARS 실험 결과와 유사한 경향을 나타냈다.

Bacillus subtilis MJP1이 생산하는 항세균 물질의 분리.정제 및 특성규명 (Purification and Characterization of Antibacterial Compound Produced by Bacillus subtilis MJP1)

  • 임은정;양은주;장해춘
    • 한국미생물·생명공학회지
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    • 제38권1호
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    • pp.84-92
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    • 2010
  • B. subtilis MJP1이 생산하는 항균물질을 분리 정제하기 위하여 SPE, IEC, GFC를 통한 정제를 수행하였다. 정제된 항세균 물질은 tricine SDS-PAGE에서 하나의 band임을 확인 한 후 N-말단 아미노산 서열분석을 하였으나 N-말단이 blocking 되어 그 서열을 분석할 수 없였다. 이에 그 내부서열을 알아보기 위한 LC를 이용한 ESI-MS/MS를 시행하였으나 내부서열도 확인할 수 없었고, UPLC를 이용한 ESI-MS/MS를 시행한 결과 항세균 활성 물질은 분자량이 매우 유사한 2개의 peptide(3356.54 Da, 3400.5244 Da)가 존재함을 확인하였다. 정제된 항세균 물질의 항균 spectrum을 조사한 결과, L. monocytogenes에 가장 강한 항균활성을 나타내며 이외에 B. subtilis, S. aureus subsp. aureus, E. faecalis 등의 Gram 양성균에서 항균활성을 나타내였다. 정제된 B. subtilis 항세균 물질은 pH 3.0부터 pH 9.0 범위에서는 안정하였으며 $4^{\circ}C$, $30^{\circ}C$, $50^{\circ}C$에서 24시간, $100^{\circ}C$에서 5분 동안 매우 안정하였고, $70^{\circ}C$에서 24 시간, $100^{\circ}C$에서 30분 동안 처리한 구간부터 역가가 감소하여 $121^{\circ}C$에서 15분 동안 처리한 구간에서는 역가가 완전히 소실되었다. 효소 안정성 실험에서 정제된 항세균 물질은 일부 단백분해효소에 의해 분해되어 역가를 상실하였으며, lipase나 $\alpha$-amylase에서는 안정함을 나타냈다. 이로부터 정제된 항세균 물질이 넓은 pH 범위에서 안정하고, 비교적 높은 온도에서도 활성을 유지한다는 점을 관찰할 수 있었으며, 단백분해효소에 의해 분해되므로 bacteriocin임을 확인하였다. 본 연구를 통하여 B. subtilis MJP1으로부터 분리 정제된 bacteriocin은 class IIa군의 특성과 유사하며, B. subtilis MJP1은 본 분리 bacteriocin 이외에도 다른 항세균 물질과 항진균 물질을 생산하는 균주임을 알 수 있었다.