• Molecules and Cells
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• 제19권1호
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• pp.97-103
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• 2005

The role of residue C323 in catalysis by human glutamate dehydrogenase isozymes (hGDH1 and hGDH2) was examined by substituting Arg, Gly, Leu, Met, or Tyr at C323 by cassette mutagenesis using synthetic human GDH isozyme genes. As a result, the $K_m$ of the enzyme for NADH and ${\alpha}-ketoglutarate$ increased up to 1.6-fold and 1.1-fold, respectively. It seems likely that C323 is not responsible for substrate-binding or coenzyme-binding. The efficiency ($k_{cat}/K_m$) of the mutant enzymes was only 11-14% of that of the wild-type isozymes, mainly due to a decrease in $k_{cat}$ values. There was a linear relationship between incorporation of [$^{14}C$]p-chloromercuribenzoic acid and loss of enzyme activity that extrapolated to a stoichiometry of one mol of [$^{14}C$] incorporated per mol of monomer for wild type hGDHs. No incorporation of [$^{14}C$]p-chloromercuribenzoic acid was observed with the C323 mutants. ADP and GTP had no effect on the binding of p-chloromercuribenzoic acid, suggesting that C323 is not directly involved in allosteric regulation. There were no differences between the two hGDH isozymes in sensitivities to mutagenesis at C323. Our results suggest that C323 plays an important role in catalysis by human GDH isozymes.

• Bulletin of the Korean Chemical Society
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• 제25권12호
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• pp.1881-1888
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• 2004

A series of $NiO-TiO_2$/$WO_3$ catalysts was prepared by drying powdered $Ni(OH)_2-Ti(OH)_4$ with ammonium metatungstate aqueous solution, followed by calcining in air at high temperature. Characterization of prepared catalysts was performed by using FTIR, Raman, XPS, XRD, and DSC and by measuring surface area. Upon the addition of tungsten oxide to titania up to 25 wt%, the specific surface area and acidity of catalysts increased in proportion to the tungsten oxide content due to the interaction between tungsten oxide and titania. Since the -$TiO_2$/stabilizes the tungsten oxide species, for the samples equal to or less than 25 wt%, tungsten oxide was well dispersed on the surface of titania, but for the samples containing above 25 wt%, the triclinic phase of $WO_3$ was observed at calcination temperature above 400 $^{\circ}C$. The catalytic activities of 10-NiO-$TiO_2$/$WO_3$ for 2-propanol dehydration and cumene dealkylation were correlated with the acidity of catalysts measured by ammonia chemisorption method. NiO may attract reactants and enhance the local concentration of reactants near the acid sites, consequently showing the increased catalytic activities.

• Bulletin of the Korean Chemical Society
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• 제30권4호
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• pp.917-923
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• 2009

The maize lipoxgyenase-1 is a non-traditional dual positional specific enzyme and the reaction proceeds via enzyme-initiated catalysis. Bioinformatic analysis indicated that the maize lipoxygenase-1 is structurally more similar to soybean LOX1 than pea LOXN2 in that it has an additional external loop (residues 318-351) in the carboxy-terminal catalytic domain. We analyzed the dependence of product distribution on concentration of linoleic acid and monitored the formation of hydroperoxyoctadecadienoic acid as a function of enzyme concentration. Product distribution was strongly influenced by substrate concentration, such that kinetically-controlled regioisomers were enriched and thermodynamically-controlled regioisomers were depleted at high substrate concentration. Kinetic studies indicated that the formation of hydroperoxyoctadecadienoic acid saturated rapidly in an enzyme concentration-dependent manner, which implied that reactivation by reoxidation of inactive Fe(II) failed to occur. Our results support the previously proposed enzyme-initiated catalytic mechanism of the maize lipoxgyenase-1 and reveals that a substrate molecule serves as a hydrogen atom donor in its enzyme-initiated catalysis.

• 공업화학
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• 제10권1호
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• pp.154-159
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• 1999

수중 금속이온 착화용 공업세정제를 비롯하여 산업적으로 다양한 용도로 폭넓게 사용되고 있는 EDTA (ethylenediaminetetraacetic acid)는 수처리시 금속이온들을 제거할 경우에 방해요인으로 작용하므로, EDTA를 우선적으로 분해하여 착화결합을 끊어야 금속이온들의 제거가 용이해진다. 본 연구에서는, $TiO_2$ (Degussa P-25)를 사용하여 1.79 mM의 초기 Cu(II)-EDTA 수용액 농도와 $20^{\circ}C$의 호기성 분위기 하에서, 촉매의 양과 초기의 수용액 pH가 Cu(II)-EDTA 착물의 산화에 미치는 영향을 고찰하였다. $TiO_2$량이 2.0 g/L일 경우에 EDTA, Cu와 TOC 감소율이 최대로 나타났고, DETA의 촉매표면 흡착은 $TiO_2$ 표면전하에 의해 영향을 받으며 광-촉매 반응에 의한 EDTA의 분해는 광-조사전의 촉매표면 흡착에 의존하는 것으로 보였다.

• Bulletin of the Korean Chemical Society
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• 제18권2호
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• pp.203-208
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• 1997

A series of MgO-SiO2 catalysts were prepared by coprecipitation from the mixed solution of magnesium chloride and sodium silicate. Some of the sample were modified with 1 N H2SO4 and used as modified catalysts. The addition of MgO to SiO2 caused the increase of acidity and the shift of O-H and Si-O stretching bands of the silanol group to a lower frequency in proportion to the MgO content. The acid structure of MgO-SiO2 agreed with that proposed by Tanabe et al.. Catalytic activity for 2-propanol dehydration increased in relation to the increase of acidity and band shift to a lower frequency.

• 한국미생물·생명공학회지
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• 제31권2호
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• pp.140-144
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• 2003

신호펩디드 가수분해는 모든 생물에 필수적인 단백질로 N-말단에 신호서열을 가진 단백질들의 신호서열을 잘라내는 효소로 serine과 lysine을 활성부위로 하는 특이한 dyad serine 효소류로 알려져있다. 최근에 신호펩디드 가수분해효소의 특성으로 새로운 항생제 이용 가능성 때문에 그 활성 메카니즘의 연구가 중요시되고 있다. 본 연구는 E. coli 신호펩디드 효소가 serine/lysine/aspartic acid로 하는 전형적인 triad serine 효소류의 메카니즘을 갖는다는 가정하에 Type Ⅰ 신호펩디드류의 하나인 E. coli에서 aspartic acid 99을 alanine으로 치환하여 효소의 enzymatic activity를 조사하였다. 그 결과 D99잔기는 E. coli Type Ⅰ 신호펩디드 효소의 활성메카니즘에 직접적으로 관여한다기보다는 그 효소를 구조적으로 안정화하는데 중요한 역할을 할 가능성이 있는 것으로 암시되어진다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2016년도 제50회 동계 정기학술대회 초록집
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• pp.128.2-128.2
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• 2016

본 발표에서는 DFT를 사용하여 개미산으로부터 수소 생산용 Pd 기반 합금 촉매의 합리적 설계를 다룰 것이다. 특히, 합금 촉매 효과 [ligand (electronic) 및 strain effect)]가 어떻게 개미산으로부터 수소 생산의 반응성과 선택도에 영향을 미칠 수 있는지를 조사하였다. 이러한 결과는 높은 촉매 성능을 달성하기 위해서 다성분 촉매의 표면 활성을 타당하게 제어하는 것이 얼마는 중요한지를 보여준다 [J. Phys. Chem. C, 118, 22254-22560 (2014), J. Nanosci. and Nanotech., 15, 8233-8237 (2015), ACS Catalysis 6 (1), 134-142 (2016)].

• 한국세라믹학회지
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• 제25권5호
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• pp.425-430
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• 1988

In this study, aluminum sec-butoxide, aluminum iso-propoxide were mixed with alcohol such as, secbutanol, iso-propanol. And then Acetyl Acetone, water were added to make Acetyl bond and OH bond. After that, Polymeric alumina sol was synthesized from catalysis reaction with strong acid typically HCl. These alumina soil was dried at 8$0^{\circ}C$~9$0^{\circ}C$ to have a optmum viscosty for spinning, spinned at spinner, and then sintered to make polycrystalline alumina fiber.

• Bulletin of the Korean Chemical Society
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• 제31권9호
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• pp.2449-2450
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• 2010

• Bulletin of the Korean Chemical Society
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• 제31권11호
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• pp.3156-3158
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• 2010

Stable and non-hygroscopic polystyrene supported aluminium triflate (Ps-$Al(OTf)_3$), which is prepared easily from cheap and commercially available compounds was found to be an environmentally friendly heterogeneous catalyst for Friedel-Crafts acylation of arenes using acid chlorides in the absence of solvent under mild reaction conditions. The catalyst can be reused up to five times after simple washing with dichloromethane.