• 한국응용과학기술학회지
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• 제31권3호
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• pp.345-351
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• 2014

Dinitramide($N(NO_2)_2$)염 화합물은 현재 고체 산화제로 로켓추진제의 중요한 원료 물질 중 하나이며, 환경 및 인체에 독성이 적은 친환경 에너지물질로 알려져 군사적 목적 외에 다양한 가스발생제로서 사용되고 있다. 특히 무기염이 아닌 유기염인 Guanidine 염(GDN)은 수분에 대한 안정성이 향상되어 안정적 보관 및 제조가 가능하므로 고순도 물질의 대량 생산이 가능하다. GDN의 출발물질로 guanidine의 음이온 염인 acetate, chloride, carbonate, nitrate, sulfate를 사용하여, GDN(GDN-1,2,3,4,5)을 최대 99%의 수율로 합성하였고, 이들의 물성을 다양한 분석기기를 이용하여 평가하였다. 흡수파장은 3452, 3402, 3354, 3278, 3208, 1642, 1570, 1492, 1416, 1337, 1179, $1000cm^{-1}$이 공통적으로 관찰되었으며, 열적 특성 변화는 $130^{\circ}C$에서 일어나기 시작하며 $150^{\circ}C{\sim}160^{\circ}C$에서는 발열반응과 함께 물질의 변화가 관찰되었다.

• Bulletin of the Korean Chemical Society
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• 제33권7호
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• pp.2352-2358
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• 2012

A high-nitrogen energetic salt, 1-amino-1-hydrazino-2,2-dinitroethylene guanidine salt [G(AHDNE)], was synthesized by reacting of 1-amino-1-hydrazino-2,2-dinitroethylene (AHDNE) and guanidine hydrochloride in sodium hydroxide aqueous solution. The theoretical investigation on G(AHDNE) was carried out by B3LYP/$6-311+G^*$ method. The thermal behaviors of G(AHDNE) were studied with DSC and TG-DTG methods, and the result presents an intense exothermic decomposition process. The enthalpy, apparent activation energy and pre-exponential constant of the process are $-1060J\;g^{-1}$, $148.7kJ\;mol^{-1}$ and $10^{15.90}s^{-1}$, respectively. The critical temperature of thermal explosion of G(AHDNE) is $152.63^{\circ}C$. The specific heat capacity of G(AHDNE) was studied with micro-DSC method and theoretical calculation method, and the molar heat capacity is $314.69J\;mol^{-1}K^{-1}$ at 298.15 K. Adiabatic time-to-explosion of G(AHDNE) was calculated to be a certain value between 60-72 s. The detonation velocity and detonation pressure were also estimated. G(AHDNE) presents good performances.

• 한국미생물·생명공학회지
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• 제19권3호
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• pp.308-312
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• 1991

B.thuringiensis subsp. darmstadiensis 73E10-2의 내독소에 대한 화학적 처리에서 고농도의 중성염(4M NaBr), 유기용매(50% acetone), 변성제(4M urea) 및 중성 계면활성제(10% triton X-100)로 내독소를 처리하였을 때 모기유충에 대한 독력의 소실이 거의 나타나지 않았으나, guanidine HCL이나 $CCl_4$ 또는 양이온 및 음이온 계면활성제로 처리함으로써 그 독력이 크게 소실되었다. 또한, 내독소의 sulfhydryl기의 변형은 모기유충에 대한 독력에 영향을 나타내지 못하였으나, lysine기 변형으로 내독소의 독력이 거의 완전히 소실되었다.

• 생명과학회지
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• 제27권11호
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• pp.1324-1330
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• 2017

최근 염분의 섭취와 관련하여 건강에 대한 우려가 늘어남에 따라, 염미대체제에 대한 소비자들의 관심이 급증하고 있으며, 세계적으로 경쟁력 있는 천연 저염제품의 개발이 필요한 실정이다. 최근 연구를 통해 식물성 및 동물성 원료 배합을 통해 가수분해물을 조제하여 최적 화합물을 얻는 것에 성공하였다. 본 연구에서는 염미성 펩타이드 분말내 arginine을 함유한 염미성 펩타이드를 규명하고 정량 하고자 하였다. L-arginine 또는 arginine을 포함한 펩타이드를 표준물질로 하여 $^{13}C$-NMR로 분석한 결과 유사한 위치에 구아니딘기 탄소가 시그널(L-arginine: 156.8 ppm, Arg-Ala: 156.4 ppm, Arg-Ser: 156.4 ppm)이 나타남을 확인하였고, 이를 통해 간편하고 신속하게 arginine 함유 펩타이드 정량분석이 가능할 것으로 기대된다.

• BMB Reports
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• 제28권6호
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• pp.477-483
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• 1995

The recombinant human interferon alpha 2a ($rhIFN-{\alpha}2a$), expressed in Saccharomyces cerevtsiae, was purified from insoluble aggregates. The inclusion body of $rhIFN-{\alpha}$ was solubilized by guanidine salt in the presence of disulfide reducing agent. The refolding of denatured $rhIFN-{\alpha}2a$ was achieved by simple dilution. The authentic interferon alpha, which has two correctly matched disulfide bonds, was seperated from incompletely oxidized $IFN-{\alpha}$ and dimeric $IFN-{\alpha}$ by use of a CM-Sepharose column, followed by size exclusion columns at two different pH conditions. The purified protein has been subjected to detailed physicochemical characterization including sequence determination. Unlike other $rhIFN-{\alpha}2a$ from E. coli reported, the $rhIFN-{\alpha}2a$ from S. cerevisiae has no methionine residue at its N-terminus originating from the start codon, ATG. The pI of the protein was determined to be 6.05 with a single band in the pI gel, which demonstrated that the purified $rhIFN-{\alpha}$ was homogeneous. The structural study using circular dichroism showed that the protein retains its three dimensional structure in the wide range of pH conditions between pH 3 and 9, and only minor strucural deformation was observed at pH 1.0.

• 공업화학
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• 제27권4호
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• pp.397-401
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• 2016

새로운 고체산화제 화합물인 pyridinium dinitramide (Py-DN)는 환경 및 인체에 독성이 적은 비염소계의 에너지물질로서 고체 추진제 뿐만 아니라 단일계 추진제로 활용이 가능한 high performance green propellant (HPGP) 물질이다. 합성반응은 술팜산칼륨(potassium sulfamate, $NH_2SO_3K$)을 출발물질로 시작하였으며, 합성된 Py-DN의 화학적인 구조특성을 적외선분광법과 가시광선-자외선분광법으로 관찰하였다. 또한, 유사한 물성의 친환경 고체산화제인 ammonium dinitramide[ADN, $NH_4N(NO_2)_2$]와 guanidine dinitramide[GDN, $NH_2C(NH_2)NH_2N(NO_2)_2$]의 열특성을 TG/DSC로 분석하여 상대 비교하였다. 본 연구에서 합성한 Py-DN염의 흡열온도는 $77.4^{\circ}C$, 분해온도는 $144.7^{\circ}C$, 발열에너지는 1739 J/g으로 기존의 DN계열 물질보다 열적 반응이 빠르므로 분해온도가 상대적으로 낮아 단일계 추진제의 촉매 분해 시 촉매의 예열온도를 낮출 수 있어 로켓추력기의 연료로 활용할 경우, 낮은 분해온도 적용성에 장점이 있다.

• BMB Reports
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• 제35권2호
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• pp.143-154
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• 2002

The structural and functional aspects of ervatamin B were studied in solution. Ervatamin B belongs to the $\alpha+\beta$ class of proteins. The intrinsic fluorescence emission maximum of the enzyme was at 350 nm under neutral conditions, and at 355 nm under denaturing conditions. Between pH 1.0-2.5 the enzyme exists in a partially unfolded state with minimum or no tertiary structure, and no proteolytic activity. At still lower pH, the enzyme regains substantial secondary structure, which is predominantly $\beta$-sheet conformation and shows a strong binding to 8-anilino-1-napthalene-sulfonic acid (ANS). In the presence of salt, the enzyme attains a similar state directly from the native state. Under neutral conditions, the enzyme was stable in urea, while the guanidine hydrochloride (GuHCl) induced equilibrium unfolding was cooperative. The GuHCl induced unfolding transition curves at pH 3.0 and 4.0 were non-coincidental, indicating the presence of intermediates in the unfolding pathway. This was substantiated by strong ANS binding that was observed at low concentrations of GuHCl at both pH 3.0 and 4.0. The urea induced transition curves at pH 3.0 were, however, coincidental, but non-cooperative. This indicates that the different structural units of the enzyme unfold in steps through intermediates. This observation is further supported by two emission maxima in ANS binding assay during urea denaturation. Hence, denaturant induced equilibrium unfolding pathway of ervatamin B, which differs from the acid induced unfolding pathway, is not a simple two-state transition but involves intermediates which probably accumulate at different stages of protein folding and hence adds a new dimension to the unfolding pathway of plant proteases of the papain superfamily.

• Maxillofacial Plastic and Reconstructive Surgery
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• 제19권3호
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• pp.265-286
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• 1997

Bone morphogenetic proteins(BMPs) are a group of transforming growth factor beta(TGF-${\beta}$)-related factors and multifunctional proteins, especially the only known biologic factors capable of inducing endochondral bone formation at an extraskeletal site. This study was performed to investigate the effect of the partially purified porcine BMP(pBMP) at an ectopic site. PBMP was partially purified from porcine bone matrix and its activity was monitored by an in vivo bioassay. The purification method utilized extraction of the bone-inducing activity with 4M guanidine, followed by chromatography on heparin-Sepharose. Active fractions were assayed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. And the fractions were reconstituted with inactive insoluble collagenous bone matrix from rats, acid soluble type I collagen from rat tail and chondroitin-6-sulfate sodium salt and implanted into the pectroralis muscle pouches of Sprague-Dawley rats. And the carrier complex was implanted on the opposite side as control. The rats were sacrificed at the day of 1st, 3rd, 5th, 7th, 11th, 14th and 21st after implantation and examined histologically, radiologically and biochemically. And alkaline phosphatase activity and calcium content were used as indices of bone formation. The results were as follows ; 1. Active fractions were localized in a zone between 31 and 40 KDa on SDS-PAGE. 2. The implanted 3.0mg of the partially purified pBMP induced cartilage and bone in the muscle tissue of rats through an endochondral ossification process. 3. Inactive insoluble bone matrix, type I collagen and chondroitin-6-sulfate have functioned as carriers for pBMP, but revealed some foreign body reactions. 4. Soft X-ray didn't reveal significant change between the experimental and the control group. 5. The alkaline phosphatase activities in the experimental group of 5th, 7th, 11th, 14th and 21st were increased significantly compared with control (p<0.01) with the peak in the group of 11th day. 6. With time, the calcium content of the experimental group increased. And the calcium contents in the experimental group of 11th, 14th and 21st were increased significantly compared with control (p<0.01).