• Title/Summary/Keyword: Carboxyl groups

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Chemical Properties and Spectroscopic Characteristics of Humic Fractions Isolated from Commercial Organic Fertilizers (국산(國産) 유기질비료(有機質肥料)의 부식조성(腐植組成) 및 분광학적(分光學的) 특성(特性))

  • Kim, Jeong-Je;Yang, Jae-E;Shin, Young-Oh
    • Korean Journal of Soil Science and Fertilizer
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    • v.29 no.1
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    • pp.44-52
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    • 1996
  • Humic substances of 17 organic fertilizers available on the market were the objects of study. The list of ingredients for formulation of them comprised fish meal. bone meal, oil-cakes, brewer's grains, peat, sawdust, wood bark, zeolite, soil conditioner, live-stock droppings, amino acid fermentation byproduct, chaff, limestone and others. Humic and fulvic acids were isolated from those substances and given chemical and spectroscopic analyses. Nutritional values of the organic fertilizers showed big diversity. Humification of organic matter was incomplete for some of the fertilizers as indicated by a high C/N ratio. Extractable humic acid percentage was higher, in general, than that of fulvic acid. Also the relative content of humin increased with advanced humification. Total acidity was closely related to phenolic hydroxyl groups. Relationships between carboxyl and hydroxyl groups. and carboxyl and alcoholic hydroxyl groups were very significant. Ultraviolet and visible light absorption spectra of humic and fulvic acids were substantially similar. The types of humic acids were B. P, and Rp. Two humic acids of the 17 samples belonged to B type. 3 to P type and all the rest to Rp type.

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Immunoglobulin Can Be Functionally Regulated by Protein Carboxylmethylation in Fc Region

  • Park Jong-Sun;Cho Jae-Youl;Kim Sung-Soo;Bae Hyun-Jin;Han Jeung-Whan;Lee Hyang-Woo;Hong Sung-Youl
    • Archives of Pharmacal Research
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    • v.29 no.5
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    • pp.384-393
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    • 2006
  • Protein carboxylmethylation methylates the free carboxyl groups in various substrate proteins by protein carboxyl O-methyltransferase (PCMT) and is one of the post-translational modifications. There have been many studies on protein carboxylmethylation. However, the precise functional role in mammalian systems is unclear. In this study, immunoglobulin, a specific form of $\gamma-globulin$, which is a well-known substrate for PCMT, was chosen to investigate the regulatory roles of protein carboxylmethylation in the immune system. It was found that the anti-BSA antibody could be carboxylmethylated via spleen PCMT to a level similar to $\gamma-globulin$. This carboxylmethylation increased the hydrophobicity of the anti-BSA antibody up to 11.4%, and enhanced the antigen-binding activity of this antibody up to 24.6%. In particular, the Fc region showed a higher methyl accepting capacity with 80% of the whole structure level. According to the amino acid sequence alignment, indeed, 7 aspartic acids and 5 glutamic acids, as potential carboxylmethylation sites, were found to be conserved in the Fc portion in the human, mouse and rabbit. The carboxylmethylation of the anti-BSA antibody was reversibly demethylated under a higher pH and long incubation time. Therefore, these results suggest that protein carboxylmethylation may reversibly regulate the antibody-mediated immunological events via the Fc region.

Preparation of $\etha$-N-[(2-Chloroethyl) nitrosocarbamoyl]-L-lysine ($\etha$-N-[(2-Chloroethyl) nitrosocarbamoyl]-L-lysine의 합성)

  • 김정균;조인섭
    • YAKHAK HOEJI
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    • v.27 no.2
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    • pp.177-179
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    • 1983
  • A copper complex of $\epsilon$-N-[(2-chloroethyl)carbamoyl]-L-lysine was prepared by the treatment of the L-lysine copper complex with 2-chloroethyl isocyanate in cold water. Within the L-lysine copper complex molecule, the $\alpha-amino$ and carboxyl groups are bounded to $Cu^{2+}$ but the $\epsilon-amino$ group is free and can react with carbamoylating agents. A potential antitumor agent, $\epsilon-N-[(2-chloroethyl)$ nitrosocarbamoyl]-L-lysine was synthesized by nitrosation of this copper complex with Na $NO_{2}$ in anhydrous formic acid, followed by the passage of $H_{2}$S gas.

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A Study on the Surface Degradation Properties of Epoxy / Glass fiber Treated with Ultraviolet Rays (자외선 처리된 Epoxy/Glass Fiber의 표면 열화 특성에 관한 연구)

  • Lee, Baek-Su;Lee, Deok-Chul
    • The Transactions of the Korean Institute of Electrical Engineers C
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    • v.48 no.2
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    • pp.86-91
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    • 1999
  • In order to analyse the degradation process of epoxy/glass fiber for outdoor condition, FRP laminate was exposed to the wavelength of ultraviolet rays and evaluated by comparing contact angle, surface resistivity, surface potential decay, and ESCA spectrum respectively. As irradiation energy are increased, the surface properties were steeply decreased in the range of 300[nm]. But the measured values within the scope of400[nm]∼440[nm] showed a increase as compared with the untreated ones. Also, fromthe result of ESCA spectrum, it was confirmed plenty of oxygen groups on the spot showing the maximum decrease of surface properties and the existence of ether groups on the surface of coloring phase. We can conclude that the degradation phenomena on the surface of epoxy composites are dominated by the induction of ester and carboxyl groups.

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오존에 의한 토양유기물질의 구조적 변화 특성

  • 정해룡;배기진;최희철
    • Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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    • 2001.04a
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    • pp.45-48
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    • 2001
  • The packed column experiments were conducted with a field soil, collected directly from the aquifer located at Bonchon industrial complex in K-city in order to characterize SOM reaction with ozone and to delineate the transformation of water soluble SOM after ozonation. As reaction time increased, water soluble organic matter increased, and this organic matter was in the range of 500∼1000 dalton. pH of extractants decreased with the increase of ozonation time. This Is because aromtic compounds in SOM were oxidized and carboxylic acid groups were formed. From the FT-IR spectra, the content of carboxylate increased as ozone injection time increased and hydroxyl group, which represents phenolic and alcoholic hydroxyl groups decreased. This is because oxidative ring fission formed carboxyl acid groups. This result provides a good agreement with pH decrease.

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Improvement of CF/ABS Composite Properties by Anodic Oxidation of Pitch based C-type Carbon Fiber

  • Yang, Xiao Ping;Wang, Cheng Zhong;Yu, Yun Hua;Ryu, Seung-Kon
    • Carbon letters
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    • v.3 no.2
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    • pp.80-84
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    • 2002
  • The surface treatment of C-type isotropic pitch-based carbon fiber was carried out by anodic oxidation in 5 wt% $NH_4NO_3$ electrolyte. The changes of fiber surface and carbon fiber/ABS resin composites were characterized by SEM, XPS and mechanical properties test. The oxygen functional groups on the surface, such as hydroxyl (-C-OH), carboxyl (-COOH) groups etc., increased after oxidation. Tensile strength, flexural strength and modulus of carbon fiber/ABS composites were also enhanced. However, the impact strength decreased with the improvement of the surface adhesion between CF and matrix.

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Comparison of Surface Characteristics and Adsorption Characteristics of Activated Carbons Changed by Acid and Base Modification (산과 염기의 개질에 의해 변화된 활성탄의 표면특성과 흡착특성 비교)

  • Lee, Song-Woo;Lee, Min-Gyu;Park, Sang-Bo
    • Journal of Environmental Science International
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    • v.17 no.5
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    • pp.565-571
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    • 2008
  • The surface properties of activated carbon modified by acids and base were studied. The influence of the surface chemistry on the adsorption of benzene and acetone vapor on modified activated carbons has been investigated The modified activated carbons were obtained by treatment with acetic acid ($CH_3COOH$), nitric acid ($HNO_3$) and sodium hydroxide (NaOH). The modified activated carbons had similar porosity but different surface chemistry and adsorption characteristics. The total surface acidity (sum of functional groups) of activated carbon (AC-AN) treated by nitric acid was 2.6 times larger than that of activated carbon (AC) before the acid treatment. Especially, carboxyl group was much developed by nitric acid treatment. The benzene equilibrium adsorption capacity of AC-AN decreased 20% more than that of AC. However, the acetone equilibrium adsorption capacity of AC-AN increased 20% more than that of AC because of the large increase of carboxyl group and acidity.

Studies on acid protease produced from Aspergillus tubingensis II (Aspergillus tubingensis의 acid protease에 관한 연구 II)

  • Chung, Yun-Su;Ko, Dong-Sung;Cho, Young;Lee, Keum-Soo
    • Korean Journal of Microbiology
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    • v.20 no.4
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    • pp.189-194
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    • 1982
  • Acid protease produced from Aspergillus tubingensis was pruified by ethanol fractionation, dialysis, and DEAE cellulose column chromatography. As a result of purification its specific activity increased to 5.4 times, and percent recovery was 39. The kinetic constants of the enzyme were studied. Km and Vmax was $1.5{\times}10^{-7}M\;and\;0.11{\Delta}O.D/min$ , respectively, when casein was used as substrate. The order of Km value of several proteins is : casein

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Identification of Catalytic Amino Acid Residues by Chemical Modification in Dextranase

  • Ko, Jin-A;Nam, Seung-Hee;Kim, Doman;Lee, Jun-Ho;Kim, Young-Min
    • Journal of Microbiology and Biotechnology
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    • v.26 no.5
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    • pp.837-845
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    • 2016
  • A novel endodextranase isolated from Paenibacillus sp. was found to produce isomaltotetraose and small amounts of cycloisomaltooligosaccharides with a degree of polymerization of 7-14 from dextran. To determine the active site, the enzyme was modified with 1-ethyl-3-[3-(dimethylamino)-propyl]-carbodiimide (EDC) and α-epoxyalkyl α-glucosides (EAGs), an affinity labeling reagent. The inactivation followed pseudo first-order kinetics. Kinetic analysis and chemical modification using EDC and EAGs indicated that carboxyl groups are essential for the enzymatic activity. Three Asp and one Glu residues were identified as candidate catalytic amino acids, since these residues are completely conserved across the GH family of 66 enzymes. Replacement of Asp189, Asp340, or Glu412 completely abolished the enzyme activity, indicating that these residues are essential for catalytic activity.

Heavy Metal Removal Capacity of Chemically Modified Alginic Acid (화학적으로 개질된 알긴산의 중금속 제거능)

  • Lee, Soon-Hong;Kim, Kwang-Kook;Lee, Sang-Hoon
    • Journal of Korean Society on Water Environment
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    • v.21 no.6
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    • pp.569-574
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    • 2005
  • In this study, alginic acid that had an high affinity for a heavy metal and was noted for biological adsorbent was modified by an oxidizer, $KMnO_4$. Chemical modification changed hydroxyl of the alginic acid into carboxyl and compare with alginic acid, modified alginic acid exhibited a characteristics that carboxyl groups are comparatively high. For the use of them as an adsorbent, beads were prepared by dropping alginic acid and modified alginic acid solution in dilute 2 wt% $CaCl_2$ solution for non water soluble. The amount of removed $Cu^{2+}$ and $Pb^{2+}$ by modified alginic acid beads showed 84.7 mg and 90.9 mg per gram of beads, respectively. And it showed the amount of adsorbed heavy metal ions 10~20% higher than that of alginic acid beads in range of pH 4~7. In particular, modified alginic acid have a good adsorption capacity for $Cu^{2+}$ and $Pb^{2+}$ by Freundlich adsorption isotherm. According to this study, it is verified that alginic acid that is a nature high molecular substance improved capacity for actual application by increased heavy metal adsorption capacity by chemical modification.