• 제목/요약/키워드: Biological Synthesis

검색결과 1,242건 처리시간 0.023초

물여뀌 에탄올 추출물의 미백 효과 (Whitening Activities of Ethanol Extract from Polygonum amphibium L.)

  • 황병수;이승영;강창희;한웅;오영택;유상미;김민진;김철환;엄정혜;정상철;이욱재;안영희;정용태
    • 한국미생물·생명공학회지
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    • 제47권2호
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    • pp.195-200
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    • 2019
  • The purpose of this study was to investigate the melanogenesis inhibiting activity of the ethanol extract from Polygonum amphibium L. Firstly, the n-hexane (Hx), chloroform ($CHCl_3$), ethyl acetate (EA), n-butanol (BuOH), and water (Water) fractions were isolated from the P. amphibium L. ethanol extract. The efficacy of melanogenesis was found to significantly decrease via the EA and BuOH fractions when compared to the control in B16F10 cells. EA particularly showed the lowest melanin content in B16F10 cells when compared to all the other extracts. Concentration-dependent inhibition of melanin synthesis was also observed in the EA fraction at concentrations below $50{\mu}g/ml$, which did not exhibit cytotoxicity in B16F10 cells. Notably, the expression of three key proteins (tyrosinase, tyrosinase-related protein-1 (TRP-1), and TRP-2), which are involved in melanogenesis, were significantly decreased via the EA fraction. EA also inhibited body pigmentation in vivo in a zebrafish model. Overall, we demonstrated melanogenesis suppression using the EA fraction from P. amphibium L., which could be a potential candidate for an antimelanogenesis agent.

Artificial Radical Generating and Scavenging Systems: Synthesis and Utilization of Photo-Fenton Regent in Biological Systems

  • Matsugo, Seiichi
    • Journal of Photoscience
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    • 제9권2호
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    • pp.138-141
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    • 2002
  • A photo-labile compound which is bioinactive but, upon irradiation with light, yields bioactive species is called as "caged compound". Photolysis of caged compounds generating bioactive species, has become a general method to produce a desired amounts of bioactive species in the specific time interval at the desired place or area of the target biological systems. For this purpose, we designed and synthesized caged hydroxyl radical., "Photo-Fenton Reagent" NP-IIl. NP-IIl has a strong absorption maximum at 377 nm and yields hydroxyl radicals upon UV light irradiation. The antioxidant activity of the ${\alpha}$ -lipoic acid and other naturally occurring compounds has been examined by using NP-IIl as a molecular probe. For example, upon photoirradiation of NP-lII with BSA or apolipoprotein of human low density (LDL), the significant oxidative modifications were observed in both cases. The oxidation was completely suppressed in the presence of ${\alpha}$-lipoic acid, which clearly demonstrates the strong hydroxyl radical scavenging activity of ${\alpha}$-lipoic acid. Other applications of NP-lII will also be described

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비고리 알릴아민 화합물의 입체선택적 이중알코올화 반응 (Stereocontrolled Dihydroxylation Reactions of Acyclic Allylic Amines)

  • 전종호;신나라;김영규
    • 공업화학
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    • 제25권5호
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    • pp.437-446
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    • 2014
  • 비고리 알릴아민 화합물의 이중알코올화 반응은 아미노 다이올 구조를 도입할 수 있는 효율적인 합성법으로 아미노 다이올 구조를 포함하는 다양한 생리활성 천연물의 효율적인 합성에 적용될 수 있다. 본 리뷰에서는 기질 그 자체, 혹은 카이랄 리간드를 이용한 다양한 입체선택적 이중알코올화 반응들을 소개하고 이를 실제 천연물의 합성에 적용한 최근의 반응 결과들을 살펴보고자 한다.

Synthesis and Biological Evaluation of Novel Isopropyl 2-thiazolopyrimidine-6-carboxylate Derivatives

  • Kotaiah, Y.;Krishna, N. Hari;Raju, K. Naga;Rao, C.V.;Jonnalagadda, S.B.;Maddila, Suresh
    • 대한화학회지
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    • 제56권1호
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    • pp.68-73
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    • 2012
  • In the present study, we have synthesized novel Isopropyl 2-(4-substitutedbenzylidene)-5-methyl-3-oxo-7-phenyl-3,7-dihydro-2H-thiazolo[3,2-a]-pyrimidine-6-carboxylate derivatives (6a-j). Elemental analysis, IR, $^1H$ NMR and mass spectral data elucidated structure of newly synthesized compounds. The newly synthesized compounds were screened for antiinflammatory and anti microbial studies. Their biological activity data of the 10 compounds indicates that two compounds posses potent anti-inflammatory and five have antimicrobial activities.

Identification of Genes for Mycothiol Biosynthesis in Streptomyces coelicolor A3(2)

  • Park Joo-Hong;Cha Chang-Jun;Roe Jung-Hye
    • Journal of Microbiology
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    • 제44권1호
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    • pp.121-125
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    • 2006
  • Mycothiol is a low molecular weight thiol compound produced by a number of actinomycetes, and has been suggested to serve both anti-oxidative and detoxifying roles. To investigate the metabolism and the role of mycothiol in Streptomyces coelicolor, the biosynthetic genes (mshA, B, C, and D) were predicted based on sequence homology with the mycobacterial genes and confirmed experimentally. Disruption of the mshA, C, and D genes by PCR targeting mutagenesis resulted in no synthesis of mycothiol, whereas the mshB mutation reduced its level to about $10\%$ of the wild type. The results indicate that the mshA, C, and D genes encode non-redundant biosynthetic enzymes, whereas the enzymatic activity of MshB (acetylase) is shared by at least one other gene product, most likely the mca gene product (amidase).

Synthesis and optical determination of chemosensor toward Cu(II) and Hg(II)

  • Yu, Hyung-Wook;Wang, Sheng;Son, Young-A
    • 한국염색가공학회:학술대회논문집
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    • 한국염색가공학회 2011년도 제44차 학술발표회
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    • pp.68-68
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    • 2011
  • A new chemosensor based on rhodamine B (1) for $Hg^{2+}$ and $Cu^{2+}$ was synthesized by one-step condensation reaction of rhodamine B hydrazide and Azo dye. Studying for its fluorogenic and colorimetric behaviors towards various metal ions, extreme sensitivity and selectivity were achieved by the detection of $Hg^{2+}$ and $Cu^{2+}$ over other commonly coexistent metal ions, which were accompanied by ring opening of a rhodamine spirocycle framework. In acetonitrile, the presence of $Hg^{2+}$ and $Cu^{2+}$ induces the formation of a Dye 1-ion complex, which was deduced by spectroscopy.

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Synthesis and the Absolute Configurations of Isoflavanone Enantiomers

  • Won, Dong-Ho;Shin, Bok-Kyu;Han, Jae-Hong
    • Journal of Applied Biological Chemistry
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    • 제51권1호
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    • pp.17-19
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    • 2008
  • Isoflavanone has been synthesized from the reduction of isoflavone in nearly quantitative yield. Isoflavone with seven equivalents of ammonium formate in the presence of Pd/C in ethanol under $N_2$ atmosphere exclusively produced the two-electron reduced product in two hours. It was characterized by various spectroscopic methods, including UV-VIS, EI-MS, $^1H$-NMR, $^{13}C$-NMR and $^1H$, $^1H$-COSY. The racemic mixture was separated by Sumi-Chiral column chromatography and the absolute configurations of the enantiomers were characterized by circular dichroism spectroscopy.

깊은 공융 용매 (DESs) 물성과 응용 (Properties of Deep Eutectic Solvents (DESs) and Their Applications)

  • 서호성;박병흥
    • 융복합기술연구소 논문집
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    • 제5권2호
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    • pp.43-48
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    • 2015
  • Deep eutectic solvents (DESs) are now broadly understood as a new kind of ionic liquid (IL) because they exhibit many characteristics and properties similar with ILs. The DESs made of quaternary ammonium salt blended with one of hydrogen bonding donor (HBD) compounds behave as ILs even at very low temperature. In this study, properties such as density, viscosity, surface tension, conductivity, and electrochemical behavior of DESs were reported and their applications were reviewed. Study on DESs has been drawn attention on application in metal finishing, but these solvents can be used in a variety of synthesis, and their potentials have been demonstrated in various areas. DESs are expected to offer applicability by extending the types of salts and hydrogen bond donor mixtures.

On-off Dewatering Control for Lipase-catalyzed Synthesis of n-Butyl Oleate in n-Hexane by Tubular Type Pervaporation System

  • Kwon, Seok-Joon;Rhee, Joon-Shick
    • Journal of Microbiology and Biotechnology
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    • 제8권2호
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    • pp.165-170
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    • 1998
  • Lipase-catalyzed esterification of n-butyl oleate was carried out in n-hexane as a model reaction. The optimal activity of Candida rugosa lipase was shown in a water activity ($a_w$) range of 0.52 to 0.65 at $30^{\circ}C$. The water produced from the esterification was removed by a tubular type pervaporation system. The rate of ester formed from the enzymatic esterification was allowed to be the same as the rate of water removal by maintaining an optimal $a_w$ of the reaction system using an on-off dewatering control device. The reaction rate and yield with a$a_w$ control were increased two folds higher than the respective values for the uncontrolled reaction.

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Carpenter bee pheromone의 2-methyl-5(S)-hexanolide의 부분 입체선택적 합성 (The diastereoselective synthesis of 2-methyl-5(S)-hexanolide)

  • 장재혁;이상준;김정한
    • Applied Biological Chemistry
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    • 제37권1호
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    • pp.25-29
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    • 1994
  • Ethyl acetoacetate를 빵효모가 환원해 생산한 ethyl-(S)-3-hydroxy-butyrate(2a)를 키 랄 출발물질로 하여 수목에 피해를 끼치는 해충인 carpenter bee의 수컷이 분비하는 성 페로몬인 cis-2-methyl-5-hexanolide(1)을 diastereomer로 합성하였다. 역합성적 분석을 통한 합성계획으로부터 T-Goal로 Wittig반응을 잡고 출발물질을 환원하여 얻은 알데히드 4와 triethyl 2-phosphonopropionate(7)을 Horner-Emmons반응시켜 ${\alpha},{\beta}$-불포화 에스테르 5를 얻은 뒤 catalytic hydrogenation과 lactonization을 시켜 carpenter bee 페로몬 1을 전체수율 37%로 쉽고 간단하게 합성하였다.

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