• 제목/요약/키워드: purine nucleoside

검색결과 41건 처리시간 0.033초

Serratia marsecscens 와 Lactobacillus plantarum Purine Nucleoside Phosphorylase의 생합성에 대한 요산의 조절 (The Regulation of Uric Acid on the Biosynthesis of Serratia marcescens and Lactobacillus plantarum Purine Nucleoside Phosphorylase)

  • 최병범
    • 한국식품과학회지
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    • 제33권3호
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    • pp.361-365
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    • 2001
  • 최소 배지와 MRS 배지에 여러 퓨린 뉴클레오시드을 첨가하여 각각 호기적과 혐기적 조건하에서 배양시킨 Serratia marcescens ATCC 25419와 Lactobacillus plantarum ATCC 8014 세포 추출물에서 PNP의 비활성도를 조사한 결과 이노신은 5 mM 이상의 농도에서 Serratia PNP의 비활성도를 대조군과 비교하여 30% 정도 감소시켰으나, Lactobacillus PNP의 비활성도를 60% 이상 증가시켰다. 히포잔틴은 $0.1{\sim}0.5\;mM$의 낮은 농도에서는 Serratia PNP의 비활성도에 거의 영향을 주지 않았으나, 5 mM 이상의 농도에서는 45% 정도를 감소시켰다. 하지만 히포잔틴은 $0.1{\sim}1\;mM$의 낮은 농도에서는 Lactobacillus PNP의 비활성도를 20%, $1{\sim}15\;mM$의 농도에서는 $50{\sim}65%$ 정도 증가시켰다. 한편, 요산은 0.5 mM의 농도에서 Serratia와 Lactobacillus PNP의 비활성도를 20% 정도 증가시킨 반면, $5{\sim}10\;mM$의 농도에서 $20{\sim}25%$ 정도, 그리고 15 mM의 농도에서는 $60{\sim}80%$ 감소시켰다. 이러한 결과들로부터 5 mM 이상 농도의 이노신과 히포잔틴은 Serratia PNP의 비활성도를 30%이상 감소시킨 반면, Lactobacillus PNP의 비활성도를 60% 이상 증가시켰으며 낮은 농도(0.5 mM)의 요산은 효소의 비활성도를 증가시키고 높은 농도(15 mM)의 요산은 감소시키는 등 퓨린 뉴클레오티드 분해 대사 과정에서 요산은 Serratia marcescens와 Lactobacillus plantarum PNP 생합성의 조절 역할을 하는 것으로 사료된다.

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부추 잎으로부터 Adenosine의 분리와 유리 아미노산 조성 (Isolation of Adenosine and Free Amino Acid Composition from the Leaves of Allium tuberosum)

  • Park, Jae-Sue;Kim, Jae-Yeun;Lee, Ji-Hyon;Young, Han-Suk;Lee, Tae-Woong
    • 한국식품영양과학회지
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    • 제21권3호
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    • pp.286-290
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    • 1992
  • 부추 잎으로부터 purine nucleoside인 adenosine을 분리하고 그 구조를 기기적인 분석방법에 의하여 동정하였으며 또한 유리 아미노산 관련 화합물들의 조성과 상대함량을 표준품과 동일 조건하에서 아미노산 자동 분석 기기로 비교 검토하였다. 가장 함량이 많은 유리 아미노산들은 ala-nine, glutamic acid, aspartic acid 그리고 valine이었다.

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Identificaiton of the dITP- and XTP-Hydrolyzing Protein from Escherichia coli

  • Chung, Ji-Hyung;Park, Hyun-Young;Lee, Jong-Ho;Jang, Yang-Soo
    • BMB Reports
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    • 제35권4호
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    • pp.403-408
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    • 2002
  • A hypothetical 21.0 kDa protein (ORF O197) from Escherichia coli K-12 was cloned, purified, and characterized. The protein sequence of ORF O197(termed EcO197) shares a 33.5% identity with that of a novel NTPase from Methanococcus jannaschii. The EcO197 protein was purified using Ni-NTA affinity chromatography, protease digestion, and gel filtration column. It hydrolyzed nucleoside triphosphates with an O6 atom-containing purine base to nucleoside monophosphate and pyrophosphate. The EcO197 protein had a strong preference for deoxyinosine triphosphate (dITP) and xanthosine triphosphate (XTP), while it had little activity in the standard nucleoside triphosphates (dATP, dCTP, dGTP, and dTTP). These aberrant nucleotides can be produced by oxidative deamination from purine nucleotides in cells; they are potentially mutagenic. The mutation protection mechanisms are caused by the incorporation into DNA of unwelcome nucleotides that are formed spontaneously. The EcO197 protein may function to eliminate specifically damaged purine nucleotide that contains the 6-keto group. This protein appears to be the first eubacterial dITP-and XTP-hydrolyzing enzyme that has been identified.

Racemic Synthesis of Novel 6'-Methylene-5'-norcarbocyclic Purine Phosphonic Acid Analogues via Mitsunobu Reaction

  • Kim, Eun-Ae;Liu, Lian Jin;Hong, Joon-Hee
    • Bulletin of the Korean Chemical Society
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    • 제32권8호
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    • pp.2689-2694
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    • 2011
  • Novel 5'-norcarbocyclic adenine and guanine phosphonic acid analogues with 6'-electronegative moiety such as unsaturated C-C bond were designed and synthesized from commercially available 2-methylene-propane-1,3-diol (4). Regioselective Mitsunobu reaction successfully proceeded from an allylic functional group (${\pm}$)-12b at low reaction temperature in polar cosolvent (DMF/1,4-dioxane) to give purine phosphonate analogues (${\pm}$)-13 and (${\pm}$)-20. The purine nucleoside phosphonate and phosphonic acid analogues were subjected to antiviral screening against HIV-1. Guanine analogue (${\pm}$)-23 shows significant anti-HIV activity in PBM cell lines ($EC_{50}=8.1\;{\mu}M$).

Flavobacterium meningosepticum이 생산하는 Nucleoside Oxidase의 정제 및 Stoichiometry (Purification and the Stoichiometry of Nucleoside Oxidase from Flavobacterium meningosepticum)

  • 최양문;조홍연;양한철
    • 한국미생물·생명공학회지
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    • 제21권1호
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    • pp.23-29
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    • 1993
  • 토양으로부터 nucleoside oxidase 생산균주를 분리하고 Flavobacterium meningosepticum으로 동정하였다. 생산균주의 cell free extract로부터 본 효소를 정제배율 180배, 수율 18로 전기영동적으로 균일하게 정제하였으며 정제효소의 기질 특이성을 검토한 결과 nucleoside만을 산화시키는 전형적인 nucleoside oxidase이었다. Adenosine을 기질로 한 표준효소반응계에서 stoichiometry를 검토한 결과 본 효소는 lmol adenosine을 중간 생성물인 adenosice 5'-aldeh-yde로 산화 후 1 mol adenosine 5'-carboxylic acid까지 2단계로 산화시키면서 동시에 2 mol H2O2를 생성하는 새로운 type의 nucleoside oxidase로 확인되었다. 본 효소의 높은 기질 특이성과 H2O2를 생성하는 반응성은 nucleoside의 신속 간편한 효소학적정량볍 및 임상진단용 시약의 개발에 응용될 수 있음을 시사하였다.

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DEGRADATION OF NUCLEIC ACIDS BY CELL-FREE EXTRACT OF MIXED RUMEN PROTOZOA OF BUFFALO RUMEN

  • Sinha, P.R.;Dutta, S.M..
    • Asian-Australasian Journal of Animal Sciences
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    • 제1권4호
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    • pp.219-222
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    • 1988
  • Degradation of deoxyribonucleic acid(DNA) and ribonucleic acid(RNA) by cell-free extract of mixed rumen protozoa of buffalo rumen was investigated. DNA was observed to be degraded rapidly during an initial incubation period of 2 hr with simultaneous appearance of degradation products. RNA on the other hand recorded a rapid degradation during an initial incubation period of 1 hr. RNA degradation products appeared upto an incubation period of 2 hr. DNA was observed to degrade into oligo- and mononucleotides. pyrimidine nucleosides, purine nucleoside adenosine and bases xanthine, hypoxanthine and thymine. Degradation products of RNA comprised of pyrimidine nucleosides, purine nucleoside, adenosine and bases xanthine, hypoxanthine and uracil besides oligo- and mononucleotides.

Synthesis of Novel 2'(β)-Methyl-5'-deoxyapiose Nucleoside Phosphonic Acid Analogues as Antiviral Agents

  • Hong, Joon Hee
    • 통합자연과학논문집
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    • 제8권1호
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    • pp.48-55
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    • 2015
  • Novel 2'(${\beta}$)-methyl-5'-deoxyapiose purine phosphonic acid analogues were designed and synthesized from 2-propanone-1,3-diacetate. Condensation successfully proceeded from a glycosyl donor 9 under Vorbr${\ddot{u}}$ggen conditions. Condensation of aldehyde 14 with Wittig reagent [(diethoxyphosphinyl)methylidene] triphenylphosphorane gave the desired nucleoside phosphonate analogues 15. Ammonolysis and hydrolysis of phosphonates gave the nucleoside phosphonic acid analogue 17 and 19. The synthesized nucleoside analogues were subjected to antiviral screening against HIV-1. The adenine analogue 19 exhibited weak in vitro activities against HIV-1.

Efficient Synthesis of Novel 4'-Trifluoromethyl-5'-norcarbocyclic Purine Phosphonic Acid Analogs by Using the Ruppert-Prakash Reaction

  • Kim, Seyeon;Kim, Eunae;Yoo, Jin Cheol;Hong, Joon Hee
    • Bulletin of the Korean Chemical Society
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    • 제35권9호
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    • pp.2743-2748
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    • 2014
  • Novel 4'-trifluoromethyl-5'-norcarbocyclic purine phosphonic acid analogs were efficiently synthesized from commercially available 1,3-dihydroxy cyclopentane (5). Trifluoromethylation was successfully performed by using the Ruppert-Prakash reaction. The purine nucleosidic bases were efficiently coupled by using the Mitsunobu reaction. The synthesized adenosine phosphonic acids analogs 13 and 16 were screened for antiviral activity against human immunodeficiency virus-1 (HIV-1). Adenine derivative 13 exhibited significant anti-HIV-1 activity.

The Increment of Purine Specific Sodium Nucleoside Cotransporter mRNA in Experimental Fibrotic Liver Induced by Bile Duct Ligation and Scission

  • Lee, Sung-Hee;Chae, Keon-Sang;Nan, Ji-Xing;Sohn, Dong-Hwan
    • Archives of Pharmacal Research
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    • 제23권6호
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    • pp.613-619
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    • 2000
  • We investigated the expression profiles of rat fibrotic liver induced by bile duct ligation and scission (BDL/S) using the 3'-directed cDNA libraries. The possibility that the 3'-directed cDNA library represents the mRNA population faithfully was examined by northern blots. During the northern analysis based on fibrotic liver expression profile, we found for the first time that purine specific sodium nucleoside cotransporter (SPNT) was upregulated in BDL/S-induced fibrotic liver. To determine whether the accumulation of bile juice could affect the expression of SPNT mRNA or not, we examined the change of SPNT mRNA expression at 3, 14, 28 days after BDL/S operation. No change in SPNT expression was observed in rat liver at 3 days after surgery. In contrast, there were significant increases in SPNT expression at 14 and 28 days after surgery. We also examined whether chronic liver damage affected SPNT mRNA expression. SPNT mRNA level was significantly increased in BDL/S-induced fibrotic rat liver, whereas no significant change was obserbed in fibrotic livers chronically exposed to carbon tetrachloride or dimethylnitrosamine. From the above results, although further study might be needed, it was considered that the increment of SPNT mRNA in BDL/S liver morphological compatibility to human was remarkable.

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