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      KCI등재 SCIE SCOPUS

      Development of New Assay for Sucrose Phosphorylase and Its Application to the Characterization of Bifidobacterium longum SJ32 Sucrose Phosphorylase

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      https://www.riss.kr/link?id=A104496543

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      다국어 초록 (Multilingual Abstract)

      Sucrose phosphorylase, a hexosyltransferase,that is an important enzyme in starch and sucrose metabolisms, reversibly catalyzes the conversion of sucrose and orthophosphate to fructose and α-D-glucose-1-phosphate. A simple assay method for sucrose ph...

      Sucrose phosphorylase, a hexosyltransferase,that is an important enzyme in starch and sucrose metabolisms, reversibly catalyzes the conversion of sucrose and orthophosphate to fructose and α-D-glucose-1-phosphate.
      A simple assay method for sucrose phosphorylase using 3,5-dinitrosalicylic acid (DNS) was developed. Its effectiveness was compared with that of a previously used NAD method. The results establish that the DNS method is comparable to the NAD method for the assay of sucrose phosphorylase. In particular, analysis of the enzyme activity level of sucrose phosphorylase (SPase) from Bifidobacterium longum SJ32 revealed that the DNS method is not only simple and accurate, but it also is a time-saving method for assaying sucrose phosphorylase activity. Most importantly, the DNS method is stable in broad pH ranges (pH 4-10), whereas the NAD method showed inaccurate profiles in the alkaline pH ranges (pH 8-10). Kinetic studies on SPase from B. longum SJ32 were performed using the simple DNS method developed in this study.

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      참고문헌 (Reference)

      1 Miller G, "Use of dinitrosalisylic acid (DNS) for determination of reducing sugars" 31 : 426-428, 1959

      2 Mueller M, "The role Asp-295 in the catalytic mechanism of Leuconostoc mesentroides sucrose phosphoylase probed with site-directed mutagenesis" 581 : 1403-1408, 2007

      3 Reid S, "Sucrose utilisation in bacteria: Genetic organisation and regulation" 67 : 312-321, 2005

      4 Kasperowicz A, "Sucrose phosphorylase of the rumen bacterium Pseudobutyrivibrio ruminis stran A" 107 : 812-820, 2009

      5 Shin MH, "Strategies for producing recombinant sucrose phosphorylase originating from Bifidobacterium longum in Escherichia coli JM109" Elsevier 43 : 822-828, 2008

      6 Koga T, "Purification and some properties of sucrose phosphorylase from Leuconostoc mesenteroides" 55 : 1805-1810, 1991

      7 Silverstein R, "Purification and mechanism of action of sucrose phosphorylase" 242 : 1338-1346, 1967

      8 Guibert A, "Production and purification of sucrose phosphorylase from Leuconostoc mesenteroides application to the production of glucose-1-phosphate" 542 : 307-311, 1988

      9 Van Den Broek L, "Physicochemical and transglucosylation properties of recombinant sucrose phosphorylase from Bifidobacterium adolescentis DSM20083" 65 : 219-227, 2004

      10 Lee JH, "Molecular cloning of a gene encoding the sucrose phosphorylase from Leuconostoc mesenterodies B-1149 and the expression in Escherichia coli" 36 : 612-620, 2006

      1 Miller G, "Use of dinitrosalisylic acid (DNS) for determination of reducing sugars" 31 : 426-428, 1959

      2 Mueller M, "The role Asp-295 in the catalytic mechanism of Leuconostoc mesentroides sucrose phosphoylase probed with site-directed mutagenesis" 581 : 1403-1408, 2007

      3 Reid S, "Sucrose utilisation in bacteria: Genetic organisation and regulation" 67 : 312-321, 2005

      4 Kasperowicz A, "Sucrose phosphorylase of the rumen bacterium Pseudobutyrivibrio ruminis stran A" 107 : 812-820, 2009

      5 Shin MH, "Strategies for producing recombinant sucrose phosphorylase originating from Bifidobacterium longum in Escherichia coli JM109" Elsevier 43 : 822-828, 2008

      6 Koga T, "Purification and some properties of sucrose phosphorylase from Leuconostoc mesenteroides" 55 : 1805-1810, 1991

      7 Silverstein R, "Purification and mechanism of action of sucrose phosphorylase" 242 : 1338-1346, 1967

      8 Guibert A, "Production and purification of sucrose phosphorylase from Leuconostoc mesenteroides application to the production of glucose-1-phosphate" 542 : 307-311, 1988

      9 Van Den Broek L, "Physicochemical and transglucosylation properties of recombinant sucrose phosphorylase from Bifidobacterium adolescentis DSM20083" 65 : 219-227, 2004

      10 Lee JH, "Molecular cloning of a gene encoding the sucrose phosphorylase from Leuconostoc mesenterodies B-1149 and the expression in Escherichia coli" 36 : 612-620, 2006

      11 Seo DH, "Molecular Cloning of the Amylosucrase Gene from a Moderate Thermophilic Bacterium Deinococcus geothermalis and Analysis of Its Dual Enzyme Activity" Woodhead Publishing Limited 125-140, 2008

      12 Tedokon M, "Enzymatic assay of inorganic phosphate with use of sucrose phosphorylase and phosphoglucomutase" 38 : 512-515, 1992

      13 Lee JW, "Development of sucrose-utilizing Escherichia coli K-12 strain by cloning beta-fructofuranosidases and its application for l-threonine production" SPRINGER 88 (88): 905-913, 2010

      14 Kogure M, "Determination of sucrose using sucrose phosphorylase in a flowinjection system" 337 : 107-111, 1997

      15 Sprogøe D, "Crystal structure of sucrose phosphorylase from Bifidobacterium adolescentis" 43 : 1156-1162, 2004

      16 Kim M, "CLONING AND EXPRESSION OF SUCROSE PHOSPHORYLASE GENE FROM BIFIDOBACTERIUM LONGUM IN E-COLI AND CHARACTERIZATION OF THE RECOMBINANT ENZYME" 25 : 1211-1217, 200308

      17 Birnberg P, "A one-step enzymatic assay for sucrose with sucrose phosphorylase" 142 : 556-561, 1984

      18 Henrissat B, "A classification of glycosyl hydrolases based on amino acid sequence similarities" 280 : 309-316, 1991

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      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-11-23 학회명변경 영문명 : Korean Society Of Food Science And Biotechnology -> Korean Society of Food Science and Technology KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-07-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.75 0.17 0.56
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.49 0.43 0.364 0.06
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