{"title":"黑曲霉醛糖1- epimase的纯化及性质研究","authors":"Shinichi Kinoshita, Keiichi Kadota, Hisaharu Taguchi","doi":"10.1016/0005-2744(81)90040-1","DOIUrl":null,"url":null,"abstract":"<div><p><em>Aspergillus niger</em> ATCC 6274 was selected as an aldose 1-epimerase (EC 5.1.3.3) producer from 45 stock cultures of <em>A. niger</em>. The aldose 1-epimerase was purified 115-fold to apparent homogeneity from cell extracts with a yield of 2.6%. The molecular weight was calculated to be 260 000 and that of the subunit to be 130 000. The enzyme preparation was active at pH 5–7. The <em>K</em><sub>m</sub> value was 50 mM and the <em>V</em> value was 1200 units/mg toward α-<span>d</span>-glucose. This enzyme catalyzed mutarotation of the following substrates; α-<span>d</span>-glucose, β-<span>d</span>-fructose, β-<span>l</span>-arabinose and β-<span>d</span>-galactose. The time required for glucose determination with a glucose oxidase reagent was significantly shortened by the addition of aldose 1-epimerase.</p></div>","PeriodicalId":100159,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Enzymology","volume":"662 2","pages":"Pages 285-290"},"PeriodicalIF":0.0000,"publicationDate":"1981-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0005-2744(81)90040-1","citationCount":"8","resultStr":"{\"title\":\"Purification and properties of aldose 1-epimerase from aspergillus niger\",\"authors\":\"Shinichi Kinoshita, Keiichi Kadota, Hisaharu Taguchi\",\"doi\":\"10.1016/0005-2744(81)90040-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>Aspergillus niger</em> ATCC 6274 was selected as an aldose 1-epimerase (EC 5.1.3.3) producer from 45 stock cultures of <em>A. niger</em>. The aldose 1-epimerase was purified 115-fold to apparent homogeneity from cell extracts with a yield of 2.6%. The molecular weight was calculated to be 260 000 and that of the subunit to be 130 000. The enzyme preparation was active at pH 5–7. The <em>K</em><sub>m</sub> value was 50 mM and the <em>V</em> value was 1200 units/mg toward α-<span>d</span>-glucose. This enzyme catalyzed mutarotation of the following substrates; α-<span>d</span>-glucose, β-<span>d</span>-fructose, β-<span>l</span>-arabinose and β-<span>d</span>-galactose. The time required for glucose determination with a glucose oxidase reagent was significantly shortened by the addition of aldose 1-epimerase.</p></div>\",\"PeriodicalId\":100159,\"journal\":{\"name\":\"Biochimica et Biophysica Acta (BBA) - Enzymology\",\"volume\":\"662 2\",\"pages\":\"Pages 285-290\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1981-12-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0005-2744(81)90040-1\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochimica et Biophysica Acta (BBA) - Enzymology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0005274481900401\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochimica et Biophysica Acta (BBA) - Enzymology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0005274481900401","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Purification and properties of aldose 1-epimerase from aspergillus niger
Aspergillus niger ATCC 6274 was selected as an aldose 1-epimerase (EC 5.1.3.3) producer from 45 stock cultures of A. niger. The aldose 1-epimerase was purified 115-fold to apparent homogeneity from cell extracts with a yield of 2.6%. The molecular weight was calculated to be 260 000 and that of the subunit to be 130 000. The enzyme preparation was active at pH 5–7. The Km value was 50 mM and the V value was 1200 units/mg toward α-d-glucose. This enzyme catalyzed mutarotation of the following substrates; α-d-glucose, β-d-fructose, β-l-arabinose and β-d-galactose. The time required for glucose determination with a glucose oxidase reagent was significantly shortened by the addition of aldose 1-epimerase.