{"title":"水热菌mn -超氧化物歧化酶和II类富马酸酶基因的克隆与序列分析","authors":"Hidemasa Motoshima , Etsuo Minagawa, Fuji Tsukasaki, Shuichi Kaminogawa","doi":"10.1016/S0922-338X(98)80028-7","DOIUrl":null,"url":null,"abstract":"<div><p>A 6955-bp sequence of a <em>Pst</em>I-<em>Hin</em>dIII DNA fragment containing the manganese-superoxide dismutase (MnSOD) gene of <em>Thermus aquaticus</em> YT-1 was determined. The gene (<em>sod</em>) encoded a polypeptide consisting of 204 amino acid residues (the mature enzyme without the initiation methionine) with a calculated Mr of 22,773. The deduced amino acid sequence of the <em>sod</em> gene showed 92% identity to that of <em>Thermus thermophilus</em> HB8 determined chemically. The <em>sod</em> gene was well expressed in <em>Escherichia coli</em> and a heat-stable active enzyme was produced. An open reading frame encoding fumarase was found 91 bp upstream of the MnSOD gene in tandem form. The <em>fum</em> gene encoded a polypeptide consisting of 466 amino acid residues with a calculated <em>M</em><sub>r</sub> of 50,950. The deduced amino acid sequence of the <em>fum</em> gene product has similarity to that of the <em>fumC</em> of <em>E. coli</em> (57% identity), suggesting that this gene encodes a class II type fumarase.</p></div>","PeriodicalId":15696,"journal":{"name":"Journal of Fermentation and Bioengineering","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1998-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0922-338X(98)80028-7","citationCount":"6","resultStr":"{\"title\":\"Cloning and nucleotide sequencing of genes encoding Mn-superoxide dismutase and class II fumarase from Thermus aquaticus YT-1\",\"authors\":\"Hidemasa Motoshima , Etsuo Minagawa, Fuji Tsukasaki, Shuichi Kaminogawa\",\"doi\":\"10.1016/S0922-338X(98)80028-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A 6955-bp sequence of a <em>Pst</em>I-<em>Hin</em>dIII DNA fragment containing the manganese-superoxide dismutase (MnSOD) gene of <em>Thermus aquaticus</em> YT-1 was determined. The gene (<em>sod</em>) encoded a polypeptide consisting of 204 amino acid residues (the mature enzyme without the initiation methionine) with a calculated Mr of 22,773. The deduced amino acid sequence of the <em>sod</em> gene showed 92% identity to that of <em>Thermus thermophilus</em> HB8 determined chemically. The <em>sod</em> gene was well expressed in <em>Escherichia coli</em> and a heat-stable active enzyme was produced. An open reading frame encoding fumarase was found 91 bp upstream of the MnSOD gene in tandem form. The <em>fum</em> gene encoded a polypeptide consisting of 466 amino acid residues with a calculated <em>M</em><sub>r</sub> of 50,950. The deduced amino acid sequence of the <em>fum</em> gene product has similarity to that of the <em>fumC</em> of <em>E. coli</em> (57% identity), suggesting that this gene encodes a class II type fumarase.</p></div>\",\"PeriodicalId\":15696,\"journal\":{\"name\":\"Journal of Fermentation and Bioengineering\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1998-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0922-338X(98)80028-7\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Fermentation and Bioengineering\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0922338X98800287\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fermentation and Bioengineering","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0922338X98800287","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Cloning and nucleotide sequencing of genes encoding Mn-superoxide dismutase and class II fumarase from Thermus aquaticus YT-1
A 6955-bp sequence of a PstI-HindIII DNA fragment containing the manganese-superoxide dismutase (MnSOD) gene of Thermus aquaticus YT-1 was determined. The gene (sod) encoded a polypeptide consisting of 204 amino acid residues (the mature enzyme without the initiation methionine) with a calculated Mr of 22,773. The deduced amino acid sequence of the sod gene showed 92% identity to that of Thermus thermophilus HB8 determined chemically. The sod gene was well expressed in Escherichia coli and a heat-stable active enzyme was produced. An open reading frame encoding fumarase was found 91 bp upstream of the MnSOD gene in tandem form. The fum gene encoded a polypeptide consisting of 466 amino acid residues with a calculated Mr of 50,950. The deduced amino acid sequence of the fum gene product has similarity to that of the fumC of E. coli (57% identity), suggesting that this gene encodes a class II type fumarase.