首页> 中文期刊> 《微生物学报》 >深海太平洋火色杆菌琼胶降解基因分析和琼胶酶Aga0950的表达及酶学性质

深海太平洋火色杆菌琼胶降解基因分析和琼胶酶Aga0950的表达及酶学性质

         

摘要

[Objective] An agarase gene,aga0590,was found in the fine genomics mapping of a deep-sea bacterium Flamrneovirga pacifica WPAGA1 using bioinformatics analysis.Recombinant Aga0950 was characterized with heterologous expression in E.coli.[Methods] Genomic sequencing of Flammeovirga pacifica WPAGA1 was performed by Illumina HiSeq2500 and agarase genes were annotated with BLAST.Subsequently,Aga0950 was obtained with heterologous expression in E.coli BL21 (DE3) and the agar-degrading activity was determined by dinitrosalicylic acid method.Enzymatic products of the agarase were analyzed by thin-layer chromatography and ion chromatography.[Results] Thirteen agarase genes with amino acid homologies from 60% to 85% were detected in the genome of Flammeovirga pacifica WPAGA1.The elected gene aga0950,which was aligned with highest identities of 67% in NCBI-nr database,possessed typical sequence characteristics of glucoside hydrolase family 16 (GH16).The specific activity of Aga0950 was 51770 U/mg,and the end-products of agar degradation by Aga0950 were neoagarotetraose (NA4) and neoagarohexaose (NA6).The optimum temperature and pH of Aga0950 was 50 ℃ and a range of 4.0 to 10.0,respectively.Meanwhile,rAga0950 showed outstanding temperature and pH stability.Activities of Aga0950 was enhanced by Co2+ and Mn2+ (1 mmol/L),while that was strongly inhibited by Cu2+.[Conclusion] Flammeovirga pacifica WPAGA1 has abundant polysaccharide-degrading genes.The agarase Aga0950 was indentified with high agar-degrading activity and excellent stability against acid,alkali and thermo.%[目的]对深海太平洋火色杆菌(Flammeovirga pacifica WPAGA1)全基因组进行生物信息学分析,筛选获得琼胶酶基因aga0950,采用基因工程手段对该基因的功能和性质进行验证和分析.[方法]采用Illumina HiSeq2500测序技术进行基因组测序分析;采用克隆表达和镍柱纯化方法获得纯aga0950基因表达产物;采用薄层层析(TLC)和离子色谱(IC)法分析酶降解琼胶产物;采用二硝基水杨酸法(DNS)测定琼胶酶活性.[结果]基因组序列分析表明,菌株WPAGA1全基因组拥有13个β-琼胶酶相关基因;氨基酸序列比对显示,同源性为60%-85%,其中aga0950是具有GH16家族典型特征的基因,同源性为67%.纯化的重组酶Aga0950比活力达51770 U/mg,具有高效降解琼胶活性,降解终产物为新琼四糖和新琼六糖;最适温度为50℃,最适pH为4.0-10.0;Co2+、Mn2+和Fe3+促进酶活,Cu2+抑制酶活.[结论]深海菌株WPAGA1具有丰富的琼胶酶基因;属于GH16家族的琼胶酶基因aga0950表达产物具有高效降解胶琼活性和良好的热、酸、碱稳定性.

著录项

  • 来源
    《微生物学报》 |2018年第3期|411-422|共12页
  • 作者单位

    华侨大学化工学院,生物工程与技术系,福建厦门361021;

    国家海洋局第三海洋研究所,海洋生物遗传资源重点实验室,福建厦门 361005;

    国家海洋局第三海洋研究所,海洋生物遗传资源重点实验室,福建厦门 361005;

    国家海洋局第三海洋研究所,海洋生物遗传资源重点实验室,福建厦门 361005;

    华侨大学化工学院,生物工程与技术系,福建厦门361021;

    国家海洋局第三海洋研究所,海洋生物遗传资源重点实验室,福建厦门 361005;

    华侨大学化工学院,生物工程与技术系,福建厦门361021;

  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类
  • 关键词

    琼胶酶; 琼胶寡糖; 基因组; 太平洋火色杆菌;

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