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首页> 外文期刊>Plant Molecular Biology Reporter >Characterization of O-Acetylserine(Thiol)Lyase-Encoding Genes Reveals Their Distinct but Cooperative Expression in Cysteine Synthesis of Soybean [Glycine max (L.) Merr.]
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Characterization of O-Acetylserine(Thiol)Lyase-Encoding Genes Reveals Their Distinct but Cooperative Expression in Cysteine Synthesis of Soybean [Glycine max (L.) Merr.]

机译:表征O-乙酰丝氨酸(硫醇)酶的基因揭示了它们在大豆半胱氨酸合成中的独特但​​协同表达的作用[Glycine max(L.)Merr。]

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摘要

In plants, the terminal step of cysteine biosynthesis is catalyzed by O-acetylserine(thiol)lyase (OAS-TL, EC 2.5.1.47). However, to date, there is limited information on those genes involved in this pathway in soybean. In this study, six soybean OAS-TL-like genes were obtained and designated as GmOAS-TL1, 2, 3, 4, 6, and 7. Phylogenetic analysis indicated that GmOAS-TL1, 2, 6, and 7 were similar and showed homology to cytosolic isoforms, while GmOAS-TL3 and 4 were homologous to β-cyanoalanine synthase (CAS, EC 4.4.1.9)-like and a plastidic isoform, respectively. Both genes seemed to belong to a small gene family as confirmed by Southern blot analysis. Expression of GmOAS-TL1, 3, 4, and 6 in the Escherichia coli cys? auxotroph resulted in bacterial growth and exhibited high enzymatic activity. Reverse transcription polymerase chain reaction analysis indicated that varying levels of expression were detected in different tissues and with distinct profiles. During the stage of seed-filling, expression patterns showed a cooperative trend that corresponded with total OAS-TL enzymatic activity. However, the enzymatic activity was highly negatively correlated with cysteine content in the developing seeds. These results suggest that cysteine synthesis in soybean might be an operation of multiple OAS-TL genes with homeostasis mechanisms for self-regulation. This finding should enhance our understanding of the molecular basis of soybean cysteine biosynthesis.
机译:在植物中,半胱氨酸生物合成的最终步骤是由O-乙酰丝氨酸(硫醇)裂解酶催化的(OAS-TL,EC 2.5.1.47)。然而,迄今为止,关于大豆中与该途径有关的那些基因的信息有限。在这项研究中,获得了六个大豆OAS-TL样基因,分别命名为GmOAS-TL1、2、3、4、6和7。系统进化分析表明,GmOAS-TL1、2、6和7相似并显示与胞质亚型同源,而GmOAS-TL3和4与β-氰丙氨酸合酶(CAS,EC 4.4.1.9)和质体亚型同源。如Southern印迹分析所证实,这两个基因似乎都属于一个小的基因家族。 GmOAS-TL1、3、4和6在大肠杆菌半胱氨酸营养缺陷型中的表达导致细菌的生长并表现出很高的酶促活性。逆转录聚合酶链反应分析表明,在不同组织中检测到不同水平的表达,并且具有不同的特征。在种子充实阶段,表达模式表现出与总OAS-TL酶活性相对应的协同趋势。然而,酶活性与正在发育的种子中的半胱氨酸含量高度负相关。这些结果表明,大豆中的半胱氨酸合成可能是多个具有自我调节机制的OAS-TL基因的运行。这一发现将增强我们对大豆半胱氨酸生物合成分子基础的理解。

著录项

  • 来源
    《Plant Molecular Biology Reporter》 |2008年第4期|277-291|共15页
  • 作者单位

    National Center for Soybean Improvement National Key Laboratory of Crop Genetics and Germplasm Enhancement Nanjing Agricultural University Nanjing 210095 People’s Republic of China;

    National Center for Soybean Improvement National Key Laboratory of Crop Genetics and Germplasm Enhancement Nanjing Agricultural University Nanjing 210095 People’s Republic of China;

    National Center for Soybean Improvement National Key Laboratory of Crop Genetics and Germplasm Enhancement Nanjing Agricultural University Nanjing 210095 People’s Republic of China;

    National Center for Soybean Improvement National Key Laboratory of Crop Genetics and Germplasm Enhancement Nanjing Agricultural University Nanjing 210095 People’s Republic of China;

    National Center for Soybean Improvement National Key Laboratory of Crop Genetics and Germplasm Enhancement Nanjing Agricultural University Nanjing 210095 People’s Republic of China;

    National Center for Soybean Improvement National Key Laboratory of Crop Genetics and Germplasm Enhancement Nanjing Agricultural University Nanjing 210095 People’s Republic of China;

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

    Cysteine synthesis; Expression; O-acetylserine(thiol)lyase; Soybean Glycine max (L.) Merr.;

    机译:半胱氨酸合成;表达;O-乙酰丝氨酸(硫醇)裂解酶;大豆[Glycine max(L.)Merr。];

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