首页> 外文学位 >Cloning and characterization of protocatechuate 3,4-dioxygenase genes from Bradyrhizobium japonicum USDA110.
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Cloning and characterization of protocatechuate 3,4-dioxygenase genes from Bradyrhizobium japonicum USDA110.

机译:日本根瘤菌USDA110原儿茶酸3,4-二加氧酶基因的克隆和鉴定。

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摘要

Cloning of Protocatechuate 3,4-dioxygenase genes (PCD) from Bradyrhizobium japonicum USDA110 was achieved by screening a genomic library using a heterologous PCD gene probe from Pseudomonas cepacia. The cloned PCD gene from B. japonicum was characterized by enzyme assay and sequence analysis. The nucleotide sequence revealed that there are two open reading frames of 651 bp and 561 bp which encode polypeptides with predicted molecular weights of 25 kilo daltons and 20 kilo daltons. DNA sequence comparisons revealed that the PCD gene from B. japonicum USDA110 shows 51-57% sequence homology with three other PCD genes. Deduced amino acid sequence comparison revealed that the PCD from B. japonicum has diverged compared to PCD from Pseudomonas putida, Acinetobacter calcoaceticus and P. cepacia. The authenticity of the cloned B. japonicum PCD gene was confirmed by complementing P. cepacia DBO167 strain mutant for the PCD gene. The functional significance of chromosomal PCD gene of B. japonicum was determined, by construction of mutants for PCD gene and comparison of the survival of mutant with the wild B. japonicum in soil. Restriction enzyme analysis and Southern hybridization using kanamycin resistance gene probe revealed the presence of mutagen Tn5 inserted into the PCD gene. The mutant PCD gene was used to replace the chromosomal PCD gene by marker exchange technique. The verification of constructed mutants was established by testing for its inability to grow on basal media containing parahydroxybenzoic acid as sole carbon source and its ability to grow on complete medium containing kanamycin. Southern hybridizations were also performed using PCD gene probe and NPTII gene probe. Results from the above experiments showed the integration of Tn5 on the chromosome of B. japonicum and disruption of the PCD gene in the mutant B. japonicum. The survival and competition problem of B. japonicum USDA110 was studied by interacting the plant with the wild and mutant B. japonicum, and enumeration of B. japonicum from soil samples. This study revealed that PCD gene has an important role in the saprophytic survival of B. japonicum in the rhizosphere.
机译:通过使用洋葱假单胞菌的异源PCD基因探针筛选基因组文库,实现了从日本根瘤菌USDA110克隆原儿茶酸3,4-二加氧酶基因(PCD)。通过酶分析和序列分析表征了从日本芽孢杆菌克隆的PCD基因。核苷酸序列显示有两个651 bp和561 bp的开放阅读框,它们编码预测分子量分别为25千道尔顿和20千道尔顿的多肽。 DNA序列比较显示,来自日本芽孢杆菌USDA110的PCD基因与其他三个PCD基因显示51-57%的序列同源性。推导的氨基酸序列比较显示,与来自恶臭假单胞菌,钙乙酸不动杆菌和洋葱假单胞菌的PCD相比,日本芽孢杆菌的PCD有所不同。克隆的日本血吸虫的PCD基因的真实性是通过补充洋葱伯氏假单胞菌DBO167菌株突变体来确认的。通过构建PCD基因突变体并比较突变体与野生日本根瘤菌在土壤中的存活情况,确定了日本根瘤菌染色体PCD基因的功能意义。限制酶分析和使用卡那霉素抗性基因探针的Southern杂交揭示了插入PCD基因中的诱变Tn5的存在。通过标记交换技术,将突变的PCD基因用于取代染色体PCD基因。通过测试其不能在含有对羟基苯甲酸作为唯一碳源的基础培养基上生长,以及其在含有卡那霉素的完全培养基上生长的能力,来建立构建的突变体的验证。还使用PCD基因探针和NPTII基因探针进行Southern杂交。上述实验的结果表明,在日本血吸虫的染色体上Tn5的整合和突变日本血吸虫的PCD基因的破坏。通过将植物与野生和突变的日本血吸虫相互作用,并从土壤样品中枚举日本血吸虫,研究了日本血吸虫USDA110的生存和竞争问题。这项研究表明,PCD基因在根瘤菌的腐生生活中具有重要作用。

著录项

  • 作者

    Kotagiri, Shailaja.;

  • 作者单位

    Michigan Technological University.;

  • 授予单位 Michigan Technological University.;
  • 学科 Molecular biology.
  • 学位 Ph.D.
  • 年度 1994
  • 页码 87 p.
  • 总页数 87
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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