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Investigations into the function and dispensability of the teichoic acid polymerase from Bacillus subtilis 168.

机译:研究枯草芽孢杆菌168中的chochochoic酸聚合酶的功能和可分散性。

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摘要

The emergence of bacterial resistance to virtually all known antibiotics poses a serious threat to human health. As pharmaceutical companies retreat from the drug discovery field, it falls to academia to identify and validate novel antibacterial targets. Teichoic acids are a ubiquitous feature of Gram-positive cell walls that may represent such a target. This thesis focuses on the dispensability and function of the teichoic acid polymerase from the model organism Bacillus subtilis.;Conditional complementation of a thermosensitive mutant and a tagF deletion strain confirmed that polymerase activity is required for growth. In addition, cell wall analysis and the inability of teichuronic acid to compensate for a tagF lesion showed that the importance of teichoic acid biosynthesis involves more than simply providing an anionic determinant in the cell wall.;The TagF enzyme was purified for the first time for in vitro biochemical analysis. A novel polymerase assay was developed that allowed for the determination of steady-state kinetic parameters while preserving the reaction product for further characterization. Thus, polymerase activity was conclusively attributed to TagF for the first time. The dependence of TagF activity on pH, combined with mutational analysis, identified several critical residues. In vivo complementation experiments showed that equivalent residues were also critical for the function of the related TagB enzyme. This analysis showed that TagF serves as a model for other poorly characterized teichoic acid synthetic enzymes and gave the first clues about the mechanism of polymerization.;Teichoic acid polymerization was also studied in the absence of membrane. This work demonstrated that TagF did not require membrane association for activity, but that this association was involved in regulating polymer length. Further analysis showed that length regulation likely did not require accessory proteins, a feature that could distinguish teichoic acid polymerization from similar processes in Gram-negative bacteria.
机译:对几乎所有已知抗生素的细菌耐药性的出现对人类健康构成了严重威胁。随着制药公司从药物发现领域撤退,它落到了学术界来识别和验证新型抗菌靶标。 Teichoic acid是革兰氏阳性细胞壁普遍存在的特征,可以代表这样的靶标。本论文主要研究枯草芽孢杆菌模型中硫磷酸聚合酶的可分配性和功能。热敏突变体和tagF缺失菌株的条件互补证实了生长需要聚合酶活性。此外,细胞壁分析和四聚硫氰酸无法补偿tagF病损表明,chochochoic acid生物合成的重要性不仅仅在于在细胞壁中提供阴离子决定簇.TagF酶首次被纯化用于体外生化分析。开发了一种新颖的聚合酶测定法,该测定法可用于确定稳态动力学参数,同时保留反应产物用于进一步表征。因此,聚合酶活性首次被归因于TagF。 TagF活性对pH的依赖性,结合突变分析,确定了几个关键残基。体内互补实验表明,等效残基对于相关TagB酶的功能也至关重要。该分析表明,TagF可以作为其他表征较差的潮草酸合成酶的模型,并提供了有关聚合机理的第一条线索。在没有膜的情况下也研究了潮草酸聚合。这项工作表明TagF不需要膜缔合的活性,但这种缔合涉及调节聚合物的长度。进一步的分析表明,长度调节可能不需要辅助蛋白,这一特征可以将回潮酸聚合与革兰氏阴性细菌的类似过程区分开。

著录项

  • 作者

    Schertzer, Jeffrey W.;

  • 作者单位

    McMaster University (Canada).;

  • 授予单位 McMaster University (Canada).;
  • 学科 Biology Molecular.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 113 p.
  • 总页数 113
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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