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Chemotaxis to pyrimidines and s-triazines in Pseudomonas and Escherichia coli.

机译:在假单胞菌和大肠杆菌中趋化于嘧啶和s-三嗪。

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摘要

Chemotaxis, the ability of motile bacteria to detect and respond to specific chemicals in the environment, can help bacteria find an optimal niche for their survival and growth. This dissertation describes chemotactic responses to two groups of structurally related compounds, s-triazines and pyrimidines, in Escherichia coli and Pseudomonas species.;E. coli was chemotactically attracted to the pyrimidines thymine and uracil, as well as the s-triazine compounds N-isopropylammelide and cyanuric acid. E. coli mutants lacking the methyl-accepting chemotaxis protein (MCP) Tap lost the ability to respond to both pyrimidines and s-triazines. These data indicate that pyrimidines and triazines are detected by the same chemoreceptor (Tap) in E. coli . Pyrimidines are the closest naturally-occurring structures to triazines. Because E. coli uses pyrimidines but not s-triazines as sole sources of nitrogen, we propose that chemotaxis towards s -triazines is due to fortuitous recognition by the pyrimidine chemoreceptor in E. coli.;Pseudomonas sp. strain ADP utilizes the man-made s-triazine herbicide atrazine as sole nitrogen source. This strain was attracted to the s-triazines atrazine, hydroxyatrazine, N-isopropylammelide and cyanuric acid. The response was not induced during growth with atrazine, and atrazine metabolism was not required for the chemotactic response. Strain ADP, as well as Pseudomonas putida strains F1 and PRS2000, responded to cytosine, but did not respond or responded very weakly to thymine and uracil. McpC, a newly identified MCP gene, was demonstrated to encode the cytosine chemoreceptor in strain F1. P. putida strains F1 and PRS2000 also responded to s-triazines, and McpC is involved in chemotaxis responses towards N-isopropylammelide in F1.;In addition to the characterization of s-triazine and pyrimidine chemotaxis, this work analyzed the putative MCPs in P. putida F1 and uncovered specific chemotaxis and aerotaxis functions for several MCPs.
机译:趋化性是能动细菌检测和响应环境中特定化学物质的能力,可以帮助细菌找到存活和生长的最佳环境。本论文描述了在大肠杆菌和假单胞菌属中对两组结构相关化合物s-三嗪和嘧啶的趋化反应。大肠杆菌被趋化性地吸引到嘧啶胸腺嘧啶和尿嘧啶,以及S-三嗪化合物N-异丙基氨化物和氰尿酸。缺乏甲基接受趋化蛋白(MCP)Tap的大肠杆菌突变体失去了对嘧啶和s-三嗪的反应能力。这些数据表明嘧啶和三嗪在大肠杆菌中被同一化学感受器(Tap)检测到。嘧啶是最接近三嗪的天然结构。因为大肠杆菌使用嘧啶而不是s-三嗪作为唯一的氮源,所以我们认为对s-三嗪的趋化性是由于大肠杆菌中嘧啶化学感受器的偶然识别所致。 ADP菌株利用人造S-三嗪除草剂at去津作为唯一的氮源。该菌株被S-三嗪阿特拉津,羟基阿特拉津,N-异丙基酰胺和氰尿酸所吸引。阿特拉津在生长过程中未诱导该应答,趋化应答不需要阿特拉津代谢。 ADP菌株以及恶臭假单胞菌F1和PRS2000菌株对胞嘧啶有反应,但对胸腺嘧啶和尿嘧啶没有反应或反应很弱。新发现的MCP基因McpC被证明编码F1菌株的胞嘧啶化学感受器。恶臭假单胞菌菌株F1和PRS2000也对s-三嗪有反应,而McpC参与了F1对N-异丙基氨化物的趋化反应。恶臭F1并发现了几种MCP的特定趋化性和空气趋化性功能。

著录项

  • 作者

    Liu, Xianxian.;

  • 作者单位

    University of California, Davis.;

  • 授予单位 University of California, Davis.;
  • 学科 Biology Molecular.;Biology Microbiology.;Biology Physiology.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 217 p.
  • 总页数 217
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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