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Mapping nif genes of Rhodobacter capsulatus, and characterization of a mutant with a pleiotropic defect in nitrogen metabolism.

机译:映射荚膜红细菌的nif基因,并表征氮代谢中具有多效性缺陷的突变体。

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摘要

Mutations affecting the ability of the photosynthetic bacterium Rhodobacter capsulatus to fix nitrogen (Nif{dollar}sp-{dollar}) have previously been mapped into six linkage groups (I-VI) by transduction with gene transfer agent (GTA). Because this vector carries only 4600 bp of DNA, linkage can only be demonstrated for short chromosomal distances. In order to demonstrate linkage on a larger scale, the self-transmissible plasmid, pBLM2, which has chromosome mobilizing ability in R. capsulatus, was used to map these six linkage groups relative to a number of auxotrophic markers. In this way, nif genes were found to lie in three regions of the chromosome. GTA linkage groups IV and VI were found to reside in the same region, based on their common linkages to adenosine and tryptophan markers. A second region was found to contain GTA groups I and V, both of which were linked by conjugation to isoleucine/valine and leucine markers. In a third region, group III was found to be located near the structural gene for glutamine synthetase (glnA).; A seventh GTA linkage group, containing mutations which cause pleiotropic defects in nitrogen metabolism, was also found to lie in the same region with group III and glnA. Mutants in this group have functional nitrogenase and normal regulation of nif gene expression. However, they are unable to grow on N{dollar}sb2{dollar} or on most amino acids. The only nitrogen sources found to allow photosynthetic growth of these mutants were ammonium and asparagine. One of these mutants was studied in more detail and found to be able to grow aerobically on most nitrogen sources. Studies of gene expression, using a lac gene fusion, indicated that the gene altered in this mutant may be under the control of an ntrC-like gene, and that it also may regulate its own synthesis. Information from the lac fusion also suggests that there may be two genes in group VII, both of which are required for growth on low levels of ammonia.
机译:先前已经通过基因转移剂(GTA)的转导将影响光合细菌荚膜红细菌固定氮(Nif {dollar} sp- {dollar})的能力的突变定位为六个连接基团(I-VI)。由于该载体仅携带4600 bp的DNA,因此只能在较短的染色体距离上显示连锁。为了更大程度地证明连接,使用在荚膜红斑狼疮中具有染色体动员能力的自传递质粒pBLM2绘制了这六个连接基团相对于许多营养缺陷型标记的图谱。以这种方式,发现nif基因位于染色体的三个区域中。基于它们与腺苷和色氨酸标记的共同连接,发现GTA连接基团IV和VI位于同一区域。发现第二区域包含GTA I和V组,两者通过与异亮氨酸/缬氨酸和亮氨酸标记物缀合而连接。在第三区域中,发现III组位于谷氨酰胺合成酶(glnA)的结构基因附近。还发现第七个GTA连锁组与第三组和glnA处于同一区域,该组包含引起氮代谢多效缺陷的突变。该组突变体具有功能性固氮酶和nif基因表达的正常调节。但是,它们无法在N {dolb} sb2 {dollar}或大多数氨基酸上生长。能够使这些突变体光合作用生长的唯一氮源是铵和天冬酰胺。对这些突变体之一进行了更详细的研究,发现它们能够在大多数氮源上有氧生长。使用lac基因融合进行的基因表达研究表明,在该突变体中改变的基因可能处于类似ntrC的基因的控制之下,并且还可能调节其自身的合成。从lac融合获得的信息还表明,第VII组中可能存在两个基因,这两个基因都是在低氨水平下生长所必需的。

著录项

  • 作者

    Goldenberg, Ann.;

  • 作者单位

    University of Missouri - Columbia.;

  • 授予单位 University of Missouri - Columbia.;
  • 学科 Biology Genetics.
  • 学位 Ph.D.
  • 年度 1988
  • 页码 174 p.
  • 总页数 174
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 遗传学;
  • 关键词

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