Genetic Analysis of Mg-tetrapyrrole Biosynthesis

四吡咯镁生物合成的遗传分析

基本信息

  • 批准号:
    6472590
  • 负责人:
  • 金额:
    $ 24.07万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1996
  • 资助国家:
    美国
  • 起止时间:
    1996-06-01 至 2006-03-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): The tetrapyrrole biosynthetic pathway is responsible for synthesizing important metabolities such as vitamin B12, hemes, bilins and chlorophylls. The "common trunk" of the pathway, from 5-aminolevulinate to protoporphyrin IX, has received much attention owing to the fact that a number of heredity diseases (porphyrias) are caused by the overproduction of heme precursors. Clinical manifestations of overproducing these intermediates range from simple skin lesions, to psychotic disorders, to death. The vitamin B12 branch of the pathway has also received recent attention genes involved in vitamin B12 synthesis characterized from Pseudomonas denitrificans and in Salmonella typhimurium. In contrast to the wealth of information on heme and vitamin B12 synthesis, information is just emerging on the synthesis of the Mg-tetrapyrrole family of chlorophylls. In this proposal, we outline plans to perform detailed biochemical and genetic analysis of the Mg-tetrapyrrole biosynthetic pathway. This analysis includes (i) biochemical characterization of enzymes from the Mg-tetrapyrrole branch of the biosynthetic pathway, (ii) biochemical and genetic characterization of a redox responding transcription factor that regulates expression of heme, Mg-tetrapyrroles and carotenoid biosynthesis genes, as well as polypeptides that comprise the light harvesting-II portion of the photosystem. A thorough understanding of the tetrapyrrole biosynthetic pathway has some far ranging practical implications, such as the design of herbicides that target enzymes in the Mg tetrapyrrole pathway, and the health implications of overproducing tetrapyrrole end-products such as vitamin B12 and heme. It should also not be overlooked that tetrapyrrole driven photosynthesis is the primary route of capturing and supplying energy to living cells and, consequently, it is the most important source of energy in our technological world.
描述(由申请人提供):四吡咯生物合成途径为

项目成果

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CARL Eugene BAUER其他文献

CARL Eugene BAUER的其他文献

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{{ truncateString('CARL Eugene BAUER', 18)}}的其他基金

Regulatory Circuits Controlling Development of Dormant Microbial Cysts
控制休眠微生物囊肿发育的调节电路
  • 批准号:
    8605881
  • 财政年份:
    2012
  • 资助金额:
    $ 24.07万
  • 项目类别:
Regulatory Circuits Controlling Development of Dormant Microbial Cysts
控制休眠微生物囊肿发育的调节电路
  • 批准号:
    8215581
  • 财政年份:
    2012
  • 资助金额:
    $ 24.07万
  • 项目类别:
Regulatory Circuits Controlling Development of Dormant Microbial Cysts
控制休眠微生物囊肿发育的调节电路
  • 批准号:
    8415958
  • 财政年份:
    2012
  • 资助金额:
    $ 24.07万
  • 项目类别:
Regulatory Circuits Controlling Development of Dormant Microbial Cysts
控制休眠微生物囊肿发育的调节电路
  • 批准号:
    8789366
  • 财政年份:
    2012
  • 资助金额:
    $ 24.07万
  • 项目类别:
CONTINUED HIGH RESOLUTION STRUCTURAL ANALYSIS OF APPA
APPA 的持续高分辨率结构分析
  • 批准号:
    7181920
  • 财政年份:
    2005
  • 资助金额:
    $ 24.07万
  • 项目类别:
CONTINUED HIGH RESOLUTION STRUCTURAL ANALYSIS OF APPA
APPA 的持续高分辨率结构分析
  • 批准号:
    6978212
  • 财政年份:
    2004
  • 资助金额:
    $ 24.07万
  • 项目类别:
MACROMOLECULAR CRYSTALLOGRAPHY OF APPA
APPA 的高分子晶体学
  • 批准号:
    6978209
  • 财政年份:
    2004
  • 资助金额:
    $ 24.07万
  • 项目类别:
PROKARYOTIC SWARM CELL DIFFERENTIATION & PHOTOPERCEPTION
原核群体细胞分化
  • 批准号:
    6019474
  • 财政年份:
    1998
  • 资助金额:
    $ 24.07万
  • 项目类别:
PROKARYOTIC SWARM CELL DIFFERENTIATION & PHOTOPERCEPTION
原核群体细胞分化
  • 批准号:
    2681474
  • 财政年份:
    1998
  • 资助金额:
    $ 24.07万
  • 项目类别:
PROKARYOTIC SWARM CELL DIFFERENTIATION & PHOTOPERCEPTION
原核群体细胞分化
  • 批准号:
    6386977
  • 财政年份:
    1998
  • 资助金额:
    $ 24.07万
  • 项目类别:

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