Difference between revisions of "PMID:349355"

From omp dev
Jump to: navigation, search
(New PMID: Page!)
 
 
Line 1: Line 1:
PMID on Demand placeholder
+
{{RightTOC}}
 +
 
 +
<!--box uid=d41d8cd98f00b204e9800998ecf8427e.6659.G55ae8fec607a1-->
 +
<!--
 +
******************************************************************************************
 +
*
 +
*  ** PLEASE DON'T EDIT THIS TABLE DIRECTLY.  Use the edit table link under the table. **
 +
*
 +
****************************************************************************************** -->
 +
{|  id="G55ae8fec607a1"  class=" tableEdit PMID_info_table" 
 +
 
 +
|-
 +
!align=left align='left' bgcolor='#CCCCFF' |Citation
 +
||
 +
'''Chippaux, M, Giudici, D, Abou-Jaoudé, A, Casse, F and Pascal, MC'''  (1978) Laboratoire de Chimie Bactérienne C.N.R.S., Marsielle, France. ''Mol. Gen. Genet.'' '''160''':225-9
 +
|-
 +
!align=left align='left' bgcolor='#CCCCFF' |Abstract
 +
||
 +
Mutants of E. coli, completely devoid of nitrite reductase activity with glucose or formate as donor were studied. Biochemical analysis indicates that they are simultaneously affected in nitrate reductase, nitrite reductase, fumarate reductase and hydrogenase activities as well as in cytochrome C552 biosynthesis. The use of an antiserum specific for nitrate reductase shows that the nitrate reductase protein is probably missing. A single mutation is responsible for this phenotype: the gene affected, nir R, is located close to tyr R i.e. at 29 min on the chromosomal map.
 +
|-
 +
!align=left align='left' bgcolor='#CCCCFF' |Links
 +
||
 +
[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=349355 PubMed]
 +
 
 +
|-
 +
!align=left align='left' bgcolor='#CCCCFF' |Keywords
 +
||
 +
Escherichia coli/enzymology; Escherichia coli/genetics; Escherichia coli/metabolism; Fumarates; Genes; Glucose/metabolism; Mutation; NADH, NADPH Oxidoreductases/genetics; Nitrate Reductases/genetics; Nitrite Reductases/genetics; Oxidoreductases/genetics
 +
 
 +
|- class="tableEdit_footer"
 +
|<span class="tableEdit_editLink plainlinks">[{{SERVER}}{{SCRIPTPATH}}?title=Special:TableEdit&id=d41d8cd98f00b204e9800998ecf8427e.6659.G55ae8fec607a1&page=6659&pagename={{FULLPAGENAMEE}}&type=1&template=PMID_info_table edit table]</span> ||
 +
|}
 +
<noinclude>
 +
 
 +
</noinclude>
 +
<!--box uid=d41d8cd98f00b204e9800998ecf8427e.6659.G55ae8fec607a1-->
 +
 
 +
==Main Points of the Paper ==
 +
{{LitSignificance}}
 +
 
 +
== Materials and Methods Used ==
 +
{{LitMaterials}}
 +
 
 +
==Phenotype Annotations==
 +
{{AnnotationTableHelp}}
 +
<protect><!--box uid=d41d8cd98f00b204e9800998ecf8427e.6659.A55ae8fec8d739-->
 +
<!--
 +
******************************************************************************************
 +
*
 +
*  ** PLEASE DON'T EDIT THIS TABLE DIRECTLY.  Use the edit table link under the table. **
 +
*
 +
****************************************************************************************** -->
 +
{| border="2" cellpadding="4" cellspacing="0" style="margin: 1em 1em 1em 0; border: 1px #aaa solid; border-collapse: collapse;"  id="A55ae8fec8d739"  class=" tableEdit Phenotype_Table_2" 
 +
|- align='left' bgcolor='#CCCCFF'
 +
!|Phenotype of!!Taxon Information!!Genotype Information (if known)!!Condition Information!!OMP ID!!OMP Term Name!!ECO ID!!ECO Term Name!!Notes!!Status
 +
 
 +
|- class="tableEdit_footer"
 +
|<span class="tableEdit_editLink plainlinks">[{{SERVER}}{{SCRIPTPATH}}?title=Special:TableEdit&id=d41d8cd98f00b204e9800998ecf8427e.6659.A55ae8fec8d739&page=6659&pagename={{FULLPAGENAMEE}}&type=0&template=Phenotype_Table_2 edit table]</span> || || || || || || || || ||
 +
|}
 +
<noinclude>
 +
 
 +
</noinclude>
 +
<!--box uid=d41d8cd98f00b204e9800998ecf8427e.6659.A55ae8fec8d739--></protect>
 +
 
 +
==Notes==
 +
 
 +
==References==
 +
{{RefHelp}}
 +
<references/>
 +
 
 +
 
 +
[[Category:Publication]] [[Category:Papers referenced in the LaRossa chapter]]

Latest revision as of 13:32, 21 July 2015

Citation

Chippaux, M, Giudici, D, Abou-Jaoudé, A, Casse, F and Pascal, MC (1978) Laboratoire de Chimie Bactérienne C.N.R.S., Marsielle, France. Mol. Gen. Genet. 160:225-9

Abstract

Mutants of E. coli, completely devoid of nitrite reductase activity with glucose or formate as donor were studied. Biochemical analysis indicates that they are simultaneously affected in nitrate reductase, nitrite reductase, fumarate reductase and hydrogenase activities as well as in cytochrome C552 biosynthesis. The use of an antiserum specific for nitrate reductase shows that the nitrate reductase protein is probably missing. A single mutation is responsible for this phenotype: the gene affected, nir R, is located close to tyr R i.e. at 29 min on the chromosomal map.

Links

PubMed

Keywords

Escherichia coli/enzymology; Escherichia coli/genetics; Escherichia coli/metabolism; Fumarates; Genes; Glucose/metabolism; Mutation; NADH, NADPH Oxidoreductases/genetics; Nitrate Reductases/genetics; Nitrite Reductases/genetics; Oxidoreductases/genetics



Main Points of the Paper

Please summarize the main points of the paper.

Materials and Methods Used

Please list the materials and methods used in this paper (strains, plasmids, antibodies, etc).

Phenotype Annotations

See Help:AnnotationTable for details on how to edit this table.
<protect>

Phenotype of Taxon Information Genotype Information (if known) Condition Information OMP ID OMP Term Name ECO ID ECO Term Name Notes Status


</protect>

Notes

References

See Help:References for how to manage references in omp dev.