Difference between revisions of "PMID:11435407"

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(Table edited by Azweifel via TableEdit)
(Materials and Methods Used)
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== Materials and Methods Used ==
 
== Materials and Methods Used ==
 +
*Phenotype Microarrays
 +
**ES- measuring carbon catabolism
 +
**EN- measuring nitrogen catabolism
 +
**EPS- measuring phosphate and sulfur catabolism
 +
**EA- measuring auxotrophy (growth stimulation by nutrients)
 +
**ES1, 2, and 3- measuring alterations in sensitivity or resistance to toxic chemicals
 
*OmniLog instrument  
 
*OmniLog instrument  
 
**read and record the color change
 
**read and record the color change

Revision as of 13:55, 29 April 2011

Citation

Bochner, BR, Gadzinski, P and Panomitros, E (2001) Phenotype microarrays for high-throughput phenotypic testing and assay of gene function.Genome Res. 11:1246-55

Abstract

The bacterium Escherichia coli is used as a model cellular system to test and validate a new technology called Phenotype MicroArrays (PMs). PM technology is a high-throughput technology for simultaneous testing of a large number of cellular phenotypes. It consists of preconfigured well arrays in which each well tests a different cellular phenotype and an automated instrument that continuously monitors and records the response of the cells in all wells of the arrays. For example, nearly 700 phenotypes of E. coli can be assayed by merely pipetting a cell suspension into seven microplate arrays. PMs can be used to directly assay the effects of genetic changes on cells, especially gene knock-outs. Here, we provide data on phenotypic analysis of six strains and show that we can detect expected phenotypes as well as, in some cases, unexpected phenotypes.

Links

PubMed Online version:10.1101/gr.186501

Keywords

Escherichia coli; Gene Deletion; Cellular Respiration; Phenomics; Mutation; Oligonucleotide Array Sequence Analysis; Phenotype; Phenotype Microarray

Main Points of the Paper

Please summarize the main points of the paper.

Materials and Methods Used

  • Phenotype Microarrays
    • ES- measuring carbon catabolism
    • EN- measuring nitrogen catabolism
    • EPS- measuring phosphate and sulfur catabolism
    • EA- measuring auxotrophy (growth stimulation by nutrients)
    • ES1, 2, and 3- measuring alterations in sensitivity or resistance to toxic chemicals
  • OmniLog instrument
    • read and record the color change
  • Color CCD camera
    • provide quantitative and kinetic information about the response of the cells

Phenotype Annotations

See Help:AnnotationTable for details on how to edit this table.
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Species Taxon ID Strain Gene (if known) OMP Phenotype Details Evidence Notes

Escherichia coli

fb753

xylA

  • abolished utilization of xylose as a C source
  • absent cellular respiration using xylose

Metabolic Activity

Biolog phenotype microarray

Biochemical Assay

Figure 2

Escherichia coli

fb753

xylA

  • abolished utilization of maltose as a C source
  • absent cellular respiration using maltose

Metabolic Activity

Biolog phenotype microarray

Biochemical Assay

Figure 2

Escherichia coli

fb753

xylA

  • abolished utilization of maltotriose as a C source
  • absent cellular respiration using maltotriose

Metabolic Activity

Biolog phenotype microarray

Biochemical Assay

Figure 2

Escherichia coli

NCBI:83333

EP014

ynjB::Tn10

  • abolished utilization of L-arginine as a N source

Metabolic Activity

Biolog phenotype microarray

Biochemical Assay

Figure 2

Escherichia coli

NCBI:83333

EP014

ynjB::Tn10

  • abolished utilization of ornithine as a N source

Metabolic Activity

Biolog phenotype microarray

Biochemical Assay

Figure 2

</protect>

Notes

References

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