PMID:8432721: Difference between revisions
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!align=left align='left' bgcolor='#CCCCFF' |Citation | |||
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'''Vander Horn, PB, Backstrom, AD, Stewart, V and Begley, TP''' (1993) Structural genes for thiamine biosynthetic enzymes (thiCEFGH) in Escherichia coli K-12. ''J. Bacteriol.'' '''175''':982-92 | |||
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!align=left align='left' bgcolor='#CCCCFF' |Abstract | |||
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Escherichia coli K-12 synthesizes thiamine pyrophosphate (vitamin B1) de novo. Two precursors [4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate and 4-amino-5-hydroxymethyl-2-methylpyrimidine pyrophosphate] are coupled to form thiamine monophosphate, which is then phosphorylated to make thiamine pyrophosphate. Previous studies have identified two classes of thi mutations, clustered at 90 min on the genetic map, which result in requirements for the thiazole or the hydroxymethylpryimidine. We report here our initial molecular genetic analysis of the thi cluster. We cloned the thi cluster genes and examined their organization, structure, and function by a combination of phenotypic testing, complementation analysis, polypeptide expression, and DNA sequencing. We found five tightly linked genes, designated thiCEFGH. The thiC gene product is required for the synthesis of the hydroxymethylpyrimidine. The thiE, thiF, thiG, and thiH gene products are required for synthesis of the thiazole. These mutants did not respond to 1-deoxy-D-threo-2-pentulose, indicating that they are blocked in the conversion of this precursor compound to the thiazole itself. | |||
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=8432721 PubMed] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC193010 PMC193010] | |||
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!align=left align='left' bgcolor='#CCCCFF' |Keywords | |||
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Amino Acid Sequence; Base Sequence; Chromosome Mapping; Cloning, Molecular; DNA, Bacterial/genetics; Escherichia coli/genetics; Escherichia coli Proteins; Genes, Bacterial; Genetic Complementation Test; Molecular Sequence Data; Nucleotidyltransferases/genetics; Restriction Mapping; Sequence Alignment; Thiamine/biosynthesis | |||
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==Main Points of the Paper == | |||
{{LitSignificance}} | |||
== Materials and Methods Used == | |||
{{LitMaterials}} | |||
==Phenotype Annotations== | |||
{{AnnotationTableHelp}} | |||
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==Notes== | |||
==References== | |||
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[[Category:Publication]] | |||
Latest revision as of 19:32, 17 July 2015
| Citation |
Vander Horn, PB, Backstrom, AD, Stewart, V and Begley, TP (1993) Structural genes for thiamine biosynthetic enzymes (thiCEFGH) in Escherichia coli K-12. J. Bacteriol. 175:982-92 |
|---|---|
| Abstract |
Escherichia coli K-12 synthesizes thiamine pyrophosphate (vitamin B1) de novo. Two precursors [4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate and 4-amino-5-hydroxymethyl-2-methylpyrimidine pyrophosphate] are coupled to form thiamine monophosphate, which is then phosphorylated to make thiamine pyrophosphate. Previous studies have identified two classes of thi mutations, clustered at 90 min on the genetic map, which result in requirements for the thiazole or the hydroxymethylpryimidine. We report here our initial molecular genetic analysis of the thi cluster. We cloned the thi cluster genes and examined their organization, structure, and function by a combination of phenotypic testing, complementation analysis, polypeptide expression, and DNA sequencing. We found five tightly linked genes, designated thiCEFGH. The thiC gene product is required for the synthesis of the hydroxymethylpyrimidine. The thiE, thiF, thiG, and thiH gene products are required for synthesis of the thiazole. These mutants did not respond to 1-deoxy-D-threo-2-pentulose, indicating that they are blocked in the conversion of this precursor compound to the thiazole itself. |
| Links | |
| Keywords |
Amino Acid Sequence; Base Sequence; Chromosome Mapping; Cloning, Molecular; DNA, Bacterial/genetics; Escherichia coli/genetics; Escherichia coli Proteins; Genes, Bacterial; Genetic Complementation Test; Molecular Sequence Data; Nucleotidyltransferases/genetics; Restriction Mapping; Sequence Alignment; Thiamine/biosynthesis |
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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
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| Phenotype of | Taxon Information | Genotype Information (if known) | Condition Information | OMP ID | OMP Term Name | ECO ID | ECO Term Name | Notes | Status |
|---|---|---|---|---|---|---|---|---|---|
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Notes
References
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