| http://purl.uniprot.org/citations/1856676 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/1856676 | http://www.w3.org/2000/01/rdf-schema#comment | "Isoelectric focusing was used to compare the complement of phosphoglucose isomerase isoenzymes in a wild-type strain of Saccharomyces cerevisiae and in a strain with a deletion in the PGI1 structural gene. Deletion of the PGI1 gene did not result in the absence of the high-Km isoenzyme I but the low-Km isoenzyme II was absent. Hence, the isoenzymes must be the products of two genes. If PGI1 were the sole structural gene its deletion would result in the disappearance of both isoenzymes. After a temperature shift-up a cdc30-bearing strain had cell cycle arrested and contained only 8% of the polysaccharide in the wild-type. Phosphoglucose isomerase is required for the synthesis of fructose 6-phosphate (F6-P), a precursor of the cell wall components chitin and mannoprotein ('mannan'), which are a polysaccharide and contain polysaccharide, respectively. Since the cdc30 mutation confers a temperature-sensitive phosphoglucose isomerase, the likely explanation for cell cycle arrest caused by this mutation is that the defective phosphoglucose isomerase results in a reduction of F6-P and hence an inability to synthesize the mannan and chitin needed for cytokinesis and cell separation. Revertants of a pgi1-1 bearing strain were selected for their ability to grow on glucose at 25 degrees C and this yielded a number of different phenotypes. Amongst the isolates was a strain which had undergone an intragenic reversion at the pgi1 locus, designated pgi1-1,100. This mutation permits growth and cell division at 25 degrees C but results in cell cycle arrest at 36 degrees C.(ABSTRACT TRUNCATED AT 250 WORDS)"xsd:string |
| http://purl.uniprot.org/citations/1856676 | http://purl.org/dc/terms/identifier | "doi:10.1099/00221287-137-4-765"xsd:string |
| http://purl.uniprot.org/citations/1856676 | http://purl.uniprot.org/core/author | "Dickinson J.R."xsd:string |
| http://purl.uniprot.org/citations/1856676 | http://purl.uniprot.org/core/date | "1991"xsd:gYear |
| http://purl.uniprot.org/citations/1856676 | http://purl.uniprot.org/core/name | "J Gen Microbiol"xsd:string |
| http://purl.uniprot.org/citations/1856676 | http://purl.uniprot.org/core/pages | "765-770"xsd:string |
| http://purl.uniprot.org/citations/1856676 | http://purl.uniprot.org/core/title | "Biochemical and genetic studies on the function of, and relationship between, the PGI1- and CDC30-encoded phosphoglucose isomerases in Saccharomyces cerevisiae."xsd:string |
| http://purl.uniprot.org/citations/1856676 | http://purl.uniprot.org/core/volume | "137"xsd:string |
| http://purl.uniprot.org/citations/1856676 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/1856676 |
| http://purl.uniprot.org/citations/1856676 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/1856676 |
| http://purl.uniprot.org/uniprot/#_P12709-mappedCitation-1856676 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/1856676 |
| http://purl.uniprot.org/uniprot/P12709 | http://purl.uniprot.org/core/mappedCitation | http://purl.uniprot.org/citations/1856676 |