Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractMicrocombustion of ng Amounts of Carbon in Non-Volatile Materials for isotope Ratio Evaluation    Next AbstractControlled-release pheromone dispenser for use in traps to monitor flight activity of false codling moth »

Eur J Biochem


Title:Characterization of the essential yeast gene encoding N-acetylglucosamine-phosphate mutase
Author(s):Hofmann M; Boles E; Zimmermann FK;
Address:"Institut fur Mikrobiologie, Technische Hochschule Darmstadt, Germany"
Journal Title:Eur J Biochem
Year:1994
Volume:221
Issue:2
Page Number:741 - 747
DOI: 10.1111/j.1432-1033.1994.tb18787.x
ISSN/ISBN:0014-2956 (Print) 0014-2956 (Linking)
Abstract:"A previously cloned gene of Saccharomyces cerevisiae, which complements the growth defect of a phosphoglucomutase (pgm1 delta/pgm2 delta) double deletion mutant on a pure galactose medium [Boles, E., Liebetrau, W., Hofmann, M. & Zimmermann, F. K. (1994) Eur. J. Biochem. 220, 83-96], was identified as the structural gene encoding N-acetylglucosamine-phosphate mutase. The complete nucleotide sequence of the gene, AGM1, and surrounding regions were determined. AGM1 codes for a predicted 62-kDa protein with 557 amino acids and is located on chromosome V adjacent to the known gene PRB1 encoding protease B. No extended nucleotide or amino acid sequence similarities could be found in the databases, except for a small region of amino acids with high similarity to the active-site consensus sequence of hexosephosphate mutases. Three putative pheromone-responsive elements have been identified in the upstream region of the AGM1 gene. The gene is essential for cell viability. An agm1 deletion mutant progresses through only approximately five cell cycles to form a 'string' of undivided cells with an abnormal cell morphology resembling glucosamine auxotrophic mutants. Expression of the AGM1 gene on a multi-copy plasmid led to a significantly increased N-acetylglucosamine-phosphate mutase activity. Unlike over-expression of the AGM1 gene in a pgm1/pgm2 double deletion mutant which could restore phosphoglucomutase activity, over-expression of the PGM2 gene encoding the major isoenzyme of phosphoglucomutase did not increase N-acetylglucosamine-phosphate-mutase activity and did not restore growth of agm1 deletion mutant cells. Our observations indicate that the different hexosephosphate mutases of S. cerevisiae have partially overlapping substrate specificities but, nevertheless, distinct physiological functions"
Keywords:"Amino Acid Sequence Base Sequence Cloning, Molecular Gene Deletion Gene Expression *Genes, Fungal Molecular Sequence Data Phosphoglucomutase/genetics/metabolism Phosphotransferases (Phosphomutases)/chemistry/*genetics/metabolism Plasmids Saccharomyces cer;"
Notes:"MedlineHofmann, M Boles, E Zimmermann, F K eng Research Support, Non-U.S. Gov't England 1994/04/15 Eur J Biochem. 1994 Apr 15; 221(2):741-7. doi: 10.1111/j.1432-1033.1994.tb18787.x"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 25-11-2024