1887

Abstract

A DNA clone containing a putative enolase gene was isolated from a genomic DNA library of the anaerobic fungus . It was deduced from sequence comparisons that the enolase gene was interrupted by a large 331 bp intron. The enolase gene, termed , has an ORF of 1308 bp and encodes a predicted 436 amino acid protein. The deduced amino acid sequence shows high identity (715-71%) to those of enolases from the yeasts and . The G+ C content of the enolase coding sequence (438 mol%) is considerably higher than the G + C content of the intervening sequence (142 mol%) or the 5′ and 3′ non-translated flanking sequences (152 and 47 mol%, respectively). The codon usage of the enolase gene was very biased as has been found for the highly expressed genes of yeast and filamentous fungi. The gene has all the canonical features (polyadenylation signal, intron splicing boundaries) of genes isolated from aerobic filamentous fungi. Only one enolase gene could be detected in genomic DNA by Southern analysis with a homologous probe. RNA analysis detected a single enolase transcript of about 16 kb. When mycelium was grown on glucose, levels of enolase mRNA were markedly increased by comparison with enolase mRNA levels in mycelium grown on cellulose, suggesting that expression of the enolase gene was transcriptionally regulated by the carbon source.

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/content/journal/micro/10.1099/13500872-141-6-1301
1995-06-01
2019-10-14
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http://instance.metastore.ingenta.com/content/journal/micro/10.1099/13500872-141-6-1301
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