ABSTRACT
The nucleotide sequence of the 2544-bp PstI fragment carrying the glucoamylase gene of Saccharomycopsis fibuligera KZ, designated as GLA1, has been determined. When compared with the nucleotide sequence of the GLU1 gene one nucleotide substitution was found in the 321- bp of the 5'-flanking region: 24 nucleotides were altered within the 1557 bp of the structural gene causing the deduced protein products of both genes to differ in three amino acids in the signal-peptide region and in eight amino acids of the mature protein. Six nucleotide insertions and 27 substitutions were in the 663 bp of the 3'-flanking region. The gene product expressed and secreted in Saccharomyces cerevisiae into the functional enzyme was not homogeneous. In situ detection of the enzyme in a polyacrylamide gel revealed two dominant and three minor bands.
Subject(s)
Genes, Fungal , Glucan 1,4-alpha-Glucosidase/genetics , Saccharomycopsis/genetics , Amino Acid Sequence , Base Sequence , Cloning, Molecular/methods , DNA, Bacterial/genetics , Escherichia coli/genetics , Molecular Sequence Data , Plasmids , Protein Sorting Signals/genetics , Restriction Mapping , Saccharomycopsis/enzymologyABSTRACT
From soil samples collected in the jungles of Ninh Binh Province of the Vietnamese Democratic Republic, 97 isolates belonging to 54 species of Fungi imperfecti were obtained and screened for the production of antibiotics. The isolates were identified as belonging to the orders Melanconiales, Moniliales, Sphaeropsidales and Mycelia sterilia. In the species studied a very high incidence of antiprotozoal activities were observed.
