Affiliation:
1. National Research Institute of Brewing, 7-3-1, Kagamiyama, Higashihiroshima, Hiroshima 739-0046, Japan
Abstract
ABSTRACT
We cloned the genomic DNA and cDNA of
bglA
, which encodes β-glucosidase in
Aspergillus kawachii
, based on a partial amino acid sequence of purified cell wall-bound β-glucosidase CB-1. The nucleotide sequence of the cloned
bglA
gene revealed a 2,933-bp open reading frame with six introns that encodes an 860-amino-acid protein. Based on the deduced amino acid sequence, we concluded that the
bglA
gene encodes cell wall-bound β-glucosidase CB-1. The amino acid sequence exhibited high levels of homology with the amino acid sequences of fungal β-glucosidases classified in subfamily B. We expressed the
bglA
cDNA in
Saccharomyces cerevisiae
and detected the recombinant β-glucosidase in the periplasm fraction of the recombinant yeast.
A. kawachii
can produce two extracellular β-glucosidases (EX-1 and EX-2) in addition to the cell wall-bound β-glucosidase.
A. kawachii
in which the
bglA
gene was disrupted produced none of the three β-glucosidases, as determined by enzyme assays and a Western blot analysis. Thus, we concluded that the
bglA
gene encodes both extracellular and cell wall-bound β-glucosidases in
A. kawachii
.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
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