Affiliation:
1. National Research Institute of Brewing, 3-7-1 Kagamiyama, Higashihiroshima 739-0046, Japan
Abstract
ABSTRACT
Yeast
Saccharomyces cerevisiae
cells generally cannot synthesize biotin, a vitamin required for many carboxylation reactions. Although sake yeasts, which are used for Japanese sake brewing, are classified as
S. cerevisiae
, they do not require biotin for their growth. In this study, we identified a novel open reading frame (ORF) in the genome of one strain of sake yeast that we speculated to be involved in biotin synthesis. Homologs of this gene are widely distributed in the genomes of sake yeasts. However, they are not found in many laboratory strains and strains used for wine making and beer brewing. This ORF was named
BIO6
because it has 52% identity with
BIO3
, a biotin biosynthesis gene of a laboratory strain. Further research showed that yeasts without the
BIO6
gene are auxotrophic for biotin, whereas yeasts holding the
BIO6
gene are prototrophic for biotin. The
BIO6
gene was disrupted in strain A364A, which is a laboratory strain with one copy of the
BIO6
gene. Although strain A364A is prototrophic for biotin, a
BIO6
disrupted mutant was found to be auxotrophic for biotin. The
BIO6
disruptant was able to grow in biotin-deficient medium supplemented with 7-keto-8-amino-pelargonic acid (KAPA), while the
bio3
disruptant was not able to grow in this medium. These results suggest that Bio6p acts in an unknown step of biotin synthesis before KAPA synthesis. Furthermore, we demonstrated that expression of the
BIO6
gene, like that of other biotin synthesis genes, was upregulated by depletion of biotin. We conclude that the
BIO6
gene is a novel biotin biosynthesis gene of
S. cerevisiae
.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Reference39 articles.
1. Adams A. D. E. Gottschling C. Kaiser and T. Stearns. 1997. Methods in yeast genetics. Cold Spring Harbor Laboratory Press Cold Spring Harbor N.Y.
2. Baldet, P., and M. L. Ruffet. 1996. Biotin synthesis in higher plants: isolation of a cDNA encoding Arabidopsis thaliana bioB-gene product equivalent by functional complementation of a biotin auxotroph mutant bioB105 of Escherichia coli K12. C. R. Acad. Sci. Ser. III319:99-106.
3. Becker, D. M., and L. Guarente. 1991. High-efficiency transformation of yeast by electroporation. Methods Enzymol.194:182-187.
4. Betz, H., H. Hinze, and H. Holzer. 1974. Isolation and properties of two inhibitors of proteinase B from yeast. J. Biol. Chem.249:4515-4521.
5. Cloning, sequencing, and characterization of the Bacillus subtilis biotin biosynthetic operon
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