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Applied and Environmental Microbiology, March 1999, p. 1168-1174, Vol. 65, No. 3
Instituto de Biotecnología INBIOTEC,
Received 9 September 1998/Accepted 28 December 1998
Four expression cassettes containing strong fungal promoters, a
signal sequence for protein translocation, a KEX protease cleavage
site, and a synthetic gene (tha) encoding the sweet protein thaumatin II were used to overexpress this protein in Aspergillus awamori lpr66, a PepA protease-deficient strain. The best
expression results were obtained with the gdhA promoter of
A. awamori or with the gpdA promoter of
Aspergillus nidulans. There was good correlation of
tha gene dosage, transcript levels, and thaumatin secretion. The thaumatin gene was expressed as a transcript of the
expected size in each construction (1.9 or 1.4 kb), and the transcript
levels and thaumatin production rate decayed at the end of the growth
phase, except in the double transformant TB2b1-44-GD5, in which
secretion of thaumatin continued until 96 h. The recombinant thaumatin secreted by a high-production transformant was purified to
homogeneity, giving one major component and two minor components. In
all cases, cleavage of the fused protein occurred at the KEX recognition sequence. This work provides new expression systems in
A. awamori that result in very high levels of thaumatin production.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Thaumatin Production in Aspergillus
awamori by Use of Expression Cassettes with Strong Fungal
Promoters and High Gene Dosage
*
Corresponding author. Mailing address: Area de
Microbiología, Facultad de Biología, Universidad de
León, 24071 León, Spain. Phone: (34-987) 291505. Fax:
(34-987) 291506. E-mail: degjmm{at}unileon.es.
Applied and Environmental Microbiology, March 1999, p. 1168-1174, Vol. 65, No. 3
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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