Eukaryotic Cell, August 2006, p. 1441-1445, Vol. 5, No. 8
1535-9778/06/$08.00+0 doi:10.1128/EC.00160-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, São Paulo, Brazil,1 Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, São Paulo, Brazil2
Received 12 April 2006/ Accepted 6 June 2006
Mutations in the human HPD gene (encoding 4-hydroxyphenylpyruvic acid dioxygenase) cause hereditary tyrosinemia type 3 (HT3). We deleted the Aspergillus nidulans homologue (hpdA). We showed that the mutant strain is not able to grow in the presence of phenylalanine and that it accumulates increased concentrations of tyrosine and 4-hydroxyphenylpyruvic acid, mimicking the human HT3 phenotype.
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