The Pichia pastoris HIS4 gene: nucleotide sequence,creation of a non-reverting his4 deletion mutant,and development of HIS4-based replicating and integrating plasmids |
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Authors: | Denis I. Crane Stephen J. Gould |
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Affiliation: | (1) The Kennedy Krieger Research Institute, 707 North Broadway, 21205 Baltimore, MD, USA;(2) The Faculty of Science and Technology, Griffith University, Nathan, 4111 Brisbane, QLD, Australia;(3) The Department of Cell Biology and Anatomy, Johns Hopkins University School of Medicine, 21205 Baltimore, MD, USA |
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Abstract: | We have obtained a clone of the Pichia pastoris HIS4 gene and have determined its nucleotide sequence. Based upon its deduced amino-acid sequence, the product of the P. pastoris HIS4 gene has the same structural organization as the Saccharomyces cerevisiae His4 protein and appears to encode a trifunctional enzyme catalyzing the second (phosphoribosyl-ATP pyrophosphohydrolase), third (phosphoribosyl-AMP cyclohydrolase), and tenth (histidinol dehydrogenase) steps in histidine biosynthesis. The chromosomal copy of the HIS4 gene was disrupted by homologous recombination, creating the strain SGY58. The his4 deletion mutation in this strain lacks the entire coding region of this gene and has a reversion rate that is undetectable. A set of complementary plasmids that carry the HIS4 gene was also developed. Among these are nine E. coli-P. pastoris shuttle vectors that transform the His4 deletion mutant at high efficiency and an integration vector for creating site-specific alterations of the P. pastoris genome. |
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Keywords: | Histidinol dehydrogenase Phosphoribosyl-AMP cyclohydrolase Phosphoribosyl-ATP pyrophosphohydrolase Transformation system Selectable marker |
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