Crane D I, Gould S J
Kennedy Krieger Research Institute, Baltimore, MD 21205.
Curr Genet. 1994 Nov-Dec;26(5-6):443-50. doi: 10.1007/BF00309932.
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 delta 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 delta deletion mutant at high efficiency and an integration vector for creating site-specific alterations of the P. pastoris genome.
我们已获得巴斯德毕赤酵母HIS4基因的一个克隆,并确定了其核苷酸序列。根据推导的氨基酸序列,巴斯德毕赤酵母HIS4基因的产物与酿酒酵母His4蛋白具有相同的结构组织,且似乎编码一种三功能酶,催化组氨酸生物合成中的第二步(磷酸核糖基-ATP焦磷酸水解酶)、第三步(磷酸核糖基-AMP环水解酶)和第十步(组氨醇脱氢酶)反应。通过同源重组破坏了HIS4基因的染色体拷贝,构建了菌株SGY58。该菌株中的his4δ缺失突变体缺少该基因的整个编码区,且回复率无法检测到。还构建了一组携带HIS4基因的互补质粒。其中包括九个能高效转化his4δ缺失突变体的大肠杆菌-巴斯德毕赤酵母穿梭载体,以及一个用于对巴斯德毕赤酵母基因组进行位点特异性改造的整合载体。