Kato M, Iefuji H, Miyake K, Iimura Y
National Research Institute of Brewing, Higashi-Hiroshima, Japan.
Appl Microbiol Biotechnol. 1997 Nov;48(5):621-5. doi: 10.1007/s002530051105.
A transformation system for Hansenula fabianii J640, a commonly used wastewater treatment yeast, was constructed. As a host cell, a uracil auxotrophic mutant designated as H. fabianii J640 u-1, which was confirmed to have a mutation at the locus of the gene for orotidine-5'-phosphate (OMP) decarboxylase (URA3), was obtained by positive selection using 5-fluoroorotic acid. A plasmid named pHFura3, which includes a 795-bp open-reading frame of the OMP decarboxylase H. fabianii, was obtained by complementation of the Escherichia coli pyrF mutant, pHFura3 could transform H. fabianii J640 u-1 by a non-homologous and frequently multicopy integration into the host genomic DNA.
构建了用于常用废水处理酵母法比安毕赤酵母J640的转化系统。作为宿主细胞,通过使用5-氟乳清酸进行正向选择,获得了一个尿嘧啶营养缺陷型突变体,命名为法比安毕赤酵母J640 u-1,经证实该突变体在乳清酸核苷-5'-磷酸(OMP)脱羧酶(URA3)基因位点发生了突变。通过互补大肠杆菌pyrF突变体获得了一个名为pHFura3的质粒,该质粒包含法比安毕赤酵母OMP脱羧酶的795 bp开放阅读框,pHFura3可通过非同源且频繁的多拷贝整合到宿主基因组DNA中来转化法比安毕赤酵母J640 u-1。