Goosen T, Bloemheuvel G, Gysler C, de Bie D A, van den Broek H W, Swart K
Department of Genetics, Agricultural University, Wageningen, The Netherlands.
Curr Genet. 1987;11(6-7):499-503. doi: 10.1007/BF00384612.
A homologous transformation system for the filamentous fungus Aspergillus niger has been developed, based on the orotidine-5'-phosphate-decarboxylase gene. A. niger Pyr- mutants have been selected from 5-fluoro-orotic acid resistant mutants. These mutants were found to comprise two complementation groups, pyrA and pyrB. The A. niger OMP-decarboxylase gene was isolated from a gene library by heterologous hybridization with the Neurospora crassa pyr4 gene. The cloned gene is capable to transform A. nidulans pyrG mutants at high frequencies. Transformation of A. niger pyrA mutants occurs with moderate frequencies (about 50 transformants/micrograms DNA) whereas the pyrB mutants cannot be complemented with the cloned OMP-decarboxylase gene. Analysis of the DNA of the A. niger PyrA+ transformants showed that transformation resulted in integration of the vector DNA into the genome by homologous recombination. Both gene replacements and integration of one or more copies of the complete vector have been observed.
基于乳清苷-5'-磷酸脱羧酶基因,已开发出一种用于丝状真菌黑曲霉的同源转化系统。从对5-氟乳清酸有抗性的突变体中筛选出了黑曲霉Pyr-突变体。发现这些突变体包含两个互补组,pyrA和pyrB。通过与粗糙脉孢菌pyr4基因进行异源杂交,从基因文库中分离出黑曲霉OMP脱羧酶基因。克隆的基因能够高频转化构巢曲霉pyrG突变体。黑曲霉pyrA突变体的转化频率适中(约50个转化体/微克DNA),而pyrB突变体不能被克隆的OMP脱羧酶基因互补。对黑曲霉PyrA+转化体的DNA分析表明,转化导致载体DNA通过同源重组整合到基因组中。已观察到基因替换以及完整载体一个或多个拷贝的整合。