Gouka R J, van Hartingsveldt W, Bovenberg R A, van den Hondel C A, van Gorcom R F
TNO Medical Biological Laboratory, Rijswijk, The Netherlands.
J Biotechnol. 1991 Sep;20(2):189-99. doi: 10.1016/0168-1656(91)90227-m.
A new homologous transformation system for the filamentous fungus Penicillium chrysogenum is described. The system is based on complementation of niaD mutants using the nitrate reductase structural gene (niaD) of P. chrysogenum. Spontaneous niaD mutants were identified after selection for chlorate resistance, in growth tests and subsequent complementation with the niaD gene of Aspergillus oryzae. The P. chrysogenum niaD gene was isolated from a genomic library using the Aspergillus nidulans niaD gene as a probe. After subcloning of the hybridizing fragment, the vector obtained, pPC1-1, was capable of transforming a P. chrysogenum niaD mutant at an average of 40 transformants per micrograms of circular DNA. Southern analysis of genomic DNA from a number of transformants showed that pPC1-1 DNA was integrated predominantly at sites other than the niaD locus. Using hybridization analysis it was shown that the niaD gene of P. chrysogenum is clustered with the nitrite reductase gene (niiA). From analysis of the nucleotide sequences of parts of the niaD and niiA genes of P. chrysogenum and comparison of these sequences with nucleotide sequences of the corresponding A. nidulans genes it was deduced that the P. chrysogenum genes are divergently transcribed.
本文描述了一种用于产黄青霉的新型同源转化系统。该系统基于利用产黄青霉的硝酸还原酶结构基因(niaD)对niaD突变体进行互补。在氯酸盐抗性筛选、生长测试以及随后用米曲霉的niaD基因进行互补后,鉴定出自发的niaD突变体。以构巢曲霉的niaD基因为探针,从基因组文库中分离出产黄青霉的niaD基因。对杂交片段进行亚克隆后,得到的载体pPC1 - 1能够以每微克环状DNA平均40个转化体的频率转化产黄青霉的niaD突变体。对多个转化体的基因组DNA进行Southern分析表明,pPC1 - 1 DNA主要整合在niaD基因座以外的位点。通过杂交分析表明,产黄青霉的niaD基因与亚硝酸还原酶基因(niiA)成簇。通过对产黄青霉niaD和niiA基因部分核苷酸序列的分析,并将这些序列与相应的构巢曲霉基因的核苷酸序列进行比较,推断出产黄青霉的基因是反向转录的。