Kolar M, Holzmann K, Weber G, Leitner E, Schwab H
Institut für Biotechnologie, Arbeitsgruppe Genetik, TU Graz, Austria.
J Biotechnol. 1991 Jan;17(1):67-80. doi: 10.1016/0168-1656(91)90027-s.
The isopenicillin N synthetase gene (pcbC) was isolated from a genomic library of Penicillium chrysogenum BC39813, a penicillin production strain. The nucleotide sequence, including 555 bp upstream of the translation start site was determined. Various deletions within the pcbC 5'-region were constructed and linked to the Escherichia coli lacZ gene. An Aspergillus nidulans argB strain was transformed with DNA of these constructions. The region essential for promoter function could be localized between positions -307 and -89 by analyzing beta-galactosidase expression of transformants containing a single copy of the corresponding plasmid integrated at the homologous argB locus. A region responsible for regulatory effects concerning nitrogen metabolism was identified by determining beta-galactosidase activities in cell-lysates of transformants cultivated under varying growth conditions. Two major transcription start sites at positions -131 and -132, as well as a further upstream located site at position -397 +/- 1 could be located by primer extension studies employing RNA isolated from P. chrysogenum BC39813.
异青霉素N合成酶基因(pcbC)是从产青霉素菌株产黄青霉BC39813的基因组文库中分离得到的。测定了包括翻译起始位点上游555 bp的核苷酸序列。构建了pcbC 5'-区域内的各种缺失片段,并将其与大肠杆菌lacZ基因连接。用这些构建体的DNA转化构巢曲霉argB菌株。通过分析在同源argB位点整合有单拷贝相应质粒的转化体的β-半乳糖苷酶表达,可将启动子功能所必需的区域定位在-307和-89位之间。通过测定在不同生长条件下培养的转化体细胞裂解物中的β-半乳糖苷酶活性,鉴定了一个与氮代谢调节作用有关的区域。利用从产黄青霉BC39813分离的RNA进行引物延伸研究,可确定位于-131和-132位的两个主要转录起始位点,以及位于-397 +/- 1位的另一个上游位点。