Gutiérrez S, Díez B, Alvarez E, Barredo J L, Martín J F
Department of Ecology, Faculty of Biology, University of León, Spain.
Mol Gen Genet. 1991 Jan;225(1):56-64. doi: 10.1007/BF00282642.
No DNA sequence homologous to the penDE gene of Penicillium chrysogenum was found in the genome of three different strains of Cephalosporium acremonium. The pcbC-penDE gene cluster of P. chrysogenum complemented the isopenicillin N synthase deficiency of C. acremonium mutant N2 and resulted in the production of penicillin, in addition to cephalosporin, in cultures supplemented with phenylacetic acid. The penicillin formed was identified as benzylpenicillin by HPLC and NMR studies. The penDE gene of P. chrysogenum is expressed in C. acremonium forming a transcript of 1.15 kb. The transcript is processed and translated in C. acremonium resulting in the formation of acyl CoA: isopenicillin N acyl transferase. When the penDE gene was introduced into a cephalosporin producing strain, the total titre of beta-lactam antibiotics comprised distinct proportions of penicillin and cephalosporin in different transformants. Analysis of the hybridization patterns of the DNA of C. acremonium transformed with the pcbC or penDE genes indicated that integration occurs by non-homologous recombination.
在三种不同的顶头孢霉菌株的基因组中,未发现与产黄青霉penDE基因同源的DNA序列。产黄青霉的pcbC - penDE基因簇弥补了顶头孢霉菌突变体N2的异青霉素N合酶缺陷,并且在添加苯乙酸的培养物中,除了头孢菌素外,还产生了青霉素。通过HPLC和NMR研究鉴定所形成的青霉素为苄青霉素。产黄青霉的penDE基因在顶头孢霉菌中表达,形成一个1.15 kb的转录本。该转录本在顶头孢霉菌中进行加工和翻译,从而形成酰基辅酶A:异青霉素N酰基转移酶。当将penDE基因导入头孢菌素生产菌株时,在不同的转化体中,β-内酰胺抗生素的总滴度包含不同比例的青霉素和头孢菌素。对用pcbC或penDE基因转化的顶头孢霉菌DNA的杂交模式分析表明,整合是通过非同源重组发生的。